Aythya fuligula isolate bAytFul2 chromosome 19, 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\nCM020318.1.\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.
GTPase activating Rap/RanGAP domain like 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
GTPase activating Rap/RanGAP domain like 3, transcript variant X3
GTPase activating Rap/RanGAP domain like 3, transcript variant X7
GTPase activating Rap/RanGAP domain like 3, transcript variant X9
GTPase activating Rap/RanGAP domain like 3, transcript variant X2
GTPase activating Rap/RanGAP domain like 3, 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 3 samples with support for all annotated introns
GTPase-activating Rap/Ran-GAP domain-like protein 3 isoform X1
GTPase-activating Rap/Ran-GAP domain-like protein 3 isoform X3
GTPase-activating Rap/Ran-GAP domain-like protein 3 isoform X7
GTPase-activating Rap/Ran-GAP domain-like protein 3 isoform X9
GTPase-activating Rap/Ran-GAP domain-like protein 3 isoform X2
GTPase-activating Rap/Ran-GAP domain-like protein 3 isoform X4
GTPase activating Rap/RanGAP domain like 3, transcript variant X8
GTPase-activating Rap/Ran-GAP domain-like protein 3 isoform X8
GTPase activating Rap/RanGAP domain like 3, transcript variant X5
GTPase activating Rap/RanGAP domain like 3, transcript variant X6
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
GTPase-activating Rap/Ran-GAP domain-like protein 3 isoform X5
GTPase-activating Rap/Ran-GAP domain-like protein 3 isoform X6
solute carrier family 2, facilitated glucose transporter member 8
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 3 bases in 3 codons; 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
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 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: F-box/WD repeat-containing protein 2
beta-1,4-galactosyltransferase galt-1-like, transcript variant X3
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
beta-1,4-galactosyltransferase galt-1-like, transcript variant X5
beta-1,4-galactosyltransferase galt-1-like, transcript variant X6
beta-1,4-galactosyltransferase galt-1-like, transcript variant X4
beta-1,4-galactosyltransferase galt-1-like isoform X2
beta-1,4-galactosyltransferase galt-1-like, transcript variant X2
beta-1,4-galactosyltransferase galt-1-like, transcript variant X1
beta-1,4-galactosyltransferase galt-1-like isoform X1
Ral GEF with PH domain and SH3 binding motif 1, transcript variant X5
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
Ral GEF with PH domain and SH3 binding motif 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 1 sample with support for all annotated introns
Ral GEF with PH domain and SH3 binding motif 1, transcript variant X4
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
Ral GEF with PH domain and SH3 binding motif 1, transcript variant X1
Ral GEF with PH domain and SH3 binding motif 1, transcript variant X2
Ral GEF with PH domain and SH3 binding motif 1, transcript variant X6
ras-specific guanine nucleotide-releasing factor RalGPS1 isoform X1
Ral GEF with PH domain and SH3 binding motif 1, transcript variant X7
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
ras-specific guanine nucleotide-releasing factor RalGPS1 isoform X2
angiopoietin like 2, 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 3 samples with support for all annotated introns
angiopoietin like 2, transcript variant X2
zinc finger and BTB domain containing 34
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; deleted 2 bases in 2 codons; 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, including 3 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger and BTB domain-containing protein 34
zinc finger and BTB domain containing 43
zinc finger and BTB domain-containing protein 43
LIM homeobox transcription factor 1 beta
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
LIM homeobox transcription factor 1-beta
multivesicular body subunit 12B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
multivesicular body subunit 12B, transcript variant X1
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
multivesicular body subunit 12B, transcript variant X2
multivesicular body subunit 12B isoform X1
multivesicular body subunit 12B 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 3 samples with support for all annotated introns
pre-B-cell leukemia transcription factor 3 isoform X1
pre-B-cell leukemia transcription factor 3 isoform 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 3 samples with support for all annotated introns
pre-B-cell leukemia transcription factor 3 isoform X3
MAPK associated protein 1, transcript variant X1
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
MAPK associated protein 1, transcript variant X2
target of rapamycin complex 2 subunit MAPKAP1 isoform X1
target of rapamycin complex 2 subunit MAPKAP1 isoform X2
GTPase activating protein and VPS9 domains 1, transcript variant X3
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
GTPase activating protein and VPS9 domains 1, transcript variant X4
GTPase activating protein and VPS9 domains 1, transcript variant X5
GTPase activating protein and VPS9 domains 1, transcript variant X2
GTPase activating protein and VPS9 domains 1, transcript variant X6
GTPase activating protein and VPS9 domains 1, transcript variant X9
GTPase activating protein and VPS9 domains 1, transcript variant X8
GTPase activating protein and VPS9 domains 1, transcript variant X7
GTPase activating protein and VPS9 domains 1, transcript variant X1
GTPase-activating protein and VPS9 domain-containing protein 1 isoform X4
GTPase-activating protein and VPS9 domain-containing protein 1 isoform X3
GTPase-activating protein and VPS9 domain-containing protein 1 isoform X2
GTPase-activating protein and VPS9 domain-containing protein 1 isoform X1
heat shock protein family A (Hsp70) member 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 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 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 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 6 catalytic subunit
actin related protein 2/3 complex subunit 5 like
actin-related protein 2/3 complex subunit 5-like protein
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
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
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
nuclear receptor subfamily 6 group A member 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear receptor subfamily 6 group A member 1 isoform X3
nuclear receptor subfamily 6 group A member 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
nuclear receptor subfamily 6 group A member 1, transcript variant X2
nuclear receptor subfamily 6 group A member 1 isoform X1
nuclear receptor subfamily 6 group A member 1 isoform X2
nuclear receptor subfamily 5 group A member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 69% coverage of the annotated genomic feature by RNAseq alignments
NIMA related kinase 6, transcript variant X1
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
NIMA related kinase 6, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
DENN domain containing 1A, transcript variant X1
DENN domain containing 1A, transcript variant X4
DENN domain containing 1A, transcript variant X2
DENN domain containing 1A, transcript variant X3
DENN domain containing 1A, transcript variant X5
DENN domain containing 1A, transcript variant X6
DENN domain-containing protein 1A isoform X1
DENN domain-containing protein 1A isoform X4
DENN domain-containing protein 1A isoform X2
DENN domain-containing protein 1A isoform X3
DENN domain-containing protein 1A isoform X5
DENN domain-containing protein 1A isoform X6
crumbs cell polarity complex component 2, transcript variant X2
crumbs cell polarity complex component 2, transcript variant X1
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 1 sample with support for all annotated introns
spermatid perinuclear RNA binding protein, transcript variant X2
spermatid perinuclear RNA binding protein, transcript variant X3
spermatid perinuclear RNA binding protein, transcript variant X4
spermatid perinuclear RNA binding protein, transcript variant X1
spermatid perinuclear RNA binding protein, transcript variant X8
spermatid perinuclear RNA binding protein, transcript variant X5
spermatid perinuclear RNA binding protein, transcript variant X6
spermatid perinuclear RNA binding protein, transcript variant X7
spermatid perinuclear RNA-binding protein isoform X5
spermatid perinuclear RNA-binding protein isoform X1
spermatid perinuclear RNA-binding protein isoform X2
spermatid perinuclear RNA-binding protein isoform X3
spermatid perinuclear RNA-binding protein isoform X4
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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and BTB domain containing 26, 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 1 sample with support for all annotated introns
zinc finger and BTB domain containing 26, transcript variant X2
zinc finger and BTB domain containing 26, transcript variant X1
zinc finger and BTB domain-containing protein 26
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
zinc finger and BTB domain-containing protein 6
ring finger and CCCH-type domains 2, transcript variant X1
ring finger and CCCH-type domains 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00579
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
ribosome-recycling factor, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
NADH:ubiquinone oxidoreductase subunit A8
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 8
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 68% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 96% 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 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: tubulin polyglutamylase TTLL11
DAB2 interacting protein, 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
disabled homolog 2-interacting protein isoform X3
DAB2 interacting protein, transcript variant X2
DAB2 interacting protein, transcript variant X1
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
DAB2 interacting protein, transcript variant X6
DAB2 interacting protein, transcript variant X4
DAB2 interacting protein, transcript variant X5
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
disabled homolog 2-interacting protein isoform X2
disabled homolog 2-interacting protein isoform X1
disabled homolog 2-interacting protein isoform X4
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
erythrocyte band 7 integral membrane protein
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
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: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 11 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
26S proteasome non-ATPase regulatory subunit 5
putative UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase LOC100288842
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
potassium sodium-activated channel subfamily T member 1, transcript variant X7
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 2 samples with support for all annotated introns
potassium sodium-activated channel subfamily T member 1, transcript variant X8
potassium channel subfamily T member 1 isoform X7
potassium channel subfamily T member 1 isoform X8
potassium sodium-activated channel subfamily T member 1, transcript variant X1
potassium sodium-activated channel subfamily T member 1, transcript variant X6
potassium sodium-activated channel subfamily T member 1, transcript variant X3
potassium sodium-activated channel subfamily T member 1, transcript variant X4
potassium sodium-activated channel subfamily T member 1, transcript variant X2
potassium sodium-activated channel subfamily T member 1, transcript variant X5
potassium channel subfamily T member 1 isoform X1
potassium channel subfamily T member 1 isoform X6
potassium channel subfamily T member 1 isoform X3
potassium channel subfamily T member 1 isoform X4
potassium channel subfamily T member 1 isoform X2
potassium channel subfamily T member 1 isoform X5
calmodulin regulated spectrin associated protein 1, transcript variant X2
calmodulin regulated spectrin associated protein 1, transcript variant X1
calmodulin-regulated spectrin-associated protein 1 isoform X2
calmodulin-regulated spectrin-associated protein 1 isoform X1
UBA domain containing 1, transcript variant X2
UBA domain containing 1, transcript variant X1
ubiquitin-associated domain-containing protein 1 isoform X2
ubiquitin-associated domain-containing protein 1 isoform X1
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
NACC family member 2, transcript variant X3
NACC family member 2, transcript variant X4
NACC family member 2, transcript variant X2
NACC family member 2, transcript variant X1
transmembrane protein 250, transcript variant X2
transmembrane protein 250, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
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
G protein signaling modulator 1, transcript variant X1
G-protein-signaling modulator 1 isoform X1
G protein signaling modulator 1, transcript variant X2
G-protein-signaling modulator 1 isoform X2
G protein signaling modulator 1, transcript variant X3
G-protein-signaling modulator 1 isoform 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 3 samples with support for all annotated introns
caspase recruitment domain family member 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
caspase recruitment domain-containing protein 9
small nuclear RNA activating complex polypeptide 4
snRNA-activating protein complex subunit 4
endosome associated trafficking regulator 1
endosome-associated-trafficking regulator 1
peptidase, mitochondrial processing subunit alpha
mitochondrial-processing peptidase subunit alpha
inositol polyphosphate-5-phosphatase E, transcript variant X1
inositol polyphosphate-5-phosphatase E, transcript variant X3
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
inositol polyphosphate-5-phosphatase E, transcript variant X2
phosphatidylinositol polyphosphate 5-phosphatase type IV
SEC16 homolog A, endoplasmic reticulum export factor, transcript variant X4
SEC16 homolog A, endoplasmic reticulum export factor, transcript variant X2
SEC16 homolog A, endoplasmic reticulum export factor, transcript variant X3
SEC16 homolog A, endoplasmic reticulum export factor, transcript variant X1
SEC16 homolog A, endoplasmic reticulum export factor, transcript variant X5
protein transport protein Sec16A isoform X4
protein transport protein Sec16A isoform X2
protein transport protein Sec16A isoform X3
protein transport protein Sec16A isoform X1
protein transport protein Sec16A isoform X5
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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
neurogenic locus notch homolog protein 1 isoform X2
neurogenic locus notch homolog protein 1 isoform X1
EGF like domain multiple 7, transcript variant X2
EGF like domain multiple 7, transcript variant X1
EGF like domain multiple 7, transcript variant X3
1-acylglycerol-3-phosphate O-acyltransferase 2
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
1-acyl-sn-glycerol-3-phosphate acyltransferase beta
COORDINATES: nucleotide motif:Rfam:12.0:RF00560
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
SWI5 homologous recombination repair protein
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
CDKN1A interacting zinc finger protein 1, transcript variant X2
CDKN1A interacting zinc finger protein 1, transcript variant X1
CDKN1A interacting zinc finger protein 1, transcript variant X3
CDKN1A interacting zinc finger protein 1, transcript variant X5
CDKN1A interacting zinc finger protein 1, transcript variant X6
cip1-interacting zinc finger protein isoform X1
cip1-interacting zinc finger protein isoform X2
cip1-interacting zinc finger protein isoform X4
cip1-interacting zinc finger protein isoform X5
CDKN1A interacting zinc finger protein 1, transcript variant X4
cip1-interacting zinc finger protein isoform X3
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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
spectrin alpha, non-erythrocytic 1, transcript variant X3
spectrin alpha, non-erythrocytic 1, transcript variant X6
spectrin alpha, non-erythrocytic 1, transcript variant X2
spectrin alpha, non-erythrocytic 1, transcript variant X5
spectrin alpha, non-erythrocytic 1, transcript variant X1
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
spectrin alpha, non-erythrocytic 1, transcript variant X4
spectrin alpha chain, non-erythrocytic 1 isoform X1
spectrin alpha chain, non-erythrocytic 1 isoform X2
spectrin alpha chain, non-erythrocytic 1 isoform X4
spectrin alpha chain, non-erythrocytic 1 isoform X5
spectrin alpha chain, non-erythrocytic 1 isoform X3
zinc finger DHHC-type palmitoyltransferase 12
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
SPOUT domain containing methyltransferase 1
putative methyltransferase C9orf114 homolog
kynurenine aminotransferase 1, transcript variant X1
kynurenine aminotransferase 1, transcript variant X2
leucine rich repeat containing 8 VRAC subunit A, transcript variant X3
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 1 sample with support for all annotated introns
leucine rich repeat containing 8 VRAC subunit A, transcript variant X2
leucine rich repeat containing 8 VRAC subunit A, transcript variant X4
leucine rich repeat containing 8 VRAC subunit A, transcript variant X1
volume-regulated anion channel subunit LRRC8A
phytanoyl-CoA dioxygenase domain containing 1
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
phytanoyl-CoA dioxygenase domain-containing protein 1
SH3 domain containing GRB2 like, endophilin B2, transcript variant X3
SH3 domain containing GRB2 like, endophilin B2, transcript variant X8
SH3 domain containing GRB2 like, endophilin B2, transcript variant X6
SH3 domain containing GRB2 like, endophilin B2, transcript variant X4
SH3 domain containing GRB2 like, endophilin B2, transcript variant X2
SH3 domain containing GRB2 like, endophilin B2, transcript variant X5
SH3 domain containing GRB2 like, endophilin B2, transcript variant X1
SH3 domain containing GRB2 like, endophilin B2, transcript variant X7
dolichyldiphosphatase 1, transcript variant X1
dolichyldiphosphatase 1, transcript variant X2
carnitine O-acetyltransferase, transcript variant X2
carnitine O-acetyltransferase, transcript variant X1
carnitine O-acetyltransferase isoform X2
carnitine O-acetyltransferase isoform X1
protein phosphatase 2 phosphatase activator, transcript variant X1
protein phosphatase 2 phosphatase activator, transcript variant X2
serine/threonine-protein phosphatase 2A activator isoform X1
serine/threonine-protein phosphatase 2A activator isoform 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
immediate early response gene 5-like protein
N-terminal Xaa-Pro-Lys N-methyltransferase 1, transcript variant X2
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
N-terminal Xaa-Pro-Lys N-methyltransferase 1, transcript variant X1
N-terminal Xaa-Pro-Lys N-methyltransferase 1, transcript variant X3
N-terminal Xaa-Pro-Lys N-methyltransferase 1
ankyrin repeat and SOCS box containing 6
paired related homeobox 2, 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 3 samples with support for all annotated introns
paired related homeobox 2, transcript variant X2
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, including 2 samples with support for all annotated introns
paired mesoderm homeobox protein 2 isoform X1
paired mesoderm homeobox protein 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 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: 11 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
telomere length and silencing protein 1 homolog
ubiquitin specific peptidase 20, transcript variant X3
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
ubiquitin specific peptidase 20, transcript variant X1
ubiquitin specific peptidase 20, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 20
formin binding protein 1, transcript variant X3
formin binding protein 1, transcript variant X14
formin binding protein 1, transcript variant X12
formin binding protein 1, transcript variant X11
formin binding protein 1, transcript variant X10
formin binding protein 1, transcript variant X9
formin binding protein 1, transcript variant X4
formin binding protein 1, transcript variant X8
formin binding protein 1, transcript variant X7
formin binding protein 1, transcript variant X6
formin binding protein 1, transcript variant X5
formin binding protein 1, transcript variant X2
formin binding protein 1, transcript variant X1
formin binding protein 1, transcript variant X13
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
far upstream element binding protein 3, transcript variant X1
far upstream element binding protein 3, transcript variant X3
far upstream element binding protein 3, transcript variant X2
far upstream element-binding protein 3 isoform X1
far upstream element-binding protein 3 isoform X3
far upstream element-binding protein 3 isoform X2
ABL proto-oncogene 1, non-receptor tyrosine kinase, transcript variant X1
ABL proto-oncogene 1, non-receptor tyrosine kinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
fibrinogen C domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 78 member A
proline rich coiled-coil 2B, transcript variant X1
proline rich coiled-coil 2B, transcript variant X4
proline rich coiled-coil 2B, transcript variant X3
proline rich coiled-coil 2B, transcript variant X5
proline rich coiled-coil 2B, transcript variant X2
protein O-mannosyltransferase 1, transcript variant X2
protein O-mannosyltransferase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 74% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Rap guanine nucleotide exchange factor 1, transcript variant X8
Rap guanine nucleotide exchange factor 1, transcript variant X7
Rap guanine nucleotide exchange factor 1, transcript variant X5
Rap guanine nucleotide exchange factor 1, transcript variant X2
Rap guanine nucleotide exchange factor 1, transcript variant X6
Rap guanine nucleotide exchange factor 1, transcript variant X4
Rap guanine nucleotide exchange factor 1, transcript variant X1
Rap guanine nucleotide exchange factor 1, transcript variant X3
rap guanine nucleotide exchange factor 1 isoform X8
rap guanine nucleotide exchange factor 1 isoform X7
rap guanine nucleotide exchange factor 1 isoform X5
rap guanine nucleotide exchange factor 1 isoform X2
rap guanine nucleotide exchange factor 1 isoform X6
rap guanine nucleotide exchange factor 1 isoform X4
rap guanine nucleotide exchange factor 1 isoform X1
rap guanine nucleotide exchange factor 1 isoform X3
mediator of RNA polymerase II transcription subunit 27
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
cilia and flagella associated protein 77
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cilia- and flagella-associated protein 77
DEAD-box helicase 31, transcript variant X2
DEAD-box helicase 31, transcript variant X1
probable ATP-dependent RNA helicase DDX31 isoform X2
probable ATP-dependent RNA helicase DDX31 isoform X1
general transcription factor IIIC subunit 4
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, including 3 samples with support for all annotated introns
general transcription factor 3C polypeptide 4
adenylate kinase 8, transcript variant X2
adenylate kinase 8, transcript variant X1
adenylate kinase 8, transcript variant X3
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 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 37% coverage of the annotated genomic feature by RNAseq alignments
TSC complex subunit 1, transcript variant X3
TSC complex subunit 1, transcript variant X2
TSC complex subunit 1, transcript variant X1
growth factor independent 1B transcriptional repressor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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: 4 Proteins
general transcription factor IIIC subunit 5
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
general transcription factor 3C polypeptide 5
ral guanine nucleotide dissociation stimulator, transcript variant X4
ral guanine nucleotide dissociation stimulator, transcript variant X2
ral guanine nucleotide dissociation stimulator, transcript variant X3
ral guanine nucleotide dissociation stimulator, transcript variant X1
ral guanine nucleotide dissociation stimulator isoform X4
ral guanine nucleotide dissociation stimulator isoform X2
ral guanine nucleotide dissociation stimulator isoform X3
ral guanine nucleotide dissociation stimulator isoform X1
globoside alpha-1,3-N-acetylgalactosaminyltransferase 1 (FORS blood group)
globoside alpha-1,3-N-acetylgalactosaminyltransferase 1
mediator complex subunit 22, transcript variant X2
mediator complex subunit 22, transcript variant X1
mediator of RNA polymerase II transcription subunit 22 isoform X2
mediator of RNA polymerase II transcription subunit 22 isoform X1
mediator complex subunit 22, transcript variant X3
mediator of RNA polymerase II transcription subunit 22 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00069
COORDINATES: nucleotide motif:Rfam:12.0:RF00049
serine/threonine kinase like domain containing 1, transcript variant X1
serine/threonine kinase like domain containing 1, transcript variant X2
serine/threonine kinase like domain containing 1, transcript variant X3
serine/threonine kinase like domain containing 1, transcript variant X4
serine/threonine kinase-like domain-containing protein STKLD1 isoform X1
serine/threonine kinase-like domain-containing protein STKLD1 isoform X2
serine/threonine kinase-like domain-containing protein STKLD1 isoform X3
serine/threonine kinase-like domain-containing protein STKLD1 isoform X4
ADAM metallopeptidase with thrombospondin type 1 motif 13
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
A disintegrin and metalloproteinase with thrombospondin motifs 13
calcium channel flower domain containing 1
solute carrier family 2, facilitated glucose transporter member 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
family with sequence similarity 163 member B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
vav guanine nucleotide exchange factor 2, transcript variant X4
vav guanine nucleotide exchange factor 2, transcript variant X2
vav guanine nucleotide exchange factor 2, transcript variant X3
vav guanine nucleotide exchange factor 2, transcript variant X1
vav guanine nucleotide exchange factor 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide exchange factor VAV2 isoform X4
guanine nucleotide exchange factor VAV2 isoform X2
guanine nucleotide exchange factor VAV2 isoform X3
guanine nucleotide exchange factor VAV2 isoform X1
guanine nucleotide exchange factor VAV2 isoform X5
bromodomain containing 3, transcript variant X1
bromodomain containing 3, transcript variant 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
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
retinoid X receptor alpha, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
retinoic acid receptor RXR-alpha isoform X1
retinoid X receptor alpha, transcript variant X2
retinoic acid receptor RXR-alpha isoform X2
collagen type V alpha 1 chain, transcript variant 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 2 samples with support for all annotated introns
collagen type V alpha 1 chain, transcript variant X2
protein phosphatase 1 regulatory subunit 26, transcript variant X3
protein phosphatase 1 regulatory subunit 26, transcript variant X2
protein phosphatase 1 regulatory subunit 26, transcript variant X1
protein phosphatase 1 regulatory subunit 26
TruB pseudouridine synthase family member 2
mitochondrial mRNA pseudouridine synthase TRUB2
ubiquinone biosynthesis protein COQ4 homolog, mitochondrial
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon UCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
long-chain fatty acid transport protein 4
cerebral endothelial cell adhesion molecule, transcript variant X3
cerebral endothelial cell adhesion molecule, transcript variant X2
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
cerebral endothelial cell adhesion molecule, transcript variant X1
inactive glycosyltransferase 25 family member 3 isoform X1
inactive glycosyltransferase 25 family member 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 49% coverage of the annotated genomic feature by RNAseq alignments
SH2 domain containing 3C, transcript variant X1
SH2 domain containing 3C, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SH2 domain-containing protein 3C isoform X1
SH2 domain-containing protein 3C isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
folylpolyglutamate synthase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 6
alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6
ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 4
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 2 samples with support for all annotated introns
alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3-N-acetyl-galactosaminide alpha-2,6-sialyltransferase
phosphatidylinositol-4-phosphate 5-kinase like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 39% 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: phosphatidylinositol 4-phosphate 5-kinase-like protein 1
dolichyl-phosphate mannosyltransferase subunit 2, regulatory
dolichol phosphate-mannose biosynthesis regulatory protein
family with sequence similarity 102 member A, transcript variant X2
family with sequence similarity 102 member A, transcript variant X1
solute carrier family 25 member 25, transcript variant X1
solute carrier family 25 member 25, transcript variant X2
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X1
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X2
solute carrier family 25 member 25, transcript variant X3
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, including 2 samples with support for all annotated introns
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
multiple epidermal growth factor-like domains protein 9
CDK5 regulatory subunit associated protein 2
CDK5 regulatory subunit-associated protein 2
BMP/retinoic acid inducible neural specific 1
BMP/retinoic acid-inducible neural-specific protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
tripartite motif containing 32, transcript variant X3
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
tripartite motif containing 32, transcript variant X2
tripartite motif containing 32, transcript variant X1
E3 ubiquitin-protein ligase TRIM32 isoform X1
E3 ubiquitin-protein ligase TRIM32 isoform 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
tumor necrosis factor ligand superfamily member 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tumor necrosis factor ligand superfamily member 15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 48% 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 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
syntaxin binding protein 1, transcript variant X2
syntaxin binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
probable low affinity copper uptake protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
voltage-dependent N-type calcium channel subunit alpha-1B-like, transcript variant X8
voltage-dependent N-type calcium channel subunit alpha-1B-like, transcript variant X10
voltage-dependent N-type calcium channel subunit alpha-1B-like, transcript variant X6
voltage-dependent N-type calcium channel subunit alpha-1B-like, transcript variant X7
voltage-dependent N-type calcium channel subunit alpha-1B-like, transcript variant X3
voltage-dependent N-type calcium channel subunit alpha-1B-like, transcript variant X4
voltage-dependent N-type calcium channel subunit alpha-1B-like, transcript variant X5
voltage-dependent N-type calcium channel subunit alpha-1B-like, transcript variant X1
voltage-dependent N-type calcium channel subunit alpha-1B-like, transcript variant X2
voltage-dependent N-type calcium channel subunit alpha-1B-like isoform X8
voltage-dependent N-type calcium channel subunit alpha-1B-like isoform X10
voltage-dependent N-type calcium channel subunit alpha-1B-like isoform X6
voltage-dependent N-type calcium channel subunit alpha-1B-like isoform X7
voltage-dependent N-type calcium channel subunit alpha-1B-like isoform X3
voltage-dependent N-type calcium channel subunit alpha-1B-like isoform X4
voltage-dependent N-type calcium channel subunit alpha-1B-like isoform X5
voltage-dependent N-type calcium channel subunit alpha-1B-like isoform X1
voltage-dependent N-type calcium channel subunit alpha-1B-like isoform X2
voltage-dependent N-type calcium channel subunit alpha-1B-like, transcript variant X9
voltage-dependent N-type calcium channel subunit alpha-1B-like isoform X9
euchromatic histone lysine methyltransferase 1, transcript variant X2
euchromatic histone lysine methyltransferase 1, transcript variant X6
euchromatic histone lysine methyltransferase 1, transcript variant X7
euchromatic histone lysine methyltransferase 1, transcript variant X5
euchromatic histone lysine methyltransferase 1, transcript variant X13
euchromatic histone lysine methyltransferase 1, transcript variant X9
euchromatic histone lysine methyltransferase 1, transcript variant X3
euchromatic histone lysine methyltransferase 1, transcript variant X10
euchromatic histone lysine methyltransferase 1, transcript variant X8
euchromatic histone lysine methyltransferase 1, transcript variant X1
euchromatic histone lysine methyltransferase 1, transcript variant X11
euchromatic histone lysine methyltransferase 1, transcript variant X12
euchromatic histone lysine methyltransferase 1, transcript variant X4
histone-lysine N-methyltransferase EHMT1 isoform X2
histone-lysine N-methyltransferase EHMT1 isoform X7
histone-lysine N-methyltransferase EHMT1 isoform X3
histone-lysine N-methyltransferase EHMT1 isoform X8
histone-lysine N-methyltransferase EHMT1 isoform X6
histone-lysine N-methyltransferase EHMT1 isoform X1
histone-lysine N-methyltransferase EHMT1 isoform X4
histone-lysine N-methyltransferase EHMT1 isoform X5
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 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
negative elongation factor complex member B
ectonucleoside triphosphate diphosphohydrolase 2-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 197 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
family with sequence similarity 166 member A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 3% coverage of the annotated genomic feature by RNAseq alignments
discoidin domain-containing receptor 2-like, transcript variant X2
discoidin domain-containing receptor 2-like, transcript variant X1
discoidin domain-containing receptor 2-like isoform X1
discoidin domain-containing receptor 2-like, transcript variant X3
discoidin domain-containing receptor 2-like isoform X2
torsin family 4 member A, transcript variant X3
torsin family 4 member A, transcript variant X1
torsin family 4 member A, transcript variant X2
torsin family 4 member A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 78% coverage of the annotated genomic feature by RNAseq alignments
NMDA receptor synaptonuclear signaling and neuronal migration factor, transcript variant X2
NMDA receptor synaptonuclear signaling and neuronal migration factor, transcript variant X5
NMDA receptor synaptonuclear signaling and neuronal migration factor, transcript variant X4
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
NMDA receptor synaptonuclear signaling and neuronal migration factor, transcript variant X3
NMDA receptor synaptonuclear signaling and neuronal migration factor, transcript variant X1
NMDA receptor synaptonuclear signaling and neuronal migration factor isoform X2
NMDA receptor synaptonuclear signaling and neuronal migration factor isoform X3
NMDA receptor synaptonuclear signaling and neuronal migration factor isoform X1
NMDA receptor synaptonuclear signaling and neuronal migration factor isoform X5
NMDA receptor synaptonuclear signaling and neuronal migration factor isoform X4
patatin like phospholipase domain containing 7
patatin-like phospholipase domain-containing protein 7
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
39S ribosomal protein L41, mitochondrial
zinc finger MYND domain-containing protein 19
COORDINATES: nucleotide motif:Rfam:12.0:RF00302
leucine rich repeat and sterile alpha motif containing 1, transcript variant X1
leucine rich repeat and sterile alpha motif containing 1, transcript variant X2
E3 ubiquitin-protein ligase LRSAM1 isoform X1
E3 ubiquitin-protein ligase LRSAM1 isoform X2
FKBP prolyl isomerase 15, transcript variant X2
FKBP prolyl isomerase 15, transcript variant X4
FKBP prolyl isomerase 15, transcript variant X3
FKBP prolyl isomerase 15, transcript variant X1
solute carrier family 31 member 1, transcript variant X1
solute carrier family 31 member 1, transcript variant X3
solute carrier family 31 member 1, transcript variant X2
anaphase-promoting complex subunit CDC26
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
U4/U6 small nuclear ribonucleoprotein Prp4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
B box and SPRY domain-containing protein
haloacid dehalogenase like hydrolase domain containing 3
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
haloacid dehalogenase-like hydrolase domain-containing protein 3
DNA polymerase epsilon 3, accessory subunit, transcript variant X1
DNA polymerase epsilon 3, accessory subunit, transcript variant X2
DNA polymerase epsilon 3, accessory subunit, transcript variant X3
regulator of G protein signaling 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
regulator of G-protein signaling 3 isoform X1
regulator of G protein signaling 3, transcript variant X4
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
regulator of G protein signaling 3, 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 1 sample with support for all annotated introns
regulator of G-protein signaling 3 isoform X2
regulator of G protein signaling 3, transcript variant X3
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 2 samples with support for all annotated introns
regulator of G-protein signaling 3 isoform X3
regulator of G protein signaling 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
regulator of G-protein signaling 3 isoform X4
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein 618, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 618, transcript variant X3
zinc finger protein 618, transcript variant X2
zinc finger protein 618, transcript variant X4
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X12
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 1 sample with support for all annotated introns
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X1
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X6
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X8
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X7
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 1 sample with support for all annotated introns
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X11
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X9
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X3
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X2
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X5
glutamate ionotropic receptor NMDA type subunit 1, 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 1 sample with support for all annotated introns
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X10
glutamate receptor ionotropic, NMDA 1 isoform X1
glutamate receptor ionotropic, NMDA 1 isoform X5
glutamate receptor ionotropic, NMDA 1 isoform X7
glutamate receptor ionotropic, NMDA 1 isoform X10
glutamate receptor ionotropic, NMDA 1 isoform X6
glutamate receptor ionotropic, NMDA 1 isoform X9
glutamate receptor ionotropic, NMDA 1 isoform X2
glutamate receptor ionotropic, NMDA 1 isoform X4
glutamate receptor ionotropic, NMDA 1 isoform X3
glutamate receptor ionotropic, NMDA 1 isoform X8
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: 1 Protein
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: leucine-rich repeat-containing protein 26
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein 208, transcript variant X1
ring finger protein 208, transcript variant X2
NADPH dependent diflavin oxidoreductase 1, transcript variant X4
NADPH dependent diflavin oxidoreductase 1, transcript variant X1
NADPH dependent diflavin oxidoreductase 1, transcript variant X2
NADPH dependent diflavin oxidoreductase 1, transcript variant X3
NADPH-dependent diflavin oxidoreductase 1
ectonucleoside triphosphate diphosphohydrolase 8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ectonucleoside triphosphate diphosphohydrolase 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
exonuclease 3'-5' domain containing 3, transcript variant X2
exonuclease 3'-5' domain containing 3, transcript variant X1
exonuclease 3'-5' domain containing 3, transcript variant X3
notch-regulated ankyrin repeat-containing protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 3 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: 7 Proteins, and 88% 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: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 11% 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: apical endosomal glycoprotein
endothelial differentiation related factor 1
endothelial differentiation-related factor 1
TNF receptor associated factor 2, transcript variant X1
TNF receptor associated factor 2, transcript variant X4
TNF receptor associated factor 2, transcript variant X3
TNF receptor associated factor 2, transcript variant X6
TNF receptor associated factor 2, transcript variant X2
TNF receptor associated factor 2, transcript variant X5
TNF receptor-associated factor 2 isoform X1
TNF receptor-associated factor 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
extracellular fatty acid-binding protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins
neural proliferation, differentiation and control 1
neural proliferation differentiation and control protein 1
POU domain, class 5, transcription factor 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 70% 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: 5 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
ATP binding cassette subfamily A member 2, transcript variant X1
ATP binding cassette subfamily A member 2, transcript variant X4
ATP binding cassette subfamily A member 2, transcript variant X5
ATP binding cassette subfamily A member 2, transcript variant X3
ATP binding cassette subfamily A member 2, transcript variant X2
ATP-binding cassette sub-family A member 2 isoform X1
ATP-binding cassette sub-family A member 2 isoform X4
ATP-binding cassette sub-family A member 2 isoform X5
ATP-binding cassette sub-family A member 2 isoform X3
ATP-binding cassette sub-family A member 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
chloride intracellular channel protein 3
ectonucleoside triphosphate diphosphohydrolase 2, transcript variant X2
ectonucleoside triphosphate diphosphohydrolase 2, transcript variant X1
ectonucleoside triphosphate diphosphohydrolase 2, transcript variant X3
ectonucleoside triphosphate diphosphohydrolase 2, transcript variant X4
ectonucleoside triphosphate diphosphohydrolase 2 isoform X2
ectonucleoside triphosphate diphosphohydrolase 2 isoform X1
ectonucleoside triphosphate diphosphohydrolase 2 isoform X3
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
suppressor APC domain-containing protein 2
UDP-N-acetylglucosamine pyrophosphorylase 1 like 1
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
UDP-N-acetylhexosamine pyrophosphorylase-like protein 1
mannosidase alpha class 1B member 1, transcript variant X1
mannosidase alpha class 1B member 1, transcript variant X2
endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase isoform X1
endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase isoform X2
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
dual specificity testis-specific protein kinase 2-like, transcript variant X18
dual specificity testis-specific protein kinase 2-like, transcript variant X16
dual specificity testis-specific protein kinase 2-like, transcript variant X17
dual specificity testis-specific protein kinase 2-like, transcript variant X6
dual specificity testis-specific protein kinase 2-like, transcript variant X3
dual specificity testis-specific protein kinase 2-like, transcript variant X9
dual specificity testis-specific protein kinase 2-like, transcript variant X5
dual specificity testis-specific protein kinase 2-like, transcript variant X11
dual specificity testis-specific protein kinase 2-like, transcript variant X2
dual specificity testis-specific protein kinase 2-like, transcript variant X8
dual specificity testis-specific protein kinase 2-like, transcript variant X4
dual specificity testis-specific protein kinase 2-like, transcript variant X7
dual specificity testis-specific protein kinase 2-like, transcript variant X10
dual specificity testis-specific protein kinase 2-like, transcript variant X14
dual specificity testis-specific protein kinase 2-like, transcript variant X12
dual specificity testis-specific protein kinase 2-like, transcript variant X13
dual specificity testis-specific protein kinase 2-like, transcript variant X1
dual specificity testis-specific protein kinase 2-like isoform X1
dual specificity testis-specific protein kinase 2-like, transcript variant X15
dual specificity testis-specific protein kinase 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
FYVE, RhoGEF and PH domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC116496792, transcript variant X1
uncharacterized LOC116496792, transcript variant X2