Carcharodon carcharias isolate sCarCar2 chromosome 32, 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\nCM029996.1.\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.
thrombospondin type-1 domain-containing protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
leucine-rich repeat-containing protein 49, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
leucine-rich repeat-containing protein 49, 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
leucine-rich repeat-containing protein 49, transcript variant X1
leucine-rich repeat-containing protein 49, transcript variant X4
leucine-rich repeat-containing protein 49, transcript variant X5
leucine-rich repeat-containing protein 49 isoform X2
leucine-rich repeat-containing protein 49 isoform X3
leucine-rich repeat-containing protein 49 isoform X1
leucine-rich repeat-containing protein 49 isoform X4
leucine-rich repeat-containing protein 49 isoform X5
La ribonucleoprotein 6, translational regulator a
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
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
TM2 domain containing 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 1 sample with support for all annotated introns
TM2 domain-containing protein 3 isoform X4
TM2 domain containing 3, transcript variant X7
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
TM2 domain containing 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
TM2 domain containing 3, transcript variant X1
TM2 domain containing 3, transcript variant X3
TM2 domain containing 3, 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 4 samples with support for all annotated introns
TM2 domain-containing protein 3 isoform X7
TM2 domain-containing protein 3 isoform X6
TM2 domain-containing protein 3 isoform X1
TM2 domain containing 3, transcript variant X5
TM2 domain-containing protein 3 isoform X3
TM2 domain-containing protein 3 isoform X2
TM2 domain-containing protein 3 isoform X5
TM2 domain containing 3, transcript variant X8
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
TM2 domain-containing protein 3 isoform X8
threonine--tRNA ligase 1, cytoplasmic-like, 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 2 samples with support for all annotated introns
threonine--tRNA ligase 1, cytoplasmic-like
threonine--tRNA ligase 1, cytoplasmic-like, transcript variant X2
tight junction protein ZO-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 3 samples with support for all annotated introns
tight junction protein ZO-1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tight junction protein ZO-1-like, transcript variant X7
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 3 samples with support for all annotated introns
tight junction protein ZO-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 1 sample with support for all annotated introns
tight junction protein ZO-1-like, transcript variant X2
tight junction protein ZO-1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tight junction protein ZO-1-like isoform X2
tight junction protein ZO-1-like isoform X1
tight junction protein ZO-1-like isoform X3
tight junction protein ZO-1-like isoform X5
tight junction protein ZO-1-like isoform X6
tight junction protein ZO-1-like, transcript variant X5
tight junction protein ZO-1-like isoform X4
family with sequence similarity 189 member A1, 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 2 samples with support for all annotated introns
family with sequence similarity 189 member A1, transcript variant X2
family with sequence similarity 189 member A1, transcript variant X3
family with sequence similarity 189 member A1, transcript variant X4
family with sequence similarity 189 member A1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
amyloid beta (A4) precursor protein-binding, family A, member 2b, transcript variant X2
amyloid beta (A4) precursor protein-binding, family A, member 2b, transcript variant X5
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
amyloid beta (A4) precursor protein-binding, family A, member 2b, 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 3 samples with support for all annotated introns
amyloid beta (A4) precursor protein-binding, family A, member 2b, transcript variant X1
amyloid beta (A4) precursor protein-binding, family A, member 2b, transcript variant X3
amyloid-beta A4 precursor protein-binding family A member 2 isoform X3
amyloid-beta A4 precursor protein-binding family A member 2 isoform X2
amyloid-beta A4 precursor protein-binding family A member 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins
M-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein)
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
U3 small nucleolar ribonucleoprotein protein MPP10
FANCD2 and FANCI associated nuclease 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 4 samples with support for all annotated introns
FANCD2 and FANCI associated nuclease 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
FANCD2 and FANCI associated nuclease 1, transcript variant X2
fanconi-associated nuclease 1 isoform X1
fanconi-associated nuclease 1 isoform X2
fanconi-associated nuclease 1 isoform X3
myotubularin related protein 10, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
myotubularin related protein 10, transcript variant X1
myotubularin related protein 10, 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 2 samples with support for all annotated introns
myotubularin-related protein 10 isoform X2
myotubularin-related protein 10 isoform X1
myotubularin-related protein 10 isoform X3
transient receptor potential cation channel subfamily M member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 2% 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, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
OTU deubiquitinase 7A, transcript variant X2
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
OTU deubiquitinase 7A, transcript variant X4
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
OTU deubiquitinase 7A, transcript variant X3
OTU deubiquitinase 7A, 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 1 sample with support for all annotated introns
OTU deubiquitinase 7A, transcript variant X5
OTU domain-containing protein 7A isoform X1
OTU domain-containing protein 7A isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 3-like
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: tRNAscan-SE.
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
ADP-dependent glucokinase, transcript variant X1
ADP-dependent glucokinase, transcript variant X2
ADP-dependent glucokinase, transcript variant X5
ADP-dependent glucokinase, transcript variant X3
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
ADP-dependent glucokinase, transcript variant X4
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
ADP-dependent glucokinase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Bardet-Biedl syndrome 4, transcript variant X3
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
Bardet-Biedl syndrome 4, transcript variant X1
Bardet-Biedl syndrome 4, transcript variant X2
Bardet-Biedl syndrome 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Bardet-Biedl syndrome 4 protein isoform X2
Bardet-Biedl syndrome 4 protein isoform X1
Bardet-Biedl syndrome 4 protein isoform X3
E3 ubiquitin-protein ligase ARIH1, 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
E3 ubiquitin-protein ligase ARIH1, transcript variant X2
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
E3 ubiquitin-protein ligase ARIH1, transcript variant X3
E3 ubiquitin-protein ligase ARIH1, transcript variant X4
E3 ubiquitin-protein ligase ARIH1 isoform X2
E3 ubiquitin-protein ligase arih1 isoform X1
E3 ubiquitin-protein ligase ARIH1 isoform X3
E3 ubiquitin-protein ligase ARIH1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
peptidylprolyl isomerase B (cyclophilin B)
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 4 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00600
leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
nuclear receptor subfamily 2, group E, member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
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
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
SUMO peptidase family member, NEDD8 specific, transcript variant X1
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 4 samples with support for all annotated introns
SUMO peptidase family member, NEDD8 specific, transcript variant 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 2 samples with support for all annotated introns
SUMO peptidase family member, NEDD8 specific, transcript variant X3
SUMO peptidase family member, NEDD8 specific, transcript variant X2
SUMO peptidase family member, NEDD8 specific, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
IQ motif containing GTPase activating protein 1, transcript variant X2
IQ motif containing GTPase activating protein 1, transcript variant X1
ras GTPase-activating-like protein IQGAP1 isoform X1
ras GTPase-activating-like protein IQGAP1 isoform X2
CREB regulated transcription coactivator 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
CREB regulated transcription coactivator 3, transcript variant X2
CREB regulated transcription coactivator 3, transcript variant X4
CREB regulated transcription coactivator 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
CREB-regulated transcription coactivator 3 isoform X2
CREB-regulated transcription coactivator 3 isoform X1
CREB-regulated transcription coactivator 3 isoform X3
CREB regulated transcription coactivator 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
CREB-regulated transcription coactivator 3 isoform X4
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: 8 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
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
FES proto-oncogene, tyrosine kinase, 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
FES proto-oncogene, tyrosine kinase, 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
FES proto-oncogene, tyrosine kinase, 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
FES proto-oncogene, tyrosine kinase, transcript variant X3
tyrosine-protein kinase Fes/Fps isoform X1
tyrosine-protein kinase Fes/Fps isoform X2
mannosidase, alpha, class 2A, member 2, 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
mannosidase, alpha, class 2A, member 2, transcript variant X2
protein shisa-like-1a, transcript variant X2
protein shisa-like-1a, transcript variant X1
protein shisa-like-1a, transcript variant X3
protein unc-45 homolog A-like, transcript variant X2
protein unc-45 homolog A-like, 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 4 samples with support for all annotated introns
protein unc-45 homolog A-like isoform X1
protein unc-45 homolog A-like isoform X2
RCC1 domain-containing protein 1-like, transcript variant X1
RCC1 domain-containing protein 1-like, transcript variant X2
RCC1 domain-containing protein 1-like, transcript variant X3
RCC1 domain-containing protein 1-like isoform X1
RCC1 domain-containing protein 1-like isoform X2
calcium and integrin-binding protein 1-like, transcript variant X3
calcium and integrin-binding protein 1-like, transcript variant X2
calcium and integrin-binding protein 1-like, transcript variant X1
calcium and integrin-binding protein 1-like isoform X1
calcium and integrin-binding protein 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
tubulin tyrosine ligase-like family, member 6, 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 1 sample with support for all annotated introns
tubulin tyrosine ligase-like family, member 6, transcript variant X5
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
tubulin tyrosine ligase-like family, member 6, transcript variant X1
tubulin tyrosine ligase-like family, member 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tubulin tyrosine ligase-like family, member 6, transcript variant X4
tubulin polyglutamylase ttll6 isoform X2
tubulin polyglutamylase ttll6 isoform X1
tubulin polyglutamylase ttll6 isoform X3
tubulin polyglutamylase ttll6 isoform X4
tubulin polyglutamylase ttll6 isoform X5
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
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
guanosine-3',5'-bis(diphosphate) 3'-pyrophosphohydrolase MESH1
VPS33B late endosome and lysosome associated, 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 4 samples with support for all annotated introns
VPS33B late endosome and lysosome associated, transcript variant X2
vacuolar protein sorting-associated protein 33B isoform X1
vacuolar protein sorting-associated protein 33B isoform X2
protein regulator of cytokinesis 1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein regulator of cytokinesis 1b, transcript variant X1
protein regulator of cytokinesis 1b, transcript variant X4
protein regulator of cytokinesis 1b, transcript variant X3
protein regulator of cytokinesis 1b isoform X1
protein regulator of cytokinesis 1b isoform X3
protein regulator of cytokinesis 1b isoform X4
protein regulator of cytokinesis 1b isoform X2
creatine kinase U-type, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
creatine kinase U-type, mitochondrial-like, transcript variant X1
creatine kinase U-type, mitochondrial-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
creatine kinase U-type, mitochondrial-like, transcript variant X3
creatine kinase U-type, mitochondrial-like, transcript variant X5
creatine kinase U-type, mitochondrial-like, transcript variant X6
creatine kinase U-type, mitochondrial-like isoform X1
creatine kinase U-type, mitochondrial-like isoform X2
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like, transcript variant X11
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
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like, transcript variant X1
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
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-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 3 samples with support for all annotated introns
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like, transcript variant X5
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 2 samples with support for all annotated introns
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like, transcript variant X7
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
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like, transcript variant X6
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
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like, transcript variant X8
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
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like, transcript variant X9
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like, transcript variant X10
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
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like, transcript variant X4
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 1 sample with support for all annotated introns
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 1-like isoform X3
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like, transcript variant X2
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 2 samples with support for all annotated introns
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like isoform X10
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 1-like isoform X1
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like isoform X2
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like isoform X4
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like isoform X6
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 1-like isoform X5
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like isoform X7
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like isoform X8
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2-like isoform X9
microtubule-associated protein 1A-like, transcript variant X3
microtubule-associated protein 1A-like, transcript variant X1
microtubule-associated protein 1A-like, transcript variant X2
microtubule-associated protein 1A-like isoform X1
microtubule-associated protein 1A-like isoform X2
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
tubulin, gamma complex associated protein 4, transcript variant X1
tubulin, gamma complex associated protein 4, 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
gamma-tubulin complex component 4 isoform X2
gamma-tubulin complex component 4 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
cocaine- and amphetamine-regulated transcript protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
tetratricopeptide repeat domain 23, transcript variant X1
tetratricopeptide repeat domain 23, transcript variant X2
tetratricopeptide repeat protein 23 isoform X1
tetratricopeptide repeat protein 23 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00007
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
family with sequence similarity 169 member B
SH2 domain-containing adapter protein F-like, transcript variant X1
SH2 domain-containing adapter protein F-like, transcript variant X2
SH2 domain-containing adapter protein F-like isoform X2
SH2 domain-containing adapter protein D-like isoform X1
neuronal acetylcholine receptor subunit beta-4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 115 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neuronal acetylcholine receptor subunit alpha-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 110 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin-like 7a (bone marrow stromal cell-derived)
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
pseudopodium-enriched atypical kinase 1, 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
pseudopodium-enriched atypical kinase 1, transcript variant X2
inactive tyrosine-protein kinase PEAK1 isoform X2
inactive tyrosine-protein kinase PEAK1 isoform X1
pseudopodium-enriched atypical kinase 1, transcript variant X3
inactive tyrosine-protein kinase PEAK1 isoform X3
high mobility group 20A, transcript variant X2
high mobility group 20A, transcript variant X4
high mobility group 20A, 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 3 samples with support for all annotated introns
high mobility group 20A, transcript variant X1
high mobility group 20A, transcript variant X6
high mobility group 20A, transcript variant X5
high mobility group protein 20A isoform X3
high mobility group protein 20A isoform X4
high mobility group protein 20A isoform X1
high mobility group protein 20A isoform X2
high mobility group protein 20A isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
proline-serine-threonine phosphatase-interacting protein 1-like
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
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
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
S-phase cyclin A-associated protein in the ER, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
S-phase cyclin A-associated protein in the ER, transcript variant X1
S-phase cyclin A-associated protein in the ER, transcript variant X4
S-phase cyclin A-associated protein in the ER, transcript variant X3
S phase cyclin A-associated protein in the endoplasmic reticulum isoform X2
S phase cyclin A-associated protein in the endoplasmic reticulum isoform X1
S phase cyclin A-associated protein in the endoplasmic reticulum isoform X4
S phase cyclin A-associated protein in the endoplasmic reticulum isoform X3
insulin gene enhancer protein ISL-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 93% 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: insulin gene enhancer protein ISL-2-like
electron transfer flavoprotein subunit alpha
electron transfer flavoprotein subunit alpha, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
pro-neuregulin-4, membrane-bound isoform-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 1 sample 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
unc-51 like kinase 3, transcript variant X1
unc-51 like kinase 3, 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
unc-51 like kinase 3, transcript variant X2
serine/threonine-protein kinase ULK3 isoform X1
serine/threonine-protein kinase ULK3 isoform X2
serine/threonine-protein kinase ULK3 isoform X3
secretory carrier-associated membrane protein 2-like
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
stomatin (EPB72)-like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
stomatin (EPB72)-like 1, transcript variant X5
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
stomatin (EPB72)-like 1, transcript variant X3
stomatin (EPB72)-like 1, transcript variant X2
stomatin (EPB72)-like 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
immunoglobulin superfamily containing leucine-rich repeat 2
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, including 1 sample with support for all annotated introns
immunoglobulin superfamily containing leucine-rich repeat protein 2
signaling receptor and transporter of retinol STRA6, transcript variant X1
signaling receptor and transporter of retinol STRA6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 33
COORDINATES: nucleotide motif:Rfam:12.0:RF00563
cholesterol side-chain cleavage enzyme, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins
telomere repeat binding bouquet formation protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
telomere repeats-binding bouquet formation protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 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: 15 Proteins, and 56% 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
sorbitol dehydrogenase-like, 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
sorbitol dehydrogenase-like, transcript variant X1
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
sorbitol dehydrogenase-like, transcript variant X2
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 1 sample with support for all annotated introns
sorbitol dehydrogenase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins
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
C-terminal Src kinase, transcript variant X3
C-terminal Src kinase, transcript variant X4
C-terminal Src kinase, transcript variant X2
C-terminal Src kinase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
C-terminal Src kinase, transcript variant X1
collagen and calcium-binding EGF domain-containing protein 1-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
collagen and calcium-binding EGF domain-containing protein 1-like, transcript variant X2
collagen and calcium-binding EGF domain-containing protein 1-like isoform X1
collagen and calcium-binding EGF domain-containing protein 1-like isoform X2
collagen and calcium-binding EGF domain-containing protein 1-like, transcript variant X4
collagen and calcium-binding EGF domain-containing protein 1-like, transcript variant X3
collagen and calcium-binding EGF domain-containing protein 1-like isoform X3
collagen and calcium-binding EGF domain-containing protein 1-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 192 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
enhancer of mRNA decapping 3 homolog (S. cerevisiae), transcript variant X1
enhancer of mRNA decapping 3 homolog (S. cerevisiae), transcript variant X2
enhancer of mRNA-decapping protein 3 isoform X2
enhancer of mRNA-decapping protein 3 isoform X1
flagellar attachment zone protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
AT rich interactive domain 3B (BRIGHT-like)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 64% coverage of the annotated genomic feature by RNAseq alignments
AT-rich interactive domain-containing protein 3B
ribonuclease P protein subunit p25-like protein
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
cytochrome c oxidase subunit 5A, mitochondrial-like
family with sequence similarity 219 member B, transcript variant X1
family with sequence similarity 219 member B, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
CUGBP Elav-like family member 6, transcript variant X28
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 6, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 6, transcript variant X20
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 6, transcript variant X19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 6, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 6, transcript variant X18
CUGBP Elav-like family member 6, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 6, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 6, transcript variant X22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 6, transcript variant X9
CUGBP Elav-like family member 6, transcript variant X21
CUGBP Elav-like family member 6, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4 isoform X28
CUGBP Elav-like family member 4 isoform X8
CUGBP Elav-like family member 4 isoform X20
CUGBP Elav-like family member 4 isoform X2
CUGBP Elav-like family member 4 isoform X19
CUGBP Elav-like family member 4 isoform X1
CUGBP Elav-like family member 4 isoform X5
CUGBP Elav-like family member 4 isoform X18
CUGBP Elav-like family member 4 isoform X6
CUGBP Elav-like family member 4 isoform X10
CUGBP Elav-like family member 4 isoform X22
CUGBP Elav-like family member 4 isoform X9
CUGBP Elav-like family member 4 isoform X21
CUGBP Elav-like family member 4 isoform X7
CUGBP Elav-like family member 6, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 6, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 6, transcript variant X26
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 6, transcript variant X17
CUGBP Elav-like family member 6, transcript variant X16
CUGBP Elav-like family member 6, transcript variant X27
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 6, transcript variant X13
CUGBP Elav-like family member 6, transcript variant X25
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 17% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 6, transcript variant X4
CUGBP Elav-like family member 6, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 6, transcript variant X24
CUGBP Elav-like family member 6, transcript variant X11
CUGBP Elav-like family member 6, transcript variant X23
CUGBP Elav-like family member 4 isoform X15
CUGBP Elav-like family member 4 isoform X14
CUGBP Elav-like family member 4 isoform X26
CUGBP Elav-like family member 4 isoform X3
CUGBP Elav-like family member 4 isoform X17
CUGBP Elav-like family member 4 isoform X16
CUGBP Elav-like family member 4 isoform X27
CUGBP Elav-like family member 4 isoform X13
CUGBP Elav-like family member 4 isoform X25
CUGBP Elav-like family member 4 isoform X4
CUGBP Elav-like family member 4 isoform X12
CUGBP Elav-like family member 4 isoform X24
CUGBP Elav-like family member 4 isoform X11
CUGBP Elav-like family member 4 isoform X23
protein mono-ADP-ribosyltransferase PARP6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
pyruvate kinase M1/2a, transcript variant X3
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 4 samples with support for all annotated introns
pyruvate kinase M1/2a, transcript variant X2
pyruvate kinase M1/2a, transcript variant X4
pyruvate kinase M1/2a, transcript variant X1
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 4 samples with support for all annotated introns
39S ribosomal protein L33, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
dual oxidase 1-like, transcript variant 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 1 sample with support for all annotated introns
dual oxidase 1-like, transcript variant X1
dual oxidase 1-like, transcript variant X3
secretory carrier-associated membrane protein 5, transcript variant X1
secretory carrier-associated membrane protein 5, transcript variant X8
secretory carrier-associated membrane protein 5, transcript variant X7
secretory carrier-associated membrane protein 5, transcript variant X6
secretory carrier-associated membrane protein 5, transcript variant X5
secretory carrier-associated membrane protein 5, transcript variant X4
secretory carrier-associated membrane protein 5, transcript variant X3
secretory carrier-associated membrane protein 5, transcript variant X2
secretory carrier-associated membrane protein 5 isoform X1
secretory carrier-associated membrane protein 5 isoform X3
secretory carrier-associated membrane protein 5 isoform X2
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, including 2 samples with support for all annotated introns
neuroplastin-like, 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
neuroplastin-like, 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
phosphopantothenoylcysteine decarboxylase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phosphopantothenoylcysteine decarboxylase, transcript variant X3
phosphopantothenoylcysteine decarboxylase, transcript variant X5
phosphopantothenoylcysteine decarboxylase, transcript variant X6
phosphopantothenoylcysteine decarboxylase, transcript variant X2
phosphopantothenoylcysteine decarboxylase isoform X2
phosphopantothenoylcysteine decarboxylase isoform X1
phosphopantothenoylcysteine decarboxylase isoform X3
phosphopantothenoylcysteine decarboxylase isoform X6
phosphopantothenoylcysteine decarboxylase isoform X5
phosphopantothenoylcysteine decarboxylase, transcript variant X4
phosphopantothenoylcysteine decarboxylase isoform X4
chromosome 32 C15orf39 homolog, transcript variant X6
chromosome 32 C15orf39 homolog, transcript variant X1
chromosome 32 C15orf39 homolog, transcript variant X2
chromosome 32 C15orf39 homolog, transcript variant X4
chromosome 32 C15orf39 homolog, transcript variant X3
chromosome 32 C15orf39 homolog, transcript variant X5
uncharacterized protein C15orf39 homolog isoform X1
uncharacterized protein C15orf39 homolog isoform X2
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
zinc finger CCCH domain-containing protein 10-like, transcript variant X1
zinc finger CCCH domain-containing protein 10-like, transcript variant X2
zinc finger CCCH domain-containing protein 10-like
COMM domain containing 4, transcript variant X1
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
COMM domain-containing protein 4 isoform X1
COMM domain containing 4, transcript variant X2
COMM domain-containing protein 4 isoform X2
nei-like DNA glycosylase 1, 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 4 samples with support for all annotated introns
nei-like DNA glycosylase 1, 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
nei-like DNA glycosylase 1, transcript variant X3
RNA-binding protein with multiple splicing 2, transcript variant X1
RNA-binding protein with multiple splicing 2, transcript variant X3
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 4 samples with support for all annotated introns
RNA-binding protein with multiple splicing 2, transcript variant X2
RNA-binding protein with multiple splicing 2 isoform X3
RNA-binding protein with multiple splicing 2 isoform X1
RNA-binding protein with multiple splicing 2 isoform X2
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: 14 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 4 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: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ornithine decarboxylase antizyme 2-like
ras-related protein Rab-8B-like, transcript variant X1
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
ras-related protein Rab-8B-like, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
APH1B gamma secretase subunit, transcript variant X1
APH1B gamma secretase subunit, transcript variant X2
gamma-secretase subunit Aph-1b isoform X1
gamma-secretase subunit Aph-1b isoform X2
ubiquitin specific peptidase 3, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 3 isoform X1
ubiquitin specific peptidase 3, transcript variant X2
ubiquitin specific peptidase 3, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 3 isoform X2
F-box and leucine-rich repeat protein 22
HECT and RLD domain containing E3 ubiquitin protein ligase family member 1, transcript variant X8
HECT and RLD domain containing E3 ubiquitin protein ligase family member 1, transcript variant X5
HECT and RLD domain containing E3 ubiquitin protein ligase family member 1, transcript variant X7
HECT and RLD domain containing E3 ubiquitin protein ligase family member 1, transcript variant X10
HECT and RLD domain containing E3 ubiquitin protein ligase family member 1, transcript variant X3
HECT and RLD domain containing E3 ubiquitin protein ligase family member 1, transcript variant X4
HECT and RLD domain containing E3 ubiquitin protein ligase family member 1, transcript variant X6
HECT and RLD domain containing E3 ubiquitin protein ligase family member 1, transcript variant X11
HECT and RLD domain containing E3 ubiquitin protein ligase family member 1, transcript variant X9
HECT and RLD domain containing E3 ubiquitin protein ligase family member 1, transcript variant X1
HECT and RLD domain containing E3 ubiquitin protein ligase family member 1, transcript variant X2
probable E3 ubiquitin-protein ligase HERC1 isoform X7
probable E3 ubiquitin-protein ligase HERC1 isoform X4
probable E3 ubiquitin-protein ligase HERC1 isoform X6
probable E3 ubiquitin-protein ligase HERC1 isoform X9
probable E3 ubiquitin-protein ligase HERC1 isoform X2
probable E3 ubiquitin-protein ligase HERC1 isoform X3
probable E3 ubiquitin-protein ligase HERC1 isoform X5
probable E3 ubiquitin-protein ligase HERC1 isoform X10
probable E3 ubiquitin-protein ligase HERC1 isoform X8
probable E3 ubiquitin-protein ligase HERC1 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00548
death-associated protein kinase 2b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
death-associated protein kinase 2 isoform X2
death-associated protein kinase 2b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
death-associated protein kinase 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
TBC1 domain family, member 2B, 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 4 samples with support for all annotated introns
TBC1 domain family, member 2B, transcript variant X1
TBC1 domain family, member 2B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85% coverage of the annotated genomic feature by RNAseq alignments
calcium and integrin binding family member 2, transcript variant X1
calcium and integrin binding family member 2, transcript variant X2
calcium and integrin-binding family member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
leucine-rich repeat-containing protein 61
isocitrate dehydrogenase (NAD(+)) 3 catalytic subunit alpha, transcript variant X2
isocitrate dehydrogenase (NAD(+)) 3 catalytic subunit alpha, transcript variant X1
isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial isoform X1
isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial isoform X2
uncharacterized LOC121271973, transcript variant X2
uncharacterized LOC121271973, transcript variant X1
uncharacterized protein LOC121271973 isoform X1
uncharacterized protein LOC121271973 isoform 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 4 samples with support for all annotated introns
cellular retinoic acid binding protein 1a, transcript variant X2
cellular retinoic acid binding protein 1a, transcript variant X1
cellular retinoic acid-binding protein 1a isoform X1
cellular retinoic acid-binding protein 1a isoform X2
solute carrier family 25 member 44a, transcript variant X5
solute carrier family 25 member 44a, transcript variant X3
solute carrier family 25 member 44a, transcript variant X1
solute carrier family 25 member 44a, 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
solute carrier family 25 member 44a, transcript variant X4
solute carrier family 25 member 44a isoform X4
solute carrier family 25 member 44a isoform X2
solute carrier family 25 member 44a isoform X1
solute carrier family 25 member 44a isoform X3
iron-responsive element binding protein 2, transcript variant X3
iron-responsive element-binding protein 2 isoform X2
iron-responsive element binding protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
iron-responsive element binding protein 2, transcript variant X2
iron-responsive element-binding protein 2 isoform X1
hydroxylysine kinase-like, transcript variant X1
hydroxylysine kinase-like, transcript variant X5
hydroxylysine kinase-like, transcript variant X3
hydroxylysine kinase-like, transcript variant X2
hydroxylysine kinase-like, transcript variant X4
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
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
uncharacterized LOC121271932, 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
uncharacterized LOC121271932, transcript variant X2
uncharacterized protein LOC121271932 isoform X2
uncharacterized protein LOC121271932 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins
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
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit DAD1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
deoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial-like, 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
deoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial-like, transcript variant X2
deoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial-like isoform X1
deoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial-like isoform X2
uncharacterized LOC121272035, transcript variant X2
uncharacterized LOC121272035, transcript variant X1
solute carrier family 12 member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 12 member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 12 member 1 isoform X2
solute carrier family 12 member 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 609-like, transcript variant X2
zinc finger protein 609-like, transcript variant X4
zinc finger protein 609-like, transcript variant X1
zinc finger protein 609-like, transcript variant X5
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 1 sample with support for all annotated introns
zinc finger protein 609-like, 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
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
protein tyrosine phosphatase non-receptor type 9a
tyrosine-protein phosphatase non-receptor type 9
SIN3 transcription regulator family member Aa, transcript variant X2
SIN3 transcription regulator family member Aa, transcript variant X1
SIN3 transcription regulator family member Aa, transcript variant X3
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
SIN3 transcription regulator family member Aa, transcript variant X5
SIN3 transcription regulator family member Aa isoform X1
SIN3 transcription regulator family member Aa isoform X2
SIN3 transcription regulator family member Aa isoform X4
SIN3 transcription regulator family member Aa, transcript variant X4
SIN3 transcription regulator family member Aa isoform X3
mannosidase, alpha, class 2C, member 1, transcript variant X1
mannosidase, alpha, class 2C, member 1, transcript variant X2
uncharacterized LOC121272037, transcript variant X2
uncharacterized LOC121272037, transcript variant X1
sorting nexin-27-like, transcript variant X1
sorting nexin-27-like, transcript variant X2
AP-3 complex subunit beta-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
AP-3 complex subunit beta-2, transcript variant X2
AP-3 complex subunit beta-2, transcript variant X3
AP-3 complex subunit beta-2, transcript variant X4
cytoplasmic polyadenylation element-binding protein 1-like, transcript variant X6
cytoplasmic polyadenylation element-binding protein 1-like, 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 4 samples with support for all annotated introns
cytoplasmic polyadenylation element-binding protein 1-like, transcript variant X5
cytoplasmic polyadenylation element-binding protein 1-like, transcript variant X1
cytoplasmic polyadenylation element-binding protein 1-like, transcript variant X2
cytoplasmic polyadenylation element-binding protein 1-like, transcript variant X3
cytoplasmic polyadenylation element-binding protein 1-like isoform X1
cytoplasmic polyadenylation element-binding protein 1-like isoform X2
cytoplasmic polyadenylation element-binding protein 1-B-like isoform X3
cytoplasmic polyadenylation element-binding protein 1-like, transcript variant X7
cytoplasmic polyadenylation element-binding protein 1-like isoform X4
synaptic vesicle glycoprotein 2, transcript variant X2
synaptic vesicle glycoprotein 2, transcript variant X3
synaptic vesicle glycoprotein 2, transcript variant X1
synaptic vesicle glycoprotein 2C isoform X3
synaptic vesicle glycoprotein 2C isoform X2
synaptic vesicle glycoprotein 2C isoform X1
casein kinase I-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
casein kinase I-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
casein kinase I-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
casein kinase I-like, transcript variant X3
casein kinase I-like, transcript variant X5
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
uncharacterized protein LOC100034462 homolog, transcript variant X4
uncharacterized protein LOC100034462 homolog, transcript variant X1
uncharacterized protein si:dkey-24l11.2 isoform X1
uncharacterized protein si:dkey-24l11.2 isoform X3
uncharacterized protein LOC100034462 homolog, transcript variant X3
uncharacterized protein LOC100034462 homolog, transcript variant X2
uncharacterized protein si:dkey-24l11.2 isoform X2
uncharacterized protein LOC100034462 homolog, transcript variant X5
uncharacterized protein si:dkey-24l11.2 isoform X4
uncharacterized protein LOC100034462 homolog, transcript variant X6
uncharacterized protein si:dkey-24l11.2 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
SEC11 homolog A, signal peptidase complex subunit
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
signal peptidase complex catalytic subunit SEC11A
zinc finger protein 592, transcript variant X2
zinc finger protein 592, transcript variant X1
MALT paracaspase 3, transcript variant X3
MALT paracaspase 3, transcript variant X2
MALT paracaspase 3, transcript variant X1
MALT paracaspase 3, transcript variant X4
mucosa-associated lymphoid tissue lymphoma translocation protein 1 isoform X3
mucosa-associated lymphoid tissue lymphoma translocation protein 1 isoform X2
mucosa-associated lymphoid tissue lymphoma translocation protein 1 isoform X1
mucosa-associated lymphoid tissue lymphoma translocation protein 1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
semaphorin-4D-like, transcript variant X2
semaphorin-4D-like, transcript variant X3
semaphorin-4D-like, transcript variant X1
general transcription factor IIA, 2, transcript variant X1
transcription initiation factor IIA subunit 2 isoform X1
general transcription factor IIA, 2, transcript variant X2
transcription initiation factor IIA subunit 2 isoform X2
interactor of little elongator complex ELL subunit 2, 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 4 samples with support for all annotated introns
interactor of little elongator complex ELL subunit 2, transcript variant X2
little elongation complex subunit 2 isoform X1
little elongation complex subunit 2 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 2 samples with support for all annotated introns
maestro heat-like repeat-containing protein family member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
tropomyosin 1 (alpha), transcript variant X5
tropomyosin 1 (alpha), transcript variant X4
tropomyosin 1 (alpha), transcript variant 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
tropomyosin 1 (alpha), transcript variant X3
tropomyosin 1 (alpha), transcript variant X1
tropomyosin 1 (alpha), transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
tropomyosin 1 (alpha), transcript variant X6
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
tropomyosin 1 (alpha), transcript variant X10
tropomyosin 1 (alpha), transcript variant X9
tropomyosin 1 (alpha), transcript variant X8
tropomyosin 1 (alpha), transcript variant X7
serine beta-lactamase-like protein LACTB, mitochondrial
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 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: 80 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns