Stegostoma fasciatum isolate 6-17 chromosome 37, sSteFas1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Chondrichthyes; Elasmobranchii; Galeomorphii; Galeoidea; Orectolobiformes; Stegostomatidae; Stegostoma.
REFSEQ INFORMATION: The reference sequence is identical to\nCM039263.1.\nAssembly name: sSteFas1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Squalomix on 2022/02/17. The\noriginal whole-genome shotgun project has the accession\nJAFIRC000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Squalomix\nAssembly Date :: 22-FEB-2021\nAssembly Method :: Platanus v. 1.2.4; P_RNA_scaffolder v.\n commit 7941e0f on May 30, at github;\n 3D-DNA v. 180922\nAssembly Name :: sSteFas1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 95.8x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Stegostoma fasciatum Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
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, including 2 samples with support for all annotated introns
ribonuclease inhibitor-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 1 sample with support for all annotated introns
ribonuclease inhibitor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
small G protein signaling modulator 3, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
small G protein signaling modulator 3, transcript variant X2
ATP-sensitive inward rectifier potassium channel 12-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 115 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ATP-sensitive inward rectifier potassium channel 12-like, transcript variant X3
ATP-sensitive inward rectifier potassium channel 12-like, transcript variant X1
ATP-sensitive inward rectifier potassium channel 12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
probable ATP-dependent RNA helicase DDX17, transcript variant X1
probable ATP-dependent RNA helicase DDX17 isoform X1
probable ATP-dependent RNA helicase DDX17, 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 23 samples with support for all annotated introns
probable ATP-dependent RNA helicase DDX17 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
meiotic recombination protein DMC1/LIM15 homolog
Sad1 and UNC84 domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Sad1 and UNC84 domain containing 2, 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 3 samples with support for all annotated introns
Sad1 and UNC84 domain containing 2, 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
platelet-derived growth factor subunit B-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 11 samples with support for all annotated introns
platelet-derived growth factor subunit B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
platelet-derived growth factor subunit B-like isoform X1
platelet-derived growth factor subunit B-like isoform X2
extracellular serine/threonine protein kinase FAM20C-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
chibby homolog 1 (Drosophila), 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 23 samples with support for all annotated introns
chibby homolog 1 (Drosophila), 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 17 samples with support for all annotated introns
protein FAM227A-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
protein FAM227A-like, transcript variant X1
protein FAM227A-like, transcript variant X3
protein FAM227A-like, transcript variant X4
TGF-beta activated kinase 1/MAP3K7 binding protein 1
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like, transcript variant X2
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like isoform X2
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like, transcript variant X5
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like, transcript variant X1
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like, transcript variant X4
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like, transcript variant X3
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like, transcript variant X6
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like isoform X1
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like isoform X3
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like, transcript variant X7
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like isoform X4
MICAL-like 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
MICAL-like protein 1, transcript variant X1
chromosome 37 C22orf23 homolog, 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 10 samples with support for all annotated introns
chromosome 37 C22orf23 homolog, 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 4 samples with support for all annotated introns
monocarboxylate transporter 3-like, transcript variant X2
monocarboxylate transporter 3-like, transcript variant X3
monocarboxylate transporter 3-like, transcript variant X1
monocarboxylate transporter 3-like, transcript variant X4
monocarboxylate transporter 3-like isoform X1
monocarboxylate transporter 3-like, transcript variant X5
monocarboxylate transporter 3-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
translocase of outer mitochondrial membrane 22 homolog (yeast)
mitochondrial import receptor subunit TOM22 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00007
ribosomal RNA-processing protein 7 homolog A
polymerase delta-interacting protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transcription factor 20, 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 8 samples with support for all annotated introns
transcription factor 20, 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
transcription factor 20, transcript variant X5
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
transcription factor 20, 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 6 samples with support for all annotated introns
transcription factor 20, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
germ cell-specific gene 1-like protein, 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
germ cell-specific gene 1-like protein, transcript variant X2
family with sequence similarity 234 member B, 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 4 samples with support for all annotated introns
family with sequence similarity 234 member B, 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 13 samples with support for all annotated introns
family with sequence similarity 234 member B, transcript variant X2
family with sequence similarity 234 member B, transcript variant X5
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
family with sequence similarity 234 member B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 59, transcript variant X7
DEAD (Asp-Glu-Ala-Asp) box polypeptide 59, transcript variant X6
DEAD (Asp-Glu-Ala-Asp) box polypeptide 59, transcript variant X3
DEAD (Asp-Glu-Ala-Asp) box polypeptide 59, transcript variant X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 59, transcript variant X5
DEAD (Asp-Glu-Ala-Asp) box polypeptide 59, transcript variant X8
DEAD (Asp-Glu-Ala-Asp) box polypeptide 59, transcript variant X4
DEAD (Asp-Glu-Ala-Asp) box polypeptide 59, transcript variant X1
probable ATP-dependent RNA helicase DDX59 isoform X1
probable ATP-dependent RNA helicase DDX59 isoform X2
putative RNA-binding protein Luc7-like 2, transcript variant X4
putative RNA-binding protein Luc7-like 2, transcript variant X5
putative RNA-binding protein Luc7-like 2, transcript variant X1
putative RNA-binding protein Luc7-like 2, transcript variant X2
putative RNA-binding protein Luc7-like 2 isoform X1
putative RNA-binding protein Luc7-like 2 isoform X2
putative RNA-binding protein Luc7-like 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
putative RNA-binding protein Luc7-like 2, transcript variant X7
putative RNA-binding protein Luc7-like 2, transcript variant X6
putative RNA-binding protein Luc7-like 2, transcript variant X3
putative RNA-binding protein Luc7-like 2 isoform X3
putative RNA-binding protein Luc7-like 2 isoform X4
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: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
NADH:ubiquinone oxidoreductase subunit A6
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 6
minichromosome maintenance complex component 5, 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 7 samples with support for all annotated introns
DNA replication licensing factor MCM5 isoform X1
minichromosome maintenance complex component 5, transcript variant X2
DNA replication licensing factor MCM5 isoform X2
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 15 samples with support for all annotated introns
FAD-dependent oxidoreductase domain containing 2, transcript variant X3
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
FAD-dependent oxidoreductase domain containing 2, transcript variant X4
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
FAD-dependent oxidoreductase domain containing 2, 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 3 samples with support for all annotated introns
FAD-dependent oxidoreductase domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
FAD-dependent oxidoreductase domain containing 2, transcript variant X5
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 5 samples with support for all annotated introns
FAD-dependent oxidoreductase domain containing 2, 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 2 samples with support for all annotated introns
FAD-dependent oxidoreductase domain-containing protein 2 isoform X2
FAD-dependent oxidoreductase domain-containing protein 2 isoform X1
FAD-dependent oxidoreductase domain-containing protein 2 isoform X3
solute carrier family 25 member 38b, transcript variant X1
mitochondrial glycine transporter B isoform X1
solute carrier family 25 member 38b, transcript variant X2
mitochondrial glycine transporter B isoform X2
small nucleolar RNA SNORA62/SNORA6 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00091
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
HMG box domain containing 4a, transcript variant X3
HMG box domain containing 4a, transcript variant X6
HMG box domain containing 4a, transcript variant X2
HMG box domain containing 4a, transcript variant X1
HMG box domain containing 4a, transcript variant X5
HMG box domain containing 4a, transcript variant X4
HMG domain-containing protein 4a isoform X1
HMG domain-containing protein 4a isoform X2
HMG domain-containing protein 4a isoform X3
HMG box domain containing 4a, transcript variant X7
HMG domain-containing protein 4a isoform X4
target of myb1 membrane trafficking protein, transcript variant X1
target of myb1 membrane trafficking protein, transcript variant X2
target of myb1 membrane trafficking protein, transcript variant X3
target of myb1 membrane trafficking protein, transcript variant X4
coiled-coil domain-containing protein 134-like
sterol regulatory element binding transcription factor 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
sterol regulatory element-binding protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
TRIO and F-actin binding protein b, transcript variant X1
TRIO and F-actin binding protein b, transcript variant X6
TRIO and F-actin binding protein b, transcript variant X3
TRIO and F-actin binding protein b, transcript variant X2
TRIO and F-actin binding protein b, transcript variant X4
TRIO and F-actin binding protein b, transcript variant X5
TRIO and F-actin binding protein b isoform X1
TRIO and F-actin binding protein b isoform X3
TRIO and F-actin binding protein b isoform X2
TRIO and F-actin binding protein b isoform X4
TRIO and F-actin binding protein b isoform X5
TRIO and F-actin binding protein b, transcript variant X7
TRIO and F-actin binding protein b isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
histone H1.0-like, transcript variant X1
histone H1.0-like, transcript variant X2
uncharacterized protein LOC125447125 isoform X1
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
2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial
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
ankyrin repeat and fibronectin type-III domain-containing protein 1-like, transcript variant X4
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
ankyrin repeat and fibronectin type-III domain-containing protein 1-like, transcript variant X3
ankyrin repeat and fibronectin type-III domain-containing protein 1-like, 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
ankyrin repeat and fibronectin type-III domain-containing protein 1-like, transcript variant X1
ankyrin repeat and fibronectin type-III domain-containing protein 1-like, transcript variant X5
ankyrin repeat and fibronectin type-III domain-containing protein 1-like
X-prolyl aminopeptidase 3, mitochondrial, transcript variant X1
X-prolyl aminopeptidase 3, mitochondrial, 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 12 samples with support for all annotated introns
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
histone acetyltransferase p300-like, transcript variant X2
histone acetyltransferase p300-like, transcript variant X1
histone acetyltransferase p300-like isoform X2
histone acetyltransferase p300-like isoform X1
lethal(3)malignant brain tumor-like protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lethal(3)malignant brain tumor-like protein 2 isoform X3
lethal(3)malignant brain tumor-like protein 2, 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 2 samples with support for all annotated introns
lethal(3)malignant brain tumor-like protein 2, 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
lethal(3)malignant brain tumor-like protein 2 isoform X2
lethal(3)malignant brain tumor-like protein 2 isoform X1
chondroadherin-like protein, 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
chondroadherin-like protein, 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ran GTPase-activating protein 1-like
zinc finger CCCH domain-containing protein 7B-like
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 19 samples with support for all annotated introns
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 22 samples with support for all annotated introns
protein Tob2-like, transcript variant X1
protein Tob2-like, transcript variant X3
protein Tob2-like, transcript variant X2
protein Tob2-like, transcript variant X4
protein Tob2-like, transcript variant X5
PHD finger-like domain-containing protein 5A
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 8 samples with support for all annotated introns
polymerase (RNA) III (DNA directed) polypeptide H, transcript variant X4
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 24 samples with support for all annotated introns
DNA-directed RNA polymerase III subunit RPC8 isoform X2
polymerase (RNA) III (DNA directed) polypeptide H, transcript variant X2
polymerase (RNA) III (DNA directed) polypeptide H, transcript variant X1
polymerase (RNA) III (DNA directed) polypeptide H, transcript variant X3
DNA-directed RNA polymerase III subunit RPC8 isoform X1
cold shock domain-containing protein C2-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
cold shock domain-containing protein C2-like, 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 10 samples with support for all annotated introns
cold shock domain-containing protein C2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
myocardin-related transcription factor A-like, transcript variant X4
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 9 samples with support for all annotated introns
myocardin-related transcription factor A-like, 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 1 sample with support for all annotated introns
myocardin-related transcription factor A-like isoform X1
myocardin-related transcription factor A-like, transcript variant X3
myocardin-related transcription factor A-like isoform X3
myocardin-related transcription factor A-like isoform X4
myocardin-related transcription factor A-like, transcript variant X2
myocardin-related transcription factor A-like isoform X2
peroxisomal membrane protein PMP34-like, transcript variant X2
peroxisomal membrane protein PMP34-like, transcript variant X1
peroxisomal membrane protein PMP34-like isoform X2
peroxisomal membrane protein PMP34-like isoform X1
cytochrome b-c1 complex subunit 2, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
X-ray repair complementing defective repair in Chinese hamster cells 6
X-ray repair cross-complementing protein 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
proliferation associated nuclear element
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125447170, transcript variant X1
uncharacterized LOC125447170, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC125447170 isoform X1
uncharacterized protein LOC125447170 isoform 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
translocase of inner mitochondrial membrane 8 homolog B (yeast)
mitochondrial import inner membrane translocase subunit Tim8 B
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
tumor necrosis factor ligand superfamily member 13B-like
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
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 20 samples with support for all annotated introns
suppressor of cytokine signaling 1-like, 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 1 sample with support for all annotated introns
suppressor of cytokine signaling 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
suppressor of cytokine signaling 1-like, transcript variant X7
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
suppressor of cytokine signaling 1-like, transcript variant X6
suppressor of cytokine signaling 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 5 samples with support for all annotated introns
suppressor of cytokine signaling 1-like, 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
suppressor of cytokine signaling 1-like, transcript variant X4
suppressor of cytokine signaling 1-like, transcript variant X8
transfer RNA opal suppressor (anticodon UCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
glutamate receptor ionotropic, NMDA 2B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
activating transcription factor 7-interacting protein 1-like, transcript variant X8
activating transcription factor 7-interacting protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
activating transcription factor 7-interacting protein 1-like, transcript variant X6
activating transcription factor 7-interacting protein 1-like, transcript variant X11
activating transcription factor 7-interacting protein 1-like, transcript variant X10
activating transcription factor 7-interacting protein 1-like, transcript variant X12
activating transcription factor 7-interacting 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 7 samples with support for all annotated introns
activating transcription factor 7-interacting protein 1-like, transcript variant X4
activating transcription factor 7-interacting protein 1-like, transcript variant X3
activating transcription factor 7-interacting protein 1-like, transcript variant X5
activating transcription factor 7-interacting protein 1-like, transcript variant X7
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 6 samples with support for all annotated introns
activating transcription factor 7-interacting protein 1-like, transcript variant X9
activating transcription factor 7-interacting protein 1-like isoform X2
activating transcription factor 7-interacting protein 1-like isoform X3
activating transcription factor 7-interacting protein 1-like isoform X4
activating transcription factor 7-interacting protein 1-like isoform X1
ankyrin repeat domain-containing protein 54
eukaryotic translation initiation factor 3, subunit 6 interacting protein
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 24 samples with support for all annotated introns
eukaryotic translation initiation factor 3 subunit L
MIEF1 upstream open reading frame protein-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 24 samples with support for all annotated introns
MIEF1 upstream open reading frame protein-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 20 samples with support for all annotated introns
MIEF1 upstream open reading frame protein-like isoform X1
MIEF1 upstream open reading frame protein-like isoform 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 23 samples with support for all annotated introns
cyclic AMP-dependent transcription factor ATF-4
mercaptopyruvate sulfurtransferase, transcript variant X2
mercaptopyruvate sulfurtransferase, transcript variant X1
3-mercaptopyruvate sulfurtransferase isoform X2
3-mercaptopyruvate sulfurtransferase isoform X1
BTB/POZ domain-containing protein KCTD5-like, transcript variant X1
BTB/POZ domain-containing protein KCTD5-like, transcript variant X3
BTB/POZ domain-containing protein KCTD5-like, transcript variant X2
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
BTB/POZ domain-containing protein KCTD5-like isoform X2
BTB/POZ domain-containing protein KCTD5-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
cytokine receptor common subunit beta-like, 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 5 samples with support for all annotated introns
cytokine receptor common subunit beta-like, transcript variant X2
cytokine receptor common subunit beta-like
caspase recruitment domain-containing protein 11-like, 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
caspase recruitment domain-containing protein 11-like, transcript variant X3
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
caspase recruitment domain-containing protein 11-like, 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 2 samples with support for all annotated introns
caspase recruitment domain-containing protein 11-like isoform X1
caspase recruitment domain-containing protein 11-like isoform X3
caspase recruitment domain-containing protein 11-like isoform X2
guanine nucleotide-binding protein subunit alpha-12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 107 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
beta-1,3-N-acetylglucosaminyltransferase lunatic fringe-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 29-like, transcript variant X2
protein phosphatase 1 regulatory subunit 29-like, transcript variant X1
protein phosphatase 1 regulatory subunit 29-like, transcript variant X3
protein phosphatase 1 regulatory subunit 29-like, transcript variant X7
protein phosphatase 1 regulatory subunit 29-like, transcript variant X5
protein phosphatase 1 regulatory subunit 29-like, transcript variant X4
protein phosphatase 1 regulatory subunit 29-like, transcript variant X6
protein phosphatase 1 regulatory subunit 29-like
discs, large (Drosophila) homolog-associated protein 5
COORDINATES: nucleotide motif:Rfam:12.0:RF00563
transmembrane protein 184ba, 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 16 samples with support for all annotated introns
transmembrane protein 184ba, 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 18 samples with support for all annotated introns
transcription factor MafK-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
transcription factor MafK-like, transcript variant X2
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 2 samples with support for all annotated introns
transcription factor MafK-like, transcript variant X4
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 1 sample with support for all annotated introns
transcription factor MafK-like, transcript variant X3
phospholipase A2, group VI (cytosolic, calcium-independent), 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 10 samples with support for all annotated introns
phospholipase A2, group VI (cytosolic, calcium-independent), 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 10 samples with support for all annotated introns
phospholipase A2, group VI (cytosolic, calcium-independent), transcript variant X2
85/88 kDa calcium-independent phospholipase A2 isoform X1
85/88 kDa calcium-independent phospholipase A2 isoform X2
phospholipase A2, group VI (cytosolic, calcium-independent), 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
85/88 kDa calcium-independent phospholipase A2 isoform X3
brain-specific angiogenesis inhibitor 1-associated protein 2-like protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
complement C1q tumor necrosis factor-related protein 6-like, transcript variant X1
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 4 samples with support for all annotated introns
complement C1q tumor necrosis factor-related protein 6-like isoform X1
complement C1q tumor necrosis factor-related protein 6-like, transcript variant X2
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 7 samples with support for all annotated introns
complement C1q tumor necrosis factor-related protein 1-like isoform X2
somatostatin receptor type 5-like, transcript variant X4
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 4 samples with support for all annotated introns
somatostatin receptor type 5-like, transcript variant X3
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 6 samples with support for all annotated introns
somatostatin receptor type 5-like, transcript variant X2
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
somatostatin receptor type 5-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 1 sample with support for all annotated introns
somatostatin receptor type 5-like, transcript variant X1
somatostatin receptor type 5-like, transcript variant X5
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
somatostatin receptor type 5-like isoform X2
somatostatin receptor type 5-like isoform X1
somatostatin receptor type 5-like isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00096
ras-related C3 botulinum toxin substrate 1-like
ras-related C3 botulinum toxin substrate 1-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
ras-related C3 botulinum toxin substrate 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 215 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ras-related C3 botulinum toxin substrate 1-like isoform X2
ras-related C3 botulinum toxin substrate 1-like isoform X1
cdc42 effector protein 1-like, 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 6 samples with support for all annotated introns
cdc42 effector protein 1-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 9 samples with support for all annotated introns
cdc42 effector protein 1-like, transcript variant X4
cdc42 effector protein 1-like, transcript variant X3
cdc42 effector protein 1-like isoform X2
cdc42 effector protein 1-like isoform X1
golgi-associated, gamma adaptin ear containing, ARF binding protein 1
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 22 samples with support for all annotated introns
ADP-ribosylation factor-binding protein GGA1
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
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 7 samples with support for all annotated introns
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
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 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 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: 4 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
ferritin, heavy subunit-like, transcript variant X3
ferritin, heavy subunit-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ferritin, heavy subunit-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 154 Proteins, and 90% 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: 184 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 279 Proteins, and 87% 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: 82 Proteins, and 58% 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 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: 21 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: 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: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
serine/threonine-protein phosphatase 6 regulatory subunit 3-like, 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 19 samples with support for all annotated introns
serine/threonine-protein phosphatase 6 regulatory subunit 3-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 23 samples with support for all annotated introns
serine/threonine-protein phosphatase 6 regulatory subunit 3-like
serine/threonine-protein kinase BRSK2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
MOB kinase activator 2-like, transcript variant X6
MOB kinase activator 2-like, transcript variant X4
MOB kinase activator 2-like, transcript variant X3
MOB kinase activator 2-like, transcript variant X5
MOB kinase activator 2-like, transcript variant X1
MOB kinase activator 2-like, transcript variant X2
dual specificity protein phosphatase 8-like
cyclin-dependent kinase inhibitor 1B-like
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 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential cation channel, subfamily M, member 4a
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
transient receptor potential cation channel subfamily M member 4a
uncharacterized LOC125447241, transcript variant X2
uncharacterized protein LOC125447241 isoform X2
uncharacterized LOC125447241, transcript variant X3
uncharacterized protein LOC125447241 isoform X3
uncharacterized LOC125447241, transcript variant X5
uncharacterized protein LOC125447241 isoform X5
uncharacterized LOC125447241, transcript variant X4
uncharacterized protein LOC125447241 isoform X4
uncharacterized LOC125447241, transcript variant X1
uncharacterized protein LOC125447241 isoform X1
ras-related and estrogen-regulated growth inhibitor-like, transcript variant X1
ras-related and estrogen-regulated growth inhibitor-like isoform X1
ras-related and estrogen-regulated growth inhibitor-like, transcript variant X2
ras-related and estrogen-regulated growth inhibitor-like isoform X2
transportin-3-like, transcript variant X3
transportin-3-like, transcript variant X1
transportin-3-like, transcript variant X4
transportin-3-like, transcript variant X2
transportin-3-like, transcript variant X5
carnitine O-palmitoyltransferase 1, liver isoform-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 13 samples with support for all annotated introns
carnitine O-palmitoyltransferase 1, liver isoform-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
carnitine O-palmitoyltransferase 1, liver isoform-like, transcript variant X3
carnitine O-palmitoyltransferase 1, liver isoform-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 5 samples with support for all annotated introns
carnitine O-palmitoyltransferase 1, liver isoform-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
carnitine O-palmitoyltransferase 1, liver isoform-like isoform X2
carnitine O-palmitoyltransferase 1, liver isoform-like isoform X1
uncharacterized LOC125447123, transcript variant X5
uncharacterized LOC125447123, transcript variant X3
uncharacterized LOC125447123, transcript variant X6
uncharacterized LOC125447123, transcript variant X4
uncharacterized LOC125447123, 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 16 samples with support for all annotated introns
uncharacterized LOC125447123, 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 19 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 12 samples with support for all annotated introns
tumor protein p53-inducible protein 11-like, 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 5 samples with support for all annotated introns
tumor protein p53-inducible protein 11-like, 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 14 samples with support for all annotated introns
tumor protein p53-inducible protein 11-like
paired box protein Pax-6-like, transcript variant X3
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
paired box protein Pax-6-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, including 1 sample with support for all annotated introns
paired box protein Pax-6-like, transcript variant X2
paired box protein Pax-6-like, transcript variant X1
paired box protein Pax-6-like isoform X2
paired box protein Pax-6-like isoform X1
paired box protein Pax-6-like isoform X3
paired box protein Pax-6-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
reticulocalbin 3, EF-hand calcium binding domain, transcript variant X3
reticulocalbin 3, EF-hand calcium binding domain, transcript variant X1
reticulocalbin 3, EF-hand calcium binding domain, transcript variant X2
reticulocalbin 3, EF-hand calcium binding domain, transcript variant X5
reticulocalbin 3, EF-hand calcium binding domain, transcript variant X4
nitric oxide synthase interacting protein, transcript variant X1
nitric oxide synthase interacting protein, transcript variant X2
nitric oxide synthase-interacting protein
proline rich Gla (G-carboxyglutamic acid) 2, transcript variant X3
proline rich Gla (G-carboxyglutamic acid) 2, transcript variant X1
proline rich Gla (G-carboxyglutamic acid) 2, transcript variant X2
transmembrane gamma-carboxyglutamic acid protein 2 isoform X1
transmembrane gamma-carboxyglutamic acid protein 2 isoform X2
mediator complex subunit 25, transcript variant X1
mediator complex subunit 25, transcript variant X2
mediator complex subunit 25, transcript variant X3
mediator complex subunit 25, transcript variant X4
mediator of RNA polymerase II transcription subunit 25 isoform X1
mediator of RNA polymerase II transcription subunit 25 isoform X2
mediator of RNA polymerase II transcription subunit 25 isoform X3
mediator of RNA polymerase II transcription subunit 25 isoform X4
protein kinase C and casein kinase substrate in neurons protein 3, transcript variant X4
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 10 samples with support for all annotated introns
protein kinase C and casein kinase substrate in neurons protein 3, transcript variant X3
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 15 samples with support for all annotated introns
protein kinase C and casein kinase substrate in neurons protein 3, transcript variant X2
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 12 samples with support for all annotated introns
protein kinase C and casein kinase substrate in neurons protein 3, 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 15 samples with support for all annotated introns
protein kinase C and casein kinase substrate in neurons protein 3, transcript variant X1
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 20 samples with support for all annotated introns
protein kinase C and casein kinase substrate in neurons protein 3 isoform X1
protein kinase C and casein kinase substrate in neurons protein 1 isoform X2
uncharacterized LOC125447203, transcript variant X2
uncharacterized LOC125447203, 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 13 samples with support for all annotated introns
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 22 samples with support for all annotated introns
polymerase (DNA directed), delta 1, catalytic subunit, transcript variant X3
polymerase (DNA directed), delta 1, catalytic subunit, transcript variant X2
polymerase (DNA directed), delta 1, catalytic subunit, transcript variant X1
transcription factor Spi-B-like, transcript variant X3
transcription factor Spi-B-like, transcript variant X4
transcription factor Spi-B-like, transcript variant X2
transcription factor Spi-B-like, transcript variant X1
transcription factor Spi-B-like isoform X1
transcription factor PU.1-like isoform X4
transcription factor Spi-B-like isoform X2
transcription factor PU.1-like isoform X3
myosin binding protein Ca, transcript variant X2
myosin binding protein Ca, transcript variant X1
ER membrane protein complex subunit 10, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
ER membrane protein complex subunit 10, 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 23 samples with support for all annotated introns
ER membrane protein complex subunit 10, transcript variant X1
ER membrane protein complex subunit 10 isoform X1
ER membrane protein complex subunit 10 isoform X2
ETS-related transcription factor Elf-5-like, transcript variant X3
ETS-related transcription factor Elf-5-like, transcript variant X1
ETS-related transcription factor Elf-5-like, transcript variant X2
ETS-related transcription factor Elf-5-like isoform X3
ETS-related transcription factor Elf-2-like isoform X1
ETS-related transcription factor Elf-5-like isoform X2
E3 SUMO-protein ligase ZBED1-like, transcript variant X1
E3 SUMO-protein ligase ZBED1-like isoform X1
E3 SUMO-protein ligase ZBED1-like, transcript variant X3
E3 SUMO-protein ligase ZBED1-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 6 samples with support for all annotated introns
E3 SUMO-protein ligase ZBED1-like isoform X2
leucine rich repeat containing 4Ba, transcript variant X2
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 8 samples with support for all annotated introns
leucine rich repeat containing 4Ba, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
leucine rich repeat containing 4Ba, 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 11 samples with support for all annotated introns
leucine rich repeat containing 4Ba, transcript variant X3
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 7 samples with support for all annotated introns
leucine rich repeat containing 4Ba, transcript variant X5
leucine rich repeat containing 4Ba, transcript variant X4
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
leucine-rich repeat-containing protein 4B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 48% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/arginine-rich splicing factor 3-like
synaptotagmin III, 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
synaptotagmin III, transcript variant X1
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 4 samples with support for all annotated introns
synaptotagmin III, transcript variant X2
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 2 samples with support for all annotated introns
synaptotagmin III, transcript variant X4
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
putative uncharacterized protein C19orf81, transcript variant X1
putative uncharacterized protein C19orf81, transcript variant X3
putative uncharacterized protein C19orf81 isoform X1
putative uncharacterized protein C19orf81 isoform X3
putative uncharacterized protein C19orf81, transcript variant X2
putative uncharacterized protein C19orf81 isoform X2
SH3 and multiple ankyrin repeat domains protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
epidermal growth factor receptor kinase substrate 8-like protein 1, 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 6 samples with support for all annotated introns
epidermal growth factor receptor kinase substrate 8-like protein 1, transcript variant X3
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 7 samples with support for all annotated introns
epidermal growth factor receptor kinase substrate 8-like protein 1 isoform X1
epidermal growth factor receptor kinase substrate 8-like protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
epidermal growth factor receptor kinase substrate 8-like protein 1 isoform X2
epidermal growth factor receptor kinase substrate 8-like protein 1, 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 8 samples with support for all annotated introns
epidermal growth factor receptor kinase substrate 8-like protein 1 isoform X3
excitatory amino acid transporter 2-like, transcript variant X3
excitatory amino acid transporter 2-like, transcript variant X2
excitatory amino acid transporter 2-like, transcript variant X1
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 1 sample with support for all annotated introns
excitatory amino acid transporter 2-like isoform X2
excitatory amino acid transporter 2-like isoform X1
excitatory amino acid transporter 2-like isoform X3
uncharacterized LOC125447133, transcript variant X1
uncharacterized LOC125447133, transcript variant X3
uncharacterized LOC125447133, transcript variant X5
uncharacterized LOC125447133, transcript variant X6
uncharacterized LOC125447133, 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 2 samples with support for all annotated introns
uncharacterized LOC125447133, transcript variant X4
uncharacterized protein LOC125447133 isoform X2
uncharacterized protein LOC125447133 isoform X1
aldehyde dehydrogenase 16 family, member A1
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 20 samples with support for all annotated introns
aldehyde dehydrogenase family 16 member A1
PIH1 domain containing 1, 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 21 samples with support for all annotated introns
PIH1 domain containing 1, 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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 171 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
U1 small nuclear ribonucleoprotein 70 kDa
protein phosphatase 1 regulatory subunit 12C-like, transcript variant X3
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 8 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 12C-like, transcript variant X2
protein phosphatase 1 regulatory subunit 12C-like, 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
protein phosphatase 1 regulatory subunit 12C-like isoform X3
protein phosphatase 1 regulatory subunit 12C-like isoform X2
protein phosphatase 1 regulatory subunit 12C-like isoform X1
troponin T, slow skeletal muscle-like, transcript variant X3
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 7 samples with support for all annotated introns
troponin T, slow skeletal muscle-like, transcript variant X1
troponin T, slow skeletal muscle-like, transcript variant X4
troponin T, slow skeletal muscle-like, transcript variant X2
troponin T, slow skeletal muscle-like isoform X4
troponin T, slow skeletal muscle-like isoform X3
troponin T, slow skeletal muscle-like isoform X2
troponin T, slow skeletal muscle-like isoform X1
dynein axonemal assembly factor 3-like, 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 13 samples with support for all annotated introns
dynein axonemal assembly factor 3-like, transcript variant X2
dynein axonemal assembly factor 3-like, 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 1 sample with support for all annotated introns
synaptotagmin-1-like, transcript variant X2
synaptotagmin-1-like, transcript variant X1
synaptotagmin-1-like, transcript variant X5
synaptotagmin-1-like, transcript variant X4
synaptotagmin-1-like, transcript variant X3
potassium voltage-gated channel subfamily A member 2-like
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
kinesin-like protein KIF18B, transcript variant X1
kinesin-like protein KIF18B, transcript variant X2
kinesin-like protein KIF18B, transcript variant X3
kinesin-like protein KIF18B, transcript variant X4
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 6 samples with support for all annotated introns
lin-7 homolog B (C. elegans), 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 3 samples with support for all annotated introns
lin-7 homolog B (C. elegans), transcript variant X3
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
lin-7 homolog B (C. elegans), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
transcription intermediary factor 1-beta-like, transcript variant X1
transcription intermediary factor 1-beta-like, transcript variant X2
transcription intermediary factor 1-beta-like, transcript variant X3
transcription intermediary factor 1-beta-like isoform X1
transcription intermediary factor 1-beta-like isoform X2
transcription intermediary factor 1-beta-like isoform X3
charged multivesicular body protein 2A, 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 24 samples with support for all annotated introns
charged multivesicular body protein 2A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 265 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: 228 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 250 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 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: 7 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 135 Proteins, and 49% 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 71% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 186 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
calcium voltage-gated channel subunit alpha1 Ia, 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
calcium voltage-gated channel subunit alpha1 Ia, transcript variant X1
calcium voltage-gated channel subunit alpha1 Ia, transcript variant X2
voltage-dependent T-type calcium channel subunit alpha-1I isoform X1
voltage-dependent T-type calcium channel subunit alpha-1I isoform X3
voltage-dependent T-type calcium channel subunit alpha-1I isoform X2
uncharacterized protein LOC436988 homolog
arf-GAP with dual PH domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins
16 kDa beta-galactoside-binding lectin-like
ATP synthase subunit f, mitochondrial-like, transcript variant X1
ATP synthase subunit f, mitochondrial-like, transcript variant X2
ATP synthase subunit f, mitochondrial-like isoform X2
ATP synthase subunit f, mitochondrial-like isoform X1
probable G-protein coupled receptor 146, transcript variant X4
probable G-protein coupled receptor 146, transcript variant X3
probable G-protein coupled receptor 146, 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 3 samples with support for all annotated introns
probable G-protein coupled receptor 146, transcript variant X1
probable G-protein coupled receptor 146 isoform X1
probable G-protein coupled receptor 146 isoform X2
lysoplasmalogenase-like protein TMEM86A, transcript variant X2
lysoplasmalogenase-like protein TMEM86A, transcript variant X1
lysoplasmalogenase-like protein TMEM86A isoform X1
lysoplasmalogenase-like protein TMEM86A isoform X2
ras-related protein R-Ras2-like, transcript variant X1
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 24 samples with support for all annotated introns
ras-related protein R-Ras2-like, 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 14 samples with support for all annotated introns
ras-related protein R-Ras2-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 7 samples with support for all annotated introns
ras-related protein R-Ras2-like isoform X1
ras-related protein R-Ras2-like isoform X2
ATP-sensitive inward rectifier potassium channel 11-like, transcript variant X1
ATP-sensitive inward rectifier potassium channel 11-like, transcript variant X2
ATP-sensitive inward rectifier potassium channel 11-like isoform X1
ATP-sensitive inward rectifier potassium channel 11-like isoform X2
SR-related CTD-associated factor 1, 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 6 samples with support for all annotated introns
SR-related CTD-associated factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
SR-related CTD-associated factor 1, 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 19 samples with support for all annotated introns
SR-related CTD-associated factor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine/arginine repetitive matrix protein 2
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 24 samples with support for all annotated introns
insulin-like growth factor II, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
insulin-like growth factor II isoform X1
insulin-like growth factor II, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
insulin-like growth factor II isoform 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
uncharacterized protein bcl2l12 isoform X1
apoptosis facilitator Bcl-2-like protein 14 isoform X2
DNA-directed RNA polymerases I, II, and III subunit RPABC5
tetraspanin-4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
tetraspanin-4-like, transcript variant X2
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 7 samples with support for all annotated introns
adaptor related protein complex 2 subunit alpha 1, transcript variant X1
adaptor related protein complex 2 subunit alpha 1, transcript variant X2
adaptor related protein complex 2 subunit alpha 1, transcript variant X3
adaptor related protein complex 2 subunit alpha 1, transcript variant X4
fuzzy planar cell polarity protein, 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
fuzzy planar cell polarity protein, transcript variant X1
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: Gnomon. Supporting evidence includes similarity to: 81 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
potassium voltage-gated channel subfamily C member 1-like, 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 3 samples with support for all annotated introns
potassium voltage-gated channel subfamily C member 1-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 5 samples with support for all annotated introns
potassium voltage-gated channel subfamily C member 1-like, transcript variant X2
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
potassium voltage-gated channel subfamily C member 1-like, transcript variant X4
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
potassium voltage-gated channel subfamily C member 1-like isoform X2
potassium voltage-gated channel subfamily C member 1-like isoform X1
potassium voltage-gated channel subfamily C member 1-like isoform X4
potassium voltage-gated channel subfamily C member 1-like isoform X3
TBC1 domain family, member 17, 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 23 samples with support for all annotated introns
TBC1 domain family, member 17, 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 15 samples with support for all annotated introns
AKT1 substrate 1 (proline-rich), transcript variant X1
proline-rich AKT1 substrate 1 isoform X1
AKT1 substrate 1 (proline-rich), transcript variant X2
proline-rich AKT1 substrate 1 isoform X2
receptor-type tyrosine-protein phosphatase H-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 218 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: 218 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: 218 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ferritin heavy chain, oocyte isoform-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 348 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: 295 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: 17 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 346 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 283 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 96% 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: 186 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
ferritin, middle subunit-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 297 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 289 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
ferritin, middle subunit-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 111 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
ferritin, middle subunit-like isoform X1
ferritin, middle subunit-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 318 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: 266 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 343 Proteins, and 74% 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, and 55% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 191 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 240 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: 80 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 294 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
trinucleotide repeat-containing gene 6B protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
calcium channel, voltage-dependent, gamma subunit 2a
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 9 samples with support for all annotated introns
intraflagellar transport 27 homolog (Chlamydomonas), transcript variant X2
intraflagellar transport protein 27 homolog isoform X2
intraflagellar transport 27 homolog (Chlamydomonas), 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 23 samples with support for all annotated introns
intraflagellar transport protein 27 homolog isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00593
synaptogyrin-1-like, transcript variant X1
synaptogyrin-1-like, transcript variant X2
synaptogyrin-1-like, 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 1 sample with support for all annotated introns
eukaryotic translation initiation factor 3, subunit D
eukaryotic translation initiation factor 3 subunit D
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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
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
GTP-binding protein 1-like, transcript variant X1
GTP-binding protein 1-like, transcript variant X2
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
neuronal pentraxin-2-like, transcript variant X5
neuronal pentraxin-2-like, transcript variant X1
neuronal pentraxin-2-like, transcript variant X3
neuronal pentraxin-2-like, transcript variant X2
neuronal pentraxin-2-like, transcript variant X4
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 19 samples with support for all annotated introns
matrix Gla protein-like, transcript variant X1
matrix Gla protein-like, transcript variant X2
osteocalcin 2-like, transcript variant X1
osteocalcin 2-like, transcript variant X3
osteocalcin 2-like, transcript variant X4
osteocalcin 2-like, transcript variant X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 47
probable ATP-dependent RNA helicase DDX47
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 17 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
G-protein coupled receptor family C group 5 member B-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 10 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 3-like, transcript variant X7
CCR4-NOT transcription complex subunit 3-like, transcript variant X6
CCR4-NOT transcription complex subunit 3-like, transcript variant X1
CCR4-NOT transcription complex subunit 3-like, transcript variant X2
CCR4-NOT transcription complex subunit 3-like, transcript variant X3
CCR4-NOT transcription complex subunit 3-like, transcript variant X4
CCR4-NOT transcription complex subunit 3-like, transcript variant X5
CCR4-NOT transcription complex subunit 3-like isoform X3
CCR4-NOT transcription complex subunit 3-like isoform X2
CCR4-NOT transcription complex subunit 3-like isoform X1
retinal cone rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma-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 1 sample with support for all annotated introns
retinal cone rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma-like isoform X2
retinal cone rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma-like, transcript variant X1
retinal cone rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma-like isoform X1
coiled-coil domain containing 96, transcript variant X5
coiled-coil domain containing 96, 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 4 samples with support for all annotated introns
coiled-coil domain containing 96, transcript variant X1
coiled-coil domain containing 96, transcript variant X4
coiled-coil domain containing 96, 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 16 samples with support for all annotated introns
coiled-coil domain-containing protein 96 isoform X2
coiled-coil domain-containing protein 96 isoform X1
coiled-coil domain-containing protein 96 isoform X3
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
formation of mitochondrial complex V assembly factor 1 homolog
RNA binding protein fox-1 homolog 2-like, transcript variant X7
RNA binding protein fox-1 homolog 2-like, transcript variant X11
RNA binding protein fox-1 homolog 2-like, transcript variant X1
RNA binding protein fox-1 homolog 2-like, transcript variant X3
RNA binding protein fox-1 homolog 2-like, transcript variant X4
RNA binding protein fox-1 homolog 2-like, transcript variant X2
RNA binding protein fox-1 homolog 2-like, transcript variant X9
RNA binding protein fox-1 homolog 2-like, transcript variant X6
RNA binding protein fox-1 homolog 2-like, transcript variant X10
RNA binding protein fox-1 homolog 2-like, transcript variant X8
RNA binding protein fox-1 homolog 1-like isoform X4
RNA binding protein fox-1 homolog 1-like isoform X10
RNA binding protein fox-1 homolog 1-like isoform X3
RNA binding protein fox-1 homolog 1-like isoform X6
RNA binding protein fox-1 homolog 1-like isoform X1
RNA binding protein fox-1 homolog 1-like isoform X2
RNA binding protein fox-1 homolog 1-like isoform X8
RNA binding protein fox-1 homolog 1-like isoform X5
RNA binding protein fox-1 homolog 2-like isoform X9
RNA binding protein fox-1 homolog 2-like isoform X7
RNA binding protein fox-1 homolog 2-like, 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 12 samples with support for all annotated introns
THAP domain containing 7, transcript variant X3
THAP domain containing 7, transcript variant X5
THAP domain containing 7, transcript variant X2
THAP domain containing 7, transcript variant X4
THAP domain containing 7, transcript variant X8
THAP domain containing 7, transcript variant X6
THAP domain containing 7, transcript variant X7
THAP domain containing 7, transcript variant X1
THAP domain-containing protein 7 isoform X1
THAP domain-containing protein 7 isoform X2
zinc finger and BTB domain-containing protein 20-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 12 samples with support for all annotated introns
ribosomal protein S11, transcript variant X1
ribosomal protein S11, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00211
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like, transcript variant X3
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like, 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 2 samples with support for all annotated introns
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like, transcript variant X1
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like isoform X3
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like isoform X2
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like isoform X1
pleckstrin homology domain-containing family A member 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
pleckstrin homology domain-containing family A member 7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 15B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 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: 79% coverage of the annotated genomic feature by RNAseq alignments
tubby protein homolog, 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 2 samples with support for all annotated introns
tubby protein homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125446983, transcript variant X3
uncharacterized LOC125446983, transcript variant X1
uncharacterized LOC125446983, 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 9 samples with support for all annotated introns
branched chain amino-acid transaminase 2, mitochondrial, transcript variant X2
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 8 samples with support for all annotated introns
branched chain amino-acid transaminase 2, mitochondrial, 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 22 samples with support for all annotated introns
branched-chain-amino-acid aminotransferase, mitochondrial
cytidine deaminase-like, transcript variant X2
cytidine deaminase-like, transcript variant X1
sodium-dependent neutral amino acid transporter B(0)AT2-like
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 6 samples with support for all annotated introns
leukocyte antigen CD37-like, transcript variant X2
leukocyte antigen CD37-like, transcript variant X4
leukocyte antigen CD37-like, transcript variant X1
leukocyte antigen CD37-like, transcript variant X3
leukocyte antigen CD37-like, transcript variant X5
transcriptional enhancer factor TEF-1-like, transcript variant X2
transcriptional enhancer factor TEF-1-like, transcript variant X4
transcriptional enhancer factor TEF-1-like, transcript variant X7
transcriptional enhancer factor TEF-1-like, 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 1 sample with support for all annotated introns
transcriptional enhancer factor TEF-1-like, transcript variant X6
transcriptional enhancer factor TEF-1-like, transcript variant X1
transcriptional enhancer factor TEF-1-like, transcript variant X3
transcriptional enhancer factor TEF-1-like isoform X5
transcriptional enhancer factor TEF-1-like isoform X3
transcriptional enhancer factor TEF-1-like isoform X4
transcriptional enhancer factor TEF-1-like isoform X1
transcriptional enhancer factor TEF-1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
tuberoinfundibular peptide of 39 residues
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68% coverage of the annotated genomic feature by RNAseq alignments
glycogen [starch] synthase, muscle-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glycogen [starch] synthase, muscle-like, transcript variant X2
glycogen [starch] synthase, muscle-like, transcript variant X3
glycogen [starch] synthase, muscle-like, transcript variant X4
glycogen [starch] synthase, muscle-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
circularly permutated Ras protein 1-like, transcript variant X1
circularly permutated Ras protein 1-like, transcript variant X3
circularly permutated Ras protein 1-like, transcript variant X4
circularly permutated Ras protein 1-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 11 samples with support for all annotated introns
circularly permutated Ras protein 1-like isoform X1
circularly permutated Ras protein 1-like isoform X2
circularly permutated Ras protein 1-like isoform X3