Cervus elaphus chromosome 25, mCerEla1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Laurasiatheria; Artiodactyla; Ruminantia; Pecora; Cervidae; Cervinae; Cervus.
REFSEQ INFORMATION: The reference sequence is identical to\nOU343102.1.\nAssembly name: mCerEla1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2021/07/07. The original whole-genome shotgun project has the\naccession CAJVBL000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Cervus elaphus Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
ankyrin repeat domain-containing protein 26-like
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
COORDINATES: polyA evidence [ECO:0006239]
slit guidance ligand 3, transcript variant X1
slit guidance ligand 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF01210
eukaryotic translation initiation factor 4B-like
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
spindle apparatus coiled-coil protein 1, transcript variant X4
spindle apparatus coiled-coil protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 ESTs, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
spindle apparatus coiled-coil protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 ESTs, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
spindle apparatus coiled-coil protein 1, transcript variant X5
spindle apparatus coiled-coil protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 5 ESTs, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
dedicator of cytokinesis 2, transcript variant X2
dedicator of cytokinesis protein 2 isoform X2
dedicator of cytokinesis 2, transcript variant X1
dedicator of cytokinesis protein 2 isoform X1
inhibitory synaptic factor family member 2B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 89% 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, 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA cysteine (anticodon ACA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
chromosome 25 C5orf58 homolog, transcript variant X1
chromosome 25 C5orf58 homolog, transcript variant X10
putative uncharacterized protein C5orf58 homolog isoform X1
chromosome 25 C5orf58 homolog, transcript variant X7
chromosome 25 C5orf58 homolog, transcript variant X3
chromosome 25 C5orf58 homolog, transcript variant X2
chromosome 25 C5orf58 homolog, transcript variant X8
chromosome 25 C5orf58 homolog, transcript variant X4
chromosome 25 C5orf58 homolog, transcript variant X9
chromosome 25 C5orf58 homolog, transcript variant X11
chromosome 25 C5orf58 homolog, transcript variant X5
chromosome 25 C5orf58 homolog, transcript variant X6
chromosome 25 C5orf58 homolog, transcript variant X12
putative uncharacterized protein C5orf58 homolog isoform X2
lymphocyte cytosolic protein 2, transcript variant X2
lymphocyte cytosolic protein 2, transcript variant X1
lymphocyte cytosolic protein 2, transcript variant X4
lymphocyte cytosolic protein 2, transcript variant X3
lymphocyte cytosolic protein 2 isoform X4
lymphocyte cytosolic protein 2 isoform X3
lymphocyte cytosolic protein 2 isoform X2
lymphocyte cytosolic protein 2 isoform X1
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
potassium voltage-gated channel interacting protein 1, transcript variant X1
Kv channel-interacting protein 1 isoform X1
potassium calcium-activated channel subfamily M regulatory beta subunit 1
calcium-activated potassium channel subunit beta-1
potassium voltage-gated channel interacting protein 1, transcript variant X4
potassium voltage-gated channel interacting protein 1, transcript variant X2
potassium voltage-gated channel interacting protein 1, transcript variant X3
Kv channel-interacting protein 1 isoform X2
Kv channel-interacting protein 1 isoform X3
Kv channel-interacting protein 1 isoform X4
gamma-aminobutyric acid type A receptor subunit pi, transcript variant X1
gamma-aminobutyric acid type A receptor subunit pi, transcript variant X2
gamma-aminobutyric acid receptor subunit pi isoform X2
gamma-aminobutyric acid receptor subunit pi isoform X1
RAN binding protein 17, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RAN binding protein 17, transcript variant X4
RAN binding protein 17, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
RAN binding protein 17, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 4 ESTs, 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
F-box and WD repeat domain containing 11, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 ESTs, 21 Proteins, 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 Protein, and 16% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
F-box and WD repeat domain containing 11, transcript variant X5
F-box and WD repeat domain containing 11, transcript variant X4
F-box and WD repeat domain containing 11, transcript variant X1
F-box and WD repeat domain containing 11, transcript variant X7
F-box and WD repeat domain containing 11, transcript variant X6
F-box and WD repeat domain containing 11, transcript variant X3
F-box/WD repeat-containing protein 11 isoform X5
F-box/WD repeat-containing protein 11 isoform X3
F-box/WD repeat-containing protein 11 isoform X2
F-box/WD repeat-containing protein 11 isoform X1
F-box/WD repeat-containing protein 11 isoform X4
serine/threonine kinase 10, transcript variant X2
serine/threonine kinase 10, transcript variant X1
serine/threonine kinase 10, transcript variant X3
serine/threonine-protein kinase 10 isoform X1
serine/threonine-protein kinase 10 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
EF-hand calcium-binding domain-containing protein 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
neuralized E3 ubiquitin protein ligase 1B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72% coverage of the annotated genomic feature by RNAseq alignments
endoplasmic reticulum-golgi intermediate compartment 1
endoplasmic reticulum-Golgi intermediate compartment protein 1
ribosomal protein L26 like 1, transcript variant X1
ribosomal protein L26 like 1, transcript variant X2
CREB3 regulatory factor, transcript variant X1
CREB3 regulatory factor, transcript variant X2
uncharacterized LOC122683788, transcript variant X11
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 5 samples with support for all annotated introns
uncharacterized LOC122683788, transcript variant X15
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 2 samples with support for all annotated introns
uncharacterized LOC122683788, transcript variant X6
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
uncharacterized LOC122683788, transcript variant X10
uncharacterized LOC122683788, transcript variant X5
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
uncharacterized LOC122683788, transcript variant X13
uncharacterized LOC122683788, transcript variant X14
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
uncharacterized LOC122683788, transcript variant X12
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 LOC122683788, transcript variant X7
uncharacterized LOC122683788, transcript variant X4
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 6 samples with support for all annotated introns
uncharacterized LOC122683788, transcript variant X9
uncharacterized LOC122683788, transcript variant X8
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 LOC122683788, transcript variant X1
uncharacterized LOC122683788, transcript variant X2
uncharacterized LOC122683788, transcript variant X3
uncharacterized protein LOC122683788 isoform X2
uncharacterized protein LOC122683788 isoform X3
uncharacterized protein LOC122683788 isoform X1
uncharacterized LOC122683788, transcript variant X16
biorientation of chromosomes in cell division 1
biorientation of chromosomes in cell division protein 1
uncharacterized LOC122683794, transcript variant X1
uncharacterized LOC122683794, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00406
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cytoplasmic polyadenylation element binding protein 4, transcript variant X1
cytoplasmic polyadenylation element binding protein 4, transcript variant X3
cytoplasmic polyadenylation element binding protein 4, transcript variant X2
cytoplasmic polyadenylation element-binding protein 4 isoform X1
cytoplasmic polyadenylation element-binding protein 4 isoform X2
cytoplasmic polyadenylation element-binding protein 4 isoform X3
chromosome 25 C5orf47 homolog, transcript variant X1
chromosome 25 C5orf47 homolog, transcript variant X2
uncharacterized protein C5orf47 homolog isoform X2
uncharacterized protein C5orf47 homolog isoform X1
neuronal vesicle trafficking associated 2
neuronal vesicle trafficking-associated protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
family with sequence similarity 169 member A, transcript variant X1
family with sequence similarity 169 member A, transcript variant X4
family with sequence similarity 169 member A, transcript variant X6
family with sequence similarity 169 member A, transcript variant X2
family with sequence similarity 169 member A, transcript variant X7
family with sequence similarity 169 member A, transcript variant X5
family with sequence similarity 169 member A, transcript variant X3
soluble lamin-associated protein of 75 kDa isoform X1
soluble lamin-associated protein of 75 kDa isoform X2
soluble lamin-associated protein of 75 kDa isoform X3
family with sequence similarity 169 member A, transcript variant X8
soluble lamin-associated protein of 75 kDa isoform X4
ribosome biogenesis protein NSA2 homolog
GTP dependent ribosome recycling factor mitochondrial 2, transcript variant X2
GTP dependent ribosome recycling factor mitochondrial 2, transcript variant X1
ribosome-releasing factor 2, mitochondrial isoform X1
ribosome-releasing factor 2, mitochondrial isoform X2
GTP dependent ribosome recycling factor mitochondrial 2, transcript variant X3
GTP dependent ribosome recycling factor mitochondrial 2, transcript variant X4
ribosome-releasing factor 2, mitochondrial isoform X3
GTP dependent ribosome recycling factor mitochondrial 2, transcript variant X5
ribosome-releasing factor 2, mitochondrial isoform X4
beta-hexosaminidase subunit beta-like, transcript variant X1
beta-hexosaminidase subunit beta-like isoform X1
beta-hexosaminidase subunit beta-like, transcript variant X2
beta-hexosaminidase subunit beta-like isoform X2
ectodermal-neural cortex 1, transcript variant X2
ectodermal-neural cortex 1, transcript variant X1
uncharacterized LOC122683854, 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 6 samples with support for all annotated introns
uncharacterized LOC122683854, transcript variant X4
uncharacterized LOC122683854, transcript variant X1
uncharacterized LOC122683854, transcript variant X6
uncharacterized LOC122683854, transcript variant 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 8 samples with support for all annotated introns
uncharacterized LOC122683854, transcript variant X5
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
transfer RNA arginine (anticodon UCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Rho guanine nucleotide exchange factor 28, transcript variant X6
Rho guanine nucleotide exchange factor 28, transcript variant X5
Rho guanine nucleotide exchange factor 28, transcript variant X1
Rho guanine nucleotide exchange factor 28, transcript variant X2
Rho guanine nucleotide exchange factor 28, transcript variant X3
Rho guanine nucleotide exchange factor 28, transcript variant X4
Rho guanine nucleotide exchange factor 28, transcript variant X7
rho guanine nucleotide exchange factor 28 isoform X5
rho guanine nucleotide exchange factor 28 isoform X1
rho guanine nucleotide exchange factor 28 isoform X2
rho guanine nucleotide exchange factor 28 isoform X3
rho guanine nucleotide exchange factor 28 isoform X4
rho guanine nucleotide exchange factor 28 isoform X6
UTP15 small subunit processome component
U3 small nucleolar RNA-associated protein 15 homolog
basic transcription factor 3, transcript variant X2
basic transcription factor 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transmembrane protein 171, transcript variant X1
transmembrane protein 171, transcript variant X2
FCH and mu domain containing endocytic adaptor 2
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
zinc finger protein 366, transcript variant X1
zinc finger protein 366, transcript variant X2
pentatricopeptide repeat domain 2, transcript variant X1
pentatricopeptide repeat domain 2, transcript variant X2
pentatricopeptide repeat domain 2, transcript variant X3
pentatricopeptide repeat-containing protein 2, mitochondrial isoform X2
pentatricopeptide repeat-containing protein 2, mitochondrial isoform X1
pentatricopeptide repeat-containing protein 2, mitochondrial isoform X3
mitochondrial ribosomal protein S27, transcript variant X1
28S ribosomal protein S27, mitochondrial isoform X1
mitochondrial ribosomal protein S27, transcript variant X2
28S ribosomal protein S27, mitochondrial isoform X2
microtubule associated protein 1B, transcript variant X1
microtubule associated protein 1B, transcript variant X2
microtubule-associated protein 1B isoform X1
microtubule-associated protein 1B isoform X2
cocaine- and amphetamine-regulated transcript protein
methylcrotonyl-CoA carboxylase subunit 2
methylcrotonoyl-CoA carboxylase beta chain, mitochondrial
B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB, transcript variant X2
B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB, transcript variant X1
transcription factor TFIIIB component B'' homolog isoform X2
transcription factor TFIIIB component B'' homolog isoform X1
survival of motor neuron 2, centromeric, transcript variant X2
survival of motor neuron 2, centromeric, transcript variant X1
survival of motor neuron 2, centromeric, transcript variant X3
NLR family apoptosis inhibitory protein, transcript variant X3
NLR family apoptosis inhibitory protein, transcript variant X1
NLR family apoptosis inhibitory protein, transcript variant X2
baculoviral IAP repeat-containing protein 1 isoform X2
baculoviral IAP repeat-containing protein 1 isoform X1
general transcription factor IIH subunit 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 21 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
MARVEL domain containing 2, transcript variant X2
MARVEL domain containing 2, transcript variant X3
MARVEL domain containing 2, transcript variant X1
RAD17 checkpoint clamp loader component, transcript variant X1
RAD17 checkpoint clamp loader component, transcript variant X4
RAD17 checkpoint clamp loader component, transcript variant X2
RAD17 checkpoint clamp loader component, transcript variant X3
cell cycle checkpoint protein RAD17 isoform X1
cell cycle checkpoint protein RAD17 isoform X2
adenylate kinase 6, transcript variant X2
adenylate kinase 6, transcript variant X1
TATA-box binding protein associated factor 9
transcription initiation factor TFIID subunit 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain containing 125, transcript variant X1
coiled-coil domain containing 125, transcript variant X4
coiled-coil domain containing 125, transcript variant X3
coiled-coil domain containing 125, transcript variant X2
coiled-coil domain containing 125, transcript variant X5
coiled-coil domain containing 125, transcript variant X6
coiled-coil domain-containing protein 125
serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit beta-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit beta-like
mitochondrial import inner membrane translocase subunit Tim23-like
cyclin dependent kinase 7, transcript variant X1
cyclin dependent kinase 7, transcript variant X3
cyclin dependent kinase 7, transcript variant X2
28S ribosomal protein S36, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
phosphoinositide-3-kinase regulatory subunit 1, transcript variant X1
phosphoinositide-3-kinase regulatory subunit 1, transcript variant X3
phosphoinositide-3-kinase regulatory subunit 1, transcript variant X2
phosphatidylinositol 3-kinase regulatory subunit alpha isoform X1
phosphatidylinositol 3-kinase regulatory subunit alpha isoform X3
phosphatidylinositol 3-kinase regulatory subunit alpha isoform X2
microtubule associated serine/threonine kinase family member 4, transcript variant X4
microtubule associated serine/threonine kinase family member 4, transcript variant X3
microtubule associated serine/threonine kinase family member 4, transcript variant X2
microtubule associated serine/threonine kinase family member 4, transcript variant X1
microtubule associated serine/threonine kinase family member 4, transcript variant X7
microtubule associated serine/threonine kinase family member 4, transcript variant X9
microtubule associated serine/threonine kinase family member 4, transcript variant X5
microtubule associated serine/threonine kinase family member 4, transcript variant X6
microtubule associated serine/threonine kinase family member 4, transcript variant X10
microtubule associated serine/threonine kinase family member 4, transcript variant X8
microtubule associated serine/threonine kinase family member 4, transcript variant X12
microtubule associated serine/threonine kinase family member 4, transcript variant X11
microtubule-associated serine/threonine-protein kinase 4 isoform X4
microtubule-associated serine/threonine-protein kinase 4 isoform X3
microtubule-associated serine/threonine-protein kinase 4 isoform X2
microtubule-associated serine/threonine-protein kinase 4 isoform X1
microtubule-associated serine/threonine-protein kinase 4 isoform X9
microtubule-associated serine/threonine-protein kinase 4 isoform X7
microtubule-associated serine/threonine-protein kinase 4 isoform X5
microtubule-associated serine/threonine-protein kinase 4 isoform X10
microtubule-associated serine/threonine-protein kinase 4 isoform X6
microtubule-associated serine/threonine-protein kinase 4 isoform X12
microtubule-associated serine/threonine-protein kinase 4 isoform X8
microtubule-associated serine/threonine-protein kinase 4 isoform X11
splicing regulatory glutamic acid and lysine rich protein 1, transcript variant X2
splicing regulatory glutamic acid and lysine rich protein 1, transcript variant X1
splicing regulatory glutamic acid and lysine rich protein 1, transcript variant X3
splicing regulatory glutamic acid and lysine rich protein 1, transcript variant X4
splicing regulatory glutamine/lysine-rich protein 1 isoform X2
splicing regulatory glutamine/lysine-rich protein 1 isoform X1
splicing regulatory glutamine/lysine-rich protein 1 isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein FAM114A2-like
erbb2 interacting protein, transcript variant X8
erbb2 interacting protein, transcript variant X7
erbb2 interacting protein, transcript variant X6
erbb2 interacting protein, transcript variant X5
erbb2 interacting protein, transcript variant X4
erbb2 interacting protein, transcript variant X3
erbb2 interacting protein, transcript variant X1
erbb2 interacting protein, transcript variant X2
transfer RNA glycine (anticodon CCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
small glutamine rich tetratricopeptide repeat co-chaperone beta, transcript variant X1
small glutamine rich tetratricopeptide repeat co-chaperone beta, transcript variant X3
small glutamine-rich tetratricopeptide repeat-containing protein beta isoform X1
small glutamine-rich tetratricopeptide repeat-containing protein beta isoform X3
small glutamine rich tetratricopeptide repeat co-chaperone beta, transcript variant X2
small glutamine-rich tetratricopeptide repeat-containing protein beta isoform X2
trafficking protein particle complex subunit 13, transcript variant X4
trafficking protein particle complex subunit 13, transcript variant X3
trafficking protein particle complex subunit 13, transcript variant X2
trafficking protein particle complex subunit 13, transcript variant X1
trafficking protein particle complex subunit 13 isoform X4
trafficking protein particle complex subunit 13 isoform X3
trafficking protein particle complex subunit 13 isoform X2
trafficking protein particle complex subunit 13 isoform X1
tripartite motif containing 23, transcript variant X1
E3 ubiquitin-protein ligase TRIM23 isoform X1
tripartite motif containing 23, transcript variant X4
tripartite motif containing 23, transcript variant X3
tripartite motif containing 23, transcript variant X2
E3 ubiquitin-protein ligase TRIM23 isoform 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 10 samples with support for all annotated introns
peptidylprolyl isomerase domain and WD repeat containing 1, transcript variant X1
peptidylprolyl isomerase domain and WD repeat containing 1, transcript variant X2
peptidylprolyl isomerase domain and WD repeat-containing protein 1 isoform X1
peptidylprolyl isomerase domain and WD repeat-containing protein 1 isoform X2
centromere protein K, transcript variant X4
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 9 samples with support for all annotated introns
centromere protein K, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
centromere protein K, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
centromere protein K, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
ADAM metallopeptidase with thrombospondin type 1 motif 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 ESTs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ADAM metallopeptidase with thrombospondin type 1 motif 6, transcript variant X8
ADAM metallopeptidase with thrombospondin type 1 motif 6, transcript variant X9
ADAM metallopeptidase with thrombospondin type 1 motif 6, transcript variant X7
ADAM metallopeptidase with thrombospondin type 1 motif 6, transcript variant X5
ADAM metallopeptidase with thrombospondin type 1 motif 6, transcript variant X6
ADAM metallopeptidase with thrombospondin type 1 motif 6, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ADAM metallopeptidase with thrombospondin type 1 motif 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ADAM metallopeptidase with thrombospondin type 1 motif 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 ESTs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 6 isoform X1
A disintegrin and metalloproteinase with thrombospondin motifs 6 isoform X3
A disintegrin and metalloproteinase with thrombospondin motifs 6 isoform X2
A disintegrin and metalloproteinase with thrombospondin motifs 6 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
CWC27 spliceosome associated cyclophilin, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
CWC27 spliceosome associated cyclophilin, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
spliceosome-associated protein CWC27 homolog isoform X2
CWC27 spliceosome associated cyclophilin, transcript variant X1
spliceosome-associated protein CWC27 homolog isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 20 ESTs, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
SREK1 interacting protein 1, transcript variant X2
SREK1 interacting protein 1, transcript variant X1
SREK1 interacting protein 1, transcript variant X3
regulator of G protein signaling 7 binding protein, transcript variant X1
regulator of G protein signaling 7 binding protein, transcript variant X2
regulator of G-protein signaling 7-binding protein isoform X1
regulator of G-protein signaling 7-binding protein isoform X2
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ring finger protein 180, transcript variant X3
ring finger protein 180, transcript variant X2
ring finger protein 180, transcript variant X4
ring finger protein 180, transcript variant X1
ring finger protein 180, transcript variant X6
ring finger protein 180, transcript variant X5
E3 ubiquitin-protein ligase RNF180 isoform X2
E3 ubiquitin-protein ligase RNF180 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 15 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 10 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat-containing protein 70
DIM1 rRNA methyltransferase and ribosome maturation factor, transcript variant X1
DIM1 rRNA methyltransferase and ribosome maturation factor, transcript variant X2
probable dimethyladenosine transferase isoform X1
DIM1 rRNA methyltransferase and ribosome maturation factor, transcript variant X3
probable dimethyladenosine transferase isoform X2
DIM1 rRNA methyltransferase and ribosome maturation factor, transcript variant X4
probable dimethyladenosine transferase isoform X3
probable dimethyladenosine transferase isoform X4
kinesin family member 2A, transcript variant X5
kinesin family member 2A, transcript variant X1
kinesin family member 2A, transcript variant X4
kinesin family member 2A, transcript variant X3
kinesin family member 2A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 82% coverage of the annotated genomic feature by RNAseq alignments
zinc finger SWIM-type containing 6, transcript variant X1
zinc finger SWIM-type containing 6, transcript variant X2
zinc finger SWIM domain-containing protein 6 isoform X1
zinc finger SWIM domain-containing protein 6 isoform X2
ESX-1 secretion-associated protein EspI-like, transcript variant X1
ESX-1 secretion-associated protein EspI-like isoform X1
ESX-1 secretion-associated protein EspI-like, transcript variant X2
uncharacterized protein LOC122683756 isoform X2
small integral membrane protein 15, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, and 62% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
small integral membrane protein 15 isoform X1
small integral membrane protein 15, transcript variant X2
small integral membrane protein 15, transcript variant X3
small integral membrane protein 15 isoform X2
NADH:ubiquinone oxidoreductase complex assembly factor 2
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
ERCC excision repair 8, CSA ubiquitin ligase complex subunit, transcript variant X3
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 13 samples with support for all annotated introns
DNA excision repair protein ERCC-8 isoform X3
ERCC excision repair 8, CSA ubiquitin ligase complex subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
ERCC excision repair 8, CSA ubiquitin ligase complex subunit, transcript variant X2
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 25 samples with support for all annotated introns
DNA excision repair protein ERCC-8 isoform X1
DNA excision repair protein ERCC-8 isoform X2
ERCC excision repair 8, CSA ubiquitin ligase complex subunit, transcript variant X5
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 16 samples with support for all annotated introns
ERCC excision repair 8, CSA ubiquitin ligase complex subunit, transcript variant X4
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 22 samples with support for all annotated introns
DNA excision repair protein ERCC-8 isoform X4
ELOVL fatty acid elongase 7, transcript variant X2
ELOVL fatty acid elongase 7, transcript variant X1
elongation of very long chain fatty acids protein 7
phosphodiesterase 4D, transcript variant X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X3
phosphodiesterase 4D, transcript variant X5
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X5
phosphodiesterase 4D, transcript variant X1
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X1
phosphodiesterase 4D, transcript variant X4
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X4
phosphodiesterase 4D, transcript variant X9
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X9
phosphodiesterase 4D, transcript variant X6
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X6
phosphodiesterase 4D, transcript variant X7
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X7
phosphodiesterase 4D, transcript variant X2
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X2
phosphodiesterase 4D, transcript variant X8
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X8
phosphodiesterase 4D, transcript variant X10
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X10
RAB3C, member RAS oncogene family, transcript variant X2
RAB3C, member RAS oncogene family, transcript variant X1
transfer RNA serine (anticodon GGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
GRB2 binding adaptor protein, transmembrane, transcript variant X2
GRB2 binding adaptor protein, transmembrane, transcript variant X1
transcriptional enhancer factor TEF-4-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transcriptional enhancer factor TEF-4-like
GC-rich promoter binding protein 1, transcript variant X3
GC-rich promoter binding protein 1, transcript variant X1
GC-rich promoter binding protein 1, transcript variant X2
mesoderm induction early response protein 3
mitogen-activated protein kinase kinase kinase 1, transcript variant X1
mitogen-activated protein kinase kinase kinase 1, transcript variant X2
mitogen-activated protein kinase kinase kinase 1, transcript variant X3
mitogen-activated protein kinase kinase kinase 1 isoform X1
mitogen-activated protein kinase kinase kinase 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat domain 55, transcript variant X1
ankyrin repeat domain 55, transcript variant X4
ankyrin repeat domain 55, transcript variant X2
ankyrin repeat domain 55, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat domain-containing protein 55
family with sequence similarity 104 member B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
COORDINATES: nucleotide motif:Rfam:12.0:RF00405
interleukin 6 cytokine family signal transducer, transcript variant X1
interleukin 6 cytokine family signal transducer, transcript variant X2
interleukin 6 cytokine family signal transducer, transcript variant X3
interleukin-6 receptor subunit beta isoform X1
interleukin-6 receptor subunit beta isoform X2
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
DEAD-box helicase 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
DEAD-box helicase 4, transcript variant X2
DEAD-box helicase 4, transcript variant X3
probable ATP-dependent RNA helicase DDX4 isoform X2
probable ATP-dependent RNA helicase DDX4 isoform X1
solute carrier family 38 member 9, transcript variant X6
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 23 samples with support for all annotated introns
solute carrier family 38 member 9, transcript variant X2
solute carrier family 38 member 9, transcript variant X1
solute carrier family 38 member 9, transcript variant X3
solute carrier family 38 member 9, transcript variant X4
solute carrier family 38 member 9, transcript variant X5
sodium-coupled neutral amino acid transporter 9 isoform X1
sodium-coupled neutral amino acid transporter 9 isoform X2
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 19 samples with support for all annotated introns
phospholipid phosphatase 1, transcript variant X2
phospholipid phosphatase 1, transcript variant X3
phospholipid phosphatase 1, transcript variant X1
DExH-box helicase 29, transcript variant X1
DExH-box helicase 29, transcript variant X2
ATP-dependent RNA helicase DHX29 isoform X1
ATP-dependent RNA helicase DHX29 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
multiciliate differentiation and DNA synthesis associated cell cycle protein
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
uncharacterized LOC122683580, transcript variant X1
uncharacterized LOC122683580, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: cell division cycle protein 20 homolog B
glutathione peroxidase 8 (putative), transcript variant X3
glutathione peroxidase 8 (putative), transcript variant X1
glutathione peroxidase 8 (putative), transcript variant X2
probable glutathione peroxidase 8 isoform X2
probable glutathione peroxidase 8 isoform X1
probable glutathione peroxidase 8 isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00598
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00108
heat shock protein family B (small) member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 ESTs, 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
transfer RNA alanine (anticodon GGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
NADH:ubiquinone oxidoreductase subunit S4
NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 40% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
molybdopterin synthase catalytic subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
integrin subunit alpha 1, transcript variant X1
integrin subunit alpha 1, transcript variant X2
pelota mRNA surveillance and ribosome rescue factor
poly(ADP-ribose) polymerase family member 8, transcript variant X4
poly(ADP-ribose) polymerase family member 8, transcript variant X3
poly(ADP-ribose) polymerase family member 8, transcript variant X1
poly(ADP-ribose) polymerase family member 8, transcript variant X2
protein mono-ADP-ribosyltransferase PARP8 isoform X4
protein mono-ADP-ribosyltransferase PARP8 isoform X3
protein mono-ADP-ribosyltransferase PARP8 isoform X1
protein mono-ADP-ribosyltransferase PARP8 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 32% 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 49% coverage of the annotated genomic feature by RNAseq alignments
hyperpolarization activated cyclic nucleotide gated potassium channel 1
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1
39S ribosomal protein S30, mitochondrial
nicotinamide nucleotide transhydrogenase, transcript variant X3
nicotinamide nucleotide transhydrogenase, transcript variant X2
nicotinamide nucleotide transhydrogenase, transcript variant X1
poly(A) binding protein interacting protein 1, transcript variant X3
poly(A) binding protein interacting protein 1, transcript variant X1
poly(A) binding protein interacting protein 1, transcript variant X2
polyadenylate-binding protein-interacting protein 1 isoform X1
polyadenylate-binding protein-interacting protein 1 isoform X2
polyadenylate-binding protein-interacting protein 1 isoform X3
chromosome 25 C5orf34 homolog, transcript variant X3
chromosome 25 C5orf34 homolog, transcript variant X4
chromosome 25 C5orf34 homolog, transcript variant X5
chromosome 25 C5orf34 homolog, transcript variant X1
chromosome 25 C5orf34 homolog, transcript variant X2
transmembrane protein 267, transcript variant X1
transmembrane protein 267, transcript variant X5
transmembrane protein 267, transcript variant X2
transmembrane protein 267, transcript variant X3
transmembrane protein 267, transcript variant X4
C-C motif chemokine ligand 28, transcript variant X3
C-C motif chemokine ligand 28, transcript variant X2
C-C motif chemokine ligand 28, transcript variant X1
3-hydroxy-3-methylglutaryl-CoA synthase 1, transcript variant X2
3-hydroxy-3-methylglutaryl-CoA synthase 1, transcript variant X1
hydroxymethylglutaryl-CoA synthase, cytoplasmic
NIM1 serine/threonine protein kinase, transcript variant X1
NIM1 serine/threonine protein kinase, transcript variant X3
NIM1 serine/threonine protein kinase, transcript variant X2
zinc finger protein 131, transcript variant X2
zinc finger protein 131, transcript variant X4
zinc finger protein 131, transcript variant X3
zinc finger protein 131, transcript variant X5
zinc finger protein 131, transcript variant X6
zinc finger protein 131, transcript variant X1
zinc finger protein 131, transcript variant X7
zinc finger protein 131, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 ESTs, 8 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain containing 152, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
coiled-coil domain containing 152, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
coiled-coil domain containing 152, transcript variant X2
coiled-coil domain-containing protein 152
growth hormone receptor, transcript variant X6
growth hormone receptor, transcript variant X3
growth hormone receptor, transcript variant X4
growth hormone receptor, transcript variant X5
growth hormone receptor, transcript variant X8
growth hormone receptor, transcript variant X7
growth hormone receptor, transcript variant X2
growth hormone receptor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 ESTs, 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: 5 mRNAs, 21 ESTs, 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
chromosome 25 C5orf51 homolog, transcript variant X2
chromosome 25 C5orf51 homolog, transcript variant X1
UPF0600 protein C5orf51 homolog isoform X2
UPF0600 protein C5orf51 homolog isoform X1
succinyl-CoA:3-ketoacid coenzyme A transferase 1, mitochondrial
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
phosphatidylinositol specific phospholipase C X domain containing 3, transcript variant X2
PI-PLC X domain-containing protein 3 isoform X2
phosphatidylinositol specific phospholipase C X domain containing 3, transcript variant X1
PI-PLC X domain-containing protein 3 isoform X1
ATP-binding cassette sub-family E member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 7 ESTs, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
maestro heat like repeat family member 2B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, and 51% coverage of the annotated genomic feature by RNAseq alignments
maestro heat-like repeat-containing protein family member 2B
caspase recruitment domain family member 6, transcript variant X2
caspase recruitment domain family member 6, transcript variant X1
caspase recruitment domain-containing protein 6 isoform X2
caspase recruitment domain-containing protein 6 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00577
protein kinase AMP-activated catalytic subunit alpha 1, transcript variant X1
5'-AMP-activated protein kinase catalytic subunit alpha-1 isoform X1
protein kinase AMP-activated catalytic subunit alpha 1, transcript variant X3
protein kinase AMP-activated catalytic subunit alpha 1, transcript variant X2
protein kinase AMP-activated catalytic subunit alpha 1, transcript variant X4
5'-AMP-activated protein kinase catalytic subunit alpha-1 isoform X2
5'-AMP-activated protein kinase catalytic subunit alpha-1 isoform X3
tetratricopeptide repeat domain 33, transcript variant X2
tetratricopeptide repeat domain 33, transcript variant X1
tetratricopeptide repeat domain 33, transcript variant X3
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 1 sample with support for all annotated introns
eukaryotic translation initiation factor 2 subunit 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: eukaryotic translation initiation factor 2 subunit 3-like
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 12 samples with support for all annotated introns
transfer RNA tyrosine (anticodon AUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
DAB adaptor protein 2, transcript variant X4
DAB adaptor protein 2, transcript variant X1
DAB adaptor protein 2, transcript variant X3
DAB adaptor protein 2, transcript variant X2
DAB adaptor protein 2, transcript variant X5
FYN binding protein 1, transcript variant X1
FYN binding protein 1, transcript variant X3
FYN binding protein 1, transcript variant X2
RPTOR independent companion of MTOR complex 2, transcript variant X1
RPTOR independent companion of MTOR complex 2, transcript variant X2
rapamycin-insensitive companion of mTOR isoform X1
rapamycin-insensitive companion of mTOR isoform X2
RPTOR independent companion of MTOR complex 2, transcript variant X3
rapamycin-insensitive companion of mTOR isoform X3
oncostatin M receptor, transcript variant X1
oncostatin M receptor, transcript variant X3
oncostatin M receptor, transcript variant X2
oncostatin-M-specific receptor subunit beta isoform X1
oncostatin-M-specific receptor subunit beta isoform X2
LIF receptor subunit alpha, transcript variant X4
LIF receptor subunit alpha, transcript variant X1
leukemia inhibitory factor receptor isoform X1
LIF receptor subunit alpha, transcript variant X3
LIF receptor subunit alpha, transcript variant X2
LIF receptor subunit alpha, transcript variant X5
leukemia inhibitory factor receptor isoform X2
EGF like, fibronectin type III and laminin G domains
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00416
glial cell derived neurotrophic factor, transcript variant X7
glial cell derived neurotrophic factor, transcript variant X10
glial cell derived neurotrophic factor, transcript variant X2
glial cell derived neurotrophic factor, transcript variant X6
glial cell line-derived neurotrophic factor isoform X2
glial cell line-derived neurotrophic factor isoform X4
glial cell derived neurotrophic factor, transcript variant X1
glial cell line-derived neurotrophic factor isoform X1
glial cell derived neurotrophic factor, transcript variant X3
glial cell derived neurotrophic factor, transcript variant X4
glial cell derived neurotrophic factor, transcript variant X5
glial cell derived neurotrophic factor, transcript variant X9
glial cell line-derived neurotrophic factor isoform X3
glial cell line-derived neurotrophic factor isoform X6
glial cell derived neurotrophic factor, transcript variant X8
glial cell line-derived neurotrophic factor isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 63% coverage of the annotated genomic feature by RNAseq alignments
ciliogenesis and planar polarity effector 1, transcript variant X2
ciliogenesis and planar polarity effector 1, transcript variant X1
ciliogenesis and planar polarity effector 1, transcript variant X8
ciliogenesis and planar polarity effector 1, transcript variant X9
ciliogenesis and planar polarity effector 1, transcript variant X11
ciliogenesis and planar polarity effector 1, transcript variant X4
ciliogenesis and planar polarity effector 1, transcript variant X10
ciliogenesis and planar polarity effector 1, transcript variant X5
ciliogenesis and planar polarity effector 1, transcript variant X6
ciliogenesis and planar polarity effector 1, transcript variant X3
ciliogenesis and planar polarity effector 1, transcript variant X7
ciliogenesis and planar polarity effector 1, transcript variant X13
ciliogenesis and planar polarity effector 1, transcript variant X14
ciliogenesis and planar polarity effector 1, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ciliogenesis and planar polarity effector 1 isoform X1
ciliogenesis and planar polarity effector 1 isoform X7
ciliogenesis and planar polarity effector 1 isoform X8
ciliogenesis and planar polarity effector 1 isoform X10
ciliogenesis and planar polarity effector 1 isoform X3
ciliogenesis and planar polarity effector 1 isoform X9
ciliogenesis and planar polarity effector 1 isoform X4
ciliogenesis and planar polarity effector 1 isoform X5
ciliogenesis and planar polarity effector 1 isoform X2
ciliogenesis and planar polarity effector 1 isoform X6
ciliogenesis and planar polarity effector 1 isoform X12
ciliogenesis and planar polarity effector 1 isoform X13
ciliogenesis and planar polarity effector 1 isoform X11
NIPBL cohesin loading factor, transcript variant X3
NIPBL cohesin loading factor, transcript variant X1
NIPBL cohesin loading factor, transcript variant X2
solute carrier family 1 member 3, transcript variant X1
solute carrier family 1 member 3, transcript variant X2
excitatory amino acid transporter 1 isoform X1
excitatory amino acid transporter 1 isoform X2
uncharacterized LOC122683544, transcript variant X2
uncharacterized LOC122683544, transcript variant X1
RAN binding protein 3 like, transcript variant X5
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 8 samples with support for all annotated introns
RAN binding protein 3 like, transcript variant X2
RAN binding protein 3 like, transcript variant X3
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 3 samples with support for all annotated introns
RAN binding protein 3 like, transcript variant X4
RAN binding protein 3 like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
RAN binding protein 3 like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
NAD kinase 2, mitochondrial, transcript variant X1
NAD kinase 2, mitochondrial, transcript variant X2
NAD kinase 2, mitochondrial, transcript variant X3
S-phase kinase associated protein 2, transcript variant X1
S-phase kinase associated protein 2, transcript variant X2
S-phase kinase-associated protein 2 isoform X1
S-phase kinase-associated protein 2 isoform X2
LMBR1 domain containing 2, transcript variant X1
LMBR1 domain containing 2, transcript variant X2
LMBR1 domain containing 2, transcript variant X3
LMBR1 domain containing 2, transcript variant X4
G-protein coupled receptor-associated protein LMBRD2 isoform X3
G-protein coupled receptor-associated protein LMBRD2 isoform X1
G-protein coupled receptor-associated protein LMBRD2 isoform X2
LMBR1 domain containing 2, transcript variant X5
G-protein coupled receptor-associated protein LMBRD2 isoform X5
G-protein coupled receptor-associated protein LMBRD2 isoform X4
UDP glycosyltransferase family 3 member A2, transcript variant X2
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 1 sample with support for all annotated introns
UDP glycosyltransferase family 3 member A2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 ESTs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
UDP-glucuronosyltransferase 3A2 isoform X2
UDP-glucuronosyltransferase 3A2 isoform X1
UDP glycosyltransferase family 3 member A1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 10 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: UDP-glucuronosyltransferase 3A1
calcyphosine like, transcript variant X2
calcyphosine like, transcript variant X1
sperm flagellar 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sperm flagellar 2, transcript variant X6
sperm flagellar 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sperm flagellar 2, 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 1 sample with support for all annotated introns
sperm flagellar 2, transcript variant X2
sperm flagellar 2, transcript variant X3
prolactin receptor, transcript variant X2
prolactin receptor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 9 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
alanine--glyoxylate aminotransferase 2, transcript variant X1
alanine--glyoxylate aminotransferase 2, transcript variant X2
alanine--glyoxylate aminotransferase 2, mitochondrial isoform X1
alanine--glyoxylate aminotransferase 2, mitochondrial isoform X2
DnaJ heat shock protein family (Hsp40) member C21
ribosome biogenesis protein BRX1 homolog
RAD1 checkpoint DNA exonuclease, transcript variant X1
RAD1 checkpoint DNA exonuclease, transcript variant X3
RAD1 checkpoint DNA exonuclease, transcript variant X2
tetratricopeptide repeat domain 23 like, transcript variant X1
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
tetratricopeptide repeat domain 23 like, transcript variant X2
tetratricopeptide repeat protein 23-like isoform X1
tetratricopeptide repeat protein 23-like isoform X2
tetratricopeptide repeat domain 23 like, transcript variant X3
tetratricopeptide repeat protein 23-like isoform X3
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC122683629, transcript variant X1
uncharacterized LOC122683629, transcript variant X2
retinoic acid induced 14, transcript variant X4
retinoic acid induced 14, transcript variant X1
retinoic acid induced 14, transcript variant X9
retinoic acid induced 14, transcript variant X5
retinoic acid induced 14, transcript variant X11
retinoic acid induced 14, transcript variant X13
retinoic acid induced 14, transcript variant X12
retinoic acid induced 14, transcript variant X6
retinoic acid induced 14, transcript variant X2
retinoic acid induced 14, transcript variant X3
retinoic acid induced 14, transcript variant X7
retinoic acid induced 14, transcript variant X8
retinoic acid induced 14, transcript variant X10
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 ESTs, 22 Proteins, 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: 55% coverage of the annotated genomic feature by RNAseq alignments
C1q and TNF related 3, transcript variant X2
C1q and TNF related 3, transcript variant X1
C1q and TNF related 3, transcript variant X3
complement C1q tumor necrosis factor-related protein 3 isoform X1
complement C1q tumor necrosis factor-related protein 3 isoform X2
complement C1q tumor necrosis factor-related protein 3 isoform X3
myosin regulatory light polypeptide 9-like
solute carrier family 45 member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
solute carrier family 45 member 2, transcript variant X2
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 2 samples with support for all annotated introns
membrane-associated transporter protein isoform X1
membrane-associated transporter protein isoform X2
ADAM metallopeptidase with thrombospondin type 1 motif 12, transcript variant X2
ADAM metallopeptidase with thrombospondin type 1 motif 12, transcript variant X1
ADAM metallopeptidase with thrombospondin type 1 motif 12, transcript variant X3
A disintegrin and metalloproteinase with thrombospondin motifs 12 isoform X2
A disintegrin and metalloproteinase with thrombospondin motifs 12 isoform X1
A disintegrin and metalloproteinase with thrombospondin motifs 12 isoform X3
ATP synthase subunit g, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
threonyl-tRNA synthetase 1, transcript variant X1
threonyl-tRNA synthetase 1, transcript variant X2
threonine--tRNA ligase 1, cytoplasmic isoform X1
threonine--tRNA ligase 1, cytoplasmic isoform X2
natriuretic peptide receptor 3, transcript variant X1
natriuretic peptide receptor 3, transcript variant X2
atrial natriuretic peptide receptor 3 isoform X2
atrial natriuretic peptide receptor 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
activated RNA polymerase II transcriptional coactivator p15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
zinc finger RNA binding protein, transcript variant X1
zinc finger RNA binding protein, transcript variant X2
zinc finger RNA binding protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
zinc finger RNA-binding protein isoform X1
zinc finger RNA-binding protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
PDZ domain containing 2, transcript variant X4
PDZ domain containing 2, transcript variant X3
PDZ domain containing 2, transcript variant X2
PDZ domain containing 2, transcript variant X1
PDZ domain containing 2, transcript variant X5
PDZ domain containing 2, transcript variant X6
PDZ domain containing 2, transcript variant X7
PDZ domain containing 2, transcript variant X9
PDZ domain containing 2, transcript variant X8
PDZ domain-containing protein 2 isoform X4
PDZ domain-containing protein 2 isoform X3
PDZ domain-containing protein 2 isoform X2
PDZ domain-containing protein 2 isoform X1
PDZ domain-containing protein 2 isoform X5
PDZ domain-containing protein 2 isoform X6
PDZ domain-containing protein 2 isoform X8
PDZ domain-containing protein 2 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
chromosome 25 C5orf22 homolog, transcript variant X1
chromosome 25 C5orf22 homolog, transcript variant X3
chromosome 25 C5orf22 homolog, transcript variant X2
UPF0489 protein C5orf22 homolog isoform X1
UPF0489 protein C5orf22 homolog isoform X2
UPF0489 protein C5orf22 homolog isoform X3
drosha ribonuclease III, transcript variant X1
drosha ribonuclease III, transcript variant X2
drosha ribonuclease III, transcript variant X4
drosha ribonuclease III, transcript variant X3
drosha ribonuclease III, transcript variant X5
uncharacterized LOC122683905, transcript variant X1
uncharacterized LOC122683905, transcript variant X2
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: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 34 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: 1 mRNA, 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00403
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 5 Proteins, 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: 5 mRNAs, 2 ESTs, 26 Proteins, and 92% 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: 13 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
MLV-related proviral Env polyprotein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC122683762, transcript variant X2
uncharacterized LOC122683762, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122683859, transcript variant X5
uncharacterized LOC122683859, transcript variant X6
uncharacterized LOC122683859, transcript variant X2
uncharacterized LOC122683859, transcript variant X3
uncharacterized LOC122683859, transcript variant X1
uncharacterized LOC122683859, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 ESTs, 4 Proteins, 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: 6 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
transcription initiation factor TFIID subunit 11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, 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: 42 Proteins
brain abundant membrane attached signal protein 1
transfer RNA serine (anticodon ACU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
reticulophagy regulator 1, transcript variant X1
reticulophagy regulator 1, transcript variant X2
zinc finger protein 622, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
zinc finger protein 622, transcript variant X1
membrane associated ring-CH-type finger 11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 4 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
F-box and leucine rich repeat protein 7, transcript variant X1
F-box and leucine rich repeat protein 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
ANKH inorganic pyrophosphate transport regulator
OTU deubiquitinase with linear linkage specificity
OTU deubiquitinase with linear linkage specificity like
trio Rho guanine nucleotide exchange factor, transcript variant X1
trio Rho guanine nucleotide exchange factor, transcript variant X2
triple functional domain protein isoform X1
triple functional domain protein isoform X2
trio Rho guanine nucleotide exchange factor, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 28 ESTs, 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
triple functional domain protein isoform X4
trio Rho guanine nucleotide exchange factor, transcript variant X3
triple functional domain protein isoform X3
methylmalonic aciduria and homocystinuria type D homolog, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 62% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00568
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 4 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
lysosomal-associated transmembrane protein 4B-like
mitochondrial import receptor subunit TOM20 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ankyrin repeat domain-containing protein 33B
translation initiation factor IF-2-like, transcript variant X7
translation initiation factor IF-2-like, transcript variant X8
translation initiation factor IF-2-like, transcript variant X5
translation initiation factor IF-2-like, transcript variant X3
translation initiation factor IF-2-like, transcript variant X6
translation initiation factor IF-2-like, transcript variant X4
translation initiation factor IF-2-like, transcript variant X2
translation initiation factor IF-2-like, transcript variant X1
uncharacterized protein LOC122683890 isoform X3
uncharacterized protein LOC122683890 isoform X6
uncharacterized protein LOC122683890 isoform X5
translation initiation factor IF-2-like isoform X7
translation initiation factor IF-2-like isoform X2
translation initiation factor IF-2-like isoform X4
translation initiation factor IF-2-like isoform X1
rhophilin associated tail protein 1 like
membrane associated ring-CH-type finger 6
carboxymethylenebutenolidase homolog, transcript variant X2
carboxymethylenebutenolidase homolog, transcript variant X1
carboxymethylenebutenolidase homolog, transcript variant X3
ATP synthase c subunit lysine N-methyltransferase, transcript variant X2
ATP synthase subunit C lysine N-methyltransferase isoform X2
ATP synthase c subunit lysine N-methyltransferase, transcript variant X1
ATP synthase subunit C lysine N-methyltransferase isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF01156
5-methyltetrahydrofolate-homocysteine methyltransferase reductase, transcript variant X2
5-methyltetrahydrofolate-homocysteine methyltransferase reductase, transcript variant X6
5-methyltetrahydrofolate-homocysteine methyltransferase reductase, transcript variant X7
5-methyltetrahydrofolate-homocysteine methyltransferase reductase, transcript variant X5
5-methyltetrahydrofolate-homocysteine methyltransferase reductase, transcript variant X1
5-methyltetrahydrofolate-homocysteine methyltransferase reductase, transcript variant X4
5-methyltetrahydrofolate-homocysteine methyltransferase reductase, transcript variant X3
methionine synthase reductase isoform X2
methionine synthase reductase isoform X3
methionine synthase reductase isoform X1
FAST kinase domains 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
FAST kinase domains 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
FAST kinase domains 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
FAST kinase domains 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
FAST kinase domain-containing protein 3, mitochondrial isoform X1
FAST kinase domain-containing protein 3, mitochondrial isoform X2
adenylate cyclase 2, transcript variant X3
adenylate cyclase 2, transcript variant X2
adenylate cyclase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST
terminal nucleotidyltransferase 4A, transcript variant X2
terminal nucleotidyltransferase 4A, transcript variant X1
terminal nucleotidyltransferase 4A isoform X2
terminal nucleotidyltransferase 4A isoform X1
RNA cytosine C(5)-methyltransferase NSUN2
COORDINATES: nucleotide motif:Rfam:12.0:RF00156
ubiquitin conjugating enzyme E2 Q family like 1, transcript variant X1
ubiquitin-conjugating enzyme E2Q-like protein 1 isoform X1
ubiquitin conjugating enzyme E2 Q family like 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
ubiquitin-conjugating enzyme E2Q-like protein 1 isoform X2
mediator complex subunit 10, transcript variant X2
mediator complex subunit 10, transcript variant X3
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 27 samples with support for all annotated introns
mediator complex subunit 10, transcript variant X1
mediator of RNA polymerase II transcription subunit 10 isoform X2
mediator of RNA polymerase II transcription subunit 10 isoform X1
interactor of little elongation complex ELL subunit 1, transcript variant X2
interactor of little elongation complex ELL subunit 1, transcript variant X1
little elongation complex subunit 1 isoform X2
little elongation complex subunit 1 isoform X1
ADAM metallopeptidase with thrombospondin type 1 motif 16, transcript variant X2
ADAM metallopeptidase with thrombospondin type 1 motif 16, transcript variant X1
A disintegrin and metalloproteinase with thrombospondin motifs 16 isoform X2
A disintegrin and metalloproteinase with thrombospondin motifs 16 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
iroquois homeobox 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
iroquois-class homeodomain protein IRX-1 isoform X2
iroquois homeobox 1, transcript variant X1
iroquois-class homeodomain protein IRX-1 isoform X1
iroquois homeobox 2, transcript variant X2
iroquois homeobox 2, transcript variant X1
iroquois-class homeodomain protein IRX-2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs
iroquois homeobox 4, transcript variant X1
iroquois homeobox 4, transcript variant X2
iroquois-class homeodomain protein IRX-4 isoform X1
iroquois-class homeodomain protein IRX-4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77% coverage of the annotated genomic feature by RNAseq alignments
NADH:ubiquinone oxidoreductase subunit S6
NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial
lysophosphatidylcholine acyltransferase 1
solute carrier family 6 member 3, transcript variant X2
solute carrier family 6 member 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium-dependent dopamine transporter isoform X1
sodium-dependent dopamine transporter isoform X2
cleft lip and palate transmembrane protein 1-like protein isoform X1
cleft lip and palate transmembrane protein 1-like protein isoform X2
telomerase reverse transcriptase, transcript variant X1
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 5 samples with support for all annotated introns
telomerase reverse transcriptase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
telomerase reverse transcriptase, transcript variant X3
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 2 samples with support for all annotated introns
telomerase reverse transcriptase isoform X1
telomerase reverse transcriptase isoform X2
telomerase reverse transcriptase isoform X3
solute carrier family 6 member 18, transcript variant X1
solute carrier family 6 member 18, transcript variant X2
inactive sodium-dependent neutral amino acid transporter B(0)AT3 isoform X1
inactive sodium-dependent neutral amino acid transporter B(0)AT3 isoform X2
solute carrier family 6 member 19, transcript variant X3
solute carrier family 6 member 19, transcript variant X2
solute carrier family 6 member 19, transcript variant X4
solute carrier family 6 member 19, transcript variant X1
sodium-dependent neutral amino acid transporter B(0)AT1
solute carrier family 12 member 7, transcript variant X1
solute carrier family 12 member 7, transcript variant X2
solute carrier family 12 member 7 isoform X1
solute carrier family 12 member 7 isoform X2
solute carrier family 12 member 7, transcript variant X5
solute carrier family 12 member 7, transcript variant X3
solute carrier family 12 member 7, transcript variant X4
solute carrier family 12 member 7 isoform X3
solute carrier family 12 member 7 isoform X4
solute carrier family 12 member 7 isoform X5
NKD inhibitor of WNT signaling pathway 2, transcript variant X1
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 26 samples with support for all annotated introns
NKD inhibitor of WNT signaling pathway 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
protein naked cuticle homolog 2 isoform X2
protein naked cuticle homolog 2 isoform X1
thyroid hormone receptor interactor 13, transcript variant X1
thyroid hormone receptor interactor 13, transcript variant X3
thyroid hormone receptor interactor 13, transcript variant X2
pachytene checkpoint protein 2 homolog isoform X3
pachytene checkpoint protein 2 homolog isoform X2
pachytene checkpoint protein 2 homolog isoform X1
bromodomain containing 9, transcript variant X1
bromodomain containing 9, transcript variant X2
bromodomain containing 9, transcript variant X3
bromodomain containing 9, transcript variant X4
bromodomain-containing protein 9 isoform X1
bromodomain-containing protein 9 isoform X2
bromodomain-containing protein 9 isoform X3
bromodomain-containing protein 9 isoform X4
tubulin polymerization promoting protein, transcript variant X2
tubulin polymerization promoting protein, transcript variant X1
tubulin polymerization promoting protein, transcript variant X4
tubulin polymerization promoting protein, transcript variant X3
tubulin polymerization-promoting protein
centrosomal protein 72, transcript variant X8
centrosomal protein 72, transcript variant X4
centrosomal protein 72, transcript variant X2
centrosomal protein 72, transcript variant X3
centrosomal protein 72, transcript variant X6
centrosomal protein 72, transcript variant X5
centrosomal protein 72, transcript variant X1
centrosomal protein 72, transcript variant X7
centrosomal protein of 72 kDa isoform X4
centrosomal protein of 72 kDa isoform X2
centrosomal protein of 72 kDa isoform X3
centrosomal protein of 72 kDa isoform X6
centrosomal protein of 72 kDa isoform X1
centrosomal protein of 72 kDa isoform X7
centrosomal protein of 72 kDa isoform X8
centrosomal protein of 72 kDa isoform X5
uncharacterized LOC122683862, transcript variant X2
uncharacterized LOC122683862, transcript variant X1
solute carrier family 9 member A3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
solute carrier family 9 member A3, transcript variant X1
exocyst complex component 3, transcript variant X2
exocyst complex component 3, transcript variant X1
aryl-hydrocarbon receptor repressor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
aryl-hydrocarbon receptor repressor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
aryl hydrocarbon receptor repressor isoform X1
aryl hydrocarbon receptor repressor isoform X2
programmed cell death 6, transcript variant X1
programmed cell death 6, transcript variant X2
programmed cell death protein 6 isoform X2
programmed cell death protein 6 isoform X1
succinate dehydrogenase complex flavoprotein subunit A
succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial
coiled-coil domain-containing protein 127
leucine-rich repeat-containing protein 14B