Rhincodon typus isolate 14 chromosome 40, sRhiTyp1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Chondrichthyes; Elasmobranchii; Galeomorphii; Galeoidea; Orectolobiformes; Rhincodontidae; Rhincodon.
REFSEQ INFORMATION: The reference sequence is identical to\nCM038837.1.\nAssembly name: sRhiTyp1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Squalomix on 2022/02/03. The\noriginal whole-genome shotgun project has the accession\nJAHMAH000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Squalomix\nAssembly Date :: 22-FEB-2021\nAssembly Method :: Supernova v. 2.1.1; P_RNA_scaffolder v.\n commit 7941e0f; Tigmint v. 1.1.2; ARKS v.\n 1.1.0; 3D-DNA v. 180922\nAssembly Name :: sRhiTyp1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 46.7x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Rhincodon typus Annotation Release\n 101\nAnnotation Version :: 101\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: 30 Proteins
uncharacterized protein LOC550500 homolog
COORDINATES: polyA evidence [ECO:0006239]
electrogenic sodium bicarbonate cotransporter 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase, transcript variant X2
methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase, transcript variant X1
bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase, mitochondrial isoform X2
bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase, mitochondrial isoform X1
heterogeneous nuclear ribonucleoprotein H3-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein H3-like, transcript variant X3
heterogeneous nuclear ribonucleoprotein H3-like, transcript variant X5
heterogeneous nuclear ribonucleoprotein H3-like, transcript variant X4
heterogeneous nuclear ribonucleoprotein H3-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein H3-like isoform X3
heterogeneous nuclear ribonucleoprotein H3-like isoform X1
heterogeneous nuclear ribonucleoprotein H3-like isoform X4
heterogeneous nuclear ribonucleoprotein H3-like isoform X2
heterogeneous nuclear ribonucleoprotein H3-like isoform X5
uncharacterized LOC125487336, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125487336, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125487336, transcript variant X4
uncharacterized LOC125487336, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 long SRA reads, and 61% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
methylcytosine dioxygenase TET3-like, transcript variant X1
methylcytosine dioxygenase TET3-like, transcript variant X3
methylcytosine dioxygenase TET3-like, transcript variant X4
methylcytosine dioxygenase TET3-like, transcript variant X5
methylcytosine dioxygenase TET3-like, transcript variant X2
methylcytosine dioxygenase tet3-like isoform X1
methylcytosine dioxygenase tet3-like isoform X2
methylcytosine dioxygenase TET3-like isoform X3
uncharacterized LOC125487338, transcript variant X3
uncharacterized LOC125487338, transcript variant X2
uncharacterized LOC125487338, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
histone acetyltransferase KAT6A, transcript variant X2
histone acetyltransferase KAT6A, transcript variant X1
histone acetyltransferase KAT6A, transcript variant X3
histone acetyltransferase KAT6A isoform X1
histone acetyltransferase KAT6A isoform X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
BAG family molecular chaperone regulator 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 6 Proteins, and 98% 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: 184 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
G protein-coupled receptor kinase 5-like, transcript variant X4
G protein-coupled receptor kinase 5-like, transcript variant X1
G protein-coupled receptor kinase 5-like, transcript variant X3
G protein-coupled receptor kinase 5-like, transcript variant X2
G protein-coupled receptor kinase 5-like isoform X1
G protein-coupled receptor kinase 5-like isoform X3
G protein-coupled receptor kinase 5-like isoform X2
G protein-coupled receptor kinase 5-like, transcript variant X5
G protein-coupled receptor kinase 5-like, transcript variant X6
G protein-coupled receptor kinase 5-like, transcript variant X7
G protein-coupled receptor kinase 5-like isoform X4
G protein-coupled receptor kinase 5-like isoform X5
U6 snRNA-associated Sm-like protein LSm1
nudix (nucleoside diphosphate linked moiety X)-type motif 18, transcript variant X1
nudix (nucleoside diphosphate linked moiety X)-type motif 18, transcript variant X2
nudix (nucleoside diphosphate linked moiety X)-type motif 18, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 3C-like
DNA replication complex GINS protein SLD5
charged multivesicular body protein 7, transcript variant X2
charged multivesicular body protein 7, transcript variant X1
charged multivesicular body protein 7 isoform X2
charged multivesicular body protein 7 isoform X1
leucine-rich repeat LGI family, member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
dematin actin binding protein, transcript variant X4
dematin actin binding protein, transcript variant X6
dematin actin binding protein, transcript variant X2
dematin actin binding protein, transcript variant X1
dematin actin binding protein, transcript variant X3
dematin actin binding protein, transcript variant X5
actin filament-associated protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
FHF complex subunit HOOK interacting protein 2A-like, transcript variant X2
FHF complex subunit HOOK interacting protein 2A-like, transcript variant X1
FHF complex subunit HOOK interacting protein 2A-like isoform X1
FHF complex subunit HOOK interacting protein 2A-like isoform X2
BRF2 RNA polymerase III transcription initiation factor subunit, transcript variant X6
BRF2 RNA polymerase III transcription initiation factor subunit, transcript variant X3
BRF2 RNA polymerase III transcription initiation factor subunit, transcript variant X4
BRF2 RNA polymerase III transcription initiation factor subunit, transcript variant X1
BRF2 RNA polymerase III transcription initiation factor subunit, transcript variant X7
BRF2 RNA polymerase III transcription initiation factor subunit, transcript variant X5
BRF2 RNA polymerase III transcription initiation factor subunit, transcript variant X2
transcription factor IIIB 50 kDa subunit
uncharacterized LOC109923083, transcript variant X1
uncharacterized LOC109923083, transcript variant X2
uncharacterized protein LOC109923083 isoform X1
uncharacterized protein LOC109923083 isoform X2
STAM-binding protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
STAM-binding protein-like, transcript variant X4
STAM-binding protein-like, transcript variant X5
STAM-binding protein-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 6 samples with support for all annotated introns
STAM-binding protein-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
plasminogen activator, tissue, transcript variant X2
plasminogen activator, tissue, transcript variant X1
tissue-type plasminogen activator isoform X2
tissue-type plasminogen activator isoform X1
inhibitor of nuclear factor kappa B kinase subunit beta, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 36 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
inhibitor of nuclear factor kappa B kinase subunit beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 36 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
inhibitor of nuclear factor kappa B kinase subunit beta, transcript variant X4
inhibitor of nuclear factor kappa B kinase subunit beta, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 36 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
inhibitor of nuclear factor kappa-B kinase subunit beta isoform X1
inhibitor of nuclear factor kappa-B kinase subunit beta isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 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: 2 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
voltage-dependent anion channel 3, transcript variant X1
voltage-dependent anion channel 3, transcript variant X2
voltage-dependent anion-selective channel protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 19 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
outer mitochondrial transmembrane helix translocase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
outer mitochondrial transmembrane helix translocase-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
outer mitochondrial transmembrane helix translocase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
outer mitochondrial transmembrane helix translocase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
outer mitochondrial transmembrane helix translocase-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
outer mitochondrial transmembrane helix translocase-like isoform X2
outer mitochondrial transmembrane helix translocase-like isoform X1
polymerase (RNA) III (DNA directed) polypeptide D, transcript variant X2
polymerase (RNA) III (DNA directed) polypeptide D, transcript variant X1
DNA-directed RNA polymerase III subunit RPC4
phytanoyl-CoA hydroxylase-interacting protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 134 long SRA reads, 35 Proteins, and 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: 1 long SRA read, 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat domain 39, transcript variant X1
ankyrin repeat domain 39, transcript variant X2
ankyrin repeat domain-containing protein 39
chromosome 40 C2orf42 homolog, transcript variant X7
chromosome 40 C2orf42 homolog, transcript variant X3
chromosome 40 C2orf42 homolog, transcript variant X2
chromosome 40 C2orf42 homolog, transcript variant X5
chromosome 40 C2orf42 homolog, transcript variant X6
chromosome 40 C2orf42 homolog, transcript variant X4
chromosome 40 C2orf42 homolog, transcript variant X1
TIA1 cytotoxic granule-associated RNA binding protein
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon CCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
prolactin-releasing peptide receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins
rab11 family-interacting protein 1-like, transcript variant X1
rab11 family-interacting protein 1-like, transcript variant X2
rab11 family-interacting protein 1-like isoform X1
rab11 family-interacting protein 1-like isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: NPC1-like intracellular cholesterol transporter 1
uncharacterized sb:cb288, transcript variant X2
uncharacterized sb:cb288, transcript variant X1
uncharacterized protein sb:cb288 isoform X1
uncharacterized protein sb:cb288 isoform X2
LIM domain-binding protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
LIM domain-binding protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 86% coverage of the annotated genomic feature by RNAseq alignments
potassium channel tetramerization domain containing 9a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71% coverage of the annotated genomic feature by RNAseq alignments
inositol polyphosphate-5-phosphatase A-like, transcript variant X2
inositol polyphosphate-5-phosphatase A-like, transcript variant X1
inositol polyphosphate-5-phosphatase A-like isoform X2
inositol polyphosphate-5-phosphatase A-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
dual specificity protein phosphatase 1-B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
poly(ADP-ribose) glycohydrolase-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
poly(ADP-ribose) glycohydrolase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
poly(ADP-ribose) glycohydrolase-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
poly(ADP-ribose) glycohydrolase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
poly(ADP-ribose) glycohydrolase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
poly(ADP-ribose) glycohydrolase-like isoform X2
poly(ADP-ribose) glycohydrolase-like isoform X1
poly(ADP-ribose) glycohydrolase-like isoform X4
poly(ADP-ribose) glycohydrolase-like isoform X3
StAR-related lipid transfer (START) domain containing 7, transcript variant X5
StAR-related lipid transfer (START) domain containing 7, transcript variant X6
StAR-related lipid transfer (START) domain containing 7, transcript variant X4
StAR-related lipid transfer (START) domain containing 7, transcript variant X1
StAR-related lipid transfer (START) domain containing 7, transcript variant X2
StAR-related lipid transfer (START) domain containing 7, transcript variant X3
stAR-related lipid transfer protein 7, mitochondrial
COORDINATES: nucleotide motif:Rfam:12.0:RF00599
2-oxoglutarate dehydrogenase complex component E1, transcript variant X2
2-oxoglutarate dehydrogenase complex component E1, transcript variant X4
2-oxoglutarate dehydrogenase complex component E1, transcript variant X1
2-oxoglutarate dehydrogenase complex component E1, transcript variant X3
2-oxoglutarate dehydrogenase complex component E1 isoform X2
2-oxoglutarate dehydrogenase complex component E1 isoform X4
2-oxoglutarate dehydrogenase complex component E1 isoform X1
2-oxoglutarate dehydrogenase complex component E1 isoform X3
zinc finger MIZ domain-containing protein 1-like
peptidyl-prolyl cis-trans isomerase-like
vesicle-associated membrane protein 8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
surfactant protein Bb, transcript variant X2
surfactant protein Bb, transcript variant X1
pulmonary surfactant-associated protein B isoform X2
pulmonary surfactant-associated protein B isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58% coverage of the annotated genomic feature by RNAseq alignments
PH and SEC7 domain-containing protein 4-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 57 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 long SRA read, and 94% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: max dimerization protein 1-like
small nuclear ribonucleoprotein 27 (U4/U6.U5), transcript variant X2
small nuclear ribonucleoprotein 27 (U4/U6.U5), transcript variant X1
U4/U6.U5 small nuclear ribonucleoprotein 27 kDa protein isoform X2
U4/U6.U5 small nuclear ribonucleoprotein 27 kDa protein isoform X1
beta-adducin-like, transcript variant X6
beta-adducin-like, transcript variant X5
beta-adducin-like, transcript variant X7
beta-adducin-like, transcript variant X4
beta-adducin-like, transcript variant X3
beta-adducin-like, transcript variant X2
beta-adducin-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 73% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
deleted in malignant brain tumors 1 protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 long SRA reads, 26 Proteins, and 99% 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: 39 long SRA reads, 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
secreted frizzled-related protein 1, transcript variant X1
secreted frizzled-related protein 1, transcript variant X2
secreted frizzled-related protein 1 isoform X1
secreted frizzled-related protein 1 isoform X2
zinc finger, matrin-type 4a, transcript variant X1
zinc finger, matrin-type 4a, transcript variant X3
zinc finger, matrin-type 4a, 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 3 samples with support for all annotated introns
zinc finger matrin-type protein 4 isoform X1
zinc finger matrin-type protein 4 isoform X3
zinc finger matrin-type protein 4 isoform X2
zinc finger, matrin-type 4a, transcript variant X4
zinc finger matrin-type protein 4 isoform X4
transcriptional and immune response regulator-like
indoleamine 2,3-dioxygenase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
indoleamine 2,3-dioxygenase 1, transcript variant X2
disintegrin and metalloproteinase domain-containing protein 9
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 6 samples with support for all annotated introns
pleckstrin homology domain-containing family A member 2
transforming, acidic coiled-coil containing protein 1, transcript variant X4
transforming, acidic coiled-coil containing protein 1, transcript variant X1
transforming, acidic coiled-coil containing protein 1, transcript variant X3
transforming, acidic coiled-coil containing protein 1, transcript variant X2
transforming, acidic coiled-coil containing protein 1, transcript variant X5
transforming acidic coiled-coil-containing protein 1 isoform X3
transforming acidic coiled-coil-containing protein 1 isoform X1
transforming acidic coiled-coil-containing protein 1 isoform X2
transforming acidic coiled-coil-containing protein 1 isoform X4
fibroblast growth factor receptor 1-like
leucine zipper-EF-hand containing transmembrane protein 2
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
LETM1 domain-containing protein LETM2, mitochondrial
nuclear receptor binding SET domain protein 3, transcript variant X2
nuclear receptor binding SET domain protein 3, transcript variant X4
nuclear receptor binding SET domain protein 3, transcript variant X6
nuclear receptor binding SET domain protein 3, transcript variant X8
nuclear receptor binding SET domain protein 3, transcript variant X3
nuclear receptor binding SET domain protein 3, transcript variant X1
nuclear receptor binding SET domain protein 3, transcript variant X7
nuclear receptor binding SET domain protein 3, transcript variant X5
nuclear receptor binding SET domain protein 3, transcript variant X9
histone-lysine N-methyltransferase NSD3 isoform X3
histone-lysine N-methyltransferase NSD3 isoform X5
histone-lysine N-methyltransferase NSD3 isoform X1
histone-lysine N-methyltransferase NSD3 isoform X4
histone-lysine N-methyltransferase NSD3 isoform X2
histone-lysine N-methyltransferase NSD3 isoform X6
mitochondrial ribosomal protein S24, transcript variant X2
mitochondrial ribosomal protein S24, transcript variant X1
28S ribosomal protein S24, mitochondrial isoform X2
28S ribosomal protein S24, mitochondrial isoform X1
calcium/calmodulin-dependent protein kinase type II subunit beta-like
polymerase (DNA directed), mu, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
polymerase (DNA directed), mu, transcript variant X5
polymerase (DNA directed), mu, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
polymerase (DNA directed), mu, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 23 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
polymerase (DNA directed), mu, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
polymerase (DNA directed), mu, transcript variant X6
DNA-directed DNA/RNA polymerase mu isoform X4
DNA-directed DNA/RNA polymerase mu isoform X3
DNA-directed DNA/RNA polymerase mu isoform X1
DNA-directed DNA/RNA polymerase mu isoform X2
DNA-directed DNA/RNA polymerase mu isoform X5
glucosamine (N-acetyl)-6-sulfatase (Sanfilippo disease IIID), b, transcript variant X1
glucosamine (N-acetyl)-6-sulfatase (Sanfilippo disease IIID), b, transcript variant X2
glucosamine (N-acetyl)-6-sulfatase (Sanfilippo disease IIID), b isoform X1
glucosamine (N-acetyl)-6-sulfatase (Sanfilippo disease IIID), b isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 240 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized protein LOC767682 homolog
fumarylacetoacetate hydrolase domain containing 2A, transcript variant X3
fumarylacetoacetate hydrolase domain containing 2A, transcript variant X1
fumarylacetoacetate hydrolase domain containing 2A, transcript variant X2
fumarylacetoacetate hydrolase domain-containing protein 2A isoform X1
fumarylacetoacetate hydrolase domain-containing protein 2A isoform X2
fumarylacetoacetate hydrolase domain-containing protein 2A isoform X3
glycerol-3-phosphate acyltransferase 2, mitochondrial, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glycerol-3-phosphate acyltransferase 2, mitochondrial, transcript variant X5
glycerol-3-phosphate acyltransferase 2, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
glycerol-3-phosphate acyltransferase 2, mitochondrial, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
glycerol-3-phosphate acyltransferase 2, mitochondrial, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
glycerol-3-phosphate acyltransferase 2, mitochondrial, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
glycerol-3-phosphate acyltransferase 2, mitochondrial isoform X5
glycerol-3-phosphate acyltransferase 2, mitochondrial isoform X4
glycerol-3-phosphate acyltransferase 2, mitochondrial isoform X2
glycerol-3-phosphate acyltransferase 2, mitochondrial isoform X1
glycerol-3-phosphate acyltransferase 2, mitochondrial isoform X6
glycerol-3-phosphate acyltransferase 2, mitochondrial, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
glycerol-3-phosphate acyltransferase 2, mitochondrial isoform X3
ELMO/CED-12 domain containing 3, transcript variant X5
ELMO/CED-12 domain containing 3, transcript variant X6
ELMO/CED-12 domain containing 3, transcript variant X3
ELMO/CED-12 domain containing 3, transcript variant X2
ELMO/CED-12 domain containing 3, transcript variant X1
ELMO/CED-12 domain containing 3, transcript variant X4
ELMO domain-containing protein 3 isoform X2
ELMO domain-containing protein 3 isoform X1
ELMO/CED-12 domain containing 3, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ELMO domain-containing protein 3 isoform X3
inactive carboxypeptidase-like protein X2
polymerase (DNA directed), delta 2, regulatory subunit
myosin, light chain 7, regulatory, transcript variant X2
myosin, light chain 7, regulatory, transcript variant X1
myosin regulatory light chain 2, atrial isoform isoform X2
myosin regulatory light chain 2, atrial isoform isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
chromaffin granule amine transporter-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
TELO2 interacting protein 2, transcript variant X1
TELO2 interacting protein 2, transcript variant X2
MAK16 homolog (S. cerevisiae), transcript variant X2
MAK16 homolog (S. cerevisiae), transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF01210
ring finger protein 122, transcript variant X2
ring finger protein 122, transcript variant X1
ring finger protein 122, transcript variant X3
ring finger protein 122, transcript variant X4
gamma-glutamyl hydrolase, transcript variant X2
gamma-glutamyl hydrolase, transcript variant X4
gamma-glutamyl hydrolase, transcript variant X3
gamma-glutamyl hydrolase, transcript variant X6
gamma-glutamyl hydrolase, transcript variant X5
gamma-glutamyl hydrolase, transcript variant X1
inositol 1,4,5-trisphosphate receptor-interacting protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 long SRA reads, 2 Proteins, and 80% 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: 9 long SRA reads, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cytosolic iron-sulfur assembly component 1, transcript variant X1
cytosolic iron-sulfur assembly component 1, transcript variant X2
probable cytosolic iron-sulfur protein assembly protein ciao1 isoform X1
probable cytosolic iron-sulfur protein assembly protein ciao1 isoform X2
small nuclear ribonucleoprotein 200 (U5)
U5 small nuclear ribonucleoprotein 200 kDa helicase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sodium-dependent phosphate transporter 1, transcript variant X3
sodium-dependent phosphate transporter 1, transcript variant X1
sodium-dependent phosphate transporter 1, transcript variant X2
sodium-dependent phosphate transporter 1 isoform X1
sodium-dependent phosphate transporter 1 isoform X2
transmembrane emp24 domain-containing protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
MAM and LDL-receptor class A domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
probable ATP-dependent RNA helicase DDX56
cell division cycle associated 2, transcript variant X1
cell division cycle associated 2, transcript variant X4
cell division cycle associated 2, transcript variant X2
cell division cycle associated 2, transcript variant X6
cell division cycle-associated protein 2 isoform X1
cell division cycle-associated protein 2 isoform X4
cell division cycle-associated protein 2 isoform X2
cell division cycle-associated protein 2 isoform X6
cell division cycle associated 2, transcript variant X3
cell division cycle associated 2, transcript variant X5
cell division cycle associated 2, transcript variant X7
cell division cycle associated 2, transcript variant X8
cell division cycle-associated protein 2 isoform X3
cell division cycle-associated protein 2 isoform X5
cell division cycle-associated protein 2 isoform X7
cell division cycle associated 2, transcript variant X9
cell division cycle-associated protein 2 isoform X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B alpha isoform, transcript variant X4
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B alpha isoform, transcript variant X3
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B alpha isoform, transcript variant X1
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B alpha isoform isoform X1
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B alpha isoform isoform X3
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B alpha isoform, transcript variant X2
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B alpha isoform isoform X2
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B alpha isoform isoform X4
BCL2/adenovirus E1B 19 kDa protein-interacting protein 3-like
dihydropyrimidinase-related protein 2, transcript variant X3
dihydropyrimidinase-related protein 2, transcript variant X1
dihydropyrimidinase-related protein 2, transcript variant X2
dihydropyrimidinase-related protein 2 isoform X1
dihydropyrimidinase-related protein 2 isoform X2
dihydropyrimidinase-related protein 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
leucine-rich repeat transmembrane neuronal protein 4-like, transcript variant X2
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 6 samples with support for all annotated introns
leucine-rich repeat transmembrane neuronal protein 4-like isoform X2
leucine-rich repeat transmembrane neuronal protein 4-like, 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 2 samples with support for all annotated introns
leucine-rich repeat transmembrane neuronal protein 4-like isoform X3
leucine-rich repeat transmembrane neuronal protein 4-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 7 samples with support for all annotated introns
leucine-rich repeat transmembrane neuronal protein 4-like isoform X1
receptor expression-enhancing protein 1-like, transcript variant X2
receptor expression-enhancing protein 1-like, transcript variant X1
receptor expression-enhancing protein 1-like
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C, transcript variant X4
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C, transcript variant X5
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C, transcript variant X2
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C, transcript variant X3
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C, transcript variant X1
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C, transcript variant X6
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C, transcript variant X7
E3 ubiquitin-protein ligase MARCHF5-like
cytoplasmic polyadenylation element-binding protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
pituitary homeobox 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
pituitary homeobox 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
AP2 associated kinase 1b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
AP2 associated kinase 1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
AP2-associated protein kinase 1 isoform X1
AP2-associated protein kinase 1 isoform X2
NFU1 iron-sulfur cluster scaffold homolog (S. cerevisiae), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 171 long SRA reads, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
NFU1 iron-sulfur cluster scaffold homolog, mitochondrial isoform X1
NFU1 iron-sulfur cluster scaffold homolog (S. cerevisiae), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
NFU1 iron-sulfur cluster scaffold homolog, mitochondrial isoform X2
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 1, transcript variant X3
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 1, transcript variant X1
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 1, transcript variant X4
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 1, transcript variant X2
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 1 isoform X1
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 1 isoform X2
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 1 isoform X3
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 1 isoform X4
disintegrin and metalloproteinase domain-containing protein 8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 22 Proteins
CDP-diacylglycerol synthase (phosphatidate cytidylyltransferase) 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ectonucleoside triphosphate diphosphohydrolase 4, transcript variant X2
ectonucleoside triphosphate diphosphohydrolase 4, transcript variant X3
ectonucleoside triphosphate diphosphohydrolase 4, transcript variant X5
ectonucleoside triphosphate diphosphohydrolase 4, transcript variant X1
ectonucleoside triphosphate diphosphohydrolase 4, transcript variant X4
ectonucleoside triphosphate diphosphohydrolase 4 isoform X1
ectonucleoside triphosphate diphosphohydrolase 4 isoform X2
homeobox protein koza-like, transcript variant X6
homeobox protein koza-like, transcript variant X5
homeobox protein koza-like, transcript variant X4
homeobox protein koza-like, transcript variant X2
homeobox protein koza-like, transcript variant X3
homeobox protein koza-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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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 3 samples with support for all annotated introns
mitoferrin-1-like, transcript variant X1
mitoferrin-1-like, transcript variant X2
mitoferrin-1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
zinc metalloproteinase-disintegrin-like ecarin
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97 Proteins, and 94% 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: 13 Proteins
DDHD domain containing 2, transcript variant X3
DDHD domain containing 2, transcript variant X2
DDHD domain containing 2, transcript variant X1
DDHD domain containing 2, transcript variant X4
phospholipid phosphatase 4-like, transcript variant X1
phospholipid phosphatase 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
steroidogenic acute regulatory protein, mitochondrial
ash2 like, histone lysine methyltransferase complex subunit, transcript variant X3
ash2 like, histone lysine methyltransferase complex subunit, transcript variant X2
ash2 like, histone lysine methyltransferase complex subunit, transcript variant X1
ash2 like, histone lysine methyltransferase complex subunit, transcript variant X4
set1/Ash2 histone methyltransferase complex subunit ASH2 isoform X3
set1/Ash2 histone methyltransferase complex subunit ASH2 isoform X2
set1/Ash2 histone methyltransferase complex subunit ASH2 isoform X1
set1/Ash2 histone methyltransferase complex subunit ASH2 isoform X4
ash2 like, histone lysine methyltransferase complex subunit, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
set1/Ash2 histone methyltransferase complex subunit ASH2 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
eukaryotic translation initiation factor 4E-binding protein 1-like
rho-related BTB domain-containing protein 2
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
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: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
bridging integrator 3, transcript variant X3
bridging integrator 3, transcript variant X2
bridging integrator 3, transcript variant X1
leucine zipper putative tumor suppressor 1-like
small nuclear ribonucleoprotein polypeptide G
aspartate aminotransferase, cytoplasmic-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
germ cell-less, spermatogenesis associated
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
GDNF family receptor alpha-2-like, transcript variant X2
GDNF family receptor alpha-2-like, transcript variant X3
GDNF family receptor alpha-2-like, transcript variant X1
GDNF family receptor alpha-2-like isoform X2
GDNF family receptor alpha-2-like isoform X1
GDNF family receptor alpha-2-like isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
docking protein 2-like, transcript variant X2
docking protein 2-like, transcript variant X1
polysaccharide biosynthesis domain containing 1, transcript variant X1
polysaccharide biosynthesis domain containing 1, transcript variant X2
F-box/WD repeat-containing protein 1A isoform X3
F-box/WD repeat-containing protein 1A isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins
nucleoplasmin-like, transcript variant X1
nucleoplasmin-like, transcript variant X3
nucleoplasmin-like, transcript variant X2
adhesion G protein-coupled receptor A2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
calcium-activated potassium channel subunit alpha-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
aspartate dehydrogenase domain containing
aspartate dehydrogenase domain-containing protein
AT-rich interactive domain-containing protein 5B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
AT-rich interactive domain-containing protein 5B-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
AT-rich interactive domain-containing protein 5B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 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: 8 long SRA reads, 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: 4 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 4 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: 5 long SRA reads, 9 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: 40 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 39 member 14, transcript variant X3
solute carrier family 39 member 14, transcript variant X1
solute carrier family 39 member 14, transcript variant X2
solute carrier family 39 member 14, transcript variant X4
serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: serine/threonine-protein phosphatase 2B catalytic subunit gamma isoform-like
PDZ and LIM domain 2 (mystique), transcript variant X2
PDZ and LIM domain 2 (mystique), transcript variant X3
PDZ and LIM domain 2 (mystique), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cell division cycle and apoptosis regulator protein 1-like, transcript variant X1
cell division cycle and apoptosis regulator protein 1-like, transcript variant X3
cell division cycle and apoptosis regulator protein 1-like, transcript variant X2
cell division cycle and apoptosis regulator protein 1-like, transcript variant X4
cell division cycle and apoptosis regulator protein 1-like isoform X1
cell division cycle and apoptosis regulator protein 1-like isoform X3
cell division cycle and apoptosis regulator protein 1-like isoform X2
cell division cycle and apoptosis regulator protein 1-like isoform X4
transcription factor 7-like 2, transcript variant X2
transcription factor 7-like 2, transcript variant X1
transcription factor 7-like 2 isoform X2
transcription factor 7-like 1-A isoform X1
ubiquitin-conjugating enzyme E2 D4-like, transcript variant X1
ubiquitin-conjugating enzyme E2 D4-like isoform X1
ubiquitin-conjugating enzyme E2 D4-like, transcript variant X2
ubiquitin-conjugating enzyme E2 D4-like isoform 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X6
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X7
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X8
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X2
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X5
NACHT, LRR and PYD domains-containing protein 12-like isoform X1
NACHT, LRR and PYD domains-containing protein 12-like isoform X2
NACHT, LRR and PYD domains-containing protein 12-like isoform X4
NACHT, LRR and PYD domains-containing protein 12-like isoform X3
NACHT, LRR and PYD domains-containing protein 12-like isoform X5
NACHT, LRR and PYD domains-containing protein 12-like isoform X6
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 12-like isoform X7