Hypomesus transpacificus isolate Combined female chromosome 25, 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\nCM038996.1.\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.
cholinergic receptor, nicotinic, beta 1 (muscle)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
complement C1q tumor necrosis factor-related protein 4-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
cholinergic receptor, nicotinic, beta 1 (muscle) like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: polyA evidence [ECO:0006239]
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
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
cornifelin homolog B-like, transcript variant X2
cornifelin homolog B-like, transcript variant X1
cornifelin homolog B-like, 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 7 samples with support for all annotated introns
placenta-specific gene 8 protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
placenta-specific gene 8 protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
placenta-specific gene 8 protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
placenta-specific gene 8 protein-like isoform X3
UDP glucuronosyltransferase 5 family, polypeptide G1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76 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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
prostaglandin D2 receptor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
prostaglandin D2 receptor 2, 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 28 samples with support for all annotated introns
fragile X mental retardation, autosomal homolog 2, transcript variant X1
fragile X mental retardation, autosomal homolog 2, transcript variant X3
fragile X mental retardation, autosomal homolog 2, transcript variant X2
fragile X mental retardation, autosomal homolog 2, transcript variant X4
fragile X mental retardation syndrome-related protein 2 isoform X1
fragile X mental retardation syndrome-related protein 2 isoform X3
fragile X mental retardation syndrome-related protein 2 isoform X2
fragile X mental retardation syndrome-related protein 2 isoform X4
transmembrane protein 272-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 44 samples with support for all annotated introns
transmembrane protein 272-like, transcript variant X3
transmembrane protein 272-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 7 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC124487017, 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 1 sample with support for all annotated introns
uncharacterized LOC124487017, transcript variant X2
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.
active breakpoint cluster region-related protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124486990, 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 5 samples with support for all annotated introns
uncharacterized LOC124486990, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC124486990, 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
uncharacterized LOC124486990, transcript variant X2
uncharacterized protein LOC124486990 isoform X1
uncharacterized protein LOC124486990 isoform X2
uncharacterized LOC124486990, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC124486990, 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 2 samples with support for all annotated introns
uncharacterized protein LOC124486990 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC794943 homolog
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 45 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 33 samples with support for all annotated introns
very long-chain specific acyl-CoA dehydrogenase, mitochondrial
LOW QUALITY PROTEIN: segment polarity protein dishevelled homolog DVL-2
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 42 samples with support for all annotated introns
ArfGAP with FG repeats 2, transcript variant X1
ArfGAP with FG repeats 2, transcript variant X3
ArfGAP with FG repeats 2, transcript variant X2
arf-GAP domain and FG repeat-containing protein 2 isoform X2
arf-GAP domain and FG repeat-containing protein 2 isoform X3
arf-GAP domain and FG repeat-containing protein 2 isoform X1
solute carrier family 16 member 13, 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 14 samples with support for all annotated introns
solute carrier family 16 member 13, 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 4 samples with support for all annotated introns
solute carrier family 16 member 13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
BCL6B transcription repressor, transcript variant X1
BCL6B transcription repressor, transcript variant X2
B-cell CLL/lymphoma 6 member B protein isoform X1
thyroid hormone receptor interactor 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
thyroid hormone receptor interactor 6, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
thyroid hormone receptor interactor 6, transcript variant X3
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 14 samples with support for all annotated introns
thyroid hormone receptor interactor 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
thyroid receptor-interacting protein 6 isoform X1
thyroid receptor-interacting protein 6 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC553698 homolog
SLX1 homolog B, structure-specific endonuclease subunit
structure-specific endonuclease subunit SLX1
uncharacterized LOC124487125, transcript variant X2
uncharacterized LOC124487125, transcript variant X1
uncharacterized protein LOC124487125 isoform X2
uncharacterized protein LOC124487125 isoform X1
uncharacterized LOC124487124, transcript variant X2
uncharacterized LOC124487124, transcript variant X1
uncharacterized protein LOC124487124 isoform X2
uncharacterized protein LOC124487124 isoform X1
uncharacterized protein si:ch211-212k18.6
ADAM metallopeptidase domain 19a, transcript variant X1
ADAM metallopeptidase domain 19a, transcript variant X2
disintegrin and metalloproteinase domain-containing protein 19 isoform X1
disintegrin and metalloproteinase domain-containing protein 19 isoform X2
leucine-rich repeats and calponin homology (CH) domain containing 4, 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
leucine-rich repeat and calponin homology domain-containing protein 4 isoform X2
leucine-rich repeats and calponin homology (CH) domain containing 4, transcript variant X1
leucine-rich repeat and calponin homology domain-containing protein 4 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
zinc finger MYND domain-containing protein 15-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
progestin and adipoQ receptor family member 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
period circadian clock 1b, transcript variant X2
period circadian clock 1b, transcript variant X1
period circadian protein homolog 1b isoform X2
period circadian protein homolog 1b isoform 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 43 samples with support for all annotated introns
uncharacterized protein LOC557813 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
serine (or cysteine) peptidase inhibitor, clade H, member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine (or cysteine) peptidase inhibitor, clade H, member 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 10 samples with support for all annotated introns
serine (or cysteine) peptidase inhibitor, clade H, member 2 isoform X1
serine (or cysteine) peptidase inhibitor, clade H, member 2 isoform X2
octapeptide-repeat protein T2, transcript variant X1
uncharacterized abhydrolase domain-containing protein DDB_G0269086 isoform X1
octapeptide-repeat protein T2, transcript variant X2
octapeptide-repeat protein T2 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: GRB10-interacting GYF protein 1
POP7 homolog, ribonuclease P/MRP subunit, transcript variant X2
POP7 homolog, ribonuclease P/MRP subunit, transcript variant X1
zona pellucida sperm-binding protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
UFM1-specific peptidase 1 (non-functional)
endonuclease domain-containing 1 protein-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 41 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 33 samples with support for all annotated introns
endonuclease domain-containing 1 protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
interferon-induced very large GTPase 1, transcript variant X2
interferon-induced very large GTPase 1, transcript variant X1
interferon-induced very large GTPase 1, transcript variant X4
interferon-induced very large GTPase 1, transcript variant X3
interferon-induced very large GTPase 1 isoform X1
interferon-induced very large GTPase 1 isoform X3
interferon-induced very large GTPase 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 99% 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: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
cGMP-specific 3',5'-cyclic phosphodiesterase
MAD2 mitotic arrest deficient-like 1 (yeast)
mitotic spindle assembly checkpoint protein MAD2A
arylsulfatase family, member J, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
arylsulfatase family, member J, 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
calcium/calmodulin-dependent protein kinase (CaM kinase) II delta 1, transcript variant X1
calcium/calmodulin-dependent protein kinase (CaM kinase) II delta 1, transcript variant X3
calcium/calmodulin-dependent protein kinase (CaM kinase) II delta 1, transcript variant X2
calcium/calmodulin-dependent protein kinase (CaM kinase) II delta 1, transcript variant X5
calcium/calmodulin-dependent protein kinase (CaM kinase) II delta 1, transcript variant X9
calcium/calmodulin-dependent protein kinase (CaM kinase) II delta 1, transcript variant X7
calcium/calmodulin-dependent protein kinase (CaM kinase) II delta 1, transcript variant X11
calcium/calmodulin-dependent protein kinase (CaM kinase) II delta 1, transcript variant X4
calcium/calmodulin-dependent protein kinase (CaM kinase) II delta 1, transcript variant X8
calcium/calmodulin-dependent protein kinase (CaM kinase) II delta 1, transcript variant X6
calcium/calmodulin-dependent protein kinase (CaM kinase) II delta 1, transcript variant X10
calcium/calmodulin-dependent protein kinase type II delta 1 chain isoform X4
calcium/calmodulin-dependent protein kinase type II delta 1 chain isoform X8
calcium/calmodulin-dependent protein kinase type II delta 1 chain isoform X2
calcium/calmodulin-dependent protein kinase type II delta 1 chain isoform X6
calcium/calmodulin-dependent protein kinase type II delta 1 chain isoform X10
calcium/calmodulin-dependent protein kinase type II delta 1 chain isoform X1
calcium/calmodulin-dependent protein kinase type II delta 1 chain isoform X5
calcium/calmodulin-dependent protein kinase type II delta 1 chain isoform X9
calcium/calmodulin-dependent protein kinase type II delta 1 chain isoform X3
calcium/calmodulin-dependent protein kinase type II delta 1 chain isoform X7
calcium/calmodulin-dependent protein kinase type II delta 1 chain isoform X11
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
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
LOW QUALITY PROTEIN: zinc finger protein 16-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
pellino E3 ubiquitin protein ligase family member 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
E3 ubiquitin-protein ligase pellino homolog 1 isoform X1
pellino E3 ubiquitin protein ligase family member 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
pellino E3 ubiquitin protein ligase family member 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
pellino E3 ubiquitin protein ligase family member 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pellino E3 ubiquitin protein ligase family member 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
pellino E3 ubiquitin protein ligase family member 3, transcript variant X4
E3 ubiquitin-protein ligase pellino homolog 1 isoform X2
E3 ubiquitin-protein ligase pellino homolog 1 isoform X3
tyrosine-protein kinase receptor TYRO3, transcript variant X2
tyrosine-protein kinase receptor TYRO3, transcript variant X1
tyrosine-protein kinase receptor TYRO3 isoform X2
tyrosine-protein kinase receptor TYRO3 isoform X1
EH domain binding protein 1-like 1a, transcript variant X3
EH domain binding protein 1-like 1a, transcript variant X8
EH domain binding protein 1-like 1a, transcript variant X9
EH domain binding protein 1-like 1a, transcript variant X1
EH domain binding protein 1-like 1a, transcript variant X4
EH domain binding protein 1-like 1a, transcript variant X5
uncharacterized protein ehbp1l1a isoform X1
EH domain-binding protein 1-like protein 1 isoform X9
nascent polypeptide-associated complex subunit alpha, muscle-specific form isoform X8
uncharacterized protein ehbp1l1a isoform X3
uncharacterized protein ehbp1l1a isoform X4
uncharacterized protein ehbp1l1a isoform X5
EH domain binding protein 1-like 1a, transcript variant X2
uncharacterized protein ehbp1l1a isoform X2
EH domain binding protein 1-like 1a, transcript variant X6
EH domain binding protein 1-like 1a, transcript variant X7
uncharacterized protein ehbp1l1a isoform X6
uncharacterized protein ehbp1l1a isoform X7
potassium channel, subfamily K, member 7
TAF6-like RNA polymerase II, p300/CBP-associated factor (PCAF)-associated factor
TAF6-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 6L
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
metastasis associated 1 family, member 2
LOW QUALITY PROTEIN: metastasis-associated protein MTA2
echinoderm microtubule-associated protein-like 3 isoform X3
echinoderm microtubule-associated protein-like 3 isoform X1
echinoderm microtubule-associated protein-like 3 isoform X2
ECSIT signaling integrator, transcript variant X1
ECSIT signaling integrator, transcript variant X2
evolutionarily conserved signaling intermediate in Toll pathway, mitochondrial isoform X1
evolutionarily conserved signaling intermediate in Toll pathway, mitochondrial isoform X2
zinc finger translocation associated, 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 5 samples with support for all annotated introns
zinc finger translocation-associated protein isoform X1
zinc finger translocation associated, transcript variant X2
zinc finger translocation-associated protein isoform X2
zinc finger translocation associated, 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 6 samples with support for all annotated introns
zinc finger translocation-associated protein isoform 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 2 samples with support for all annotated introns
multiple endocrine neoplasia I, transcript variant X1
multiple endocrine neoplasia I, transcript variant X2
multiple endocrine neoplasia I, transcript variant X3
mitogen-activated protein kinase kinase kinase kinase 2, transcript variant X1
mitogen-activated protein kinase kinase kinase kinase 2, transcript variant X4
mitogen-activated protein kinase kinase kinase kinase 2, transcript variant X3
mitogen-activated protein kinase kinase kinase kinase 2, transcript variant X2
mitogen-activated protein kinase kinase kinase kinase 2, transcript variant X5
mitogen-activated protein kinase kinase kinase kinase 2 isoform X1
mitogen-activated protein kinase kinase kinase kinase 2 isoform X4
mitogen-activated protein kinase kinase kinase kinase 2 isoform X3
mitogen-activated protein kinase kinase kinase kinase 2 isoform X2
mitogen-activated protein kinase kinase kinase kinase 2 isoform X5
RNA-binding protein 4.1-like, transcript variant X1
RNA-binding protein 4.1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
RNA-binding protein 4.1-like, transcript variant X3
RNA-binding protein 4.1-like, transcript variant X4
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 5 samples with support for all annotated introns
splicing factor 1, transcript variant X1
splicing factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
spermatogenesis associated 6-like protein
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
tRNA methyltransferase 10 homolog A-like, 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
tRNA methyltransferase 10 homolog A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized protein LOC124486969 isoform X1
tRNA methyltransferase 10 homolog A-like 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 44 samples with support for all annotated introns
RNA (guanine-9-)-methyltransferase domain-containing protein 2
RAP1, GTP-GDP dissociation stimulator 1, transcript variant X1
RAP1, GTP-GDP dissociation stimulator 1, transcript variant X5
RAP1, GTP-GDP dissociation stimulator 1, transcript variant X3
RAP1, GTP-GDP dissociation stimulator 1, transcript variant X2
RAP1, GTP-GDP dissociation stimulator 1, transcript variant X4
rap1 GTPase-GDP dissociation stimulator 1 isoform X1
rap1 GTPase-GDP dissociation stimulator 1 isoform X3
rap1 GTPase-GDP dissociation stimulator 1 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 3 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 19 samples with support for all annotated introns
Fras1 related extracellular matrix 1a, transcript variant X3
Fras1 related extracellular matrix 1a, transcript variant X1
Fras1 related extracellular matrix 1a, transcript variant X6
Fras1 related extracellular matrix 1a, transcript variant X8
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 14 samples with support for all annotated introns
Fras1 related extracellular matrix 1a, transcript variant X2
Fras1 related extracellular matrix 1a, transcript variant X5
Fras1 related extracellular matrix 1a, transcript variant X4
FRAS1-related extracellular matrix protein 1a isoform X1
FRAS1-related extracellular matrix protein 1a isoform X2
FRAS1-related extracellular matrix protein 1a isoform X4
Fras1 related extracellular matrix 1a, transcript variant X7
FRAS1-related extracellular matrix protein 1a isoform X3
zinc finger DHHC-type palmitoyltransferase 21, transcript variant X2
zinc finger DHHC-type palmitoyltransferase 21, transcript variant X3
zinc finger DHHC-type palmitoyltransferase 21, transcript variant X1
nuclear factor 1 B-type-like, transcript variant X4
nuclear factor 1 B-type-like, transcript variant X3
nuclear factor 1 B-type-like, transcript variant X6
nuclear factor 1 B-type-like, transcript variant X2
nuclear factor 1 B-type-like, transcript variant X5
nuclear factor 1 B-type-like, transcript variant X1
nuclear factor 1 B-type-like, transcript variant X8
nuclear factor 1 B-type-like, transcript variant X7
B-cell scaffold protein with ankyrin repeats-like, transcript variant X12
B-cell scaffold protein with ankyrin repeats-like, transcript variant X11
B-cell scaffold protein with ankyrin repeats-like, transcript variant X2
B-cell scaffold protein with ankyrin repeats-like, transcript variant X9
B-cell scaffold protein with ankyrin repeats-like, transcript variant X14
B-cell scaffold protein with ankyrin repeats-like, transcript variant X13
B-cell scaffold protein with ankyrin repeats-like, transcript variant X3
B-cell scaffold protein with ankyrin repeats-like, transcript variant X10
B-cell scaffold protein with ankyrin repeats-like, transcript variant X8
B-cell scaffold protein with ankyrin repeats-like, transcript variant X6
B-cell scaffold protein with ankyrin repeats-like, transcript variant X7
B-cell scaffold protein with ankyrin repeats-like, transcript variant X4
B-cell scaffold protein with ankyrin repeats-like, transcript variant X5
B-cell scaffold protein with ankyrin repeats-like, transcript variant X1
B-cell scaffold protein with ankyrin repeats-like isoform X4
B-cell scaffold protein with ankyrin repeats-like isoform X3
B-cell scaffold protein with ankyrin repeats-like isoform X2
B-cell scaffold protein with ankyrin repeats-like isoform X1
serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform-like, transcript variant X3
serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform-like, transcript variant X1
serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform-like, transcript variant X2
serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform-like isoform X3
serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform-like isoform X1
serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform-like isoform X2
cell wall integrity and stress response component 4-like, transcript variant X2
cell wall integrity and stress response component 4-like, transcript variant X1
cell wall integrity and stress response component 4-like, transcript variant X3
cell wall integrity and stress response component 4-like isoform X1
cell wall integrity and stress response component 4-like isoform X3
cell wall integrity and stress response component 4-like isoform X2
ubiquitin thioesterase OTUB1-like, transcript variant X1
ubiquitin thioesterase OTUB1-like, transcript variant X2
ubiquitin thioesterase OTUB1-like isoform X1
ubiquitin thioesterase OTUB1-like isoform X2
aconitase 1, soluble, transcript variant X4
aconitase 1, soluble, transcript variant X1
aconitase 1, soluble, transcript variant X2
aconitase 1, soluble, transcript variant X3
cytoplasmic aconitate hydratase isoform X2
cytoplasmic aconitate hydratase isoform X1
leucine-rich melanocyte differentiation-associated protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
oligosaccharyltransferase complex subunit
oligosaccharyltransferase complex subunit ostc
sodium/potassium/calcium exchanger 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase, transcript variant X1
Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase, 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 21 samples with support for all annotated introns
Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase, 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 35 samples with support for all annotated introns
O-phosphoseryl-tRNA(Sec) selenium transferase isoform X1
O-phosphoseryl-tRNA(Sec) selenium transferase isoform X3
O-phosphoseryl-tRNA(Sec) selenium transferase isoform X4
Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
O-phosphoseryl-tRNA(Sec) selenium transferase isoform X2
O-phosphoseryl-tRNA(Sec) selenium transferase isoform X5
leucine-rich repeat LGI family, member 2a
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
leucine-rich repeat LGI family member 2a
TBC1 domain family, member 14, transcript variant X1
TBC1 domain family, member 14, transcript variant X2
TBC1 domain family, member 14, transcript variant X4
TBC1 domain family, member 14, transcript variant X3
TBC1 domain family, member 14, transcript variant X5
KIAA0232 ortholog, transcript variant X1
KIAA0232 ortholog, transcript variant X2
uncharacterized protein KIAA0232 homolog isoform X1
uncharacterized protein KIAA0232 homolog isoform X2
uncharacterized LOC124487175, 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 10 samples with support for all annotated introns
uncharacterized LOC124487175, 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 40 samples with support for all annotated introns
uncharacterized LOC124487175, 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 42 samples with support for all annotated introns
uncharacterized protein LOC124487175 isoform X2
uncharacterized protein LOC124487175 isoform X1
recombination signal binding protein for immunoglobulin kappa J region b
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 43 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 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: stromal interaction molecule 2
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 6 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 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: 9 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124486931, 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 36 samples with support for all annotated introns
uncharacterized LOC124486931, transcript variant X3
uncharacterized protein LOC124486931 isoform X3
uncharacterized LOC124486931, 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 13 samples with support for all annotated introns
uncharacterized LOC124486931, transcript variant X2
uncharacterized protein LOC124486931 isoform X1
uncharacterized protein LOC124486931 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
PC-esterase domain-containing protein 1A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 28% coverage of the annotated genomic feature by RNAseq alignments
RAS guanyl-releasing protein 2-like, transcript variant X6
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
RAS guanyl-releasing protein 2-like, transcript variant X5
RAS guanyl-releasing protein 2-like, transcript variant X8
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 6 samples with support for all annotated introns
RAS guanyl-releasing protein 2-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
RAS guanyl-releasing protein 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
RAS guanyl-releasing protein 2-like isoform X5
RAS guanyl-releasing protein 2-like isoform X4
RAS guanyl-releasing protein 2-like isoform X6
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
RAS guanyl-releasing protein 2-like, 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 4 samples with support for all annotated introns
RAS guanyl-releasing protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
RAS guanyl-releasing protein 2-like, transcript variant X1
RAS guanyl-releasing protein 2-like isoform X3
RAS guanyl-releasing protein 2-like isoform X2
RAS guanyl-releasing protein 2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
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 38 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
MLLT3 super elongation complex subunit, 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
MLLT3 super elongation complex subunit, 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 4
chromosome 25 C4orf54 homolog, transcript variant X3
chromosome 25 C4orf54 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
chromosome 25 C4orf54 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 28 samples with support for all annotated introns
chromosome 25 C4orf54 homolog, transcript variant X5
chromosome 25 C4orf54 homolog, transcript variant X4
uncharacterized protein C4orf54 homolog isoform X2
uncharacterized protein C4orf54 homolog isoform X1
uncharacterized protein C4orf54 homolog isoform X4
uncharacterized protein C4orf54 homolog isoform X3
chromosome 25 C4orf54 homolog, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
chromosome 25 C4orf54 homolog, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein C4orf54 homolog isoform X5
uncharacterized protein C4orf54 homolog isoform X6
La ribonucleoprotein 7, transcriptional regulator, transcript variant X1
La ribonucleoprotein 7, transcriptional regulator, transcript variant X2
DENN/MADD domain containing 4C, transcript variant X3
DENN/MADD domain containing 4C, transcript variant X5
DENN/MADD domain containing 4C, transcript variant X1
DENN/MADD domain containing 4C, transcript variant X4
DENN/MADD domain containing 4C, transcript variant X7
DENN/MADD domain containing 4C, transcript variant X2
DENN domain-containing protein 4C isoform X1
DENN domain-containing protein 4C isoform X2
DENN domain-containing protein 4C isoform X3
DENN domain-containing protein 4C isoform X4
DENN domain-containing protein 4C isoform X6
DENN/MADD domain containing 4C, transcript variant X6
DENN domain-containing protein 4C isoform X5
uncharacterized LOC124487166, transcript variant X3
uncharacterized LOC124487166, 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 11 samples with support for all annotated introns
uncharacterized LOC124487166, transcript variant X1
peroxisome proliferator-activated receptor gamma, coactivator 1 alpha
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 5 bases in 4 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 5 bases in 4 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: peroxisome proliferator-activated receptor gamma coactivator 1-alpha
glucosidase, beta, acid 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
glucosidase, beta, acid 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
adhesion G protein-coupled receptor A3, transcript variant X1
adhesion G protein-coupled receptor A3, transcript variant X2
adhesion G protein-coupled receptor A3 isoform X1
adhesion G protein-coupled receptor A3 isoform X2
potassium voltage-gated channel interacting protein 4a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium voltage-gated channel interacting protein 4a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Kv channel-interacting protein 4 isoform X1
potassium voltage-gated channel interacting protein 4a, transcript variant X5
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 31 samples with support for all annotated introns
Kv channel-interacting protein 4 isoform X4
potassium voltage-gated channel interacting protein 4a, transcript variant X6
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 3 samples with support for all annotated introns
Kv channel-interacting protein 4 isoform X5
potassium voltage-gated channel interacting protein 4a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Kv channel-interacting protein 4 isoform X3
potassium voltage-gated channel interacting protein 4a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Kv channel-interacting protein 4 isoform X2
SEC24 homolog D, COPII coat complex component
proline-rich extensin-like protein EPR1 isoform X3
inactive ubiquitin carboxyl-terminal hydrolase 53, transcript variant X1
inactive ubiquitin carboxyl-terminal hydrolase 53, transcript variant X2
inactive ubiquitin carboxyl-terminal hydrolase 53
uncharacterized LOC124487084, transcript variant X1
uncharacterized LOC124487084, transcript variant X2
receptor-type tyrosine-protein phosphatase delta-like, transcript variant X9
receptor-type tyrosine-protein phosphatase delta-like, transcript variant X8
receptor-type tyrosine-protein phosphatase delta-like, transcript variant X7
receptor-type tyrosine-protein phosphatase delta-like, transcript variant X6
receptor-type tyrosine-protein phosphatase delta-like, transcript variant X4
receptor-type tyrosine-protein phosphatase delta-like, transcript variant X5
receptor-type tyrosine-protein phosphatase delta-like, transcript variant X2
receptor-type tyrosine-protein phosphatase delta-like, transcript variant X3
receptor-type tyrosine-protein phosphatase delta-like, transcript variant X1
receptor-type tyrosine-protein phosphatase delta-like isoform X9
receptor-type tyrosine-protein phosphatase delta-like isoform X8
receptor-type tyrosine-protein phosphatase delta-like isoform X7
receptor-type tyrosine-protein phosphatase delta-like isoform X6
receptor-type tyrosine-protein phosphatase delta-like isoform X4
receptor-type tyrosine-protein phosphatase delta-like isoform X5
receptor-type tyrosine-protein phosphatase delta-like isoform X2
receptor-type tyrosine-protein phosphatase delta-like isoform X3
receptor-type tyrosine-protein phosphatase delta-like isoform X1
5,6-dihydroxyindole-2-carboxylic acid oxidase-like
multiple PDZ domain protein-like, transcript variant X1
multiple PDZ domain protein-like, 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 8 samples with support for all annotated introns
multiple PDZ domain protein-like isoform X1
multiple PDZ domain protein-like isoform X2
adhesion G protein-coupled receptor L3-like, transcript variant X3
adhesion G protein-coupled receptor L3-like, transcript variant X9
adhesion G protein-coupled receptor L3-like, transcript variant X1
adhesion G protein-coupled receptor L3-like, transcript variant X7
adhesion G protein-coupled receptor L3-like, transcript variant X2
adhesion G protein-coupled receptor L3-like, transcript variant X4
adhesion G protein-coupled receptor L3-like, transcript variant X8
adhesion G protein-coupled receptor L3-like isoform X3
adhesion G protein-coupled receptor L3-like isoform X8
adhesion G protein-coupled receptor L3-like isoform X1
adhesion G protein-coupled receptor L3-like isoform X6
adhesion G protein-coupled receptor L3-like isoform X2
adhesion G protein-coupled receptor L3-like isoform X4
adhesion G protein-coupled receptor L3-like isoform X7
adhesion G protein-coupled receptor L3-like, transcript variant X5
adhesion G protein-coupled receptor L3-like, transcript variant X6
adhesion G protein-coupled receptor L3-like isoform X5
phospholipid-transporting ATPase ABCA1-like, transcript variant X2
phospholipid-transporting ATPase ABCA1-like, transcript variant X1
phospholipid-transporting ATPase ABCA1-like, transcript variant X5
phospholipid-transporting ATPase ABCA1-like, transcript variant X3
phospholipid-transporting ATPase ABCA1-like, transcript variant X4
phospholipid-transporting ATPase ABCA1-like isoform X2
phospholipid-transporting ATPase ABCA1-like isoform X1
phospholipid-transporting ATPase ABCA1-like isoform X3
trans-2,3-enoyl-CoA reductase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
trans-2,3-enoyl-CoA reductase-like isoform X2
trans-2,3-enoyl-CoA reductase-like, transcript variant X1
trans-2,3-enoyl-CoA reductase-like, transcript variant X3
trans-2,3-enoyl-CoA reductase-like isoform X3
trans-2,3-enoyl-CoA reductase-like isoform X1
caspase activity and apoptosis inhibitor 1
ELAV like neuron-specific RNA binding protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ELAV like neuron-specific RNA binding protein 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 1 sample with support for all annotated introns
ELAV like neuron-specific RNA binding protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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: 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: glucosidase 2 subunit beta-like
doublesex- and mab-3-related transcription factor A1-like
fatty acid-binding protein, intestinal-like
RNA-binding protein with multiple splicing-like, transcript variant X4
RNA-binding protein with multiple splicing-like, transcript variant X3
RNA-binding protein with multiple splicing-like, transcript variant X1
RNA-binding protein with multiple splicing-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
RNA-binding protein with multiple splicing-like
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
uncharacterized RNA-binding protein C23E6.01c-like, transcript variant X2
uncharacterized RNA-binding protein C23E6.01c-like, transcript variant X1
uncharacterized RNA-binding protein C23E6.01c-like isoform X2
uncharacterized protein LOC124487088 isoform X1
major facilitator superfamily domain containing 8
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
major facilitator superfamily domain-containing protein 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
claudin domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
N-acyl-aromatic-L-amino acid amidohydrolase (carboxylate-forming) B-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 1 sample with support for all annotated introns
oxysterol-binding protein 1-like, transcript variant X2
oxysterol-binding protein 1-like, transcript variant X3
oxysterol-binding protein 1-like, transcript variant X1
oxysterol-binding protein 1-like isoform X2
oxysterol-binding protein 1-like isoform X1
transfer RNA arginine (anticodon UCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
coronin, actin binding protein, 1B, transcript variant X1
coronin, actin binding protein, 1B, transcript variant X4
coronin, actin binding protein, 1B, transcript variant X2
coronin, actin binding protein, 1B, transcript variant X3
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Myb/SANT-like DNA-binding domain containing 1
myb/SANT-like DNA-binding domain-containing protein 1
regulator of G protein signaling 12a, 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 13 samples with support for all annotated introns
regulator of G protein signaling 12a, 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 25 samples with support for all annotated introns
hepatocyte growth factor activator, transcript variant X1
hepatocyte growth factor activator, transcript variant X2
hepatocyte growth factor activator isoform X1
hepatocyte growth factor activator isoform X2
protein Dok-7-like, transcript variant X1
protein Dok-7-like, 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 2 samples with support for all annotated introns
protein Dok-7-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
G-protein coupled receptor 26-like, transcript variant X2
G-protein coupled receptor 26-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
G-protein coupled receptor 78-like isoform X2
G-protein coupled receptor 26-like isoform X1
probable tRNA (uracil-O(2)-)-methyltransferase
tyrosine kinase, non-receptor, 1, transcript variant X2
tyrosine kinase, non-receptor, 1, transcript variant X1
non-receptor tyrosine-protein kinase TNK1
phospholipid scramblase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
phospholipid scramblase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
phospholipid scramblase 1-like isoform X2
phospholipid scramblase 1-like isoform X1
elongator acetyltransferase complex subunit 5, transcript variant X2
elongator acetyltransferase complex subunit 5, transcript variant X1
CTD nuclear envelope phosphatase 1A-like
gamma-aminobutyric acid receptor-associated protein
G protein pathway suppressor 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
G protein pathway suppressor 2-like, transcript variant X2
G protein pathway suppressor 2-like isoform X1
G protein pathway suppressor 2-like isoform X2
eukaryotic translation initiation factor 5A-1
solute carrier family 2, facilitated glucose transporter member 4-like
cellular tumor antigen p53-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
cellular tumor antigen p53-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
cellular tumor antigen p53-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase H, transcript variant X1
receptor-type tyrosine-protein phosphatase eta isoform X1
receptor-type tyrosine-protein phosphatase H, 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 33 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase H isoform X2
capping protein (actin filament), gelsolin-like b, transcript variant X1
capping protein (actin filament), gelsolin-like b, transcript variant X2
capping protein (actin filament), gelsolin-like b isoform X1
capping protein (actin filament), gelsolin-like b isoform X2
DNA-directed RNA polymerase II subunit RPB1
zinc finger and BTB domain containing 4, transcript variant X2
zinc finger and BTB domain containing 4, transcript variant X4
zinc finger and BTB domain containing 4, transcript variant X3
zinc finger and BTB domain containing 4, transcript variant X6
zinc finger and BTB domain containing 4, transcript variant X1
zinc finger and BTB domain containing 4, transcript variant X5
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 9 samples with support for all annotated introns
high density lipoprotein binding protein b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 15b, transcript variant X2
Rho guanine nucleotide exchange factor 15b, transcript variant X1
rho guanine nucleotide exchange factor 15 isoform X1
rho guanine nucleotide exchange factor 15 isoform X2
low density lipoprotein receptor adapter protein 1
thialysine N-epsilon-acetyltransferase-like, 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 32 samples with support for all annotated introns
thialysine N-epsilon-acetyltransferase-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 32 samples with support for all annotated introns
thialysine N-epsilon-acetyltransferase-like isoform X2
diamine acetyltransferase 1-like isoform X1
TNF superfamily member 12, transcript variant X1
TNF superfamily member 12, transcript variant X2
tumor necrosis factor ligand superfamily member 12 isoform X1
tumor necrosis factor ligand superfamily member 12 isoform X2
chromodomain helicase DNA binding protein 3, transcript variant X7
chromodomain helicase DNA binding protein 3, transcript variant X5
chromodomain-helicase-DNA-binding protein 3 isoform X7
chromodomain-helicase-DNA-binding protein 3 isoform X5
chromodomain helicase DNA binding protein 3, transcript variant X4
chromodomain helicase DNA binding protein 3, transcript variant X2
chromodomain helicase DNA binding protein 3, transcript variant X3
chromodomain helicase DNA binding protein 3, transcript variant X1
chromodomain helicase DNA binding protein 3, transcript variant X6
chromodomain-helicase-DNA-binding protein 3 isoform X3
chromodomain-helicase-DNA-binding protein 3 isoform X4
chromodomain-helicase-DNA-binding protein 3 isoform X2
chromodomain-helicase-DNA-binding protein 3 isoform X1
chromodomain-helicase-DNA-binding protein 3 isoform X6
cytochrome b5 domain-containing protein 1
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
N-alpha-acetyltransferase 38, NatC auxiliary subunit, 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, including 45 samples with support for all annotated introns
N-alpha-acetyltransferase 38, NatC auxiliary subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
N-alpha-acetyltransferase 38, NatC auxiliary subunit isoform X1
N-alpha-acetyltransferase 38, NatC auxiliary subunit isoform X2
DnaJ (Hsp40) homolog, subfamily C, member 3b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
TRAF interacting protein with forkhead associated domain
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 52 samples with support for all annotated introns
TRAF-interacting protein with FHA domain-containing protein A
RNA-binding protein 4B-like, transcript variant X2
RNA-binding protein 4B-like, transcript variant X1
uncharacterized LOC124487153, transcript variant X3
uncharacterized LOC124487153, transcript variant X2
uncharacterized LOC124487153, transcript variant X1
uncharacterized protein LOC124487153 isoform X3
uncharacterized protein LOC124487153 isoform X2
uncharacterized protein LOC124487153 isoform X1
uncharacterized LOC124487156, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC124487156, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC124487156, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized protein LOC124487156 isoform X1
uncharacterized protein LOC124487156 isoform X2
uncharacterized LOC124487157, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
uncharacterized LOC124487157, 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 3 samples with support for all annotated introns
uncharacterized protein LOC124487157 isoform X2
uncharacterized protein LOC124487157 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC124487149, transcript variant X3
uncharacterized LOC124487149, transcript variant X1
uncharacterized protein LOC124487149 isoform X3
uncharacterized protein LOC124487149 isoform X1
uncharacterized LOC124487149, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC124487149 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
Ig kappa chain V region K29-213-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
Ig kappa chain V region K29-213-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
T cell receptor alpha chain MC.7.G5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
T cell receptor alpha chain MC.7.G5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
T cell receptor alpha chain MC.7.G5-like, transcript variant X3
T cell receptor alpha chain MC.7.G5-like isoform X2
uncharacterized protein LOC124487147 isoform X1
T cell receptor alpha chain MC.7.G5-like isoform X3
T cell receptor alpha variable 13-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124487146, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC124487146, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124487146, transcript variant X3
uncharacterized protein LOC124487146 isoform X2
uncharacterized protein LOC124487146 isoform X1
uncharacterized protein LOC124487146 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
polymeric immunoglobulin receptor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
polymeric immunoglobulin receptor-like, transcript variant X1
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
polymeric immunoglobulin receptor-like isoform X2
polymeric immunoglobulin receptor-like isoform X1
immunoglobulin superfamily member 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
immunoglobulin superfamily member 3-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
immunoglobulin superfamily member 3-like, transcript variant X1
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 32 samples with support for all annotated introns
uncharacterized protein LOC124487148 isoform X3
immunoglobulin superfamily member 3-like isoform X2
immunoglobulin superfamily member 3-like isoform X1
immunoglobulin superfamily member 3-like, transcript variant X3
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 37 samples with support for all annotated introns
uncharacterized LOC124487050, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC124487050, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC124487050 isoform X2
uncharacterized protein LOC124487050 isoform X1
LOW QUALITY PROTEIN: dedicator of cytokinesis protein 11
interleukin-13 receptor subunit alpha-2-like, transcript variant X1
interleukin-13 receptor subunit alpha-2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
interleukin-13 receptor subunit alpha-2-like, transcript variant X4
interleukin-13 receptor subunit alpha-2-like, transcript variant X2
interleukin-13 receptor subunit alpha-2-like isoform X1
interleukin-13 receptor subunit alpha-2-like isoform X2
interleukin-13 receptor subunit alpha-2-like isoform X3
dedicator of cytokinesis protein 11-like, transcript variant X6
dedicator of cytokinesis protein 11-like, transcript variant X8
dedicator of cytokinesis protein 11-like, transcript variant X9
dedicator of cytokinesis protein 11-like, transcript variant X7
dedicator of cytokinesis protein 11-like isoform X6
dedicator of cytokinesis protein 11-like, 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 27 samples with support for all annotated introns
dedicator of cytokinesis protein 11-like, transcript variant X1
dedicator of cytokinesis protein 11-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 19 samples with support for all annotated introns
dedicator of cytokinesis protein 11-like, transcript variant X4
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
dedicator of cytokinesis protein 11-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
dedicator of cytokinesis protein 11-like isoform X3
dedicator of cytokinesis protein 11-like isoform X1
dedicator of cytokinesis protein 11-like isoform X2
dedicator of cytokinesis protein 11-like isoform X4
dedicator of cytokinesis protein 11-like isoform X5
interleukin-13 receptor subunit alpha-2-like
kirre like nephrin family adhesion molecule 1a, 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 41 samples with support for all annotated introns
kirre like nephrin family adhesion molecule 1a, 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 40 samples with support for all annotated introns
NADH:ubiquinone oxidoreductase core subunit S2
NADH dehydrogenase [ubiquinone] iron-sulfur protein 2, mitochondrial
high affinity immunoglobulin epsilon receptor subunit gamma-like, transcript variant X1
high affinity immunoglobulin epsilon receptor subunit gamma-like isoform X1
high affinity immunoglobulin epsilon receptor subunit gamma-like, transcript variant X2
high affinity immunoglobulin epsilon receptor subunit gamma-like isoform X2
nectin cell adhesion molecule 4a, transcript variant X1
nectin cell adhesion molecule 4a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
equilibrative nucleoside transporter 2-like
serine/threonine-protein phosphatase PP1-beta catalytic subunit
v-rel avian reticuloendotheliosis viral oncogene homolog A
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 48 samples with support for all annotated introns
DR1-associated protein 1 (negative cofactor 2 alpha)
mitogen-activated protein kinase kinase kinase 11
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