Rhincodon typus isolate 14 chromosome 24, 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\nCM038821.1.\nAssembly name: sRhiTyp1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Squalomix on 2022/02/03. The\noriginal whole-genome shotgun project has the accession\nJAHMAH000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Squalomix\nAssembly Date :: 22-FEB-2021\nAssembly Method :: Supernova v. 2.1.1; P_RNA_scaffolder v.\n commit 7941e0f; Tigmint v. 1.1.2; ARKS v.\n 1.1.0; 3D-DNA v. 180922\nAssembly Name :: sRhiTyp1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 46.7x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Rhincodon typus Annotation Release\n 101\nAnnotation Version :: 101\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
ring finger protein 185, transcript variant X1
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 2 samples with support for all annotated introns
ring finger protein 185, 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 1 sample with support for all annotated introns
ring finger protein 185, transcript variant X4
ring finger protein 185, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ring finger protein 185, transcript variant X3
ring finger protein 185, transcript variant X6
E3 ubiquitin-protein ligase RNF185 isoform X1
E3 ubiquitin-protein ligase RNF185 isoform X5
E3 ubiquitin-protein ligase RNF185 isoform X2
E3 ubiquitin-protein ligase RNF185 isoform X4
E3 ubiquitin-protein ligase RNF185 isoform X6
E3 ubiquitin-protein ligase RNF185 isoform X3
phosphoinositide-3-kinase interacting protein 1, transcript variant X3
phosphoinositide-3-kinase interacting protein 1, transcript variant X1
phosphoinositide-3-kinase interacting protein 1, transcript variant X4
phosphoinositide-3-kinase interacting protein 1, transcript variant X2
phosphoinositide-3-kinase-interacting protein 1 isoform X1
phosphoinositide-3-kinase-interacting protein 1 isoform X2
phosphoinositide-3-kinase-interacting protein 1 isoform X3
integral membrane protein DGCR2/IDD-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 2 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 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, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized protein si:ch211-225b11.4
uncharacterized protein C22orf15, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized protein C22orf15, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein C22orf15, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein C22orf15, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein C22orf15, transcript variant X5
uncharacterized protein C22orf15 isoform X1
uncharacterized protein C22orf15 isoform X2
uncharacterized protein C22orf15 isoform X4
uncharacterized protein C22orf15 isoform X3
coiled-coil-helix-coiled-coil-helix domain containing 10
coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1a, transcript variant X1
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1a, transcript variant X3
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1a, transcript variant X5
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1a, transcript variant X2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1a, transcript variant X4
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A isoform X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A isoform X3
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A isoform X5
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1 isoform X2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 32 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: 6 long SRA reads, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
PH_BCR_vertebrate and RhoGAP_Bcr domain-containing protein, transcript variant X1
PH_BCR_vertebrate and RhoGAP_Bcr domain-containing protein, transcript variant X2
PH_BCR_vertebrate and RhoGAP_Bcr domain-containing protein isoform X1
PH_BCR_vertebrate and RhoGAP_Bcr domain-containing protein isoform X2
sperm antigen with calponin homology and coiled-coil domains 1-like a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ureidopropionase, beta, transcript variant X2
ureidopropionase, beta, transcript variant X1
ureidopropionase, beta, transcript variant X3
small nuclear ribonucleoprotein D3 polypeptide
mediator of RNA polymerase II transcription subunit 15
uncharacterized protein LOC101885505 homolog, transcript variant X1
uncharacterized protein LOC101885505 homolog, transcript variant X3
uncharacterized protein LOC101885505 homolog, transcript variant X2
coiled-coil domain-containing protein 74B
sphingomyelin phosphodiesterase 4, transcript variant X5
sphingomyelin phosphodiesterase 4, transcript variant X4
sphingomyelin phosphodiesterase 4, transcript variant X2
sphingomyelin phosphodiesterase 4, transcript variant X3
sphingomyelin phosphodiesterase 4, transcript variant X1
sphingomyelin phosphodiesterase 4 isoform X5
sphingomyelin phosphodiesterase 4 isoform X4
sphingomyelin phosphodiesterase 4 isoform X2
sphingomyelin phosphodiesterase 4 isoform X3
sphingomyelin phosphodiesterase 4 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 88% 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 86% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine-protein phosphatase 4 catalytic subunit-like, transcript variant X1
serine/threonine-protein phosphatase 4 catalytic subunit-like, transcript variant X4
serine/threonine-protein phosphatase 4 catalytic subunit-like, transcript variant X2
serine/threonine-protein phosphatase 4 catalytic subunit-like, transcript variant X3
serine/threonine-protein phosphatase 4 catalytic subunit-like, transcript variant X5
serine/threonine-protein phosphatase 4 catalytic subunit-like isoform X1
serine/threonine-protein phosphatase 4 catalytic subunit-like isoform X2
serine/threonine-protein phosphatase 4 catalytic subunit-like isoform X3
v-crk avian sarcoma virus CT10 oncogene homolog-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
calcineurin binding protein 1, transcript variant X2
calcineurin binding protein 1, transcript variant X3
calcineurin binding protein 1, transcript variant X1
calcineurin-binding protein cabin-1 isoform X2
calcineurin-binding protein cabin-1 isoform X3
calcineurin-binding protein cabin-1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 51
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 11-like, transcript variant X1
solute carrier family 2, facilitated glucose transporter member 11-like isoform X1
solute carrier family 2, facilitated glucose transporter member 11-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 11-like isoform X2
POZ/BTB and AT hook containing zinc finger 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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
POZ/BTB and AT hook containing zinc finger 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
POZ (BTB) and AT hook-containing zinc finger 1 isoform X2
POZ (BTB) and AT hook-containing zinc finger 1 isoform X1
developmentally regulated GTP binding protein 1
developmentally-regulated GTP-binding protein 1
phosphatidylserine decarboxylase, transcript variant X5
phosphatidylserine decarboxylase, transcript variant X4
phosphatidylserine decarboxylase, transcript variant X2
phosphatidylserine decarboxylase, transcript variant X1
phosphatidylserine decarboxylase, transcript variant X6
phosphatidylserine decarboxylase, transcript variant X3
phosphatidylserine decarboxylase proenzyme, mitochondrial isoform X3
phosphatidylserine decarboxylase proenzyme, mitochondrial isoform X2
phosphatidylserine decarboxylase proenzyme, mitochondrial isoform X4
phosphatidylserine decarboxylase proenzyme, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
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
uncharacterized wu:fi75a02, transcript variant X3
uncharacterized wu:fi75a02, transcript variant X1
uncharacterized protein wu:fi75a02 isoform X1
uncharacterized protein wu:fi75a02 isoform X2
uncharacterized wu:fi75a02, 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
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
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
DEP domain containing 5, GATOR1 subcomplex subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 74% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
guanine nucleotide binding protein (G protein), alpha z polypeptide
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 129 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
guanine nucleotide-binding protein G(z) subunit alpha
RAB36, member RAS oncogene family, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 20 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
RAB36, member RAS oncogene family, transcript variant X3
RAB36, member RAS oncogene family, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RAB36, member RAS oncogene family, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DNA topoisomerase III beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
DNA topoisomerase III beta, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DNA topoisomerase III beta, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein phosphatase, Mg2+/Mn2+ dependent, 1F
RING-type E3 ubiquitin-protein ligase PPIL2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
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 6 samples with support for all annotated introns
immunoglobulin lambda-1 light chain-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
39S ribosomal protein L40, mitochondrial
peptidyl-prolyl cis-trans isomerase FKBP8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 93% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin recognition factor in ER associated degradation 1, transcript variant X5
ubiquitin recognition factor in ER associated degradation 1, transcript variant X4
ubiquitin recognition factor in ER associated degradation 1, transcript variant X2
ubiquitin recognition factor in ER associated degradation 1, transcript variant X3
ubiquitin recognition factor in ER associated degradation 1, transcript variant X1
ubiquitin recognition factor in ER-associated degradation protein 1 isoform X4
ubiquitin recognition factor in ER-associated degradation protein 1 isoform X3
ubiquitin recognition factor in ER-associated degradation protein 1 isoform X2
ubiquitin recognition factor in ER-associated degradation protein 1 isoform X1
CDC45 cell division cycle 45 homolog (S. cerevisiae), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
CDC45 cell division cycle 45 homolog (S. cerevisiae), 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 2 samples with support for all annotated introns
cell division control protein 45 homolog isoform X1
cell division control protein 45 homolog isoform X2
transfer RNA phenylalanine (anticodon AAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized protein LOC393431 homolog, transcript variant X2
uncharacterized protein LOC393431 homolog, transcript variant X1
uncharacterized protein LOC393431 homolog, transcript variant X3
glycoprotein Ib platelet subunit beta, transcript variant X1
glycoprotein Ib platelet subunit beta, transcript variant X3
glycoprotein Ib platelet subunit beta, transcript variant X2
glycoprotein Ib platelet subunit beta, transcript variant X4
platelet glycoprotein Ib beta chain isoform X1
platelet glycoprotein Ib beta chain isoform X3
platelet glycoprotein Ib beta chain isoform X2
platelet glycoprotein Ib beta chain isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 92% 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: 15 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 105 Proteins, and 71% 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 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: immunoglobulin gamma-1 heavy chain-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments
ribosomal protein, large, P0, transcript variant X1
ribosomal protein, large, P0, transcript variant X2
cytosolic thiouridylase subunit 1 homolog (S. pombe), transcript variant X1
cytosolic thiouridylase subunit 1 homolog (S. pombe), transcript variant X2
cytosolic thiouridylase subunit 1 homolog (S. pombe), transcript variant X3
cytosolic thiouridylase subunit 1 homolog (S. pombe), transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 22 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: 1 long SRA read, 22 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
NAD-dependent protein lipoamidase sirtuin-4, mitochondrial
mitochondrial fission regulator 1-like, transcript variant X2
mitochondrial fission regulator 1-like, transcript variant X1
uncharacterized protein LOC109928128 isoform X1
mitochondrial fission regulator 1-like isoform X2
leucine-zipper-like transcription regulator 1
leucine-zipper-like transcriptional regulator 1
apoptosis-inducing factor 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
apoptosis-inducing factor 3, transcript variant X2
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
mitotic spindle organizing protein 2B, transcript variant X1
mitotic spindle organizing protein 2B, transcript variant X4
mitotic spindle organizing protein 2B, transcript variant X2
mitotic spindle organizing protein 2B, transcript variant X3
mitotic-spindle organizing protein 2 isoform X2
mitotic-spindle organizing protein 2 isoform X1
oxysterol-binding protein 2-like, transcript variant X1
oxysterol-binding protein 2-like, transcript variant X2
oxysterol-binding protein 2-like isoform X1
oxysterol-binding protein 2-like isoform X2
oxysterol-binding protein 2-like, transcript variant X6
oxysterol-binding protein 2-like, transcript variant X3
oxysterol-binding protein 2-like isoform X3
oxysterol-binding protein 2-like, transcript variant X4
oxysterol-binding protein 2-like, transcript variant X5
oxysterol-binding protein 2-like isoform X4
oxysterol-binding protein 2-like isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59% coverage of the annotated genomic feature by RNAseq alignments
calponin homology domain-containing protein DDB_G0272472
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
coiled-coil domain containing 117, transcript variant X1
coiled-coil domain containing 117, transcript variant X5
coiled-coil domain containing 117, transcript variant X4
coiled-coil domain containing 117, transcript variant X2
coiled-coil domain containing 117, transcript variant X3
coiled-coil domain-containing protein 117 isoform X1
coiled-coil domain-containing protein 117 isoform X2
transcobalamin II, transcript variant X1
transcobalamin II, transcript variant X2
transcobalamin II, transcript variant X4
transcobalamin II, transcript variant X5
transcobalamin II, transcript variant X3
transcobalamin II, transcript variant X6
ADP-ribose pyrophosphatase, mitochondrial-like
protein kinase, AMP-activated, beta 1 non-catalytic subunit, a, transcript variant X1
protein kinase, AMP-activated, beta 1 non-catalytic subunit, a, transcript variant X3
protein kinase, AMP-activated, beta 1 non-catalytic subunit, a, transcript variant X2
protein kinase, AMP-activated, beta 1 non-catalytic subunit, a, transcript variant X4
protein kinase, AMP-activated, beta 1 non-catalytic subunit, a, transcript variant X5
5'-AMP-activated protein kinase subunit beta-1a isoform X1
5'-AMP-activated protein kinase subunit beta-1a isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
BICD family like cargo adaptor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
BICD family like cargo adaptor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
BICD family-like cargo adapter 1 isoform X2
BICD family-like cargo adapter 1 isoform X1
citron rho-interacting serine/threonine kinase a
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
solute carrier family 2, facilitated glucose transporter member 11b
solute carrier family 2, facilitated glucose transporter member 11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 98% 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 long SRA reads, 39 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 long SRA reads, 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 11-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 11-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 11-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 11-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 11-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cytochrome c oxidase subunit 6A, mitochondrial-like
dynein light chain LC6, flagellar outer arm
2-methoxy-6-polyprenyl-1,4-benzoquinol methylase, mitochondrial
ring finger protein 10, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ring finger protein 10, transcript variant X1
ring finger protein 10, transcript variant X2
ring finger protein 10, transcript variant X3
ring finger protein 10, transcript variant X4
glutamyl-tRNA amidotransferase subunit C
glutamyl-tRNA(Gln) amidotransferase subunit C, mitochondrial
POP5 homolog, ribonuclease P/MRP subunit
calcium-binding protein 1, transcript variant X3
calcium-binding protein 1, transcript variant X2
calcium-binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 93% 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: 1 long SRA read, 20 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
short-chain specific acyl-CoA dehydrogenase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins
synergin gamma-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
synergin gamma-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
dual specificity protein phosphatase 18-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: dual specificity protein phosphatase 18-like
sushi domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sushi domain containing 2, transcript variant X2
sushi domain-containing protein 2 isoform X1
sushi domain-containing protein 2 isoform X2
kringle containing transmembrane protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
kringle containing transmembrane protein 1, transcript variant X2
zinc and ring finger 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc and ring finger 3, transcript variant X3
zinc and ring finger 3, 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 7 samples with support for all annotated introns
E3 ubiquitin-protein ligase znrf3 isoform X2
E3 ubiquitin-protein ligase znrf3 isoform X3
E3 ubiquitin-protein ligase znrf3 isoform X1
coiled-coil domain-containing protein 60, transcript variant X2
coiled-coil domain-containing protein 60, transcript variant X3
coiled-coil domain-containing protein 60, transcript variant X1
coiled-coil domain-containing protein 60 isoform X2
coiled-coil domain-containing protein 60 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 88% coverage of the annotated genomic feature by RNAseq alignments
serine/arginine repetitive matrix protein 4
SDS3 homolog, SIN3A corepressor complex component, transcript variant X1
SDS3 homolog, SIN3A corepressor complex component, transcript variant X3
SDS3 homolog, SIN3A corepressor complex component, transcript variant X2
sin3 histone deacetylase corepressor complex component SDS3 isoform X1
sin3 histone deacetylase corepressor complex component SDS3 isoform X2
sin3 histone deacetylase corepressor complex component SDS3 isoform X3
serine/threonine-protein kinase TAO3 isoform X1
serine/threonine-protein kinase TAO3 isoform X2
serine/threonine-protein kinase TAO3 isoform X3
phosphatidylethanolamine binding protein 1
phosphatidylethanolamine-binding protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 42% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
nitric oxide synthase 1 (neuronal), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
nitric oxide synthase 1 (neuronal), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
replication factor C (activator 1) 5, transcript variant X1
replication factor C (activator 1) 5, transcript variant X2
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 5 samples with support for all annotated introns
replication factor C subunit 5 isoform X1
replication factor C subunit 5 isoform X2
WD repeat and SOCS box containing 2, transcript variant X3
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 6 samples with support for all annotated introns
WD repeat and SOCS box containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
WD repeat and SOCS box containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
WD repeat and SOCS box-containing protein 2 isoform X3
WD repeat and SOCS box-containing protein 2 isoform X2
WD repeat and SOCS box-containing protein 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 7 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein, transmembrane 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ring finger protein, transmembrane 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RING finger and transmembrane domain-containing protein 2 isoform X1
RING finger and transmembrane domain-containing protein 2 isoform X2
SREBF pathway regulator in golgi 1, transcript variant X1
SREBF pathway regulator in golgi 1, transcript variant X2
SREBP regulating gene protein isoform X2
SREBP regulating gene protein isoform X1
mediator of RNA polymerase II transcription subunit 13-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
uncharacterized LOC125486010, 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 3 samples with support for all annotated introns
uncharacterized LOC125486010, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125486010, transcript variant X3
uncharacterized LOC125486010, transcript variant X1
transfer RNA histidin (anticodon AUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125485939, transcript variant X2
uncharacterized LOC125485939, transcript variant X1
T-box transcription factor TBX5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
T-box transcription factor TBX5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
T-box transcription factor TBX5-like isoform X1
T-box transcription factor TBX5-like isoform X2
RNA binding motif protein 19, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
RNA binding motif protein 19, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
probable RNA-binding protein 19 isoform X2
RNA binding motif protein 19, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
probable RNA-binding protein 19 isoform X1
probable RNA-binding protein 19 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 81% 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: 11 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
solute carrier family 8 member B1, transcript variant X1
solute carrier family 8 member B1, transcript variant X2
solute carrier family 8 member B1, 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
mitochondrial sodium/calcium exchanger protein isoform X1
mitochondrial sodium/calcium exchanger protein isoform X2
mitochondrial sodium/calcium exchanger protein isoform X3
two pore segment channel 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
two pore segment channel 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
two pore segment channel 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
IQ motif containing D, transcript variant X1
IQ motif containing D, transcript variant X2
RBPJ-interacting and tubulin-associated protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
RBPJ-interacting and tubulin-associated protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
RBPJ-interacting and tubulin-associated protein 1, transcript variant X3
RBPJ-interacting and tubulin-associated protein 1 isoform X1
RBPJ-interacting and tubulin-associated protein 1 isoform X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 54
coiled-coil domain-containing protein 42 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
activating signal cointegrator 1 complex subunit 2-like
spliceosome associated factor 3, U4/U6 recycling protein
squamous cell carcinoma antigen recognized by T-cells 3
iron-sulfur cluster assembly enzyme ISCU, mitochondrial
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
myotubularin related protein 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
myotubularin related protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
myotubularin related protein 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
myotubularin related protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
myotubularin related protein 3, transcript variant X4
myotubularin related protein 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 long SRA reads, 19 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
myotubularin related protein 3, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 long SRA reads, 22 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
myotubularin-related protein 3 isoform X1
myotubularin-related protein 3 isoform X6
myotubularin-related protein 3 isoform X2
myotubularin-related protein 3 isoform X7
myotubularin-related protein 3 isoform X4
myotubularin-related protein 3 isoform X3
myotubularin-related protein 3 isoform X5
DEAH (Asp-Glu-Ala-His) box polypeptide 37
probable ATP-dependent RNA helicase DHX37
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
acetoacetyl-CoA synthetase, transcript variant X2
acetoacetyl-CoA synthetase, transcript variant X5
acetoacetyl-CoA synthetase, transcript variant X4
acetoacetyl-CoA synthetase, transcript variant X1
acetoacetyl-CoA synthetase, transcript variant X3
transmembrane protein 132D, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane protein 132D, transcript variant X3
transmembrane protein 132D, transcript variant X2
glycosyltransferase 1 domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glycosyltransferase 1 domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
glycosyltransferase 1 domain containing 1, transcript variant X2
glycosyltransferase 1 domain-containing protein 1 isoform X2
glycosyltransferase 1 domain-containing protein 1 isoform X1
glycosyltransferase 1 domain-containing protein 1 isoform X3
huntingtin-interacting protein 1-related protein
vacuolar protein sorting-associated protein 37B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain containing 62, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
coiled-coil domain containing 62, transcript variant X2
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 1 sample with support for all annotated introns
coiled-coil domain-containing protein 62
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: hydroxycarboxylic acid receptor 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins
LOW QUALITY PROTEIN: 26S proteasome complex subunit SEM1
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
uncharacterized protein LOC562347 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized protein si:ch211-110p13.9
zinc finger, CCHC domain containing 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 long SRA reads, 17 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
zinc finger, CCHC domain containing 8, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
zinc finger, CCHC domain containing 8, transcript variant X1
zinc finger, CCHC domain containing 8, transcript variant X3
zinc finger CCHC domain-containing protein 8 isoform X2
zinc finger CCHC domain-containing protein 8 isoform X1
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: arginine/serine-rich coiled-coil protein 2
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
CAP-GLY domain containing linker protein 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
CAP-Gly domain-containing linker protein 1
VPS33A core subunit of CORVET and HOPS complexes, transcript variant X1
VPS33A core subunit of CORVET and HOPS complexes, transcript variant X3
VPS33A core subunit of CORVET and HOPS complexes, transcript variant X2
VPS33A core subunit of CORVET and HOPS complexes, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
vacuolar protein sorting-associated protein 33A isoform X1
vacuolar protein sorting-associated protein 33A isoform X2
diablo IAP-binding mitochondrial protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
diablo IAP-binding mitochondrial protein, transcript variant X1
diablo IAP-binding mitochondrial protein, transcript variant X2
diablo IAP-binding mitochondrial protein isoform X3
diablo IAP-binding mitochondrial protein isoform X1
diablo IAP-binding mitochondrial protein isoform X2
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 4
leucine-rich repeat-containing protein 43
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
BAF chromatin remodeling complex subunit BCL7A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
B-cell CLL/lymphoma 7 protein family member A isoform X2
BAF chromatin remodeling complex subunit BCL7A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
BAF chromatin remodeling complex subunit BCL7A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
B-cell CLL/lymphoma 7 protein family member A isoform X1
B-cell CLL/lymphoma 7 protein family member A isoform X3
proteasome 26S subunit, non-ATPase 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
proteasome 26S subunit, non-ATPase 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 long SRA reads, 17 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
26S proteasome non-ATPase regulatory subunit 9 isoform X1
26S proteasome non-ATPase regulatory subunit 9 isoform X2
cilia and flagella associated protein 251
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cilia- and flagella-associated protein 251
SET domain containing 1B, histone lysine methyltransferase a, transcript variant X2
SET domain containing 1B, histone lysine methyltransferase a, transcript variant X3
SET domain containing 1B, histone lysine methyltransferase a, transcript variant X1
histone-lysine N-methyltransferase SETD1B-A isoform X2
histone-lysine N-methyltransferase SETD1B-A isoform X1
ras homolog family member F, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 47 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ras homolog family member F, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 long SRA reads, 72 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
rho-related GTP-binding protein RhoF isoform X1
rho-related GTP-binding protein RhoF isoform X2
transmembrane protein 120B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 21 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transmembrane protein 120B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
MORN repeat containing 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
MORN repeat containing 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
MORN repeat-containing protein 3 isoform X2
MORN repeat-containing protein 3 isoform X1
calcium release-activated calcium channel protein 1, transcript variant X2
calcium release-activated calcium channel protein 1, transcript variant X1
calcium release-activated calcium channel protein 1 isoform X1
calcium release-activated calcium channel protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
anaphase promoting complex subunit 5, transcript variant X1
anaphase promoting complex subunit 5, transcript variant X3
anaphase promoting complex subunit 5, transcript variant X2
calcium/calmodulin-dependent protein kinase kinase 2
P2X purinoceptor 4-like, transcript variant X2
P2X purinoceptor 4-like, transcript variant X1
P2X purinoceptor 4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 18 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
intraflagellar transport 81 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
intraflagellar transport 81 homolog, 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
intraflagellar transport protein 81 homolog isoform X1
intraflagellar transport protein 81 homolog isoform X2
ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2b, transcript variant X2
ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2b, transcript variant X1
sarcoplasmic/endoplasmic reticulum calcium ATPase 2 isoform X2
sarcoplasmic/endoplasmic reticulum calcium ATPase 2 isoform X1
anaphase promoting complex subunit 7, transcript variant X1
anaphase promoting complex subunit 7, transcript variant X2
anaphase-promoting complex subunit 7 isoform X1
anaphase-promoting complex subunit 7 isoform X2
ubiquitin-conjugating enzyme E2G 1b (UBC7 homolog, yeast)
actin related protein 2/3 complex, subunit 3
actin-related protein 2/3 complex subunit 3
VPS29 retromer complex component, transcript variant X2
VPS29 retromer complex component, transcript variant X1
vacuolar protein sorting-associated protein 29 isoform X2
vacuolar protein sorting-associated protein 29 isoform X1
tectonic family member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
tectonic family member 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tectonic family member 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 7 samples with support for all annotated introns
protein phosphatase 1, catalytic subunit, gamma isozyme
serine/threonine-protein phosphatase PP1-gamma catalytic subunit A
coiled-coil domain-containing protein 63-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 72% coverage of the annotated genomic feature by RNAseq alignments
myosin regulatory light chain 2, ventricular/cardiac muscle isoform
sesquipedalian-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 1 sample with support for all annotated introns
sesquipedalian-1-like, transcript variant X2
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 2 samples with support for all annotated introns
sesquipedalian-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68% coverage of the annotated genomic feature by RNAseq alignments
BRCA1-associated protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
BRCA1-associated protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
BRCA1-associated protein, transcript variant X2
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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 23 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92 Proteins
coiled-coil domain containing 157, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
coiled-coil domain containing 157, transcript variant X2
coiled-coil domain-containing protein 157 isoform X1
coiled-coil domain-containing protein 157 isoform X2
ring finger protein 215, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ring finger protein 215, 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
ring finger protein 215, transcript variant X3
ring finger protein 215, transcript variant X4
ring finger protein 215, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
mitochondrial fission process 1, transcript variant X1
mitochondrial fission process protein 1 isoform X1
mitochondrial fission process 1, transcript variant X4
mitochondrial fission process protein 1 isoform X4
mitochondrial fission process 1, transcript variant X2
mitochondrial fission process protein 1 isoform X2
mitochondrial fission process 1, transcript variant X3
mitochondrial fission process protein 1 isoform X3
zona pellucida sperm-binding protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase DTX1, transcript variant X1
E3 ubiquitin-protein ligase DTX1, transcript variant X2
E3 ubiquitin-protein ligase DTX1 isoform X1
E3 ubiquitin-protein ligase DTX1 isoform X2
E3 ubiquitin-protein ligase DTX1, transcript variant X3
E3 ubiquitin-protein ligase DTX1 isoform X3
ABC transporter B family member 1-like, transcript variant X2
ABC transporter B family member 1-like, transcript variant X1
ABC transporter B family member 1-like, transcript variant X3
ABC transporter B family member 1-like isoform X1
ABC transporter B family member 1-like isoform X2
EMI domain-containing protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
EMI domain-containing protein 1, 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 5 samples with support for all annotated introns
EMI domain-containing protein 1, transcript variant X5
EMI domain-containing protein 1, transcript variant X3
EMI domain-containing protein 1, transcript variant X4
EMI domain-containing protein 1 isoform X2
EMI domain-containing protein 1 isoform X1
EMI domain-containing protein 1 isoform X5
EMI domain-containing protein 1 isoform X3
EMI domain-containing protein 1 isoform X4
rhomboid domain containing 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
rhomboid domain containing 3, transcript variant X4
rhomboid domain containing 3, transcript variant X1
rhomboid domain containing 3, transcript variant X3
rhomboid domain-containing protein 3 isoform X1
rhomboid domain-containing protein 3 isoform X2
growth arrest-specific 2 like 1, transcript variant X1
growth arrest-specific 2 like 1, transcript variant X2
uncharacterized protein LOC564476 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, and 69% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized protein zgc:193801 isoform X1
uncharacterized protein LOC564476 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein zgc:193801 isoform X2
THO complex subunit 5 homolog isoform X2
THO complex subunit 5 homolog isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins
proline dehydrogenase 1, mitochondrial-like, transcript variant X1
proline dehydrogenase 1, mitochondrial-like, transcript variant X2
proline dehydrogenase 1, mitochondrial-like isoform X1
proline dehydrogenase 1, mitochondrial-like isoform X2
scavenger receptor class F, member 2, transcript variant X2
scavenger receptor class F, member 2, transcript variant X1
uncharacterized LOC125485957, transcript variant X2
uncharacterized LOC125485957, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transcriptional activator MN1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 98% 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 long SRA reads, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transcriptional activator MN1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC125485969, transcript variant X1
uncharacterized LOC125485969, transcript variant X2
tetratricopeptide repeat protein 28-like
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
SRR1 domain containing, transcript variant X1
SRR1 domain containing, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
protein-tyrosine sulfotransferase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein-tyrosine sulfotransferase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein-tyrosine sulfotransferase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 33 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein-tyrosine sulfotransferase 2, transcript variant X4
protein-tyrosine sulfotransferase 2, transcript variant X5
beta-crystallin B2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
beta-crystallin B2-like, transcript variant X2
crystallin, beta B3, transcript variant X2
crystallin, beta B3, transcript variant X3
crystallin, beta B3, transcript variant X1
uncharacterized LOC109923141, transcript variant X1
uncharacterized LOC109923141, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
2'-5'-oligoadenylate synthase-like protein 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
LOW QUALITY PROTEIN: 2'-5'-oligoadenylate synthase-like protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 7 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
DNA polymerase epsilon catalytic subunit A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
phosphatidylinositol 4,5-bisphosphate 5-phosphatase A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
probable E3 ubiquitin-protein ligase HECTD4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
TRAF-type zinc finger domain-containing protein 1, transcript variant X2
TRAF-type zinc finger domain-containing protein 1, transcript variant X1
TRAF-type zinc finger domain-containing protein 1 isoform X2
TRAF-type zinc finger domain-containing protein 1 isoform X1
N-alpha-acetyltransferase 25, NatB auxiliary subunit
endoplasmic reticulum resident protein 29
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 83% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: transmembrane protein 116
MAP kinase-activated protein kinase 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 12 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized LOC125485922, transcript variant X2
uncharacterized LOC125485922, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 long SRA reads, 12 Proteins, and 97% 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: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC568894 homolog
acyl-CoA dehydrogenase family member 10, transcript variant X1
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 3 samples with support for all annotated introns
acyl-CoA dehydrogenase family member 10, transcript variant X2
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
acyl-CoA dehydrogenase family member 10 isoform X1
acyl-CoA dehydrogenase family member 10, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
acyl-CoA dehydrogenase family member 10 isoform X2
uncharacterized LOC125485926, transcript variant X2
uncharacterized LOC125485926, transcript variant X1
sodium- and chloride-dependent GABA transporter 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
protein tyrosine phosphatase non-receptor type 11a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
tyrosine-protein phosphatase non-receptor type 11
uncharacterized LOC125485943, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125485943, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 81% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein phosphatase Slingshot homolog 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 15 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 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: 1 long SRA read, 66 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat domain 13A, transcript variant X2
ankyrin repeat domain 13A, transcript variant X1
ankyrin repeat domain-containing protein 13A
G protein-coupled receptor kinase interacting ArfGAP 2a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 25 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
trichoplein keratin filament-binding protein
ARF GTPase-activating protein GIT2-like, transcript variant X1
ARF GTPase-activating protein GIT2-like, transcript variant X2
ARF GTPase-activating protein GIT2-like, transcript variant X3
ARF GTPase-activating protein GIT2-like isoform X3
ARF GTPase-activating protein GIT2-like isoform X2
ARF GTPase-activating protein GIT2-like isoform X1
family with sequence similarity 222 member Aa
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mevalonate kinase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mevalonate kinase, transcript variant X4
mevalonate kinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
mevalonate kinase, transcript variant X9
mevalonate kinase, transcript variant X6
mevalonate kinase, transcript variant X7
mevalonate kinase, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 66% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mevalonate kinase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mevalonate kinase, transcript variant X10
mevalonate kinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin protein ligase E3B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ubiquitin protein ligase E3B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
ubiquitin protein ligase E3B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 16 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: 10 Proteins
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
alkB homolog 2, alpha-ketoglutarate dependent dioxygenase
ubiquitin carboxyl-terminal hydrolase 30, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 long SRA reads, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 30, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 30, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 30
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: small G protein signaling modulator 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
aspartate beta-hydroxylase domain-containing protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
aspartate beta-hydroxylase domain-containing protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
aspartate beta-hydroxylase domain-containing protein 2-like
HPS4 biogenesis of lysosomal organelles complex 3 subunit 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 long SRA reads, 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
HPS4 biogenesis of lysosomal organelles complex 3 subunit 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DiGeorge syndrome critical region gene 6, transcript variant X4
DiGeorge syndrome critical region gene 6, transcript variant X5
DiGeorge syndrome critical region gene 6, transcript variant X1
DiGeorge syndrome critical region gene 6, transcript variant X2
DiGeorge syndrome critical region gene 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
leucine rich repeat containing 74B, transcript variant X2
leucine rich repeat containing 74B, transcript variant X5
leucine rich repeat containing 74B, transcript variant X1
leucine rich repeat containing 74B, transcript variant X7
leucine-rich repeat-containing protein 74B isoform X5
leucine-rich repeat-containing protein 74B isoform X2
leucine-rich repeat-containing protein 74B isoform X1
leucine-rich repeat-containing protein 74B isoform X7
leucine rich repeat containing 74B, transcript variant X4
leucine rich repeat containing 74B, transcript variant X3
leucine rich repeat containing 74B, transcript variant X6
leucine-rich repeat-containing protein 74B isoform X4
leucine-rich repeat-containing protein 74B isoform X3
leucine-rich repeat-containing protein 74B isoform X6
leucine rich repeat containing 74B, transcript variant X8
leucine-rich repeat-containing protein 74B isoform X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 19 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
stromal cell-derived factor 2-like protein 1
YdjC chitooligosaccharide deacetylase homolog, transcript variant X2
YdjC chitooligosaccharide deacetylase homolog, transcript variant X1
putative phosphatidylinositol 4-kinase alpha-like protein P2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 long SRA reads, 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phosphatidylinositol 4-kinase alpha-like
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, including 11 samples with support for all annotated introns
phosphatidylinositol 4-kinase, catalytic, alpha a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
phosphatidylinositol 4-kinase, catalytic, alpha a, 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 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phosphatidylinositol 4-kinase alpha isoform X2
phosphatidylinositol 4-kinase alpha isoform X1
serpin peptidase inhibitor, clade D (heparin cofactor), member 1
somatomedin-B and thrombospondin type-1 domain-containing protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 79% coverage of the annotated genomic feature by RNAseq alignments
clathrin, heavy chain-like 1, transcript variant X3
clathrin, heavy chain-like 1, transcript variant X2
clathrin, heavy chain-like 1, transcript variant X1
T-box transcription factor 1, transcript variant X3
T-box transcription factor TBX1 isoform X3
T-box transcription factor 1, transcript variant X1
T-box transcription factor 1, transcript variant X2
T-box transcription factor TBX1 isoform X1
T-box transcription factor TBX1 isoform X2
T-box transcription factor 1, transcript variant X4
T-box transcription factor 1, transcript variant X5
T-box transcription factor TBX1 isoform X4
T-box transcription factor TBX1 isoform X5
guanine nucleotide binding protein (G protein), beta polypeptide 1-like, transcript variant X3
guanine nucleotide binding protein (G protein), beta polypeptide 1-like, transcript variant X2
guanine nucleotide binding protein (G protein), beta polypeptide 1-like, transcript variant X1
guanine nucleotide-binding protein subunit beta-like protein 1 isoform X1
guanine nucleotide-binding protein subunit beta-like protein 1 isoform X2
thioredoxin reductase 2, tandem duplicate 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
transport and golgi organization 2 homolog (Drosophila), transcript variant X2
transport and golgi organization 2 homolog (Drosophila), transcript variant X1
transport and golgi organization 2 homolog (Drosophila), transcript variant X3
transport and Golgi organization protein 2 homolog isoform X1
transport and Golgi organization protein 2 homolog isoform X2
microprocessor complex subunit DGCR8-like, transcript variant X1
microprocessor complex subunit DGCR8-like, transcript variant X2
microprocessor complex subunit DGCR8-like, transcript variant X3
microprocessor complex subunit DGCR8-like isoform X1
microprocessor complex subunit DGCR8-like isoform X2
microprocessor complex subunit DGCR8-like isoform X3
tRNA (uracil-5-)-methyltransferase homolog A
RAN binding protein 1, transcript variant X3
RAN binding protein 1, transcript variant X2
ran-specific GTPase-activating protein isoform X2
RAN binding protein 1, transcript variant X1
ran-specific GTPase-activating protein isoform X1
ran-specific GTPase-activating protein isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
PGAM family member 5, serine/threonine protein phosphatase, mitochondrial, transcript variant X1
PGAM family member 5, serine/threonine protein phosphatase, mitochondrial, transcript variant X2
PGAM family member 5, serine/threonine protein phosphatase, mitochondrial, transcript variant X4
serine/threonine-protein phosphatase PGAM5, mitochondrial isoform X1
serine/threonine-protein phosphatase PGAM5, mitochondrial isoform X2
PGAM family member 5, serine/threonine protein phosphatase, mitochondrial, transcript variant X3
serine/threonine-protein phosphatase PGAM5, mitochondrial isoform X3
serine/threonine-protein phosphatase PGAM5, mitochondrial isoform X4
ankyrin repeat and LEM domain containing 2, transcript variant X2
ankyrin repeat and LEM domain containing 2, transcript variant X3
ankyrin repeat and LEM domain containing 2, transcript variant X1
ankyrin repeat and LEM domain containing 2, transcript variant X6
ankyrin repeat and LEM domain-containing protein 2 isoform X3
ankyrin repeat and LEM domain-containing protein 2 isoform X1
ankyrin repeat and LEM domain-containing protein 2 isoform X5
ankyrin repeat and LEM domain-containing protein 2 isoform X2
ankyrin repeat and LEM domain containing 2, transcript variant X5
ankyrin repeat and LEM domain containing 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
ankyrin repeat and LEM domain-containing protein 2 isoform X4
uncharacterized protein si:dkey-112e17.1
checkpoint with forkhead and ring finger domains, E3 ubiquitin protein ligase
autism susceptibility gene 2 protein-like, transcript variant X1
autism susceptibility gene 2 protein-like isoform X1
autism susceptibility gene 2 protein-like, transcript variant X10
autism susceptibility gene 2 protein-like, transcript variant X4
autism susceptibility gene 2 protein-like, transcript variant X2
autism susceptibility gene 2 protein-like, transcript variant X5
autism susceptibility gene 2 protein-like, transcript variant X6
autism susceptibility gene 2 protein-like, transcript variant X8
autism susceptibility gene 2 protein-like, transcript variant X7
autism susceptibility gene 2 protein-like, transcript variant X9
autism susceptibility gene 2 protein-like, transcript variant X3
autism susceptibility gene 2 protein-like, transcript variant X12
autism susceptibility gene 2 protein-like isoform X10
autism susceptibility gene 2 protein-like isoform X4
autism susceptibility gene 2 protein-like isoform X2
autism susceptibility gene 2 protein-like isoform X5
autism susceptibility gene 2 protein-like isoform X6
autism susceptibility gene 2 protein-like isoform X8
autism susceptibility gene 2 protein-like isoform X7
autism susceptibility gene 2 protein-like isoform X9
autism susceptibility gene 2 protein-like isoform X3
autism susceptibility gene 2 protein-like, transcript variant X11
autism susceptibility gene 2 protein-like, transcript variant X13
autism susceptibility gene 2 protein-like isoform X12
autism susceptibility gene 2 protein-like isoform X11
fibrosin-1-like protein, transcript variant X3
fibrosin-1-like protein, transcript variant X2
fibrosin-1-like protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 4 Proteins, and 99% 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, and 90% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00562
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 long SRA reads, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
E1A-binding protein p400-like, transcript variant X4
E1A-binding protein p400-like, transcript variant X5
E1A-binding protein p400-like, transcript variant X2
E1A-binding protein p400-like, transcript variant X3
E1A-binding protein p400-like, transcript variant X1
E1A-binding protein p400-like isoform X4
E1A-binding protein p400-like isoform X5
E1A-binding protein p400-like isoform X2
E1A-binding protein p400-like isoform X3
E1A-binding protein p400-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 long SRA reads, 26 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
unc-51 like autophagy activating kinase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
adhesion G-protein coupled receptor D1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
splicing factor SWAP, transcript variant X1
splicing factor SWAP, transcript variant X4
splicing factor SWAP, transcript variant X2
splicing factor SWAP, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
splicing factor, suppressor of white-apricot homolog isoform X1
splicing factor, suppressor of white-apricot homolog isoform X3
splicing factor, suppressor of white-apricot homolog isoform X2
splicing factor SWAP, transcript variant X5
splicing factor SWAP, transcript variant X6
splicing factor, suppressor of white-apricot homolog isoform X4
membrane-associated phosphatidylinositol transfer protein 2, transcript variant X1
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 5 samples with support for all annotated introns
membrane-associated phosphatidylinositol transfer protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
membrane-associated phosphatidylinositol transfer protein 2 isoform X2
membrane-associated phosphatidylinositol transfer protein 2 isoform X1
M-phase phosphoprotein 9-like, transcript variant X2
M-phase phosphoprotein 9-like, transcript variant X3
M-phase phosphoprotein 9-like, transcript variant X4
M-phase phosphoprotein 9-like, transcript variant X1
M-phase phosphoprotein 9-like isoform X2
M-phase phosphoprotein 9-like isoform X3
M-phase phosphoprotein 9-like isoform X4
M-phase phosphoprotein 9-like isoform X1
mitochondrial translation release factor in rescue, transcript variant X2
mitochondrial translation release factor in rescue, transcript variant X1
mitochondrial translation release factor in rescue, transcript variant X3
mitochondrial translation release factor in rescue, transcript variant X4
mitochondrial translation release factor in rescue
2-oxoglutarate and iron-dependent oxygenase domain containing 2, transcript variant X3
2-oxoglutarate and iron-dependent oxygenase domain containing 2, transcript variant X4
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 2 isoform X4
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 2 isoform X3
2-oxoglutarate and iron-dependent oxygenase domain containing 2, transcript variant X6
2-oxoglutarate and iron-dependent oxygenase domain containing 2, transcript variant X1
2-oxoglutarate and iron-dependent oxygenase domain containing 2, transcript variant X5
2-oxoglutarate and iron-dependent oxygenase domain containing 2, transcript variant X2
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 2 isoform X5
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 2 isoform X2
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 2 isoform X1
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 2 isoform X6
uncharacterized protein LOC503528 homolog, transcript variant X1
uncharacterized protein LOC503528 homolog, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized protein LOC503528 homolog, transcript variant X3
uncharacterized protein LOC503528 homolog, transcript variant X4
uncharacterized protein LOC503528 homolog, transcript variant X2
uncharacterized protein zgc:113436 isoform X1
uncharacterized protein zgc:113436 isoform X3
uncharacterized protein zgc:113436 isoform X2
membrane-associated phosphatidylinositol transfer protein 2-like
ADP-ribosylation factor-like 6 interacting protein 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
ADP-ribosylation factor-like protein 6-interacting protein 4 isoform X2
ADP-ribosylation factor-like 6 interacting protein 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ADP-ribosylation factor-like protein 6-interacting protein 4 isoform X1
ADP-ribosylation factor-like 6 interacting protein 4, transcript variant X3
ADP-ribosylation factor-like protein 6-interacting protein 4 isoform X3
piwi-like RNA-mediated gene silencing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
piwi-like RNA-mediated gene silencing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
Rab interacting lysosomal protein-like 1, transcript variant X2
Rab interacting lysosomal protein-like 1, transcript variant X4
Rab interacting lysosomal protein-like 1, transcript variant X1
Rab interacting lysosomal protein-like 1, transcript variant X3
transmembrane emp24 domain-containing protein 2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 55, transcript variant X3
DEAD (Asp-Glu-Ala-Asp) box polypeptide 55, transcript variant X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 55, transcript variant X1
ATP-dependent RNA helicase DDX55 isoform X1
ATP-dependent RNA helicase DDX55 isoform X2
eukaryotic translation initiation factor 2B, subunit 1 alpha
translation initiation factor eIF-2B subunit alpha
general transcription factor IIH, polypeptide 3, transcript variant X1
general transcription factor IIH subunit 3 isoform X1
general transcription factor IIH, polypeptide 3, transcript variant X2
general transcription factor IIH subunit 3 isoform X2
V-type proton ATPase 116 kDa subunit a 2-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 41 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain containing 92, transcript variant X5
coiled-coil domain containing 92, transcript variant X2
coiled-coil domain containing 92, transcript variant X6
coiled-coil domain containing 92, transcript variant X4
coiled-coil domain containing 92, transcript variant X3
coiled-coil domain containing 92, transcript variant X8
coiled-coil domain containing 92, transcript variant X7
coiled-coil domain containing 92, transcript variant X1
coiled-coil domain-containing protein 92 isoform X1
coiled-coil domain-containing protein 92 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
scavenger receptor class B member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 33 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments