Hypomesus transpacificus isolate Combined female chromosome 20, 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\nCM038991.1.\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.
choline-phosphate cytidylyltransferase B-like, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
choline-phosphate cytidylyltransferase B-like, transcript variant X1
choline-phosphate cytidylyltransferase B-like isoform X1
choline-phosphate cytidylyltransferase B-like isoform X2
organic solute transporter subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
palmitoyltransferase ZDHHC20-B-like, transcript variant X4
palmitoyltransferase ZDHHC20-B-like, transcript variant X3
palmitoyltransferase ZDHHC20-B-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
palmitoyltransferase ZDHHC20-B-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 5 samples with support for all annotated introns
palmitoyltransferase ZDHHC20-B-like, 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 6 samples with support for all annotated introns
palmitoyltransferase ZDHHC20-B-like, transcript variant X7
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
palmitoyltransferase ZDHHC20-B-like, transcript variant X6
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 36 samples with support for all annotated introns
palmitoyltransferase ZDHHC20-B-like isoform X2
palmitoyltransferase ZDHHC20-B-like isoform X1
palmitoyltransferase ZDHHC20-B-like isoform X3
APC membrane recruitment protein 2, 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 4 samples with support for all annotated introns
APC membrane recruitment protein 2, transcript variant X2
pleckstrin homology-like domain, family B, member 2a, transcript variant X6
pleckstrin homology-like domain, family B, member 2a, transcript variant X5
pleckstrin homology-like domain, family B, member 2a, transcript variant X7
pleckstrin homology-like domain, family B, member 2a, transcript variant X4
pleckstrin homology-like domain, family B, member 2a, transcript variant X3
pleckstrin homology-like domain, family B, member 2a, transcript variant X2
pleckstrin homology-like domain, family B, member 2a, transcript variant X1
pleckstrin homology-like domain family B member 2 isoform X3
pleckstrin homology-like domain family B member 2 isoform X5
pleckstrin homology-like domain family B member 2 isoform X2
pleckstrin homology-like domain family B member 2 isoform X4
pleckstrin homology-like domain family B member 2 isoform X1
pleckstrin homology-like domain, family B, member 2a, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
pleckstrin homology-like domain family B member 2 isoform X6
protein Aster-B-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
protein Aster-B-like, transcript variant X2
protein Aster-B-like, transcript variant X4
protein Aster-B-like, transcript variant X3
protein Aster-B-like, transcript variant X1
dishevelled-binding antagonist of beta-catenin 3a, 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 34 samples with support for all annotated introns
dishevelled-binding antagonist of beta-catenin 3a, 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 7 samples with support for all annotated introns
dishevelled-binding antagonist of beta-catenin 3a, 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 25 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
myotonin-protein kinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
myotonin-protein kinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized protein LOC100124596 homolog
putative transcription factor ovo-like protein 3
v-akt murine thymoma viral oncogene homolog 2, like, transcript variant X1
v-akt murine thymoma viral oncogene homolog 2, like, transcript variant X2
v-akt murine thymoma viral oncogene homolog 2, like isoform X1
v-akt murine thymoma viral oncogene homolog 2, like isoform X2
leucine rich repeat containing 32, transcript variant X1
transforming growth factor beta activator LRRC32 isoform X1
leucine rich repeat containing 32, transcript variant X2
transforming growth factor beta activator LRRC32 isoform X2
EMSY transcriptional repressor, BRCA2 interacting
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
BRCA2-interacting transcriptional repressor EMSY
kelch-like family member 35, transcript variant X2
kelch-like family member 35, transcript variant X1
myelin protein zero-like 1 like, transcript variant X4
myelin protein zero-like 1 like, transcript variant X3
myelin protein zero-like 1 like isoform X3
myelin protein zero-like 1 like isoform X2
myelin protein zero-like 1 like, transcript variant X2
myelin protein zero-like 1 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 18 samples with support for all annotated introns
myelin protein zero-like 1 like isoform X1
Rho GTPase activating protein 32b, transcript variant X1
Rho GTPase activating protein 32b, transcript variant X2
Rho GTPase activating protein 32b, transcript variant X3
rho GTPase-activating protein 32 isoform X1
rho GTPase-activating protein 32 isoform X2
rho GTPase-activating protein 32 isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein turtle homolog B
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
non-SMC condensin II complex, subunit D3
vacuolar protein sorting 26 homolog B, like, transcript variant X1
vacuolar protein sorting 26 homolog B, like, transcript variant X2
vacuolar protein sorting-associated protein 26B-like
fasciculation and elongation protein zeta 1 (zygin I)
fasciculation and elongation protein zeta-1
endothelial cell adhesion molecule a, transcript variant X1
endothelial cell adhesion molecule a, transcript variant X2
endothelial cell adhesion molecule a isoform X1
endothelial cell adhesion molecule a isoform X2
myb/SANT-like DNA-binding domain-containing protein 2
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 36 samples with support for all annotated introns
roundabout, axon guidance receptor, homolog 3 (Drosophila)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
roundabout, axon guidance receptor, homolog 4 (Drosophila)
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: roundabout homolog 1
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 42 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
MKS transition zone complex subunit 1, transcript variant X2
MKS transition zone complex subunit 1, transcript variant X1
Meckel syndrome type 1 protein isoform X1
Meckel syndrome type 1 protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
inactive peptidyl-prolyl cis-trans isomerase FKBP6
uncharacterized protein LOC795694 homolog
replication factor C (activator 1) 2, 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 39 samples with support for all annotated introns
replication factor C (activator 1) 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized protein LOC566445 homolog
thread biopolymer filament subunit alpha
uncharacterized protein C11orf87 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 10, 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 7 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 10, transcript variant X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 10, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 10, 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 3 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 10, transcript variant X4
DEAD (Asp-Glu-Ala-Asp) box polypeptide 10, 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 12 samples with support for all annotated introns
probable ATP-dependent RNA helicase DDX10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
centromere/kinetochore protein zw10 homolog
G protein-activated inward rectifier potassium channel 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ubiquitin specific peptidase 28, transcript variant X1
ubiquitin specific peptidase 28, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 28 isoform X2
ubiquitin carboxyl-terminal hydrolase 28 isoform X1
5-hydroxytryptamine (serotonin) receptor 3B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
5-hydroxytryptamine (serotonin) receptor 3A
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 3 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 16-A-like
neural cell adhesion molecule 1a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
neural cell adhesion molecule 1a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
neural cell adhesion molecule 1a, transcript variant X2
neural cell adhesion molecule 1a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neural cell adhesion molecule 1a, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
neural cell adhesion molecule 1a, 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 18 samples with support for all annotated introns
neural cell adhesion molecule 1a, transcript variant X7
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 29 samples with support for all annotated introns
neural cell adhesion molecule 1a, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
neural cell adhesion molecule 1a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
neural cell adhesion molecule 1a isoform X8
neural cell adhesion molecule 1a isoform X4
neural cell adhesion molecule 1a isoform X7
neural cell adhesion molecule 1a isoform X3
neural cell adhesion molecule 1a isoform X2
neural cell adhesion molecule 1a isoform X6
neural cell adhesion molecule 1a isoform X1
neural cell adhesion molecule 1a isoform X5
neural cell adhesion molecule 1a isoform X11
neural cell adhesion molecule 1a, transcript variant X10
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 19 samples with support for all annotated introns
neural cell adhesion molecule 1a, transcript variant X9
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 27 samples with support for all annotated introns
neural cell adhesion molecule 1a isoform X10
neural cell adhesion molecule 1a isoform X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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 31 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 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: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
opioid binding protein/cell adhesion molecule-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 1 sample with support for all annotated introns
opioid binding protein/cell adhesion molecule-like, transcript variant X3
opioid binding protein/cell adhesion molecule-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
opioid-binding protein/cell adhesion molecule isoform X2
opioid-binding protein/cell adhesion molecule isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
tetratricopeptide repeat domain 1, transcript variant X1
tetratricopeptide repeat domain 1, transcript variant X2
fatty acid binding protein 6, ileal (gastrotropin)
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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
prefoldin subunit 1, transcript variant X1
prefoldin subunit 1, transcript variant X2
heterogeneous nuclear ribonucleoprotein H1, like, transcript variant X2
heterogeneous nuclear ribonucleoprotein H1, like, transcript variant X3
heterogeneous nuclear ribonucleoprotein H1, like, transcript variant X1
heterogeneous nuclear ribonucleoprotein H1, like isoform X2
heterogeneous nuclear ribonucleoprotein H1, like isoform X3
heterogeneous nuclear ribonucleoprotein H1, like isoform X1
heterogeneous nuclear ribonucleoprotein H1, like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein H1, like isoform X4
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 39 samples with support for all annotated introns
ankyrin repeat and KH domain containing 1, transcript variant X9
ankyrin repeat and KH domain containing 1, transcript variant X3
ankyrin repeat and KH domain containing 1, transcript variant X1
ankyrin repeat and KH domain containing 1, transcript variant X2
ankyrin repeat and KH domain containing 1, transcript variant X8
ankyrin repeat and KH domain containing 1, transcript variant X4
ankyrin repeat and KH domain containing 1, transcript variant X5
ankyrin repeat and KH domain containing 1, transcript variant X10
ankyrin repeat and KH domain containing 1, transcript variant X6
ankyrin repeat and KH domain containing 1, transcript variant X7
ankyrin repeat and KH domain containing 1, transcript variant X12
ankyrin repeat and KH domain containing 1, transcript variant X11
ankyrin repeat and KH domain-containing protein 1 isoform X1
ankyrin repeat and KH domain-containing protein 1 isoform X6
ankyrin repeat and KH domain-containing protein 1 isoform X2
ankyrin repeat and KH domain-containing protein 1 isoform X3
ankyrin repeat and KH domain-containing protein 1 isoform X8
ankyrin repeat and KH domain-containing protein 1 isoform X4
ankyrin repeat and KH domain-containing protein 1 isoform X5
ankyrin repeat and KH domain-containing protein 1 isoform X10
ankyrin repeat and KH domain-containing protein 1 isoform X7
ankyrin repeat and KH domain-containing protein 1 isoform X9
eukaryotic translation initiation factor 4E binding protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
eukaryotic translation initiation factor 4E-binding protein 3
methionine adenosyltransferase II, beta, transcript variant X2
methionine adenosyltransferase 2 subunit beta isoform X2
methionine adenosyltransferase II, beta, transcript variant X1
methionine adenosyltransferase 2 subunit beta isoform X1
cysteine-rich and transmembrane domain-containing protein 1-like, transcript variant X1
cysteine-rich and transmembrane domain-containing protein 1-like, transcript variant X2
cysteine-rich and transmembrane domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glutamate receptor, ionotropic, AMPA 1b, transcript variant X1
glutamate receptor, ionotropic, AMPA 1b, transcript variant X2
trafficking protein particle complex subunit 14
uncharacterized protein LOC767741 homolog
polyunsaturated fatty acid lipoxygenase ALOX15B
macrophage mannose receptor 1-like, 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 1 sample with support for all annotated introns
macrophage mannose receptor 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
macrophage mannose receptor 1-like, 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 33 samples with support for all annotated introns
macrophage mannose receptor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
macrophage mannose receptor 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
macrophage mannose receptor 1-like isoform X1
macrophage mannose receptor 1-like isoform X2
eva-1 homolog C (C. elegans), 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 28 samples with support for all annotated introns
eva-1 homolog C (C. elegans), 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 28 samples with support for all annotated introns
cilia and flagella associated protein 298, transcript variant X2
cilia- and flagella-associated protein 298 isoform X2
cilia and flagella associated protein 298, 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 13 samples with support for all annotated introns
cilia- and flagella-associated protein 298 isoform X1
GrpE-like 2, mitochondrial, transcript variant X1
GrpE-like 2, mitochondrial, transcript variant X2
grpE protein homolog 2, mitochondrial isoform X1
grpE protein homolog 2, mitochondrial isoform X2
actin filament associated protein 1-like 1b, transcript variant X2
actin filament associated protein 1-like 1b, transcript variant X1
actin filament-associated protein 1-like 1b isoform X2
actin filament-associated protein 1-like 1b isoform X1
actin binding LIM protein family, member 3
beta-2 adrenergic receptor-like, transcript variant X2
beta-2 adrenergic receptor-like, transcript variant X1
beta-2 adrenergic receptor-like isoform X1
beta-2 adrenergic receptor-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
interleukin 12B, b, transcript variant X1
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 24 samples with support for all annotated introns
interleukin 12B, b, transcript variant X2
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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ubiquitin-like domain containing CTD phosphatase 1
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 41 samples with support for all annotated introns
ubiquitin-like domain-containing CTD phosphatase 1
RING finger protein 145-like, transcript variant X1
RING finger protein 145-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 38 samples with support for all annotated introns
clathrin interactor 1-like, transcript variant X1
clathrin interactor 1-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
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
transcription elongation regulator 1b (CA150), 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 43 samples with support for all annotated introns
transcription elongation regulator 1b (CA150), 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 39 samples with support for all annotated introns
transcription elongation regulator 1b (CA150), transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
transcription elongation regulator 1b (CA150), transcript variant X3
transcription elongation regulator 1 isoform X1
transcription elongation regulator 1 isoform X2
transcription elongation regulator 1 isoform X4
transcription elongation regulator 1 isoform X3
protein phosphatase 2, regulatory subunit B, beta b
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
BCL2 interacting protein 1b, transcript variant X2
BCL2 interacting protein 1b, transcript variant X1
vesicle transport protein SEC20 isoform X1
vesicle transport protein SEC20 isoform X2
biorientation of chromosomes in cell division 1, 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 25 samples with support for all annotated introns
biorientation of chromosomes in cell division 1, 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 44 samples with support for all annotated introns
biorientation of chromosomes in cell division protein 1
HIV-1 Tat specific factor 1, transcript variant X1
HIV-1 Tat specific factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
interferon regulatory factor 1b, transcript variant X1
interferon regulatory factor 1b, transcript variant X2
interferon regulatory factor 1b isoform X1
interferon regulatory factor 1b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
interferon regulatory factor 1b isoform X2
acyl-CoA synthetase long chain family member 6, 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
acyl-CoA synthetase long chain family member 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
long-chain-fatty-acid--CoA ligase 6 isoform X1
long-chain-fatty-acid--CoA ligase 6 isoform X2
uncharacterized LOC124482714, transcript variant X1
uncharacterized LOC124482714, transcript variant X4
uncharacterized LOC124482714, transcript variant X3
uncharacterized LOC124482714, transcript variant X2
uncharacterized protein LOC124482714 isoform X1
uncharacterized protein LOC124482714 isoform X2
uncharacterized protein LOC124482714 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC124482718, 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 25 samples with support for all annotated introns
uncharacterized LOC124482718, 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 20 samples with support for all annotated introns
uncharacterized protein LOC124482718 isoform X2
uncharacterized protein LOC124482718 isoform X1
folliculin interacting protein 1, transcript variant X1
folliculin interacting protein 1, transcript variant X3
folliculin interacting protein 1, transcript variant X4
folliculin interacting protein 1, transcript variant X5
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, including 42 samples with support for all annotated introns
folliculin-interacting protein 1 isoform X1
folliculin-interacting protein 1 isoform X3
folliculin-interacting protein 1 isoform X4
folliculin-interacting protein 1 isoform X5
folliculin interacting protein 1, transcript variant X2
folliculin-interacting protein 1 isoform X2
Rap guanine nucleotide exchange factor (GEF) 6, transcript variant X1
Rap guanine nucleotide exchange factor (GEF) 6, transcript variant X3
Rap guanine nucleotide exchange factor (GEF) 6, transcript variant X2
rap guanine nucleotide exchange factor 6 isoform X1
rap guanine nucleotide exchange factor 6 isoform X3
rap guanine nucleotide exchange factor 6 isoform X2
Rap guanine nucleotide exchange factor (GEF) 6, transcript variant X4
rap guanine nucleotide exchange factor 6 isoform X4
Rap guanine nucleotide exchange factor (GEF) 6, transcript variant X5
rap guanine nucleotide exchange factor 6 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
tyrosine-protein phosphatase non-receptor type 7-like
T cell immunoglobulin and mucin domain containing 4
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 10 samples with support for all annotated introns
T-cell immunoglobulin and mucin domain-containing protein 4
RNA binding motif protein 27, 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 11 samples with support for all annotated introns
RNA binding motif protein 27, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins
POU domain, class 4, transcription factor 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
RAD50 homolog, double strand break repair protein
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: DNA repair protein RAD50
dopamine receptor D1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dopamine receptor D1b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
neuronal vesicle trafficking associated 2
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 3 samples with support for all annotated introns
neuronal vesicle trafficking-associated protein 2
cytoplasmic polyadenylation element binding protein 4b, transcript variant X2
cytoplasmic polyadenylation element binding protein 4b, transcript variant X1
cytoplasmic polyadenylation element-binding protein 4b isoform X1
cytoplasmic polyadenylation element-binding protein 4b isoform X2
RNA binding motif protein 14a, transcript variant X4
RNA binding motif protein 14a, transcript variant X3
RNA binding motif protein 14a, transcript variant X2
RNA binding motif protein 14a, transcript variant X1
RNA binding motif protein 14a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
Ras and Rab interactor 1a, transcript variant X1
Ras and Rab interactor 1a, 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 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon GCU); 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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 2-like
LOW QUALITY PROTEIN: A disintegrin and metalloproteinase with thrombospondin motifs 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
regulator of G protein signaling 14b, transcript variant X2
regulator of G protein signaling 14b, transcript variant X1
regulator of G protein signaling 14b, transcript variant X3
regulator of G-protein signaling 14 isoform X2
regulator of G-protein signaling 14 isoform X1
regulator of G-protein signaling 14 isoform X3
bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1-like, transcript variant X4
bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1-like, transcript variant X1
bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1-like, transcript variant X2
bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1-like, transcript variant X3
bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1-like
CD74 molecule, major histocompatibility complex, class II invariant chain b, transcript variant X1
CD74 molecule, major histocompatibility complex, class II invariant chain b, transcript variant X5
CD74 molecule, major histocompatibility complex, class II invariant chain b, transcript variant X3
CD74 molecule, major histocompatibility complex, class II invariant chain b, transcript variant X6
CD74 molecule, major histocompatibility complex, class II invariant chain b, transcript variant X2
CD74 molecule, major histocompatibility complex, class II invariant chain b, transcript variant X8
CD74 molecule, major histocompatibility complex, class II invariant chain b, transcript variant X4
CD74 molecule, major histocompatibility complex, class II invariant chain b, transcript variant X7
CD74 molecule, major histocompatibility complex, class II invariant chain b isoform X1
CD74 molecule, major histocompatibility complex, class II invariant chain b isoform X2
SLC35A4 upstream open reading frame protein-like
amyloid beta (A4) precursor protein-binding, family B, member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
amyloid-beta A4 precursor protein-binding family B member 3
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon CUC); 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: 9 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
vascular endothelial growth factor c, transcript variant X1
vascular endothelial growth factor c, transcript variant X2
vascular endothelial growth factor C isoform X2
vascular endothelial growth factor C isoform X1
macrophage colony-stimulating factor 1 receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
platelet-derived growth factor receptor beta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
T-cell surface antigen CD2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
T-cell surface antigen CD2-like, transcript variant X2
T-cell surface antigen CD2-like, transcript variant X1
uncharacterized protein LOC124482643 isoform X3
uncharacterized protein LOC124482643 isoform X2
T-cell surface antigen CD2-like isoform X1
T-cell immunoglobulin and mucin domain-containing protein 4-like
hepatocyte cell adhesion molecule-like, transcript variant X1
hepatocyte cell adhesion molecule-like, transcript variant X2
hepatocyte cell adhesion molecule-like isoform X1
hepatocyte cell adhesion molecule-like isoform X2
calcium/calmodulin-dependent protein kinase II alpha
calcium/calmodulin-dependent protein kinase type II subunit alpha
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
nucleolar protein dao-5-like, transcript variant X1
nucleolar protein dao-5-like, transcript variant X2
NADH:ubiquinone oxidoreductase subunit A2
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 2
arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 1, transcript variant X3
arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 1, transcript variant X2
arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 1, transcript variant X1
arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 1 isoform X2
arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 1 isoform X1
arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
mitogen-activated protein kinase kinase kinase kinase 6
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
high mobility group box 3b, transcript variant X2
high mobility group box 3b, transcript variant X1
mitochondrial ornithine transporter 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
short transient receptor potential channel 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
ALG13 UDP-N-acetylglucosaminyltransferase subunit
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
putative bifunctional UDP-N-acetylglucosamine transferase and deubiquitinase ALG13
dachshund homolog 2-like, transcript variant X2
dachshund homolog 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
rab proteins geranylgeranyltransferase component A 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
uncharacterized protein LOC550336 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
autophagy related 4A, cysteine peptidase
nascent polypeptide-associated complex subunit alpha, muscle-specific form
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
wiskott-Aldrich syndrome protein family member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
chloride channel, voltage-sensitive 5a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
chloride channel, voltage-sensitive 5a, 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
H(+)/Cl(-) exchange transporter 5 isoform X2
H(+)/Cl(-) exchange transporter 5 isoform X1
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform-like
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
phosphatidylinositol-binding clathrin assembly protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
cytokine receptor common subunit gamma-like, transcript variant X1
cytokine receptor common subunit gamma-like, transcript variant X4
cytokine receptor common subunit gamma-like, transcript variant X3
cytokine receptor common subunit gamma-like, transcript variant X2
cytokine receptor common subunit gamma-like isoform X3
cytokine receptor common subunit gamma-like isoform X1
cytokine receptor common subunit gamma-like isoform X4
cytokine receptor common subunit gamma-like isoform X2
cytokine receptor common subunit gamma-like
golgin subfamily A member 6-like protein 6
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
Bardet-Biedl syndrome 1, transcript variant X1
Bardet-Biedl syndrome 1, transcript variant X2
Bardet-Biedl syndrome 1 protein isoform X1
Bardet-Biedl syndrome 1 protein isoform 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 5 samples with support for all annotated introns
equilibrative nucleoside transporter 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
equilibrative nucleoside transporter 2-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 38 samples with support for all annotated introns
equilibrative nucleoside transporter 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
trichohyalin-like, transcript variant X1
trichohyalin-like, transcript variant X2
uncharacterized protein LOC792578 homolog, transcript variant X3
uncharacterized protein LOC792578 homolog, transcript variant X2
immunoglobulin superfamily member 11 isoform X2
uncharacterized protein LOC792578 homolog, 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 22 samples with support for all annotated introns
immunoglobulin superfamily member 11 isoform X1
immunoglobulin superfamily member 11 isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
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: pecanex-like protein 3
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: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
CD209 antigen-like protein E, 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 34 samples with support for all annotated introns
CD209 antigen-like protein E, 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 35 samples with support for all annotated introns
RAS guanyl-releasing protein 2-like, transcript variant X2
RAS guanyl-releasing protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
endothelial cell surface expressed chemotaxis and apoptosis regulator, transcript variant X4
endothelial cell surface expressed chemotaxis and apoptosis regulator, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
endothelial cell surface expressed chemotaxis and apoptosis regulator, transcript variant X1
endothelial cell surface expressed chemotaxis and apoptosis regulator, 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 37 samples with support for all annotated introns
endothelial cell-specific chemotaxis regulator isoform X3
endothelial cell-specific chemotaxis regulator isoform X2
endothelial cell-specific chemotaxis regulator isoform X1
DnaJ (Hsp40) homolog, subfamily C, member 18
bromodomain containing 8a, transcript variant X2
bromodomain containing 8a, transcript variant X1
bromodomain containing 8a, transcript variant X3
bromodomain-containing protein 8 isoform X2
bromodomain-containing protein 8 isoform X1
bromodomain-containing protein 8 isoform X3
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
kinesin family member 20A, transcript variant X2
kinesin family member 20A, transcript variant X1
kinesin family member 20A, 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 36 samples with support for all annotated introns
kinesin family member 20A, transcript variant X3
CDC23 (cell division cycle 23, yeast, homolog)
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 42 samples with support for all annotated introns
GDNF family receptor alpha-4-like, transcript variant X2
GDNF family receptor alpha-4-like, transcript variant X1
pre-mRNA 3'-end-processing factor FIP1-like
uncharacterized protein LOC100038774 homolog
uncharacterized protein LOC562682 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC553498 homolog
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
U3 small nucleolar RNA-associated protein 14 homolog A
zinc finger and BTB domain containing 20
zinc finger and BTB domain-containing protein 20
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
Rho GTPase activating protein 31, transcript variant X2
Rho GTPase activating protein 31, transcript variant X1
rho GTPase-activating protein 31 isoform X2
rho GTPase-activating protein 31 isoform X1
UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
cationic amino acid transporter 2 family protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cationic amino acid transporter 2 family protein
eukaryotic translation initiation factor 4E family member 1B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
eukaryotic translation initiation factor 4E-1B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
abhydrolase domain containing 10, depalmitoylase a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mitochondrial translational initiation factor 3
translation initiation factor IF-3, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
V-type proton ATPase catalytic subunit A
palmitoyltransferase ZDHHC23-A-like, transcript variant X2
palmitoyltransferase ZDHHC23-A-like, transcript variant X3
palmitoyltransferase ZDHHC23-A-like, transcript variant X1
palmitoyltransferase ZDHHC23-A-like isoform X1
palmitoyltransferase ZDHHC23-A-like isoform X2
palmitoyltransferase ZDHHC23-A-like isoform X3
thiosulfate:glutathione sulfurtransferase-like
zinc finger Y-chromosomal protein 1, transcript variant X1
zinc finger Y-chromosomal protein 1, transcript variant X2
zinc finger Y-chromosomal protein 1 isoform X2
zinc finger Y-chromosomal protein 1 isoform X1
apolipoprotein O, a, transcript variant X1
apolipoprotein O, a, transcript variant X3
apolipoprotein O, a, transcript variant X2
apolipoprotein O, a, transcript variant X4
spermidine/spermine N1-acetyltransferase 1a, duplicate 2
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: diamine acetyltransferase 1a.2
pyruvate dehydrogenase E1 subunit alpha 1a, transcript variant X1
pyruvate dehydrogenase E1 subunit alpha 1a, transcript variant X2
pyruvate dehydrogenase E1 subunit alpha 1a, transcript variant X3
pyruvate dehydrogenase E1 subunit alpha 1a isoform X1
pyruvate dehydrogenase E1 subunit alpha 1a isoform X2
pyruvate dehydrogenase E1 subunit alpha 1a isoform X3
ribosomal protein S6 kinase a, polypeptide 3a, transcript variant X3
ribosomal protein S6 kinase a, polypeptide 3a, transcript variant X2
ribosomal protein S6 kinase alpha-1 isoform X2
ribosomal protein S6 kinase a, polypeptide 3a, transcript variant X1
ribosomal protein S6 kinase alpha-1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
golgin subfamily A member 6-like protein 22
uncharacterized protein LOC336578 homolog
serine/arginine repetitive matrix protein 1
SH3 domain-containing kinase-binding protein 1, transcript variant X1
SH3 domain-containing kinase-binding protein 1, transcript variant X3
SH3 domain-containing kinase-binding protein 1, transcript variant X2
SH3 domain-containing kinase-binding protein 1, transcript variant X5
SH3 domain-containing kinase-binding protein 1, transcript variant X6
SH3 domain-containing kinase-binding protein 1, transcript variant X8
SH3 domain-containing kinase-binding protein 1, 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 7 samples with support for all annotated introns
SH3 domain-containing kinase-binding protein 1, transcript variant X7
SH3 domain-containing kinase-binding protein 1 isoform X2
SH3 domain-containing kinase-binding protein 1 isoform X4
SH3 domain-containing kinase-binding protein 1 isoform X1
SH3 domain-containing kinase-binding protein 1 isoform X3
lipase, member Ia, transcript variant X2
lipase, member Ia, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 82
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
aristaless-related homeobox protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 9 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
ferredoxin-fold anticodon binding domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ferredoxin-fold anticodon binding domain containing 1, 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
ferredoxin-fold anticodon-binding domain-containing protein 1 isoform X1
ferredoxin-fold anticodon-binding domain-containing protein 1 isoform X2
BAF chromatin remodeling complex subunit BCL7B a, transcript variant X3
BAF chromatin remodeling complex subunit BCL7B a, transcript variant X1
BAF chromatin remodeling complex subunit BCL7B a, transcript variant X4
BAF chromatin remodeling complex subunit BCL7B a, transcript variant X2
B-cell CLL/lymphoma 7 protein family member B-A isoform X4
B-cell CLL/lymphoma 7 protein family member B-A isoform X3
B-cell CLL/lymphoma 7 protein family member B-A isoform X2
B-cell CLL/lymphoma 7 protein family member B-A isoform X1
NOP2/Sun RNA methyltransferase 5, transcript variant X2
NOP2/Sun RNA methyltransferase 5, transcript variant X1
probable 28S rRNA (cytosine-C(5))-methyltransferase isoform X1
probable 28S rRNA (cytosine-C(5))-methyltransferase isoform X2
POM121 transmembrane nucleoporin, 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 26 samples with support for all annotated introns
POM121 transmembrane nucleoporin, 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 42 samples with support for all annotated introns
nuclear envelope pore membrane protein POM 121 isoform X2
nuclear envelope pore membrane protein POM 121 isoform X1
serine/threonine/tyrosine interacting-like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine/tyrosine-interacting-like protein 1 isoform X1
serine/threonine/tyrosine interacting-like 1, transcript variant X2
SMG8 nonsense mediated mRNA decay factor
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
serine/threonine/tyrosine interacting-like 1, 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 35 samples with support for all annotated introns
serine/threonine/tyrosine-interacting-like protein 1 isoform X2
transmembrane protein 120Aa, transcript variant X1
transmembrane protein 120Aa, transcript variant X2
phosphatidylinositol-binding clathrin assembly protein-like, transcript variant X8
phosphatidylinositol-binding clathrin assembly protein-like, transcript variant X4
phosphatidylinositol-binding clathrin assembly protein-like, transcript variant X6
phosphatidylinositol-binding clathrin assembly protein-like, transcript variant X7
phosphatidylinositol-binding clathrin assembly protein-like, transcript variant X12
phosphatidylinositol-binding clathrin assembly protein-like, transcript variant X11
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 32 samples with support for all annotated introns
phosphatidylinositol-binding clathrin assembly protein-like, transcript variant X1
phosphatidylinositol-binding clathrin assembly protein-like, transcript variant X3
phosphatidylinositol-binding clathrin assembly protein-like, transcript variant X5
phosphatidylinositol-binding clathrin assembly protein-like, transcript variant X2
phosphatidylinositol-binding clathrin assembly protein-like, transcript variant X10
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
phosphatidylinositol-binding clathrin assembly protein-like, transcript variant X9
phosphatidylinositol-binding clathrin assembly protein-like isoform X8
phosphatidylinositol-binding clathrin assembly protein-like isoform X9
phosphatidylinositol-binding clathrin assembly protein-like isoform X12
phosphatidylinositol-binding clathrin assembly protein-like isoform X1
phosphatidylinositol-binding clathrin assembly protein-like isoform X4
phosphatidylinositol-binding clathrin assembly protein-like isoform X3
phosphatidylinositol-binding clathrin assembly protein-like isoform X6
phosphatidylinositol-binding clathrin assembly protein-like isoform X5
phosphatidylinositol-binding clathrin assembly protein-like isoform X7
phosphatidylinositol-binding clathrin assembly protein-like isoform X2
phosphatidylinositol-binding clathrin assembly protein-like isoform X10
phosphatidylinositol-binding clathrin assembly protein-like isoform X11
coiled-coil domain containing 83, transcript variant X2
coiled-coil domain containing 83, transcript variant X1
coiled-coil domain-containing protein 83
uncharacterized protein LOC768125 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 38 samples with support for all annotated introns
adenosine deaminase domain containing 2, transcript variant X1
adenosine deaminase domain containing 2, 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 2 samples with support for all annotated introns
adenosine deaminase domain containing 2, transcript variant X2
adenosine deaminase domain-containing protein 2 isoform X1
adenosine deaminase domain-containing protein 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
protein phosphatase 1, regulatory (inhibitor) subunit 14Aa
exocyst complex component 3-like 2a, transcript variant X1
exocyst complex component 3-like 2a, transcript variant X2
MAP/microtubule affinity-regulating kinase 4a
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: MAP/microtubule affinity-regulating kinase 4
solute carrier family 8 member 2a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 8 member 2a, transcript variant X1
solute carrier family 8 member 2a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
serine and arginine rich splicing factor 7a
heterogeneous nuclear ribonucleoprotein L, transcript variant X2
heterogeneous nuclear ribonucleoprotein L, transcript variant X3
heterogeneous nuclear ribonucleoprotein L, transcript variant X1
heterogeneous nuclear ribonucleoprotein L, transcript variant X4
heterogeneous nuclear ribonucleoprotein L, transcript variant X5
heterogeneous nuclear ribonucleoprotein L isoform X2
heterogeneous nuclear ribonucleoprotein L isoform X3
heterogeneous nuclear ribonucleoprotein L isoform X1
heterogeneous nuclear ribonucleoprotein L isoform X4
heterogeneous nuclear ribonucleoprotein L isoform X5
cation channel sperm-associated protein subunit gamma-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
interferon regulatory factor 2-binding protein 1-like
basic helix-loop-helix family, member a9
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
class A basic helix-loop-helix protein 9
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