Aythya fuligula isolate bAytFul2 chromosome 17, bAytFul2.pri, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Archelosauria; Archosauria; Dinosauria; Saurischia; Theropoda; Coelurosauria; Aves; Neognathae; Galloanserae; Anseriformes; Anatidae; Aythyinae; Aythya.
REFSEQ INFORMATION: The reference sequence is identical to\nCM020316.1.\nAssembly name: bAytFul2.pri\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Vertebrate Genomes Project on\n2019/12/31. The original whole-genome shotgun project has the\naccession WNMM00000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Vertebrate Genomes Project\nAssembly Date :: 20-SEP-2019\nAssembly Method :: FALCON v. 2018.31.08-03.06; FALCON-Unzip\n v. 6.0.0.47841; purge_haplotigs v.\n v1.0.3+ 1.Nov.2018; scaff10x v. 4.1.0;\n Bionano Solve DLS v. 3.2.1; Salsa HiC v.\n 2.2; Arrow smrtanalysis Pacbio polishing\n & gap filling v. 6.0.0.47841; longranger\n align v. 2.2.2; freebayes Illumina\n polishing v. 1.3; gEVAL manual curation\n v. 2019-09-20; VGP assembly pipeline\n individual v. 1.5\nAssembly Name :: bAytFul2.pri\nDiploid :: Principal pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 64.03x\nSequencing Technology :: PacBio Sequel I CLR; Illumina NovaSeq;\n Arima Genomics Hi-C; Bionano Genomics DLS\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Aythya fuligula Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.3\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Patrik Ellstrom, Mahmoud Naguib, Josef Jarhult
Derived by automated computational analysis using gene prediction method: Gnomon.
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; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 86% 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; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: sushi domain-containing protein 2
kringle containing transmembrane protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
kringle containing transmembrane protein 1, transcript variant X2
kringle containing transmembrane protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
kringle containing transmembrane protein 1, transcript variant X4
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: 6 Proteins, and 98% 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; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: E3 ubiquitin-protein ligase ZNRF3
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
X-box binding protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
X-box binding protein 1, 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
coiled-coil domain-containing protein 117
solute carrier family 2, facilitated glucose transporter member 11-like, transcript variant X1
solute carrier family 2, facilitated glucose transporter member 11-like, transcript variant X2
solute carrier family 2, facilitated glucose transporter member 11-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 11-like, transcript variant X4
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 3 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 11-like isoform X1
solute carrier family 2, facilitated glucose transporter member 11-like isoform X2
solute carrier family 2, facilitated glucose transporter member 11-like, transcript variant X5
solute carrier family 2, facilitated glucose transporter member 11-like isoform X3
solute carrier family 2, facilitated glucose transporter member 11-like isoform X4
HscB mitochondrial iron-sulfur cluster cochaperone
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
iron-sulfur cluster co-chaperone protein HscB
checkpoint kinase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
checkpoint kinase 2, transcript variant X4
checkpoint kinase 2, transcript variant X1
checkpoint kinase 2, transcript variant X3
serine/threonine-protein kinase Chk2 isoform X1
serine/threonine-protein kinase Chk2 isoform X2
tetratricopeptide repeat domain 28, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tetratricopeptide repeat domain 28, transcript variant X1
tetratricopeptide repeat protein 28 isoform X1
tetratricopeptide repeat domain 28, transcript variant X3
tetratricopeptide repeat domain 28, transcript variant X4
tetratricopeptide repeat protein 28 isoform X2
tetratricopeptide repeat protein 28 isoform X3
tetratricopeptide repeat domain 28, 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 3 samples with support for all annotated introns
tetratricopeptide repeat protein 28 isoform X4
phosphatidylinositol transfer protein beta, transcript variant X1
phosphatidylinositol transfer protein beta, transcript variant X2
phosphatidylinositol transfer protein beta isoform isoform X1
phosphatidylinositol transfer protein beta isoform isoform X2
MN1 proto-oncogene, transcriptional regulator
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 11% 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
HPS4 biogenesis of lysosomal organelles complex 3 subunit 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
aspartate beta-hydroxylase domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
aspartate beta-hydroxylase domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 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: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
crystallin beta B2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
crystallin beta B2, transcript variant X1
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, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein KIAA1671 homolog
small G protein signaling modulator 1, transcript variant X2
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
small G protein signaling modulator 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
small G protein signaling modulator 1 isoform X2
small G protein signaling modulator 1 isoform X1
sodium-dependent serotonin transporter-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins
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
ankyrin repeat domain-containing protein 13A
ARF GTPase-activating protein GIT2 isoform X1
ARF GTPase-activating protein GIT2 isoform X5
ARF GTPase-activating protein GIT2 isoform X7
ARF GTPase-activating protein GIT2 isoform X8
ARF GTPase-activating protein GIT2 isoform X2
ARF GTPase-activating protein GIT2 isoform X3
ARF GTPase-activating protein GIT2 isoform X6
ARF GTPase-activating protein GIT2 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
trichoplein keratin filament-binding protein
transient receptor potential cation channel subfamily V member 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 2% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 222 member A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin protein ligase E3B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ubiquitin protein ligase E3B, transcript variant X1
potassium channel tetramerization domain containing 10, transcript variant X1
potassium channel tetramerization domain containing 10, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3 isoform X1
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 44% 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 12% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
alkB homolog 2, alpha-ketoglutarate dependent dioxygenase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin specific peptidase 30, transcript variant X2
ubiquitin specific peptidase 30, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 30 isoform X2
ubiquitin carboxyl-terminal hydrolase 30 isoform X1
D-amino acid oxidase, transcript variant X2
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
D-amino acid oxidase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
slingshot protein phosphatase 1, transcript variant X4
protein phosphatase Slingshot homolog 1 isoform X3
slingshot protein phosphatase 1, transcript variant X1
slingshot protein phosphatase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
slingshot protein phosphatase 1, transcript variant X2
protein phosphatase Slingshot homolog 1 isoform X2
protein phosphatase Slingshot homolog 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% 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 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
iron-sulfur cluster assembly enzyme ISCU, mitochondrial
spliceosome associated factor 3, U4/U6 recycling protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
squamous cell carcinoma antigen recognized by T-cells 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein tyrosine phosphatase non-receptor type 11
tyrosine-protein phosphatase non-receptor type 11
HECT domain E3 ubiquitin protein ligase 4, transcript variant X1
HECT domain E3 ubiquitin protein ligase 4, transcript variant X3
HECT domain E3 ubiquitin protein ligase 4, transcript variant X2
HECT domain E3 ubiquitin protein ligase 4, transcript variant X4
probable E3 ubiquitin-protein ligase HECTD4 isoform X1
probable E3 ubiquitin-protein ligase HECTD4 isoform X3
probable E3 ubiquitin-protein ligase HECTD4 isoform X2
probable E3 ubiquitin-protein ligase HECTD4 isoform X4
HECT domain E3 ubiquitin protein ligase 4, transcript variant X5
probable E3 ubiquitin-protein ligase HECTD4 isoform X5
TRAF-type zinc finger domain containing 1
TRAF-type zinc finger domain-containing protein 1
N-alpha-acetyltransferase 25, NatB auxiliary subunit, transcript variant X1
N-alpha-acetyltransferase 25, NatB auxiliary subunit, transcript variant X2
N-alpha-acetyltransferase 25, NatB auxiliary subunit isoform X1
N-alpha-acetyltransferase 25, NatB auxiliary subunit isoform X2
endoplasmic reticulum resident protein 29
disintegrin and metalloproteinase domain-containing protein 20-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 6% 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 Proteins, and 3% coverage of the annotated genomic feature by RNAseq alignments
MAPK activated protein kinase 5, transcript variant X1
MAPK activated protein kinase 5, transcript variant X2
MAP kinase-activated protein kinase 5 isoform X2
MAP kinase-activated protein kinase 5 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 65% 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 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 59% 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: deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: SH2B adapter protein 3
PH domain containing endocytic trafficking adaptor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 36% 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: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
myosin regulatory light chain 2, ventricular/cardiac muscle isoform
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 63
protein phosphatase 1 catalytic subunit gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine/threonine-protein phosphatase PP1-gamma catalytic subunit
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 2 samples with support for all annotated introns
RAD9 checkpoint clamp component B, transcript variant X2
RAD9 checkpoint clamp component B, transcript variant X3
RAD9 checkpoint clamp component B, transcript variant X1
RAD9 checkpoint clamp component B, transcript variant X4
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 1 sample with support for all annotated introns
RAD9 checkpoint clamp component B, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cell cycle checkpoint control protein RAD9B isoform X2
cell cycle checkpoint control protein RAD9B isoform X3
cell cycle checkpoint control protein RAD9B isoform X1
cell cycle checkpoint control protein RAD9B isoform X4
cell cycle checkpoint control protein RAD9B isoform X5
VPS29 retromer complex component, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
VPS29 retromer complex component, transcript variant X1
vacuolar protein sorting-associated protein 29 isoform X1
vacuolar protein sorting-associated protein 29 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
arginine and serine rich coiled-coil 2, transcript variant X1
arginine and serine rich coiled-coil 2, transcript variant X2
arginine/serine-rich coiled-coil protein 2 isoform X1
arginine/serine-rich coiled-coil protein 2 isoform X2
arginine and serine rich coiled-coil 2, transcript variant X3
arginine/serine-rich coiled-coil protein 2 isoform X3
zinc finger CCHC-type containing 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger CCHC-type containing 8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger CCHC domain-containing protein 8 isoform X2
zinc finger CCHC domain-containing protein 8 isoform X1
CAP-Gly domain containing linker protein 1, transcript variant X1
CAP-Gly domain containing linker protein 1, transcript variant X2
CAP-Gly domain containing linker protein 1, transcript variant X6
CAP-Gly domain containing linker protein 1, transcript variant X10
CAP-Gly domain containing linker protein 1, transcript variant X7
CAP-Gly domain containing linker protein 1, transcript variant X4
CAP-Gly domain containing linker protein 1, transcript variant X5
CAP-Gly domain containing linker protein 1, transcript variant X8
CAP-Gly domain containing linker protein 1, transcript variant X9
CAP-Gly domain containing linker protein 1, transcript variant X3
CAP-Gly domain containing linker protein 1, transcript variant X12
CAP-Gly domain containing linker protein 1, transcript variant X11
CAP-Gly domain-containing linker protein 1 isoform X1
CAP-Gly domain-containing linker protein 1 isoform X2
CAP-Gly domain-containing linker protein 1 isoform X6
CAP-Gly domain-containing linker protein 1 isoform X10
CAP-Gly domain-containing linker protein 1 isoform X7
CAP-Gly domain-containing linker protein 1 isoform X4
CAP-Gly domain-containing linker protein 1 isoform X5
CAP-Gly domain-containing linker protein 1 isoform X8
CAP-Gly domain-containing linker protein 1 isoform X9
CAP-Gly domain-containing linker protein 1 isoform X3
CAP-Gly domain-containing linker protein 1 isoform X11
VPS33A core subunit of CORVET and HOPS complexes
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
vacuolar protein sorting-associated protein 33A
diablo IAP-binding mitochondrial protein
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat-containing protein 43
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
BAF chromatin remodeling complex subunit BCL7A
B-cell CLL/lymphoma 7 protein family member A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
cilia- and flagella-associated protein 251
26S proteasome non-ATPase regulatory subunit 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SET domain containing 1B, histone lysine methyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
histone-lysine N-methyltransferase SETD1B
ras homolog family member F, filopodia associated
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
ORAI calcium release-activated calcium modulator 1, transcript variant X1
ORAI calcium release-activated calcium modulator 1, transcript variant X2
calcium release-activated calcium channel protein 1 isoform X1
calcium release-activated calcium channel protein 1 isoform X2
lysine demethylase 2B, transcript variant X2
lysine demethylase 2B, transcript variant X1
lysine demethylase 2B, transcript variant X5
lysine demethylase 2B, transcript variant X3
lysine demethylase 2B, transcript variant X8
lysine demethylase 2B, transcript variant X6
lysine demethylase 2B, transcript variant X4
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 2 samples with support for all annotated introns
lysine-specific demethylase 2B isoform X1
lysine-specific demethylase 2B isoform X4
lysine-specific demethylase 2B isoform X2
lysine-specific demethylase 2B isoform X7
lysine-specific demethylase 2B isoform X5
lysine-specific demethylase 2B isoform X3
lysine demethylase 2B, transcript variant X7
lysine-specific demethylase 2B isoform X6
anaphase promoting complex subunit 5, transcript variant X1
anaphase promoting complex subunit 5, transcript variant X2
anaphase-promoting complex subunit 5 isoform X1
anaphase-promoting complex subunit 5 isoform X2
calcium/calmodulin dependent protein kinase kinase 2, transcript variant X3
calcium/calmodulin dependent protein kinase kinase 2, transcript variant X2
calcium/calmodulin dependent protein kinase kinase 2, transcript variant X1
calcium/calmodulin dependent protein kinase kinase 2, transcript variant X5
calcium/calmodulin dependent protein kinase kinase 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
calcium/calmodulin dependent protein kinase kinase 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
calcium/calmodulin dependent protein kinase kinase 2, transcript variant X4
calcium/calmodulin-dependent protein kinase kinase 2 isoform X1
calcium/calmodulin-dependent protein kinase kinase 2 isoform X2
calcium/calmodulin-dependent protein kinase kinase 2 isoform X3
calcium/calmodulin-dependent protein kinase kinase 2 isoform X4
purinergic receptor P2X 4, transcript variant X1
purinergic receptor P2X 4, transcript variant X2
intraflagellar transport protein 81 homolog
ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sarcoplasmic/endoplasmic reticulum calcium ATPase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
actin related protein 2/3 complex subunit 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
actin-related protein 2/3 complex subunit 3
GPN-loop GTPase 3, transcript variant X1
GPN-loop GTPase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
density regulated re-initiation and release factor
coiled-coil domain-containing protein 62
huntingtin interacting protein 1 related
huntingtin-interacting protein 1-related protein
vacuolar protein sorting-associated protein 37B
ATP binding cassette subfamily B member 9
ATP-binding cassette sub-family B member 9
2-oxoglutarate and iron dependent oxygenase domain containing 2, transcript variant X1
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 2 isoform X1
2-oxoglutarate and iron dependent oxygenase domain containing 2, transcript variant X2
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 2 isoform X2
ADP ribosylation factor like GTPase 6 interacting protein 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ADP ribosylation factor like GTPase 6 interacting protein 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ADP-ribosylation factor-like protein 6-interacting protein 4
phosphatidylinositol transfer protein membrane associated 2, transcript variant X4
phosphatidylinositol transfer protein membrane associated 2, transcript variant X6
phosphatidylinositol transfer protein membrane associated 2, transcript variant X5
phosphatidylinositol transfer protein membrane associated 2, transcript variant X1
phosphatidylinositol transfer protein membrane associated 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phosphatidylinositol transfer protein membrane associated 2, transcript variant X3
membrane-associated phosphatidylinositol transfer protein 2 isoform X4
membrane-associated phosphatidylinositol transfer protein 2 isoform X3
membrane-associated phosphatidylinositol transfer protein 2 isoform X2
membrane-associated phosphatidylinositol transfer protein 2 isoform X1
chromosome 17 C12orf65 homolog, transcript variant X1
chromosome 17 C12orf65 homolog, transcript variant X4
chromosome 17 C12orf65 homolog, transcript variant X3
chromosome 17 C12orf65 homolog, transcript variant X2
probable peptide chain release factor C12orf65 homolog, mitochondrial
cyclin dependent kinase 2 associated protein 1, transcript variant X1
cyclin dependent kinase 2 associated protein 1, transcript variant X4
cyclin dependent kinase 2 associated protein 1, transcript variant X3
cyclin dependent kinase 2 associated protein 1, transcript variant X5
cyclin dependent kinase 2 associated protein 1, transcript variant X2
cyclin-dependent kinase 2-associated protein 1 isoform X1
cyclin-dependent kinase 2-associated protein 1 isoform X2
strawberry notch homolog 1, transcript variant X3
strawberry notch homolog 1, transcript variant X2
strawberry notch homolog 1, transcript variant X4
strawberry notch homolog 1, transcript variant X1
protein strawberry notch homolog 1 isoform X1
protein strawberry notch homolog 1 isoform X2
lysine methyltransferase 5A, transcript variant X2
lysine methyltransferase 5A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
N-lysine methyltransferase KMT5A isoform X1
N-lysine methyltransferase KMT5A isoform X2
Rab interacting lysosomal protein like 2
small nuclear ribonucleoprotein U11/U12 subunit 35, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
small nuclear ribonucleoprotein U11/U12 subunit 35, transcript variant X1
small nuclear ribonucleoprotein U11/U12 subunit 35, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
U11/U12 small nuclear ribonucleoprotein 35 kDa protein
Rab interacting lysosomal protein like 1, transcript variant X1
Rab interacting lysosomal protein like 1, transcript variant X2
transmembrane p24 trafficking protein 2, transcript variant X1
transmembrane p24 trafficking protein 2, transcript variant X2
transmembrane emp24 domain-containing protein 2 isoform X1
transmembrane emp24 domain-containing protein 2 isoform X2
eukaryotic translation initiation factor 2B subunit alpha
translation initiation factor eIF-2B subunit alpha
general transcription factor IIH subunit 3, transcript variant X1
general transcription factor IIH subunit 3, transcript variant X2
general transcription factor IIH subunit 3 isoform X1
general transcription factor IIH subunit 3 isoform X2
tectonic family member 2, transcript variant X1
tectonic family member 2, transcript variant X2
tectonic family member 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain containing 92, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
coiled-coil domain containing 92, transcript variant X4
coiled-coil domain containing 92, transcript variant X1
coiled-coil domain containing 92, transcript variant X2
coiled-coil domain containing 92, transcript variant X5
coiled-coil domain containing 92, transcript variant X3
coiled-coil domain-containing protein 92
nuclear receptor corepressor 2, transcript variant X14
nuclear receptor corepressor 2, transcript variant X13
nuclear receptor corepressor 2, transcript variant X6
nuclear receptor corepressor 2, transcript variant X11
nuclear receptor corepressor 2, transcript variant X12
nuclear receptor corepressor 2, transcript variant X5
nuclear receptor corepressor 2, transcript variant X3
nuclear receptor corepressor 2, transcript variant X4
nuclear receptor corepressor 2, transcript variant X10
nuclear receptor corepressor 2, transcript variant X7
nuclear receptor corepressor 2, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
nuclear receptor corepressor 2, transcript variant X8
nuclear receptor corepressor 2, transcript variant X1
nuclear receptor corepressor 2, transcript variant X2
nuclear receptor corepressor 2 isoform X13
nuclear receptor corepressor 2 isoform X12
nuclear receptor corepressor 2 isoform X5
nuclear receptor corepressor 2 isoform X10
nuclear receptor corepressor 2 isoform X11
nuclear receptor corepressor 2 isoform X4
nuclear receptor corepressor 2 isoform X2
nuclear receptor corepressor 2 isoform X3
nuclear receptor corepressor 2 isoform X9
nuclear receptor corepressor 2 isoform X6
nuclear receptor corepressor 2 isoform X8
nuclear receptor corepressor 2 isoform X7
nuclear receptor corepressor 2 isoform X1
scavenger receptor class B member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
scavenger receptor class B member 1 isoform X1
scavenger receptor class B member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
scavenger receptor class B member 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 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: 1 Protein, and 59% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phosphatidylinositol 4,5-bisphosphate 5-phosphatase A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
DNA polymerase epsilon, catalytic subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
DNA polymerase epsilon catalytic subunit A
apoptosis inducing factor mitochondria associated 3, transcript variant X1
apoptosis inducing factor mitochondria associated 3, transcript variant X2
apoptosis inducing factor mitochondria associated 3, transcript variant X3
purinergic receptor P2X 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
purinergic receptor P2X 6, transcript variant X1
purinergic receptor P2X 6, transcript variant X4
purinergic receptor P2X 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat-containing protein 74B
solute carrier family 7 member 4, transcript variant X1
solute carrier family 7 member 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 82% 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: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: scavenger receptor class F member 2
proline dehydrogenase 1, mitochondrial-like
oxysterol binding protein 2, transcript variant X2
oxysterol binding protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
oxysterol binding protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
pescadillo ribosomal biogenesis factor 1
coiled-coil domain-containing protein 157-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 13% 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 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: coiled-coil domain-containing protein 157-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
cytosolic arginine sensor for mTORC1 subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
acyl-CoA dehydrogenase family member 11-like
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
myotubularin related protein 3, transcript variant X4
myotubularin related protein 3, transcript variant X5
myotubularin related protein 3, transcript variant X1
myotubularin related protein 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
myotubularin related protein 3, transcript variant X2
myotubularin-related protein 3 isoform X2
myotubularin-related protein 3 isoform X1
activating signal cointegrator 1 complex subunit 2
zinc finger matrin-type 5, transcript variant X1
zinc finger matrin-type 5, transcript variant X2
pleckstrin homology domain-containing family A member 4-like, transcript variant X1
pleckstrin homology domain-containing family A member 4-like, transcript variant X3
pleckstrin homology domain-containing family A member 4-like, transcript variant X2
pleckstrin homology domain-containing family A member 4-like
adaptor related protein complex 1 subunit beta 1, transcript variant X1
adaptor related protein complex 1 subunit beta 1, transcript variant X2
adaptor related protein complex 1 subunit beta 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF01200
EWS RNA binding protein 1, transcript variant X2
EWS RNA binding protein 1, transcript variant X1
EWS RNA binding protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 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: 8 Proteins
WD repeat and SOCS box-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
kinase suppressor of Ras 2, transcript variant X1
kinase suppressor of Ras 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
kinase suppressor of Ras 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nitric oxide synthase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nitric oxide synthase 1, 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 1 sample with support for all annotated introns
calcineurin B homologous protein 3 isoform X1
calcineurin B homologous protein 3 isoform X2
RING finger and transmembrane domain-containing protein 2
mediator of RNA polymerase II transcription subunit 13-like
T-box transcription factor 3, transcript variant X1
T-box transcription factor TBX3 isoform X1
T-box transcription factor 3, transcript variant X2
T-box transcription factor TBX3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
serine dehydratase like, transcript variant X1
serine dehydratase like, transcript variant X2
mitochondrial sodium/calcium exchanger protein
two pore segment channel 1, transcript variant X1
two pore segment channel 1, transcript variant X2
two pore calcium channel protein 1 isoform X1
two pore calcium channel protein 1 isoform X2
cilia and flagella associated protein 73
cilia- and flagella-associated protein 73
V-set and immunoglobulin domain containing 10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
V-set and immunoglobulin domain-containing protein 10
phosphatidylethanolamine binding protein 1
phosphatidylethanolamine-binding protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine/threonine-protein kinase TAO3 isoform X2
serine/threonine-protein kinase TAO3 isoform X1
SDS3 homolog, SIN3A corepressor complex component
sin3 histone deacetylase corepressor complex component SDS3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
serine/arginine repetitive matrix protein 4
heat shock protein family B (small) member 8, transcript variant X1
heat shock protein family B (small) member 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 60
protein kinase AMP-activated non-catalytic subunit beta 1
5'-AMP-activated protein kinase subunit beta-1
citron rho-interacting serine/threonine kinase, transcript variant X7
citron rho-interacting serine/threonine kinase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
citron rho-interacting serine/threonine kinase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
citron rho-interacting serine/threonine kinase, transcript variant X3
citron rho-interacting serine/threonine kinase, transcript variant X4
citron rho-interacting serine/threonine kinase, transcript variant X2
citron rho-interacting serine/threonine kinase, transcript variant X1
citron rho-interacting serine/threonine kinase, transcript variant X8
citron Rho-interacting kinase isoform X7
citron Rho-interacting kinase isoform X6
citron Rho-interacting kinase isoform X5
citron Rho-interacting kinase isoform X3
citron Rho-interacting kinase isoform X4
citron Rho-interacting kinase isoform X2
citron Rho-interacting kinase isoform X1
citron Rho-interacting kinase isoform X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ribosomal protein lateral stalk subunit P0
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NAD-dependent protein lipoamidase sirtuin-4, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
musashi RNA binding protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
musashi RNA binding protein 1, transcript variant X1
RNA-binding protein Musashi homolog 1 isoform X2
RNA-binding protein Musashi homolog 1 isoform X1
cytochrome c oxidase subunit 6A1, mitochondrial
glutamyl-tRNA amidotransferase subunit C
glutamyl-tRNA(Gln) amidotransferase subunit C, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 101 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
2-methoxy-6-polyprenyl-1,4-benzoquinol methylase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dynein light chain LC6, flagellar outer arm-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95 Proteins, and 35% 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 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
POP5 homolog, ribonuclease P/MRP subunit
calcium binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
calcium binding protein 1, transcript variant X2
calcium binding protein 1, transcript variant X4
calcium binding protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
short-chain specific acyl-CoA dehydrogenase, mitochondrial
signal peptide peptidase like 3, transcript variant X2
signal peptide peptidase like 3, transcript variant X1
signal peptide peptidase-like 3 isoform X2
signal peptide peptidase-like 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 14% 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 18% coverage of the annotated genomic feature by RNAseq alignments
hepatocyte nuclear factor 1-alpha isoform X1
hepatocyte nuclear factor 1-alpha isoform X2
ring finger protein 185, transcript variant X3
ring finger protein 185, transcript variant X1
ring finger protein 185, transcript variant X2
LIM domain kinase 2, transcript variant X1
LIM domain kinase 2, transcript variant X2
LIM domain kinase 2, transcript variant X3
phosphoinositide-3-kinase interacting protein 1
phosphoinositide-3-kinase-interacting protein 1
POZ/BTB and AT hook containing zinc finger 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
POZ/BTB and AT hook containing zinc finger 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
POZ-, AT hook-, and zinc finger-containing protein 1 isoform X2
POZ-, AT hook-, and zinc finger-containing protein 1 isoform X1
POZ/BTB and AT hook containing zinc finger 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
POZ-, AT hook-, and zinc finger-containing protein 1 isoform X3
developmentally regulated GTP binding protein 1
developmentally-regulated GTP-binding protein 1
eukaryotic translation initiation factor 4E nuclear import factor 1, transcript variant X4
eukaryotic translation initiation factor 4E nuclear import factor 1, transcript variant X2
eukaryotic translation initiation factor 4E nuclear import factor 1, transcript variant X3
eukaryotic translation initiation factor 4E nuclear import factor 1, transcript variant X1
eukaryotic translation initiation factor 4E transporter isoform X4
eukaryotic translation initiation factor 4E transporter isoform X2
eukaryotic translation initiation factor 4E transporter isoform X3
eukaryotic translation initiation factor 4E transporter isoform 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
phosphatidylserine decarboxylase, transcript variant X4
phosphatidylserine decarboxylase, transcript variant X3
phosphatidylserine decarboxylase, transcript variant X2
phosphatidylserine decarboxylase, transcript variant X5
phosphatidylserine decarboxylase, transcript variant X1
phosphatidylserine decarboxylase proenzyme, mitochondrial isoform X2
phosphatidylserine decarboxylase proenzyme, mitochondrial isoform X3
phosphatidylserine decarboxylase proenzyme, mitochondrial isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 1 base in 1 codon; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: melanotransferrin-like
DEP domain containing 5, GATOR1 subcomplex subunit, transcript variant X1
DEP domain containing 5, GATOR1 subcomplex subunit, transcript variant X5
DEP domain containing 5, GATOR1 subcomplex subunit, transcript variant X10
DEP domain containing 5, GATOR1 subcomplex subunit, transcript variant X6
DEP domain containing 5, GATOR1 subcomplex subunit, transcript variant X3
DEP domain containing 5, GATOR1 subcomplex subunit, transcript variant X8
DEP domain containing 5, GATOR1 subcomplex subunit, transcript variant X2
DEP domain containing 5, GATOR1 subcomplex subunit, transcript variant X7
DEP domain containing 5, GATOR1 subcomplex subunit, transcript variant X4
DEP domain containing 5, GATOR1 subcomplex subunit, transcript variant X9
GATOR complex protein DEPDC5 isoform X10
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein eta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 99% 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 93% coverage of the annotated genomic feature by RNAseq alignments
G protein subunit alpha z, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
G protein subunit alpha z, transcript variant X1
guanine nucleotide-binding protein G(z) subunit alpha
BCR activator of RhoGEF and GTPase, transcript variant X2
BCR activator of RhoGEF and GTPase, transcript variant X1
sperm antigen with calponin homology and coiled-coil domains 1 like, transcript variant X3
sperm antigen with calponin homology and coiled-coil domains 1 like, transcript variant X1
sperm antigen with calponin homology and coiled-coil domains 1 like, transcript variant X2
adenosine A2a receptor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
adenosine A2a receptor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
small nuclear ribonucleoprotein D3 polypeptide, transcript variant X1
small nuclear ribonucleoprotein D3 polypeptide, transcript variant X2
leucine-rich repeat-containing protein 75B
gamma-glutamyltransferase 1, transcript variant X1
gamma-glutamyltransferase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
gamma-glutamyltransferase 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
gamma-glutamyltransferase 1, transcript variant X5
glutathione hydrolase 1 proenzyme isoform X1
gamma-glutamyltransferase 1, transcript variant X3
glutathione hydrolase 1 proenzyme isoform X4
glutathione hydrolase 1 proenzyme isoform X2
gamma-glutamyltransferase 1, transcript variant X4
glutathione hydrolase 1 proenzyme isoform X3
sphingomyelin phosphodiesterase 4, transcript variant X1
sphingomyelin phosphodiesterase 4, transcript variant X2
sphingomyelin phosphodiesterase 4 isoform X1
sphingomyelin phosphodiesterase 4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
mediator of RNA polymerase II transcription subunit 15
kelch like family member 22, transcript variant X1
kelch like family member 22, transcript variant X2
CRK like proto-oncogene, adaptor protein
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
calcineurin binding protein 1, transcript variant X2
calcineurin binding protein 1, transcript variant X3
calcineurin binding protein 1, transcript variant X1
calcineurin-binding protein cabin-1 isoform X2
calcineurin-binding protein cabin-1 isoform X3
calcineurin-binding protein cabin-1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
macrophage migration inhibitory factor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
solute carrier family 2, facilitated glucose transporter member 11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
solute carrier family 2, facilitated glucose transporter member 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil-helix-coiled-coil-helix domain containing 10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial
uncharacterized protein C22orf15 homolog
V-set pre-B cell surrogate light chain 3
vacuolar protein sorting-associated protein 29-like
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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
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: uncharacterized protein LOC116496188
immunoglobulin lambda-1 light chain-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins
DiGeorge syndrome critical region gene 2, transcript variant X2
DiGeorge syndrome critical region gene 2, transcript variant X1
integral membrane protein DGCR2/IDD isoform X2
integral membrane protein DGCR2/IDD isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins
testis-specific serine/threonine-protein kinase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 59% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63% coverage of the annotated genomic feature by RNAseq alignments
thyroid adenoma-associated protein homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67% coverage of the annotated genomic feature by RNAseq alignments
somatomedin-B and thrombospondin type-1 domain-containing protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 56% coverage of the annotated genomic feature by RNAseq alignments
tricarboxylate transport protein, mitochondrial
clathrin heavy chain like 1, transcript variant X1
clathrin heavy chain like 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serpin family D member 1, transcript variant X2
serpin family D member 1, transcript variant X1
HIC ZBTB transcriptional repressor 2, transcript variant X2
HIC ZBTB transcriptional repressor 2, transcript variant X1
YdjC chitooligosaccharide deacetylase homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
stromal cell-derived factor 2-like protein 1
protein phosphatase, Mg2+/Mn2+ dependent 1F
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, including 3 samples with support for all annotated introns
RING-type E3 ubiquitin-protein ligase PPIL2
39S ribosomal protein L40, mitochondrial
ubiquitin recognition factor in ER associated degradation 1, transcript variant X1
ubiquitin recognition factor in ER associated degradation 1, transcript variant X2
ubiquitin recognition factor in ER-associated degradation protein 1 isoform X1
ubiquitin recognition factor in ER-associated degradation protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cell division control protein 45 homolog
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: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide-binding protein subunit beta-like protein 1
thioredoxin reductase 2, transcript variant X2
thioredoxin reductase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
thioredoxin reductase 2, mitochondrial isoform X1
thioredoxin reductase 2, mitochondrial isoform X2
catechol-O-methyltransferase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
catechol-O-methyltransferase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
catechol-O-methyltransferase, transcript variant X2
catechol-O-methyltransferase, transcript variant X4
catechol-O-methyltransferase, transcript variant X3
catechol-O-methyltransferase, transcript variant X1
ARVCF delta catenin family member, transcript variant X3
ARVCF delta catenin family member, transcript variant X6
ARVCF delta catenin family member, transcript variant X5
ARVCF delta catenin family member, transcript variant X4
ARVCF delta catenin family member, transcript variant X7
ARVCF delta catenin family member, transcript variant X1
ARVCF delta catenin family member, transcript variant X14
ARVCF delta catenin family member, transcript variant X10
ARVCF delta catenin family member, transcript variant X2
ARVCF delta catenin family member, transcript variant X9
ARVCF delta catenin family member, transcript variant X13
ARVCF delta catenin family member, transcript variant X8
ARVCF delta catenin family member, transcript variant X12
ARVCF delta catenin family member, transcript variant X11
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X5
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X4
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X3
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X2
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X1
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X9
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X7
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X6
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X8
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X10
transport and golgi organization 2 homolog, transcript variant X1
transport and golgi organization 2 homolog, transcript variant X2
transport and golgi organization 2 homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transport and golgi organization 2 homolog, transcript variant X3
transport and Golgi organization protein 2 homolog
tRNA (uracil-5-)-methyltransferase homolog A
COORDINATES: nucleotide motif:Rfam:12.0:RF00599
zinc finger DHHC-type palmitoyltransferase 8
PGAM family member 5, mitochondrial serine/threonine protein phosphatase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein phosphatase PGAM5, mitochondrial
ankyrin repeat and LEM domain containing 2, transcript variant X2
ankyrin repeat and LEM domain containing 2, transcript variant X1
ankyrin repeat and LEM domain-containing protein 2 isoform X1
ankyrin repeat and LEM domain-containing protein 2 isoform X2
uncharacterized LOC116496131, transcript variant X1
uncharacterized LOC116496131, transcript variant X2
uncharacterized protein LOC116496131 isoform X1
uncharacterized protein LOC116496131 isoform X2
checkpoint with forkhead and ring finger domains, transcript variant X2
checkpoint with forkhead and ring finger domains, transcript variant X1
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase 9 isoform X1
polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X2
polypeptide N-acetylgalactosaminyltransferase 9 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
E1A binding protein p400, transcript variant X1
E1A binding protein p400, transcript variant X10
E1A binding protein p400, transcript variant X7
E1A binding protein p400, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
E1A binding protein p400, transcript variant X6
E1A binding protein p400, transcript variant X11
E1A binding protein p400, transcript variant X9
E1A binding protein p400, transcript variant X8
E1A binding protein p400, transcript variant X3
E1A binding protein p400, transcript variant X4
E1A binding protein p400, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
E1A binding protein p400, transcript variant X2
E1A-binding protein p400-like, transcript variant X2
E1A-binding protein p400-like, transcript variant X1
E1A-binding protein p400-like isoform X2
E1A-binding protein p400-like isoform X1
E1A-binding protein p400-like, transcript variant X3
E1A-binding protein p400-like isoform X3
E1A-binding protein p400-like, transcript variant X4
E1A-binding protein p400-like isoform X4
COORDINATES: nucleotide motif:Rfam:12.0:RF00562
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
pseudouridine synthase 1, transcript variant X1
pseudouridine synthase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
unc-51 like autophagy activating kinase 1, transcript variant X2
unc-51 like autophagy activating kinase 1, transcript variant X3
unc-51 like autophagy activating kinase 1, transcript variant X1
serine/threonine-protein kinase ULK1 isoform X2
serine/threonine-protein kinase ULK1 isoform X3
serine/threonine-protein kinase ULK1 isoform X1
matrix metallopeptidase 17, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
matrix metallopeptidase 17, transcript variant X2
splicing factor SWAP, transcript variant X1
splicing factor SWAP, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
splicing factor SWAP, transcript variant X2
splicing factor, suppressor of white-apricot homolog isoform X1
splicing factor, suppressor of white-apricot homolog isoform X3
splicing factor, suppressor of white-apricot homolog isoform X2
adhesion G protein-coupled receptor D1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
adhesion G protein-coupled receptor D1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
adhesion G-protein coupled receptor D1 isoform X2
adhesion G-protein coupled receptor D1 isoform X1
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: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RIMS binding protein 2, transcript variant X6
RIMS binding protein 2, transcript variant X2
RIMS binding protein 2, transcript variant X4
RIMS binding protein 2, transcript variant X8
RIMS binding protein 2, transcript variant X1
RIMS binding protein 2, transcript variant X9
RIMS binding protein 2, transcript variant X3
RIMS binding protein 2, transcript variant X5
RIMS binding protein 2, transcript variant X7
RIMS binding protein 2, transcript variant X10
RIMS binding protein 2, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 132D, transcript variant X1
transmembrane protein 132D, transcript variant X2
transmembrane protein 132D, transcript variant X3
glycosyltransferase 1 domain containing 1
glycosyltransferase 1 domain-containing protein 1
transmembrane protein 132C, transcript variant X2
transmembrane protein 132C, transcript variant X3
transmembrane protein 132C, transcript variant X1
DEAH-box helicase 37, transcript variant X1
probable ATP-dependent RNA helicase DHX37 isoform X1
DEAH-box helicase 37, transcript variant X2
probable ATP-dependent RNA helicase DHX37 isoform X2
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC116496023, transcript variant X2
uncharacterized LOC116496023, transcript variant X5
uncharacterized LOC116496023, transcript variant X4
uncharacterized LOC116496023, transcript variant X1
uncharacterized LOC116496023, transcript variant X6
uncharacterized LOC116496023, transcript variant X3
uncharacterized LOC116496023, transcript variant X7