Hypomesus transpacificus isolate Combined female chromosome 16, 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\nCM038987.1.\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.
rho guanine nucleotide exchange factor 18-like, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
rho guanine nucleotide exchange factor 18-like, transcript variant X3
rho guanine nucleotide exchange factor 18-like, transcript variant X1
rho guanine nucleotide exchange factor 18-like isoform X3
rho guanine nucleotide exchange factor 18-like isoform X1
rho guanine nucleotide exchange factor 18-like isoform X2
insulin receptor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
insulin receptor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
unconventional SNARE in the ER 1 homolog (S. cerevisiae)
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 44 samples with support for all annotated introns
cell wall protein DAN4-like, transcript variant X3
cell wall protein DAN4-like, transcript variant X2
cell wall protein DAN4-like, transcript variant X1
uncharacterized protein LOC124478763 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
DAZ interacting zinc finger protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 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: tRNAscan-SE.
transfer RNA proline (anticodon UGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
high density lipoprotein binding protein a, transcript variant X3
high density lipoprotein binding protein a, transcript variant X2
high density lipoprotein binding protein a, transcript variant X1
high density lipoprotein binding protein a isoform X3
high density lipoprotein binding protein a isoform X2
high density lipoprotein binding protein a isoform X1
FERM, RhoGEF and pleckstrin domain protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
FERM, ARHGEF and pleckstrin domain-containing protein 2
BCL2 family apoptosis regulator BOK a, transcript variant X4
BCL2 family apoptosis regulator BOK a, transcript variant X2
BCL2 family apoptosis regulator BOK a, transcript variant X3
BCL2 family apoptosis regulator BOK a, transcript variant X1
BCL2 family apoptosis regulator BOK a, transcript variant X5
bcl-2-related ovarian killer protein homolog A isoform X1
bcl-2-related ovarian killer protein homolog A isoform X2
autophagy related 4B, cysteine peptidase, transcript variant X1
autophagy related 4B, cysteine peptidase, transcript variant X2
autophagy related 4B, cysteine peptidase, transcript variant X3
deoxythymidylate kinase (thymidylate kinase)
alanine--glyoxylate and serine--pyruvate aminotransferase a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
alanine--glyoxylate and serine--pyruvate aminotransferase a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
alanine--glyoxylate and serine--pyruvate aminotransferase a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
alanine--glyoxylate and serine--pyruvate aminotransferase a
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 19 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 99% coverage of the annotated genomic feature by RNAseq alignments
selenocysteine lyase, transcript variant X2
selenocysteine lyase, transcript variant X1
selenocysteine lyase, transcript variant X5
selenocysteine lyase, transcript variant X4
selenocysteine lyase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
kelch-like family member 30, transcript variant X1
kelch-like family member 30, transcript variant X3
kelch-like family member 30, transcript variant X4
kelch-like family member 30, transcript variant X2
ciliary rootlet coiled-coil, rootletin family member 2
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: 3 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
syntaxin 11b, tandem duplicate 1, transcript variant X2
syntaxin 11b, tandem duplicate 1, transcript variant X1
monofunctional C1-tetrahydrofolate synthase, mitochondrial-like
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 43 samples with support for all annotated introns
solute carrier organic anion transporter family member 2A1-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 31 samples with support for all annotated introns
solute carrier organic anion transporter family member 2A1-like isoform X1
solute carrier organic anion transporter family member 2A1-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 2 samples with support for all annotated introns
solute carrier organic anion transporter family member 2A1-like isoform X2
RAB6B, member RAS oncogene family a, 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
RAB6B, member RAS oncogene family a, 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 24 samples with support for all annotated introns
RAB6B, member RAS oncogene family a, transcript variant X3
RAB6B, member RAS oncogene family a, transcript variant X4
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 23 samples with support for all annotated introns
RAB6B, member RAS oncogene family a isoform X3
RAB6B, member RAS oncogene family a isoform X4
RAB6B, member RAS oncogene family a isoform X1
RAB6B, member RAS oncogene family a isoform X2
uncharacterized protein LOC559250 homolog
transfer RNA proline (anticodon CGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
centrosomal protein 63, 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 33 samples with support for all annotated introns
centrosomal protein 63, transcript variant X1
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 33 samples with support for all annotated introns
centrosomal protein 63, transcript variant X3
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 13 samples with support for all annotated introns
centrosomal protein of 63 kDa isoform X1
centrosomal protein of 63 kDa isoform X2
centrosomal protein of 63 kDa isoform X3
angiomotin like 2a, transcript variant X1
angiomotin like 2a, transcript variant X2
Sin3A-associated protein a, 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 38 samples with support for all annotated introns
Sin3A-associated protein a, 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 40 samples with support for all annotated introns
histone deacetylase complex subunit SAP130a isoform X1
histone deacetylase complex subunit SAP130a isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
uracil nucleotide/cysteinyl leukotriene receptor
phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 1
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
BCL6A transcription repressor a, transcript variant X3
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 3 samples with support for all annotated introns
BCL6A transcription repressor a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
BCL6A transcription repressor a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
BCL6A transcription repressor a, transcript variant X4
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 41 samples with support for all annotated introns
BCL6A transcription repressor a, transcript variant X5
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 41 samples with support for all annotated introns
BCL6A transcription repressor a isoform X2
BCL6A transcription repressor a isoform X1
BCL6A transcription repressor a isoform X3
BCL6A transcription repressor a isoform X4
uncharacterized LOC124478571, transcript variant X2
uncharacterized LOC124478571, transcript variant X1
LIM domain containing preferred translocation partner in lipoma
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
tumor protein p63-regulated gene 1 protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
zinc finger and BTB domain containing 11
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
zinc finger and BTB domain-containing protein 11
ATPase Na+/K+ transporting subunit beta 1a
sodium/potassium-transporting ATPase subunit beta-1a
NME/NM23 family member 7, transcript variant X1
NME/NM23 family member 7, transcript variant X2
nucleoside diphosphate kinase 7 isoform X2
nucleoside diphosphate kinase 7 isoform X1
NME/NM23 family member 7, 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 16 samples with support for all annotated introns
nucleoside diphosphate kinase 7 isoform X3
translocase of inner mitochondrial membrane 13 homolog (yeast)
mitochondrial import inner membrane translocase subunit Tim13
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: 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.
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 43 samples with support for all annotated introns
Jun proto-oncogene, AP-1 transcription factor subunit
CARD- and ANK-containing Inflammasome Adaptor Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
CARD- and ANK-domain containing inflammasome adapter protein
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 34 samples with support for all annotated introns
uncharacterized protein LOC557342 homolog, transcript variant X1
uncharacterized protein LOC557342 homolog, 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 33 samples with support for all annotated introns
uncharacterized protein LOC557342 homolog, 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 40 samples with support for all annotated introns
uncharacterized protein si:dkey-86e18.1 isoform X1
uncharacterized protein si:dkey-86e18.1 isoform X2
Fas ligand (TNF superfamily, member 6), 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 40 samples with support for all annotated introns
Fas ligand (TNF superfamily, member 6), 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 41 samples with support for all annotated introns
tumor necrosis factor ligand superfamily member 6 isoform X1
tumor necrosis factor ligand superfamily member 6 isoform X2
FAM20B glycosaminoglycan xylosylkinase, 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 43 samples with support for all annotated introns
FAM20B glycosaminoglycan xylosylkinase, 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 20 samples with support for all annotated introns
uncharacterized protein LOC405808 homolog
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 44 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
deleted in malignant brain tumors 1 protein-like
nuclear receptor ROR-beta-like, transcript variant X1
nuclear receptor ROR-beta-like, transcript variant X3
nuclear receptor ROR-beta-like, transcript variant X2
nuclear receptor ROR-beta-like isoform X1
nuclear receptor ROR-beta-like isoform X3
nuclear receptor ROR-beta-like isoform 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 43 samples with support for all annotated introns
tumor necrosis factor, alpha-induced protein 8-like 1
tumor necrosis factor alpha-induced protein 8-like protein 1
SIN3 transcription regulator family member B
xenotropic and polytropic retrovirus receptor 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
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
acyl-CoA-binding domain-containing protein 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments
sterol O-acyltransferase 1, transcript variant X1
sterol O-acyltransferase 1, transcript variant X2
c-abl oncogene 2, non-receptor tyrosine kinase, transcript variant X1
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 42 samples with support for all annotated introns
c-abl oncogene 2, non-receptor tyrosine kinase, 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 14 samples with support for all annotated introns
c-abl oncogene 2, non-receptor tyrosine kinase, transcript variant X3
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 42 samples with support for all annotated introns
c-abl oncogene 2, non-receptor tyrosine kinase, transcript variant X5
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 43 samples with support for all annotated introns
c-abl oncogene 2, non-receptor tyrosine kinase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
oxysterol binding protein-like 9, transcript variant X2
oxysterol binding protein-like 9, transcript variant X1
oxysterol binding protein-like 9, transcript variant X3
oxysterol-binding protein-related protein 9 isoform X2
oxysterol-binding protein-related protein 9 isoform X1
oxysterol-binding protein-related protein 9 isoform X3
oxysterol binding protein-like 9, transcript variant X4
oxysterol-binding protein-related protein 9 isoform X4
oxysterol binding protein-like 9, transcript variant X7
oxysterol binding protein-like 9, transcript variant X6
oxysterol-binding protein-related protein 9 isoform X6
oxysterol-binding protein-related protein 9 isoform X7
oxysterol binding protein-like 9, transcript variant X5
oxysterol-binding protein-related protein 9 isoform X5
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00284
COORDINATES: nucleotide motif:Rfam:12.0:RF00152
small nucleolar RNA snR60/Z15/Z230/Z193/J17
COORDINATES: nucleotide motif:Rfam:12.0:RF00309
COORDINATES: nucleotide motif:Rfam:12.0:RF00592
COORDINATES: nucleotide motif:Rfam:12.0:RF00281
epidermal growth factor receptor pathway substrate 15, 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 39 samples with support for all annotated introns
epidermal growth factor receptor pathway substrate 15, 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 43 samples with support for all annotated introns
epidermal growth factor receptor substrate 15-like 1 isoform X1
epidermal growth factor receptor substrate 15 isoform 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 40 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 89% 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
inactive N-acetylated-alpha-linked acidic dipeptidase-like protein 2
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
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
F-box-like/WD repeat-containing protein TBL1XR1a
calcium-activated potassium channel subunit beta-2, transcript variant X2
calcium-activated potassium channel subunit beta-2, transcript variant X1
calcium-activated potassium channel subunit beta-2 isoform X1
calcium-activated potassium channel subunit beta-2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
lysosome-associated membrane glycoprotein 3
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
methylcrotonoyl-CoA carboxylase subunit alpha, mitochondrial
ATPase phospholipid transporting 11B (putative), transcript variant X1
phospholipid-transporting ATPase IF isoform X1
ATPase phospholipid transporting 11B (putative), 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 14 samples with support for all annotated introns
phospholipid-transporting ATPase IF isoform 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 41 samples with support for all annotated introns
inaD-like protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
inaD-like protein, 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 23 samples with support for all annotated introns
inaD-like protein, transcript variant X2
single-stranded DNA-binding protein 3-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: 2 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: single-stranded DNA-binding protein 3-like
NFX1-type zinc finger-containing protein 1
DEAD (Asp-Glu-Ala-Asp) box polypeptide 27, transcript variant X1
probable ATP-dependent RNA helicase DDX27 isoform X1
DEAD (Asp-Glu-Ala-Asp) box polypeptide 27, 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 42 samples with support for all annotated introns
probable ATP-dependent RNA helicase DDX27 isoform X2
small nuclear ribonucleoprotein polypeptides B and B1
small nuclear ribonucleoprotein-associated proteins B and B'
E3 ubiquitin-protein ligase RNF182, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF182, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF182, 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 31 samples with support for all annotated introns
regulator of G-protein signaling 9-binding protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
deoxynucleotidyltransferase terminal-interacting protein 1, transcript variant X7
deoxynucleotidyltransferase terminal-interacting protein 1, transcript variant X2
deoxynucleotidyltransferase terminal-interacting protein 1, transcript variant X6
deoxynucleotidyltransferase terminal-interacting protein 1, transcript variant X3
deoxynucleotidyltransferase terminal-interacting protein 1, transcript variant X5
deoxynucleotidyltransferase terminal-interacting protein 1, transcript variant X1
deoxynucleotidyltransferase terminal-interacting protein 1, transcript variant X4
deoxynucleotidyltransferase terminal-interacting protein 1 isoform X2
deoxynucleotidyltransferase terminal-interacting protein 1 isoform X1
phosphorylated CTD interacting factor 1, transcript variant X2
phosphorylated CTD interacting factor 1, transcript variant X1
mRNA (2'-O-methyladenosine-N(6)-)-methyltransferase
phospholipid transfer protein, transcript variant X2
phospholipid transfer protein, transcript variant X1
phospholipid transfer protein isoform X1
phospholipid transfer protein, transcript variant X3
phospholipid transfer protein isoform X2
cytochrome c1, heme protein, mitochondrial
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 4 bases in 3 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: endoplasmic reticulum-Golgi intermediate compartment protein 3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 3 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: reactive oxygen species modulator 1
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00581
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
CSE1 chromosome segregation 1-like (yeast)
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 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: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
uncharacterized protein C6orf132 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TRAF3-interacting JNK-activating modulator-like, 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 14 samples with support for all annotated introns
TRAF3-interacting JNK-activating modulator-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 38 samples with support for all annotated introns
TRAF3-interacting JNK-activating modulator-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
TRAF3-interacting JNK-activating modulator-like
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
epidermal growth factor receptor kinase substrate 8-like protein 3
adenosine monophosphate deaminase 2a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
adenosine monophosphate deaminase 2a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
adenosine monophosphate deaminase 2a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
adenosine monophosphate deaminase 2a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
adenosine monophosphate deaminase 2a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
adenosine monophosphate deaminase 2a, transcript variant X6
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 21 samples with support for all annotated introns
guanine nucleotide-binding protein G(t) subunit alpha-2-like
guanine nucleotide-binding protein G(i) subunit alpha-3-like
G-protein coupled receptor 61-like, transcript variant X1
G-protein coupled receptor 61-like, transcript variant X2
amphoterin-induced protein 1-like, 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 3 samples with support for all annotated introns
amphoterin-induced protein 1-like, transcript variant X1
amphoterin-induced protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
sodium-dependent neutral amino acid transporter SLC6A17-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transcription factor AP-2 gamma (activating enhancer binding protein 2 gamma), transcript variant X3
transcription factor AP-2 gamma (activating enhancer binding protein 2 gamma), transcript variant X5
transcription factor AP-2 gamma (activating enhancer binding protein 2 gamma), transcript variant X4
transcription factor AP-2 gamma (activating enhancer binding protein 2 gamma), transcript variant X2
transcription factor AP-2 gamma (activating enhancer binding protein 2 gamma), transcript variant X1
transcription factor AP-2 gamma isoform X5
transcription factor AP-2 gamma isoform X3
transcription factor AP-2 gamma isoform X4
transcription factor AP-2 gamma isoform X2
transcription factor AP-2 gamma isoform X1
glucosaminyl (N-acetyl) transferase family member 7, transcript variant X1
glucosaminyl (N-acetyl) transferase family member 7, transcript variant X2
beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 7 isoform X1
beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 7 isoform X2
EYA transcriptional coactivator and phosphatase 2, transcript variant X2
EYA transcriptional coactivator and phosphatase 2, transcript variant X1
EYA transcriptional coactivator and phosphatase 2, transcript variant X3
itchy E3 ubiquitin protein ligase a, transcript variant X3
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 20 samples with support for all annotated introns
itchy E3 ubiquitin protein ligase a, transcript variant X1
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 43 samples with support for all annotated introns
itchy E3 ubiquitin protein ligase a, transcript variant X2
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 36 samples with support for all annotated introns
N-terminal EF-hand calcium binding protein 3, transcript variant X1
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
N-terminal EF-hand calcium-binding protein 1 isoform X1
N-terminal EF-hand calcium binding protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
N-terminal EF-hand calcium-binding protein 1 isoform 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 42 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 26 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 34 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 46
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
sarcoglycan, beta (dystrophin-associated glycoprotein)
uncharacterized protein LOC124478625 isoform X2
uncharacterized protein LOC124478625 isoform X3
uncharacterized protein LOC124478625 isoform X4
DCN1, defective in cullin neddylation 1, domain containing 4 (S. cerevisiae), transcript variant X1
DCN1, defective in cullin neddylation 1, domain containing 4 (S. cerevisiae), transcript variant X2
DCN1, defective in cullin neddylation 1, domain containing 4 (S. cerevisiae), transcript variant X4
DCN1, defective in cullin neddylation 1, domain containing 4 (S. cerevisiae), transcript variant X3
furry homolog, like, transcript variant X7
furry homolog, like, transcript variant X1
furry homolog, like, transcript variant X2
furry homolog, like, transcript variant X3
furry homolog, like, transcript variant X5
furry homolog, like, transcript variant X6
furry homolog, like, 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 2 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 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SLAIN motif family, member 2, transcript variant X4
SLAIN motif family, member 2, transcript variant X3
SLAIN motif family, member 2, transcript variant X2
SLAIN motif family, member 2, transcript variant X1
SLAIN motif-containing protein 2 isoform X4
SLAIN motif-containing protein 2 isoform X3
SLAIN motif-containing protein 2 isoform X2
SLAIN motif-containing protein 2 isoform X1
palladin, cytoskeletal associated protein
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
carbonyl reductase 4, transcript variant X1
carbonyl reductase 4, transcript variant X2
carbonyl reductase family member 4 isoform X2
carbonyl reductase family member 4 isoform X1
NIMA-related kinase 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
NIMA-related kinase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NIMA-related kinase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NIMA-related kinase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
serine/threonine-protein kinase Nek1 isoform X3
serine/threonine-protein kinase Nek1 isoform X2
serine/threonine-protein kinase Nek1 isoform 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 43 samples with support for all annotated introns
coiled-coil and C2 domain containing 2A, transcript variant X2
coiled-coil and C2 domain containing 2A, transcript variant X3
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 5 samples with support for all annotated introns
coiled-coil and C2 domain containing 2A, 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 4 samples with support for all annotated introns
coiled-coil and C2 domain-containing protein 2A isoform X2
coiled-coil and C2 domain-containing protein 2A isoform X1
NACHT, LRR and PYD domains-containing protein 12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 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 98% coverage of the annotated genomic feature by RNAseq alignments
vitelline membrane outer layer protein 1 homolog
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
complement C1q tumor necrosis factor-related protein 7, transcript variant X1
complement C1q tumor necrosis factor-related protein 7, transcript variant X2
complement C1q tumor necrosis factor-related protein 7 isoform X1
complement C1q tumor necrosis factor-related protein 7 isoform X2
cytoplasmic polyadenylation element-binding protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
pancreas/duodenum homeobox protein 1-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 17 samples with support for all annotated introns
platelet-derived growth factor receptor, alpha polypeptide
LOW QUALITY PROTEIN: platelet-derived growth factor receptor alpha
KIT proto-oncogene, receptor tyrosine kinase a, transcript variant X1
KIT proto-oncogene, receptor tyrosine kinase a, transcript variant X2
mast/stem cell growth factor receptor kita isoform X1
mast/stem cell growth factor receptor kita isoform X2
KIT proto-oncogene, receptor tyrosine kinase a, transcript variant X3
mast/stem cell growth factor receptor kita isoform X3
kinase insert domain receptor (a type III receptor tyrosine kinase), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
kinase insert domain receptor (a type III receptor tyrosine kinase), transcript variant X1
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
vascular endothelial growth factor receptor 2 isoform X2
vascular endothelial growth factor receptor 2 isoform X1
steroid 5 alpha-reductase 3, transcript variant X1
steroid 5 alpha-reductase 3, transcript variant X2
steroid 5 alpha-reductase 3, transcript variant X3
steroid 5 alpha-reductase 3, transcript variant X4
clock circadian regulator a, transcript variant X3
clock circadian regulator a, transcript variant X4
clock circadian regulator a, transcript variant X1
clock circadian regulator a, transcript variant X2
circadian locomoter output cycles protein kaput isoform X2
circadian locomoter output cycles protein kaput isoform X3
circadian locomoter output cycles protein kaput isoform X1
uncharacterized LOC124478501, transcript variant X1
uncharacterized LOC124478501, 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 13 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 5 bases in 5 codons; deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 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 5 bases in 5 codons; deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: exocyst complex component 1-like
exocyst complex component 1-like, transcript variant X1
exocyst complex component 1-like, transcript variant X6
exocyst complex component 1-like, transcript variant X4
exocyst complex component 1-like, transcript variant X5
exocyst complex component 1-like, transcript variant X7
exocyst complex component 1-like, transcript variant X2
exocyst complex component 1-like, transcript variant X3
exocyst complex component 1-like isoform X1
exocyst complex component 1-like isoform X4
exocyst complex component 1-like isoform X2
exocyst complex component 1-like isoform X3
exocyst complex component 1-like isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
large 60S subunit nuclear export GTPase 1
family with sequence similarity 43 member A
ectoderm-neural cortex protein 1-like, transcript variant X1
ectoderm-neural cortex protein 1-like, transcript variant X2
ectoderm-neural cortex protein 1-like isoform X1
ectoderm-neural cortex protein 1-like isoform X2
uncharacterized protein LOC337599 homolog, transcript variant X1
uncharacterized protein LOC337599 homolog, 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 43 samples with support for all annotated introns
homocysteine S-methyltransferase isoform X1
homocysteine S-methyltransferase isoform X2
basic immunoglobulin-like variable motif-containing protein, transcript variant X2
basic immunoglobulin-like variable motif-containing protein, transcript variant X1
basic immunoglobulin-like variable motif-containing protein isoform X2
basic immunoglobulin-like variable motif-containing protein isoform X1
uncharacterized protein LOC555526 homolog
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 4 samples with support for all annotated introns
inosine-uridine preferring nucleoside hydrolase
transmembrane protein 131, transcript variant X1
transmembrane protein 131, transcript variant X2
von Willebrand factor A domain-containing protein 3B-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 2 samples with support for all annotated introns
von Willebrand factor A domain-containing protein 3B-like, transcript variant X2
von Willebrand factor A domain-containing protein 3B-like, transcript variant X3
von Willebrand factor A domain-containing protein 3B-like isoform X1
von Willebrand factor A domain-containing protein 3B-like isoform X2
von Willebrand factor A domain-containing protein 3B-like isoform X3
cyclic nucleotide gated channel subunit alpha 3a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
cyclic nucleotide-gated channel cone photoreceptor subunit alpha
gamma-aminobutyric acid receptor subunit beta-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit alpha-5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit gamma-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
epidermal growth factor receptor substrate 15-like 1
RAD23 homolog A, nucleotide excision repair protein b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
RAD23 homolog A, nucleotide excision repair protein b, transcript variant 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, including 19 samples with support for all annotated introns
RAD23 homolog A, nucleotide excision repair protein b isoform X2
RAD23 homolog A, nucleotide excision repair protein b isoform X1
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized protein C19orf44 homolog
calcium homeostasis endoplasmic reticulum protein, transcript variant X4
calcium homeostasis endoplasmic reticulum protein, transcript variant X5
calcium homeostasis endoplasmic reticulum protein, transcript variant X2
calcium homeostasis endoplasmic reticulum protein, transcript variant X3
calcium homeostasis endoplasmic reticulum protein, transcript variant X1
calcium homeostasis endoplasmic reticulum protein, transcript variant X6
calcium homeostasis endoplasmic reticulum protein, transcript variant X7
calcium homeostasis endoplasmic reticulum protein, transcript variant X8
calcium homeostasis endoplasmic reticulum protein isoform X4
calcium homeostasis endoplasmic reticulum protein isoform X5
calcium homeostasis endoplasmic reticulum protein isoform X2
calcium homeostasis endoplasmic reticulum protein isoform X3
calcium homeostasis endoplasmic reticulum protein isoform X1
calcium homeostasis endoplasmic reticulum protein isoform X6
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 12 samples with support for all annotated introns
megakaryocyte-associated tyrosine kinase
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 34 samples with support for all annotated introns
megakaryocyte-associated tyrosine-protein kinase
ATCAY kinesin light chain interacting caytaxin a
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
muscle-specific beta 1 integrin binding protein, transcript variant X1
muscle-specific beta 1 integrin binding protein, transcript variant X2
muscle-specific beta 1 integrin binding protein isoform X1
muscle-specific beta 1 integrin binding protein isoform X2
TSC22 domain family 2, transcript variant X1
TSC22 domain family protein 2 isoform X1
TSC22 domain family 2, transcript variant X2
TSC22 domain family protein 2 isoform X2
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
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; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: E3 ubiquitin-protein ligase RNF13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
protein phosphatase 1, regulatory (inhibitor) subunit 2
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like, transcript variant X2
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like, transcript variant X1
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like isoform X1
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like isoform X2
26S proteasome non-ATPase regulatory subunit 1
5-hydroxytryptamine (serotonin) receptor 2B, G protein-coupled
COORDINATES: nucleotide motif:Rfam:12.0:RF00397
uncharacterized LOC124478790, transcript variant X4
uncharacterized LOC124478790, transcript variant X5
uncharacterized LOC124478790, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC124478790, 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 12 samples with support for all annotated introns
uncharacterized LOC124478790, transcript variant X2
uncharacterized protein LOC124478790 isoform X1
uncharacterized protein LOC124478790 isoform X3
uncharacterized protein LOC124478790 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin specific peptidase 13, 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 28 samples with support for all annotated introns
ubiquitin specific peptidase 13, 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 32 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 13 isoform X2
ubiquitin carboxyl-terminal hydrolase 13 isoform X1
NADH:ubiquinone oxidoreductase subunit B5
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 5, mitochondrial
39S ribosomal protein L47, mitochondrial
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
pre-rRNA 2'-O-ribose RNA methyltransferase FTSJ3
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 7 samples with support for all annotated introns
GRAM domain-containing protein 2B, transcript variant X1
GRAM domain-containing protein 2B, transcript variant X2
GRAM domain-containing protein 2B isoform X1
GRAM domain-containing protein 2B isoform X2
GIPC PDZ domain containing family, member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
thromboxane A2 receptor, transcript variant X1
thromboxane A2 receptor, transcript variant X3
thromboxane A2 receptor, transcript variant X2
thromboxane A2 receptor, 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 19 samples with support for all annotated introns
protein tyrosine phosphatase receptor type Sa
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 5 bases in 4 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 5 bases in 4 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: receptor-type tyrosine-protein phosphatase S
lysine (K)-specific demethylase 4B, transcript variant X1
lysine (K)-specific demethylase 4B, transcript variant X2
ubiquitin-like with PHD and ring finger domains 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
ubiquitin-like with PHD and ring finger domains 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 43 samples with support for all annotated introns
small conductance calcium-activated potassium channel protein 3-like
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 1 sample with support for all annotated introns
coiled-coil domain-containing protein 124
epithelial cell transforming 2, transcript variant X4
epithelial cell transforming 2, transcript variant X3
epithelial cell transforming 2, 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 23 samples with support for all annotated introns
epithelial cell transforming 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
guanine nucleotide exchange factor DBS-like, transcript variant X1
guanine nucleotide exchange factor DBS-like, transcript variant X2
guanine nucleotide exchange factor DBS-like, transcript variant X4
guanine nucleotide exchange factor DBS-like isoform X4
guanine nucleotide exchange factor DBS-like isoform X2
guanine nucleotide exchange factor DBS-like isoform X1
guanine nucleotide exchange factor DBS-like, transcript variant X3
guanine nucleotide exchange factor DBS-like isoform X3
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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: replication factor C subunit 4-like
rubicon autophagy regulator, 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 28 samples with support for all annotated introns
rubicon autophagy regulator, transcript variant X4
rubicon autophagy regulator, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
rubicon autophagy regulator, transcript variant X5
rubicon autophagy regulator, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
run domain Beclin-1-interacting and cysteine-rich domain-containing protein isoform X1
run domain Beclin-1-interacting and cysteine-rich domain-containing protein isoform X4
run domain Beclin-1-interacting and cysteine-rich domain-containing protein isoform X3
run domain Beclin-1-interacting and cysteine-rich domain-containing protein isoform X5
run domain Beclin-1-interacting and cysteine-rich domain-containing protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC124478643, transcript variant X2
uncharacterized LOC124478643, transcript variant X1
uncharacterized protein LOC124478643 isoform X2
uncharacterized protein LOC124478643 isoform X1
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 41 samples with support for all annotated introns
dynein light chain Tctex-type protein 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 1 sample with support for all annotated introns
hydroxylysine kinase, tandem duplicate 2, 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 32 samples with support for all annotated introns
hydroxylysine kinase, tandem duplicate 2, 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 16 samples with support for all annotated introns
ephrin type-B receptor 3-like, transcript variant X2
ephrin type-B receptor 3-like, transcript variant X3
ephrin type-B receptor 3-like, transcript variant X7
ephrin type-B receptor 3-like, transcript variant X1
ephrin type-B receptor 3-like, transcript variant X6
ephrin type-B receptor 3-like, transcript variant X4
ephrin type-B receptor 3-like, transcript variant X5
ephrin type-B receptor 3-like, transcript variant X8
ephrin type-B receptor 3-like isoform X2
ephrin type-B receptor 3-like isoform X3
ephrin type-B receptor 3-like isoform X7
ephrin type-B receptor 3-like isoform X1
ephrin type-B receptor 3-like isoform X6
ephrin type-B receptor 3-like isoform X4
ephrin type-B receptor 3-like isoform X5
ephrin type-B receptor 3-like isoform X8
major facilitator superfamily domain containing 8-like 1, transcript variant X3
major facilitator superfamily domain containing 8-like 1, transcript variant X1
major facilitator superfamily domain containing 8-like 1, transcript variant X2
major facilitator superfamily domain-containing protein 8
DNA-directed RNA polymerases I, II, and III subunit RPABC3
lisH domain-containing protein ARMC9, transcript variant X1
lisH domain-containing protein ARMC9, transcript variant X2
lisH domain-containing protein ARMC9 isoform X1
lisH domain-containing protein ARMC9 isoform X2
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7
COORDINATES: nucleotide motif:Rfam:12.0:RF00072
COORDINATES: nucleotide motif:Rfam:12.0:RF00191
natriuretic peptide C, transcript variant X4
natriuretic peptide C, transcript variant X2
natriuretic peptide C, transcript variant X3
natriuretic peptide C, transcript variant X1
alkaline phosphatase, intestinal, tandem duplicate 1, 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 10 samples with support for all annotated introns
alkaline phosphatase, intestinal, tandem duplicate 1, 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 32 samples with support for all annotated introns
alkaline phosphatase, intestinal, tandem duplicate 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
alkaline phosphatase, intestinal, tandem duplicate 1 isoform X3
alkaline phosphatase, intestinal, tandem duplicate 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
alkaline phosphatase, intestinal, tandem duplicate 1 isoform X2
alkaline phosphatase, intestinal, tandem duplicate 1, 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 9 samples with support for all annotated introns
alkaline phosphatase, intestinal, tandem duplicate 1 isoform X1
alkaline phosphatase, intestinal, tandem duplicate 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ankyrin repeat and LEM domain containing 1, transcript variant X1
ankyrin repeat and LEM domain containing 1, transcript variant X2
ankyrin repeat and LEM domain-containing protein 1 isoform X1
ankyrin repeat and LEM domain-containing protein 1 isoform X2
nuclear receptor subfamily 5, group A, member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
nuclear receptor subfamily 5 group A member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
kinesin family member 14, transcript variant X2
kinesin family member 14, transcript variant X1
DEAD (Asp-Glu-Ala-Asp) box polypeptide 59, transcript variant X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 59, transcript variant X1
probable ATP-dependent RNA helicase DDX59 isoform X2
probable ATP-dependent RNA helicase DDX59 isoform X1
calmodulin regulated spectrin-associated protein family, member 2a, transcript variant X2
calmodulin regulated spectrin-associated protein family, member 2a, transcript variant X1
calmodulin-regulated spectrin-associated protein 2a isoform X1
calmodulin-regulated spectrin-associated protein 2a isoform X2
17-beta-hydroxysteroid dehydrogenase 14-like
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 44 samples with support for all annotated introns
calmodulin regulated spectrin-associated protein family, member 2a, transcript variant X3
calmodulin-regulated spectrin-associated protein 2a isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 183 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 193 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
afadin- and alpha-actinin-binding protein-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
afadin- and alpha-actinin-binding protein-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 3 samples with support for all annotated introns
afadin- and alpha-actinin-binding protein-like, transcript variant X3
afadin- and alpha-actinin-binding protein-like isoform X1
afadin- and alpha-actinin-binding protein-like isoform X2
atrial natriuretic peptide receptor 2-like
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
lysophosphatidic acid receptor 3, transcript variant X2
lysophosphatidic acid receptor 3, transcript variant X1
lysophosphatidic acid receptor 3, transcript variant X3
lysophosphatidic acid receptor 3 isoform X1
lysophosphatidic acid receptor 3 isoform X2
mucolipin TRP cation channel 2, 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 9 samples with support for all annotated introns
mucolipin TRP cation channel 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 18 samples with support for all annotated introns
mucolipin TRP cation channel 2, transcript variant X4
mucolipin TRP cation channel 2, 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 25 samples with support for all annotated introns
mucolipin TRP cation channel 2, 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 25 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 5% coverage of the annotated genomic feature by RNAseq alignments
adhesion G protein-coupled receptor L4, 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 39 samples with support for all annotated introns
adhesion G protein-coupled receptor L4, 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 30 samples with support for all annotated introns
adhesion G protein-coupled receptor L4 isoform X1
adhesion G protein-coupled receptor L4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
neuronal growth regulator 1, transcript variant X1
neuronal growth regulator 1, transcript variant X2
uncharacterized LOC124478641, transcript variant X2
uncharacterized LOC124478641, transcript variant X1
uncharacterized LOC124478745, transcript variant X2
uncharacterized LOC124478745, transcript variant X3
uncharacterized protein LOC124478745 isoform X3
uncharacterized protein LOC124478745 isoform X2
uncharacterized LOC124478745, transcript variant X1
uncharacterized protein LOC124478745 isoform X1
zinc finger, RAN-binding domain containing 2
zinc finger Ran-binding domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
neural retina-specific leucine zipper protein
phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase
phosphoribosyl pyrophosphate amidotransferase
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 44 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 7% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 259, transcript variant X4
transmembrane protein 259, transcript variant X5
transmembrane protein 259, transcript variant X1
transmembrane protein 259, 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 19 samples with support for all annotated introns
transmembrane protein 259, 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 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61% coverage of the annotated genomic feature by RNAseq alignments
adhesion G protein-coupled receptor L2a, 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
adhesion G protein-coupled receptor L2a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
adhesion G protein-coupled receptor L2a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
adhesion G protein-coupled receptor L2 isoform X1
adhesion G protein-coupled receptor L2 isoform X2
adhesion G protein-coupled receptor L2 isoform X3
tubulin tyrosine ligase-like family, member 7, transcript variant X3
tubulin tyrosine ligase-like family, member 7, transcript variant X2
tubulin tyrosine ligase-like family, member 7, transcript variant X1
tubulin tyrosine ligase-like family, member 7, transcript variant X5
tubulin polyglutamylase TTLL7 isoform X1
tubulin polyglutamylase TTLL7 isoform X3
tubulin tyrosine ligase-like family, member 7, transcript variant X4
tubulin polyglutamylase TTLL7 isoform X2
tubulin tyrosine ligase-like family, member 7, transcript variant X6
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 13 samples with support for all annotated introns
tubulin polyglutamylase TTLL7 isoform X4
protein kinase, cAMP-dependent, catalytic, beta a, transcript variant X2
protein kinase, cAMP-dependent, catalytic, beta a, transcript variant X3
protein kinase, cAMP-dependent, catalytic, beta a isoform X2
protein kinase, cAMP-dependent, catalytic, beta a isoform X3
protein kinase, cAMP-dependent, catalytic, beta a, transcript variant X1
protein kinase, cAMP-dependent, catalytic, beta a isoform X1
sterile alpha motif domain containing 13
sterile alpha motif domain-containing protein 13
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: 3 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: deoxyribonuclease-2-beta
guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-5, transcript variant X3
guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-5, transcript variant X2
guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-5, transcript variant X1
guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 185 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
cilia and flagella associated protein 70
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 44% coverage of the annotated genomic feature by RNAseq alignments
cilia- and flagella-associated protein 70
HECT and RLD domain containing E3 ubiquitin protein ligase 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 8 bases in 7 codons
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 8 bases in 7 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: E3 ubiquitin-protein ligase HERC2
NIPA magnesium transporter 1, transcript variant X1
NIPA magnesium transporter 1, transcript variant X2
NIPA magnesium transporter 1, transcript variant X3
NIPA magnesium transporter 2, transcript variant X3
NIPA magnesium transporter 2, transcript variant X2
NIPA magnesium transporter 2, transcript variant X1
cytoplasmic FMR1-interacting protein 1 homolog
fibronectin type III domain-containing protein 9
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 14 samples with support for all annotated introns
tubulin, gamma complex associated protein 5, transcript variant X2
tubulin, gamma complex associated protein 5, transcript variant X1
gamma-tubulin complex component 5 isoform X2
gamma-tubulin complex component 5 isoform X1
carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 7, transcript variant X2
carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 7, transcript variant X1
solute carrier family 9 member 7, transcript variant X1
solute carrier family 9 member 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
phosphatidylinositol-specific phospholipase C, X domain containing 1, transcript variant X1
phosphatidylinositol-specific phospholipase C, X domain containing 1, 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 42 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 43% coverage of the annotated genomic feature by RNAseq alignments
acireductone dioxygenase 1, transcript variant X1
1,2-dihydroxy-3-keto-5-methylthiopentene dioxygenase isoform X1
acireductone dioxygenase 1, transcript variant X2
1,2-dihydroxy-3-keto-5-methylthiopentene dioxygenase isoform X2
TBC1 domain family, member 23, transcript variant X5
TBC1 domain family, member 23, transcript variant X2
TBC1 domain family, member 23, transcript variant X4
TBC1 domain family, member 23, transcript variant X1
TBC1 domain family, member 23, transcript variant X6
TBC1 domain family, member 23, transcript variant X3
translocase of outer mitochondrial membrane 70 homolog A (S. cerevisiae)
mitochondrial import receptor subunit TOM70
leukemia NUP98 fusion partner 1, transcript variant X2
leukemia NUP98 fusion partner 1, transcript variant X1
leukemia NUP98 fusion partner 1 isoform X2
leukemia NUP98 fusion partner 1 isoform X1
transmembrane protein 45a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
transmembrane protein 45a, transcript variant X1
chromodomain helicase DNA binding protein 1-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 10 samples with support for all annotated introns
chromodomain helicase DNA binding protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
chromodomain helicase DNA binding protein 1-like, transcript variant X3
chromodomain-helicase-DNA-binding protein 1-like isoform X1
chromodomain-helicase-DNA-binding protein 1-like isoform X2
chromodomain-helicase-DNA-binding protein 1-like isoform X3
WWC family member 3, transcript variant X4
WWC family member 3, transcript variant X2
WWC family member 3, transcript variant X3
WWC family member 3, 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 10 samples with support for all annotated introns
shroom family member 2a, transcript variant X2
shroom family member 2a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 16% coverage of the annotated genomic feature by RNAseq alignments
AP-1 complex subunit sigma-2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
AP-1 complex subunit sigma-2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
AP-1 complex subunit sigma-2, transcript variant X4
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 1 sample with support for all annotated introns
AP-1 complex subunit sigma-2, 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 11 samples with support for all annotated introns
AP-1 complex subunit sigma-2, transcript variant X5
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 3 samples with support for all annotated introns
AP-1 complex subunit sigma-2, transcript variant X6
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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
cyclin-dependent kinase-like 5, transcript variant X2
cyclin-dependent kinase-like 5, transcript variant X3
cyclin-dependent kinase-like 5, transcript variant X4
cyclin-dependent kinase-like 5, transcript variant X1
cyclin-dependent kinase-like 5 isoform X2
cyclin-dependent kinase-like 5 isoform X3
cyclin-dependent kinase-like 5 isoform X4
cyclin-dependent kinase-like 5 isoform X1
sex comb on midleg-like protein 2, transcript variant X1
sex comb on midleg-like protein 2, transcript variant X2
sex comb on midleg-like protein 2, transcript variant X3
sex comb on midleg-like protein 2 isoform X1
sex comb on midleg-like protein 2 isoform X2
sex comb on midleg-like protein 2 isoform X3
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
family with sequence similarity 174 member C, 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 46 samples with support for all annotated introns
family with sequence similarity 174 member C, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type IV
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: 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
PWWP domain-containing DNA repair factor 3A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
PWWP domain-containing DNA repair factor 3A-like, transcript variant X2
PWWP domain-containing DNA repair factor 3B-like isoform X2
PWWP domain-containing DNA repair factor 3A-like isoform X1
glutamate receptor, ionotropic, N-methyl-D-aspartate 3Bb
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
Fras1 related extracellular matrix 1b, transcript variant X3
Fras1 related extracellular matrix 1b, 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
Fras1 related extracellular matrix 1b, transcript variant X1
FRAS1-related extracellular matrix protein 1b