Perognathus longimembris pacificus isolate PPM17 chromosome 9, ASM2315922v1, whole genome shotgun sequence.
Perognathus longimembris pacificus (Pacific pocket mouse)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Castorimorpha; Heteromyidae; Perognathinae; Perognathus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM041272.1.\nAssembly name: ASM2315922v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the San Diego Zoo Wildlife\nAlliance on 2022/04/27. The original whole-genome shotgun project\nhas the accession JALGBO000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: San Diego Zoo Wildlife Alliance\nAssembly Date :: 2021\nAssembly Method :: Peregrine v. JUNE-2020; HiRise v.\n JULY-2020; Juicer v. DECEMBER-2020;\n Juicebox Assembly Tools v. DECEMBER-2020\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 23.0x\nSequencing Technology :: PacBio Sequel\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Perognathus longimembris pacificus\n Annotation 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##
Derived by automated computational analysis using gene prediction method: Gnomon.
family with sequence similarity 135 member A, 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 5 samples with support for all annotated introns
family with sequence similarity 135 member A, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
family with sequence similarity 135 member A, transcript variant X8
family with sequence similarity 135 member A, transcript variant X4
family with sequence similarity 135 member A, transcript variant X7
family with sequence similarity 135 member A, transcript variant X6
family with sequence similarity 135 member A, transcript variant X1
family with sequence similarity 135 member A, transcript variant X3
family with sequence similarity 135 member A, transcript variant X9
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, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62% coverage of the annotated genomic feature by RNAseq alignments
lysosomal cobalamin transport escort protein LMBD1
adhesion G protein-coupled receptor B3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83% coverage of the annotated genomic feature by RNAseq alignments
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: 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: 2 Proteins
melanocortin 2 receptor accessory protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
melanocortin-2 receptor accessory protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
cytochrome b5 reductase 4, transcript variant X2
cytochrome b5 reductase 4, transcript variant X1
cytochrome b5 reductase 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 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 90% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: NADP-dependent malic enzyme
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: 9 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: RWD domain-containing protein 2A
phosphoglucomutase 3, transcript variant X2
phosphoglucomutase 3, transcript variant X1
phosphoacetylglucosamine mutase isoform X1
phosphoacetylglucosamine mutase isoform X2
DOP1 leucine zipper like protein A, transcript variant X3
DOP1 leucine zipper like protein A, transcript variant X1
DOP1 leucine zipper like protein A, transcript variant X2
DOP1 leucine zipper like protein A, transcript variant X4
DOP1 leucine zipper like protein A, 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 3 samples with support for all annotated introns
DOP1 leucine zipper like protein A, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
inhibitor of Bruton tyrosine kinase, transcript variant X1
inhibitor of Bruton tyrosine kinase, transcript variant X2
inhibitor of Bruton tyrosine kinase isoform X1
inhibitor of Bruton tyrosine kinase isoform X2
terminal nucleotidyltransferase 5A, transcript variant X1
terminal nucleotidyltransferase 5A, transcript variant X2
terminal nucleotidyltransferase 5A isoform X1
terminal nucleotidyltransferase 5A isoform X2
branched chain keto acid dehydrogenase E1 subunit beta, transcript variant X2
branched chain keto acid dehydrogenase E1 subunit beta, transcript variant X1
2-oxoisovalerate dehydrogenase subunit beta, mitochondrial isoform X1
2-oxoisovalerate dehydrogenase subunit beta, mitochondrial 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 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 2 samples with support for all annotated introns
proline-rich protein HaeIII subfamily 1-like
TTK protein kinase, transcript variant X2
TTK protein kinase, transcript variant X1
dual specificity protein kinase TTK isoform X2
dual specificity protein kinase TTK isoform 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 1 sample with support for all annotated introns
elongation of very long chain fatty acids protein 4
SH3 domain binding glutamate rich protein like 2
SH3 domain-binding glutamic acid-rich-like protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
high mobility group nucleosomal binding domain 3, transcript variant X2
high mobility group nucleosomal binding domain 3, transcript variant X1
high mobility group nucleosomal binding domain 3, transcript variant X3
high mobility group nucleosome-binding domain-containing protein 3 isoform X1
high mobility group nucleosome-binding domain-containing protein 3 isoform X3
high mobility group nucleosome-binding domain-containing protein 3 isoform X2
pleckstrin homology domain interacting protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
interleukin 1 receptor associated kinase 1 binding protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
interleukin 1 receptor associated kinase 1 binding protein 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 12 samples with support for all annotated introns
interleukin-1 receptor-associated kinase 1-binding protein 1 isoform X2
interleukin-1 receptor-associated kinase 1-binding protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins
meiotic double-stranded break formation protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
interphotoreceptor matrix proteoglycan 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 7 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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
SUMO specific peptidase 6, transcript variant X10
SUMO specific peptidase 6, transcript variant X3
SUMO specific peptidase 6, transcript variant X9
SUMO specific peptidase 6, transcript variant X8
SUMO specific peptidase 6, transcript variant X7
SUMO specific peptidase 6, transcript variant X2
SUMO specific peptidase 6, transcript variant X1
SUMO specific peptidase 6, transcript variant X5
SUMO specific peptidase 6, transcript variant X4
SUMO specific peptidase 6, transcript variant X6
SUMO specific peptidase 6, transcript variant X12
SUMO specific peptidase 6, transcript variant X11
SUMO specific peptidase 6, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
filamin A interacting protein 1, transcript variant X3
filamin A interacting protein 1, transcript variant X1
filamin-A-interacting protein 1 isoform X3
filamin-A-interacting protein 1 isoform X1
filamin A interacting protein 1, 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 1 sample with support for all annotated introns
filamin-A-interacting protein 1 isoform X2
cytochrome c oxidase subunit 7A2, mitochondrial
collagen type XII alpha 1 chain, transcript variant X2
collagen type XII alpha 1 chain, transcript variant X1
collagen type XII alpha 1 chain, transcript variant X3
collagen type XII alpha 1 chain, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
collagen type XII alpha 1 chain, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation elongation factor 1 alpha 1
mitochondrial tRNA translation optimization 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 11 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
probable ATP-dependent RNA helicase DDX43
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
KH homology domain-containing protein 1-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: 3 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily Q member 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 14 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium voltage-gated channel subfamily Q member 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily KQT member 5 isoform X1
potassium voltage-gated channel subfamily KQT member 5 isoform X2
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
D-aspartate oxidase, transcript variant X1
D-aspartate oxidase, transcript variant X2
D-aspartate oxidase, transcript variant X6
D-aspartate oxidase, transcript variant X4
D-aspartate oxidase, transcript variant X3
D-aspartate oxidase, transcript variant X5
probable methyltransferase-like protein 24
cell division cycle 40, transcript variant X1
cell division cycle 40, transcript variant X2
pre-mRNA-processing factor 17 isoform X1
pre-mRNA-processing factor 17 isoform X2
WASP family member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
WASP family member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
WASP family member 1, transcript variant X3
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, including 6 samples with support for all annotated introns
wiskott-Aldrich syndrome protein family member 1 isoform X1
wiskott-Aldrich syndrome protein family member 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 14 Proteins
FIG4 phosphoinositide 5-phosphatase, transcript variant X2
FIG4 phosphoinositide 5-phosphatase, transcript variant X1
polyphosphoinositide phosphatase isoform X2
polyphosphoinositide phosphatase isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and BTB domain containing 24, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
zinc finger and BTB domain containing 24, 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 8 samples with support for all annotated introns
zinc finger and BTB domain containing 24, 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 8 samples with support for all annotated introns
zinc finger and BTB domain containing 24, transcript variant X4
zinc finger and BTB domain containing 24, 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
zinc finger and BTB domain-containing protein 24 isoform X1
zinc finger and BTB domain-containing protein 24 isoform X3
zinc finger and BTB domain-containing protein 24 isoform X2
ral guanine nucleotide dissociation stimulator-like
microtubule associated monooxygenase, calponin and LIM domain containing 1, transcript variant X1
microtubule associated monooxygenase, calponin and LIM domain containing 1, transcript variant X2
microtubule associated monooxygenase, calponin and LIM domain containing 1, transcript variant X3
sphingomyelin phosphodiesterase 2, transcript variant X2
sphingomyelin phosphodiesterase 2, transcript variant X1
sphingomyelin phosphodiesterase 2 isoform X2
sphingomyelin phosphodiesterase 2 isoform X1
probable inactive peptidyl-prolyl cis-trans isomerase-like 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00045
centrosomal protein 57 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
centrosomal protein 57 like 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
centrosomal protein 57 like 1, 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 5 samples with support for all annotated introns
armadillo repeat containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
armadillo repeat containing 2, 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 4 samples with support for all annotated introns
armadillo repeat-containing protein 2 isoform X1
armadillo repeat-containing protein 2 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00438
nuclear receptor subfamily 2 group E member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 Proteins
osteoclastogenesis associated transmembrane protein 1
osteopetrosis-associated transmembrane protein 1
SEC63 homolog, protein translocation regulator, transcript variant X2
SEC63 homolog, protein translocation regulator, transcript variant X1
translocation protein SEC63 homolog isoform X1
translocation protein SEC63 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
sine oculis binding protein homolog, transcript variant X2
sine oculis binding protein homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sine oculis binding protein homolog, transcript variant X3
sine oculis-binding protein homolog isoform X2
sine oculis-binding protein homolog isoform X1
sine oculis-binding protein homolog isoform X3
decaprenyl diphosphate synthase subunit 2
all trans-polyprenyl-diphosphate synthase PDSS2
mitochondrial transcription rescue factor 1, transcript variant X3
mitochondrial transcription rescue factor 1, transcript variant X2
mitochondrial transcription rescue factor 1, transcript variant X1
mitochondrial transcription rescue factor 1
low molecular weight phosphotyrosine protein phosphatase-like
glutaminyl-tRNA amidotransferase subunit QRSL1
glutamyl-tRNA(Gln) amidotransferase subunit A, mitochondrial
reticulon-4-interacting protein 1, mitochondrial
eukaryotic translation initiation factor 1-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
crystallin beta-gamma domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
beta/gamma crystallin domain-containing protein 1
autophagy related 5, transcript variant X1
autophagy related 5, transcript variant X2
PR domain zinc finger protein 1 isoform X1
PR domain zinc finger protein 1 isoform X2
blood vessel epicardial substance, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
blood vessel epicardial substance, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 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 45% 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 60% coverage of the annotated genomic feature by RNAseq alignments
HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1, transcript variant X1
HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1, transcript variant X2
E3 ubiquitin-protein ligase HACE1 isoform X1
E3 ubiquitin-protein ligase HACE1 isoform X2
HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1, transcript variant X3
E3 ubiquitin-protein ligase HACE1 isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00432
glutamate ionotropic receptor kainate type subunit 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, kainate 2 isoform X1
glutamate ionotropic receptor kainate type subunit 2, 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 1 sample with support for all annotated introns
glutamate ionotropic receptor kainate type subunit 2, transcript variant X3
glutamate receptor ionotropic, kainate 2 isoform X2
activating signal cointegrator 1 complex subunit 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
activating signal cointegrator 1 complex subunit 3, transcript variant X1
activating signal cointegrator 1 complex subunit 3 isoform X1
activating signal cointegrator 1 complex subunit 3 isoform X2
SIM bHLH transcription factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
SIM bHLH transcription factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
SIM bHLH transcription factor 1, transcript variant X3
SIM bHLH transcription factor 1, transcript variant X5
SIM bHLH transcription factor 1, transcript variant X4
SIM bHLH transcription factor 1, transcript variant X6
melanin concentrating hormone receptor 2
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: 1 Protein
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: melanin-concentrating hormone receptor 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
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: PR domain zinc finger protein 13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
thiosulfate sulfurtransferase like domain containing 3
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 10 samples with support for all annotated introns
thiosulfate sulfurtransferase/rhodanese-like domain-containing protein 3
ubiquitin specific peptidase 45, transcript variant X1
ubiquitin specific peptidase 45, transcript variant X2
ubiquitin specific peptidase 45, transcript variant X5
ubiquitin specific peptidase 45, 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 3 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 45 isoform X1
ubiquitin carboxyl-terminal hydrolase 45 isoform X2
ubiquitin carboxyl-terminal hydrolase 45 isoform X4
ubiquitin specific peptidase 45, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 45 isoform X3
PNN interacting serine and arginine rich protein, transcript variant X5
PNN interacting serine and arginine rich protein, transcript variant X2
PNN interacting serine and arginine rich protein, transcript variant X1
PNN interacting serine and arginine rich protein, transcript variant X3
PNN interacting serine and arginine rich protein, transcript variant X4
ubiquinone biosynthesis O-methyltransferase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
failed axon connections homolog, metaxin like GST domain containing
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: 5 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: failed axon connections homolog
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: TM2 domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 40% coverage of the annotated genomic feature by RNAseq alignments
F-box and leucine rich repeat protein 4, transcript variant X4
F-box and leucine rich repeat protein 4, transcript variant X3
F-box and leucine rich repeat protein 4, transcript variant X2
F-box and leucine rich repeat protein 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins
POU domain, class 3, transcription factor 2
MMS22 like, DNA repair protein, transcript variant X2
MMS22 like, DNA repair protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
MMS22 like, DNA repair protein, transcript variant X4
MMS22 like, DNA repair protein, transcript variant X6
MMS22 like, DNA repair protein, transcript variant X5
MMS22 like, DNA repair protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NADH:ubiquinone oxidoreductase complex assembly factor 4
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 4
G protein-coupled receptor 63, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
G protein-coupled receptor 63, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
four and a half LIM domains 5, transcript variant X3
four and a half LIM domains 5, transcript variant X2
four and a half LIM domains 5, transcript variant X1
four and a half LIM domains 5, transcript variant X4
four and a half LIM domains protein 5 isoform X1
four and a half LIM domains protein 5 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
fucosyltransferase 9, transcript variant X2
fucosyltransferase 9, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
fucosyltransferase 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fucosyltransferase 9, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase 9 isoform X1
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase 9 isoform X2
mannosidase endo-alpha, transcript variant X3
mannosidase endo-alpha, transcript variant X1
mannosidase endo-alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
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: 48 Proteins, and 86% 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: 17 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00568
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
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: 24 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
mitogen-activated protein kinase kinase kinase 7, transcript variant X2
mitogen-activated protein kinase kinase kinase 7, transcript variant X1
mitogen-activated protein kinase kinase kinase 7 isoform X1
mitogen-activated protein kinase kinase kinase 7 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 26% coverage of the annotated genomic feature by RNAseq alignments
BTB domain and CNC homolog 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
BTB domain and CNC homolog 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
BTB domain and CNC homolog 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
transcription regulator protein BACH2 isoform X1
transcription regulator protein BACH2 isoform X2
BTB domain and CNC homolog 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
BTB domain and CNC homolog 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transcription regulator protein BACH2 isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: gap junction alpha-10 protein
caspase 8 associated protein 2, transcript variant X2
caspase 8 associated protein 2, transcript variant X1
caspase 8 associated protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
caspase 8 associated protein 2, transcript variant X3
caspase 8 associated protein 2, transcript variant X5
midasin AAA ATPase 1, transcript variant X1
midasin AAA ATPase 1, transcript variant X2
midasin AAA ATPase 1, 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 2 samples with support for all annotated introns
ankyrin repeat domain-containing protein 6
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
gamma-aminobutyric acid type A receptor subunit rho2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 30 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit rho-2
gamma-aminobutyric acid type A receptor subunit rho1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 19 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid type A receptor subunit rho1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid type A receptor subunit rho1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit rho-1 isoform X1
gamma-aminobutyric acid receptor subunit rho-1 isoform X2
gamma-aminobutyric acid receptor subunit rho-1 isoform X3
serine and arginine rich splicing factor 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
proline rich nuclear receptor coactivator 1
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
proline-rich nuclear receptor coactivator 1
RNA guanylyltransferase and 5'-phosphatase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
RNA guanylyltransferase and 5'-phosphatase, 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 6 samples with support for all annotated introns
RNA guanylyltransferase and 5'-phosphatase, 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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sperm acrosome membrane-associated protein 1
origin recognition complex subunit 3, 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 7 samples with support for all annotated introns
origin recognition complex subunit 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
origin recognition complex subunit 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
origin recognition complex subunit 3 isoform X3
origin recognition complex subunit 3 isoform X2
origin recognition complex subunit 3 isoform X1
origin recognition complex subunit 3, transcript variant X4
origin recognition complex subunit 3 isoform X4
arginyl-tRNA synthetase 2, mitochondrial
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 11 samples with support for all annotated introns
probable arginine--tRNA ligase, mitochondrial
cilia and flagella associated protein 206, transcript variant X2
cilia and flagella associated protein 206, transcript variant X1
cilia- and flagella-associated protein 206
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
uncharacterized protein C6orf163 homolog
small integral membrane protein 8, transcript variant X4
small integral membrane protein 8, transcript variant X5
small integral membrane protein 8 isoform X2
small integral membrane protein 8, transcript variant X1
small integral membrane protein 8, transcript variant X3
small integral membrane protein 8, transcript variant X2
small integral membrane protein 8 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
gap junction protein beta 7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
gap junction protein beta 7, transcript variant X4
gap junction protein beta 7, transcript variant X2
gap junction protein beta 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 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 51% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 292, transcript variant X1
zinc finger protein 292, transcript variant X3
zinc finger protein 292, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
glycoprotein hormones, alpha polypeptide
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 22 Proteins
nuclear fragile X mental retardation-interacting protein 2-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: nuclear fragile X mental retardation-interacting protein 2-like
heterogeneous nuclear ribonucleoprotein D-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 71% 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 46% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00278
synaptotagmin binding cytoplasmic RNA interacting protein, transcript variant X5
synaptotagmin binding cytoplasmic RNA interacting protein, transcript variant X2
synaptotagmin binding cytoplasmic RNA interacting protein, transcript variant X1
synaptotagmin binding cytoplasmic RNA interacting protein, transcript variant X6
synaptotagmin binding cytoplasmic RNA interacting protein, transcript variant X3
synaptotagmin binding cytoplasmic RNA interacting protein, transcript variant X4
heterogeneous nuclear ribonucleoprotein Q isoform X1
heterogeneous nuclear ribonucleoprotein Q isoform X2
heterogeneous nuclear ribonucleoprotein Q isoform X4
heterogeneous nuclear ribonucleoprotein Q isoform X5
heterogeneous nuclear ribonucleoprotein Q isoform X6
heterogeneous nuclear ribonucleoprotein Q isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 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: 1 Protein, and 22% 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; deleted 4 bases in 3 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 74% 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
centrosomal protein 162, transcript variant X1
centrosomal protein 162, transcript variant X2
centrosomal protein of 162 kDa isoform X1
centrosomal protein of 162 kDa isoform X2
succinate dehydrogenase complex assembly factor 4
succinate dehydrogenase assembly factor 4, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
stromal membrane-associated protein 1 isoform X1
stromal membrane-associated protein 1 isoform X2
stromal membrane-associated protein 1 isoform X5
stromal membrane-associated protein 1 isoform X3
stromal membrane-associated protein 1 isoform X4
stromal membrane-associated protein 1 isoform X6
stromal membrane-associated protein 1 isoform X7
COORDINATES: nucleotide motif:Rfam:12.0:RF00561
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 16 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 2
probable ATP-dependent RNA helicase DDX5
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: probable ATP-dependent RNA helicase DDX5
opioid growth factor receptor like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
opioid growth factor receptor like 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
opioid growth factor receptor-like protein 1 isoform X1
opioid growth factor receptor-like protein 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 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 86% coverage of the annotated genomic feature by RNAseq alignments
sterile alpha motif domain-containing protein 1-like, transcript variant X4
sterile alpha motif domain-containing protein 1-like, transcript variant X3
sterile alpha motif domain-containing protein 1-like, transcript variant X2
sterile alpha motif domain-containing protein 1-like, transcript variant X1
sterile alpha motif domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
regulating synaptic membrane exocytosis 1
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: 18 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: regulating synaptic membrane exocytosis protein 1
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, including 4 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: eIF5-mimic protein 2-like
cyclin dependent kinase 19, transcript variant X3
cyclin dependent kinase 19, transcript variant X1
cyclin dependent kinase 19, transcript variant X5
cyclin dependent kinase 19, transcript variant X2
cyclin dependent kinase 19, transcript variant X4
cyclin dependent kinase 19, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
S-adenosylmethionine decarboxylase proenzyme
general transcription factor IIIC subunit 6
general transcription factor 3C polypeptide 6
ribosome production factor 2 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
ribosome production factor 2 homolog isoform X1
ribosome production factor 2 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ribosome production factor 2 homolog isoform X2
solute carrier family 16 member 10, 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 5 samples with support for all annotated introns
solute carrier family 16 member 10, transcript variant X3
solute carrier family 16 member 10, transcript variant X1
solute carrier family 16 member 10, transcript variant X2
monocarboxylate transporter 10 isoform X1
monocarboxylate transporter 10 isoform X2
monocarboxylate transporter 10 isoform X3
sodium-dependent glucose transporter 1-like
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
sodium-dependent glucose transporter 1C-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
LOW QUALITY PROTEIN: sodium-dependent glucose transporter 1C-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
REV3 like, DNA directed polymerase zeta catalytic subunit, transcript variant X2
REV3 like, DNA directed polymerase zeta catalytic subunit, transcript variant X1
REV3 like, DNA directed polymerase zeta catalytic subunit, transcript variant X4
REV3 like, DNA directed polymerase zeta catalytic subunit, transcript variant X5
DNA polymerase zeta catalytic subunit isoform X2
DNA polymerase zeta catalytic subunit isoform X1
DNA polymerase zeta catalytic subunit isoform X3
DNA polymerase zeta catalytic subunit isoform X4
REV3 like, DNA directed polymerase zeta catalytic subunit, transcript variant X3
REV3 like, DNA directed polymerase zeta catalytic subunit, transcript variant X7
REV3 like, DNA directed polymerase zeta catalytic subunit, transcript variant X6
DNA polymerase zeta catalytic subunit isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
TRAF3 interacting protein 2, transcript variant X1
TRAF3 interacting protein 2, transcript variant X2
FYN proto-oncogene, Src family tyrosine kinase, transcript variant X3
FYN proto-oncogene, Src family tyrosine kinase, transcript variant X1
FYN proto-oncogene, Src family tyrosine kinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
family with sequence similarity 229 member B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
family with sequence similarity 229 member B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
laminin subunit alpha 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
laminin subunit alpha 4, transcript variant X1
laminin subunit alpha 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 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: 28 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: 19 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 81% 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 5 bases in 4 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 4 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
10 kDa heat shock protein, mitochondrial
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
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: 11 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: nucleoporin p54-like
myristoylated alanine rich protein kinase C substrate
myristoylated alanine-rich C-kinase substrate
histone deacetylase 2, transcript variant X2
histone deacetylase 2, transcript variant X1
heparan sulfate-glucosamine 3-sulfotransferase 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
heparan sulfate glucosamine 3-O-sulfotransferase 5
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
5'-nucleotidase domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
5'-nucleotidase domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
5'-nucleotidase domain-containing protein 1 isoform X1
5'-nucleotidase domain-containing protein 1 isoform X2
collagen type X alpha 1 chain, 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
collagen type X alpha 1 chain, 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
testis-specific Y-encoded-like protein 4
testis-specific Y-encoded-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
dermatan sulfate epimerase, transcript variant X1
dermatan sulfate epimerase, transcript variant X3
dermatan sulfate epimerase, transcript variant X2
dermatan sulfate epimerase, transcript variant X4
dermatan sulfate epimerase, transcript variant X5
calcium homeostasis modulator family member 6
trafficking protein particle complex subunit 3L
trafficking protein particle complex subunit 3-like protein
calcium homeostasis modulator family member 5
calcium homeostasis modulator family member 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
RWD domain containing 1, transcript variant X1
RWD domain containing 1, transcript variant X3
RWD domain containing 1, transcript variant X2
RWD domain-containing protein 1 isoform X1
RWD domain-containing protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 31% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
radial spoke head component 4A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
radial spoke head protein 4 homolog A isoform X1
radial spoke head component 4A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
radial spoke head protein 4 homolog A isoform X2
zinc finger containing ubiquitin peptidase 1, transcript variant X1
zinc finger containing ubiquitin peptidase 1, transcript variant X4
zinc finger containing ubiquitin peptidase 1, transcript variant X3
zinc finger-containing ubiquitin peptidase 1 isoform X1
zinc finger-containing ubiquitin peptidase 1 isoform X2
zinc finger containing ubiquitin peptidase 1, transcript variant X2
karyopherin subunit alpha 5, transcript variant X3
karyopherin subunit alpha 5, transcript variant X4
karyopherin subunit alpha 5, transcript variant X2
karyopherin subunit alpha 5, transcript variant X1
karyopherin subunit alpha 5, transcript variant X5
family with sequence similarity 162 member B
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 68% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
G protein-coupled receptor class C group 6 member A, transcript variant X2
G protein-coupled receptor class C group 6 member A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
G-protein coupled receptor family C group 6 member A isoform X2
G-protein coupled receptor family C group 6 member A isoform X1
heterogeneous nuclear ribonucleoprotein A3-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein A3-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein A3-like isoform X2
heterogeneous nuclear ribonucleoprotein A3-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 8 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
spindle and kinetochore-associated protein 2-like
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
vestigial like family member 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
vestigial like family member 2, transcript variant X1
vestigial like family member 2, transcript variant X2
transcription cofactor vestigial-like protein 2 isoform X3
transcription cofactor vestigial-like protein 2 isoform X1
transcription cofactor vestigial-like protein 2 isoform X2
ROS proto-oncogene 1, receptor tyrosine kinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
ROS proto-oncogene 1, receptor tyrosine kinase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
ROS proto-oncogene 1, receptor tyrosine kinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 79% coverage of the annotated genomic feature by RNAseq alignments
proto-oncogene tyrosine-protein kinase ROS isoform X1
proto-oncogene tyrosine-protein kinase ROS isoform X3
proto-oncogene tyrosine-protein kinase ROS isoform X2
discoidin, CUB and LCCL domain containing 1, transcript variant X1
discoidin, CUB and LCCL domain containing 1, transcript variant X2
discoidin, CUB and LCCL domain-containing protein 1
golgi associated PDZ and coiled-coil motif containing, transcript variant X1
golgi associated PDZ and coiled-coil motif containing, transcript variant X2
Golgi-associated PDZ and coiled-coil motif-containing protein isoform X2
Golgi-associated PDZ and coiled-coil motif-containing protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
NUS1 dehydrodolichyl diphosphate synthase subunit, transcript variant X2
NUS1 dehydrodolichyl diphosphate synthase subunit, transcript variant X1
dehydrodolichyl diphosphate synthase complex subunit NUS1 isoform X1
dehydrodolichyl diphosphate synthase complex subunit NUS1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
centrosomal protein 85 like, transcript variant X3
centrosomal protein 85 like, transcript variant X2
centrosomal protein 85 like, transcript variant X1
centrosomal protein of 85 kDa-like isoform X2
centrosomal protein of 85 kDa-like isoform X1
centrosomal protein of 85 kDa-like isoform X3
minichromosome maintenance 9 homologous recombination repair factor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
minichromosome maintenance 9 homologous recombination repair factor, transcript variant X1
minichromosome maintenance 9 homologous recombination repair factor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
anti-silencing function 1A histone chaperone
minichromosome maintenance 9 homologous recombination repair factor, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 184 member A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
mannosidase alpha class 1A member 1, transcript variant X1
mannosidase alpha class 1A member 1, transcript variant X2
mannosyl-oligosaccharide 1,2-alpha-mannosidase IA isoform X1
mannosyl-oligosaccharide 1,2-alpha-mannosidase IA isoform X2
peptidyl-prolyl cis-trans isomerase NIMA-interacting 4-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: peptidyl-prolyl cis-trans isomerase NIMA-interacting 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
10 kDa heat shock protein, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial import inner membrane translocase subunit TIM14-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 51% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
mitochondrial import inner membrane translocase subunit TIM14-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial import inner membrane translocase subunit TIM14-like isoform X1
mitochondrial import inner membrane translocase subunit TIM14-like isoform X2
gap junction protein alpha 1, transcript variant X1
gap junction protein alpha 1, transcript variant X2
mitochondrial translation release factor in rescue-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
elongation factor 1-alpha 1-like, transcript variant X2
elongation factor 1-alpha 1-like, transcript variant X1
elongation factor 1-alpha 1-like isoform X2
elongation factor 1-alpha 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
heat shock transcription factor 2, transcript variant X1
heat shock transcription factor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 mRNAs, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
cAMP-dependent protein kinase inhibitor beta, transcript variant X1
cAMP-dependent protein kinase inhibitor beta, transcript variant X2
cAMP-dependent protein kinase inhibitor beta, transcript variant X5
cAMP-dependent protein kinase inhibitor beta, transcript variant X3
cAMP-dependent protein kinase inhibitor beta, transcript variant X4
cAMP-dependent protein kinase inhibitor beta isoform X1
cAMP-dependent protein kinase inhibitor beta isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sphingomyelin phosphodiesterase acid like 3A, transcript variant X2
sphingomyelin phosphodiesterase acid like 3A, transcript variant X1
acid sphingomyelinase-like phosphodiesterase 3a isoform X1
acid sphingomyelinase-like phosphodiesterase 3a isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 11 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
sodium/potassium transporting ATPase interacting 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 10 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
sodium/potassium-transporting ATPase subunit beta-1-interacting protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 84% 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: 2 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
HD domain containing 2, transcript variant X1
HD domain containing 2, transcript variant X2
hes related family bHLH transcription factor with YRPW motif 2
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 8 samples with support for all annotated introns
hairy/enhancer-of-split related with YRPW motif protein 2
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
nuclear receptor coactivator 7, transcript variant X1
nuclear receptor coactivator 7, transcript variant X3
nuclear receptor coactivator 7, transcript variant X4
nuclear receptor coactivator 7, transcript variant X2
nuclear receptor coactivator 7 isoform X1
nuclear receptor coactivator 7 isoform X2
nuclear receptor coactivator 7 isoform X3
nuclear receptor coactivator 7, transcript variant X5
nuclear receptor coactivator 7 isoform X4
histidine triad nucleotide binding protein 3
tRNA methyltransferase 11 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
tRNA methyltransferase 11 homolog, 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 6 samples with support for all annotated introns
tRNA (guanine(10)-N2)-methyltransferase homolog isoform X1
tRNA (guanine(10)-N2)-methyltransferase homolog isoform X3
tRNA methyltransferase 11 homolog, transcript variant X2
tRNA (guanine(10)-N2)-methyltransferase homolog isoform X2
centromere protein W, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 71% coverage of the annotated genomic feature by RNAseq alignments
centromere protein W, transcript variant X1
ring finger protein 146, transcript variant X1
ring finger protein 146, transcript variant X3
ring finger protein 146, transcript variant X2
ethylmalonyl-CoA decarboxylase 1, transcript variant X4
ethylmalonyl-CoA decarboxylase 1, transcript variant X2
ethylmalonyl-CoA decarboxylase 1, transcript variant X1
ethylmalonyl-CoA decarboxylase 1, transcript variant X3
ethylmalonyl-CoA decarboxylase isoform X1
ethylmalonyl-CoA decarboxylase isoform X2
ethylmalonyl-CoA decarboxylase isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
KIAA0408 ortholog, transcript variant X1
KIAA0408 ortholog, transcript variant X2
uncharacterized protein KIAA0408 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 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 55% coverage of the annotated genomic feature by RNAseq alignments
protein tyrosine phosphatase receptor type K, transcript variant X2
protein tyrosine phosphatase receptor type K, transcript variant X1
protein tyrosine phosphatase receptor type K, transcript variant X4
protein tyrosine phosphatase receptor type K, transcript variant X3
receptor-type tyrosine-protein phosphatase kappa isoform X4
receptor-type tyrosine-protein phosphatase kappa isoform X2
receptor-type tyrosine-protein phosphatase kappa isoform X3
receptor-type tyrosine-protein phosphatase kappa isoform X1
protein tyrosine phosphatase receptor type K, transcript variant X7
protein tyrosine phosphatase receptor type K, transcript variant X6
protein tyrosine phosphatase receptor type K, transcript variant X5
receptor-type tyrosine-protein phosphatase kappa isoform X7
receptor-type tyrosine-protein phosphatase kappa isoform X6
receptor-type tyrosine-protein phosphatase kappa isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 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: 5 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
Rho GTPase activating protein 18, transcript variant X1
Rho GTPase activating protein 18, transcript variant X2
rho GTPase-activating protein 18 isoform X1
rho GTPase-activating protein 18 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
L3MBTL histone methyl-lysine binding protein 3, transcript variant X3
L3MBTL histone methyl-lysine binding protein 3, transcript variant X1
L3MBTL histone methyl-lysine binding protein 3, transcript variant X2
lethal(3)malignant brain tumor-like protein 3 isoform X1
lethal(3)malignant brain tumor-like protein 3 isoform X2
L3MBTL histone methyl-lysine binding protein 3, transcript variant X4
lethal(3)malignant brain tumor-like protein 3 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
sterile alpha motif domain-containing protein 3
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: 1 Protein, and 34% coverage of the annotated genomic feature by RNAseq alignments
erythrocyte membrane protein band 4.1 like 2, transcript variant X10
erythrocyte membrane protein band 4.1 like 2, transcript variant X9
erythrocyte membrane protein band 4.1 like 2, transcript variant X8
erythrocyte membrane protein band 4.1 like 2, transcript variant X6
erythrocyte membrane protein band 4.1 like 2, transcript variant X4
erythrocyte membrane protein band 4.1 like 2, transcript variant X5
erythrocyte membrane protein band 4.1 like 2, transcript variant X3
erythrocyte membrane protein band 4.1 like 2, transcript variant X7
erythrocyte membrane protein band 4.1 like 2, transcript variant X1
erythrocyte membrane protein band 4.1 like 2, transcript variant X2
A-kinase anchoring protein 7, transcript variant X5
A-kinase anchoring protein 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
A-kinase anchoring protein 7, transcript variant X6
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 6 samples with support for all annotated introns
A-kinase anchoring protein 7, transcript variant X3
A-kinase anchoring protein 7, transcript variant X1
A-kinase anchoring protein 7, transcript variant X4
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
A-kinase anchoring protein 7, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
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
mediator complex subunit 23, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
mediator complex subunit 23, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 23 isoform X2
mediator of RNA polymerase II transcription subunit 23 isoform X1
ectonucleotide pyrophosphatase/phosphodiesterase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ectonucleotide pyrophosphatase/phosphodiesterase 3, transcript variant X1
ectonucleotide pyrophosphatase/phosphodiesterase family member 3 isoform X1
ectonucleotide pyrophosphatase/phosphodiesterase family member 3 isoform X2
ectonucleotide pyrophosphatase/phosphodiesterase 1, transcript variant X1
ectonucleotide pyrophosphatase/phosphodiesterase family member 1 isoform X1
ectonucleotide pyrophosphatase/phosphodiesterase 1, transcript variant X2
ectonucleotide pyrophosphatase/phosphodiesterase family member 1 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins
LOW QUALITY PROTEIN: trace amine-associated receptor 7a-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 32 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 20 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 20 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
vascular non-inflammatory molecule 3-like, transcript variant X3
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
vascular non-inflammatory molecule 3-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 3 samples with support for all annotated introns
vascular non-inflammatory molecule 3-like, transcript variant X2
vascular non-inflammatory molecule 3-like isoform X1
vascular non-inflammatory molecule 3-like isoform X3
vascular non-inflammatory molecule 3-like isoform X2
solute carrier family 18 member B1, transcript variant X2
solute carrier family 18 member B1, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00186
COORDINATES: nucleotide motif:Rfam:12.0:RF00609
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
EYA transcriptional coactivator and phosphatase 4, transcript variant X1
EYA transcriptional coactivator and phosphatase 4, transcript variant X2
EYA transcriptional coactivator and phosphatase 4, transcript variant X3
EYA transcriptional coactivator and phosphatase 4, transcript variant X4
EYA transcriptional coactivator and phosphatase 4, transcript variant X5
EYA transcriptional coactivator and phosphatase 4, transcript variant X6
COORDINATES: nucleotide motif:Rfam:12.0:RF01210
TATA-box binding protein like 1, transcript variant X1
TATA-box binding protein like 1, transcript variant X2
TATA box-binding protein-like 1 isoform X1
TATA box-binding protein-like 1 isoform X2
solute carrier family 2, facilitated glucose transporter member 12
serum/glucocorticoid regulated kinase 1, transcript variant X3
serum/glucocorticoid regulated kinase 1, transcript variant X1
serum/glucocorticoid regulated kinase 1, transcript variant X2
serine/threonine-protein kinase Sgk1 isoform X3
serine/threonine-protein kinase Sgk1 isoform X1
serine/threonine-protein kinase Sgk1 isoform X2
aldehyde dehydrogenase 8 family member A1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
aldehyde dehydrogenase 8 family member A1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
2-aminomuconic semialdehyde dehydrogenase
HBS1 like translational GTPase, 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 11 samples with support for all annotated introns
HBS1 like translational GTPase, transcript variant X3
HBS1 like translational GTPase, 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
MYB proto-oncogene, transcription factor, transcript variant X1
MYB proto-oncogene, transcription factor, transcript variant X2
transcriptional activator Myb isoform X1
transcriptional activator Myb isoform X2
Abelson helper integration site 1, transcript variant X1
Abelson helper integration site 1, transcript variant X7
Abelson helper integration site 1, transcript variant X8
Abelson helper integration site 1, transcript variant X4
Abelson helper integration site 1, transcript variant X3
Abelson helper integration site 1, transcript variant X2
Abelson helper integration site 1, transcript variant X5
Abelson helper integration site 1, transcript variant X6
Abelson helper integration site 1, transcript variant X9
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
LOW QUALITY PROTEIN: 40S ribosomal protein S25-like
small nucleolar RNA SNORA42/SNORA80 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00406
phosphodiesterase 7B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cAMP-specific 3',5'-cyclic phosphodiesterase 7B isoform X1
phosphodiesterase 7B, transcript variant X3
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 9 samples with support for all annotated introns
cAMP-specific 3',5'-cyclic phosphodiesterase 7B isoform X3
phosphodiesterase 7B, 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 5 samples with support for all annotated introns
cAMP-specific 3',5'-cyclic phosphodiesterase 7B isoform X2
BCL2 associated transcription factor 1, transcript variant X2
BCL2 associated transcription factor 1, transcript variant X5
BCL2 associated transcription factor 1, transcript variant X3
BCL2 associated transcription factor 1, transcript variant X4
BCL2 associated transcription factor 1, transcript variant X1
bcl-2-associated transcription factor 1 isoform X4
bcl-2-associated transcription factor 1 isoform X2
bcl-2-associated transcription factor 1 isoform X3
bcl-2-associated transcription factor 1 isoform X1
BCL2 associated transcription factor 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
microtubule associated protein 7, transcript variant X3
microtubule associated protein 7, transcript variant X1
microtubule associated protein 7, transcript variant X2
mitogen-activated protein kinase kinase kinase 5, transcript variant X3
mitogen-activated protein kinase kinase kinase 5, transcript variant X4
mitogen-activated protein kinase kinase kinase 5, transcript variant X5
mitogen-activated protein kinase kinase kinase 5, transcript variant X2
mitogen-activated protein kinase kinase kinase 5, transcript variant X6
mitogen-activated protein kinase kinase kinase 5, transcript variant X7
mitogen-activated protein kinase kinase kinase 5, transcript variant X1
mitogen-activated protein kinase kinase kinase 5, transcript variant X9
mitogen-activated protein kinase kinase kinase 5, transcript variant X11
mitogen-activated protein kinase kinase kinase 5 isoform X1
mitogen-activated protein kinase kinase kinase 5 isoform X5
mitogen-activated protein kinase kinase kinase 5 isoform X2
mitogen-activated protein kinase kinase kinase 5 isoform X6
mitogen-activated protein kinase kinase kinase 5 isoform X4
mitogen-activated protein kinase kinase kinase 5 isoform X3
mitogen-activated protein kinase kinase kinase 5 isoform X7
mitogen-activated protein kinase kinase kinase 5 isoform X8
mitogen-activated protein kinase kinase kinase 5, transcript variant X8
mitogen-activated protein kinase kinase kinase 5, transcript variant X12
mitogen-activated protein kinase kinase kinase 5, transcript variant X10
mitogen-activated protein kinase kinase kinase 5 isoform X9
peroxisomal biogenesis factor 7, transcript variant X3
peroxisomal biogenesis factor 7, transcript variant X1
peroxisomal biogenesis factor 7, transcript variant X2
peroxisomal biogenesis factor 7 isoform X1
peroxisomal biogenesis factor 7 isoform X2
peroxisomal biogenesis factor 7 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
interleukin 20 receptor subunit alpha, 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 7 samples with support for all annotated introns
interleukin 20 receptor subunit alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
interleukin-20 receptor subunit alpha isoform X1
interleukin-20 receptor subunit alpha isoform X2
interleukin 22 receptor subunit alpha 2, transcript variant X2
interleukin 22 receptor subunit alpha 2, transcript variant X1
interleukin-22 receptor subunit alpha-2 isoform X1
interleukin-22 receptor subunit alpha-2 isoform 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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
TNF alpha induced protein 3, 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 9 samples with support for all annotated introns
TNF alpha induced protein 3, transcript variant X2
tumor necrosis factor alpha-induced protein 3
p53 apoptosis effector related to PMP-22
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: brefeldin A-inhibited guanine nucleotide-exchange protein 3
uncharacterized LOC125357340, transcript variant X1
uncharacterized LOC125357340, transcript variant X2
coiled-coil domain-containing protein 28A
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
epithelial cell-transforming sequence 2 oncogene-like
RALBP1 associated Eps domain containing 1, transcript variant X3
RALBP1 associated Eps domain containing 1, transcript variant X2
RALBP1 associated Eps domain containing 1, transcript variant X1
RALBP1 associated Eps domain containing 1, transcript variant X5
RALBP1 associated Eps domain containing 1, transcript variant X4
ralBP1-associated Eps domain-containing protein 1 isoform X3
ralBP1-associated Eps domain-containing protein 1 isoform X5
ralBP1-associated Eps domain-containing protein 1 isoform X4
ralBP1-associated Eps domain-containing protein 1 isoform X2
ralBP1-associated Eps domain-containing protein 1 isoform 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 11 samples with support for all annotated introns
hdc homolog, cell cycle regulator, transcript variant X2
hdc homolog, cell cycle regulator, transcript variant X1
Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 71% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: ran-binding protein 9-like
COORDINATES: nucleotide motif:Rfam:12.0:RF00279
COORDINATES: nucleotide motif:Rfam:12.0:RF00393
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
vacuolar protein sorting-associated protein VTA1 homolog
adhesion G protein-coupled receptor G6, transcript variant X1
adhesion G protein-coupled receptor G6, 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
adhesion G protein-coupled receptor G6, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
adhesion G protein-coupled receptor G6, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
adhesion G-protein coupled receptor G6 isoform X1
adhesion G-protein coupled receptor G6 isoform X3
adhesion G-protein coupled receptor G6 isoform X4
adhesion G-protein coupled receptor G6 isoform X5
adhesion G protein-coupled receptor G6, transcript variant X2
adhesion G-protein coupled receptor G6 isoform X2
HIVEP zinc finger 2, transcript variant X2
HIVEP zinc finger 2, transcript variant X3
HIVEP zinc finger 2, transcript variant X5
HIVEP zinc finger 2, transcript variant X4
HIVEP zinc finger 2, transcript variant X1
HIVEP zinc finger 2, transcript variant X7
HIVEP zinc finger 2, transcript variant X6
androgen induced 1, transcript variant X2
androgen induced 1, transcript variant X1
androgen-induced gene 1 protein isoform X1
androgen-induced gene 1 protein isoform X2
LOW QUALITY PROTEIN: protein canopy homolog 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
phosphatase and actin regulator 2, transcript variant X4
phosphatase and actin regulator 2, transcript variant X2
phosphatase and actin regulator 2, transcript variant X3
phosphatase and actin regulator 2 isoform X4
phosphatase and actin regulator 2 isoform X2
phosphatase and actin regulator 2 isoform X3
phosphatase and actin regulator 2, transcript variant X1
phosphatase and actin regulator 2 isoform X1
zinc finger C2HC domain-containing protein 1B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
cytochrome c oxidase subunit 7B, mitochondrial-like
transfer RNA leucine (anticodon UAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
SNF2 histone linker PHD RING helicase, transcript variant X2
SNF2 histone linker PHD RING helicase, transcript variant X1
SNF2 histone linker PHD RING helicase, transcript variant X3
SNF2 histone linker PHD RING helicase, transcript variant X5
E3 ubiquitin-protein ligase SHPRH isoform X1
E3 ubiquitin-protein ligase SHPRH isoform X2
E3 ubiquitin-protein ligase SHPRH isoform X4
SNF2 histone linker PHD RING helicase, transcript variant X4
E3 ubiquitin-protein ligase SHPRH isoform X3
glutamate metabotropic receptor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
metabotropic glutamate receptor 1 isoform X1
glutamate metabotropic receptor 1, transcript variant X2
metabotropic glutamate receptor 1 isoform X2
syntaxin binding protein 5, transcript variant X2
syntaxin binding protein 5, transcript variant X1
syntaxin binding protein 5, transcript variant X3
syntaxin binding protein 5, transcript variant X4
syntaxin binding protein 5, transcript variant X5
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 8 samples with support for all annotated introns
sterile alpha motif domain-containing protein 5
SAM and SH3 domain containing 1, transcript variant X1
SAM and SH3 domain containing 1, transcript variant X2
SAM and SH3 domain-containing protein 1 isoform X1
SAM and SH3 domain-containing protein 1 isoform X2
SAM and SH3 domain containing 1, transcript variant X4
SAM and SH3 domain-containing protein 1 isoform X4
SAM and SH3 domain containing 1, transcript variant X3
SAM and SH3 domain-containing protein 1 isoform X3
uncharacterized LOC125357395, transcript variant X2
uncharacterized LOC125357395, transcript variant X1
TGF-beta activated kinase 1 (MAP3K7) binding protein 2, transcript variant X1
TGF-beta activated kinase 1 (MAP3K7) binding protein 2, transcript variant X2
TGF-beta activated kinase 1 (MAP3K7) binding protein 2, transcript variant X3
TGF-beta-activated kinase 1 and MAP3K7-binding protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
peptidylprolyl isomerase like 4, transcript variant X2
peptidylprolyl isomerase like 4, transcript variant X1
peptidyl-prolyl cis-trans isomerase-like 4
glycosylated integral membrane protein 1
glycoprotein integral membrane protein 1
katanin catalytic subunit A1, transcript variant X1
katanin catalytic subunit A1, transcript variant X2
katanin p60 ATPase-containing subunit A1
protein-L-isoaspartate (D-aspartate) O-methyltransferase, transcript variant X1
protein-L-isoaspartate (D-aspartate) O-methyltransferase, transcript variant X2
protein-L-isoaspartate(D-aspartate) O-methyltransferase isoform X1
protein-L-isoaspartate(D-aspartate) O-methyltransferase isoform X2
protein-L-isoaspartate (D-aspartate) O-methyltransferase, transcript variant X3
protein-L-isoaspartate(D-aspartate) O-methyltransferase isoform X3
low-density lipoprotein receptor-related protein 11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
U1 small nuclear ribonucleoprotein C-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
protein phosphatase 1 regulatory inhibitor subunit 14C
protein phosphatase 1 regulatory subunit 14C
iodotyrosine deiodinase, transcript variant X1
iodotyrosine deiodinase, 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 2 samples with support for all annotated introns
iodotyrosine deiodinase, transcript variant X3
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
pleckstrin homology and RhoGEF domain containing G1, 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 4 samples with support for all annotated introns
pleckstrin homology and RhoGEF domain containing G1, 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 2 samples with support for all annotated introns
pleckstrin homology domain-containing family G member 1 isoform X1
pleckstrin homology domain-containing family G member 1 isoform X2
methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1 like
monofunctional C1-tetrahydrofolate synthase, mitochondrial
zinc finger and BTB domain containing 2, transcript variant X3
zinc finger and BTB domain containing 2, transcript variant X1
zinc finger and BTB domain containing 2, transcript variant X2
zinc finger and BTB domain containing 2, transcript variant X4
zinc finger and BTB domain-containing protein 2 isoform X1
zinc finger and BTB domain-containing protein 2 isoform X2
required for meiotic nuclear division 1 homolog, transcript variant X2
required for meiotic nuclear division 1 homolog, transcript variant X1
required for meiotic nuclear division protein 1 homolog isoform X2
required for meiotic nuclear division protein 1 homolog isoform X1
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
coiled-coil domain-containing protein 170
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
estrogen receptor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
estrogen receptor 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
estrogen receptor 1, transcript variant X4
estrogen receptor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
estrogen receptor 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 95 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
estrogen receptor 1, transcript variant X3
estrogen receptor 1, transcript variant X6
spectrin repeat containing nuclear envelope protein 1
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 9 samples with support for all annotated introns
vasoactive intestinal peptide, transcript variant X1
vasoactive intestinal peptide, transcript variant X2
mitochondrial translation release factor 1 like, transcript variant X1
mitochondrial translation release factor 1 like, transcript variant X7
mitochondrial translation release factor 1 like, transcript variant X2
peptide chain release factor 1-like, mitochondrial isoform X1
peptide chain release factor 1-like, mitochondrial isoform X2
mitochondrial translation release factor 1 like, transcript variant X3
peptide chain release factor 1-like, mitochondrial isoform X3
mitochondrial translation release factor 1 like, transcript variant X6
mitochondrial translation release factor 1 like, transcript variant X4
mitochondrial translation release factor 1 like, transcript variant X5
peptide chain release factor 1-like, mitochondrial isoform X4
peptide chain release factor 1-like, mitochondrial isoform 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 11 samples with support for all annotated introns
opioid receptor mu 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 82 Proteins
opioid receptor mu 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 32 Proteins
opioid receptor mu 1, transcript variant X3
opioid receptor mu 1, transcript variant X1
interaction protein for cytohesin exchange factors 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
interaction protein for cytohesin exchange factors 1, transcript variant X1
interaction protein for cytohesin exchange factors 1, 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 1 sample with support for all annotated introns
interaction protein for cytohesin exchange factors 1, transcript variant X4
interaction protein for cytohesin exchange factors 1, transcript variant X3
interaction protein for cytohesin exchange factors 1, transcript variant X6
interactor protein for cytohesin exchange factors 1 isoform X2
interactor protein for cytohesin exchange factors 1 isoform X1
interactor protein for cytohesin exchange factors 1 isoform X4
interactor protein for cytohesin exchange factors 1 isoform X3
interactor protein for cytohesin exchange factors 1 isoform X5
CNKSR family member 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
CNKSR family member 3, transcript variant X1
connector enhancer of kinase suppressor of ras 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
SR-related CTD associated factor 8, transcript variant X5
SR-related CTD associated factor 8, transcript variant X9
SR-related CTD associated factor 8, transcript variant X7
SR-related CTD associated factor 8, transcript variant X8
SR-related and CTD-associated factor 8 isoform X3
SR-related and CTD-associated factor 8 isoform X7
SR-related and CTD-associated factor 8 isoform X5
SR-related and CTD-associated factor 8 isoform X6
SR-related CTD associated factor 8, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
SR-related CTD associated factor 8, transcript variant X2
SR-related CTD associated factor 8, transcript variant X1
SR-related CTD associated factor 8, transcript variant X4
SR-related CTD associated factor 8, transcript variant X6
SR-related and CTD-associated factor 8 isoform X1
SR-related and CTD-associated factor 8 isoform X4
SR-related and CTD-associated factor 8 isoform X2
TIAM Rac1 associated GEF 2, transcript variant X3
TIAM Rac1 associated GEF 2, transcript variant X6
TIAM Rac1 associated GEF 2, transcript variant X5
TIAM Rac1 associated GEF 2, transcript variant X1
TIAM Rac1 associated GEF 2, transcript variant X2
TIAM Rac1 associated GEF 2, transcript variant X4
rho guanine nucleotide exchange factor TIAM2 isoform X1
rho guanine nucleotide exchange factor TIAM2 isoform X3
rho guanine nucleotide exchange factor TIAM2 isoform X2
dimethyladenosine transferase 1, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
AT-rich interaction domain 1B, transcript variant X1
AT-rich interaction domain 1B, transcript variant X2
AT-rich interaction domain 1B, transcript variant X4
AT-rich interaction domain 1B, transcript variant X3
AT-rich interaction domain 1B, transcript variant X5
AT-rich interactive domain-containing protein 1B isoform X1
AT-rich interactive domain-containing protein 1B isoform X2
AT-rich interactive domain-containing protein 1B isoform X4
AT-rich interactive domain-containing protein 1B isoform X3
AT-rich interactive domain-containing protein 1B isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
zinc finger DHHC-type palmitoyltransferase 14, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 13 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
zinc finger DHHC-type palmitoyltransferase 14, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
zinc finger DHHC-type palmitoyltransferase 14, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
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
serine active site containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
serine active site containing 1, transcript variant X2
general transcription factor IIH subunit 5
TUB like protein 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TUB like protein 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transmembrane protein 181, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transmembrane protein 181, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: synaptotagmin-like protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
T cell activation RhoGTPase activating protein
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
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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: T-cell activation Rho GTPase-activating protein
fibronectin type III domain containing 1
LOW QUALITY PROTEIN: fibronectin type III domain-containing protein 1
superoxide dismutase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
superoxide dismutase [Mn], mitochondrial isoform X2
superoxide dismutase 2, transcript variant X1
superoxide dismutase [Mn], mitochondrial isoform X1
WT1 associated protein, transcript variant X2
WT1 associated protein, transcript variant X1
WT1 associated protein, transcript variant X3
pre-mRNA-splicing regulator WTAP isoform X1
pre-mRNA-splicing regulator WTAP isoform X2
CCHC-type zinc finger nucleic acid binding protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 mRNAs, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00401
COORDINATES: nucleotide motif:Rfam:12.0:RF00429
39S ribosomal protein L18, mitochondrial
PARN like ribonuclease domain containing exonuclease 1, transcript variant X2
PARN like ribonuclease domain containing exonuclease 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
poly(A)-specific ribonuclease PNLDC1 isoform X2
poly(A)-specific ribonuclease PNLDC1 isoform X1
mas-related G-protein coupled receptor member H-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
LOW QUALITY PROTEIN: cation-independent mannose-6-phosphate receptor
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
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 9 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 6 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 4, transcript variant X3
mitogen-activated protein kinase kinase kinase 4 isoform X3
mitogen-activated protein kinase kinase kinase 4, transcript variant X1
mitogen-activated protein kinase kinase kinase 4, transcript variant X4
mitogen-activated protein kinase kinase kinase 4, transcript variant X2
mitogen-activated protein kinase kinase kinase 4, 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 9 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 4, transcript variant X6
mitogen-activated protein kinase kinase kinase 4 isoform X1
mitogen-activated protein kinase kinase kinase 4 isoform X4
mitogen-activated protein kinase kinase kinase 4 isoform X2
mitogen-activated protein kinase kinase kinase 4 isoform X5
mitogen-activated protein kinase kinase kinase 4 isoform X6
1-acylglycerol-3-phosphate O-acyltransferase 4
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 3 samples with support for all annotated introns
1-acyl-sn-glycerol-3-phosphate acyltransferase delta
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
parkin coregulated, transcript variant X1
parkin coregulated, transcript variant X2
parkin coregulated gene protein isoform X1
parkin coregulated gene protein isoform X2
QKI, KH domain containing RNA binding, transcript variant X2
QKI, KH domain containing RNA binding, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
QKI, KH domain containing RNA binding, transcript variant X3
QKI, KH domain containing RNA binding, transcript variant X4
QKI, KH domain containing RNA binding, transcript variant X1
QKI, KH domain containing RNA binding, transcript variant X5
SH3 domain-containing protein C23A1.17-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein C6orf118 homolog
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 54% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 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 88% 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 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: T-box transcription factor T-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 23 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
ribosomal protein S6 kinase alpha-2-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: ribosomal protein S6 kinase alpha-2-like
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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
centrosomal protein 43-like, transcript variant X1
centrosomal protein 43-like, transcript variant X3
centrosomal protein 43-like, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein LOC125357614
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
centrosomal protein 43, transcript variant X7
centrosomal protein 43, transcript variant X8
centrosomal protein 43, transcript variant X9
centrosomal protein 43, transcript variant X1
centrosomal protein 43, transcript variant X3
centrosomal protein 43, transcript variant X4
centrosomal protein 43, transcript variant X5
centrosomal protein 43, transcript variant X2
centrosomal protein 43, transcript variant X6
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 81% 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 47% 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: 1 Protein, and 29% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: protein unc-93 homolog A
afadin, adherens junction formation factor, transcript variant X3
afadin, adherens junction formation factor, transcript variant X1
afadin, adherens junction formation factor, transcript variant X9
afadin, adherens junction formation factor, transcript variant X5
afadin, adherens junction formation factor, transcript variant X7
afadin, adherens junction formation factor, transcript variant X10
afadin, adherens junction formation factor, transcript variant X6
afadin, adherens junction formation factor, transcript variant X11
afadin, adherens junction formation factor, transcript variant X12
afadin, adherens junction formation factor, transcript variant X2
afadin, adherens junction formation factor, transcript variant X13
afadin, adherens junction formation factor, transcript variant X14
afadin, adherens junction formation factor, transcript variant X15
afadin, adherens junction formation factor, transcript variant X4
afadin, adherens junction formation factor, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 48% 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: 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
LOW QUALITY PROTEIN: dapper homolog 2-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
SPARC related modular calcium binding 2, transcript variant X2
SPARC related modular calcium binding 2, transcript variant X1
SPARC related modular calcium binding 2, transcript variant X4
SPARC related modular calcium binding 2, transcript variant X3
SPARC-related modular calcium-binding protein 2 isoform X1
SPARC-related modular calcium-binding protein 2 isoform X2
SPARC-related modular calcium-binding protein 2 isoform X3
SPARC-related modular calcium-binding protein 2 isoform X4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
WD repeat domain 27, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
WD repeat domain 27, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
WD repeat domain 27, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
WD repeat-containing protein 27 isoform X1
WD repeat-containing protein 27 isoform X2
PHD finger protein 10, transcript variant X1
PHD finger protein 10, transcript variant X2
ER membrane associated RNA degradation, transcript variant X2
ER membrane associated RNA degradation, transcript variant X1
ER membrane associated RNA degradation, transcript variant X3
ER membrane associated RNA degradation, transcript variant X5
ER membrane associated RNA degradation, transcript variant X4
endoplasmic reticulum membrane-associated RNA degradation protein isoform X2
endoplasmic reticulum membrane-associated RNA degradation protein isoform X1
LOW QUALITY PROTEIN: delta-like protein 1
family with sequence similarity 120B, transcript variant X3
family with sequence similarity 120B, transcript variant X2
family with sequence similarity 120B, transcript variant X12
family with sequence similarity 120B, transcript variant X6
family with sequence similarity 120B, transcript variant X7
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 3 samples with support for all annotated introns
family with sequence similarity 120B, transcript variant X13
family with sequence similarity 120B, transcript variant X1
family with sequence similarity 120B, transcript variant X5
family with sequence similarity 120B, transcript variant X4
family with sequence similarity 120B, transcript variant X9
family with sequence similarity 120B, transcript variant X11
family with sequence similarity 120B, transcript variant X10
family with sequence similarity 120B, transcript variant X8
constitutive coactivator of peroxisome proliferator-activated receptor gamma isoform X1
constitutive coactivator of peroxisome proliferator-activated receptor gamma isoform X2
constitutive coactivator of peroxisome proliferator-activated receptor gamma isoform X3
family with sequence similarity 120B, transcript variant X14
constitutive coactivator of peroxisome proliferator-activated receptor gamma isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
TATA-box binding protein, transcript variant X1
TATA-box binding protein, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 70% 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 4 bases in 3 codons; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: programmed cell death protein 2