Carcharodon carcharias isolate sCarCar2 chromosome X, sCarCar2.pri, whole genome shotgun sequence.
Carcharodon carcharias (great white shark)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Chondrichthyes; Elasmobranchii; Galeomorphii; Galeoidea; Lamniformes; Alopiidae; Carcharodon.
REFSEQ INFORMATION: The reference sequence is identical to\nCM030005.1.\nAssembly name: sCarCar2.pri\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Vertebrate Genomes Project on\n2021/03/30. The original whole-genome shotgun project has the\naccession JAGDEE000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Vertebrate Genomes Project\nAssembly Date :: 05-FEB-2021\nAssembly Method :: FALCON v. DX 2.0.1; FALCON-Unzip v. DX\n 1.2.1; purge_dups v. DX 19-08-10;\n scaff10X v. DX 2.0.3; bionano Solve v. DX\n 3.4.0; Salsa2 HiC v. DX 2.2.0; Arrow\n polishing and gap filling v. DX 7.0.1.1;\n Longranger Align DX v. 2.2.2.1; freebayes\n DX v. 19-07-11; gEVAL manual curation v.\n 2021-02-05; VGP assembly pipeline v. 1.6\nAssembly Name :: sCarCar2.pri\nDiploid :: Principal Pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 66.84x\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 :: Carcharodon carcharias Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.6\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC121273172, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC121273172, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% coverage of the annotated genomic feature by RNAseq alignments
POU domain, class 6, transcription factor 1
transcription factor CP2, transcript variant X1
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
transcription factor CP2, 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 2 samples with support for all annotated introns
R3H domain-containing protein 2, 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 1 sample with support for all annotated introns
R3H domain-containing protein 2, 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
R3H domain-containing protein 2, transcript variant X6
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
R3H domain-containing protein 2, transcript variant X5
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 4 samples with support for all annotated introns
R3H domain-containing protein 2, 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 3 samples with support for all annotated introns
R3H domain-containing protein 2, transcript variant X4
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
R3H domain-containing protein 2, transcript variant X2
R3H domain-containing protein 2 isoform X1
R3H domain-containing protein 2 isoform X2
R3H domain-containing protein 2 isoform X5
R3H domain-containing protein 2 isoform X4
R3H domain-containing protein 2 isoform X6
R3H domain-containing protein 2 isoform X3
diacylglycerol kinase beta-like, transcript variant X1
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
diacylglycerol kinase beta-like, 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
diacylglycerol kinase beta-like, 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 2 samples with support for all annotated introns
diacylglycerol kinase beta-like isoform X1
diacylglycerol kinase beta-like isoform X2
diacylglycerol kinase gamma-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
SH3 and cysteine-rich domain-containing protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00548
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 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: 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: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 69% 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
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 4 samples with support for all annotated introns
tumor necrosis factor receptor superfamily member 5-like, transcript variant X2
tumor necrosis factor receptor superfamily member 5-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tumor necrosis factor receptor superfamily member 5-like, transcript variant X1
tumor necrosis factor receptor superfamily member 5-like isoform X1
tumor necrosis factor receptor superfamily member 5-like isoform X2
uncharacterized LOC121273169, transcript variant X3
uncharacterized LOC121273169, transcript variant X2
uncharacterized LOC121273169, transcript variant X1
uncharacterized protein LOC121273169 isoform X3
uncharacterized protein LOC121273169 isoform X2
uncharacterized protein LOC121273169 isoform X1
histone acetyltransferase 1, transcript variant X2
histone acetyltransferase 1, transcript variant X1
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 4 samples with support for all annotated introns
histone acetyltransferase type B catalytic subunit isoform X2
histone acetyltransferase type B catalytic subunit isoform X1
calcitonin gene-related peptide type 1 receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
SPRY domain containing 3, 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 4 samples with support for all annotated introns
SPRY domain containing 3, transcript variant X3
SPRY domain containing 3, 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 3 samples with support for all annotated introns
SPRY domain-containing protein 3 isoform X2
SPRY domain-containing protein 3 isoform X1
insulin-like growth factor-binding protein 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2, 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
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2, transcript variant X2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2, transcript variant X1
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
SWI/SNF complex subunit SMARCC2 isoform X3
SWI/SNF complex subunit SMARCC2 isoform X2
SWI/SNF complex subunit SMARCC2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
BEN domain-containing protein 5-like, transcript variant X1
BEN domain-containing protein 5-like, transcript variant X3
BEN domain-containing protein 5-like, transcript variant X2
BEN domain-containing protein 5-like, transcript variant X4
BEN domain-containing protein 5-like isoform X1
BEN domain-containing protein 5-like isoform X3
BEN domain-containing protein 5-like isoform X2
BEN domain-containing protein 5-like isoform 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
acidic amino acid decarboxylase GADL1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 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: 22 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
natural resistance-associated macrophage protein 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
natural resistance-associated macrophage protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
natural resistance-associated macrophage protein 2-like, transcript variant X1
natural resistance-associated macrophage protein 2-like, transcript variant X4
natural resistance-associated macrophage protein 2-like isoform X1
natural resistance-associated macrophage protein 2-like isoform X2
natural resistance-associated macrophage protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
bridging integrator 2-like, 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
bridging integrator 2-like, transcript variant X3
bridging integrator 2-like, transcript variant X2
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
nck-associated protein 1-like, 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 2 samples with support for all annotated introns
nck-associated protein 1-like, 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 1 sample with support for all annotated introns
tachykinin-3-like, transcript variant X1
tachykinin-3-like, transcript variant X2
OS9 endoplasmic reticulum lectin, transcript variant X3
OS9 endoplasmic reticulum lectin, transcript variant X1
OS9 endoplasmic reticulum lectin, transcript variant X2
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 4 samples with support for all annotated introns
beta-1,4-N-acetyl-galactosaminyl transferase 1b
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
beta-1,4 N-acetylgalactosaminyltransferase 1
beta-1,4 N-acetylgalactosaminyltransferase 1-like
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: 7 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins
Golgi reassembly-stacking protein 2-like, transcript variant X1
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
Golgi reassembly-stacking protein 2-like, transcript variant X3
Golgi reassembly-stacking protein 2-like, 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 4 samples with support for all annotated introns
Golgi reassembly-stacking protein 2-like isoform X3
Golgi reassembly-stacking protein 2-like isoform X1
Golgi reassembly-stacking protein 2-like isoform X2
rho guanine nucleotide exchange factor 25-like, 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
rho guanine nucleotide exchange factor 25-like, 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
rho guanine nucleotide exchange factor 25-like, transcript variant X1
rho guanine nucleotide exchange factor 25-like, transcript variant X6
rho guanine nucleotide exchange factor 25-like, transcript variant X4
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 1 sample with support for all annotated introns
rho guanine nucleotide exchange factor 25-like, transcript variant X5
rho guanine nucleotide exchange factor 25-like isoform X3
rho guanine nucleotide exchange factor 25-like isoform X2
rho guanine nucleotide exchange factor 25-like isoform X1
rho guanine nucleotide exchange factor 25-like isoform X4
rho guanine nucleotide exchange factor 25-like isoform X6
rho guanine nucleotide exchange factor 25-like isoform X5
activin receptor type-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 131 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
activin receptor type-1-like, transcript variant X6
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
activin receptor type-1-like, transcript variant X4
activin receptor type-1-like, transcript variant X2
activin receptor type-1-like, transcript variant X5
activin receptor type-1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 131 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
activin receptor type-1B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
activin receptor type-1B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
activin receptor type-1B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
activin receptor type-1B-like isoform X1
activin receptor type-1B-like isoform X3
activin receptor type-1B-like isoform X2
trafficking regulator and scaffold protein tamalin, transcript variant X1
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
trafficking regulator and scaffold protein tamalin, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
general receptor for phosphoinositides 1-associated scaffold protein isoform X1
general receptor for phosphoinositides 1-associated scaffold protein isoform X2
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
nuclear receptor subfamily 4 group A member 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nuclear receptor subfamily 4 group A member 1-like, transcript variant X2
nuclear receptor subfamily 4 group A member 1-like isoform X1
nuclear receptor subfamily 4 group A member 1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear receptor subfamily 4 group A member 1-like isoform X2
nuclear receptor subfamily 4 group A member 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
nuclear receptor subfamily 4 group A member 1-like, transcript variant X7
nuclear receptor subfamily 4 group A member 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nuclear receptor subfamily 4 group A member 1-like isoform X3
nuclear receptor subfamily 4 group A member 1-like, transcript variant X5
nuclear receptor subfamily 4 group A member 1-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
formin-like protein 3, transcript variant X4
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 1 sample with support for all annotated introns
formin-like protein 3, 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
formin-like protein 3, transcript variant X1
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
formin-like protein 3, transcript variant X5
formin-like protein 3, transcript variant X2
retinol dehydrogenase 5 (11-cis/9-cis), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
retinol dehydrogenase 5 (11-cis/9-cis), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
retinol dehydrogenase 5 (11-cis/9-cis), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
biogenesis of lysosomal organelles complex-1, subunit 1
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 4 samples with support for all annotated introns
biogenesis of lysosome-related organelles complex 1 subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
integrin alpha-7-like, 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
integrin alpha-7-like, transcript variant X1
integrin alpha-7-like, transcript variant X2
integrin alpha-7-like, transcript variant X3
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sodium channel protein type 8 subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
RNA-binding motif, single-stranded-interacting protein 2-like, 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
RNA-binding motif, single-stranded-interacting protein 2-like, transcript variant X4
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
RNA-binding motif, single-stranded-interacting protein 2-like, transcript variant X2
RNA-binding motif, single-stranded-interacting protein 2-like isoform X1
RNA-binding motif, single-stranded-interacting protein 2-like isoform X4
RNA-binding motif, single-stranded-interacting protein 2-like isoform X2
RNA-binding motif, single-stranded-interacting protein 2-like, transcript variant X3
RNA-binding motif, single-stranded-interacting protein 2-like isoform X3
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic-like, transcript variant X2
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic-like
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1
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
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 1
acid-sensing (proton-gated) ion channel 1b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Rac GTPase activating protein 1, 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 4 samples with support for all annotated introns
Rac GTPase activating protein 1, transcript variant X1
uncharacterized si:ch211-210c8.6, 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 4 samples with support for all annotated introns
uncharacterized si:ch211-210c8.6, transcript variant X2
uncharacterized protein si:ch211-210c8.6 isoform X1
uncharacterized protein si:ch211-210c8.6 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
pre-miRNA 5'-monophosphate methyltransferase
keratin, type II cytoskeletal 8-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
keratin, type II cytoskeletal 8-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 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: 105 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: 92 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: 87 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
keratin, type I cytoskeletal 18-like, transcript variant X1
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
keratin, type I cytoskeletal 18-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 102 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
keratin, type I cytoskeletal 18-like isoform X1
keratin, type I cytoskeletal 18-like isoform X2
eukaryotic translation initiation factor 4Ba, transcript variant X1
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 4 samples with support for all annotated introns
eukaryotic translation initiation factor 4Ba, transcript variant X2
eukaryotic translation initiation factor 4Ba isoform X1
eukaryotic translation initiation factor 4Ba isoform X2
PYM homolog 1, exon junction complex associated factor, transcript variant X2
PYM homolog 1, exon junction complex associated factor, transcript variant X4
PYM homolog 1, exon junction complex associated factor, transcript variant X3
PYM homolog 1, exon junction complex associated factor, transcript variant X6
PYM homolog 1, exon junction complex associated factor, transcript variant X5
PYM homolog 1, exon junction complex associated factor, transcript variant X1
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 4 samples with support for all annotated introns
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89 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: 381 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 561 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: 559 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 510 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
limb development membrane protein 1-like
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
lysine (K)-specific methyltransferase 2D, transcript variant X2
lysine (K)-specific methyltransferase 2D, transcript variant X3
lysine (K)-specific methyltransferase 2D, transcript variant X8
lysine (K)-specific methyltransferase 2D, transcript variant X7
lysine (K)-specific methyltransferase 2D, transcript variant X1
lysine (K)-specific methyltransferase 2D, transcript variant X10
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
lysine (K)-specific methyltransferase 2D, transcript variant X11
lysine (K)-specific methyltransferase 2D, transcript variant X12
lysine (K)-specific methyltransferase 2D, transcript variant X9
lysine (K)-specific methyltransferase 2D, transcript variant X14
lysine (K)-specific methyltransferase 2D, transcript variant X13
lysine (K)-specific methyltransferase 2D, transcript variant X16
lysine (K)-specific methyltransferase 2D, transcript variant X17
lysine (K)-specific methyltransferase 2D, transcript variant X15
lysine (K)-specific methyltransferase 2D, transcript variant X4
lysine (K)-specific methyltransferase 2D, transcript variant X6
lysine (K)-specific methyltransferase 2D, transcript variant X5
histone-lysine N-methyltransferase 2D isoform X1
histone-lysine N-methyltransferase 2D isoform X3
histone-lysine N-methyltransferase 2D isoform X4
histone-lysine N-methyltransferase 2D isoform X5
histone-lysine N-methyltransferase 2D isoform X2
histone-lysine N-methyltransferase 2D isoform X7
histone-lysine N-methyltransferase 2D isoform X6
histone-lysine N-methyltransferase 2D isoform X9
histone-lysine N-methyltransferase 2D isoform X10
histone-lysine N-methyltransferase 2D isoform X8
transfer RNA opal suppressor (anticodon UCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
5'-AMP-activated protein kinase subunit gamma-1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
5'-AMP-activated protein kinase subunit gamma-1, transcript variant X1
5'-AMP-activated protein kinase subunit gamma-1 isoform X1
5'-AMP-activated protein kinase subunit gamma-1, 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
5'-AMP-activated protein kinase subunit gamma-1 isoform X2
wingless-type MMTV integration site family, member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
wingless-type MMTV integration site family, member 10b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
ADP-ribosylation factor 3-like, transcript variant X5
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 4 samples with support for all annotated introns
ADP-ribosylation factor 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 193 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ADP-ribosylation factor 3-like, transcript variant X4
ADP-ribosylation factor 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 193 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ADP-ribosylation factor 3-like, transcript variant X3
ADP-ribosylation factor 1-like isoform X2
ADP-ribosylation factor 3-like isoform X1
FKBP prolyl isomerase 11, transcript variant X2
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 1 sample with support for all annotated introns
FKBP prolyl isomerase 11, transcript variant X4
FKBP prolyl isomerase 11, transcript variant X8
FKBP prolyl isomerase 11, transcript variant X5
FKBP prolyl isomerase 11, transcript variant X6
FKBP prolyl isomerase 11, transcript variant X11
peptidyl-prolyl cis-trans isomerase FKBP11 isoform X2
peptidyl-prolyl cis-trans isomerase FKBP11 isoform X4
FKBP prolyl isomerase 11, transcript variant X9
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
FKBP prolyl isomerase 11, transcript variant X10
FKBP prolyl isomerase 11, transcript variant X1
FKBP prolyl isomerase 11, transcript variant X3
peptidyl-prolyl cis-trans isomerase FKBP11 isoform X1
peptidyl-prolyl cis-trans isomerase FKBP11 isoform X3
FKBP prolyl isomerase 11, transcript variant X7
FKBP prolyl isomerase 11, transcript variant X12
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 4 samples with support for all annotated introns
peptidyl-prolyl cis-trans isomerase FKBP11 isoform 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 3 samples with support for all annotated introns
TAR (HIV) RNA binding protein 2, transcript variant X2
TAR (HIV) RNA binding protein 2, transcript variant X1
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
RISC-loading complex subunit tarbp2 isoform X2
RISC-loading complex subunit tarbp2 isoform X1
pleckstrin homology domain-containing family A member 3-like
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
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
erb-b2 receptor tyrosine kinase 3a, transcript variant X1
erb-b2 receptor tyrosine kinase 3a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
receptor tyrosine-protein kinase erbB-3a isoform X1
receptor tyrosine-protein kinase erbB-3a isoform X2
40S ribosomal protein S26-like, 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 4 samples with support for all annotated introns
40S ribosomal protein S26-like, transcript variant X1
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
40S ribosomal protein S26-like isoform X1
40S ribosomal protein S26-like isoform X2
IKAROS family zinc finger 4, transcript variant X4
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 1 sample with support for all annotated introns
IKAROS family zinc finger 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
IKAROS family zinc finger 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
IKAROS family zinc finger 4, 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 4 samples with support for all annotated introns
uncharacterized LOC121273306, transcript variant X1
uncharacterized LOC121273306, transcript variant X2
leucine-rich repeat flightless-interacting protein 1-like
ras-related protein Rab-5B, transcript variant X2
ras-related protein Rab-5B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cyclin-dependent kinase 2, transcript variant X3
cyclin-dependent kinase 2, transcript variant X2
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
cyclin-dependent kinase 2, transcript variant X1
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
premelanosome protein a, transcript variant X1
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
premelanosome protein a, transcript variant X2
microspherule protein 1, transcript variant X1
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 4 samples with support for all annotated introns
microspherule protein 1, 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 4 samples with support for all annotated introns
microspherule protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
spermatogenesis associated serine rich 2, transcript variant X1
spermatogenesis associated serine rich 2, transcript variant X2
spermatogenesis-associated serine-rich protein 2
DnaJ (Hsp40) homolog, subfamily C, member 22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC121273174, transcript variant X1
uncharacterized LOC121273174, transcript variant X2
uncharacterized protein LOC121273174 isoform X1
uncharacterized protein LOC121273174 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
zinc finger CCCH-type containing 10, transcript variant X2
zinc finger CCCH-type containing 10, transcript variant X1
zinc finger CCCH domain-containing protein 10
zinc finger CCCH domain-containing protein 10-like, 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 2 samples with support for all annotated introns
zinc finger CCCH domain-containing protein 10-like, transcript variant X1
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 4 samples with support for all annotated introns
zinc finger CCCH domain-containing protein 10-like, transcript variant X2
zinc finger CCCH domain-containing protein 10-like
zinc finger CCCH domain-containing protein 10-like, transcript variant X32
zinc finger CCCH domain-containing protein 10-like, transcript variant X36
zinc finger CCCH domain-containing protein 10-like, transcript variant X16
zinc finger CCCH domain-containing protein 10-like, transcript variant X33
zinc finger CCCH domain-containing protein 10-like, transcript variant X30
zinc finger CCCH domain-containing protein 10-like, transcript variant X11
zinc finger CCCH domain-containing protein 10-like, transcript variant X34
zinc finger CCCH domain-containing protein 10-like, transcript variant X29
zinc finger CCCH domain-containing protein 10-like, transcript variant X12
zinc finger CCCH domain-containing protein 10-like, transcript variant X13
zinc finger CCCH domain-containing protein 10-like, transcript variant X28
zinc finger CCCH domain-containing protein 10-like, transcript variant X35
zinc finger CCCH domain-containing protein 10-like, transcript variant X5
zinc finger CCCH domain-containing protein 10-like, transcript variant X7
zinc finger CCCH domain-containing protein 10-like, transcript variant X31
zinc finger CCCH domain-containing protein 10-like, transcript variant X17
zinc finger CCCH domain-containing protein 10-like, transcript variant X19
zinc finger CCCH domain-containing protein 10-like, transcript variant X18
zinc finger CCCH domain-containing protein 10-like, transcript variant X20
zinc finger CCCH domain-containing protein 10-like, transcript variant X22
zinc finger CCCH domain-containing protein 10-like, transcript variant X21
zinc finger CCCH domain-containing protein 10-like, transcript variant X23
zinc finger CCCH domain-containing protein 10-like, transcript variant X24
zinc finger CCCH domain-containing protein 10-like, transcript variant X25
zinc finger CCCH domain-containing protein 10-like, transcript variant X8
zinc finger CCCH domain-containing protein 10-like, transcript variant X10
zinc finger CCCH domain-containing protein 10-like, transcript variant X9
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
zinc finger CCCH domain-containing protein 10-like isoform X2
zinc finger CCCH domain-containing protein 10-like, transcript variant X14
zinc finger CCCH domain-containing protein 10-like, transcript variant X15
zinc finger CCCH domain-containing protein 10-like, transcript variant X6
zinc finger CCCH domain-containing protein 10-like, transcript variant X4
uncharacterized protein LOC121273345 isoform X3
uncharacterized protein LOC121273345 isoform X4
zinc finger CCCH domain-containing protein 10-like isoform X1
zinc finger CCCH domain-containing protein 10-like, transcript variant X37
zinc finger CCCH domain-containing protein 10-like, transcript variant X27
zinc finger CCCH domain-containing protein 10-like, transcript variant X26
ATP synthase subunit epsilon, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ATP synthase subunit epsilon, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
electroneutral sodium bicarbonate exchanger 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
polypeptide N-acetylgalactosaminyltransferase 6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 6-like
chymotrypsin-like elastase family member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
cysteine/serine-rich nuclear protein 2-like, transcript variant X4
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 1 sample with support for all annotated introns
cysteine/serine-rich nuclear protein 2-like isoform X2
cysteine/serine-rich nuclear protein 2-like, transcript variant X2
cysteine/serine-rich nuclear protein 2-like, 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
cysteine/serine-rich nuclear protein 2-like, transcript variant X3
cysteine/serine-rich nuclear protein 2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
LIM domain and actin-binding protein 1-like, 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
LIM domain and actin-binding protein 1-like, transcript variant X1
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
LIM domain and actin-binding protein 1-like, transcript variant X5
LIM domain and actin-binding protein 1-like, transcript variant X4
LIM domain and actin-binding protein 1-like, transcript variant X6
LIM domain and actin-binding protein 1-like, transcript variant X7
LIM domain and actin-binding protein 1-like, transcript variant X3
LIM domain and actin-binding protein 1-like isoform X1
LIM domain and actin-binding protein 1-like isoform X3
LIM domain and actin-binding protein 1-like isoform X2
LIM domain and actin-binding protein 1-like isoform X4
LIM domain and actin-binding protein 1-like isoform X5
STE20/SPS1-related proline-alanine-rich protein kinase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
ceramide synthase 6-like, transcript variant X1
ceramide synthase 6-like, transcript variant X2
cytochrome c oxidase assembly protein COX14, transcript variant X4
cytochrome c oxidase assembly protein COX14, transcript variant X3
cytochrome c oxidase assembly protein COX14, transcript variant X2
cytochrome c oxidase assembly protein COX14, transcript variant X5
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
cytochrome c oxidase assembly protein COX14, transcript variant X1
cytochrome c oxidase assembly protein COX14 isoform X1
cytochrome c oxidase assembly protein COX14 isoform X2
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X6
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X2
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X5
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X4
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X3
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X1
bromodomain adjacent to zinc finger domain protein 2B-like isoform X3
bromodomain adjacent to zinc finger domain protein 2B-like isoform X2
bromodomain adjacent to zinc finger domain protein 2B-like isoform X1
bromodomain adjacent to zinc finger domain protein 2B-like isoform X4
bromodomain adjacent to zinc finger domain protein 2B-like isoform X5
prostaglandin E synthase 3-like, transcript variant X2
prostaglandin E synthase 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
prostaglandin E synthase 3-like isoform X2
prostaglandin E synthase 3-like isoform X1
nascent polypeptide associated complex subunit alpha, transcript variant X5
nascent polypeptide associated complex subunit alpha, transcript variant X3
nascent polypeptide associated complex subunit alpha, transcript variant X8
nascent polypeptide associated complex subunit alpha, transcript variant X7
nascent polypeptide associated complex subunit alpha, transcript variant X1
nascent polypeptide associated complex subunit alpha, transcript variant X9
nascent polypeptide associated complex subunit alpha, transcript variant X14
nascent polypeptide associated complex subunit alpha, transcript variant X10
nascent polypeptide associated complex subunit alpha, transcript variant X12
nascent polypeptide associated complex subunit alpha, transcript variant X11
nascent polypeptide associated complex subunit alpha, transcript variant X13
nascent polypeptide associated complex subunit alpha, transcript variant X4
nascent polypeptide associated complex subunit alpha, transcript variant X2
nascent polypeptide associated complex subunit alpha, transcript variant X6
nascent polypeptide associated complex subunit alpha, transcript variant X15
nascent polypeptide associated complex subunit alpha, transcript variant X16
nascent polypeptide-associated complex subunit alpha isoform X12
nascent polypeptide-associated complex subunit alpha isoform X11
nascent polypeptide-associated complex subunit alpha isoform X10
nascent polypeptide-associated complex subunit alpha isoform X6
nascent polypeptide-associated complex subunit alpha isoform X3
nascent polypeptide-associated complex subunit alpha isoform X9
nascent polypeptide-associated complex subunit alpha isoform X2
nascent polypeptide-associated complex subunit alpha isoform X8
nascent polypeptide-associated complex subunit alpha isoform X7
nascent polypeptide-associated complex subunit alpha isoform X5
nascent polypeptide-associated complex subunit alpha isoform X4
nascent polypeptide-associated complex subunit alpha isoform X1
DNA primase subunit 1, transcript variant X3
DNA primase subunit 1, transcript variant X2
DNA primase subunit 1, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
zinc finger and BTB domain-containing protein 39-like, transcript variant X2
zinc finger and BTB domain-containing protein 39-like, transcript variant X1
zinc finger and BTB domain-containing protein 39-like
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1-like, transcript variant X1
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1-like, transcript variant X2
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1-like isoform X1
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cyclin-dependent kinase 4, transcript variant X2
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
cyclin-dependent kinase 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
E3 ubiquitin-protein ligase MARCHF9-like
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, including 2 samples with support for all annotated introns
methyltransferase like 1, transcript variant X5
methyltransferase like 1, transcript variant X1
methyltransferase like 1, transcript variant X2
tRNA (guanine-N(7)-)-methyltransferase isoform X1
tRNA (guanine-N(7)-)-methyltransferase isoform X2
methyltransferase like 1, transcript variant X4
methyltransferase like 1, transcript variant X3
tRNA (guanine-N(7)-)-methyltransferase isoform X3
tRNA (guanine-N(7)-)-methyltransferase isoform X4
25-hydroxyvitamin D-1 alpha hydroxylase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
EEF1A lysine methyltransferase 3-like, transcript variant X4
EEF1A lysine methyltransferase 3-like, transcript variant X1
EEF1A lysine methyltransferase 3-like, transcript variant X2
EEF1A lysine methyltransferase 3-like, transcript variant X5
EEF1A lysine methyltransferase 3-like, transcript variant X3
EEF1A lysine methyltransferase 3-like, transcript variant X6
Ts translation elongation factor, mitochondrial, 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 4 samples with support for all annotated introns
Ts translation elongation factor, mitochondrial, transcript variant X3
Ts translation elongation factor, mitochondrial, transcript variant X2
elongation factor Ts, mitochondrial isoform X1
elongation factor Ts, mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
poly(A) specific ribonuclease subunit PAN2, transcript variant X1
poly(A) specific ribonuclease subunit PAN2, transcript variant X3
poly(A) specific ribonuclease subunit PAN2, transcript variant X2
poly(A) specific ribonuclease subunit PAN2, transcript variant X7
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X5
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X1
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X2
poly(A) specific ribonuclease subunit PAN2, transcript variant X4
poly(A) specific ribonuclease subunit PAN2, transcript variant X6
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X4
poly(A) specific ribonuclease subunit PAN2, transcript variant X5
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X3
poly(A) specific ribonuclease subunit PAN2, transcript variant X8
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X6
inositol polyphosphate 1-phosphatase-like, transcript variant X1
inositol polyphosphate 1-phosphatase-like, transcript variant X3
inositol polyphosphate 1-phosphatase-like, transcript variant X2
inositol polyphosphate 1-phosphatase-like
SAP domain containing ribonucleoprotein, transcript variant X1
SAP domain containing ribonucleoprotein, transcript variant X2
SAP domain-containing ribonucleoprotein isoform X1
SAP domain-containing ribonucleoprotein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 129 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
ORMDL sphingolipid biosynthesis regulator 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ORMDL sphingolipid biosynthesis regulator 2, transcript variant X2
ORMDL sphingolipid biosynthesis regulator 2, transcript variant X1
ORMDL sphingolipid biosynthesis regulator 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
DnaJ (Hsp40) homolog, subfamily C, member 14, transcript variant X2
DnaJ (Hsp40) homolog, subfamily C, member 14, transcript variant X4
DnaJ (Hsp40) homolog, subfamily C, member 14, transcript variant X5
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
DnaJ (Hsp40) homolog, subfamily C, member 14, transcript variant X3
DnaJ (Hsp40) homolog, subfamily C, member 14, transcript variant X1
nuclear envelope integral membrane protein 1
signal transducer and activator of transcription 5B-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
signal transducer and activator of transcription 5B-like, transcript variant X6
signal transducer and activator of transcription 5B-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
signal transducer and activator of transcription 5B-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
signal transducer and activator of transcription 5B-like, transcript variant X2
signal transducer and activator of transcription 5B-like, transcript variant X1
signal transducer and activator of transcription 5B-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
signal transducer and activator of transcription 5B-like, transcript variant X3
signal transducer and activator of transcription 5B-like isoform X2
signal transducer and activator of transcription 5B-like isoform X1
glutaminase kidney isoform, mitochondrial-like, transcript variant X1
glutaminase liver isoform, mitochondrial-like isoform X1
glutaminase kidney isoform, mitochondrial-like, transcript variant X2
glutaminase kidney isoform, mitochondrial-like isoform X2
signal transducer and activator of transcription 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 138 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
signal transducer and activator of transcription 1-like, transcript variant X5
signal transducer and activator of transcription 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 138 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
signal transducer and activator of transcription 1-like, transcript variant X2
signal transducer and activator of transcription 1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
signal transducer and activator of transcription 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 138 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
signal transducer and activator of transcription 1-like isoform X3
signal transducer and activator of transcription 1-like isoform X1
signal transducer and activator of transcription 1-like isoform X2
unconventional myosin-Ib-like, transcript variant X2
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
unconventional myosin-Ib-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
unconventional myosin-Ib-like isoform X2
unconventional myosin-Ib-like isoform X1
E3 ubiquitin-protein ligase NRDP1, transcript variant X1
E3 ubiquitin-protein ligase NRDP1, transcript variant X2
E3 ubiquitin-protein ligase NRDP1, transcript variant X3
transfer RNA serine (anticodon CGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
E3 ubiquitin-protein ligase NRDP1, transcript variant X6
E3 ubiquitin-protein ligase NRDP1, transcript variant X4
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
E3 ubiquitin-protein ligase NRDP1, transcript variant X5
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
E3 ubiquitin-protein ligase NRDP1, transcript variant X7
E3 ubiquitin-protein ligase NRDP1 isoform X2
E3 ubiquitin-protein ligase NRDP1 isoform X3
gamma-crystallin M2-like, transcript variant X2
gamma-crystallin M2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit C-like, transcript variant X1
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit C-like isoform X1
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit C-like, 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
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit C-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 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: 14 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins
low-density lipoprotein receptor-related protein 1-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
DNA-damage-inducible transcript 3, transcript variant X2
DNA-damage-inducible transcript 3, transcript variant X3
DNA-damage-inducible transcript 3, transcript variant X1
DNA damage-inducible transcript 3 protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments