Homo sapiens chromosome 21, GRCh38 Primary Assembly.
Derived by automated computational analysis using gene prediction method: Gnomon.
sorting nexin 18 pseudogene 10; Derived by automated computational analysis using gene prediction method: Curated Genomic.
MT-CO1 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
asparagine synthetase pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ankyrin repeat domain 20 family, member A16, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
microRNA 3648; Derived by automated computational analysis using gene prediction method: BestRefSeq.
microRNA 3687; Derived by automated computational analysis using gene prediction method: BestRefSeq.
tektin 4 pseudogene 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ankyrin repeat domain 57 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
sorting nexin 18 pseudogene 11; Derived by automated computational analysis using gene prediction method: Curated Genomic.
sorting nexin 18 pseudogene 12; Derived by automated computational analysis using gene prediction method: Curated Genomic.
uncharacterized LOC441058; Derived by automated computational analysis using gene prediction method: BestRefSeq.
chromosome 2 open reading frame 27A pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
eukaryotic translation initiation factor 3, subunit F pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
vomeronasal 1 receptor 7 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
B melanoma antigen family, member 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transmembrane phosphatase with tensin homology; Derived by automated computational analysis using gene prediction method: BestRefSeq.
cytochrome c, somatic pseudogene 41; Derived by automated computational analysis using gene prediction method: Curated Genomic.
solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 pseudogene 4; Derived by automated computational analysis using gene prediction method: Curated Genomic.
immunoglobulin heavy variable 1/OR21-1 (non-functional); Derived by automated computational analysis using gene prediction method: Curated Genomic.
ankyrin repeat domain 30B pseudogene 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
vomeronasal 1 receptor 109 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
zinc finger protein 355, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
fibroblast growth factor 7 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ankyrin repeat domain 30B pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
microRNA 3156-3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
general transcription factor IIi, pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
vomeronasal 1 receptor 8 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
sorting nexin 19 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
olfactory receptor, family 4, subfamily K, member 11 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
olfactory receptor, family 4, subfamily K, member 12 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
A26B3; ANKRD21; CT104.1; POTE; POTE-21; POTE21
POTE ankyrin domain family, member D; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
microRNA 3118-5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
GRAM domain containing 4 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
coxsackie virus and adenovirus receptor pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
microRNA mir-8069; Derived by automated computational analysis using gene prediction method: BestRefSeq.
fem-1 homolog a (C. elegans) pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
telomeric repeat binding factor (NIMA-interacting) 1 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
family with sequence similarity 207, member C; Derived by automated computational analysis using gene prediction method: Curated Genomic.
brain cytoplasmic RNA 1 (non-protein coding) pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
glucoside xylosyltransferase 1 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
calponin 2 pseudogene 7; Derived by automated computational analysis using gene prediction method: Curated Genomic.
zinc finger protein 114 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
chromosome 21 open reading frame 15; Derived by automated computational analysis using gene prediction method: BestRefSeq.
cytochrome P450, family 4, subfamily F, polypeptide 29, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
sorting nexin 18 pseudogene 13; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ras homolog family member T1 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ankyrin repeat domain 20 family, member A11, pseudogene; Derived by automated computational analysis using gene prediction method: BestRefSeq.
neurofibromin 1 pseudogene 3; Derived by automated computational analysis using gene prediction method: Curated Genomic.
protein phosphatase 6, regulatory subunit 2 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ankyrin repeat domain 20 family, member A18, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
RNA, 5S ribosomal pseudogene 488; Derived by automated computational analysis using gene prediction method: Curated Genomic.
endoplasmic reticulum lectin 1 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
lipase, member I; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
RNA binding motif protein 11; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
ATP-binding cassette, sub-family C (CFTR/MRP), member 13, pseudogene; Derived by automated computational analysis using gene prediction method: BestRefSeq.
heat shock protein 70kDa family, member 13; Derived by automated computational analysis using gene prediction method: BestRefSeq.
SAM domain, SH3 domain and nuclear localization signals 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
SAMSN1 antisense RNA 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
uncharacterized protein ENSP00000383407-like; Derived by automated computational analysis using gene prediction method: BestRefSeq.
polymerase (RNA) II (DNA directed) polypeptide C, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
glyceraldehyde-3-phosphate dehydrogenase pseudogene 16; Derived by automated computational analysis using gene prediction method: Curated Genomic.
RNA binding motif protein, X-linked 2 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
nuclear receptor interacting protein 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
cytochrome c, somatic pseudogene 42; Derived by automated computational analysis using gene prediction method: Curated Genomic.
RAD23 homolog B-like (S. cerevisiae) pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ubiquitin specific peptidase 25; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
RNA binding protein with multiple splicing-like pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
long intergenic non-protein coding RNA 478; Derived by automated computational analysis using gene prediction method: BestRefSeq.
voltage-dependent anion channel 2 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ribosomal protein S26 pseudogene 5; Derived by automated computational analysis using gene prediction method: Curated Genomic.
microRNA 99a; Derived by automated computational analysis using gene prediction method: BestRefSeq.
microRNA let-7c; Derived by automated computational analysis using gene prediction method: BestRefSeq.
microRNA 125b-2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
NIMA-related kinase 4 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
chromosome 21 open reading frame 37; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ribosomal protein L39 pseudogene 40; Derived by automated computational analysis using gene prediction method: Curated Genomic.
coxsackie virus and adenovirus receptor; Derived by automated computational analysis using gene prediction method: BestRefSeq.
basic transcription factor 3-like 4 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
BTG family, member 3; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
C21orf91 overlapping transcript 1 (non-protein coding); Derived by automated computational analysis using gene prediction method: BestRefSeq.
chromosome 21 open reading frame 91; Derived by automated computational analysis using gene prediction method: BestRefSeq.
CHODL antisense RNA 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ribosomal protein L37 pseudogene 3; Derived by automated computational analysis using gene prediction method: Curated Genomic.
chondrolectin; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transmembrane protease, serine 15; Derived by automated computational analysis using gene prediction method: BestRefSeq.
uncharacterized LOC101927797; Derived by automated computational analysis using gene prediction method: BestRefSeq.
microRNA 548x; Derived by automated computational analysis using gene prediction method: BestRefSeq.
peptidylprolyl isomerase A (cyclophilin A) pseudogene 22; Derived by automated computational analysis using gene prediction method: Curated Genomic.
solute carrier family 6, member 6 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ribosomal protein L37 pseudogene 4; Derived by automated computational analysis using gene prediction method: Curated Genomic.
non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 3; Derived by automated computational analysis using gene prediction method: Curated Genomic.
SREK1-interacting protein 1 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
complement component 1, q subcomponent binding protein, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
farnesyl diphosphate synthase pseudogene 6; Derived by automated computational analysis using gene prediction method: Curated Genomic.
keratin 18 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ribosomal protein S3A pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
long intergenic non-protein coding RNA 320; Derived by automated computational analysis using gene prediction method: BestRefSeq.
peptidylprolyl isomerase A (cyclophilin A), pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
neural cell adhesion molecule 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
long intergenic non-protein coding RNA 317; Derived by automated computational analysis using gene prediction method: BestRefSeq.
uncharacterized LOC101927821; Derived by automated computational analysis using gene prediction method: BestRefSeq.
uncharacterized LOC101927843; Derived by automated computational analysis using gene prediction method: BestRefSeq.
long intergenic non-protein coding RNA 308; Derived by automated computational analysis using gene prediction method: BestRefSeq.
phosphoglycerate kinase 1 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
mitogen-activated protein kinase 6 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
microRNA mir-6130; Derived by automated computational analysis using gene prediction method: BestRefSeq.
zinc finger protein 299, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
Myb/SANT-like DNA-binding domain containing 2 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
D21S2088E; Derived by automated computational analysis using gene prediction method: BestRefSeq.
eukaryotic translation elongation factor 1 alpha 1 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
tubulin, alpha pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
vomeronasal 2 receptor 20 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
uncharacterized LOC101927869; Derived by automated computational analysis using gene prediction method: BestRefSeq.
uncharacterized LOC339622; Derived by automated computational analysis using gene prediction method: BestRefSeq.
CTAGE family, member 5 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
RNA, 5S ribosomal pseudogene 489; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ribosomal protein L13a pseudogene 7; Derived by automated computational analysis using gene prediction method: Curated Genomic.
long intergenic non-protein coding RNA 158; Derived by automated computational analysis using gene prediction method: BestRefSeq.
MIR155 host gene (non-protein coding); Derived by automated computational analysis using gene prediction method: BestRefSeq.
microRNA 155; Derived by automated computational analysis using gene prediction method: BestRefSeq.
long intergenic non-protein coding RNA 515; Derived by automated computational analysis using gene prediction method: BestRefSeq.
C21orf92; L39mt; MRP-L5; MRPL5; MSTP003; PRED22; PRED66; RPML5
mitochondrial ribosomal protein L39; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
C21orf43; CD322; JAM-B; JAMB; PRO245; VE-JAM; VEJAM
junctional adhesion molecule 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
RNA guanylyltransferase and 5'-phosphatase pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ferredoxin 1 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
E4TF1-60; E4TF1A; NFT2; NRF2; NRF2A; RCH04A07
GA binding protein transcription factor, alpha subunit 60kDa; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
AAA; ABETA; ABPP; AD1; APPI; CTFgamma; CVAP; PN-II; PN2
amyloid beta (A4) precursor protein; Derived by automated computational analysis using gene prediction method: BestRefSeq.
myristoylated alanine-rich protein kinase C substrate pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
cysteine/tyrosine-rich 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
ADAM metallopeptidase with thrombospondin type 1 motif, 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ADAM-TS 11; ADAM-TS 5; ADAM-TS5; ADAMTS-11; ADAMTS-5; ADAMTS11; ADMP-2
ADAM metallopeptidase with thrombospondin type 1 motif, 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
microRNA 4759; Derived by automated computational analysis using gene prediction method: BestRefSeq.
glutathione peroxidase pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
eukaryotic translation initiation factor 4A1 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ribosomal protein L10 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
nicastrin pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
long intergenic non-protein coding RNA 113; Derived by automated computational analysis using gene prediction method: BestRefSeq.
long intergenic non-protein coding RNA 314; Derived by automated computational analysis using gene prediction method: BestRefSeq.
long intergenic non-protein coding RNA 161; Derived by automated computational analysis using gene prediction method: BestRefSeq.
N-6 adenine-specific DNA methyltransferase 1 (putative); Derived by automated computational analysis using gene prediction method: BestRefSeq.
heat shock 60kDa protein 1 (chaperonin) pseudogene 7; Derived by automated computational analysis using gene prediction method: Curated Genomic.
THUMP domain containing 1 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
listerin E3 ubiquitin protein ligase 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
ribosomal protein L23 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
RWD domain containing 2B; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
ubiquitin specific peptidase 16; Derived by automated computational analysis using gene prediction method: BestRefSeq.
chaperonin containing TCP1, subunit 8 (theta); Derived by automated computational analysis using gene prediction method: BestRefSeq.
C21orf7; HC21ORF7; TAK1L; TAKL; TAKL-1; TAKL-2; TAKL-4
MAP3K7 C-terminal like; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
ribosomal protein L12 pseudogene 9; Derived by automated computational analysis using gene prediction method: Curated Genomic.
long intergenic non-protein coding RNA 189; Derived by automated computational analysis using gene prediction method: BestRefSeq.
glyceraldehyde-3-phosphate dehydrogenase pseudogene 14; Derived by automated computational analysis using gene prediction method: Curated Genomic.
BTB and CNC homology 1, basic leucine zipper transcription factor 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
glutamate receptor, ionotropic, kainate 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
GRIK1 antisense RNA 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
GRIK1 antisense RNA 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
claudin 17; Derived by automated computational analysis using gene prediction method: BestRefSeq.
long intergenic non-protein coding RNA 307; Derived by automated computational analysis using gene prediction method: BestRefSeq.
claudin 8; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ribosomal protein L8 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
keratin associated protein 24-1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 25-1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 26-1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 27-1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 23-1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 13-6, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
keratin associated protein 13-2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
microRNA 4327; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 13-1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 13-3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 13-4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 13-5, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
keratin associated protein 15-1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 19-1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 19-2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 19-3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 19-4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 19-5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 19-9, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
keratin associated protein 19-10, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
keratin associated protein 19-11, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
keratin associated protein 19-6; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 19-7; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 22-2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 6-3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 6-2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 22-1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 6-1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 20-1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 20-4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 20-2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 20-3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 21-3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 21-4, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
keratin associated protein 21-2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 21-1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 8-2, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
keratin associated protein 8-3, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
keratin associated protein 8-1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 7-1 (gene/pseudogene); Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 11-1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 19-8; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ubiquitin protein ligase E3A pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
T-cell lymphoma invasion and metastasis 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
chromosome 6 open reading frame 203 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
F-box and WD repeat domain containing 11 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ALS; ALS1; HEL-S-44; homodimer; hSod1; IPOA; SOD
superoxide dismutase 1, soluble; Derived by automated computational analysis using gene prediction method: BestRefSeq.
SR-related CTD-associated factor 4; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
high mobility group nucleosome binding domain 1 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
tumor protein, translationally-controlled 1 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
hormonally up-regulated Neu-associated kinase; Derived by automated computational analysis using gene prediction method: BestRefSeq.
long intergenic non-protein coding RNA 159; Derived by automated computational analysis using gene prediction method: BestRefSeq.
B28; C21orf45; C21orf46; FASP1; hMis18alpha; MIS18alpha
MIS18 kinetochore protein A; Derived by automated computational analysis using gene prediction method: BestRefSeq.
melanocortin 2 receptor accessory protein; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
URB1 ribosome biogenesis 1 homolog (S. cerevisiae); Derived by automated computational analysis using gene prediction method: BestRefSeq.
small nucleolar RNA, H/ACA box 80; Derived by automated computational analysis using gene prediction method: BestRefSeq.
chromosome 21 open reading frame 119; Derived by automated computational analysis using gene prediction method: BestRefSeq.
eva-1 homolog C (C. elegans); Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
exosome component 3 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
RNA, 5S ribosomal pseudogene 490; Derived by automated computational analysis using gene prediction method: Curated Genomic.
t-complex 10-like; Derived by automated computational analysis using gene prediction method: BestRefSeq.
chromosome 21 open reading frame 59; Derived by automated computational analysis using gene prediction method: BestRefSeq.
olfactory receptor, family 7, subfamily E, member 23 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
synaptojanin 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
PAXBP1 antisense RNA 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
PAX3 and PAX7 binding protein 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
chromosome 21 open reading frame 49; Derived by automated computational analysis using gene prediction method: BestRefSeq.
chromosome 21 open reading frame 62; Derived by automated computational analysis using gene prediction method: BestRefSeq.
BHLHB1; bHLHe19; OLIGO2; PRKCBP2; RACK17
oligodendrocyte lineage transcription factor 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
long intergenic non-protein coding RNA 945; Derived by automated computational analysis using gene prediction method: BestRefSeq.
oligodendrocyte transcription factor 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
uncharacterized LOC101928107; Derived by automated computational analysis using gene prediction method: BestRefSeq.
chromosome 21 open reading frame 54; Derived by automated computational analysis using gene prediction method: BestRefSeq.
interferon (alpha, beta and omega) receptor 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
IL10RB antisense RNA 1 (head to head); Derived by automated computational analysis using gene prediction method: BestRefSeq.
interleukin 10 receptor, beta; Derived by automated computational analysis using gene prediction method: BestRefSeq.
interferon (alpha, beta and omega) receptor 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
upstream transcription factor 1 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
interferon gamma receptor 2 (interferon gamma transducer 1); Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
transmembrane protein 50B; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ribosomal protein S5 pseudogene 3; Derived by automated computational analysis using gene prediction method: Curated Genomic.
DnaJ (Hsp40) homolog, subfamily C, member 28; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
basic transcription factor 3 pseudogene 6; Derived by automated computational analysis using gene prediction method: Curated Genomic.
SON DNA binding protein; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
microRNA mir-6501; Derived by automated computational analysis using gene prediction method: BestRefSeq.
downstream neighbor of SON; Derived by automated computational analysis using gene prediction method: BestRefSeq.
crystallin, zeta (quinone reductase)-like 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
intersectin 1 (SH3 domain protein); Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
ATP synthase, H+ transporting, mitochondrial F1 complex, O subunit; Derived by automated computational analysis using gene prediction method: BestRefSeq.
long intergenic non-protein coding RNA 649; Derived by automated computational analysis using gene prediction method: BestRefSeq.
uncharactered LOC400863; Derived by automated computational analysis using gene prediction method: BestRefSeq.
mitochondrial ribosomal protein S6; Derived by automated computational analysis using gene prediction method: BestRefSeq.
solute carrier family 5 (sodium/myo-inositol cotransporter), member 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ribosomal protein S5 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
long intergenic non-protein coding RNA 310; Derived by automated computational analysis using gene prediction method: BestRefSeq.
potassium voltage-gated channel, Isk-related family, member 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
small integral membrane protein 11; Derived by automated computational analysis using gene prediction method: BestRefSeq.
chromosome 21 open reading frame 140; Derived by automated computational analysis using gene prediction method: BestRefSeq.
potassium voltage-gated channel, Isk-related family, member 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
regulator of calcineurin 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
chloride intracellular channel 6; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
long intergenic non-protein coding RNA 160; Derived by automated computational analysis using gene prediction method: BestRefSeq.
uncharacterized LOC100506385; Derived by automated computational analysis using gene prediction method: BestRefSeq.
AML1; AML1-EVI-1; AMLCR1; CBFA2; EVI-1; PEBP2aB
runt-related transcription factor 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
RUNX1 intronic transcript 1 (non-protein coding); Derived by automated computational analysis using gene prediction method: BestRefSeq.
uncharacterized LOC100506403; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ribosomal protein L34 pseudogene 3; Derived by automated computational analysis using gene prediction method: Curated Genomic.
enhancer of zeste homolog 2 (Drosophila) pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
microRNA 802; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ribosomal protein S20 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
protein phosphatase 1, regulatory (inhibitor) subunit 2 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
MT-ND2 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ribosomal protein L23a pseudogene 3; Derived by automated computational analysis using gene prediction method: Curated Genomic.
SET domain containing 4; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
ribosomal modification protein rimK-like family member B pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
uncharacterized LOC100133286; Derived by automated computational analysis using gene prediction method: BestRefSeq.
carbonyl reductase 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
mediator of cell motility 1 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
CBR3 antisense RNA 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ribosomal protein S9 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
carbonyl reductase 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
dopey family member 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
ribosomal protein L3 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
serine/arginine-rich splicing factor 9 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ribosomal protein S26 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
MORC family CW-type zinc finger 3; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
CAF-1; CAF-IP60; CAF1; CAF1A; CAF1P60; MPHOSPH7; MPP7
chromatin assembly factor 1, subunit B (p60); Derived by automated computational analysis using gene prediction method: BestRefSeq.
ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2-like pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
claudin 14; Derived by automated computational analysis using gene prediction method: BestRefSeq.
proteasome (prosome, macropain) 26S subunit, non-ATPase, 4 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
single-minded family bHLH transcription factor 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase); Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
RNA, 5S ribosomal pseudogene 491; Derived by automated computational analysis using gene prediction method: Curated Genomic.
divergent-paired related homeobox pseudogene 5; Derived by automated computational analysis using gene prediction method: Curated Genomic.
mitochondrial ribosomal protein L20 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ripply transcriptional repressor 3; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
phosphatidylinositol glycan anchor biosynthesis, class P; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
tetratricopeptide repeat domain 3; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
Down syndrome critical region gene 9 (non-protein coding); Derived by automated computational analysis using gene prediction method: BestRefSeq.
Down syndrome critical region gene 3; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
BIR1; GIRK-2; GIRK2; hiGIRK2; KATP-2; KATP2; KCNJ7; KIR3.2
potassium inwardly-rectifying channel, subfamily J, member 6; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Down syndrome critical region gene 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
C21orf65; CT25.1a; CT25.1b; MMA-1; MMA-1a; MMA-1b; MMA1; MTAG2
Down syndrome critical region gene 8; Derived by automated computational analysis using gene prediction method: BestRefSeq.
cutaneous T-cell lymphoma-associated antigen 1 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
Down syndrome critical region gene 10 (non-protein coding); Derived by automated computational analysis using gene prediction method: BestRefSeq.
potassium inwardly-rectifying channel, subfamily J, member 15; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
spermatogenesis associated 20 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
v-ets avian erythroblastosis virus E26 oncogene homolog; Derived by automated computational analysis using gene prediction method: BestRefSeq.
small nuclear ribonucleoprotein polypeptide G pseudogene 13; Derived by automated computational analysis using gene prediction method: Curated Genomic.
long intergenic non-protein coding RNA 114; Derived by automated computational analysis using gene prediction method: BestRefSeq.
v-ets avian erythroblastosis virus E26 oncogene homolog 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
uncharacterized LOC101928398; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ribosomal protein SA pseudogene 64; Derived by automated computational analysis using gene prediction method: Curated Genomic.
uncharacterized LOC101928435; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ribosomal protein L23a pseudogene 12; Derived by automated computational analysis using gene prediction method: Curated Genomic.
poly(rC) binding protein 2 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
proteasome (prosome, macropain) assembly chaperone 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
bromodomain and WD repeat domain containing 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
translocase of inner mitochondrial membrane 9 homolog (yeast) pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
methyltransferase like 21A pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
BRWD1 intronic transcript 2 (non-protein coding); Derived by automated computational analysis using gene prediction method: BestRefSeq.
BRWD1 antisense RNA 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
high mobility group nucleosome binding domain 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ring finger protein (C3H2C3 type) 6 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
tryptophan rich basic protein; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
Leber congenital amaurosis 5-like; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
SH3 domain binding glutamic acid-rich protein; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
microRNA mir-6508; Derived by automated computational analysis using gene prediction method: BestRefSeq.
myosin, light chain 6 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ribosomal protein S26 pseudogene 4; Derived by automated computational analysis using gene prediction method: Curated Genomic.
KIAA1462 pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
3-GalTase 5; B3GalT-V; B3GalTx; B3T5; beta-1; beta-3-Gx-T5; beta3Gal-T5; GLCT5
UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 5; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
chromosome 21 open reading frame 88; Derived by automated computational analysis using gene prediction method: BestRefSeq.
immunoglobulin superfamily, member 5; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
Purkinje cell protein 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Down syndrome cell adhesion molecule; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
microRNA 4760; Derived by automated computational analysis using gene prediction method: BestRefSeq.
DSCAM antisense RNA 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
DSCAM intronic transcript 1 (non-protein coding); Derived by automated computational analysis using gene prediction method: BestRefSeq.
yrdC N(6)-threonylcarbamoyltransferase domain containing pseudogene 3; Derived by automated computational analysis using gene prediction method: Curated Genomic.
long intergenic non-protein coding RNA 323; Derived by automated computational analysis using gene prediction method: BestRefSeq.
microRNA 3197; Derived by automated computational analysis using gene prediction method: BestRefSeq.
AEPLC; ALP56; ASP1; ASP21; BAE2; CDA13; CEAP1; DRAP
beta-site APP-cleaving enzyme 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
placenta-specific 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
2-21; C21orf11; C21orf76; ORF9; PANDER; PRED44
family with sequence similarity 3, member B; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
myxovirus (influenza virus) resistance 2 (mouse); Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse); Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
transmembrane protease, serine 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
long intergenic non-protein coding RNA 111; Derived by automated computational analysis using gene prediction method: BestRefSeq.
long intergenic non-protein coding RNA 479; Derived by automated computational analysis using gene prediction method: BestRefSeq.
long intergenic non-protein coding RNA 112; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ANKK2; ANKRD3; DIK; NKRD3; PKK; PPS2; RIP4
receptor-interacting serine-threonine kinase 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
microRNA mir-6814; Derived by automated computational analysis using gene prediction method: BestRefSeq.
PR domain containing 15; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
C2 calcium-dependent domain containing 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
zinc finger and BTB domain containing 21; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
ZNF295 antisense RNA 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
uromodulin-like 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
chromosome 21 open reading frame 128; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ATP-binding cassette, sub-family G (WHITE), member 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
RNA, 5S ribosomal pseudogene 492; Derived by automated computational analysis using gene prediction method: Curated Genomic.
trefoil factor 3 (intestinal); Derived by automated computational analysis using gene prediction method: BestRefSeq.
trefoil factor 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
trefoil factor 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transmembrane protease, serine 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ubiquitin associated and SH3 domain containing A; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
radial spoke head 1 homolog (Chlamydomonas); Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
solute carrier family 37 (glucose-6-phosphate transporter), member 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
phosphodiesterase 9A; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
WD repeat domain 4; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
NADH dehydrogenase (ubiquinone) flavoprotein 3, 10kDa; Derived by automated computational analysis using gene prediction method: BestRefSeq.
microRNA 5692b; Derived by automated computational analysis using gene prediction method: BestRefSeq.
PBX/knotted 1 homeobox 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
cystathionine-beta-synthase; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
U2 small nuclear RNA auxiliary factor 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
mitochondrial ribosomal protein L51 pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
crystallin, alpha A; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
long intergenic non-protein coding RNA 322; Derived by automated computational analysis using gene prediction method: BestRefSeq.
salt-inducible kinase 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
long intergenic non-protein coding RNA 319; Derived by automated computational analysis using gene prediction method: BestRefSeq.
long intergenic non-protein coding RNA 313; Derived by automated computational analysis using gene prediction method: BestRefSeq.
heat shock transcription factor 2 binding protein; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
ribosomal protein L31 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
H2B histone family, member S (pseudogene); Derived by automated computational analysis using gene prediction method: Curated Genomic.
microRNA mir-6070; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ribosomal RNA processing 1B; Derived by automated computational analysis using gene prediction method: BestRefSeq.
C21orf124; C21orf97; HEL-S-1a; PKH; PNK; PRED79
pyridoxal (pyridoxine, vitamin B6) kinase; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
cystatin B (stefin B); Derived by automated computational analysis using gene prediction method: BestRefSeq.
transmembrane protein 97 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ribosomal RNA processing 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
uncharacterized LOC284837; Derived by automated computational analysis using gene prediction method: BestRefSeq.
myosin, light chain 6 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
1-acylglycerol-3-phosphate O-acyltransferase 3; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
EHOC-1; EHOC1; GT334; TMEM1; TRS130; TRS30
trafficking protein particle complex 10; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
H2A histone family, member Z pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
PWP2 periodic tryptophan protein homolog (yeast); Derived by automated computational analysis using gene prediction method: BestRefSeq.
chromosome 21 open reading frame 33; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
B7-H2; B7H2; B7RP-1; B7RP1; CD275; GL50; ICOS-L; ICOSL; LICOS
inducible T-cell co-stimulator ligand; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
DNA (cytosine-5-)-methyltransferase 3-like; Derived by automated computational analysis using gene prediction method: BestRefSeq.
autoimmune regulator; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
phosphofructokinase, liver; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
chromosome 21 open reading frame 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
EREG1; KNP3; LTRPC2; NUDT9H; NUDT9L1; TRPC7
transient receptor potential cation channel, subfamily M, member 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
transient receptor potential cation channel, subfamily M, member 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
LRRC3 antisense RNA 1 (head to head); Derived by automated computational analysis using gene prediction method: BestRefSeq.
leucine rich repeat containing 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
MT-ND6 pseudogene 21; Derived by automated computational analysis using gene prediction method: Curated Genomic.
MT-ND5 pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
thrombospondin-type laminin G domain and EAR repeats; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
TSPEAR antisense RNA 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
chromosome 21 open reading frame 90; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 10-1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 10-2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 10-3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 10-4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 10-5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 10-6; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 10-7; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 10-8; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 10-9; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 10-10; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 10-11; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 12-4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 12-3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 12-2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
inner membrane protein, mitochondrial (mitofilin) pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
keratin associated protein 12-1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 10-12; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin associated protein 10-13, pseudogene; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ubiquitin-conjugating enzyme E2G 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
uncharacterized LOC101928689; Derived by automated computational analysis using gene prediction method: BestRefSeq.
small ubiquitin-like modifier 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
pituitary tumor-transforming 1 interacting protein; Derived by automated computational analysis using gene prediction method: BestRefSeq.
CD18; LAD; LCAMB; LFA-1; MAC-1; MF17; MFI7
integrin, beta 2 (complement component 3 receptor 3 and 4 subunit); Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
ITGB2 antisense RNA 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
chromosome 21 open reading frame 67; Derived by automated computational analysis using gene prediction method: BestRefSeq.
family with sequence similarity 207, member A; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
long intergenic non-protein coding RNA 163; Derived by automated computational analysis using gene prediction method: BestRefSeq.
C21orf113; NCRNA00162; NLC1-C; NLC1C; PRED74
long intergenic non-protein coding RNA 162; Derived by automated computational analysis using gene prediction method: BestRefSeq.
signal sequence receptor, delta pseudogene 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
adenosine deaminase, RNA-specific, B1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
protein O-fucosyltransferase 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
uncharacterized LOC642852; Derived by automated computational analysis using gene prediction method: BestRefSeq.
long intergenic non-protein coding RNA 316; Derived by automated computational analysis using gene prediction method: BestRefSeq.
MT-CO1 pseudogene 3; Derived by automated computational analysis using gene prediction method: Curated Genomic.
collagen, type XVIII, alpha 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
COL18A1 antisense RNA 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
COL18A1 antisense RNA 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
microRNA mir-6815; Derived by automated computational analysis using gene prediction method: BestRefSeq.
solute carrier family 19 (folate transporter), member 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
uncharacterized LOC100129027; Derived by automated computational analysis using gene prediction method: BestRefSeq.
poly(rC) binding protein 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
uncharacterized LOC101928796; Derived by automated computational analysis using gene prediction method: BestRefSeq.
collagen, type VI, alpha 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
proteasome (prosome, macropain) subunit, alpha type, 6 pseudogene 3; Derived by automated computational analysis using gene prediction method: Curated Genomic.
collagen, type VI, alpha 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
formimidoyltransferase cyclodeaminase; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
spermatogenesis and centriole associated 1-like; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
lanosterol synthase (2,3-oxidosqualene-lanosterol cyclase); Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
C21orf85; MCM3AP-AS; MCM3APAS; MCM3APASB; NCRNA00031
MCM3AP antisense RNA 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
minichromosome maintenance complex component 3 associated protein; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
ybeY metallopeptidase (putative); Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
chromosome 21 open reading frame 58; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
KEN; MOPD2; PCN; PCNT2; PCNTB; PCTN2; SCKL4
pericentrin; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
ribosomal protein L18a pseudogene 2; Derived by automated computational analysis using gene prediction method: Curated Genomic.
DIP2 disco-interacting protein 2 homolog A (Drosophila); Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
DIP2A intronic transcript 1 (non-protein coding); Derived by automated computational analysis using gene prediction method: BestRefSeq.
S100 calcium binding protein B; Derived by automated computational analysis using gene prediction method: BestRefSeq.
protein arginine methyltransferase 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
destrin (actin depolymerizing factor) pseudogene 1; Derived by automated computational analysis using gene prediction method: Curated Genomic.
ribosomal protein L23a pseudogene 4; Derived by automated computational analysis using gene prediction method: Curated Genomic.
Linear centromere model derived predominantly from reads generated in PMID: 17803354. This region does not represent an actual centromere sequence, as long-range ordering of repeats and unmapped WGS contigs is not provided by the model. For details of model production, see http://arxiv.org/abs/1307.0035.
DNA (cytosine-5)-methyltransferase 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 97 ESTs, 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 97 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ES1 protein homolog, mitochondrial-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ES1 protein homolog, mitochondrial-like isoform X5
uncharacterized LOC102724132, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC102724132, transcript variant X1
uncharacterized protein LOC102724132 isoform X2
uncharacterized protein LOC102724132 isoform X1
ES1 protein homolog, mitochondrial-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ES1 protein homolog, mitochondrial-like isoform X7
ES1 protein homolog, mitochondrial-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ES1 protein homolog, mitochondrial-like isoform X6
uncharacterized LOC101928576, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC101928576, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ES1 protein homolog, mitochondrial-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
ES1 protein homolog, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 174 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
ES1 protein homolog, mitochondrial-like isoform X3
ES1 protein homolog, mitochondrial-like isoform X1
ES1 protein homolog, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
ES1 protein homolog, mitochondrial-like isoform X2
ES1 protein homolog, mitochondrial-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ES1 protein homolog, mitochondrial-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 187 ESTs, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
trafficking protein particle complex subunit 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 ESTs, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC102724219, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 ESTs, 1 Protein, and 87% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC102724219, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 ESTs, 1 Protein, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC102724219, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 ESTs, 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC102724219, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 ESTs, 1 Protein, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC102724219, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 ESTs, 1 Protein, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC102724219 isoform X2
uncharacterized protein LOC102724219 isoform X1
uncharacterized protein LOC102724219 isoform X3
uncharacterized protein LOC102724219 isoform X4
uncharacterized protein LOC102724219 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 11 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 64 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
putative uncharacterized protein C21orf125-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine/threonine-protein kinase SIK1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 140 ESTs, 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC102724441, transcript variant X1
uncharacterized LOC102724441, transcript variant X3
uncharacterized LOC102724441, transcript variant X4
uncharacterized LOC102724441, transcript variant X5
uncharacterized LOC102724441, transcript variant X2
uncharacterized protein LOC102724441 isoform X2
uncharacterized protein LOC102724441 isoform X1
uncharacterized protein LOC102724441 isoform X3
uncharacterized protein LOC102724441 isoform X4
uncharacterized protein LOC102724441 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 136 ESTs, 8 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
splicing factor U2AF 35 kDa subunit-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 139 ESTs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
splicing factor U2AF 35 kDa subunit-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 94 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
splicing factor U2AF 35 kDa subunit-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 75 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
splicing factor U2AF 35 kDa subunit-like isoform X2
splicing factor U2AF 35 kDa subunit-like isoform X1
splicing factor U2AF 35 kDa subunit-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
alpha-crystallin A chain-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 277 ESTs, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
alpha-crystallin A chain-like isoform X1
alpha-crystallin A chain-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 198 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
alpha-crystallin A chain-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC102724843, transcript variant X1
uncharacterized LOC102724843, transcript variant X4
uncharacterized LOC102724843, transcript variant X3
uncharacterized LOC102724843, transcript variant X5
uncharacterized LOC102724843, transcript variant X2
uncharacterized protein LOC102724843 isoform X2
uncharacterized protein LOC102724843 isoform X1
uncharacterized protein LOC102724843 isoform X3
uncharacterized protein LOC102724843 isoform X4
uncharacterized protein LOC102724843 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC102724951, transcript variant X1
uncharacterized LOC102724951, transcript variant X4
uncharacterized LOC102724951, transcript variant X3
uncharacterized LOC102724951, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 40 ESTs, 1 Protein, and 78% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC102724951, transcript variant X2
uncharacterized protein LOC102724951 isoform X2
uncharacterized protein LOC102724951 isoform X1
uncharacterized protein LOC102724951 isoform X3
uncharacterized protein LOC102724951 isoform X4
uncharacterized protein LOC102724951 isoform X5
uncharacterized LOC102723360, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 ESTs, 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC102723360, transcript variant X1
uncharacterized LOC102723360, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 ESTs, 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC102723360 isoform X2
uncharacterized protein LOC102723360 isoform X1
uncharacterized protein LOC102723360 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 12 ESTs, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein ENSP00000386791-like
potassium voltage-gated channel subfamily E member 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium voltage-gated channel subfamily E member 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
potassium voltage-gated channel subfamily E member 1-like isoform X2
potassium voltage-gated channel subfamily E member 1-like isoform X3
potassium voltage-gated channel subfamily E member 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 11 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium voltage-gated channel subfamily E member 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium voltage-gated channel subfamily E member 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
potassium voltage-gated channel subfamily E member 1-like isoform X1
potassium voltage-gated channel subfamily E member 1-like isoform X4
potassium voltage-gated channel subfamily E member 1-like isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 ESTs, 7 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 ESTs, 7 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: BestRefSeq.
tektin 4 pseudogene 2, transcript variant 2
tektin 4 pseudogene 2, transcript variant 1
tektin 4 pseudogene 2, transcript variant 3
uncharacterized LOC101930100, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC101930100, transcript variant X3
uncharacterized LOC101930100, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 30% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Curated Genomic.
transmembrane phosphatase with tensin homology, transcript variant 1
similar to RNA sequence, mRNA (same species):RefSeq:NM_199261.2
annotated by transcript or proteomic data
The RefSeq transcript has 2 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transmembrane phosphatase with tensin homology, transcript variant 2
similar to RNA sequence, mRNA (same species):RefSeq:NM_199259.2
transmembrane phosphatase with tensin homology, transcript variant 3
similar to RNA sequence, mRNA (same species):RefSeq:NM_199260.2
similar to AA sequence (same species):RefSeq:NP_954870.2
isoform alpha is encoded by transcript variant 1; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
putative tyrosine-protein phosphatase TPTE isoform alpha
similar to AA sequence (same species):RefSeq:NP_954868.1
isoform beta is encoded by transcript variant 2; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
putative tyrosine-protein phosphatase TPTE isoform beta
similar to AA sequence (same species):RefSeq:NP_954869.1
isoform gamma is encoded by transcript variant 3; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
putative tyrosine-protein phosphatase TPTE isoform gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 76% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
POTE ankyrin domain family, member D, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
POTE ankyrin domain family member D isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 7% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat domain 20 family, member A11, pseudogene
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 3 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
similar to RNA sequence, mRNA (same species):RefSeq:NM_198996.2
The RefSeq transcript has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_945347.1
The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RNA binding motif protein 11, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RNA binding motif protein 11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RNA binding motif protein 11, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RNA binding motif protein 11, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 15 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ATP-binding cassette, sub-family C (CFTR/MRP), member 13, pseudogene, transcript variant A
ATP-binding cassette, sub-family C (CFTR/MRP), member 13, pseudogene, transcript variant D
heat shock protein 70kDa family, member 13
SAM domain, SH3 domain and nuclear localization signals 1, transcript variant 2
SAM domain, SH3 domain and nuclear localization signals 1, transcript variant 1
SAM domain, SH3 domain and nuclear localization signals 1, transcript variant 3
isoform 2 is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
SAM domain-containing protein SAMSN-1 isoform 2
isoform 1 is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
SAM domain-containing protein SAMSN-1 isoform 1
isoform 3 is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
SAM domain-containing protein SAMSN-1 isoform 3
uncharacterized protein ENSP00000383407-like
similar to RNA sequence, mRNA (same species):RefSeq:NM_001256579.1
similar to AA sequence (same species):RefSeq:NP_001243508.1
putative uncharacterized protein ENSP00000383407
nuclear receptor interacting protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 183 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
nuclear receptor interacting protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 183 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
nuclear receptor interacting protein 1, transcript variant X6
nuclear receptor interacting protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 183 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
nuclear receptor-interacting protein 1 isoform X2
nuclear receptor-interacting protein 1 isoform X4
nuclear receptor-interacting protein 1 isoform X5
nuclear receptor-interacting protein 1 isoform X6
ubiquitin specific peptidase 25, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ubiquitin specific peptidase 25, transcript variant 1
ubiquitin specific peptidase 25, transcript variant 2
ubiquitin specific peptidase 25, transcript variant 3
isoform USP25m is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ubiquitin carboxyl-terminal hydrolase 25 isoform USP25m
isoform USP25b is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ubiquitin carboxyl-terminal hydrolase 25 isoform USP25b
isoform USP25a is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ubiquitin carboxyl-terminal hydrolase 25 isoform USP25a
ubiquitin specific peptidase 25, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 68 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 25 isoform X5
ubiquitin specific peptidase 25, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 61 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 25 isoform X4
long intergenic non-protein coding RNA 478, transcript variant 1
similar to RNA sequence (same species):RefSeq:NR_027790.1
The RefSeq transcript has 1 indel compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
long intergenic non-protein coding RNA 478, transcript variant 2
similar to RNA sequence (same species):RefSeq:NR_027791.1
chromosome 21 open reading frame 37, transcript variant 1
chromosome 21 open reading frame 37, transcript variant 2
transfer RNA glycine 27 (anticodon GCC); tRNA features were annotated by tRNAscan-SE; Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
coxsackie virus and adenovirus receptor, transcript variant 5
coxsackie virus and adenovirus receptor, transcript variant 1
coxsackie virus and adenovirus receptor, transcript variant 2
coxsackie virus and adenovirus receptor, transcript variant 3
coxsackie virus and adenovirus receptor, transcript variant 4
isoform 5 precursor is encoded by transcript variant 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
coxsackievirus and adenovirus receptor isoform 5 precursor
isoform 1 precursor is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
coxsackievirus and adenovirus receptor isoform 1 precursor
isoform 2 precursor is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
coxsackievirus and adenovirus receptor isoform 2 precursor
isoform 3 precursor is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
coxsackievirus and adenovirus receptor isoform 3 precursor
isoform 4 precursor is encoded by transcript variant 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
coxsackievirus and adenovirus receptor isoform 4 precursor
BTG family, member 3, transcript variant 2
BTG family, member 3, transcript variant 1
BTG family, member 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 110 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
isoform b is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
isoform a is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
C21orf91 overlapping transcript 1 (non-protein coding), transcript variant 2
C21orf91 overlapping transcript 1 (non-protein coding), transcript variant 1
chromosome 21 open reading frame 91, transcript variant 3
chromosome 21 open reading frame 91, transcript variant 2
chromosome 21 open reading frame 91, transcript variant 1
similar to RNA sequence, mRNA (same species):RefSeq:NM_001204176.1
The RefSeq transcript aligns at 97% coverage compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001204178.1
isoform a precursor is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001204175.1
similar to RNA sequence, mRNA (same species):RefSeq:NM_001204177.1
The RefSeq transcript aligns at 96% coverage compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
isoform d is encoded by transcript variant 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
isoform d is encoded by transcript variant 6; Derived by automated computational analysis using gene prediction method: BestRefSeq.
isoform c is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
isoform c is encoded by transcript variant 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_002772.2
similar to AA sequence (same species):RefSeq:NP_002763.2
long intergenic non-protein coding RNA 320, transcript variant 1
long intergenic non-protein coding RNA 320, transcript variant 2
long intergenic non-protein coding RNA 320, transcript variant 4
long intergenic non-protein coding RNA 320, transcript variant 3
neural cell adhesion molecule 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 ESTs, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
neural cell adhesion molecule 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 ESTs, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neural cell adhesion molecule 2 precursor
neural cell adhesion molecule 2 isoform X3
neural cell adhesion molecule 2 isoform X4
neural cell adhesion molecule 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 48 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neural cell adhesion molecule 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 49 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neural cell adhesion molecule 2 isoform X2
neural cell adhesion molecule 2 isoform X5
long intergenic non-protein coding RNA 317
long intergenic non-protein coding RNA 308
long intergenic non-protein coding RNA 158
long intergenic non-protein coding RNA 515
similar to RNA sequence (same species):RefSeq:NR_024092.1
mitochondrial ribosomal protein L39, transcript variant 1
similar to RNA sequence, mRNA (same species):RefSeq:NM_017446.3
mitochondrial ribosomal protein L39, transcript variant 2
similar to RNA sequence, mRNA (same species):RefSeq:NM_080794.3
similar to AA sequence (same species):RefSeq:NP_059142.2
isoform a is encoded by transcript variant 1; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
39S ribosomal protein L39, mitochondrial isoform a
similar to AA sequence (same species):RefSeq:NP_542984.2
isoform b is encoded by transcript variant 2; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
39S ribosomal protein L39, mitochondrial isoform b
mitochondrial ribosomal protein L39, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 ESTs, 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
39S ribosomal protein L39, mitochondrial isoform X1
junctional adhesion molecule 2, transcript variant 1
junctional adhesion molecule 2, transcript variant 4
junctional adhesion molecule 2, transcript variant 2
junctional adhesion molecule 2, transcript variant 3
junctional adhesion molecule 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
junctional adhesion molecule B isoform 1 precursor
junctional adhesion molecule B isoform 2 precursor
junctional adhesion molecule B isoform 3 precursor
junctional adhesion molecule B isoform X1
ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6, transcript variant 4
ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6, transcript variant 3
ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6, transcript variant 2
ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6, transcript variant 5
ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6, transcript variant 1
ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 64 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
isoform b precursor is encoded by transcript variant 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ATP synthase-coupling factor 6, mitochondrial isoform b precursor
ATP synthase-coupling factor 6, mitochondrial isoform X1
isoform a precursor is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ATP synthase-coupling factor 6, mitochondrial isoform a precursor
isoform a precursor is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
isoform a precursor is encoded by transcript variant 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
GA binding protein transcription factor, alpha subunit 60kDa, transcript variant 2
GA binding protein transcription factor, alpha subunit 60kDa, transcript variant 1
GA binding protein transcription factor, alpha subunit 60kDa, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 92 ESTs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
GA binding protein transcription factor, alpha subunit 60kDa, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 89 ESTs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
GA-binding protein alpha chain isoform X1
GA-binding protein alpha chain isoform X2
amyloid beta (A4) precursor protein, transcript variant 7
amyloid beta (A4) precursor protein, transcript variant 5
amyloid beta (A4) precursor protein, transcript variant 6
amyloid beta (A4) precursor protein, transcript variant 10
amyloid beta (A4) precursor protein, transcript variant 3
amyloid beta (A4) precursor protein, transcript variant 9
amyloid beta (A4) precursor protein, transcript variant 2
amyloid beta (A4) precursor protein, transcript variant 8
amyloid beta (A4) precursor protein, transcript variant 1
amyloid beta (A4) precursor protein, transcript variant 4
isoform e precursor is encoded by transcript variant 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
amyloid beta A4 protein isoform e precursor
isoform f precursor is encoded by transcript variant 6; Derived by automated computational analysis using gene prediction method: BestRefSeq.
amyloid beta A4 protein isoform f precursor
isoform j precursor is encoded by transcript variant 10; Derived by automated computational analysis using gene prediction method: BestRefSeq.
amyloid beta A4 protein isoform j precursor
isoform c precursor is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
amyloid beta A4 protein isoform c precursor
isoform i precursor is encoded by transcript variant 9; Derived by automated computational analysis using gene prediction method: BestRefSeq.
amyloid beta A4 protein isoform i precursor
isoform b precursor is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
amyloid beta A4 protein isoform b precursor
isoform h precursor is encoded by transcript variant 8; Derived by automated computational analysis using gene prediction method: BestRefSeq.
amyloid beta A4 protein isoform h precursor
amyloid beta A4 protein isoform a precursor
isoform d is encoded by transcript variant 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
isoform g is encoded by transcript variant 7; Derived by automated computational analysis using gene prediction method: BestRefSeq.
tigger transposable element-derived protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, and 9% coverage of the annotated genomic feature by RNAseq alignments
cysteine/tyrosine-rich 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cysteine and tyrosine-rich protein 1 precursor
cysteine/tyrosine-rich 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tigger transposable element-derived protein 1 isoform X1
cysteine/tyrosine-rich 1, transcript variant X5
cysteine/tyrosine-rich 1, transcript variant X6
ADAM metallopeptidase with thrombospondin type 1 motif, 1
similar to RNA sequence, mRNA (same species):RefSeq:NM_006988.3
A disintegrin and metalloproteinase with thrombospondin motifs 1 preproprotein preproprotein; Derived by automated computational analysis using gene prediction method: BestRefSeq.
A disintegrin and metalloproteinase with thrombospondin motifs 1 preproprotein
ADAM metallopeptidase with thrombospondin type 1 motif, 5
A disintegrin and metalloproteinase with thrombospondin motifs 5 preproprotein preproprotein; Derived by automated computational analysis using gene prediction method: BestRefSeq.
A disintegrin and metalloproteinase with thrombospondin motifs 5 preproprotein
long intergenic non-protein coding RNA 113
long intergenic non-protein coding RNA 314
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 50% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
long intergenic non-protein coding RNA 161, transcript variant 1
long intergenic non-protein coding RNA 161, transcript variant 2
N-6 adenine-specific DNA methyltransferase 1 (putative), transcript variant 3
similar to RNA sequence (same species):RefSeq:NR_047510.1
The RefSeq transcript has 7 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
N-6 adenine-specific DNA methyltransferase 1 (putative), transcript variant 2
similar to RNA sequence, mRNA (same species):RefSeq:NM_182749.3
N-6 adenine-specific DNA methyltransferase 1 (putative), transcript variant 1
similar to RNA sequence, mRNA (same species):RefSeq:NM_013240.4
similar to AA sequence (same species):RefSeq:NP_877426.3
isoform 2 is encoded by transcript variant 2; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
hemK methyltransferase family member 2 isoform 2
similar to AA sequence (same species):RefSeq:NP_037372.3
isoform 1 is encoded by transcript variant 1; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
hemK methyltransferase family member 2 isoform 1
listerin E3 ubiquitin protein ligase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 18 ESTs, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
E3 ubiquitin-protein ligase listerin isoform X1
RWD domain containing 2B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 63 ESTs, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
RWD domain-containing protein 2B isoform X1
ubiquitin specific peptidase 16, transcript variant 3
ubiquitin specific peptidase 16, transcript variant 1
ubiquitin specific peptidase 16, transcript variant 2
ubiquitin carboxyl-terminal hydrolase 16 isoform a
isoform a is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ubiquitin carboxyl-terminal hydrolase 16 isoform b
chaperonin containing TCP1, subunit 8 (theta), transcript variant 4
chaperonin containing TCP1, subunit 8 (theta), transcript variant 1
chaperonin containing TCP1, subunit 8 (theta), transcript variant 3
chaperonin containing TCP1, subunit 8 (theta), transcript variant 2
T-complex protein 1 subunit theta isoform 1
T-complex protein 1 subunit theta isoform 2
isoform 4 is encoded by transcript variant 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
T-complex protein 1 subunit theta isoform 4
T-complex protein 1 subunit theta isoform 3
MAP3K7 C-terminal like, transcript variant 1
MAP3K7 C-terminal like, transcript variant 7
MAP3K7 C-terminal like, transcript variant 3
MAP3K7 C-terminal like, transcript variant 4
MAP3K7 C-terminal like, transcript variant 2
MAP3K7 C-terminal like, transcript variant 8
MAP3K7 C-terminal like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
MAP3K7 C-terminal-like protein isoform 1
isoform 1 is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
isoform 4 is encoded by transcript variant 8; Derived by automated computational analysis using gene prediction method: BestRefSeq.
MAP3K7 C-terminal-like protein isoform 4
MAP3K7 C-terminal-like protein isoform X1
MAP3K7 C-terminal like, transcript variant 5
isoform 3 is encoded by transcript variant 7; Derived by automated computational analysis using gene prediction method: BestRefSeq.
MAP3K7 C-terminal-like protein isoform 3
MAP3K7 C-terminal like, transcript variant 6
isoform 2 is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
MAP3K7 C-terminal-like protein isoform 2
isoform 2 is encoded by transcript variant 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
isoform 2 is encoded by transcript variant 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
isoform 2 is encoded by transcript variant 6; Derived by automated computational analysis using gene prediction method: BestRefSeq.
MAP3K7 C-terminal like, transcript variant 9
isoform 5 is encoded by transcript variant 9; Derived by automated computational analysis using gene prediction method: BestRefSeq.
MAP3K7 C-terminal-like protein isoform 5
long intergenic non-protein coding RNA 189
BTB and CNC homology 1, basic leucine zipper transcription factor 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 27 ESTs, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
BTB and CNC homology 1, basic leucine zipper transcription factor 1, transcript variant X6
BTB and CNC homology 1, basic leucine zipper transcription factor 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 28 ESTs, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
BTB and CNC homology 1, basic leucine zipper transcription factor 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 27 ESTs, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
BTB and CNC homology 1, basic leucine zipper transcription factor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 101 ESTs, 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
BTB and CNC homology 1, basic leucine zipper transcription factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 102 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
BTB and CNC homology 1, basic leucine zipper transcription factor 1, transcript variant 2
BTB and CNC homology 1, basic leucine zipper transcription factor 1, transcript variant 1
BTB and CNC homology 1, basic leucine zipper transcription factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 128 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
BTB and CNC homology 1, basic leucine zipper transcription factor 1, transcript variant 3
transcription regulator protein BACH1 isoform X4
transcription regulator protein BACH1 isoform X1
transcription regulator protein BACH1 isoform X2
transcription regulator protein BACH1 isoform X3
glutamate receptor, ionotropic, kainate 1, transcript variant 2
glutamate receptor, ionotropic, kainate 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutamate receptor, ionotropic, kainate 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 ESTs, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutamate receptor, ionotropic, kainate 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutamate receptor ionotropic, kainate 1 isoform 2 precursor
glutamate receptor ionotropic, kainate 1 isoform X1
glutamate receptor ionotropic, kainate 1 isoform X2
glutamate receptor ionotropic, kainate 1 isoform X4
glutamate receptor, ionotropic, kainate 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 13 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutamate receptor, ionotropic, kainate 1, transcript variant 1
glutamate receptor ionotropic, kainate 1 isoform X3
glutamate receptor ionotropic, kainate 1 isoform 1 precursor
long intergenic non-protein coding RNA 307
similar to RNA sequence, mRNA (same species):RefSeq:NM_181612.2
keratin associated protein 7-1 (gene/pseudogene)
T-cell lymphoma invasion and metastasis 1
T-cell lymphoma invasion and metastasis 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 145 ESTs, 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
T-cell lymphoma invasion and metastasis 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 134 ESTs, 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
T-cell lymphoma invasion and metastasis 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 132 ESTs, 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
T-cell lymphoma invasion and metastasis 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 30 ESTs, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
T-lymphoma invasion and metastasis-inducing protein 1
T-lymphoma invasion and metastasis-inducing protein 1 isoform X1
T-lymphoma invasion and metastasis-inducing protein 1 isoform X2
T-lymphoma invasion and metastasis-inducing protein 1 isoform X3
T-lymphoma invasion and metastasis-inducing protein 1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 9% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 ESTs, and 58% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SR-related CTD-associated factor 4, transcript variant 2
SR-related CTD-associated factor 4, transcript variant 3
SR-related CTD-associated factor 4, transcript variant 1
SR-related CTD-associated factor 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 117 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
SR-related CTD-associated factor 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 153 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
SR-related CTD-associated factor 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 157 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
splicing factor, arginine/serine-rich 15 isoform 2
splicing factor, arginine/serine-rich 15 isoform X3
splicing factor, arginine/serine-rich 15 isoform X5
splicing factor, arginine/serine-rich 15 isoform X4
splicing factor, arginine/serine-rich 15 isoform 3
splicing factor, arginine/serine-rich 15 isoform 1
hormonally up-regulated Neu-associated kinase
hormonally up-regulated neu tumor-associated kinase
long intergenic non-protein coding RNA 159
melanocortin 2 receptor accessory protein, transcript variant 2
melanocortin 2 receptor accessory protein, transcript variant 1
melanocortin 2 receptor accessory protein, transcript variant 3
melanocortin 2 receptor accessory protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
isoform beta is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
melanocortin-2 receptor accessory protein isoform beta
melanocortin-2 receptor accessory protein isoform X1
isoform alpha is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
melanocortin-2 receptor accessory protein isoform alpha
melanocortin-2 receptor accessory protein isoform c
URB1 ribosome biogenesis 1 homolog (S. cerevisiae)
nucleolar pre-ribosomal-associated protein 1
eva-1 homolog C (C. elegans), transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 29 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
eva-1 homolog C (C. elegans), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 58 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
eva-1 homolog C (C. elegans), transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 59 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
eva-1 homolog C (C. elegans), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
eva-1 homolog C (C. elegans), transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 24 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
eva-1 homolog C (C. elegans), transcript variant 1
eva-1 homolog C (C. elegans), transcript variant 2
eva-1 homolog C (C. elegans), transcript variant 3
protein eva-1 homolog C isoform 1 precursor
protein eva-1 homolog C isoform 2 precursor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
chromosome 21 open reading frame 59, transcript variant 1
chromosome 21 open reading frame 59, transcript variant 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 135 ESTs, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 126 ESTs, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 130 ESTs, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 132 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 132 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 129 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 121 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 42 ESTs, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 41 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
PAXBP1 antisense RNA 1, transcript variant 1
PAXBP1 antisense RNA 1, transcript variant 2
PAX3 and PAX7 binding protein 1, transcript variant 1
PAX3 and PAX7 binding protein 1, transcript variant 3
PAX3 and PAX7 binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 98 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
PAX3- and PAX7-binding protein 1 isoform X1
PAX3- and PAX7-binding protein 1 isoform 1
PAX3 and PAX7 binding protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 23 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
PAX3- and PAX7-binding protein 1 isoform X2
PAX3 and PAX7 binding protein 1, transcript variant 2
PAX3- and PAX7-binding protein 1 isoform 2
chromosome 21 open reading frame 49, transcript variant 1
chromosome 21 open reading frame 49, transcript variant 2
chromosome 21 open reading frame 62, transcript variant 3
chromosome 21 open reading frame 62, transcript variant 2
chromosome 21 open reading frame 62, transcript variant 1
uncharacterized protein C21orf62 precursor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
oligodendrocyte lineage transcription factor 2
oligodendrocyte lineage transcription factor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 25 ESTs, 10 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
oligodendrocyte transcription factor 2 isoform X1
long intergenic non-protein coding RNA 945
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 ESTs, and 92% coverage of the annotated genomic feature by RNAseq alignments
interferon (alpha, beta and omega) receptor 2, transcript variant 4
interferon (alpha, beta and omega) receptor 2, transcript variant 6
interferon (alpha, beta and omega) receptor 2, transcript variant 1
interferon (alpha, beta and omega) receptor 2, transcript variant 5
interferon (alpha, beta and omega) receptor 2, transcript variant 2
interferon (alpha, beta and omega) receptor 2, transcript variant 3
interferon alpha/beta receptor 2 isoform a
isoform a is encoded by transcript variant 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
isoform c is encoded by transcript variant 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
interferon alpha/beta receptor 2 isoform c
isoform c is encoded by transcript variant 6; Derived by automated computational analysis using gene prediction method: BestRefSeq.
interferon alpha/beta receptor 2 isoform b
isoform b is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
interleukin-10 receptor subunit beta precursor
interferon (alpha, beta and omega) receptor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 149 ESTs, 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
interferon (alpha, beta and omega) receptor 1
interferon alpha/beta receptor 1 precursor
interferon alpha/beta receptor 1 isoform X1
interferon gamma receptor 2 (interferon gamma transducer 1)
interferon gamma receptor 2 (interferon gamma transducer 1), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 222 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transmembrane protein 50B, transcript variant 2
transmembrane protein 50B, transcript variant 1
DnaJ (Hsp40) homolog, subfamily C, member 28, transcript variant 2
DnaJ (Hsp40) homolog, subfamily C, member 28, transcript variant 1
DnaJ (Hsp40) homolog, subfamily C, member 28, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
dnaJ homolog subfamily C member 28 isoform X1
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 217 ESTs, 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 184 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant 4
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 191 ESTs, 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant 3
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 179 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant 1
trifunctional purine biosynthetic protein adenosine-3 isoform X2
isoform 1 is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
trifunctional purine biosynthetic protein adenosine-3 isoform 1
isoform 1 is encoded by transcript variant 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
trifunctional purine biosynthetic protein adenosine-3 isoform X1
trifunctional purine biosynthetic protein adenosine-3 isoform X3
trifunctional purine biosynthetic protein adenosine-3 isoform X4
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant 2
trifunctional purine biosynthetic protein adenosine-3 isoform 2
SON DNA binding protein, transcript variant e
similar to RNA sequence (same species):RefSeq:NR_103798.1
The RefSeq transcript has 1 substitution and 1 indel compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
SON DNA binding protein, transcript variant c
similar to RNA sequence (same species):RefSeq:NR_103797.1
SON DNA binding protein, transcript variant f
similar to RNA sequence, mRNA (same species):RefSeq:NM_138927.2
SON DNA binding protein, transcript variant h
similar to RNA sequence (same species):RefSeq:NR_103796.1
SON DNA binding protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 mRNAs, 526 ESTs, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
SON DNA binding protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 mRNAs, 341 ESTs, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
SON DNA binding protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 mRNAs, 354 ESTs, 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
SON DNA binding protein, transcript variant b
similar to RNA sequence, mRNA (same species):RefSeq:NM_032195.2
SON DNA binding protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 mRNAs, 339 ESTs, 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
similar to AA sequence (same species):RefSeq:NP_620305.2
isoform F is encoded by transcript variant f; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_115571.2
isoform B is encoded by transcript variant b; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
crystallin, zeta (quinone reductase)-like 1
intersectin 1 (SH3 domain protein), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 134 ESTs, 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
intersectin 1 (SH3 domain protein), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 mRNAs, 224 ESTs, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
intersectin 1 (SH3 domain protein), transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 mRNAs, 207 ESTs, 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
intersectin 1 (SH3 domain protein), transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 mRNAs, 216 ESTs, 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
intersectin 1 (SH3 domain protein), transcript variant 1
intersectin 1 (SH3 domain protein), transcript variant 2
isoform ITSN-l is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
isoform ITSN-s is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ATP synthase, H+ transporting, mitochondrial F1 complex, O subunit
ATP synthase subunit O, mitochondrial precursor
long intergenic non-protein coding RNA 649
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
solute carrier family 5 (sodium/myo-inositol cotransporter), member 3
similar to RNA sequence, mRNA (same species):RefSeq:NM_006933.5
similar to AA sequence (same species):RefSeq:NP_008864.3
The RefSeq protein has 2 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
long intergenic non-protein coding RNA 310, transcript variant 1
long intergenic non-protein coding RNA 310, transcript variant 2
potassium voltage-gated channel, Isk-related family, member 2
potassium voltage-gated channel subfamily E member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, and 72% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
potassium voltage-gated channel, Isk-related family, member 1, transcript variant 2
similar to RNA sequence, mRNA (same species):RefSeq:NM_000219.4
potassium voltage-gated channel, Isk-related family, member 1, transcript variant 7
similar to RNA sequence, mRNA (same species):RefSeq:NM_001270404.1
potassium voltage-gated channel, Isk-related family, member 1, transcript variant 5
similar to RNA sequence, mRNA (same species):RefSeq:NM_001270402.1
potassium voltage-gated channel, Isk-related family, member 1, transcript variant 6
similar to RNA sequence, mRNA (same species):RefSeq:NM_001270403.1
potassium voltage-gated channel, Isk-related family, member 1, transcript variant 8
similar to RNA sequence, mRNA (same species):RefSeq:NM_001270405.1
potassium voltage-gated channel, Isk-related family, member 1, transcript variant 4
similar to RNA sequence, mRNA (same species):RefSeq:NM_001127669.2
potassium voltage-gated channel, Isk-related family, member 1, transcript variant 3
similar to RNA sequence, mRNA (same species):RefSeq:NM_001127668.2
potassium voltage-gated channel, Isk-related family, member 1, transcript variant 1
similar to RNA sequence, mRNA (same species):RefSeq:NM_001127670.2
potassium voltage-gated channel subfamily E member 1
regulator of calcineurin 1, transcript variant 1
regulator of calcineurin 1, transcript variant 2
regulator of calcineurin 1, transcript variant 4
regulator of calcineurin 1, transcript variant 3
regulator of calcineurin 1, transcript variant 6
regulator of calcineurin 1, transcript variant 5
regulator of calcineurin 1, transcript variant 7
isoform e is encoded by transcript variant 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
isoform b is encoded by transcript variant 6; Derived by automated computational analysis using gene prediction method: BestRefSeq.
isoform b is encoded by transcript variant 7; Derived by automated computational analysis using gene prediction method: BestRefSeq.
regulator of calcineurin 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 12 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
regulator of calcineurin 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 57 ESTs, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
chloride intracellular channel 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 60 ESTs, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
chloride intracellular channel protein 6
chloride intracellular channel protein 6 isoform X1
long intergenic non-protein coding RNA 160
uncharacterized LOC100506385, transcript variant 1
uncharacterized LOC100506385, transcript variant 2
runt-related transcription factor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 128 ESTs, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
runt-related transcription factor 1, transcript variant 1
runt-related transcription factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 127 ESTs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
runt-related transcription factor 1, transcript variant 2
runt-related transcription factor 1 isoform X3
isoform AML1c is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
runt-related transcription factor 1 isoform AML1c
runt-related transcription factor 1 isoform X2
isoform AML1b is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
runt-related transcription factor 1 isoform AML1b
runt-related transcription factor 1, transcript variant 3
isoform AML1a is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
runt-related transcription factor 1 isoform AML1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC101928240, transcript variant X2
uncharacterized LOC101928240, transcript variant X1
RUNX1 intronic transcript 1 (non-protein coding)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, and 30% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 ESTs, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
SET domain containing 4, transcript variant 4
SET domain containing 4, transcript variant 1
SET domain containing 4, transcript variant 3
SET domain containing 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 66 ESTs, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SET domain containing 4, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 74 ESTs, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SET domain containing 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 ESTs, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
SET domain containing 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 ESTs, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SET domain containing 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 65 ESTs, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SET domain containing 4, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 ESTs, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SET domain-containing protein 4 isoform X1
SET domain-containing protein 4 isoform 1
SET domain-containing protein 4 isoform X2
SET domain-containing protein 4 isoform X3
SET domain-containing protein 4 isoform X5
SET domain-containing protein 4 isoform X9
SET domain-containing protein 4 isoform 3
SET domain containing 4, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 ESTs, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SET domain containing 4, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 ESTs, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SET domain-containing protein 4 isoform X10
SET domain containing 4, transcript variant 2
SET domain containing 4, transcript variant 5
SET domain containing 4, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 33 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SET domain-containing protein 4 isoform X11
SET domain-containing protein 4 isoform 2
isoform 4 is encoded by transcript variant 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
SET domain-containing protein 4 isoform 4
carbonyl reductase 1, transcript variant 2
carbonyl reductase 1, transcript variant 1
CBR3 antisense RNA 1, transcript variant 2
CBR3 antisense RNA 1, transcript variant 1
CBR3 antisense RNA 1, transcript variant 3
dopey family member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 52 ESTs, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
similar to RNA sequence, mRNA (same species):RefSeq:NM_005128.2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
MORC family CW-type zinc finger 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 89 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
MORC family CW-type zinc finger protein 3 isoform X2
MORC family CW-type zinc finger protein 3
MORC family CW-type zinc finger 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 89 ESTs, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
MORC family CW-type zinc finger protein 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments
chromatin assembly factor 1, subunit B (p60)
single-minded family bHLH transcription factor 2, transcript variant SIM2
single-minded family bHLH transcription factor 2, transcript variant SIM2s
long isoform is encoded by transcript variant SIM2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
short isoform is encoded by transcript variant SIM2s; Derived by automated computational analysis using gene prediction method: BestRefSeq.
holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase), transcript variant 1
holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase), transcript variant 2
holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase), transcript variant 3
holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88 ESTs, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase), transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 ESTs, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase), transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 ESTs, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase), transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 84 ESTs, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 90 ESTs, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase), transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase), transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 22 ESTs, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ripply transcriptional repressor 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 Protein, and 64% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol glycan anchor biosynthesis, class P, transcript variant 2
phosphatidylinositol glycan anchor biosynthesis, class P, transcript variant 4
phosphatidylinositol glycan anchor biosynthesis, class P, transcript variant 1
phosphatidylinositol glycan anchor biosynthesis, class P, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 50 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
phosphatidylinositol glycan anchor biosynthesis, class P, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 50 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
phosphatidylinositol N-acetylglucosaminyltransferase subunit P isoform 1
phosphatidylinositol N-acetylglucosaminyltransferase subunit P isoform 2
phosphatidylinositol N-acetylglucosaminyltransferase subunit P isoform X1
phosphatidylinositol N-acetylglucosaminyltransferase subunit P isoform X2
tetratricopeptide repeat domain 3, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 622 ESTs, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
tetratricopeptide repeat domain 3, transcript variant 2
tetratricopeptide repeat domain 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 619 ESTs, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tetratricopeptide repeat domain 3, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 625 ESTs, 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
tetratricopeptide repeat domain 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 619 ESTs, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
tetratricopeptide repeat domain 3, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 622 ESTs, 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
tetratricopeptide repeat domain 3, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 611 ESTs, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
tetratricopeptide repeat domain 3, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 88 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tetratricopeptide repeat domain 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 616 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tetratricopeptide repeat domain 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 637 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tetratricopeptide repeat domain 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 619 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tetratricopeptide repeat domain 3, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 640 ESTs, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
E3 ubiquitin-protein ligase TTC3 isoform X1
E3 ubiquitin-protein ligase TTC3 isoform X3
E3 ubiquitin-protein ligase TTC3 isoform X2
E3 ubiquitin-protein ligase TTC3 isoform X7
E3 ubiquitin-protein ligase TTC3 isoform X14
tetratricopeptide repeat domain 3, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 619 ESTs, 5 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
tetratricopeptide repeat domain 3, transcript variant 1
tetratricopeptide repeat domain 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 616 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
E3 ubiquitin-protein ligase TTC3 isoform X4
E3 ubiquitin-protein ligase TTC3 isoform X5
E3 ubiquitin-protein ligase TTC3 isoform X6
E3 ubiquitin-protein ligase TTC3 isoform X10
E3 ubiquitin-protein ligase TTC3 isoform X8
E3 ubiquitin-protein ligase TTC3 isoform X9
E3 ubiquitin-protein ligase TTC3 isoform X11
E3 ubiquitin-protein ligase TTC3 isoform X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 47% coverage of the annotated genomic feature by RNAseq alignments
Down syndrome critical region gene 9 (non-protein coding)
similar to RNA sequence, mRNA (same species):RefSeq:NM_006052.1
Down syndrome critical region gene 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 50 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Down syndrome critical region gene 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 88 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Down syndrome critical region protein 3 isoform X3
Down syndrome critical region protein 3 isoform X1
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 217 ESTs, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A, transcript variant 3
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 mRNAs, 214 ESTs, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 mRNAs, 212 ESTs, 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 mRNAs, 212 ESTs, 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A, transcript variant 2
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A, transcript variant 5
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 212 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A, transcript variant 1
dual specificity tyrosine-phosphorylation-regulated kinase 1A isoform 1
dual specificity tyrosine-phosphorylation-regulated kinase 1A isoform X4
dual specificity tyrosine-phosphorylation-regulated kinase 1A isoform X5
dual specificity tyrosine-phosphorylation-regulated kinase 1A isoform X6
dual specificity tyrosine-phosphorylation-regulated kinase 1A isoform 2
dual specificity tyrosine-phosphorylation-regulated kinase 1A isoform X7
isoform 5 is encoded by transcript variant 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
dual specificity tyrosine-phosphorylation-regulated kinase 1A isoform 5
dual specificity tyrosine-phosphorylation-regulated kinase 1A isoform 3
dual specificity tyrosine-phosphorylation-regulated kinase 1A isoform X1
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 209 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
dual specificity tyrosine-phosphorylation-regulated kinase 1A isoform X3
potassium inwardly-rectifying channel, subfamily J, member 6
G protein-activated inward rectifier potassium channel 2
similar to RNA sequence, mRNA (same species):RefSeq:NM_005867.2
Down syndrome critical region gene 8, transcript variant 4
Down syndrome critical region gene 8, transcript variant 3
Down syndrome critical region gene 8, transcript variant 5
Down syndrome critical region gene 8, transcript variant 1
Down syndrome critical region gene 8, transcript variant 2
Down syndrome critical region gene 10 (non-protein coding)
potassium inwardly-rectifying channel, subfamily J, member 15, transcript variant 8
potassium inwardly-rectifying channel, subfamily J, member 15, transcript variant 6
potassium inwardly-rectifying channel, subfamily J, member 15, transcript variant 7
potassium inwardly-rectifying channel, subfamily J, member 15, transcript variant 5
potassium inwardly-rectifying channel, subfamily J, member 15, transcript variant 4
potassium inwardly-rectifying channel, subfamily J, member 15, transcript variant 2
potassium inwardly-rectifying channel, subfamily J, member 15, transcript variant 1
potassium inwardly-rectifying channel, subfamily J, member 15, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 34 ESTs, 17 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
potassium inwardly-rectifying channel, subfamily J, member 15, transcript variant 3
potassium inwardly-rectifying channel, subfamily J, member 15, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 33 ESTs, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
potassium inwardly-rectifying channel, subfamily J, member 15, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 32 ESTs, 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
ATP-sensitive inward rectifier potassium channel 15
ATP-sensitive inward rectifier potassium channel 15 isoform X1
ATP-sensitive inward rectifier potassium channel 15 isoform X2
ATP-sensitive inward rectifier potassium channel 15 isoform X3
v-ets avian erythroblastosis virus E26 oncogene homolog, transcript variant 7
isoform 6 is encoded by transcript variant 7; Derived by automated computational analysis using gene prediction method: BestRefSeq.
v-ets avian erythroblastosis virus E26 oncogene homolog, transcript variant 2
v-ets avian erythroblastosis virus E26 oncogene homolog, transcript variant 3
v-ets avian erythroblastosis virus E26 oncogene homolog, transcript variant 5
v-ets avian erythroblastosis virus E26 oncogene homolog, transcript variant 6
v-ets avian erythroblastosis virus E26 oncogene homolog, transcript variant 4
v-ets avian erythroblastosis virus E26 oncogene homolog, transcript variant 1
isoform 3 is encoded by transcript variant 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
isoform 5 is encoded by transcript variant 6; Derived by automated computational analysis using gene prediction method: BestRefSeq.
long intergenic non-protein coding RNA 114, transcript variant 3
long intergenic non-protein coding RNA 114, transcript variant 1
similar to RNA sequence (same species):RefSeq:NR_027065.1
long intergenic non-protein coding RNA 114, transcript variant 2
similar to RNA sequence (same species):RefSeq:NR_027066.1
The RefSeq transcript has 3 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
v-ets avian erythroblastosis virus E26 oncogene homolog 2, transcript variant 2
v-ets avian erythroblastosis virus E26 oncogene homolog 2, transcript variant 1
v-ets avian erythroblastosis virus E26 oncogene homolog 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 323 ESTs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
proteasome (prosome, macropain) assembly chaperone 1, transcript variant 4
proteasome (prosome, macropain) assembly chaperone 1, transcript variant 2
proteasome (prosome, macropain) assembly chaperone 1, transcript variant 3
proteasome (prosome, macropain) assembly chaperone 1, transcript variant 1
proteasome assembly chaperone 1 isoform b
proteasome assembly chaperone 1 isoform 3
proteasome assembly chaperone 1 isoform a
bromodomain and WD repeat domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 88 ESTs, 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
bromodomain and WD repeat domain containing 1, transcript variant 1
bromodomain and WD repeat domain containing 1, transcript variant 2
bromodomain and WD repeat-containing protein 1 isoform X1
bromodomain and WD repeat-containing protein 1 isoform A
bromodomain and WD repeat-containing protein 1 isoform B
bromodomain and WD repeat domain containing 1, transcript variant 3
similar to RNA sequence, mRNA (same species):RefSeq:NM_001007246.2
bromodomain and WD repeat-containing protein 1 isoform C
BRWD1 intronic transcript 2 (non-protein coding)
high mobility group nucleosome binding domain 1
tryptophan rich basic protein, transcript variant 1
tail-anchored protein insertion receptor WRB isoform 1
tryptophan rich basic protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 131 ESTs, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
tryptophan rich basic protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 131 ESTs, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tryptophan rich basic protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 131 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
tryptophan rich basic protein, transcript variant 2
tail-anchored protein insertion receptor WRB isoform 2
tail-anchored protein insertion receptor WRB isoform X1
tail-anchored protein insertion receptor WRB isoform X2
tail-anchored protein insertion receptor WRB isoform X3
Leber congenital amaurosis 5-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 36 ESTs, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Leber congenital amaurosis 5-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 38 ESTs, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Leber congenital amaurosis 5-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 36 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Leber congenital amaurosis 5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 50 ESTs, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Leber congenital amaurosis 5-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 37 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Leber congenital amaurosis 5-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 38 ESTs, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Leber congenital amaurosis 5-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 ESTs, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Leber congenital amaurosis 5-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 36 ESTs, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC102724757, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 61% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC102724757, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, and 58% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC102724757, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, and 57% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC102724757, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 81% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SH3 domain binding glutamic acid-rich protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
SH3 domain binding glutamic acid-rich protein, transcript variant 2
SH3 domain binding glutamic acid-rich protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
SH3 domain binding glutamic acid-rich protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
SH3 domain binding glutamic acid-rich protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
SH3 domain binding glutamic acid-rich protein, transcript variant 1
similar to RNA sequence, mRNA (same species):RefSeq:NM_007341.2
similar to AA sequence (same species):RefSeq:NP_031367.1
SH3 domain-binding glutamic acid-rich protein isoform a
SH3 domain-binding glutamic acid-rich protein isoform X1
SH3 domain binding glutamic acid-rich protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
SH3 domain-binding glutamic acid-rich protein isoform X2
SH3 domain-binding glutamic acid-rich protein isoform X3
SH3 domain-binding glutamic acid-rich protein isoform X4
SH3 domain-binding glutamic acid-rich protein isoform X5
SH3 domain-binding glutamic acid-rich protein isoform b
UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, 5 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
chromosome 21 open reading frame 88, transcript variant 1
chromosome 21 open reading frame 88, transcript variant 2
UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 5, transcript variant 6
UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 5, transcript variant 3
UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 5, transcript variant 4
UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 5, transcript variant 1
UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 5, transcript variant 2
isoform b is encoded by transcript variant 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
beta-1,3-galactosyltransferase 5 isoform b
beta-1,3-galactosyltransferase 5 isoform X1
beta-1,3-galactosyltransferase 5 isoform a
isoform a is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
isoform a is encoded by transcript variant 6; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 59% coverage of the annotated genomic feature by RNAseq alignments
immunoglobulin superfamily, member 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
immunoglobulin superfamily member 5 isoform X1
Down syndrome cell adhesion molecule, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 24 ESTs, 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
Down syndrome cell adhesion molecule, transcript variant 3
Down syndrome cell adhesion molecule, transcript variant 2
Down syndrome cell adhesion molecule, transcript variant 1
Down syndrome cell adhesion molecule isoform 2 precursor
isoform CHD2-42 precursor is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Down syndrome cell adhesion molecule isoform CHD2-42 precursor
Down syndrome cell adhesion molecule isoform X1
DSCAM antisense RNA 1, transcript variant 2
DSCAM antisense RNA 1, transcript variant 1
DSCAM antisense RNA 1, transcript variant 4
DSCAM antisense RNA 1, transcript variant 3
DSCAM intronic transcript 1 (non-protein coding)
long intergenic non-protein coding RNA 323
beta-site APP-cleaving enzyme 2, transcript variant a
beta-site APP-cleaving enzyme 2, transcript variant b
beta-site APP-cleaving enzyme 2, transcript variant c
isoform A preproprotein is encoded by transcript variant a; Derived by automated computational analysis using gene prediction method: BestRefSeq.
beta-secretase 2 isoform A preproprotein
isoform C preproprotein is encoded by transcript variant c; Derived by automated computational analysis using gene prediction method: BestRefSeq.
beta-secretase 2 isoform C preproprotein
isoform B preproprotein is encoded by transcript variant b; Derived by automated computational analysis using gene prediction method: BestRefSeq.
beta-secretase 2 isoform B preproprotein
family with sequence similarity 3, member B, transcript variant 1
family with sequence similarity 3, member B, transcript variant 2
family with sequence similarity 3, member B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
family with sequence similarity 3, member B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
myxovirus (influenza virus) resistance 2 (mouse)
myxovirus (influenza virus) resistance 2 (mouse), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 66 ESTs, 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
myxovirus (influenza virus) resistance 2 (mouse), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 71 ESTs, 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
myxovirus (influenza virus) resistance 2 (mouse), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 67 ESTs, 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
interferon-induced GTP-binding protein Mx2
interferon-induced GTP-binding protein Mx2 isoform X1
interferon-induced GTP-binding protein Mx2 isoform X2
interferon-induced GTP-binding protein Mx2 isoform X3
myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse), transcript variant 1
myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 177 ESTs, 17 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse), transcript variant 2
myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse), transcript variant 3
myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 179 ESTs, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse), transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 178 ESTs, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse), transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 171 ESTs, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 183 ESTs, 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse), transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 167 ESTs, 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
interferon-induced GTP-binding protein Mx1 isoform X6
myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse), transcript variant 4
interferon-induced GTP-binding protein Mx1 isoform b
interferon-induced GTP-binding protein Mx1 isoform X1
interferon-induced GTP-binding protein Mx1 isoform X2
interferon-induced GTP-binding protein Mx1 isoform X3
interferon-induced GTP-binding protein Mx1 isoform X4
interferon-induced GTP-binding protein Mx1 isoform X5
interferon-induced GTP-binding protein Mx1 isoform a
transmembrane protease, serine 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 115 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transmembrane protease, serine 2, transcript variant X2
transmembrane protease, serine 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 116 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transmembrane protease, serine 2, transcript variant 2
transmembrane protease, serine 2, transcript variant 1
transmembrane protease serine 2 isoform X2
transmembrane protease serine 2 isoform 1
transmembrane protease serine 2 isoform X3
transmembrane protease serine 2 isoform 2
transmembrane protease serine 2 isoform X4
transmembrane protease, serine 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 14 ESTs, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane protease serine 2 isoform X5
long intergenic non-protein coding RNA 111
long intergenic non-protein coding RNA 479
long intergenic non-protein coding RNA 112
receptor-interacting serine-threonine kinase 4
receptor-interacting serine/threonine-protein kinase 4
uncharacterized LOC102724800, transcript variant X2
uncharacterized LOC102724800, transcript variant X1
PR domain containing 15, transcript variant 5
PR domain containing 15, transcript variant 2
PR domain containing 15, transcript variant 4
PR domain containing 15, transcript variant 3
PR domain containing 15, transcript variant 6
PR domain containing 15, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 81 ESTs, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PR domain containing 15, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 79 ESTs, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PR domain containing 15, transcript variant 1
PR domain zinc finger protein 15 isoform X2
PR domain zinc finger protein 15 isoform 2
PR domain zinc finger protein 15 isoform X1
PR domain zinc finger protein 15 isoform 3
PR domain zinc finger protein 15 isoform 1
C2 calcium-dependent domain containing 2, transcript variant 1
C2 calcium-dependent domain containing 2, transcript variant 2
C2 calcium-dependent domain containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 107 ESTs, 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
C2 calcium-dependent domain containing 2, transcript variant X3
C2 calcium-dependent domain containing 2, transcript variant X5
C2 domain-containing protein 2 isoform 1 precursor
C2 domain-containing protein 2 isoform X2
C2 domain-containing protein 2 isoform 2
C2 domain-containing protein 2 isoform X3
C2 domain-containing protein 2 isoform X5
zinc finger and BTB domain containing 21, transcript variant 2
zinc finger and BTB domain containing 21, transcript variant 3
zinc finger and BTB domain containing 21, transcript variant 1
zinc finger and BTB domain containing 21, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 95 ESTs, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
zinc finger and BTB domain containing 21, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
isoform S is encoded by transcript variant 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
zinc finger and BTB domain-containing protein 21 isoform S
zinc finger and BTB domain-containing protein 21 isoform X3
isoform L is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
zinc finger and BTB domain-containing protein 21 isoform L
isoform L is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
zinc finger and BTB domain-containing protein 21 isoform X1
similar to RNA sequence, mRNA (same species):RefSeq:NM_001199527.1
similar to RNA sequence, mRNA (same species):RefSeq:NM_001199528.2
similar to RNA sequence, mRNA (same species):RefSeq:NM_173568.3
similar to RNA sequence, mRNA (same species):RefSeq:NM_001004416.2
similar to AA sequence (same species):RefSeq:NP_775839.3
isoform 2 precursor is encoded by transcript variant 2; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001004416.2
isoform 1 precursor is encoded by transcript variant 1; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001186456.1
isoform 3 is encoded by transcript variant 3; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001186457.2
isoform 4 is encoded by transcript variant 4; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ATP-binding cassette, sub-family G (WHITE), member 1, transcript variant 5
ATP-binding cassette, sub-family G (WHITE), member 1, transcript variant 6
ATP-binding cassette sub-family G member 1 isoform 5
ATP-binding cassette, sub-family G (WHITE), member 1, transcript variant 7
isoform 7 is encoded by transcript variant 7; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ATP-binding cassette sub-family G member 1 isoform 7
ATP-binding cassette, sub-family G (WHITE), member 1, transcript variant 4
ATP-binding cassette, sub-family G (WHITE), member 1, transcript variant 2
ATP-binding cassette sub-family G member 1 isoform 4
ATP-binding cassette sub-family G member 1 isoform 2
ATP-binding cassette, sub-family G (WHITE), member 1, transcript variant 3
ATP-binding cassette sub-family G member 1 isoform 3
isoform 6 is encoded by transcript variant 6; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ATP-binding cassette sub-family G member 1 isoform 6
transmembrane protease, serine 3, transcript variant G
transmembrane protease, serine 3, transcript variant F
transmembrane protease, serine 3, transcript variant A
transmembrane protease, serine 3, transcript variant C
isoform 4 is encoded by transcript variant F; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transmembrane protease serine 3 isoform 4
isoform 1 is encoded by transcript variant A; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transmembrane protease serine 3 isoform 1
isoform 2 is encoded by transcript variant C; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transmembrane protease serine 3 isoform 2
transmembrane protease, serine 3, transcript variant D
isoform 3 is encoded by transcript variant D; Derived by automated computational analysis using gene prediction method: BestRefSeq.
transmembrane protease serine 3 isoform 3
ubiquitin associated and SH3 domain containing A, transcript variant 1
ubiquitin associated and SH3 domain containing A, transcript variant 2
ubiquitin associated and SH3 domain containing A, transcript variant 3
ubiquitin associated and SH3 domain containing A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 26 ESTs, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ubiquitin associated and SH3 domain containing A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ubiquitin-associated and SH3 domain-containing protein A isoform 1
ubiquitin-associated and SH3 domain-containing protein A isoform 2
ubiquitin-associated and SH3 domain-containing protein A isoform 3
ubiquitin-associated and SH3 domain-containing protein A isoform X2
radial spoke head 1 homolog (Chlamydomonas), transcript variant 2
radial spoke head 1 homolog (Chlamydomonas), transcript variant 1
radial spoke head 1 homolog (Chlamydomonas), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95 ESTs, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 37 (glucose-6-phosphate transporter), member 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 18 ESTs, 2 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 37 (glucose-6-phosphate transporter), member 1
solute carrier family 37 (glucose-6-phosphate transporter), member 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 19 ESTs, 2 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 37 (glucose-6-phosphate transporter), member 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 20 ESTs, 2 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 37 (glucose-6-phosphate transporter), member 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 105 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
solute carrier family 37 (glucose-6-phosphate transporter), member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 33 ESTs, 2 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
solute carrier family 37 (glucose-6-phosphate transporter), member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 20 ESTs, 2 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
glycerol-3-phosphate transporter isoform X3
glycerol-3-phosphate transporter isoform X1
glycerol-3-phosphate transporter isoform X2
glycerol-3-phosphate transporter isoform X5
glycerol-3-phosphate transporter isoform X6
glycerol-3-phosphate transporter isoform X7
solute carrier family 37 (glucose-6-phosphate transporter), member 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 ESTs, 2 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glycerol-3-phosphate transporter isoform X4
uncharacterized LOC101928212, transcript variant X2
uncharacterized LOC101928212, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, and 35% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 48% coverage of the annotated genomic feature by RNAseq alignments
phosphodiesterase 9A, transcript variant 5
phosphodiesterase 9A, transcript variant 1
phosphodiesterase 9A, transcript variant 2
phosphodiesterase 9A, transcript variant 18
phosphodiesterase 9A, transcript variant 9
phosphodiesterase 9A, transcript variant 14
phosphodiesterase 9A, transcript variant 17
phosphodiesterase 9A, transcript variant 20
phosphodiesterase 9A, transcript variant 6
phosphodiesterase 9A, transcript variant 13
phosphodiesterase 9A, transcript variant 12
phosphodiesterase 9A, transcript variant 19
phosphodiesterase 9A, transcript variant 16
phosphodiesterase 9A, transcript variant 3
phosphodiesterase 9A, transcript variant 4
phosphodiesterase 9A, transcript variant 11
phosphodiesterase 9A, transcript variant 8
phosphodiesterase 9A, transcript variant 7
phosphodiesterase 9A, transcript variant 10
phosphodiesterase 9A, transcript variant 15
phosphodiesterase 9A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform e
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform a
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform b
isoform o is encoded by transcript variant 18; Derived by automated computational analysis using gene prediction method: BestRefSeq.
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform o
isoform h is encoded by transcript variant 9; Derived by automated computational analysis using gene prediction method: BestRefSeq.
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform h
isoform l is encoded by transcript variant 13; Derived by automated computational analysis using gene prediction method: BestRefSeq.
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform l
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform d
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform X2
isoform n is encoded by transcript variant 17; Derived by automated computational analysis using gene prediction method: BestRefSeq.
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform n
isoform f is encoded by transcript variant 6; Derived by automated computational analysis using gene prediction method: BestRefSeq.
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform f
isoform k is encoded by transcript variant 12; Derived by automated computational analysis using gene prediction method: BestRefSeq.
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform k
isoform m is encoded by transcript variant 16; Derived by automated computational analysis using gene prediction method: BestRefSeq.
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform m
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform c
isoform i is encoded by transcript variant 10; Derived by automated computational analysis using gene prediction method: BestRefSeq.
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform i
isoform j is encoded by transcript variant 11; Derived by automated computational analysis using gene prediction method: BestRefSeq.
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform j
isoform j is encoded by transcript variant 15; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, and 78% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
isoform g is encoded by transcript variant 19; Derived by automated computational analysis using gene prediction method: BestRefSeq.
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform g
isoform g is encoded by transcript variant 8; Derived by automated computational analysis using gene prediction method: BestRefSeq.
isoform g is encoded by transcript variant 14; Derived by automated computational analysis using gene prediction method: BestRefSeq.
isoform g is encoded by transcript variant 20; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
WD repeat domain 4, transcript variant 2
WD repeat domain 4, transcript variant 7
similar to RNA sequence (same species):RefSeq:NR_048535.1
WD repeat domain 4, transcript variant 5
similar to RNA sequence, mRNA (same species):RefSeq:NM_001260476.1
WD repeat domain 4, transcript variant 4
similar to RNA sequence, mRNA (same species):RefSeq:NM_001260475.1
WD repeat domain 4, transcript variant 3
similar to RNA sequence, mRNA (same species):RefSeq:NM_001260474.1
WD repeat domain 4, transcript variant 1
similar to RNA sequence, mRNA (same species):RefSeq:NM_018669.5
WD repeat domain 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 ESTs, 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
WD repeat domain 4, transcript variant 6
similar to RNA sequence, mRNA (same species):RefSeq:NM_001260477.1
tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit WDR4 isoform 2
tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit WDR4 isoform 1
tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit WDR4 isoform X1
isoform 3 is encoded by transcript variant 4; Derived by automated computational analysis using gene prediction method: BestRefSeq.
tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit WDR4 isoform 3
isoform 3 is encoded by transcript variant 6; Derived by automated computational analysis using gene prediction method: BestRefSeq.
NADH dehydrogenase (ubiquinone) flavoprotein 3, 10kDa, transcript variant 1
NADH dehydrogenase (ubiquinone) flavoprotein 3, 10kDa, transcript variant 2
NADH dehydrogenase [ubiquinone] flavoprotein 3, mitochondrial isoform a precursor
NADH dehydrogenase [ubiquinone] flavoprotein 3, mitochondrial isoform b precursor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
PBX/knotted 1 homeobox 1, transcript variant 1
PBX/knotted 1 homeobox 1, transcript variant 2
cystathionine-beta-synthase, transcript variant 3
cystathionine-beta-synthase, transcript variant 2
cystathionine-beta-synthase, transcript variant 1
cystathionine-beta-synthase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 152 ESTs, 8 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
U2 small nuclear RNA auxiliary factor 1, transcript variant a
U2 small nuclear RNA auxiliary factor 1, transcript variant b
U2 small nuclear RNA auxiliary factor 1, transcript variant c
isoform a is encoded by transcript variant a; Derived by automated computational analysis using gene prediction method: BestRefSeq.
splicing factor U2AF 35 kDa subunit isoform a
isoform b is encoded by transcript variant b; Derived by automated computational analysis using gene prediction method: BestRefSeq.
splicing factor U2AF 35 kDa subunit isoform b
isoform c is encoded by transcript variant c; Derived by automated computational analysis using gene prediction method: BestRefSeq.
splicing factor U2AF 35 kDa subunit isoform c
crystallin, alpha A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 199 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
long intergenic non-protein coding RNA 322
uncharacterized LOC101928399, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC101928399, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
long intergenic non-protein coding RNA 319
long intergenic non-protein coding RNA 313
heat shock transcription factor 2 binding protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
heat shock transcription factor 2 binding protein
heat shock factor 2-binding protein isoform X1
ribosomal RNA processing protein 1 homolog B
pyridoxal (pyridoxine, vitamin B6) kinase
similar to RNA sequence, mRNA (same species):RefSeq:NM_003681.4
pyridoxal (pyridoxine, vitamin B6) kinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 254 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
pyridoxal (pyridoxine, vitamin B6) kinase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 mRNAs, 381 ESTs, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
pyridoxal (pyridoxine, vitamin B6) kinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 mRNAs, 382 ESTs, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
pyridoxal (pyridoxine, vitamin B6) kinase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 mRNAs, 386 ESTs, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ribosomal RNA processing protein 1 homolog A
1-acylglycerol-3-phosphate O-acyltransferase 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 ESTs, 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
1-acylglycerol-3-phosphate O-acyltransferase 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 268 ESTs, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
1-acylglycerol-3-phosphate O-acyltransferase 3, transcript variant 1
1-acylglycerol-3-phosphate O-acyltransferase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 mRNAs, 273 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
1-acylglycerol-3-phosphate O-acyltransferase 3, transcript variant 2
1-acylglycerol-3-phosphate O-acyltransferase 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 272 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
1-acylglycerol-3-phosphate O-acyltransferase 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 273 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
1-acylglycerol-3-phosphate O-acyltransferase 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 273 ESTs, 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma isoform X1
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma isoform X2
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma isoform X3
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma isoform X4
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma isoform X6
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma isoform X5
trafficking protein particle complex 10, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
trafficking protein particle complex 10, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
trafficking protein particle complex 10, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 115 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
trafficking protein particle complex subunit 10
trafficking protein particle complex subunit 10 isoform X1
trafficking protein particle complex subunit 10 isoform X3
trafficking protein particle complex subunit 10 isoform X4
trafficking protein particle complex 10, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 111 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
trafficking protein particle complex subunit 10 isoform X2
PWP2 periodic tryptophan protein homolog (yeast)
chromosome 21 open reading frame 33, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
chromosome 21 open reading frame 33, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
chromosome 21 open reading frame 33, transcript variant X5
chromosome 21 open reading frame 33, transcript variant 1
similar to RNA sequence, mRNA (same species):RefSeq:NM_004649.6
chromosome 21 open reading frame 33, transcript variant 2
similar to RNA sequence, mRNA (same species):RefSeq:NM_198155.3
chromosome 21 open reading frame 33, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
chromosome 21 open reading frame 33, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ES1 protein homolog, mitochondrial isoform X4
ES1 protein homolog, mitochondrial isoform X6
ES1 protein homolog, mitochondrial isoform X5
similar to AA sequence (same species):RefSeq:NP_004640.3
isoform Ia precursor is encoded by transcript variant 1; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ES1 protein homolog, mitochondrial isoform Ia precursor
similar to AA sequence (same species):RefSeq:NP_937798.3
isoform Ib precursor is encoded by transcript variant 2; The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ES1 protein homolog, mitochondrial isoform Ib precursor
ES1 protein homolog, mitochondrial isoform X2
ES1 protein homolog, mitochondrial isoform X3
putative proline-rich protein 21-like, transcript variant X1
putative proline-rich protein 21-like, transcript variant X2
uncharacterized protein LOC101928533 isoform X1
uncharacterized protein LOC101928533 isoform X2
inducible T-cell co-stimulator ligand, transcript variant 2
inducible T-cell co-stimulator ligand, transcript variant 3
inducible T-cell co-stimulator ligand, transcript variant 4
inducible T-cell co-stimulator ligand, transcript variant 1
inducible T-cell co-stimulator ligand, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 64 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
DNA (cytosine-5-)-methyltransferase 3-like, transcript variant 2
DNA (cytosine-5-)-methyltransferase 3-like, transcript variant 1
DNA (cytosine-5)-methyltransferase 3-like isoform 2
DNA (cytosine-5)-methyltransferase 3-like isoform 1
autoimmune regulator, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 Protein, and 56% coverage of the annotated genomic feature by RNAseq alignments
phosphofructokinase, liver, transcript variant 1
phosphofructokinase, liver, transcript variant 2
similar to RNA sequence, mRNA (same species):RefSeq:NM_002626.4
phosphofructokinase, liver, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 274 ESTs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
phosphofructokinase, liver, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 273 ESTs, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
6-phosphofructokinase, liver type isoform X2
phosphofructokinase, liver, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 276 ESTs, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
phosphofructokinase, liver, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 275 ESTs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
6-phosphofructokinase, liver type isoform X5
6-phosphofructokinase, liver type isoform X6
phosphofructokinase, liver, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 272 ESTs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
6-phosphofructokinase, liver type isoform X3
6-phosphofructokinase, liver type isoform X4
chromosome 21 open reading frame 2, transcript variant 2
chromosome 21 open reading frame 2, transcript variant 3
chromosome 21 open reading frame 2, transcript variant 1
chromosome 21 open reading frame 2, transcript variant 4
chromosome 21 open reading frame 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
chromosome 21 open reading frame 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
chromosome 21 open reading frame 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
nuclear encoded mitochondrial protein C21orf2 isoform 2
nuclear encoded mitochondrial protein C21orf2 isoform 3
nuclear encoded mitochondrial protein C21orf2 isoform 1
transient receptor potential cation channel, subfamily M, member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 59 ESTs, 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential cation channel, subfamily M, member 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 65 ESTs, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transient receptor potential cation channel, subfamily M, member 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 19 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential cation channel, subfamily M, member 2, transcript variant 2
similar to RNA sequence (same species):RefSeq:NR_038257.1
transient receptor potential cation channel, subfamily M, member 2, transcript variant 1
similar to RNA sequence, mRNA (same species):RefSeq:NM_003307.3
similar to AA sequence (same species):RefSeq:NP_003298.1
transient receptor potential cation channel subfamily M member 2
transient receptor potential cation channel subfamily M member 2 isoform X2
transient receptor potential cation channel subfamily M member 2 isoform X3
transient receptor potential cation channel subfamily M member 2 isoform X4
transient receptor potential cation channel, subfamily M, member 2
similar to RNA sequence, mRNA (same species):RefSeq:NM_030891.3
leucine-rich repeat-containing protein 3 precursor
LRRC3 downstream neighbor (non-protein coding)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 ESTs, and 13% coverage of the annotated genomic feature by RNAseq alignments
thrombospondin-type laminin G domain and EAR repeats, transcript variant 1
thrombospondin-type laminin G domain and EAR repeats, transcript variant 2
thrombospondin-type laminin G domain and EAR repeat-containing protein isoform 1 precursor
thrombospondin-type laminin G domain and EAR repeat-containing protein isoform 2
thrombospondin-type laminin G domain and EAR repeats, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 64% coverage of the annotated genomic feature by RNAseq alignments
thrombospondin-type laminin G domain and EAR repeat-containing protein isoform X1
chromosome 21 open reading frame 90, transcript variant 1
chromosome 21 open reading frame 90, transcript variant 2
similar to RNA sequence, mRNA (same species):RefSeq:NM_198693.2
similar to RNA sequence, mRNA (same species):RefSeq:NM_198687.1
similar to AA sequence (same species):RefSeq:NP_941960.1
similar to RNA sequence, mRNA (same species):RefSeq:NM_198694.2
similar to AA sequence (same species):RefSeq:NP_941967.2
The RefSeq protein has 3 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_198688.2
similar to AA sequence (same species):RefSeq:NP_941961.2
ubiquitin-conjugating enzyme E2G 2, transcript variant 3
ubiquitin-conjugating enzyme E2G 2, transcript variant 1
ubiquitin-conjugating enzyme E2G 2, transcript variant 2
ubiquitin-conjugating enzyme E2 G2 isoform 1
ubiquitin-conjugating enzyme E2 G2 isoform 2
ubiquitin-conjugating enzyme E2 G2 isoform 3
small ubiquitin-like modifier 3, transcript variant 1
small ubiquitin-like modifier 3, transcript variant 2
small ubiquitin-related modifier 3 isoform 1 precursor
small ubiquitin-related modifier 3 isoform 2
pituitary tumor-transforming 1 interacting protein, transcript variant 2
pituitary tumor-transforming 1 interacting protein, transcript variant 3
pituitary tumor-transforming 1 interacting protein, transcript variant 1
pituitary tumor-transforming gene 1 protein-interacting protein isoform 2 precursor
pituitary tumor-transforming gene 1 protein-interacting protein isoform 1 precursor
integrin, beta 2 (complement component 3 receptor 3 and 4 subunit), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 244 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
integrin, beta 2 (complement component 3 receptor 3 and 4 subunit), transcript variant 2
similar to RNA sequence, mRNA (same species):RefSeq:NM_001127491.1
integrin, beta 2 (complement component 3 receptor 3 and 4 subunit), transcript variant 1
similar to RNA sequence, mRNA (same species):RefSeq:NM_000211.3
similar to AA sequence (same species):RefSeq:NP_000202.2
similar to AA sequence (same species):RefSeq:NP_001120963.1
ITGB2 antisense RNA 1, transcript variant 1
ITGB2 antisense RNA 1, transcript variant 2
ITGB2 antisense RNA 1, transcript variant 3
ITGB2 antisense RNA 1, transcript variant 4
ITGB2 antisense RNA 1, transcript variant 5
ITGB2 antisense RNA 1, transcript variant 6
chromosome 21 open reading frame 67, transcript variant 1
chromosome 21 open reading frame 67, transcript variant 2
family with sequence similarity 207, member A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 17 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
family with sequence similarity 207, member A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
family with sequence similarity 207, member A, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
family with sequence similarity 207, member A
family with sequence similarity 207, member A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
family with sequence similarity 207, member A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
family with sequence similarity 207, member A, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
long intergenic non-protein coding RNA 163
long intergenic non-protein coding RNA 162
similar to RNA sequence (same species):RefSeq:NR_024089.1
signal sequence receptor, delta pseudogene 1
adenosine deaminase, RNA-specific, B1, transcript variant 4
adenosine deaminase, RNA-specific, B1, transcript variant 2
adenosine deaminase, RNA-specific, B1, transcript variant 8
adenosine deaminase, RNA-specific, B1, transcript variant 3
adenosine deaminase, RNA-specific, B1, transcript variant 1
adenosine deaminase, RNA-specific, B1, transcript variant 6
adenosine deaminase, RNA-specific, B1, transcript variant 7
adenosine deaminase, RNA-specific, B1, transcript variant 5
adenosine deaminase, RNA-specific, B1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 104 ESTs, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
adenosine deaminase, RNA-specific, B1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 103 ESTs, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
double-stranded RNA-specific editase 1 isoform X2
adenosine deaminase, RNA-specific, B1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 85 ESTs, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
adenosine deaminase, RNA-specific, B1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 78 ESTs, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
adenosine deaminase, RNA-specific, B1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 100 ESTs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
adenosine deaminase, RNA-specific, B1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
double-stranded RNA-specific editase 1 isoform X3
double-stranded RNA-specific editase 1 isoform X1
double-stranded RNA-specific editase 1 isoform X5
double-stranded RNA-specific editase 1 isoform X6
double-stranded RNA-specific editase 1 isoform 3
double-stranded RNA-specific editase 1 isoform 7
double-stranded RNA-specific editase 1 isoform 2
double-stranded RNA-specific editase 1 isoform X4
double-stranded RNA-specific editase 1 isoform 1
protein O-fucosyltransferase 2, transcript variant 3
protein O-fucosyltransferase 2, transcript variant 2
protein O-fucosyltransferase 2, transcript variant 1
protein O-fucosyltransferase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 117 ESTs, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein O-fucosyltransferase 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 112 ESTs, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein O-fucosyltransferase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 111 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein O-fucosyltransferase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 112 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
GDP-fucose protein O-fucosyltransferase 2 isoform C precursor
GDP-fucose protein O-fucosyltransferase 2 isoform X1
GDP-fucose protein O-fucosyltransferase 2 isoform X3
GDP-fucose protein O-fucosyltransferase 2 isoform X2
GDP-fucose protein O-fucosyltransferase 2 isoform A precursor
protein O-fucosyltransferase 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 ESTs, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
GDP-fucose protein O-fucosyltransferase 2 isoform X4
putative uncharacterized protein encoded by LINC00205-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 ESTs, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
long intergenic non-protein coding RNA 316
uncharacterized LOC101928745, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC101928745, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC101928745, transcript variant X3
collagen, type XVIII, alpha 1, transcript variant 2
similar to RNA sequence, mRNA (same species):RefSeq:NM_130445.2
similar to AA sequence (same species):RefSeq:NP_569712.2
isoform 2 precursor is encoded by transcript variant 2; The RefSeq protein has 1 indel compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
collagen alpha-1(XVIII) chain isoform 2 precursor
COL18A1 antisense RNA 1, transcript variant 2
COL18A1 antisense RNA 1, transcript variant 1
collagen, type XVIII, alpha 1, transcript variant 1
similar to RNA sequence, mRNA (same species):RefSeq:NM_030582.3
similar to AA sequence (same species):RefSeq:NP_085059.2
isoform 1 precursor is encoded by transcript variant 1; The RefSeq protein has 1 indel compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
collagen alpha-1(XVIII) chain isoform 1 precursor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 19 (folate transporter), member 1, transcript variant 2
solute carrier family 19 (folate transporter), member 1, transcript variant 1
solute carrier family 19 (folate transporter), member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 53 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
solute carrier family 19 (folate transporter), member 1, transcript variant 3
poly(rC) binding protein 3, transcript variant 1
poly(rC) binding protein 3, transcript variant 2
collagen, type VI, alpha 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 568 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
collagen, type VI, alpha 2, transcript variant 2C2
collagen, type VI, alpha 2, transcript variant 2C2a'
collagen, type VI, alpha 2, transcript variant 2C2a
isoform 2C2 precursor is encoded by transcript variant 2C2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
collagen alpha-2(VI) chain isoform 2C2 precursor
isoform 2C2a precursor is encoded by transcript variant 2C2a; Derived by automated computational analysis using gene prediction method: BestRefSeq.
collagen alpha-2(VI) chain isoform 2C2a precursor
isoform 2C2a' precursor is encoded by transcript variant 2C2a'; Derived by automated computational analysis using gene prediction method: BestRefSeq.
collagen alpha-2(VI) chain isoform 2C2a' precursor
formimidoyltransferase cyclodeaminase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
formimidoyltransferase cyclodeaminase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
formimidoyltransferase cyclodeaminase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
formimidoyltransferase cyclodeaminase, transcript variant B
formimidoyltransferase cyclodeaminase, transcript variant A
formimidoyltransferase-cyclodeaminase isoform X1
formimidoyltransferase-cyclodeaminase isoform X3
formimidoyltransferase-cyclodeaminase isoform X2
spermatogenesis and centriole associated 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 60 ESTs, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
spermatogenesis and centriole associated 1-like, transcript variant 2
spermatogenesis and centriole associated 1-like, transcript variant 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
lanosterol synthase (2,3-oxidosqualene-lanosterol cyclase), transcript variant 2
lanosterol synthase (2,3-oxidosqualene-lanosterol cyclase), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 258 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
lanosterol synthase (2,3-oxidosqualene-lanosterol cyclase), transcript variant 3
lanosterol synthase (2,3-oxidosqualene-lanosterol cyclase), transcript variant 1
lanosterol synthase (2,3-oxidosqualene-lanosterol cyclase), transcript variant 4
lanosterol synthase (2,3-oxidosqualene-lanosterol cyclase), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 212 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, and 70% coverage of the annotated genomic feature by RNAseq alignments
minichromosome maintenance complex component 3 associated protein
minichromosome maintenance complex component 3 associated protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 mRNAs, 233 ESTs, 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
minichromosome maintenance complex component 3 associated protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 mRNAs, 233 ESTs, 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
minichromosome maintenance complex component 3 associated protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 mRNAs, 234 ESTs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
minichromosome maintenance complex component 3 associated protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 mRNAs, 232 ESTs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
minichromosome maintenance complex component 3 associated protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 mRNAs, 232 ESTs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
minichromosome maintenance complex component 3 associated protein, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 217 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
germinal-center associated nuclear protein
germinal-center associated nuclear protein isoform X1
germinal-center associated nuclear protein isoform X2
germinal-center associated nuclear protein isoform X3
germinal-center associated nuclear protein isoform X4
germinal-center associated nuclear protein isoform X5
germinal-center associated nuclear protein isoform X6
ybeY metallopeptidase (putative), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 15 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ybeY metallopeptidase (putative), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 55 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
ybeY metallopeptidase (putative), transcript variant X4
ybeY metallopeptidase (putative), transcript variant 1
ybeY metallopeptidase (putative), transcript variant 2
ybeY metallopeptidase (putative), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
chromosome 21 open reading frame 58, transcript variant 2
chromosome 21 open reading frame 58, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 ESTs, and 97% coverage of the annotated genomic feature by RNAseq alignments
chromosome 21 open reading frame 58, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 19 ESTs, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
chromosome 21 open reading frame 58, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 20 ESTs, 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein C21orf58 isoform X2
uncharacterized protein C21orf58 isoform X7
chromosome 21 open reading frame 58, transcript variant 1
similar to RNA sequence, mRNA (same species):RefSeq:NM_058180.4
The RefSeq transcript has 3 indels compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
chromosome 21 open reading frame 58, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 28 ESTs, 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
chromosome 21 open reading frame 58, transcript variant 4
similar to RNA sequence, mRNA (same species):RefSeq:NM_001286476.1
chromosome 21 open reading frame 58, transcript variant 5
similar to RNA sequence, mRNA (same species):RefSeq:NM_001286477.1
The RefSeq transcript has 2 indels compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
chromosome 21 open reading frame 58, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 12 ESTs, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
chromosome 21 open reading frame 58, transcript variant 3
similar to RNA sequence, mRNA (same species):RefSeq:NM_001286463.1
chromosome 21 open reading frame 58, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 22 ESTs, 2 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein C21orf58 isoform 1
uncharacterized protein C21orf58 isoform X1
uncharacterized protein C21orf58 isoform 2
uncharacterized protein C21orf58 isoform X8
uncharacterized protein C21orf58 isoform X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 102 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 102 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 101 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 92 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DIP2 disco-interacting protein 2 homolog A (Drosophila), transcript variant 1
DIP2 disco-interacting protein 2 homolog A (Drosophila), transcript variant 7
DIP2 disco-interacting protein 2 homolog A (Drosophila), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 49 ESTs, 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DIP2 disco-interacting protein 2 homolog A (Drosophila), transcript variant 5
DIP2 disco-interacting protein 2 homolog A (Drosophila), transcript variant 2
DIP2 disco-interacting protein 2 homolog A (Drosophila), transcript variant 3
DIP2 disco-interacting protein 2 homolog A (Drosophila), transcript variant 6
DIP2 disco-interacting protein 2 homolog A (Drosophila), transcript variant 4
disco-interacting protein 2 homolog A isoform a
disco-interacting protein 2 homolog A isoform g
disco-interacting protein 2 homolog A isoform X1
disco-interacting protein 2 homolog A isoform e
disco-interacting protein 2 homolog A isoform b
disco-interacting protein 2 homolog A isoform c
disco-interacting protein 2 homolog A isoform f
disco-interacting protein 2 homolog A isoform d
DIP2A intronic transcript 1 (non-protein coding)
protein arginine methyltransferase 2, transcript variant 1
protein arginine methyltransferase 2, transcript variant 2
protein arginine methyltransferase 2, transcript variant 7
protein arginine methyltransferase 2, transcript variant 3
protein arginine methyltransferase 2, transcript variant 6
protein arginine methyltransferase 2, transcript variant 8
protein arginine methyltransferase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 217 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
protein arginine methyltransferase 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 188 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
protein arginine methyltransferase 2, transcript variant 5
protein arginine methyltransferase 2, transcript variant 4
protein arginine methyltransferase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 120 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
protein arginine methyltransferase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 183 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein arginine N-methyltransferase 2 isoform 5
protein arginine N-methyltransferase 2 isoform X2
protein arginine N-methyltransferase 2 isoform 6
protein arginine N-methyltransferase 2 isoform 1
protein arginine N-methyltransferase 2 isoform X1
protein arginine N-methyltransferase 2 isoform 2
isoform 7 is encoded by transcript variant 8; Derived by automated computational analysis using gene prediction method: BestRefSeq.
protein arginine N-methyltransferase 2 isoform 7
protein arginine N-methyltransferase 2 isoform X4
protein arginine N-methyltransferase 2 isoform 4
protein arginine N-methyltransferase 2 isoform X3
protein arginine N-methyltransferase 2 isoform 3