Rhincodon typus isolate 14 chromosome 30, 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\nCM038827.1.\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.
corticotropin-releasing factor receptor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 57 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
corticotropin-releasing factor receptor 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
corticotropin-releasing factor receptor 1-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
corticotropin-releasing factor receptor 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
corticotropin-releasing factor receptor 1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
corticotropin-releasing factor receptor 1-like, transcript variant X9
corticotropin-releasing factor receptor 1-like, transcript variant X8
corticotropin-releasing factor receptor 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
corticotropin-releasing factor receptor 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
corticotropin-releasing factor receptor 1-like isoform X2
corticotropin-releasing factor receptor 1-like isoform X3
corticotropin-releasing factor receptor 1-like isoform X1
corticotropin-releasing factor receptor 1-like isoform X4
corticotropin-releasing factor receptor 1-like isoform X5
corticotropin-releasing factor receptor 1-like isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
KAT8 regulatory NSL complex subunit 1b, transcript variant X4
KAT8 regulatory NSL complex subunit 1b, transcript variant X2
KAT8 regulatory NSL complex subunit 1b, transcript variant X1
KAT8 regulatory NSL complex subunit 1b, transcript variant X3
KAT8 regulatory NSL complex subunit 1 isoform X1
KAT8 regulatory NSL complex subunit 1 isoform X2
microtubule-associated protein tau b, transcript variant X4
microtubule-associated protein tau b, transcript variant X3
microtubule-associated protein tau b, transcript variant X1
microtubule-associated protein tau b, transcript variant X2
microtubule-associated protein tau b, transcript variant X6
microtubule-associated protein tau b, transcript variant X5
microtubule-associated protein tau isoform X3
microtubule-associated protein tau isoform X2
microtubule-associated protein tau isoform X4
microtubule-associated protein tau isoform X1
microtubule-associated protein tau isoform X6
microtubule-associated protein tau isoform 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 3 samples with support for all annotated introns
uncharacterized LOC125486609, 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 1 sample with support for all annotated introns
uncharacterized LOC125486609, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125486609, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
STE20-related kinase adapter protein alpha
parathyroid hormone/parathyroid hormone-related peptide receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein 113A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 108 long SRA reads, 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
ring finger protein 113A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 201 long SRA reads, 12 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF113A isoform X2
E3 ubiquitin-protein ligase RNF113A isoform X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like, transcript variant X2
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 8 samples with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like isoform X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like isoform X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like isoform X3
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like isoform X4
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like isoform X5
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
glycylpeptide N-tetradecanoyltransferase 1-like
dephospho-CoA kinase domain containing, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 long SRA reads, 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
dephospho-CoA kinase domain containing, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 long SRA reads, 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
dephospho-CoA kinase domain containing, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 long SRA reads, 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dephospho-CoA kinase domain-containing protein isoform X2
dephospho-CoA kinase domain-containing protein isoform X1
dephospho-CoA kinase domain containing, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 long SRA reads, 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dephospho-CoA kinase domain containing, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 long SRA reads, 9 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dephospho-CoA kinase domain containing, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 long SRA reads, 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dephospho-CoA kinase domain-containing protein isoform X3
dephospho-CoA kinase domain-containing protein isoform X4
C1q-related factor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
C1q-related factor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, 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: 85 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel, subfamily H (eag-related), member 6a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily H member 6a
translational activator of cytochrome c oxidase 1
mitogen-activated protein kinase kinase kinase 3
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
LIM domain containing 2, transcript variant X2
LIM domain containing 2, transcript variant X1
LIM domain containing 2, transcript variant X3
LIM domain-containing protein 2 isoform X2
LIM domain-containing protein 2 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 7 samples with support for all annotated introns
coiled-coil domain-containing protein 103
Ig-like V-type domain-containing protein FAM187A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
angiotensin I converting enzyme (peptidyl-dipeptidase A) 1
transmembrane ascorbate-dependent reductase CYB561, transcript variant X2
transmembrane ascorbate-dependent reductase CYB561, transcript variant X1
transmembrane ascorbate-dependent reductase CYB561, transcript variant X3
transmembrane ascorbate-dependent reductase CYB561
proline-rich protein 29-like, 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 2 samples with support for all annotated introns
proline-rich protein 29-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
proline-rich protein 29-like, transcript variant X2
uncharacterized protein LOC125486593 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62% coverage of the annotated genomic feature by RNAseq alignments
vasoactive intestinal polypeptide receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, transcript variant X6
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
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, transcript variant X4
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, transcript variant X1
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, transcript variant X2
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, transcript variant X3
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2a, 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
tousled-like kinase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 26 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
tousled-like kinase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tousled-like kinase 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
tousled-like kinase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine-protein kinase tousled-like 2 isoform X2
serine/threonine-protein kinase tousled-like 2 isoform X1
tRNA N(3)-methylcytidine methyltransferase METTL2-like
golgi SNAP receptor complex member 2, transcript variant X4
golgi SNAP receptor complex member 2, transcript variant X2
golgi SNAP receptor complex member 2, transcript variant X3
golgi SNAP receptor complex member 2, transcript variant X1
Golgi SNAP receptor complex member 2 isoform X4
Golgi SNAP receptor complex member 2 isoform X1
Golgi SNAP receptor complex member 2 isoform X3
Golgi SNAP receptor complex member 2 isoform X2
wingless-type MMTV integration site family, member 9B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
ADP-ribosylation factor 3-like, transcript variant X3
ADP-ribosylation factor 3-like, transcript variant X1
ADP-ribosylation factor 3-like, transcript variant X2
26S proteasome non-ATPase regulatory subunit 11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
mitogen-activated protein kinase kinase kinase 14a, transcript variant X2
mitogen-activated protein kinase kinase kinase 14a, transcript variant X1
mitogen-activated protein kinase kinase kinase 14
myosin light chain kinase, smooth muscle-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 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
myosin light chain kinase, smooth muscle-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 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
myosin light chain kinase, smooth muscle-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
myosin light chain kinase, smooth muscle-like isoform X1
myosin light chain kinase, smooth muscle-like isoform X3
myosin light chain kinase, smooth muscle-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 long SRA reads, 7 Proteins, and 98% 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: 66 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Rho GTPase activating protein 27, like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Rho GTPase activating protein 27, like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Rho GTPase activating protein 27, like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
rho GTPase-activating protein 12 isoform X2
rho GTPase-activating protein 12 isoform X1
rho GTPase-activating protein 15 isoform X3
pleckstrin homology domain containing, family M (with RUN domain) member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 long SRA reads, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
pleckstrin homology domain containing, family M (with RUN domain) member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 long SRA reads, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
pleckstrin homology domain containing, family M (with RUN domain) member 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
pleckstrin homology domain-containing family M member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
interferon omega-1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
interferon omega-1-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 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
interferon omega-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 8 Proteins, 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: 100% coverage of the annotated genomic feature by RNAseq alignments
RAD52 motif containing 1, transcript variant X1
RAD52 motif-containing protein 1 isoform X1
RAD52 motif containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
RAD52 motif-containing protein 1 isoform X2
B-cell antigen receptor complex-associated protein beta chain-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
B-cell antigen receptor complex-associated protein beta chain-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
B-cell antigen receptor complex-associated protein beta chain-like isoform X1
B-cell antigen receptor complex-associated protein beta chain-like isoform X2
sodium channel protein type 4 subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins, and 60% 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
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
G patch domain containing 8, transcript variant X3
G patch domain containing 8, transcript variant X1
G patch domain containing 8, transcript variant X4
G patch domain containing 8, transcript variant X2
G patch domain containing 8, transcript variant X5
G patch domain containing 8, transcript variant X6
G patch domain-containing protein 8 isoform X3
G patch domain-containing protein 8 isoform X1
G patch domain-containing protein 8 isoform X2
G patch domain-containing protein 8 isoform X4
G patch domain-containing protein 8 isoform X5
small ubiquitin like modifier 1, transcript variant X5
small ubiquitin like modifier 1, transcript variant X9
small ubiquitin like modifier 1, transcript variant X7
small ubiquitin like modifier 1, transcript variant X4
small ubiquitin like modifier 1, transcript variant X8
small ubiquitin like modifier 1, transcript variant X6
small ubiquitin-related modifier 1 isoform X9
small ubiquitin-related modifier 1 isoform X7
small ubiquitin-related modifier 1 isoform X8
small ubiquitin-related modifier 1 isoform X6
small ubiquitin-related modifier 1 isoform X5
small ubiquitin-related modifier 1 isoform X4
small ubiquitin like modifier 1, transcript variant X3
small ubiquitin like modifier 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
small ubiquitin like modifier 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
small ubiquitin-related modifier 1 isoform X2
small ubiquitin-related modifier 1 isoform X1
small ubiquitin-related modifier 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
meiosis-specific coiled-coil domain-containing protein MEIOC
coiled-coil domain-containing protein 43
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
disintegrin and metalloproteinase domain-containing protein 11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: disintegrin and metalloproteinase domain-containing protein 11-like
gap junction protein gamma 1, transcript variant X3
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 3 samples with support for all annotated introns
gap junction protein gamma 1, transcript variant X1
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 10 samples with support for all annotated introns
gap junction protein gamma 1, transcript variant X6
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
gap junction protein gamma 1, transcript variant X2
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 7 samples with support for all annotated introns
gap junction protein gamma 1, transcript variant X5
gap junction protein gamma 1, transcript variant X4
HIG1 domain family member 1A, mitochondrial-like
elongation factor Tu GTP binding domain containing 2
116 kDa U5 small nuclear ribonucleoprotein component
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
phosphoethanolamine/phosphocholine phosphatase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
phosphoethanolamine/phosphocholine phosphatase-like
phosphoethanolamine/phosphocholine phosphatase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
zinc finger protein 652-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 long SRA reads, 14 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
zinc finger protein 652-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger protein 652-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
zinc finger protein 652-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
zinc finger protein 652-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 14 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
BMP and activin membrane-bound inhibitor homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 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 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nucleolar transcription factor 1-like, transcript variant X5
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 4 samples with support for all annotated introns
nucleolar transcription factor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
nucleolar transcription factor 1-like, transcript variant X3
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 11 samples with support for all annotated introns
nucleolar transcription factor 1-like, transcript variant X4
nucleolar transcription factor 1-like, transcript variant X2
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 6 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, 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: 8 long SRA reads, and 89% coverage of the annotated genomic feature by RNAseq alignments
transmembrane and ubiquitin-like domain containing 2
transmembrane and ubiquitin-like domain-containing protein 2
ankyrin repeat and SOCS box containing 16
homologous recombination factor with OB-fold
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
homologous recombination OB-fold protein
acid-sensing (proton-gated) ion channel 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 35 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: tRNAscan-SE.
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
glucocorticoid-induced transcript 1 protein-like, transcript variant X3
glucocorticoid-induced transcript 1 protein-like, transcript variant X2
glucocorticoid-induced transcript 1 protein-like, transcript variant X1
glucocorticoid-induced transcript 1 protein-like, transcript variant X5
glucocorticoid-induced transcript 1 protein-like, transcript variant X4
glucocorticoid-induced transcript 1 protein-like isoform X5
glucocorticoid-induced transcript 1 protein-like isoform X4
glucocorticoid-induced transcript 1 protein-like isoform X3
glucocorticoid-induced transcript 1 protein-like isoform X2
glucocorticoid-induced transcript 1 protein-like isoform X1
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, 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
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, transcript variant X5
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
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, transcript variant X1
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 4 samples with support for all annotated introns
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like
uncharacterized si:ch211-131k2.2, transcript variant X2
uncharacterized si:ch211-131k2.2, transcript variant X1
uncharacterized si:ch211-131k2.2, transcript variant X3
uncharacterized protein si:ch211-131k2.2
uncharacterized LOC125486607, transcript variant X2
uncharacterized LOC125486607, transcript variant X1
pyruvate dehydrogenase (acetyl-transferring) kinase isozyme 2, mitochondrial-like
sterile alpha motif domain containing 14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
sterile alpha motif domain-containing protein 14
transfer RNA cysteine (anticodon GCA); 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 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 40% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 40% 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 long SRA read, 1 Protein, and 39% 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: 34 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
collagen, type I, alpha 1b, transcript variant X2
collagen, type I, alpha 1b, transcript variant X1
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
beta-1,4 N-acetylgalactosaminyltransferase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
beta-1,4 N-acetylgalactosaminyltransferase 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
beta-1,4 N-acetylgalactosaminyltransferase 2-like, transcript variant X1
beta-1,4 N-acetylgalactosaminyltransferase 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
beta-1,4 N-acetylgalactosaminyltransferase 2-like, transcript variant X5
beta-1,4 N-acetylgalactosaminyltransferase 2-like isoform X2
beta-1,4 N-acetylgalactosaminyltransferase 2-like, transcript variant X3
beta-1,4 N-acetylgalactosaminyltransferase 2-like isoform X3
beta-1,4 N-acetylgalactosaminyltransferase 2-like isoform X1
beta-1,4 N-acetylgalactosaminyltransferase 2-like isoform X4
beta-1,4 N-acetylgalactosaminyltransferase 2-like isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins
terminal uridylyl transferase 1, U6 snRNA-specific, transcript variant X1
terminal uridylyl transferase 1, U6 snRNA-specific, transcript variant X3
terminal uridylyl transferase 1, U6 snRNA-specific, transcript variant X2
speckle targeted PIP5K1A-regulated poly(A) polymerase isoform X1
speckle targeted PIP5K1A-regulated poly(A) polymerase isoform X2
speckle targeted PIP5K1A-regulated poly(A) polymerase isoform X3
histone deacetylase 5, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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
histone deacetylase 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
histone deacetylase 5, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
histone deacetylase 5, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
histone deacetylase 5, transcript variant X7
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 3 samples with support for all annotated introns
histone deacetylase 5, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
histone deacetylase 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 25 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
histone deacetylase 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
histone deacetylase 5, transcript variant X9
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 2 samples with support for all annotated introns
histone deacetylase 5, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glucose-6-phosphatase catalytic subunit 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 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: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
N-acetylglutamate synthase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 84 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
MAGUK p55 scaffold protein 2b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
MAGUK p55 scaffold protein 2b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
MAGUK p55 subfamily member 2b isoform X1
MAGUK p55 scaffold protein 2b, 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
MAGUK p55 subfamily member 2b isoform X2
galactoside alpha-(1,2)-fucosyltransferase 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
galactoside alpha-(1,2)-fucosyltransferase 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 4 samples with support for all annotated introns
galactoside alpha-(1,2)-fucosyltransferase 2-like, transcript variant X4
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
galactoside alpha-(1,2)-fucosyltransferase 2-like, transcript variant X2
galactoside alpha-(1,2)-fucosyltransferase 2-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 9% 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: inserted 2 bases in 2 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: all-trans-retinol 13,14-reductase
abl interactor 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 26 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
abl interactor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acyl-CoA-binding domain-containing protein 5-like, transcript variant X7
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 10 samples with support for all annotated introns
acyl-CoA-binding domain-containing protein 5-like, transcript variant X1
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 11 samples with support for all annotated introns
acyl-CoA-binding domain-containing protein 5-like, transcript variant X2
acyl-CoA-binding domain-containing protein 5-like, transcript variant X9
acyl-CoA-binding domain-containing protein 5-like, transcript variant X6
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
acyl-CoA-binding domain-containing protein 5-like, transcript variant X4
acyl-CoA-binding domain-containing protein 5-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
acyl-CoA-binding domain-containing protein 5-like, transcript variant X3
acyl-CoA-binding domain-containing protein 5-like isoform X1
acyl-CoA-binding domain-containing protein 5-like, transcript variant X8
acyl-CoA-binding domain-containing protein 5-like isoform X2
acyl-CoA-binding domain-containing protein 5-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
all-trans-retinol 13,14-reductase, transcript variant X1
all-trans-retinol 13,14-reductase isoform X1
all-trans-retinol 13,14-reductase, 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 15 samples with support for all annotated introns
all-trans-retinol 13,14-reductase isoform X2
mucin 13b, cell surface associated, transcript variant X2
mucin 13b, cell surface associated, transcript variant X1
mucin 13b, cell surface associated, transcript variant X3
mucin 13b, cell surface associated, transcript variant X4
G protein-activated inward rectifier potassium channel 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 110 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 76% coverage of the annotated genomic feature by RNAseq alignments
HAUS augmin-like complex, subunit 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
HAUS augmin-like complex, subunit 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
HAUS augmin-like complex subunit 7 isoform X2
HAUS augmin-like complex subunit 7 isoform X1
deoxyribonuclease-1-like, transcript variant X2
deoxyribonuclease-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC125486582, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 68% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125486582, transcript variant X1
uncharacterized LOC125486582, transcript variant X2
mesenchyme homeobox 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
mesenchyme homeobox 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
ETS variant transcription factor 4, transcript variant X1
ETS variant transcription factor 4, transcript variant X3
ETS variant transcription factor 4, transcript variant X4
ETS variant transcription factor 4, transcript variant X2
ETS variant transcription factor 4, transcript variant X5
ETS variant transcription factor 4, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
coiled-coil domain-containing protein 200-like, transcript variant X1
coiled-coil domain-containing protein 200-like, transcript variant 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 5 samples with support for all annotated introns
coiled-coil domain-containing protein 200-like isoform X1
uncharacterized protein LOC125486563 isoform X3
coiled-coil domain-containing protein 200-like, 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 2 samples with support for all annotated introns
coiled-coil domain-containing protein 200-like, transcript variant X2
uncharacterized protein LOC125486563 isoform X2
coiled-coil domain-containing protein 200-like, transcript variant X4
coiled-coil domain-containing protein 200-like, transcript variant X7
coiled-coil domain-containing protein 200-like, transcript variant X6
NBR1 autophagy cargo receptor a, transcript variant X2
NBR1 autophagy cargo receptor a, transcript variant X1
NBR1 autophagy cargo receptor a isoform X2
NBR1 autophagy cargo receptor a isoform X1
breast cancer type 1 susceptibility protein homolog
uncharacterized protein si:busm1-163l24.3
interferon-induced protein 35, transcript variant X1
interferon-induced protein 35, transcript variant X3
interferon-induced protein 35, transcript variant X2
interferon-induced protein 35 isoform X3
interferon-induced protein 35 isoform X2
interferon-induced protein 35 isoform X1
RUN domain containing 1, transcript variant X2
RUN domain containing 1, transcript variant X1
RUN domain-containing protein 1 isoform X2
RUN domain-containing protein 1 isoform X1
ceramide synthase 6-like, transcript variant X1
ceramide synthase 6-like, transcript variant X2
ceramide synthase 6-like, transcript variant X3
prostaglandin E synthase 3 like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 21 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
prostaglandin E synthase 3 like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 20 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
alanyl-tRNA synthetase domain containing 1, transcript variant X3
alanyl-tRNA synthetase domain containing 1, transcript variant X1
alanyl-tRNA synthetase domain containing 1, transcript variant X2
alanyl-tRNA editing protein Aarsd1 isoform X3
alanyl-tRNA editing protein Aarsd1 isoform X1
alanyl-tRNA editing protein Aarsd1 isoform X2
glucose-6-phosphatase catalytic subunit 1a, tandem duplicate 2, transcript variant X2
glucose-6-phosphatase catalytic subunit 1a, tandem duplicate 2, transcript variant X1
glucose-6-phosphatase catalytic subunit 1 isoform X2
glucose-6-phosphatase catalytic subunit 1 isoform X1
glucose-6-phosphatase catalytic subunit 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
retina-specific copper amine oxidase-like
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
cyclin N-terminal domain-containing protein 1
cytochrome c oxidase assembly factor 3 homolog, mitochondrial
WNK lysine deficient protein kinase 4a, transcript variant X1
WNK lysine deficient protein kinase 4a, transcript variant X2
serine/threonine-protein kinase WNK4 isoform X2
serine/threonine-protein kinase WNK4 isoform X1
vacuolar protein-sorting-associated protein 25
serine/threonine-protein kinase 17A-like
V-type proton ATPase 116 kDa subunit a 1, transcript variant X4
V-type proton ATPase 116 kDa subunit a 1, transcript variant X5
V-type proton ATPase 116 kDa subunit a 1, transcript variant X1
V-type proton ATPase 116 kDa subunit a 1, transcript variant X2
V-type proton ATPase 116 kDa subunit a 1, transcript variant X6
V-type proton ATPase 116 kDa subunit a 1, transcript variant X3
V-type proton ATPase 116 kDa subunit a 1, transcript variant X7
V-type proton ATPase 116 kDa subunit a 1 isoform X2
V-type proton ATPase 116 kDa subunit a 1 isoform X1
V-type proton ATPase 116 kDa subunit a 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
signal transducer and activator of transcription 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 69 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
signal transducer and activator of transcription 5a, transcript variant X1
signal transducer and activator of transcription 5a, transcript variant X4
signal transducer and activator of transcription 5a, transcript variant X3
signal transducer and activator of transcription 5a, transcript variant X2
signal transducer and activator of transcription 5A isoform X1
signal transducer and activator of transcription 5A isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
GH3 domain containing, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
GH3 domain containing, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium voltage-gated channel subfamily H member 8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
K(lysine) acetyltransferase 2A, transcript variant X1
K(lysine) acetyltransferase 2A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 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, 25 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
probable ATP-dependent RNA helicase DHX58
zinc finger protein 385C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein 385C, 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
26S proteasome non-ATPase regulatory subunit 3
DnaJ (Hsp40) homolog, subfamily C, member 7
2',3'-cyclic nucleotide 3' phosphodiesterase, transcript variant X1
2',3'-cyclic nucleotide 3' phosphodiesterase, transcript variant X4
2',3'-cyclic nucleotide 3' phosphodiesterase, transcript variant X2
2',3'-cyclic nucleotide 3' phosphodiesterase, transcript variant X3
2',3'-cyclic-nucleotide 3'-phosphodiesterase
casc3 exon junction complex subunit, transcript variant X2
casc3 exon junction complex subunit, transcript variant X8
casc3 exon junction complex subunit, transcript variant X5
casc3 exon junction complex subunit, transcript variant X3
casc3 exon junction complex subunit, transcript variant X7
casc3 exon junction complex subunit, transcript variant X6
casc3 exon junction complex subunit, transcript variant X4
casc3 exon junction complex subunit, transcript variant X1
MSL complex subunit 1a, transcript variant X1
MSL complex subunit 1a, transcript variant X2
male-specific lethal 1-like 1 isoform X2
male-specific lethal 1-like 1 isoform X1
MSL complex subunit 1a, transcript variant X3
male-specific lethal 1-like 1 isoform X3
nuclear receptor subfamily 1, group d, member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
nuclear receptor subfamily 1 group D member 1
thyroid hormone receptor alpha, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 long SRA reads, 68 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
thyroid hormone receptor alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 68 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
thyroid hormone receptor alpha, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 68 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cell division cycle 6 homolog (S. cerevisiae)
retinoic acid receptor, alpha a, transcript variant X2
retinoic acid receptor, alpha a, transcript variant X1
retinoic acid receptor, alpha a, transcript variant X4
retinoic acid receptor alpha-A isoform X1
retinoic acid receptor alpha-A isoform X3
retinoic acid receptor, alpha a, transcript variant X3
retinoic acid receptor alpha-A isoform X2
gap junction delta-3 protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gap junction delta-3 protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 34 Proteins, and 99% 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: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
leucine-rich repeat-containing protein 3B
Rap guanine nucleotide exchange factor (GEF)-like 1
rap guanine nucleotide exchange factor-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
mediator complex subunit 24, transcript variant X1
mediator complex subunit 24, transcript variant X3
mediator complex subunit 24, transcript variant X2
mediator of RNA polymerase II transcription subunit 24 isoform X3
mediator of RNA polymerase II transcription subunit 24 isoform X1
mediator of RNA polymerase II transcription subunit 24 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 52% coverage of the annotated genomic feature by RNAseq alignments
39S ribosomal protein L10, mitochondrial
oxysterol binding protein-like 7, transcript variant X1
oxysterol binding protein-like 7, 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 1 sample with support for all annotated introns
oxysterol-binding protein-related protein 7 isoform X1
oxysterol-binding protein-related protein 7 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 44 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: 7 long SRA reads, 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: 14 long SRA reads, 29 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: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
WAS/WASL interacting protein family, member 2b
WAS/WASL-interacting protein family member 2b
leucine-rich repeat-containing protein 46
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 19 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 1
F-box/LRR-repeat protein 20, transcript variant X2
F-box/LRR-repeat protein 20, transcript variant X1
F-box/LRR-repeat protein 20, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
SH3 and cysteine-rich domain-containing protein 2-like, transcript variant X1
SH3 and cysteine-rich domain-containing protein 2-like, transcript variant X2
SH3 and cysteine-rich domain-containing protein 2-like, transcript variant X3
SH3 and cysteine-rich domain-containing protein 2-like isoform X1
SH3 and cysteine-rich domain-containing protein 2-like isoform X2
SH3 and cysteine-rich domain-containing protein 2-like isoform X3
P43 5S RNA-binding protein-like, transcript variant X1
P43 5S RNA-binding protein-like, transcript variant X2
P43 5S RNA-binding protein-like isoform X2
P43 5S RNA-binding protein-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
calcium channel, voltage-dependent, beta 1 subunit, transcript variant X1
calcium channel, voltage-dependent, beta 1 subunit, transcript variant X2
voltage-dependent L-type calcium channel subunit beta-1 isoform X1
voltage-dependent L-type calcium channel subunit beta-1 isoform X2
calcium channel, voltage-dependent, beta 1 subunit, transcript variant X4
voltage-dependent L-type calcium channel subunit beta-1 isoform X4
calcium channel, voltage-dependent, beta 1 subunit, transcript variant X3
voltage-dependent L-type calcium channel subunit beta-1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC109938619, transcript variant X2
uncharacterized LOC109938619, transcript variant X3
uncharacterized LOC109938619, transcript variant X1
uncharacterized LOC109938619, transcript variant X4
uncharacterized LOC109938619, transcript variant X5
SWI5 homologous recombination repair protein, transcript variant X3
SWI5 homologous recombination repair protein, transcript variant X6
SWI5 homologous recombination repair protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 180 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
SWI5 homologous recombination repair protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 161 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
SWI5 homologous recombination repair protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
SWI5 homologous recombination repair protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
DNA repair protein SWI5 homolog isoform X3
DNA repair protein SWI5 homolog isoform X6
DNA repair protein SWI5 homolog isoform X1
DNA repair protein SWI5 homolog isoform X5
DNA repair protein SWI5 homolog isoform X2
DNA repair protein SWI5 homolog isoform X4
plexin domain-containing protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
plexin domain-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
plexin domain-containing protein 1-like isoform X1
plexin domain-containing protein 1-like isoform X2
CWC25 spliceosome associated protein homolog, transcript variant X1
CWC25 spliceosome associated protein homolog, transcript variant X2
pre-mRNA-splicing factor CWC25 homolog isoform X1
pre-mRNA-splicing factor CWC25 homolog isoform X2
phosphatidylinositol 5-phosphate 4-kinase type-2 beta, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
phosphatidylinositol 5-phosphate 4-kinase type-2 beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol 5-phosphate 4-kinase type-2 beta isoform X1
phosphatidylinositol 5-phosphate 4-kinase type-2 beta isoform X2
transfer RNA asparagine (anticodon GUU); 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: 11 long SRA reads, 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
CDGSH iron-sulfur domain-containing protein 3, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
SKI/DACH domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Rho GTPase activating protein 23a, transcript variant X1
Rho GTPase activating protein 23a, transcript variant X2
Rho GTPase activating protein 23a, transcript variant X3
rho GTPase-activating protein 23 isoform X1
rho GTPase-activating protein 23 isoform X2
rho GTPase-activating protein 23 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
39S ribosomal protein L45, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 76% 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: 4 long SRA reads, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
aminopeptidase puromycin sensitive, transcript variant X1
puromycin-sensitive aminopeptidase isoform X1
aminopeptidase puromycin sensitive, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
puromycin-sensitive aminopeptidase isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
karyopherin (importin) beta 1, transcript variant X3
karyopherin (importin) beta 1, transcript variant X2
karyopherin (importin) beta 1, transcript variant X1
karyopherin (importin) beta 1, transcript variant X4
insulin-like growth factor 2 mRNA-binding protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
insulin-like growth factor 2 mRNA-binding protein 3-B
transformer-2 protein homolog alpha-like, transcript variant X6
transformer-2 protein homolog alpha-like, transcript variant X3
transformer-2 protein homolog alpha-like, transcript variant X1
transformer-2 protein homolog alpha-like, transcript variant X5
transformer-2 protein homolog alpha-like, transcript variant X7
transformer-2 protein homolog alpha-like, transcript variant X4
transformer-2 protein homolog alpha-like isoform X6
transformer-2 protein homolog alpha-like isoform X3
transformer-2 protein homolog alpha-like isoform X1
transformer-2 protein homolog alpha-like isoform X5
transformer-2 protein homolog alpha-like isoform X7
transformer-2 protein homolog alpha-like isoform X4
transformer-2 protein homolog alpha-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
transformer-2 protein homolog alpha-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 81% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
SNF8 subunit of ESCRT-II, transcript variant X2
SNF8 subunit of ESCRT-II, transcript variant X1
vacuolar-sorting protein SNF8 isoform X1
vacuolar-sorting protein SNF8 isoform X2
ubiquitin-conjugating enzyme E2Z, transcript variant X3
ubiquitin-conjugating enzyme E2Z, transcript variant X1
ubiquitin-conjugating enzyme E2Z, transcript variant X2
calcium-binding and coiled-coil domain-containing protein 2-like, transcript variant X4
calcium-binding and coiled-coil domain-containing protein 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
calcium-binding and coiled-coil domain-containing protein 2-like, transcript variant X1
calcium-binding and coiled-coil domain-containing protein 2-like, transcript variant X3
calcium-binding and coiled-coil domain-containing protein 2-like, transcript variant X2
calcium-binding and coiled-coil domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
homeobox protein Hox-A10-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
homeobox protein Hox-A10-like, transcript variant X1
uncharacterized LOC109932173, transcript variant X2
uncharacterized LOC109932173, transcript variant X1
uncharacterized LOC109932177, transcript variant X2
uncharacterized LOC109932177, transcript variant X1
homeobox protein Hox-B4-like, transcript variant X2
homeobox protein Hox-B4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
homeobox protein Hox-A2-like, transcript variant X2
homeobox protein Hox-A2-like, transcript variant X1
src kinase-associated phosphoprotein 1-like
sorting nexin-11-like, transcript variant X3
sorting nexin-11-like, transcript variant X1
sorting nexin-11-like, transcript variant X4
sorting nexin-11-like, transcript variant X2
sorting nexin-11-like, transcript variant X5
tigger transposable element-derived protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
chromobox homolog 1b (HP1 beta homolog Drosophila), transcript variant X3
chromobox homolog 1b (HP1 beta homolog Drosophila), transcript variant X4
chromobox homolog 1b (HP1 beta homolog Drosophila), transcript variant X1
chromobox homolog 1b (HP1 beta homolog Drosophila), transcript variant X2
chromobox homolog 1b (HP1 beta homolog Drosophila), transcript variant X5
endoplasmic reticulum membrane sensor NFE2L1b
coatomer subunit zeta-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
coatomer subunit zeta-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
coatomer subunit zeta-1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
CDK5 regulatory subunit-associated protein 3
pyridoxamine 5'-phosphate oxidase, transcript variant X2
pyridoxamine 5'-phosphate oxidase, transcript variant X1
pyridoxine-5'-phosphate oxidase isoform X2
pyridoxine-5'-phosphate oxidase isoform X1
sp2 transcription factor, transcript variant X2
sp2 transcription factor, transcript variant X1
outer dynein arm docking complex subunit 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
outer dynein arm docking complex subunit 4, transcript variant X3
outer dynein arm docking complex subunit 4, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
outer dynein arm docking complex subunit 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
outer dynein arm docking complex subunit 4, transcript variant X1
outer dynein arm docking complex subunit 4, transcript variant X4
outer dynein arm-docking complex subunit 4 isoform X5
outer dynein arm-docking complex subunit 4 isoform X3
outer dynein arm-docking complex subunit 4 isoform X6
outer dynein arm-docking complex subunit 4 isoform X2
outer dynein arm-docking complex subunit 4 isoform X1
outer dynein arm-docking complex subunit 4 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 12 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
kelch-like family member 11, transcript variant X1
kelch-like family member 11, transcript variant X2
peptidyl-prolyl cis-trans isomerase FKBP10-like
junction plakoglobin-like, transcript variant X1
junction plakoglobin-like, transcript variant X2
trafficking kinesin-binding protein 1-like
eukaryotic translation initiation factor 1b-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 47% 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 80% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1, transcript variant X2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1, transcript variant X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1 isoform X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1 isoform X2
insulin-like growth factor-binding protein 4
growth factor receptor-bound protein 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
growth factor receptor-bound protein 7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein Aiolos-like, transcript variant X1
zinc finger protein Aiolos-like, transcript variant X2
zinc finger protein Aiolos-like isoform X1
zinc finger protein Aiolos-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
von Willebrand factor C domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
receptor tyrosine-protein kinase erbB-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
post-GPI attachment to proteins phospholipase 3, transcript variant X3
post-GPI attachment to proteins phospholipase 3, transcript variant X1
post-GPI attachment to proteins phospholipase 3, transcript variant X4
post-GPI attachment to proteins phospholipase 3, transcript variant X2
post-GPI attachment to proteins phospholipase 3, 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 5 samples with support for all annotated introns
post-GPI attachment to proteins phospholipase 3, transcript variant X6
post-GPI attachment to proteins factor 3 isoform X3
post-GPI attachment to proteins factor 3 isoform X1
post-GPI attachment to proteins factor 3 isoform X4
post-GPI attachment to proteins factor 3 isoform X2
post-GPI attachment to proteins factor 3 isoform X5
uncharacterized LOC125486585, transcript variant X1
uncharacterized LOC125486585, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
StAR-related lipid transfer (START) domain containing 3, transcript variant X1
StAR-related lipid transfer (START) domain containing 3, transcript variant X3
StAR-related lipid transfer (START) domain containing 3, transcript variant X7
StAR-related lipid transfer (START) domain containing 3, transcript variant X2
StAR-related lipid transfer (START) domain containing 3, transcript variant X6
StAR-related lipid transfer (START) domain containing 3, transcript variant X5
StAR-related lipid transfer (START) domain containing 3, transcript variant X8
StAR-related lipid transfer (START) domain containing 3, transcript variant X4
protein phosphatase 1, regulatory (inhibitor) subunit 1B
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, including 1 sample with support for all annotated introns
protein phosphatase 1 regulatory subunit 1B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins
receptor (G protein-coupled) activity modifying protein 2
enhancer of zeste 1 polycomb repressive complex 2 subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
pleckstrin homology, MyTH4 and FERM domain containing H3
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
pleckstrin homology domain-containing family H member 3
bifunctional coenzyme A synthase isoform X1
bifunctional coenzyme A synthase isoform X2
N-acetylglucosaminidase, alpha, transcript variant X2
N-acetylglucosaminidase, alpha, transcript variant X1
alpha-N-acetylglucosaminidase isoform X2
alpha-N-acetylglucosaminidase isoform X1