Hypomesus transpacificus isolate Combined female chromosome 21, fHypTra1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Stomiati; Osmeriformes; Osmeridae; Hypomesus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM038992.1.\nAssembly name: fHypTra1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Genomic Variation Lab at\nUniversity of California Davis on 2022/02/04. The original\nwhole-genome shotgun project has the accession JAJTOO000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Genomic Variation Lab at University of\n California Davis\nAssembly Date :: 21-APR-2021\nAssembly Method :: IPA v. 1.3.1; scaff10x v. 4.2; SALSA2 v.\n NA; Chromonomer v. 1.13\nAssembly Name :: fHypTra1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 120.0x\nSequencing Technology :: 10X; PacBio Sequel; Hi-C\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Hypomesus transpacificus Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
USA: Fish Conservation and Culture Laboratory, Discovery Bay, California
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: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
presequence translocase associated motor 16
COORDINATES: polyA evidence [ECO:0006239]
mitochondrial import inner membrane translocase subunit tim16
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 7 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 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: 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 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
glycerophosphodiester phosphodiesterase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
MAPK regulated corepressor interacting protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
heat shock protein 75 kDa, mitochondrial
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 2 codons; deleted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 2 codons; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: CREB-binding protein-like
SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae)
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 17 samples with support for all annotated introns
structure-specific endonuclease subunit SLX4
MAPK regulated corepressor interacting protein 2
glycerophosphodiester phosphodiesterase 1, transcript variant X2
glycerophosphodiester phosphodiesterase 1, transcript variant X1
glycerophosphodiester phosphodiesterase 1 isoform X1
glycerophosphodiester phosphodiesterase 1 isoform X2
transmembrane protein 186, 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 43 samples with support for all annotated introns
transmembrane protein 186, 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 8 samples with support for all annotated introns
transmembrane protein 186, 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 43 samples with support for all annotated introns
4-aminobutyrate aminotransferase, mitochondrial-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
4-aminobutyrate aminotransferase, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
4-aminobutyrate aminotransferase, mitochondrial-like, transcript variant X2
4-aminobutyrate aminotransferase, mitochondrial-like isoform X1
4-aminobutyrate aminotransferase, mitochondrial-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
chemokine (C-X-C motif) ligand 12b (stromal cell-derived factor 1)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
X-prolyl aminopeptidase (aminopeptidase P) 1, soluble
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124483509, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC124483509, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
programmed cell death 4b, transcript variant X2
programmed cell death 4b, transcript variant X1
programmed cell death protein 4b isoform X1
programmed cell death protein 4b isoform X2
SHOC2 leucine rich repeat scaffold protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
trace amine-associated receptor 13c-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 10% 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 39% coverage of the annotated genomic feature by RNAseq alignments
patatin-like phospholipase domain containing 6
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: patatin-like phospholipase domain-containing protein 6
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 29 samples with support for all annotated introns
VPS10 domain-containing receptor SorCS1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sortilin related VPS10 domain containing receptor 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
voltage-dependent calcium channel gamma-4 subunit-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
voltage-dependent calcium channel gamma-1 subunit-like
helicase with zinc finger, transcript variant X5
helicase with zinc finger, transcript variant X4
helicase with zinc finger, transcript variant X3
helicase with zinc finger, transcript variant X1
helicase with zinc finger, transcript variant X2
probable helicase with zinc finger domain isoform X4
probable helicase with zinc finger domain isoform X3
probable helicase with zinc finger domain isoform X2
probable helicase with zinc finger domain isoform X1
26S proteasome non-ATPase regulatory subunit 12
cytoplasmic phosphatidylinositol transfer protein 1-like, transcript variant X2
cytoplasmic phosphatidylinositol transfer protein 1-like, transcript variant X4
cytoplasmic phosphatidylinositol transfer protein 1-like, transcript variant X5
cytoplasmic phosphatidylinositol transfer protein 1-like, transcript variant X6
cytoplasmic phosphatidylinositol transfer protein 1-like, transcript variant X3
cytoplasmic phosphatidylinositol transfer protein 1-like isoform X3
cytoplasmic phosphatidylinositol transfer protein 1-like isoform X2
cytoplasmic phosphatidylinositol transfer protein 1-like isoform X4
cytoplasmic phosphatidylinositol transfer protein 1-like, transcript variant X1
cytoplasmic phosphatidylinositol transfer protein 1-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
cytoplasmic phosphatidylinositol transfer protein 1-like isoform X1
cytoplasmic phosphatidylinositol transfer protein 1-like isoform X6
cytoplasmic phosphatidylinositol transfer protein 1-like isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 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 5 samples with support for all annotated introns
nucleosome-remodeling factor subunit BPTF-like
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 32 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon CCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
secretory phospholipase A2 receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
phosphoribosyl pyrophosphate synthase-associated protein 1-like, transcript variant X2
phosphoribosyl pyrophosphate synthase-associated protein 1-like, transcript variant X3
phosphoribosyl pyrophosphate synthase-associated protein 1-like, transcript variant X1
phosphoribosyl pyrophosphate synthase-associated protein 1-like, transcript variant X4
phosphoribosyl pyrophosphate synthase-associated protein 1-like, transcript variant X5
phosphoribosyl pyrophosphate synthase-associated protein 1-like isoform X2
phosphoribosyl pyrophosphate synthase-associated protein 1-like isoform X1
uncharacterized si:dkey-45d16.4, 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 14 samples with support for all annotated introns
uncharacterized si:dkey-45d16.4, transcript variant X1
uncharacterized protein si:dkey-45d16.4 isoform X2
uncharacterized protein si:dkey-45d16.4 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized LOC124483553, transcript variant X3
uncharacterized LOC124483553, transcript variant X1
uncharacterized LOC124483553, 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 15 samples with support for all annotated introns
butyrophilin subfamily 3 member A1-like, 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 1 sample with support for all annotated introns
butyrophilin subfamily 3 member A1-like, transcript variant X2
butyrophilin subfamily 3 member A1-like isoform X1
butyrophilin subfamily 3 member A1-like isoform X2
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; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: (E3-independent) E2 ubiquitin-conjugating enzyme UBE2O
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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 43 samples with support for all annotated introns
acyl-CoA oxidase 1, palmitoyl, transcript variant X1
acyl-CoA oxidase 1, palmitoyl, transcript variant X2
peroxisomal acyl-coenzyme A oxidase 1 isoform X1
peroxisomal acyl-coenzyme A oxidase 1 isoform X2
signal recognition particle subunit SRP68
polymerase (DNA directed), gamma 2, accessory subunit
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 31 samples with support for all annotated introns
DNA polymerase subunit gamma-2, mitochondrial
probable ATP-dependent RNA helicase DDX5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
U3 small nucleolar RNA-associated protein 6 homolog
SUZ12 polycomb repressive complex 2 subunit b, transcript variant X1
SUZ12 polycomb repressive complex 2 subunit b, transcript variant X2
SUZ12 polycomb repressive complex 2 subunit b, 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 25 samples with support for all annotated introns
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: 46 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
ATPase family AAA domain containing 5b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ATPase family AAA domain containing 5b, transcript variant X1
ATPase family AAA domain containing 5b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
ATPase family AAA domain-containing protein 5b isoform X1
ATPase family AAA domain-containing protein 5b isoform X2
transcription elongation factor, mitochondrial
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 44 samples with support for all annotated introns
arf-GAP with dual PH domain-containing protein 2-like
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 44 samples with support for all annotated introns
ras homolog family member T1, transcript variant X1
ras homolog family member T1, transcript variant X2
ras homolog family member T1, transcript variant X3
rhomboid, veinlet-like 3 (Drosophila), 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 8 samples with support for all annotated introns
rhomboid, veinlet-like 3 (Drosophila), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
BUB3-interacting and GLEBS motif-containing protein ZNF207b
uncharacterized protein LOC100136852 homolog, transcript variant X2
uncharacterized protein LOC100136852 homolog, transcript variant X1
coxsackievirus and adenovirus receptor homolog isoform X2
uncharacterized protein zgc:174863 isoform X1
Jupiter microtubule associated homolog 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
golgi associated, gamma adaptin ear containing, ARF binding protein 3a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
ADP-ribosylation factor-binding protein GGA3a
melanin-concentrating hormone receptor 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
melanin-concentrating hormone receptor 1
ubiquitin carboxyl-terminal hydrolase 43-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
cilia and flagella associated protein 52
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
cilia- and flagella-associated protein 52
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 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 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 19 samples with support for all annotated introns
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 42 samples with support for all annotated introns
bifunctional endo-1,4-beta-xylanase XylA-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
phosphoinositide-3-kinase, regulatory subunit 5, transcript variant X3
phosphoinositide-3-kinase, regulatory subunit 5, 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 15 samples with support for all annotated introns
phosphoinositide-3-kinase, regulatory subunit 5, 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 43 samples with support for all annotated introns
phosphoinositide 3-kinase regulatory subunit 5 isoform X1
phosphoinositide 3-kinase regulatory subunit 5 isoform X2
phosphoinositide 3-kinase regulatory subunit 6, transcript variant X4
phosphoinositide 3-kinase regulatory subunit 6, transcript variant X1
phosphoinositide 3-kinase regulatory subunit 6, transcript variant X2
phosphoinositide 3-kinase regulatory subunit 6, transcript variant X7
phosphoinositide 3-kinase regulatory subunit 6, transcript variant X3
phosphoinositide 3-kinase regulatory subunit 6, transcript variant X5
phosphoinositide 3-kinase regulatory subunit 6, transcript variant X6
phosphoinositide 3-kinase regulatory subunit 6 isoform X1
phosphoinositide 3-kinase regulatory subunit 6 isoform X2
phosphoinositide-3-kinase, regulatory subunit 6a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
bMERB domain-containing protein 1 isoform X2
phosphoinositide-3-kinase, regulatory subunit 6a, 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
bMERB domain-containing protein 1 isoform X1
myosin, heavy chain 10, non-muscle, transcript variant X1
myosin, heavy chain 10, non-muscle, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
tetratricopeptide repeat domain 26, transcript variant X1
intraflagellar transport protein 56 isoform X1
tetratricopeptide repeat domain 26, 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
intraflagellar transport protein 56 isoform X2
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: cmsearch.
small nucleolar RNA SNORA62/SNORA6 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00091
DEAD (Asp-Glu-Ala-Asp) box polypeptide 39Ab
ecotropic viral integration site 5 like, 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
ecotropic viral integration site 5 like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 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 35 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mitogen-activated protein kinase kinase 7
dual specificity mitogen-activated protein kinase kinase 7
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
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 11 samples with support for all annotated introns
proline-rich protein 36, transcript variant X2
proline-rich protein 36, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
trafficking protein particle complex subunit 5, transcript variant X1
trafficking protein particle complex subunit 5, transcript variant X2
trafficking protein particle complex subunit 5
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
LOW QUALITY PROTEIN: N-acetylmuramoyl-L-alanine amidase-like
volume-regulated anion channel subunit LRRC8E
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
cyclin-dependent kinase inhibitor 2D (p19, inhibits CDK4)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
adaptor related protein complex 1 subunit mu 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 4 bases in 4 codons; 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, 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: deleted 4 bases in 4 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transcription activator BRG1
LOW QUALITY PROTEIN: cysteine protease ATG4D-like
microtubule associated serine/threonine kinase 1a
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
microtubule-associated serine/threonine-protein kinase 1
ribonuclease H2, subunit A, transcript variant X1
ribonuclease H2, subunit A, transcript variant X2
ribonuclease H2, subunit A, transcript variant X3
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X3
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 12-like isoform X1
NACHT, LRR and PYD domains-containing protein 12-like isoform X2
NACHT, LRR and PYD domains-containing protein 12-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 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 6 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
germ cell-specific gene 1-like protein isoform X1
germ cell-specific gene 1-like protein isoform X2
SEC23 homolog B, coat complex II component, transcript variant X1
SEC23 homolog B, coat complex II component, transcript variant X2
zinc finger protein Aiolos-like, transcript variant X2
zinc finger protein Aiolos-like, transcript variant X1
insulin-like growth factor-binding protein 4
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1-like isoform X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1-like isoform X2
chemokine (C-C motif) receptor 7, transcript variant X2
chemokine (C-C motif) receptor 7, transcript variant X1
C-C chemokine receptor type 7 isoform X1
C-C chemokine receptor type 7 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
uncharacterized protein LOC124483664 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
huntingtin associated protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
huntingtin associated protein 1, 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 18 samples with support for all annotated introns
trafficking kinesin-binding protein 1 isoform X1
huntingtin associated protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
huntingtin associated protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
trafficking kinesin-binding protein 1 isoform X4
trafficking kinesin-binding protein 1 isoform X3
trafficking kinesin-binding protein 1 isoform X2
uncharacterized LOC124483578, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
uncharacterized LOC124483578, transcript variant X2
junction plakoglobin a, transcript variant X1
junction plakoglobin a, transcript variant X2
ATP-sensitive inward rectifier potassium channel 12-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ATP-sensitive inward rectifier potassium channel 12-like, transcript variant X1
ATP-sensitive inward rectifier potassium channel 12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
single-pass membrane protein with aspartate-rich tail 1b
proliferation associated nuclear element
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 32 samples with support for all annotated introns
serine hydrolase-like protein, transcript variant X1
serine hydrolase-like protein isoform X1
serine hydrolase-like protein, transcript variant X2
serine hydrolase-like protein isoform X2
serine hydrolase-like protein, 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 18 samples with support for all annotated introns
uncharacterized LOC124483313, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC124483313, transcript variant X2
uncharacterized protein LOC124483313 isoform X2
uncharacterized LOC124483313, transcript variant X1
uncharacterized protein LOC124483313 isoform X1
uncharacterized protein LOC124483313 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
activating transcription factor 7 interacting protein, transcript variant X2
activating transcription factor 7 interacting protein, transcript variant X3
activating transcription factor 7 interacting protein, transcript variant X1
activating transcription factor 7-interacting protein 1 isoform X1
activating transcription factor 7-interacting protein 1 isoform X2
glutamate receptor, ionotropic, N-methyl D-aspartate 2B, genome duplicate b
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: 3 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: glutamate receptor, ionotropic, N-methyl D-aspartate 2B, genome duplicate b
uncharacterized protein LOC100151507 homolog, transcript variant X2
uncharacterized protein LOC100151507 homolog, transcript variant X1
uncharacterized protein si:ch211-243a20.3
uncharacterized protein si:ch211-243a20.4
RNA binding fox-1 homolog 2, transcript variant X2
RNA binding fox-1 homolog 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
RNA binding fox-1 homolog 2, 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 31 samples with support for all annotated introns
RNA binding fox-1 homolog 2, 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 26 samples with support for all annotated introns
RNA binding fox-1 homolog 2, transcript variant X1
RNA binding protein fox-1 homolog 2 isoform X1
RNA binding protein fox-1 homolog 2 isoform X2
RNA binding protein fox-1 homolog 2 isoform X3
retinal cone rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma-like
endoplasmic reticulum resident protein 27
bone gamma-carboxyglutamate (gla) protein, like
target of Myb protein 1-like, transcript variant X2
target of Myb protein 1-like, transcript variant X1
guided entry of tail-anchored proteins factor 3, ATPase
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 44 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
protein Hook homolog 2-like, transcript variant X1
protein Hook homolog 2-like, transcript variant X2
JunB proto-oncogene, AP-1 transcription factor subunit a, transcript variant X1
JunB proto-oncogene, AP-1 transcription factor subunit a, transcript variant X2
junB proto-oncogene, AP-1 transcription factor subunit a isoform X1
junB proto-oncogene, AP-1 transcription factor subunit a isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
prostaglandin E receptor 1a (subtype EP1)
interleukin enhancer-binding factor 3-like, transcript variant X1
interleukin enhancer-binding factor 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
interleukin enhancer-binding factor 3-like isoform X1
interleukin enhancer-binding factor 3-like isoform X2
tartrate-resistant acid phosphatase type 5a
glutaryl-CoA dehydrogenase, mitochondrial-like
solute carrier family 44 member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
solute carrier family 44 member 2, transcript variant X3
choline transporter-like protein 2 isoform X3
choline transporter-like protein 2 isoform X1
solute carrier family 44 member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
choline transporter-like protein 2 isoform X2
uncharacterized LOC124483376, transcript variant X1
uncharacterized LOC124483376, transcript variant X2
uncharacterized LOC124483376, transcript variant X3
uncharacterized protein LOC124483376 isoform X1
uncharacterized protein LOC124483376 isoform X2
uncharacterized protein LOC124483376 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124483477, transcript variant X1
uncharacterized LOC124483477, transcript variant X2
outer dynein arm docking complex subunit 3
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
coiled-coil domain-containing protein 151
ral guanine nucleotide dissociation stimulator-like 3a, transcript variant X1
ral guanine nucleotide dissociation stimulator-like 1 isoform X1
ral guanine nucleotide dissociation stimulator-like 3a, transcript variant X2
ral guanine nucleotide dissociation stimulator-like 1 isoform X2
nuclear factor, interleukin 3 regulated, member 5, transcript variant X2
nuclear factor, interleukin 3 regulated, member 5, transcript variant X1
nuclear factor, interleukin 3 regulated, member 5 isoform X2
nuclear factor, interleukin 3 regulated, member 5 isoform X1
nuclear factor interleukin-3-regulated protein-like, transcript variant X1
nuclear factor interleukin-3-regulated protein-like, transcript variant X2
nuclear factor interleukin-3-regulated protein-like
Kruppel-like factor 1 (erythroid), transcript variant X2
Kruppel-like factor 1 (erythroid), 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 23 samples with support for all annotated introns
uncharacterized LOC124483476, 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 29 samples with support for all annotated introns
uncharacterized LOC124483476, 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
uncharacterized LOC124483472, transcript variant X1
uncharacterized LOC124483472, transcript variant X3
uncharacterized LOC124483472, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
5-demethoxyubiquinone hydroxylase, mitochondrial
ATP-binding cassette, sub-family C (CFTR/MRP), member 6a
multidrug resistance-associated protein 1
centrosomal protein 20, transcript variant X1
centrosomal protein 20, transcript variant X2
myosin, heavy chain 11a, smooth muscle, transcript variant X3
myosin, heavy chain 11a, smooth muscle, transcript variant X1
myosin, heavy chain 11a, smooth muscle, transcript variant X2
nudE neurodevelopment protein 1, transcript variant X2
nudE neurodevelopment protein 1, transcript variant X1
nudE neurodevelopment protein 1, transcript variant X3
nuclear distribution protein nudE homolog 1 isoform X1
nuclear distribution protein nudE homolog 1 isoform X2
meiosis regulator and mRNA stability factor 1, transcript variant X1
meiosis regulator and mRNA stability factor 1, transcript variant X2
meiosis regulator and mRNA stability factor 1 isoform X1
meiosis regulator and mRNA stability factor 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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 41 samples with support for all annotated introns
polyadenylate-binding protein, cytoplasmic and nuclear-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
polyadenylate-binding protein, cytoplasmic and nuclear-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
polyadenylate-binding protein, cytoplasmic and nuclear-like isoform X1
polyadenylate-binding protein, cytoplasmic and nuclear-like isoform X2
putative C-type lectin domain family 20 member A, 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 1 sample with support for all annotated introns
putative C-type lectin domain family 20 member A, transcript variant X3
putative C-type lectin domain family 20 member A, transcript variant X2
putative C-type lectin domain family 20 member A isoform X1
putative C-type lectin domain family 20 member A isoform X3
putative C-type lectin domain family 20 member A isoform X2
tripartite motif-containing protein 16-like, transcript variant X2
tripartite motif-containing protein 16-like, transcript variant X1
tripartite motif-containing protein 16-like
coiled-coil domain containing 166, transcript variant X2
coiled-coil domain containing 166, transcript variant X1
uncharacterized protein ccdc166 isoform X2
uncharacterized protein ccdc166 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 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: 5 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124483462, transcript variant X2
uncharacterized protein LOC124483462 isoform X2
uncharacterized LOC124483462, transcript variant X3
uncharacterized LOC124483462, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC124483462, transcript variant X1
uncharacterized protein LOC124483462 isoform X1
uncharacterized protein LOC124483462 isoform X3
uncharacterized LOC124483474, transcript variant X1
uncharacterized LOC124483474, 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 31 samples with support for all annotated introns
uncharacterized LOC124483759, transcript variant X2
uncharacterized LOC124483759, transcript variant X1
uncharacterized protein LOC124483759 isoform X2
uncharacterized protein LOC124483759 isoform X1
uncharacterized LOC124483560, transcript variant X3
uncharacterized LOC124483560, transcript variant X6
uncharacterized LOC124483560, transcript variant X2
uncharacterized LOC124483560, transcript variant X4
uncharacterized LOC124483560, transcript variant X7
uncharacterized LOC124483560, transcript variant X1
uncharacterized LOC124483560, transcript variant X5
uncharacterized protein LOC780838 homolog
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 49 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: apolipoprotein L5-like
protein N-terminal asparagine amidohydrolase
DEAD-box helicase 17, transcript variant X2
DEAD-box helicase 17, transcript variant X3
DEAD-box helicase 17, transcript variant X1
probable ATP-dependent RNA helicase DDX17 isoform X1
probable ATP-dependent RNA helicase DDX17 isoform X2
probable ATP-dependent RNA helicase DDX17 isoform X3
golgi-associated, gamma adaptin ear containing, ARF binding protein 1
ADP-ribosylation factor-binding protein GGA1
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 7 samples with support for all annotated introns
TAF5-like RNA polymerase II, p300/CBP-associated factor (PCAF)-associated factor, transcript variant X1
TAF5-like RNA polymerase II, p300/CBP-associated factor (PCAF)-associated factor, transcript variant X2
TAF5-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 5L isoform X1
TAF5-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 5L isoform X2
uncharacterized LOC124483266, transcript variant X2
uncharacterized LOC124483266, transcript variant X1
uncharacterized protein LOC124483266 isoform X2
uncharacterized protein LOC124483266 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
uncharacterized protein C1orf100 homolog, transcript variant X2
uncharacterized protein C1orf100 homolog, transcript variant X1
uncharacterized protein C1orf100 homolog, transcript variant X3
uncharacterized protein C1orf100 homolog isoform X1
uncharacterized protein LOC124483488 isoform X2
v-akt murine thymoma viral oncogene homolog 3b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
v-akt murine thymoma viral oncogene homolog 3b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
v-akt murine thymoma viral oncogene homolog 3b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
RAC-gamma serine/threonine-protein kinase
myeloid-associated differentiation marker homolog
testis-expressed protein 2-like, transcript variant X1
testis-expressed protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 40
caspase recruitment domain family, member 14
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: caspase recruitment domain-containing protein 14
uncharacterized protein C17orf67 homolog
tripartite motif containing 25, transcript variant X5
tripartite motif containing 25, transcript variant X2
tripartite motif containing 25, transcript variant X3
tripartite motif containing 25, transcript variant X1
tripartite motif containing 25, transcript variant X4
E3 ubiquitin/ISG15 ligase TRIM25 isoform X5
E3 ubiquitin/ISG15 ligase TRIM25 isoform X2
E3 ubiquitin/ISG15 ligase TRIM25 isoform X3
E3 ubiquitin/ISG15 ligase TRIM25 isoform X1
E3 ubiquitin/ISG15 ligase TRIM25 isoform X4
immunoglobulin superfamily member 3-like, transcript variant X2
immunoglobulin superfamily member 3-like, transcript variant X1
immunoglobulin superfamily member 3-like
uncharacterized LOC124483545, transcript variant X1
uncharacterized LOC124483545, transcript variant X4
uncharacterized LOC124483545, transcript variant X3
uncharacterized LOC124483545, transcript variant X2
SEC14-like protein 1, transcript variant X2
SEC14-like protein 1, transcript variant X1
SEC14-like protein 1, transcript variant X3
regulatory associated protein of MTOR, complex 1
platelet and endothelial cell adhesion molecule 1b
LOW QUALITY PROTEIN: platelet endothelial cell adhesion molecule
protein phosphatase 1, regulatory subunit 27b, transcript variant X1
protein phosphatase 1 regulatory subunit 27b isoform X1
protein phosphatase 1, regulatory subunit 27b, transcript variant X2
protein phosphatase 1 regulatory subunit 27b isoform X2
APC11 anaphase promoting complex subunit 11 homolog (yeast)
rho GDP-dissociation inhibitor 1-like, transcript variant X1
rho GDP-dissociation inhibitor 1-like, transcript variant X4
rho GDP-dissociation inhibitor 1-like, transcript variant X3
rho GDP-dissociation inhibitor 1-like, transcript variant X2
uncharacterized LOC124483293, transcript variant X3
uncharacterized LOC124483293, transcript variant X2
uncharacterized LOC124483293, transcript variant X1
uncharacterized LOC124483293, transcript variant X4
protein phosphatase 1, regulatory subunit 12C
protein phosphatase 1 regulatory subunit 12C
nicotinate-nucleotide pyrophosphorylase [carboxylating]-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
nicotinate-nucleotide pyrophosphorylase [carboxylating]-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
nicotinate-nucleotide pyrophosphorylase [carboxylating]-like isoform X1
nicotinate-nucleotide pyrophosphorylase [carboxylating]-like isoform X2
integrin alpha-L-like, transcript variant X1
integrin alpha-L-like, transcript variant X2
integrin alpha-L-like, transcript variant X3
integrin alpha-L-like, transcript variant X4
zinc finger CCCH domain-containing protein 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
group XIIB secretory phospholipase A2-like protein
uncharacterized LOC124483435, transcript variant X1
uncharacterized LOC124483435, 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 38 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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; deleted 6 bases in 6 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; deleted 6 bases in 6 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transcription factor Sp6
CWC25 spliceosome associated protein homolog
phosphatidylinositol 5-phosphate 4-kinase type-2 beta
polycomb group RING finger protein 2-like
CDGSH iron-sulfur domain-containing protein 3, mitochondrial-like, 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 7 samples with support for all annotated introns
CDGSH iron-sulfur domain-containing protein 3, mitochondrial-like, transcript variant X2
CDGSH iron-sulfur domain-containing protein 3, mitochondrial-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
CDGSH iron-sulfur domain-containing protein 3, mitochondrial-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
CDGSH iron-sulfur domain-containing protein 3, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
CDGSH iron-sulfur domain-containing protein 3, mitochondrial-like isoform X1
CDGSH iron-sulfur domain-containing protein 3, mitochondrial-like isoform X2
CDGSH iron-sulfur domain-containing protein 3, mitochondrial-like isoform X3
protein AF-17-like, transcript variant X2
protein AF-17-like, transcript variant X1
coiled-coil domain-containing protein 85A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: centrosomal protein of 170 kDa-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
complement C1q tumor necrosis factor-related protein 3-like
WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein
inositol 1,4,5-trisphosphate receptor-interacting protein
calcium homeostasis modulator protein 1, transcript variant X2
calcium homeostasis modulator protein 1, transcript variant X3
calcium homeostasis modulator protein 1, transcript variant X4
calcium homeostasis modulator protein 1, transcript variant X1
calcium homeostasis modulator protein 1, transcript variant X5
calcium homeostasis modulator protein 1 isoform X1
calcium homeostasis modulator protein 1 isoform X2
uncharacterized protein LOC557610 homolog
programmed cell death 11, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
programmed cell death 11, 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 38 samples with support for all annotated introns
programmed cell death 11, 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 34 samples with support for all annotated introns
ATP synthase membrane subunit DAPIT, mitochondrial
TAF5 RNA polymerase II, TATA box binding protein (TBP)-associated factor
transcription initiation factor TFIID subunit 5
internexin neuronal intermediate filament protein, alpha b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
cyclin and CBS domain divalent metal cation transport mediator 2b
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 10 samples with support for all annotated introns
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 43 samples with support for all annotated introns
polymerase (DNA directed), lambda, transcript variant X1
polymerase (DNA directed), lambda, transcript variant X2
polymerase (DNA directed), lambda, transcript variant X3
deleted in primary ciliary dyskinesia homolog (mouse)
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
LOW QUALITY PROTEIN: solute carrier family 2 member 15b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 84% 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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
stromal membrane-associated protein 1-like
LOW QUALITY PROTEIN: stromal membrane-associated protein 1-like
regulating synaptic membrane exocytosis 1b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
regulating synaptic membrane exocytosis protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC124483731, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC124483731, transcript variant X2
uncharacterized LOC124483536, transcript variant X2
uncharacterized LOC124483536, 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 44 samples with support for all annotated introns
endoplasmic reticulum oxidoreductase 1 beta, transcript variant X2
endoplasmic reticulum oxidoreductase 1 beta, transcript variant X1
endoplasmic reticulum oxidoreductase 1 beta, transcript variant X3
BTB (POZ) domain containing 3a, transcript variant X2
BTB (POZ) domain containing 3a, transcript variant X1
ESF1, nucleolar pre-rRNA processing protein, homolog (S. cerevisiae)
NADH:ubiquinone oxidoreductase complex assembly factor 5
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 43 samples with support for all annotated introns
arginine-hydroxylase NDUFAF5, mitochondrial
kinesin family member 16Ba, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
kinesin family member 16Ba, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
kinesin family member 16Ba, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
kinesin family member 16Ba, 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 7 samples with support for all annotated introns
kinesin family member 16Ba, transcript variant X2
small nuclear ribonucleoprotein polypeptide B2, transcript variant X1
small nuclear ribonucleoprotein polypeptide B2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
aprataxin and PNKP like factor, transcript variant X2
aprataxin and PNKP like factor, transcript variant X3
aprataxin and PNKP like factor, transcript variant X4
aprataxin and PNKP like factor, transcript variant X5
aprataxin and PNKP like factor, transcript variant X1
aprataxin and PNK-like factor isoform X2
aprataxin and PNK-like factor isoform X3
aprataxin and PNK-like factor isoform X1
aprataxin and PNK-like factor isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
cannabinoid receptor interacting protein 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
CB1 cannabinoid receptor-interacting protein 1a
protein phosphatase 3 (formerly 2B), regulatory s1ubunit B, alpha isoform, b
ETAA1 activator of ATR kinase a, transcript variant X2
ETAA1 activator of ATR kinase a, 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 29 samples with support for all annotated introns
ewing's tumor-associated antigen 1 isoform X2
ewing's tumor-associated antigen 1 isoform X1
sprouty related EVH1 domain containing 2a
sprouty-related, EVH1 domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 305 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
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 44 samples with support for all annotated introns
E3 ubiquitin-protein ligase pellino homolog 1-like, transcript variant X2
E3 ubiquitin-protein ligase pellino homolog 1-like, transcript variant X1
E3 ubiquitin-protein ligase pellino homolog 1-like, transcript variant X3
E3 ubiquitin-protein ligase pellino homolog 1-like
VPS54 subunit of GARP complex, transcript variant X1
VPS54 subunit of GARP complex, transcript variant X2
vacuolar protein sorting-associated protein 54 isoform X1
vacuolar protein sorting-associated protein 54 isoform X2
UTP--glucose-1-phosphate uridylyltransferase-like, transcript variant X2
UTP--glucose-1-phosphate uridylyltransferase-like, transcript variant X1
UTP--glucose-1-phosphate uridylyltransferase-like isoform X1
UTP--glucose-1-phosphate uridylyltransferase-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
phenazine biosynthesis-like domain-containing protein 1, transcript variant X1
phenazine biosynthesis-like domain-containing protein 1, transcript variant X2
phenazine biosynthesis-like domain-containing protein 1 isoform X1
phenazine biosynthesis-like domain-containing protein 2 isoform X2
uncharacterized protein LOC393502 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 78% coverage of the annotated genomic feature by RNAseq alignments
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2-like, transcript variant X3
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2-like, transcript variant X1
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2-like, transcript variant X2
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2-like
copper metabolism (Murr1) domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
copper metabolism (Murr1) domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 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 48 samples with support for all annotated introns
calponin homology domain-containing protein DDB_G0272472-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 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: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
signal-induced proliferation-associated 1 like 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
signal-induced proliferation-associated 1 like 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
signal-induced proliferation-associated 1 like 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
signal-induced proliferation-associated 1 like 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
signal-induced proliferation-associated 1 like 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
signal-induced proliferation-associated 1-like protein 2 isoform X4
signal-induced proliferation-associated 1-like protein 2 isoform X2
signal-induced proliferation-associated 1-like protein 2 isoform X3
signal-induced proliferation-associated 1-like protein 2 isoform X1
uncharacterized si:dkey-238i5.2, transcript variant X3
uncharacterized si:dkey-238i5.2, transcript variant X4
uncharacterized si:dkey-238i5.2, transcript variant X2
uncharacterized si:dkey-238i5.2, transcript variant X1
uncharacterized si:dkey-238i5.2, transcript variant X5
uncharacterized protein si:dkey-238i5.2 isoform X4
uncharacterized protein si:dkey-238i5.2 isoform X3
uncharacterized protein si:dkey-238i5.2 isoform X2
uncharacterized protein si:dkey-238i5.2 isoform X1
uncharacterized protein si:dkey-238i5.2 isoform X5
ribosomal RNA processing protein 36 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
phosphofurin acidic cluster sorting protein 2, transcript variant X1
phosphofurin acidic cluster sorting protein 2, transcript variant X2
phosphofurin acidic cluster sorting protein 2 isoform X1
phosphofurin acidic cluster sorting protein 2 isoform X2
kinesin light chain 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
kinesin light chain 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 193 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
heme-binding protein soul4, transcript variant X1
heme-binding protein soul4, transcript variant X2
MAP/microtubule affinity-regulating kinase 1
Tnf receptor-associated factor 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
Tnf receptor-associated factor 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
Tnf receptor-associated factor 5, transcript variant X5
Tnf receptor-associated factor 5, transcript variant X6
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 22 samples with support for all annotated introns
Tnf receptor-associated factor 5, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
Tnf receptor-associated factor 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
TNF receptor-associated factor 5 isoform X1
TNF receptor-associated factor 5 isoform X2
potassium voltage-gated channel subfamily H member 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
potassium voltage-gated channel subfamily H member 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
potassium voltage-gated channel subfamily H member 1-like isoform X1
potassium voltage-gated channel subfamily H member 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
post-GPI attachment to proteins GalNAc transferase 4
solute carrier family 8 member 1a, transcript variant X1
solute carrier family 8 member 1a, transcript variant X3
solute carrier family 8 member 1a, transcript variant X4
solute carrier family 8 member 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase kinase 3a, transcript variant X1
mitogen-activated protein kinase kinase kinase kinase 3a, transcript variant X2
mitogen-activated protein kinase kinase kinase kinase 3 isoform X1
mitogen-activated protein kinase kinase kinase kinase 3 isoform X2
gem (nuclear organelle) associated protein 6
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 44 samples with support for all annotated introns
uncharacterized LOC124483366, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
uncharacterized LOC124483366, transcript variant X4
uncharacterized LOC124483366, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized LOC124483366, transcript variant X1
uncharacterized LOC124483366, 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 24 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein L-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
eukaryotic translation initiation factor 4A3
serum response factor a, transcript variant X2
serum response factor a, transcript variant X1
uncharacterized protein LOC563864 homolog, transcript variant X1
uncharacterized protein LOC563864 homolog, transcript variant X2
EGF-containing fibulin-like extracellular matrix protein 1 isoform X1
EGF-containing fibulin-like extracellular matrix protein 1 isoform X2
uncharacterized LOC124483607, transcript variant X2
uncharacterized LOC124483607, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
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, including 9 samples with support for all annotated introns
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA phenylalanine (anticodon AAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
uncharacterized LOC124483566, transcript variant X2
uncharacterized LOC124483566, transcript variant X1
uncharacterized LOC124483566, transcript variant X4
uncharacterized LOC124483566, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ATP-binding cassette, sub-family C (CFTR/MRP), member 10, transcript variant X2
ATP-binding cassette, sub-family C (CFTR/MRP), member 10, transcript variant X1
ATP-binding cassette sub-family C member 10 isoform X2
ATP-binding cassette sub-family C member 10 isoform X1
ATP-binding cassette, sub-family C (CFTR/MRP), member 10, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
sp2 transcription factor, transcript variant X3
sp2 transcription factor, transcript variant X1
sp2 transcription factor, transcript variant X5
sp2 transcription factor, transcript variant X4
sp2 transcription factor, transcript variant X2
sp2 transcription factor, transcript variant X7
sp2 transcription factor, transcript variant X6
suppressor of cytokine signaling 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
suppressor of cytokine signaling 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
suppressor of cytokine signaling 7 isoform X2
suppressor of cytokine signaling 7 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial ribosomal protein L45, transcript variant X1
mitochondrial ribosomal protein L45, transcript variant X2
39S ribosomal protein L45, mitochondrial isoform X2
39S ribosomal protein L45, mitochondrial isoform X1
cell division cycle 6 homolog (S. cerevisiae)
zinc finger BED domain-containing protein 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
chromosome 21 C6orf120 homolog, transcript variant X5
chromosome 21 C6orf120 homolog, transcript variant X4
chromosome 21 C6orf120 homolog, transcript variant X9
chromosome 21 C6orf120 homolog, transcript variant X2
chromosome 21 C6orf120 homolog, transcript variant X8
chromosome 21 C6orf120 homolog, transcript variant X3
chromosome 21 C6orf120 homolog, transcript variant X6
chromosome 21 C6orf120 homolog, transcript variant X1
chromosome 21 C6orf120 homolog, transcript variant X7
UPF0669 protein C6orf120 homolog isoform X3
UPF0669 protein C6orf120 homolog isoform X2
UPF0669 protein C6orf120 homolog isoform X1
aminopeptidase puromycin sensitive, transcript variant X6
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 18 samples with support for all annotated introns
aminopeptidase puromycin sensitive, transcript variant X1
aminopeptidase puromycin sensitive, transcript variant X3
aminopeptidase puromycin sensitive, transcript variant X5
aminopeptidase puromycin sensitive, transcript variant X4
aminopeptidase puromycin sensitive, transcript variant X2
puromycin-sensitive aminopeptidase isoform X1
puromycin-sensitive aminopeptidase isoform X3
puromycin-sensitive aminopeptidase isoform X5
puromycin-sensitive aminopeptidase isoform X4
puromycin-sensitive aminopeptidase isoform X2
puromycin-sensitive aminopeptidase isoform X6
uncharacterized LOC124483298, transcript variant X4
uncharacterized LOC124483298, transcript variant X2
uncharacterized LOC124483298, transcript variant X5
uncharacterized LOC124483298, transcript variant X1
uncharacterized LOC124483298, transcript variant X3
neuroblast differentiation-associated protein AHNAK
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
mitochondrial ribosomal protein L4, transcript variant X2
mitochondrial ribosomal protein L4, transcript variant X1
39S ribosomal protein L4, mitochondrial isoform X1
39S ribosomal protein L4, mitochondrial isoform X2
HYLS1 centriolar and ciliogenesis associated, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
HYLS1 centriolar and ciliogenesis associated, transcript variant X6
HYLS1 centriolar and ciliogenesis associated, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
HYLS1 centriolar and ciliogenesis associated, 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 30 samples with support for all annotated introns
HYLS1 centriolar and ciliogenesis associated, transcript variant X7
HYLS1 centriolar and ciliogenesis associated, transcript variant X2
HYLS1 centriolar and ciliogenesis associated, transcript variant X4
HYLS1 centriolar and ciliogenesis associated, transcript variant X5
HYLS1 centriolar and ciliogenesis associated, transcript variant X3
hydrolethalus syndrome protein 1 isoform X9
hydrolethalus syndrome protein 1 isoform X6
hydrolethalus syndrome protein 1 isoform X7
hydrolethalus syndrome protein 1 isoform X2
hydrolethalus syndrome protein 1 isoform X4
hydrolethalus syndrome protein 1 isoform X1
hydrolethalus syndrome protein 1 isoform X8
uncharacterized protein hyls1 isoform X5
uncharacterized protein hyls1 isoform X3
protein tyrosine phosphatase 4A1, transcript variant X2
protein tyrosine phosphatase 4A1, transcript variant X1
lengsin, lens protein with glutamine synthetase domain
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
zinc finger and BTB domain containing 45, transcript variant X3
zinc finger and BTB domain containing 45, 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 28 samples with support for all annotated introns
zinc finger and BTB domain containing 45, transcript variant X2
zinc finger and BTB domain-containing protein 45 isoform X1
zinc finger and BTB domain-containing protein 45 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
rho-related GTP-binding protein RhoU-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 103 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
centriole, cilia and spindle-associated protein a
centriole, cilia and spindle-associated protein
nuclear pore complex protein Nup133 isoform X2
nuclear pore complex protein Nup133 isoform X1
nuclear pore complex protein Nup133 isoform X3
CSC1-like protein 2, transcript variant X2
CSC1-like protein 2, transcript variant X3
CSC1-like protein 2, transcript variant X1
CSC1-like protein 2, transcript variant X4
CSC1-like protein 2, transcript variant X5
CSC1-like protein 2, transcript variant X6
CSC1-like protein 2, transcript variant X7
equilibrative nucleoside transporter 1-like, transcript variant X3
equilibrative nucleoside transporter 1-like, transcript variant X2
equilibrative nucleoside transporter 1-like, transcript variant X1
equilibrative nucleoside transporter 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC124483769, transcript variant X2
uncharacterized LOC124483769, transcript variant X1
uncharacterized protein LOC124483769 isoform X1
uncharacterized LOC124483769, transcript variant X3
uncharacterized protein LOC124483769 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124483157, transcript variant X3
uncharacterized LOC124483157, transcript variant X2
uncharacterized protein LOC124483157 isoform X3
uncharacterized protein LOC124483157 isoform X2
uncharacterized LOC124483157, transcript variant X1
uncharacterized protein LOC124483157 isoform X1
spectrin beta chain, non-erythrocytic 1-like, transcript variant X1
spectrin beta chain, non-erythrocytic 1-like isoform X1
spectrin beta chain, non-erythrocytic 1-like, transcript variant X2
spectrin beta chain, non-erythrocytic 1-like isoform X2
spectrin beta chain, non-erythrocytic 1-like, transcript variant X3
spectrin beta chain, non-erythrocytic 1-like isoform X3
echinoderm microtubule-associated protein-like 6
mitochondrial translational initiation factor 2, transcript variant X1
mitochondrial translational initiation factor 2, transcript variant X2
translation initiation factor IF-2, mitochondrial isoform X1
translation initiation factor IF-2, mitochondrial isoform X2
SDE2 telomere maintenance homolog (S. pombe), transcript variant X3
SDE2 telomere maintenance homolog (S. pombe), transcript variant X2
SDE2 telomere maintenance homolog (S. pombe), transcript variant X1
replication stress response regulator SDE2 isoform X3
replication stress response regulator SDE2 isoform X2
replication stress response regulator SDE2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
28S ribosomal protein S28, mitochondrial
uncharacterized LOC124483194, transcript variant X1
uncharacterized LOC124483194, transcript variant X2
calpain 1, (mu/I) large subunit b, 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 4 samples with support for all annotated introns
calpain 1, (mu/I) large subunit b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
calpain 1, (mu/I) large subunit b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
calpain 1, (mu/I) large subunit b, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
calpain-1 catalytic subunit b isoform X1
calpain-1 catalytic subunit b isoform X2
calpain 2, (m/II) large subunit b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
calpain 2, (m/II) large subunit b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
calpain 2, (m/II) large subunit b isoform X2
calpain 2, (m/II) large subunit b isoform X1
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; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; 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: 108 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: C-X-C chemokine receptor type 4-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger protein 239-like, transcript variant X2
zinc finger protein 239-like, transcript variant X1
uncharacterized LOC124483352, transcript variant X2
uncharacterized LOC124483352, transcript variant X1
uncharacterized LOC124483352, transcript variant X3
uncharacterized LOC124483349, transcript variant X1
uncharacterized LOC124483349, transcript variant X2
uncharacterized protein LOC124483349 isoform X1
uncharacterized protein LOC124483349 isoform X2
uncharacterized LOC124483349, transcript variant X3
uncharacterized protein LOC124483349 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
zinc finger protein 501-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 501-like, transcript variant X4
zinc finger protein 501-like, transcript variant X2
zinc finger protein 501-like, transcript variant X3
zinc finger protein 501-like, transcript variant X6
zinc finger protein 501-like, transcript variant X5
uncharacterized protein LOC124483350 isoform X4
uncharacterized protein LOC124483350 isoform X2
uncharacterized protein LOC124483350 isoform X3
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; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 9% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein LOC124483739
GTP binding protein 2b, 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 5 samples with support for all annotated introns
GTP binding protein 2b, transcript variant X1
GTP binding protein 2b, transcript variant X4
GTP binding protein 2b, transcript variant X5
GTP binding protein 2b, transcript variant X2
GTP binding protein 2b, transcript variant X6
tumor protein p53 binding protein, 2b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
tumor protein p53 binding protein, 2b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
apoptosis-stimulating of p53 protein 2b isoform X1
apoptosis-stimulating of p53 protein 2b isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
uncharacterized protein LOC561073 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 38% coverage of the annotated genomic feature by RNAseq alignments
microtubule-associated protein 1 light chain 3 gamma
microtubule-associated proteins 1A/1B light chain 3C
striatin, calmodulin binding protein, transcript variant X1
striatin, calmodulin binding protein, transcript variant X2
striatin, calmodulin binding protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
dpy-30 histone methyltransferase complex regulatory subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124483259, transcript variant X3
uncharacterized LOC124483259, transcript variant X2
uncharacterized LOC124483259, transcript variant X1
uncharacterized protein LOC124483259 isoform X3
uncharacterized protein LOC124483259 isoform X2
uncharacterized protein LOC124483259 isoform X1
piggyBac transposable element-derived protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% coverage of the annotated genomic feature by RNAseq alignments
jagged canonical Notch ligand 1a, transcript variant X1
jagged canonical Notch ligand 1a, transcript variant X2
uncharacterized LOC124483757, transcript variant X1
uncharacterized LOC124483757, transcript variant X2
steroid-5-alpha-reductase, alpha polypeptide 2a
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 19 samples with support for all annotated introns
3-oxo-5-alpha-steroid 4-dehydrogenase 2a
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 41 samples with support for all annotated introns
ribosomal RNA processing protein 1 homolog A-like, transcript variant X1
ribosomal RNA processing protein 1 homolog A-like isoform X1
ribosomal RNA processing protein 1 homolog A-like, transcript variant X2
ribosomal RNA processing protein 1 homolog A-like isoform X2
acyl carrier protein, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
endothelial zinc finger protein induced by tumor necrosis factor alpha-like, transcript variant X1
endothelial zinc finger protein induced by tumor necrosis factor alpha-like, transcript variant X3
endothelial zinc finger protein induced by tumor necrosis factor alpha-like, transcript variant X2
endothelial zinc finger protein induced by tumor necrosis factor alpha-like, transcript variant X4
endothelial zinc finger protein induced by tumor necrosis factor alpha-like, transcript variant X5
endothelial zinc finger protein induced by tumor necrosis factor alpha-like isoform X3
endothelial zinc finger protein induced by tumor necrosis factor alpha-like isoform X2
endothelial zinc finger protein induced by tumor necrosis factor alpha-like isoform X1
endothelial zinc finger protein induced by tumor necrosis factor alpha-like isoform X4
endothelial zinc finger protein induced by tumor necrosis factor alpha-like isoform X5
uncharacterized LOC124483426, transcript variant X1
uncharacterized LOC124483426, transcript variant X2
uncharacterized protein LOC124483426 isoform X2
uncharacterized protein LOC124483426 isoform X1
zinc finger protein 572-like, transcript variant X2
zinc finger protein 572-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
zinc finger protein Xfin-like isoform X1
bifunctional apoptosis regulator-like, transcript variant X3
bifunctional apoptosis regulator-like, transcript variant X1
bifunctional apoptosis regulator-like, transcript variant X2
bifunctional apoptosis regulator-like isoform X1
bifunctional apoptosis regulator-like isoform X3
bifunctional apoptosis regulator-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
zinc finger protein 260-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
zinc finger protein 260-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 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 45 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 45 samples with support for all annotated introns
zinc finger protein 23-like, transcript variant X2
zinc finger protein 23-like, transcript variant X1
gastrula zinc finger protein XlCGF57.1-like
gastrula zinc finger protein XlCGF57.1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
gastrula zinc finger protein XlCGF57.1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
gastrula zinc finger protein XlCGF57.1-like isoform X2
zinc finger and SCAN domain-containing protein 2-like, transcript variant X2
zinc finger and SCAN domain-containing protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
zinc finger and SCAN domain-containing protein 2-like
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 26 samples with support for all annotated introns
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 26 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 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: 92% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
calmodulin-regulated spectrin-associated protein 3-like
lysophosphatidic acid receptor 2b, transcript variant X5
lysophosphatidic acid receptor 2b, transcript variant X3
lysophosphatidic acid receptor 2b isoform X2
lysophosphatidic acid receptor 2b isoform X4
lysophosphatidic acid receptor 2b, transcript variant X4
lysophosphatidic acid receptor 2b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
lysophosphatidic acid receptor 2b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
lysophosphatidic acid receptor 2b isoform X3
lysophosphatidic acid receptor 2b isoform X1
bromodomain-containing protein 4-like, transcript variant X2
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 15 samples with support for all annotated introns
bromodomain-containing protein 4-like, transcript variant X3
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 21 samples with support for all annotated introns
bromodomain-containing protein 4-like, transcript variant X1
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 40 samples with support for all annotated introns
bromodomain-containing protein 4-like isoform X2
bromodomain-containing protein 4-like isoform X3
bromodomain-containing protein 4-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
pentatricopeptide repeat-containing protein 1, mitochondrial
F-box and leucine-rich repeat protein 18
uncharacterized protein LOC678627 homolog
endoplasmic reticulum to nucleus signaling 2
serine/threonine-protein kinase/endoribonuclease IRE1
carbohydrate sulfotransferase 12-like, 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 26 samples with support for all annotated introns
carbohydrate sulfotransferase 12-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
eukaryotic translation initiation factor 3, subunit Ba
BRCA1-associated ATM activator 1, transcript variant X3
BRCA1-associated ATM activator 1, 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 9 samples with support for all annotated introns
BRCA1-associated ATM activator 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
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: 145 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
LOW QUALITY PROTEIN: zinc finger protein 2 homolog
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: 131 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
LOW QUALITY PROTEIN: zinc finger protein 436-like
zinc finger protein 599-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
zinc finger protein 599-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
zinc finger protein 599-like, transcript variant X3
uncharacterized protein LOC124483395 isoform X3
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
uncharacterized LOC124483407, transcript variant X2
uncharacterized LOC124483407, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
basement membrane-specific heparan sulfate proteoglycan core protein-like