Rhincodon typus isolate 14 chromosome 17, 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\nCM038814.1.\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.
COORDINATES: polyA evidence [ECO:0006239]
receptor-associated protein of the synapse, 43kD, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
receptor-associated protein of the synapse, 43kD, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
43 kDa receptor-associated protein of the synapse isoform X2
43 kDa receptor-associated protein of the synapse isoform X1
cugbp, Elav-like family member 1, transcript variant X7
cugbp, Elav-like family member 1, transcript variant X5
cugbp, Elav-like family member 1, transcript variant X1
cugbp, Elav-like family member 1, transcript variant X6
cugbp, Elav-like family member 1, transcript variant X3
cugbp, Elav-like family member 1, transcript variant X4
cugbp, Elav-like family member 1, transcript variant X8
cugbp, Elav-like family member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
CUGBP Elav-like family member 1 isoform X7
CUGBP Elav-like family member 1 isoform X6
CUGBP Elav-like family member 1 isoform X5
CUGBP Elav-like family member 1 isoform X2
CUGBP Elav-like family member 1 isoform X3
CUGBP Elav-like family member 1 isoform X4
CUGBP Elav-like family member 1 isoform X1
ADP-ribosylation factor GTPase activating protein 2, transcript variant X2
ADP-ribosylation factor GTPase activating protein 2, transcript variant X4
ADP-ribosylation factor GTPase activating protein 2, transcript variant X3
ADP-ribosylation factor GTPase activating protein 2, transcript variant X1
ADP-ribosylation factor GTPase-activating protein 2 isoform X3
ADP-ribosylation factor GTPase-activating protein 2 isoform X2
ADP-ribosylation factor GTPase-activating protein 2 isoform X4
ADP-ribosylation factor GTPase-activating protein 2 isoform X1
ADP-ribosylation factor GTPase activating protein 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein kinase C and casein kinase substrate in neurons 3, transcript variant X2
protein kinase C and casein kinase substrate in neurons 3, transcript variant X1
protein kinase C and casein kinase substrate in neurons protein 3 isoform X1
protein kinase C and casein kinase substrate in neurons protein 3 isoform X2
lysosomal acid phosphatase-like, transcript variant X1
lysosomal acid phosphatase-like, transcript variant X2
lysosomal acid phosphatase-like isoform X1
lysosomal acid phosphatase-like isoform X2
prostatic acid phosphatase-like isoform X1
lysosomal acid phosphatase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 35 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
lysosomal acid phosphatase-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
MAP kinase-activating death domain protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
maestro heat-like repeat-containing protein family member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
formin binding protein 4, transcript variant X1
formin binding protein 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial carrier homolog 2, transcript variant X2
mitochondrial carrier homolog 2, 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
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00582
proteasome 26S subunit, ATPase 3, transcript variant X1
26S proteasome regulatory subunit 6A isoform X1
proteasome 26S subunit, ATPase 3, transcript variant X2
26S proteasome regulatory subunit 6A isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 39 member 13, transcript variant X1
solute carrier family 39 member 13, 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 5 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
carnitine palmitoyltransferase 1Ab (liver), transcript variant X1
carnitine palmitoyltransferase 1Ab (liver), transcript variant X3
carnitine palmitoyltransferase 1Ab (liver), transcript variant X4
carnitine palmitoyltransferase 1Ab (liver), transcript variant X2
carnitine O-palmitoyltransferase 1, liver isoform isoform X2
carnitine O-palmitoyltransferase 1, liver isoform isoform X1
AP-2 complex subunit alpha-2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
AP-2 complex subunit alpha-2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
AP-2 complex subunit alpha-2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
AP-2 complex subunit alpha-2-like isoform X1
AP-2 complex subunit alpha-2-like isoform X2
AP-2 complex subunit alpha-2-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 20% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 7% 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 12A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 12A-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 12A-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 12A-like, 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 6 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 12A-like isoform X2
protein phosphatase 1 regulatory subunit 12A-like isoform X4
protein phosphatase 1 regulatory subunit 12A-like isoform X3
protein phosphatase 1 regulatory subunit 12A-like isoform X1
von Willebrand factor C and EGF domain-containing protein-like
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: 3 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: 2 long SRA reads, 2 Proteins, and 97% 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 5 samples with support for all annotated introns
protein tyrosine phosphatase non-receptor type 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
tyrosine-protein phosphatase non-receptor type 5
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
protein tyrosine phosphatase receptor type Ja
receptor-type tyrosine-protein phosphatase eta
oxysterol-binding protein-related protein 8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 20 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
cysteinyl-tRNA synthetase 1, transcript variant X3
cysteinyl-tRNA synthetase 1, transcript variant X1
cysteinyl-tRNA synthetase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cysteinyl-tRNA synthetase 1, transcript variant X5
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 9 samples with support for all annotated introns
cysteinyl-tRNA synthetase 1, transcript variant X4
cysteine--tRNA ligase, cytoplasmic isoform X1
cysteine--tRNA ligase, cytoplasmic isoform X3
cysteine--tRNA ligase, cytoplasmic isoform X4
cysteine--tRNA ligase, cytoplasmic isoform X2
cysteine--tRNA ligase, cytoplasmic isoform X5
nucleosome assembly protein 1-like 4b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
nucleosome assembly protein 1-like 4b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
nucleosome assembly protein 1-like 4b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00430
nuclear pore complex protein Nup160-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
nuclear pore complex protein Nup160 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
nuclear pore complex protein Nup160 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 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
39S ribosomal protein L23, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
p53-induced death domain-containing protein 1
patatin-like phospholipase domain-containing protein 2
EF-hand calcium-binding domain-containing protein 4A-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
EF-hand calcium-binding domain-containing protein 4B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial ribosomal protein L21, transcript variant X2
mitochondrial ribosomal protein L21, transcript variant X1
39S ribosomal protein L21, mitochondrial
immunoglobulin mu DNA binding protein 2, transcript variant X4
immunoglobulin mu DNA binding protein 2, transcript variant X6
immunoglobulin mu DNA binding protein 2, transcript variant X1
immunoglobulin mu DNA binding protein 2, transcript variant X3
immunoglobulin mu DNA binding protein 2, transcript variant X2
immunoglobulin mu DNA binding protein 2, transcript variant X5
synaptotagmin XII, 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
synaptotagmin XII, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential cation channel, subfamily M, member 5
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
transient receptor potential cation channel subfamily M member 5
potassium voltage-gated channel subfamily KQT member 1
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
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
beta-1,4-N-acetyl-galactosaminyl transferase 4a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
N-acetyl-beta-glucosaminyl-glycoprotein 4-beta-N-acetylgalactosaminyltransferase 1 isoform X1
beta-1,4-N-acetyl-galactosaminyl transferase 4a, 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
N-acetyl-beta-glucosaminyl-glycoprotein 4-beta-N-acetylgalactosaminyltransferase 1 isoform X2
dual specificity protein phosphatase 8-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
dual specificity protein phosphatase 8-like, transcript variant X1
dual specificity protein phosphatase 8-like isoform X2
dual specificity protein phosphatase 8-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 1 Protein, 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: 12 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ATG13 autophagy related 13 homolog (S. cerevisiae), transcript variant X2
ATG13 autophagy related 13 homolog (S. cerevisiae), transcript variant X1
ATG13 autophagy related 13 homolog (S. cerevisiae), transcript variant X4
ATG13 autophagy related 13 homolog (S. cerevisiae), transcript variant X3
ATG13 autophagy related 13 homolog (S. cerevisiae), transcript variant X6
ATG13 autophagy related 13 homolog (S. cerevisiae), transcript variant X5
ATG13 autophagy related 13 homolog (S. cerevisiae), transcript variant X7
ATG13 autophagy related 13 homolog (S. cerevisiae), transcript variant X8
activating molecule in BECN1-regulated autophagy protein 1-like, transcript variant X1
activating molecule in BECN1-regulated autophagy protein 1-like, transcript variant X2
activating molecule in BECN1-regulated autophagy protein 1-like isoform X1
activating molecule in BECN1-regulated autophagy protein 1-like isoform X2
cholinergic receptor, muscarinic 4a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cholinergic receptor, muscarinic 4a, transcript variant X2
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 2 samples with support for all annotated introns
cAMP responsive element binding protein 3-like 1, transcript variant X1
cAMP responsive element binding protein 3-like 1, transcript variant X2
cyclic AMP-responsive element-binding protein 3-like protein 1 isoform X1
cyclic AMP-responsive element-binding protein 3-like protein 1 isoform X2
Rho GTPase activating protein 1, transcript variant X1
Rho GTPase activating protein 1, transcript variant X2
rho GTPase-activating protein 1 isoform X1
rho GTPase-activating protein 1 isoform X2
PHD finger protein 21Ab, transcript variant X2
PHD finger protein 21Ab, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
zinc finger protein 660-like, transcript variant X1
zinc finger protein 660-like, transcript variant X3
zinc finger protein 660-like, transcript variant X2
zinc finger protein 408, transcript variant X1
zinc finger protein 408, transcript variant X2
PR domain containing 11, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
PR domain containing 11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PR domain containing 11, transcript variant X5
PR domain containing 11, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PR domain containing 11, transcript variant X6
uncharacterized protein prdm11 isoform X5
PR domain containing 11, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
synaptotagmin XIII, 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 6 samples with support for all annotated introns
synaptotagmin XIII, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 long SRA reads, 18 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
low-density lipoprotein receptor class A domain-containing protein 3-like, transcript variant X2
low-density lipoprotein receptor class A domain-containing protein 3-like, transcript variant X1
low-density lipoprotein receptor class A domain-containing protein 3-like isoform X2
low-density lipoprotein receptor class A domain-containing protein 3-like isoform 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 13 samples with support for all annotated introns
peptidase domain containing associated with muscle regeneration 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 101 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56% coverage of the annotated genomic feature by RNAseq alignments
pyruvate dehydrogenase complex component X
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: pyruvate dehydrogenase protein X component, mitochondrial
methylthioribulose-1-phosphate dehydratase
ETS homologous factor-like, transcript variant X3
ETS homologous factor-like, transcript variant X2
ETS homologous factor-like, transcript variant X1
tumor protein p53 inducible protein 11b, transcript variant X1
tumor protein p53 inducible protein 11b, transcript variant X2
tetraspanin-18-like, transcript variant X3
tetraspanin-18-like, transcript variant X4
tetraspanin-18-like, transcript variant X5
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
tetraspanin-18-like, transcript variant X1
tetraspanin-18-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 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: 16 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
embryonic protein UVS.2-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 2 samples with support for all annotated introns
embryonic protein UVS.2-like, transcript variant X2
embryonic protein UVS.2-like, transcript variant X1
embryonic protein UVS.2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins
pleckstrin homology-like domain, family A, member 2, transcript variant X2
pleckstrin homology-like domain, family A, member 2, transcript variant X1
pleckstrin homology-like domain family A member 2
tumor suppressing subtransferable candidate 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 11 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: 7 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
single immunoglobulin and toll-interleukin 1 receptor (TIR) domain
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
potassium voltage-gated channel, Shaw-related subfamily, member 1a, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel, Shaw-related subfamily, member 1a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily C member 1a isoform X7
potassium voltage-gated channel subfamily C member 1a isoform X5
potassium voltage-gated channel, Shaw-related subfamily, member 1a, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel, Shaw-related subfamily, member 1a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel, Shaw-related subfamily, member 1a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel, Shaw-related subfamily, member 1a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel, Shaw-related subfamily, member 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily C member 1a isoform X6
potassium voltage-gated channel subfamily C member 1a isoform X4
potassium voltage-gated channel subfamily C member 1a isoform X3
potassium voltage-gated channel subfamily C member 1a isoform X1
potassium voltage-gated channel subfamily C member 1a isoform X2
tryptophan hydroxylase 1 (tryptophan 5-monooxygenase) a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tryptophan hydroxylase 1 (tryptophan 5-monooxygenase) a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
HPS5 biogenesis of lysosomal organelles complex 2 subunit 2, transcript variant X2
HPS5 biogenesis of lysosomal organelles complex 2 subunit 2, transcript variant X1
HPS5 biogenesis of lysosomal organelles complex 2 subunit 2, transcript variant X3
HPS5 biogenesis of lysosomal organelles complex 2 subunit 2, transcript variant X4
Hermansky-Pudlak syndrome 5 protein isoform X1
HPS5 biogenesis of lysosomal organelles complex 2 subunit 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Hermansky-Pudlak syndrome 5 protein isoform X2
general transcription factor IIH, polypeptide 1, transcript variant X4
general transcription factor IIH, polypeptide 1, transcript variant X3
general transcription factor IIH, polypeptide 1, transcript variant X1
general transcription factor IIH, polypeptide 1, transcript variant X2
general transcription factor IIH subunit 1 isoform X2
general transcription factor IIH subunit 1 isoform X1
general transcription factor IIH, polypeptide 1, transcript variant X5
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
L-lactate dehydrogenase A chain, transcript variant X1
L-lactate dehydrogenase A chain, transcript variant X2
L-lactate dehydrogenase A chain isoform X1
L-lactate dehydrogenase A chain, transcript variant X4
L-lactate dehydrogenase A chain, transcript variant X3
L-lactate dehydrogenase A chain isoform X2
UEV and lactate/malate dehyrogenase domains
ubiquitin-conjugating enzyme E2 variant 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
galanin/GMAP prepropeptide, transcript variant X1
galanin/GMAP prepropeptide, transcript variant X2
cytochrome c oxidase subunit 6A2, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 11 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
damage-specific DNA binding protein 1, transcript variant X2
damage-specific DNA binding protein 1, transcript variant X1
lysosomal membrane ascorbate-dependent ferrireductase CYB561A3-like, transcript variant X1
lysosomal membrane ascorbate-dependent ferrireductase CYB561A3-like, transcript variant X2
lysosomal membrane ascorbate-dependent ferrireductase CYB561A3-like isoform X1
lysosomal membrane ascorbate-dependent ferrireductase CYB561A3-like isoform X2
armadillo repeat containing 7, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
armadillo repeat-containing protein 7 isoform X2
armadillo repeat containing 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 107 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
armadillo repeat containing 7, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 102 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane protein 138, transcript variant X4
armadillo repeat containing 7, transcript variant X3
armadillo repeat containing 7, transcript variant X2
armadillo repeat-containing protein 7 isoform X1
transmembrane protein 138, transcript variant X5
transmembrane protein 138, transcript variant X2
transmembrane protein 138, transcript variant X1
transmembrane protein 138, transcript variant X3
transmembrane protein 216-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
transmembrane protein 216-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
transmembrane protein 216-like, transcript variant X1
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 2 samples with support for all annotated introns
transmembrane protein 216-like isoform X1
transmembrane protein 216-like isoform X2
transmembrane protein 216-like isoform X3
succinate dehydrogenase complex assembly factor 2
succinate dehydrogenase assembly factor 2, mitochondrial
transmembrane protein 80-like, transcript variant X1
transmembrane protein 80-like isoform X1
transmembrane protein 80-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
transmembrane protein 80-like isoform X2
cleavage and polyadenylation specificity factor subunit 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC109928218, transcript variant X2
uncharacterized LOC109928218, transcript variant X1
uncharacterized LOC109928235, transcript variant X1
uncharacterized LOC109928235, transcript variant X2
uncharacterized protein LOC109928235 isoform X1
uncharacterized protein LOC109928235 isoform X2
protein-glucosylgalactosylhydroxylysine glucosidase, 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 6 samples with support for all annotated introns
protein-glucosylgalactosylhydroxylysine glucosidase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein-glucosylgalactosylhydroxylysine glucosidase, 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 3 samples with support for all annotated introns
protein-glucosylgalactosylhydroxylysine glucosidase isoform X1
protein-glucosylgalactosylhydroxylysine glucosidase isoform X2
protein-glucosylgalactosylhydroxylysine glucosidase isoform X3
inner centromere protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
inner centromere protein-like, transcript variant X3
inner centromere protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
inner centromere protein-like isoform X1
inner centromere protein-like isoform X3
inner centromere protein-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 30% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
myelin regulatory factor, transcript variant X1
myelin regulatory factor, transcript variant X3
myelin regulatory factor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 119 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: 133 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
SPT2 chromatin protein domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 long SRA reads, 7 Proteins, and 97% 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: 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: 10 long SRA reads, 1 Protein, and 99% 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: 1 long SRA read, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
synaptotagmin VIIa, transcript variant X2
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
synaptotagmin VIIa, transcript variant X1
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
uncharacterized LOC125485241, transcript variant X1
uncharacterized LOC125485241, transcript variant X2
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
leucine-rich repeat-containing protein 10B, 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 8 samples with support for all annotated introns
leucine-rich repeat-containing protein 10B, 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
leucine-rich repeat-containing protein 10B
uncharacterized LOC125485282, transcript variant X1
uncharacterized LOC125485282, transcript variant X2
protein phosphatase 1, regulatory subunit 32
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 1 sample with support for all annotated introns
protein phosphatase 1 regulatory subunit 32
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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 6 samples with support for all annotated introns
epidermal growth factor receptor kinase substrate 8-like protein 2 isoform X1
epidermal growth factor receptor kinase substrate 8-like protein 2 isoform X2
glutamine amidotransferase class 1 domain containing 1, transcript variant X2
glutamine amidotransferase class 1 domain containing 1, transcript variant X1
glutamine amidotransferase-like class 1 domain-containing protein 1
troponin T, fast skeletal muscle isoforms-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 57% 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 84% coverage of the annotated genomic feature by RNAseq alignments
troponin I, fast skeletal muscle-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
troponin I, fast skeletal muscle-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 1 sample with support for all annotated introns
troponin I, fast skeletal muscle-like, transcript variant X1
troponin I, fast skeletal muscle-like isoform X1
troponin I, fast skeletal muscle-like isoform X2
synaptotagmin VIII, transcript variant X1
synaptotagmin VIII, transcript variant X2
cytosolic 5'-nucleotidase 1A-like, transcript variant X2
cytosolic 5'-nucleotidase 1A-like, transcript variant X1
cytosolic 5'-nucleotidase 1A-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
myoblast determination protein 1 homolog
Ferritin light chain, oocyte isoform-like
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
ATP-binding cassette, sub-family C (CFTR/MRP), member 8
ATP-binding cassette sub-family C member 8
ATP-sensitive inward rectifier potassium channel 11-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 122 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 11-like, transcript variant X2
ATP-sensitive inward rectifier potassium channel 11-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 122 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ATP-sensitive inward rectifier potassium channel 11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein si:ch211-256a21.4
probable inactive 1-aminocyclopropane-1-carboxylate synthase-like protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 67% coverage of the annotated genomic feature by RNAseq alignments
1-aminocyclopropane-1-carboxylate synthase-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
MOB kinase activator 2-like, transcript variant X5
MOB kinase activator 2-like, 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 2 samples with support for all annotated introns
MOB kinase activator 2-like, transcript variant X3
MOB kinase activator 2-like, transcript variant X2
MOB kinase activator 2-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
serine/threonine-protein kinase BRSK2-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: 1 Protein, and 83% 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 kinase BRSK2-like
toll interacting protein, transcript variant X2
toll interacting protein, transcript variant X1
protein phosphatase 6, regulatory subunit 3, transcript variant X1
protein phosphatase 6, regulatory subunit 3, transcript variant X3
protein phosphatase 6, regulatory subunit 3, transcript variant X2
protein phosphatase 6, regulatory subunit 3, transcript variant X4
serine/threonine-protein phosphatase 6 regulatory subunit 3 isoform X3
serine/threonine-protein phosphatase 6 regulatory subunit 3 isoform X2
serine/threonine-protein phosphatase 6 regulatory subunit 3 isoform X4
serine/threonine-protein phosphatase 6 regulatory subunit 3 isoform X1
synaptotagmin XIX, 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 1 sample with support for all annotated introns
synaptotagmin XIX, transcript variant X3
synaptotagmin XIX, transcript variant X1
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
lysine methyltransferase 5B, transcript variant X3
lysine methyltransferase 5B, transcript variant X4
lysine methyltransferase 5B, transcript variant X6
lysine methyltransferase 5B, transcript variant X5
lysine methyltransferase 5B, transcript variant X2
lysine methyltransferase 5B, transcript variant X1
lysine methyltransferase 5B, transcript variant X7
histone-lysine N-methyltransferase KMT5B isoform X2
histone-lysine N-methyltransferase KMT5B isoform X1
histone-lysine N-methyltransferase KMT5B isoform X3
uncharacterized LOC125485248, transcript variant X2
uncharacterized LOC125485248, transcript variant X1
cell wall protein DAN4-like, transcript variant X3
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
cell wall protein DAN4-like, transcript variant X1
cell wall protein DAN4-like, transcript variant X2
cell wall protein DAN4-like, transcript variant X4
cell wall protein DAN4-like, transcript variant X6
cell wall protein DAN4-like, transcript variant X7
cell wall protein DAN4-like, transcript variant X8
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 3 samples with support for all annotated introns
cell wall protein DAN4-like, transcript variant X5
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 4 samples with support for all annotated introns
uncharacterized protein C11orf24-like isoform X1
low density lipoprotein receptor-related protein 5, transcript variant X1
low density lipoprotein receptor-related protein 5, transcript variant X2
low-density lipoprotein receptor-related protein 5 isoform X1
low-density lipoprotein receptor-related protein 5 isoform X2
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ecotropic viral integration site 5 ortholog-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 91% 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 long SRA reads, 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: 1 Protein, and 100% 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
switching B cell complex subunit SWAP70b
WEE1 G2 checkpoint kinase, transcript variant X2
WEE1 G2 checkpoint kinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 long SRA reads, 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: 3 long SRA reads, 1 Protein, and 99% 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: 8 long SRA reads, 1 Protein, 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: 6 long SRA reads, 14 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
SIN3-HDAC complex-associated factor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SIN3-HDAC complex-associated factor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SIN3-HDAC complex-associated factor-like isoform X1
SIN3-HDAC complex-associated factor-like, transcript variant X3
SIN3-HDAC complex-associated factor-like isoform X2
signal peptide, CUB and EGF-like domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TMEM9 domain family, member B, transcript variant X1
TMEM9 domain family, member B, transcript variant X3
TMEM9 domain family, member B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
uncharacterized protein C11orf16 homolog
DENN domain containing 2B, 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 7 samples with support for all annotated introns
DENN domain containing 2B, transcript variant X6
DENN domain containing 2B, transcript variant X2
DENN domain containing 2B, transcript variant X1
DENN domain containing 2B, transcript variant X7
DENN domain containing 2B, transcript variant X4
DENN domain containing 2B, transcript variant X5
suppression of tumorigenicity 5 protein isoform X1
suppression of tumorigenicity 5 protein isoform X2
small nucleolar RNA SNORA3/SNORA45 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00334
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
serine/threonine kinase 33, transcript variant X1
serine/threonine kinase 33, transcript variant X5
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
serine/threonine kinase 33, transcript variant X3
serine/threonine kinase 33, transcript variant X4
serine/threonine kinase 33, transcript variant X6
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
serine/threonine kinase 33, 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
serine/threonine-protein kinase 33 isoform X1
serine/threonine-protein kinase 33 isoform X2
LIM domain only 1, transcript variant X1
LIM domain only 1, transcript variant X4
LIM domain only 1, transcript variant X5
LIM domain only 1, transcript variant X2
LIM domain only 1, transcript variant X3
LIM domain only 1, transcript variant X7
LIM domain only 1, transcript variant X6
COORDINATES: nucleotide motif:Rfam:12.0:RF00211
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 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: 24 long SRA reads, 22 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
proteasome 20S subunit alpha 1, transcript variant X2
proteasome 20S subunit alpha 1, transcript variant X1
proteasome subunit alpha type-1 isoform X1
proteasome subunit alpha type-1 isoform X2
cGMP-inhibited 3',5'-cyclic phosphodiesterase B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
calcitonin/calcitonin-related polypeptide, alpha
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 17% 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 38% coverage of the annotated genomic feature by RNAseq alignments
SRY-box transcription factor 6, transcript variant X4
SRY-box transcription factor 6, transcript variant X2
SRY-box transcription factor 6, transcript variant X3
SRY-box transcription factor 6, transcript variant X1
pleckstrin homology domain containing, family A member 7b
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
pleckstrin homology domain-containing family A member 7
protein phosphatase 1 regulatory subunit 15B-like, transcript variant X1
protein phosphatase 1 regulatory subunit 15B-like, transcript variant X2
uncharacterized protein LOC109917152 isoform X1
protein phosphatase 1 regulatory subunit 15B-like isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00016
phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 alpha
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha
nucleobindin-2-like, transcript variant X2
nucleobindin-2-like, transcript variant X1
nucleobindin-2-like, transcript variant X4
nucleobindin-2-like, transcript variant X6
nucleobindin-2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
nucleobindin-2-like, transcript variant X3
uncharacterized protein LOC100124608 homolog, transcript variant X1
uncharacterized protein LOC100124608 homolog, transcript variant X2
2-oxoglutarate-Fe(II) type oxidoreductase ppzD isoform X1
2-oxoglutarate-Fe(II) type oxidoreductase ppzD isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 87% coverage of the annotated genomic feature by RNAseq alignments
natural cytotoxicity triggering receptor 3 ligand 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 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
uncharacterized LOC109934976, transcript variant X1
uncharacterized LOC109934976, transcript variant X2
uncharacterized protein LOC109934976 isoform X1
uncharacterized protein LOC109934976 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dispanin subfamily A member 2b-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 1 sample with support for all annotated introns
dispanin subfamily A member 2b-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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized oxidoreductase YjmC-like
cytochrome c oxidase subunit 8B, mitochondrial
26S proteasome non-ATPase regulatory subunit 13
NAD-dependent protein deacetylase sirtuin-3, mitochondrial isoform X1
NAD-dependent protein deacetylase sirtuin-3, mitochondrial isoform X2
NAD-dependent protein deacetylase sirtuin-3, mitochondrial isoform X3
NAD-dependent protein deacetylase sirtuin-3, mitochondrial isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 34 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: 5 long SRA reads, 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Bet1 golgi vesicular membrane trafficking protein-like
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
deformed epidermal autoregulatory factor 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 84% 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% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
malignant fibrous histiocytoma-amplified sequence 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
malignant fibrous histiocytoma-amplified sequence 1 isoform X1
malignant fibrous histiocytoma-amplified sequence 1, transcript variant X2
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 1 sample with support for all annotated introns
malignant fibrous histiocytoma-amplified sequence 1 isoform X2
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
PHD and RING finger domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 122 long SRA reads, 10 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: 11 long SRA reads, and 32% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Ras association domain family member 7b, transcript variant X2
Ras association domain family member 7b, transcript variant X1
ras association domain-containing protein 7b
leucine rich repeat containing 56, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
leucine rich repeat containing 56, transcript variant X2
leucine rich repeat containing 56, transcript variant X4
leucine rich repeat containing 56, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat-containing protein 56 isoform X1
leucine-rich repeat-containing protein 56 isoform X2
lamin tail domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 36 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
lymphatic vessel endothelial hyaluronic receptor 1b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
murine retrovirus integration site 1 homolog, transcript variant X1
murine retrovirus integration site 1 homolog, transcript variant X2
inositol 1,4,5-triphosphate receptor associated 1 isoform X1
inositol 1,4,5-triphosphate receptor associated 1 isoform X2
inositol 1,4,5-triphosphate receptor associated 2-like
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
CTR9 homolog, Paf1/RNA polymerase II complex component
RNA polymerase-associated protein CTR9 homolog
eukaryotic translation initiation factor 4 gamma 2, transcript variant X3
eukaryotic translation initiation factor 4 gamma 2, transcript variant X4
eukaryotic translation initiation factor 4 gamma 2, transcript variant X5
eukaryotic translation initiation factor 4 gamma 2, transcript variant X1
eukaryotic translation initiation factor 4 gamma 2, transcript variant X2
eukaryotic translation initiation factor 4 gamma 2 isoform X2
eukaryotic translation initiation factor 4 gamma 2 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF01291
UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 18b
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 6 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 18
uncharacterized protein LOC555881 homolog
ubiquitin specific peptidase 47, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ubiquitin specific peptidase 47, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ubiquitin specific peptidase 47, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 47 isoform X1
ubiquitin carboxyl-terminal hydrolase 47 isoform X3
ubiquitin carboxyl-terminal hydrolase 47 isoform X4
ubiquitin specific peptidase 47, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 47 isoform X2
dickkopf-related protein 3, transcript variant X4
dickkopf-related protein 3, transcript variant X3
dickkopf-related protein 3, transcript variant X1
dickkopf-related protein 3, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 47-like
microtubule associated monooxygenase, calponin and LIM domain containing 2a, transcript variant X5
microtubule associated monooxygenase, calponin and LIM domain containing 2a, transcript variant X1
microtubule associated monooxygenase, calponin and LIM domain containing 2a, transcript variant X2
microtubule associated monooxygenase, calponin and LIM domain containing 2a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
microtubule associated monooxygenase, calponin and LIM domain containing 2a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
TEA domain family member 1b, transcript variant X2
TEA domain family member 1b, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
TEA domain family member 1b, transcript variant X1
TEA domain family member 1b, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
TEA domain family member 1b, transcript variant X3
TEA domain family member 1b, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transcriptional enhancer factor TEF-1 isoform X2
transcriptional enhancer factor TEF-1 isoform X4
transcriptional enhancer factor TEF-1 isoform X1
transcriptional enhancer factor TEF-1 isoform X3
alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase C-like
ras association domain-containing protein 10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments
aryl hydrocarbon receptor nuclear translocator-like protein 1, transcript variant X1
aryl hydrocarbon receptor nuclear translocator-like protein 1, transcript variant X2
aryl hydrocarbon receptor nuclear translocator-like protein 1
fatty acyl CoA reductase 1, transcript variant X1
fatty acyl CoA reductase 1, transcript variant X2
fatty acyl CoA reductase 1, transcript variant X3
endoplasmic reticulum-Golgi intermediate compartment protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
RAB15 effector protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RAB15 effector protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 16% 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: 15 long SRA reads, 5 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 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 30 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 long SRA reads, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein C11orf91 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
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
LOW QUALITY PROTEIN: UPF0606 protein KIAA1549L
homeodomain-interacting protein kinase 3, transcript variant X2
homeodomain-interacting protein kinase 3, transcript variant X1
homeodomain-interacting protein kinase 3 isoform X2
homeodomain-interacting protein kinase 3 isoform X1
ARL14 effector protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 long SRA reads, 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
ARL14 effector protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
mitogen-activated protein kinase 8 interacting protein 1b, transcript variant X1
mitogen-activated protein kinase 8 interacting protein 1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mitogen-activated protein kinase 8 interacting protein 1b, 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 4 samples with support for all annotated introns
C-Jun-amino-terminal kinase-interacting protein 1 isoform X1
C-Jun-amino-terminal kinase-interacting protein 1 isoform X2
C-Jun-amino-terminal kinase-interacting protein 1 isoform X3
mitogen-activated protein kinase 8 interacting protein 1b, 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
C-Jun-amino-terminal kinase-interacting protein 1 isoform X5
mitogen-activated protein kinase 8 interacting protein 1b, transcript variant X6
mitogen-activated protein kinase 8 interacting protein 1b, transcript variant X4
C-Jun-amino-terminal kinase-interacting protein 1 isoform X4
C-Jun-amino-terminal kinase-interacting protein 1 isoform X6
metallophosphoesterase domain containing 2a, transcript variant X1
metallophosphoesterase domain containing 2a, transcript variant X2
doublecortin domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
inner mitochondrial membrane peptidase subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 13 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial inner membrane protease subunit 1
DnaJ (Hsp40) homolog, subfamily C, member 24
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
elongator acetyltransferase complex subunit 4, transcript variant X1
elongator acetyltransferase complex subunit 4, transcript variant X2
elongator acetyltransferase complex subunit 4, transcript variant X3
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125485273, transcript variant X1
uncharacterized LOC125485273, transcript variant X2
uncharacterized LOC125485273, transcript variant X3
reticulocalbin 1, EF-hand calcium binding domain, 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 6 samples with support for all annotated introns
reticulocalbin 1, EF-hand calcium binding domain, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
WT1 transcription factor b, transcript variant X2
WT1 transcription factor b, transcript variant X1
WT1 transcription factor b, transcript variant X4
WT1 transcription factor b, transcript variant X3
eukaryotic translation initiation factor 3, subunit M
eukaryotic translation initiation factor 3 subunit M
coiled-coil domain-containing protein 73
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 37% coverage of the annotated genomic feature by RNAseq alignments
proline rich Gla (G-carboxyglutamic acid) 4 (transmembrane)
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
transmembrane gamma-carboxyglutamic acid protein 4
glutamine and serine rich 1, transcript variant X1
glutamine and serine rich 1, transcript variant X2
glutamine and serine-rich protein 1 isoform X1
glutamine and serine-rich protein 1 isoform X2
glutamine and serine rich 1, transcript variant X3
glutamine and serine-rich protein 1 isoform X3
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
cat eye syndrome critical region protein 2-like, transcript variant X1
cat eye syndrome critical region protein 2-like, transcript variant X2
cat eye syndrome critical region protein 2-like, transcript variant X3
cat eye syndrome critical region protein 2-like isoform X1
cat eye syndrome critical region protein 2-like isoform X2
cat eye syndrome critical region protein 2-like isoform X3
cat eye syndrome critical region protein 2-like, transcript variant X4
bromodomain-containing protein DDB_G0280777-like isoform X4
DEP domain containing 7, paralog a, transcript variant X1
DEP domain-containing protein 7 isoform X1
DEP domain containing 7, paralog a, transcript variant X2
DEP domain-containing protein 7 isoform X2
t-complex 11, testis-specific-like 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
t-complex 11, testis-specific-like 1, transcript variant X3
t-complex 11, testis-specific-like 1, transcript variant X4
t-complex 11, testis-specific-like 1, transcript variant X1
t-complex 11, testis-specific-like 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
t-complex 11, testis-specific-like 1, transcript variant X5
T-complex protein 11-like protein 1 isoform X1
T-complex protein 11-like protein 1 isoform X2
cleavage stimulation factor, 3' pre-RNA, subunit 3, transcript variant X2
cleavage stimulation factor, 3' pre-RNA, subunit 3, transcript variant X1
cleavage stimulation factor subunit 3 isoform X1
cleavage stimulation factor subunit 3 isoform X2
solute carrier family 35 member C1, transcript variant X4
solute carrier family 35 member C1, transcript variant X2
solute carrier family 35 member C1, transcript variant X3
solute carrier family 35 member C1, transcript variant X1
carbohydrate (keratan sulfate Gal-6) sulfotransferase 1, transcript variant X1
carbohydrate (keratan sulfate Gal-6) sulfotransferase 1, transcript variant X2
carbohydrate (keratan sulfate Gal-6) sulfotransferase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 4 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane protein 263-like, transcript variant X1
transmembrane protein 263-like, transcript variant X2
LIM domain only 2 (rhombotin-like 1), transcript variant X1
LIM domain only 2 (rhombotin-like 1), transcript variant X2
uncharacterized LOC109936200, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC109936200, transcript variant X3
uncharacterized LOC109936200, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
N-acetyltransferase 10, transcript variant X1
RNA cytidine acetyltransferase isoform X1
N-acetyltransferase 10, transcript variant X2
RNA cytidine acetyltransferase isoform X2
ankyrin repeat and BTB (POZ) domain containing 2b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and BTB/POZ domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 2 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
SPRY domain-containing SOCS box protein 3, transcript variant X1
SPRY domain-containing SOCS box protein 3, transcript variant X4
SPRY domain-containing SOCS box protein 3, transcript variant X2
SPRY domain-containing SOCS box protein 3, transcript variant X3
SPRY domain-containing SOCS box protein 3 isoform X1
SPRY domain-containing SOCS box protein 3 isoform X2
protein tyrosine phosphatase mitochondrial 1
phosphatidylglycerophosphatase and protein-tyrosine phosphatase 1
kelch repeat and BTB (POZ) domain containing 4
kelch repeat and BTB domain-containing protein 4
NADH:ubiquinone oxidoreductase core subunit S3
NADH dehydrogenase [ubiquinone] iron-sulfur protein 3, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 533 Proteins
V(D)J recombination-activating protein 1
intraflagellar transport associated protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 1 Protein, and 49% coverage of the annotated genomic feature by RNAseq alignments
leucine rich repeat containing 4C, genome duplicate a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tetratricopeptide repeat protein 17-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 13 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: 33 long SRA reads, 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
very-long-chain 3-oxoacyl-CoA reductase-A-like
alkB homolog 3, alpha-ketoglutarate dependent dioxygenase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 8 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
alpha-ketoglutarate-dependent dioxygenase alkB homolog 3
uncharacterized protein C11orf96 homolog
uncharacterized LOC125485239, transcript variant X1
uncharacterized LOC125485239, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
centriolar satellite-associated tubulin polyglutamylase complex regulator 1
low density lipoprotein receptor-related protein 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
low density lipoprotein receptor-related protein 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
low-density lipoprotein receptor-related protein 4 isoform X1
low-density lipoprotein receptor-related protein 4 isoform X2
low density lipoprotein receptor-related protein 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
low-density lipoprotein receptor-related protein 4 isoform X3
cytoskeleton associated protein 5, transcript variant X2
cytoskeleton associated protein 5, transcript variant X5
cytoskeleton associated protein 5, transcript variant X1
cytoskeleton associated protein 5, transcript variant X3
cytoskeleton associated protein 5, transcript variant X4
cytoskeleton-associated protein 5 isoform X1
cytoskeleton-associated protein 5 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00573
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
fin bud initiation factor b, 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 4 samples with support for all annotated introns
fin bud initiation factor b, transcript variant X1
coiled-coil domain-containing protein 34, transcript variant X2
coiled-coil domain-containing protein 34, transcript variant X1
coiled-coil domain-containing protein 34
leucine-rich repeat containing G protein-coupled receptor 4
leucine-rich repeat-containing G-protein coupled receptor 4
lin-7 homolog C (C. elegans), transcript variant X2
lin-7 homolog C (C. elegans), transcript variant X1
brain-derived neurotrophic factor, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
brain-derived neurotrophic factor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
brain-derived neurotrophic factor, transcript variant X1
brain-derived neurotrophic factor, transcript variant X10
brain-derived neurotrophic factor, transcript variant X8
brain-derived neurotrophic factor, transcript variant X5
brain-derived neurotrophic factor, transcript variant X7
brain-derived neurotrophic factor, transcript variant X9
brain-derived neurotrophic factor, transcript variant X2
brain-derived neurotrophic factor, transcript variant X6
brain-derived neurotrophic factor isoform X1
brain-derived neurotrophic factor 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: 5 long SRA reads, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: kinesin-like protein KIF18A
methyltransferase like 15, transcript variant X2
methyltransferase like 15, transcript variant X1
methyltransferase like 15, transcript variant X4
methyltransferase like 15, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
probable methyltransferase-like protein 15 isoform X1
probable methyltransferase-like protein 15 isoform X4
probable methyltransferase-like protein 15 isoform X2
methyltransferase like 15, transcript variant X3
probable methyltransferase-like protein 15 isoform X3
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, including 2 samples with support for all annotated introns
potassium voltage-gated channel, shaker-related subfamily, member 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
potassium voltage-gated channel, shaker-related subfamily, member 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium voltage-gated channel, shaker-related subfamily, member 4, transcript variant X1
potassium voltage-gated channel subfamily A member 2
follicle stimulating hormone subunit beta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins
sodium-coupled monocarboxylate transporter 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 95% 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: 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: 90% coverage of the annotated genomic feature by RNAseq alignments
leucine zipper protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
leucine zipper protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 97% 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 long SRA reads, 9 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: 33 Proteins
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 21 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
protein kinase C-binding protein NELL1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins
protein kinase C-binding protein NELL1-like, transcript variant X2
protein kinase C-binding protein NELL1-like, transcript variant X1
protein kinase C-binding protein NELL1-like isoform X2
protein kinase C-binding protein NELL1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 137 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
sodium- and chloride-dependent glycine transporter 2
protein arginine methyltransferase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 19 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein arginine methyltransferase 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 19 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
protein arginine methyltransferase 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
protein arginine methyltransferase 3, 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
protein arginine N-methyltransferase 3 isoform X2
protein arginine N-methyltransferase 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 88% 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, 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
cysteine and glycine-rich protein 3 (cardiac LIM protein), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins
cysteine and glycine-rich protein 3 (cardiac LIM protein), transcript variant X3
cysteine and glycine-rich protein 3 (cardiac LIM protein), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins
cysteine and glycine-rich protein 3 isoform X2
cysteine and glycine-rich protein 3 isoform X3
cysteine and glycine-rich protein 3 isoform X1
zinc finger DHHC-type palmitoyltransferase 13
L-lactate dehydrogenase A chain-like, transcript variant X1
L-lactate dehydrogenase A chain-like, transcript variant X2
L-lactate dehydrogenase A chain-like isoform X2
L-lactate dehydrogenase A chain-like isoform X1
zinc finger and SCAN domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: glutamine-dependent NAD(+) synthetase
two pore segment channel 2, transcript variant X3
two pore segment channel 2, transcript variant X4
two pore segment channel 2, transcript variant X5
two pore segment channel 2, transcript variant X1
two pore segment channel 2, transcript variant X6
two pore segment channel 2, transcript variant X2
two pore segment channel 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
two pore segment channel 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
LTO1 maturation factor of ABCE1, transcript variant X1
LTO1 maturation factor of ABCE1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
LTO1 maturation factor of ABCE1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
uncharacterized protein LOC767645 homolog
anoctamin 1, calcium activated chloride channel a, transcript variant X7
anoctamin 1, calcium activated chloride channel a, transcript variant X3
anoctamin 1, calcium activated chloride channel a, transcript variant X1
anoctamin 1, calcium activated chloride channel a, transcript variant X4
anoctamin 1, calcium activated chloride channel a, transcript variant X2
anoctamin 1, calcium activated chloride channel a, transcript variant X6
anoctamin 1, calcium activated chloride channel a, transcript variant X5
Fas (tnfrsf6)-associated via death domain
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 4 Proteins, and 78% 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, 26 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
SH3 and multiple ankyrin repeat domains protein 2-like, transcript variant X4
SH3 and multiple ankyrin repeat domains protein 2-like, transcript variant X3
SH3 and multiple ankyrin repeat domains protein 2-like, transcript variant X2
SH3 and multiple ankyrin repeat domains protein 2-like, transcript variant X1
SH3 and multiple ankyrin repeat domains protein 2-like isoform X4
SH3 and multiple ankyrin repeat domains protein 2-like isoform X3
SH3 and multiple ankyrin repeat domains protein 2-like isoform X2
SH3 and multiple ankyrin repeat domains protein 2-like isoform X1
golgin subfamily B member 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
golgin subfamily B member 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
golgin subfamily B member 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
golgin subfamily B member 1-like isoform X2
golgin subfamily B member 1-like isoform X3
golgin subfamily B member 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83% coverage of the annotated genomic feature by RNAseq alignments