Vulpes lagopus strain Blue_001 chromosome 16, ASM1834538v1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Laurasiatheria; Carnivora; Caniformia; Canidae; Vulpes.
Chromosome-level genome assembly of the Arctic fox (Vulpes lagopus) using PacBio sequencing and Hi-C technology
Publication Status: Available-Online prior to print
REFSEQ INFORMATION: The reference sequence is identical to\nCM031310.1.\nAssembly name: ASM1834538v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Hebei Normal University of\nScience and Technology on 2021/05/12. The original whole-genome\nshotgun project has the accession JADWOQ000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Hebei Normal University of Science and\n Technology\nAssembly Method :: WTDBG2 v. 2.5\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 121.0x\nSequencing Technology :: PacBio Sequel; Illumina NovaSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Vulpes lagopus Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.6\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.
nascent polypeptide-associated complex subunit alpha, muscle-specific form
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
chromosome alignment maintaining phosphoprotein 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 4 samples with support for all annotated introns
UPF3A regulator of nonsense mediated mRNA decay, 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 1 sample with support for all annotated introns
UPF3A regulator of nonsense mediated mRNA decay, transcript variant X6
UPF3A regulator of nonsense mediated mRNA decay, transcript variant X4
UPF3A regulator of nonsense mediated mRNA decay, 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 1 sample with support for all annotated introns
UPF3A regulator of nonsense mediated mRNA decay, transcript variant X1
regulator of nonsense transcripts 3A isoform X3
UPF3A regulator of nonsense mediated mRNA decay, transcript variant X2
UPF3A regulator of nonsense mediated mRNA decay, transcript variant X7
chromosome alignment-maintaining phosphoprotein 1
regulator of nonsense transcripts 3A isoform X4
regulator of nonsense transcripts 3A isoform X2
regulator of nonsense transcripts 3A isoform X1
UPF3A regulator of nonsense mediated mRNA decay, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
regulator of nonsense transcripts 3A isoform X5
UPF3A regulator of nonsense mediated mRNA decay, transcript variant X9
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
regulator of nonsense transcripts 3A isoform X6
UPF3A regulator of nonsense mediated mRNA decay, transcript variant X10
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
regulator of nonsense transcripts 3A isoform X7
UPF3A regulator of nonsense mediated mRNA decay, transcript variant X11
UPF3A regulator of nonsense mediated mRNA decay, transcript variant X13
UPF3A regulator of nonsense mediated mRNA decay, transcript variant X12
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
DET1- and DDB1-associated protein 1-like
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
regulator of nonsense transcripts 3A isoform X8
cell division cycle 16, transcript variant X2
cell division cycle 16, transcript variant X1
cell division cycle protein 16 homolog isoform X2
cell division cycle protein 16 homolog 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 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 77% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein C13orf46 homolog
growth arrest specific 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
growth arrest specific 6, 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 4 samples with support for all annotated introns
growth arrest-specific protein 6 isoform X1
growth arrest-specific protein 6 isoform X2
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: 11 Proteins, and 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: 2 Proteins
potassium-transporting ATPase subunit beta
transcription factor Dp-1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transcription factor Dp-1, transcript variant X1
transmembrane and coiled-coil domains 3, 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 3 samples with support for all annotated introns
transmembrane and coiled-coil domains 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transmembrane and coiled-coil domains 3, transcript variant X2
transmembrane and coiled-coil domains 3, transcript variant X4
transmembrane and coiled-coil domain-containing protein 3 isoform X2
transmembrane and coiled-coil domain-containing protein 3 isoform X1
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: 20 Proteins, and 98% 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: small ubiquitin-related modifier 2-like
defective in cullin neddylation 1 domain containing 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% 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: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: DCN1-like protein 2
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 2 samples with support for all annotated introns
protein ADP-ribosylarginine hydrolase-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lysosomal associated membrane 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 4 samples with support for all annotated introns
lysosomal associated membrane protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
lysosome-associated membrane glycoprotein 1 isoform X2
lysosome-associated membrane glycoprotein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
PCI domain containing 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PCI domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
PCI domain-containing protein 2 isoform X1
PCI domain containing 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
PCI domain containing 2, transcript variant X2
PCI domain containing 2, transcript variant X4
PCI domain-containing protein 2 isoform X2
PCI domain-containing protein 2 isoform X3
coagulation factor X, transcript variant X1
coagulation factor X, transcript variant X2
coagulation factor X, transcript variant X3
coagulation factor X, transcript variant X4
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
coagulation factor VII, transcript variant X3
coagulation factor VII, transcript variant X2
coagulation factor VII, transcript variant X1
MCF.2 cell line derived transforming sequence like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
MCF.2 cell line derived transforming sequence like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
MCF.2 cell line derived transforming sequence like, transcript variant X1
MCF.2 cell line derived transforming sequence like, transcript variant X8
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
MCF.2 cell line derived transforming sequence like, transcript variant X4
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
MCF.2 cell line derived transforming sequence like, transcript variant X3
guanine nucleotide exchange factor DBS isoform X2
guanine nucleotide exchange factor DBS isoform X6
guanine nucleotide exchange factor DBS isoform X7
guanine nucleotide exchange factor DBS isoform X4
guanine nucleotide exchange factor DBS isoform X3
guanine nucleotide exchange factor DBS isoform X1
MCF.2 cell line derived transforming sequence like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
guanine nucleotide exchange factor DBS isoform X8
MCF.2 cell line derived transforming sequence like, 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 1 sample with support for all annotated introns
MCF.2 cell line derived transforming sequence like, transcript variant X6
guanine nucleotide exchange factor DBS isoform X5
ATPase phospholipid transporting 11A, transcript variant X7
ATPase phospholipid transporting 11A, transcript variant X5
ATPase phospholipid transporting 11A, transcript variant X4
ATPase phospholipid transporting 11A, 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
ATPase phospholipid transporting 11A, transcript variant X2
ATPase phospholipid transporting 11A, transcript variant X6
ATPase phospholipid transporting 11A, transcript variant X1
phospholipid-transporting ATPase IH isoform X5
phospholipid-transporting ATPase IH isoform X1
phospholipid-transporting ATPase IH isoform X3
phospholipid-transporting ATPase IH isoform X2
phospholipid-transporting ATPase IH isoform X4
ATPase phospholipid transporting 11A, transcript variant X8
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
tubulin gamma complex associated protein 3, transcript variant X3
tubulin gamma complex associated protein 3, transcript variant X1
tubulin gamma complex associated protein 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
gamma-tubulin complex component 3 isoform X3
gamma-tubulin complex component 3 isoform X1
gamma-tubulin complex component 3 isoform X2
tubulin gamma complex associated protein 3, transcript variant X4
gamma-tubulin complex component 3 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 118 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 7, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 7, transcript variant X4
Rho guanine nucleotide exchange factor 7, transcript variant X1
Rho guanine nucleotide exchange factor 7, 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 2 samples with support for all annotated introns
Rho guanine nucleotide exchange factor 7, 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 1 sample with support for all annotated introns
rho guanine nucleotide exchange factor 7 isoform X4
rho guanine nucleotide exchange factor 7 isoform X1
rho guanine nucleotide exchange factor 7 isoform X7
rho guanine nucleotide exchange factor 7 isoform X3
rho guanine nucleotide exchange factor 7 isoform X6
Rho guanine nucleotide exchange factor 7, transcript variant X5
Rho guanine nucleotide exchange factor 7, transcript variant X2
rho guanine nucleotide exchange factor 7 isoform X5
rho guanine nucleotide exchange factor 7 isoform X2
ankyrin repeat domain 10, transcript variant X1
ankyrin repeat domain 10, transcript variant X2
ankyrin repeat domain 10, transcript variant X3
ankyrin repeat domain-containing protein 10 isoform X1
ankyrin repeat domain-containing protein 10 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
inhibitor of growth family member 1, 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 4 samples with support for all annotated introns
inhibitor of growth family member 1, transcript variant X1
inhibitor of growth protein 1 isoform X2
inhibitor of growth protein 1 isoform X1
cysteinyl-tRNA synthetase 2, mitochondrial, transcript variant X2
cysteinyl-tRNA synthetase 2, mitochondrial, transcript variant X1
probable cysteine--tRNA ligase, mitochondrial isoform X2
probable cysteine--tRNA ligase, mitochondrial isoform X1
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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: ATP-dependent (S)-NAD(P)H-hydrate dehydratase
uncharacterized LOC121477153, transcript variant X2
uncharacterized LOC121477153, transcript variant X1
uncharacterized LOC121476875, transcript variant X1
uncharacterized LOC121476875, transcript variant X2
insulin receptor substrate 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
insulin receptor substrate 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
insulin receptor substrate 2, transcript variant X1
uncharacterized LOC121477054, transcript variant X1
uncharacterized LOC121477054, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
TNF superfamily member 13b, transcript variant X3
TNF superfamily member 13b, transcript variant X2
TNF superfamily member 13b, transcript variant X1
tumor necrosis factor ligand superfamily member 13B isoform X3
tumor necrosis factor ligand superfamily member 13B isoform X2
tumor necrosis factor ligand superfamily member 13B isoform 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
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
NALCN channel auxiliary factor 1, transcript variant X1
NALCN channel auxiliary factor 1, transcript variant X2
transmembrane protein FAM155A isoform X1
transmembrane protein FAM155A isoform X2
basic salivary proline-rich protein 2-like
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: 7 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
putative methyltransferase-like protein 21E pseudogene
ERCC excision repair 5, endonuclease, transcript variant X3
ERCC excision repair 5, endonuclease, transcript variant X4
ERCC excision repair 5, endonuclease, transcript variant X2
ERCC excision repair 5, endonuclease, transcript variant X1
DNA repair protein complementing XP-G cells isoform X4
DNA repair protein complementing XP-G cells isoform X3
DNA repair protein complementing XP-G cells isoform X2
DNA repair protein complementing XP-G cells isoform X1
ERCC excision repair 5, endonuclease, transcript variant X9
ERCC excision repair 5, endonuclease, transcript variant X5
DNA repair protein complementing XP-G cells isoform X7
DNA repair protein complementing XP-G cells isoform X5
ERCC excision repair 5, endonuclease, transcript variant X7
ERCC excision repair 5, endonuclease, transcript variant X6
ERCC excision repair 5, endonuclease, transcript variant X8
DNA repair protein complementing XP-G cells isoform X6
basic, immunoglobulin-like variable motif containing, transcript variant X3
basic, immunoglobulin-like variable motif containing, transcript variant X2
basic, immunoglobulin-like variable motif containing, transcript variant X4
basic, immunoglobulin-like variable motif containing, transcript variant X1
basic immunoglobulin-like variable motif-containing protein isoform X2
basic immunoglobulin-like variable motif-containing protein isoform X1
protein O-glucosyltransferase 2, transcript variant X1
protein O-glucosyltransferase 2 isoform X1
protein O-glucosyltransferase 2, transcript variant X2
protein O-glucosyltransferase 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 88% 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, 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: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 168
protein-lysine methyltransferase METTL21C
short transmembrane mitochondrial protein 1-like
tripeptidyl peptidase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tripeptidyl peptidase 2, transcript variant X1
tripeptidyl peptidase 2, transcript variant X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00601
fibroblast growth factor 14, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
fibroblast growth factor 14, transcript variant X3
fibroblast growth factor 14, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium leak channel, non-selective, transcript variant X5
sodium leak channel, non-selective, transcript variant X4
sodium leak channel, non-selective, transcript variant X3
sodium leak channel, non-selective, 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 2 samples with support for all annotated introns
sodium leak channel, non-selective, transcript variant X2
sodium leak channel non-selective protein isoform X1
sodium leak channel non-selective protein isoform X3
sodium leak channel non-selective protein isoform X2
sodium leak channel non-selective protein isoform X4
sodium leak channel, non-selective, transcript variant X6
sodium leak channel non-selective protein isoform X5
mitochondrial import inner membrane translocase subunit Tim17-B-like
COORDINATES: nucleotide motif:Rfam:12.0:RF00139
transmembrane O-mannosyltransferase targeting cadherins 4, transcript variant X2
transmembrane O-mannosyltransferase targeting cadherins 4, transcript variant X3
transmembrane O-mannosyltransferase targeting cadherins 4, transcript variant X5
transmembrane O-mannosyltransferase targeting cadherins 4, transcript variant X6
transmembrane O-mannosyltransferase targeting cadherins 4, transcript variant X1
transmembrane O-mannosyltransferase targeting cadherins 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein O-mannosyl-transferase TMTC4 isoform X1
protein O-mannosyl-transferase TMTC4 isoform X2
gamma-glutamylamine cyclotransferase, transcript variant X2
gamma-glutamylamine cyclotransferase, 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 2 samples with support for all annotated introns
gamma-glutamylamine cyclotransferase, transcript variant X5
gamma-glutamylamine cyclotransferase, transcript variant X1
gamma-glutamylamine cyclotransferase, transcript variant X4
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
gamma-glutamylaminecyclotransferase isoform X1
heterogeneous nuclear ribonucleoprotein D-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
gamma-glutamylaminecyclotransferase isoform X2
propionyl-CoA carboxylase alpha chain, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 22 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
Zic family member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Zic family member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
citramalyl-CoA lyase, transcript variant X4
citramalyl-CoA lyase, transcript variant X3
citramalyl-CoA lyase, transcript variant X2
citramalyl-CoA lyase, transcript variant X1
citramalyl-CoA lyase, transcript variant X5
citramalyl-CoA lyase, mitochondrial isoform X1
citramalyl-CoA lyase, mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ubiquitin-associated domain-containing protein 2
dedicator of cytokinesis 9, transcript variant X4
dedicator of cytokinesis 9, transcript variant X25
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
dedicator of cytokinesis 9, transcript variant X12
dedicator of cytokinesis 9, transcript variant X14
dedicator of cytokinesis 9, transcript variant X18
dedicator of cytokinesis 9, transcript variant X19
dedicator of cytokinesis protein 9 isoform X4
dedicator of cytokinesis protein 9 isoform X14
dedicator of cytokinesis protein 9 isoform X25
dedicator of cytokinesis protein 9 isoform X12
dedicator of cytokinesis protein 9 isoform X18
dedicator of cytokinesis protein 9 isoform X19
dedicator of cytokinesis 9, transcript variant X1
dedicator of cytokinesis 9, transcript variant X3
dedicator of cytokinesis 9, transcript variant X8
dedicator of cytokinesis 9, transcript variant X11
dedicator of cytokinesis 9, transcript variant X7
dedicator of cytokinesis 9, transcript variant X10
dedicator of cytokinesis 9, transcript variant X16
dedicator of cytokinesis 9, transcript variant X9
dedicator of cytokinesis 9, transcript variant X23
dedicator of cytokinesis 9, transcript variant X17
dedicator of cytokinesis 9, transcript variant X2
dedicator of cytokinesis protein 9 isoform X1
dedicator of cytokinesis protein 9 isoform X3
dedicator of cytokinesis protein 9 isoform X8
dedicator of cytokinesis protein 9 isoform X11
dedicator of cytokinesis protein 9 isoform X7
dedicator of cytokinesis protein 9 isoform X10
dedicator of cytokinesis protein 9 isoform X16
dedicator of cytokinesis protein 9 isoform X9
dedicator of cytokinesis protein 9 isoform X23
dedicator of cytokinesis protein 9 isoform X17
dedicator of cytokinesis protein 9 isoform X2
dedicator of cytokinesis 9, transcript variant X5
dedicator of cytokinesis 9, transcript variant X21
dedicator of cytokinesis 9, transcript variant X6
dedicator of cytokinesis 9, transcript variant X22
dedicator of cytokinesis 9, transcript variant X15
dedicator of cytokinesis 9, transcript variant X13
dedicator of cytokinesis 9, transcript variant X24
dedicator of cytokinesis 9, transcript variant X20
dedicator of cytokinesis protein 9 isoform X5
dedicator of cytokinesis protein 9 isoform X21
dedicator of cytokinesis protein 9 isoform X6
dedicator of cytokinesis protein 9 isoform X22
dedicator of cytokinesis protein 9 isoform X15
dedicator of cytokinesis protein 9 isoform X13
dedicator of cytokinesis protein 9 isoform X24
dedicator of cytokinesis protein 9 isoform X20
serine/threonine kinase 24, transcript variant X2
serine/threonine-protein kinase 24 isoform X2
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
serine/threonine kinase 24, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine-protein kinase 24 isoform X1
FERM, ARH/RhoGEF and pleckstrin domain protein 1
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: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: FERM, ARHGEF and pleckstrin domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 151 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC121477162, transcript variant X2
uncharacterized LOC121477162, transcript variant X1
muscleblind like splicing regulator 2, transcript variant X2
muscleblind like splicing regulator 2, transcript variant X5
muscleblind like splicing regulator 2, transcript variant X1
muscleblind like splicing regulator 2, transcript variant X3
muscleblind like splicing regulator 2, transcript variant X6
muscleblind like splicing regulator 2, transcript variant X4
muscleblind like splicing regulator 2, transcript variant X8
muscleblind like splicing regulator 2, transcript variant X7
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
heparan sulfate 6-O-sulfotransferase 3, transcript variant X1
heparan sulfate 6-O-sulfotransferase 3, transcript variant X2
heparan sulfate 6-O-sulfotransferase 3, transcript variant X3
heparan-sulfate 6-O-sulfotransferase 3 isoform X2
heparan-sulfate 6-O-sulfotransferase 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
UDP-glucose glycoprotein glucosyltransferase 2
UDP-glucose:glycoprotein glucosyltransferase 2
DnaJ heat shock protein family (Hsp40) member C3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
DAZ interacting zinc finger protein 1, transcript variant X1
DAZ interacting zinc finger protein 1, transcript variant X2
DAZ interacting zinc finger protein 1, transcript variant X3
DAZ interacting zinc finger protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
ATP binding cassette subfamily C member 4, transcript variant X1
ATP binding cassette subfamily C member 4, transcript variant X2
ATP-binding cassette sub-family C member 4
uncharacterized LOC121476805, transcript variant X1
uncharacterized LOC121476805, transcript variant X2
uncharacterized LOC121477029, transcript variant X1
uncharacterized LOC121477029, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 118 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
G protein-coupled receptor 180, transcript variant X3
G protein-coupled receptor 180, transcript variant X2
G protein-coupled receptor 180, transcript variant X6
G protein-coupled receptor 180, transcript variant X4
G protein-coupled receptor 180, transcript variant X1
G protein-coupled receptor 180, transcript variant X5
integral membrane protein GPR180 isoform X4
integral membrane protein GPR180 isoform X2
integral membrane protein GPR180 isoform X1
integral membrane protein GPR180 isoform X3
transfer RNA phenylalanine (anticodon GAA); 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: 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: 19 Proteins, and 58% 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 29% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 62% 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 21% 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 68% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
SLIT and NTRK like family member 5, transcript variant X2
SLIT and NTRK like family member 5, transcript variant X4
SLIT and NTRK like family member 5, transcript variant X1
SLIT and NTRK like family member 5, transcript variant X3
mitochondrial import inner membrane translocase subunit TIM14-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 7% 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, and 68% 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
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: 1 Protein, 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: 15 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 9% 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 45% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC121476768
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 78% 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: 29 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 16% 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: 40S ribosomal protein S19-B-like
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: 25 Proteins
sprouty RTK signaling antagonist 2, transcript variant X2
sprouty RTK signaling antagonist 2, 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: 2 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: mitochondrial carrier homolog 2-like
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
microtubule-associated serine/threonine-protein kinase 4-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
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
RNA binding motif protein 26, transcript variant X11
RNA binding motif protein 26, transcript variant X6
RNA binding motif protein 26, transcript variant X1
RNA binding motif protein 26, transcript variant X3
RNA binding motif protein 26, transcript variant X2
RNA binding motif protein 26, transcript variant X5
RNA binding motif protein 26, transcript variant X4
RNA binding motif protein 26, transcript variant X12
RNA binding motif protein 26, transcript variant X9
RNA binding motif protein 26, transcript variant X7
RNA binding motif protein 26, transcript variant X13
RNA binding motif protein 26, transcript variant X8
RNA binding motif protein 26, transcript variant X15
RNA binding motif protein 26, transcript variant X10
RNA binding motif protein 26, transcript variant X14
non-POU domain-containing octamer-binding protein-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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: non-POU domain-containing octamer-binding protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins
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: 9 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
POU domain, class 4, transcription factor 1
endothelin receptor type B, transcript variant X2
endothelin receptor type B, transcript variant X1
SLAIN motif family member 1, transcript variant X2
SLAIN motif family member 1, transcript variant X1
SLAIN motif-containing protein 1 isoform X2
SLAIN motif-containing protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
F-box and leucine rich repeat protein 3, transcript variant X2
F-box and leucine rich repeat protein 3, transcript variant X1
ceroid-lipofuscinosis neuronal protein 5
potassium channel tetramerization domain containing 12
BTB/POZ domain-containing protein KCTD12
uncharacterized LOC121477158, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC121477158, transcript variant X1
uncharacterized LOC121477158, transcript variant X2
uncharacterized LOC121477158, transcript variant X3
uncharacterized LOC121477064, transcript variant X3
uncharacterized LOC121477064, transcript variant X2
uncharacterized LOC121477064, transcript variant X1
ubiquitin C-terminal hydrolase L3, transcript variant X1
ubiquitin C-terminal hydrolase L3, transcript variant X2
ubiquitin carboxyl-terminal hydrolase isozyme L3 isoform X1
ubiquitin carboxyl-terminal hydrolase isozyme L3 isoform X2
COMM domain containing 6, transcript variant X1
COMM domain-containing protein 6 isoform X1
COMM domain containing 6, transcript variant X2
COMM domain-containing protein 6 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
TBC1 domain family member 4, transcript variant X1
TBC1 domain family member 4, transcript variant X2
TBC1 domain family member 4, transcript variant X3
TBC1 domain family member 4, transcript variant X4
TBC1 domain family member 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
Kruppel like factor 12, transcript variant X3
Kruppel like factor 12, 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 3 samples with support for all annotated introns
Kruppel like factor 12, 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
Kruppel like factor 12, transcript variant X4
progesterone immunomodulatory binding factor 1, transcript variant X4
progesterone immunomodulatory binding factor 1, transcript variant X1
progesterone immunomodulatory binding factor 1, transcript variant X2
progesterone immunomodulatory binding factor 1, transcript variant X3
progesterone immunomodulatory binding factor 1, transcript variant X6
progesterone-induced-blocking factor 1 isoform X2
progesterone-induced-blocking factor 1 isoform X1
progesterone-induced-blocking factor 1 isoform X3
progesterone immunomodulatory binding factor 1, transcript variant X5
DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease, transcript variant X3
DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease, transcript variant X1
DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease, transcript variant X2
exosome complex exonuclease RRP44 isoform X3
exosome complex exonuclease RRP44 isoform X1
exosome complex exonuclease RRP44 isoform 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
uncharacterized LOC121477127, transcript variant X3
uncharacterized LOC121477127, transcript variant X1
uncharacterized LOC121477127, transcript variant X2
uncharacterized LOC121477127, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
kelch like family member 1, transcript variant X1
kelch like family member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 70-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 49% 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: 1 Protein, and 48% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ethylmalonyl-CoA decarboxylase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
ATP synthase-coupling factor 6, mitochondrial-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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 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: 32 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 5 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 2% 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 5 bases in 5 codons; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC121476906
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
tudor domain containing 3, transcript variant X7
tudor domain containing 3, transcript variant X3
tudor domain containing 3, transcript variant X1
tudor domain containing 3, transcript variant X6
tudor domain containing 3, transcript variant X5
tudor domain containing 3, transcript variant X8
tudor domain-containing protein 3 isoform X1
tudor domain-containing protein 3 isoform X5
tudor domain containing 3, transcript variant X4
tudor domain containing 3, transcript variant X2
tudor domain-containing protein 3 isoform X3
tudor domain-containing protein 3 isoform X2
tudor domain-containing protein 3 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
diaphanous related formin 3, transcript variant X2
diaphanous related formin 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 43% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 35% 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 3 bases in 2 codons; deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SGT1 homolog, MIS12 kinetochore complex assembly cochaperone
E74 like ETS transcription factor 1, transcript variant X4
E74 like ETS transcription factor 1, transcript variant X1
E74 like ETS transcription factor 1, transcript variant X2
E74 like ETS transcription factor 1, transcript variant X3
ETS-related transcription factor Elf-1 isoform X2
ETS-related transcription factor Elf-1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
WW domain binding protein 4, transcript variant X2
WW domain binding protein 4, transcript variant X1
kelch repeat and BTB domain-containing protein 6
kelch repeat and BTB domain-containing protein 7
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial translation release factor 1, transcript variant X1
mitochondrial translation release factor 1, transcript variant X2
mitochondrial translation release factor 1, transcript variant X3
mitochondrial translation release factor 1, transcript variant X4
peptide chain release factor 1, mitochondrial
N-alpha-acetyltransferase 16, NatA auxiliary subunit, transcript variant X3
N-alpha-acetyltransferase 16, NatA auxiliary subunit, transcript variant X4
N-alpha-acetyltransferase 16, NatA auxiliary subunit, transcript variant X1
N-alpha-acetyltransferase 16, NatA auxiliary subunit, transcript variant X2
N-alpha-acetyltransferase 16, NatA auxiliary subunit, transcript variant X5
N-alpha-acetyltransferase 16, NatA auxiliary subunit isoform X3
N-alpha-acetyltransferase 16, NatA auxiliary subunit isoform X1
N-alpha-acetyltransferase 16, NatA auxiliary subunit isoform X2
N-alpha-acetyltransferase 16, NatA auxiliary subunit isoform X4
regulator of cell cycle, transcript variant X2
regulator of cell cycle, transcript variant X1
von Willebrand factor A domain containing 8
von Willebrand factor A domain-containing protein 8
uncharacterized LOC121476829, transcript variant X2
uncharacterized LOC121476829, transcript variant X1
diacylglycerol kinase eta, transcript variant X1
diacylglycerol kinase eta, transcript variant X4
diacylglycerol kinase eta, transcript variant X3
diacylglycerol kinase eta, transcript variant X2
A-kinase anchoring protein 11, transcript variant X3
A-kinase anchoring protein 11, transcript variant X5
A-kinase anchoring protein 11, transcript variant X1
A-kinase anchoring protein 11, transcript variant X7
A-kinase anchoring protein 11, transcript variant X2
A-kinase anchoring protein 11, transcript variant X4
A-kinase anchoring protein 11, transcript variant X6
tumor necrosis factor ligand superfamily member 11
family with sequence similarity 216 member B, transcript variant X1
family with sequence similarity 216 member B, transcript variant X2
epithelial stromal interaction 1, transcript variant X2
epithelial stromal interaction 1, transcript variant X1
epithelial stromal interaction 1, transcript variant X3
epithelial-stromal interaction protein 1 isoform X2
epithelial-stromal interaction protein 1 isoform X1
epithelial-stromal interaction protein 1 isoform X3
DnaJ heat shock protein family (Hsp40) member C15
malignant T-cell-amplified sequence 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
ecto-NOX disulfide-thiol exchanger 1, transcript variant X1
ecto-NOX disulfide-thiol exchanger 1, transcript variant X2
ecto-NOX disulfide-thiol exchanger 1 isoform X1
ecto-NOX disulfide-thiol exchanger 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 122
laccase domain containing 1, transcript variant X1
laccase domain containing 1, transcript variant X3
laccase domain containing 1, transcript variant X4
laccase domain containing 1, transcript variant X2
purine nucleoside phosphorylase LACC1 isoform X1
purine nucleoside phosphorylase LACC1 isoform X2
purine nucleoside phosphorylase LACC1 isoform X3
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: small integral membrane protein 2
stress associated endoplasmic reticulum protein family member 2, transcript variant X1
stress associated endoplasmic reticulum protein family member 2, transcript variant X2
stress-associated endoplasmic reticulum protein 2 isoform X2
stress-associated endoplasmic reticulum protein 2 isoform X1
TSC22 domain family member 1, transcript variant X1
TSC22 domain family member 1, transcript variant X9
TSC22 domain family member 1, transcript variant X8
TSC22 domain family protein 1 isoform X1
TSC22 domain family protein 1 isoform X6
TSC22 domain family protein 1 isoform X7
TSC22 domain family member 1, transcript variant X2
TSC22 domain family member 1, transcript variant X4
TSC22 domain family member 1, transcript variant X5
TSC22 domain family member 1, transcript variant X6
TSC22 domain family member 1, transcript variant X3
TSC22 domain family protein 1 isoform X3
TSC22 domain family protein 1 isoform X4
TSC22 domain family protein 1 isoform X2
TSC22 domain family member 1, transcript variant X7
TSC22 domain family protein 1 isoform X5
uncharacterized LOC121476774, transcript variant X2
uncharacterized LOC121476774, transcript variant X3
uncharacterized LOC121476774, transcript variant X1
nuclear fragile X mental retardation-interacting protein 1
uncharacterized LOC121477103, transcript variant X2
uncharacterized LOC121477103, transcript variant X1
general transcription factor IIF subunit 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
potassium channel tetramerization domain containing 4
COORDINATES: nucleotide motif:Rfam:12.0:RF00404
COORDINATES: nucleotide motif:Rfam:12.0:RF00322
tumor protein, translationally-controlled 1
translationally-controlled tumor protein
solute carrier family 25 member 30, 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 3 samples with support for all annotated introns
solute carrier family 25 member 30, transcript variant X1
conserved oligomeric Golgi complex subunit 3
chibby family member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
chibby family member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 14% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC121477124, transcript variant X2
uncharacterized LOC121477124, transcript variant X1
siah E3 ubiquitin protein ligase family member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC121477124, transcript variant X3
zinc finger CCCH-type containing 13, transcript variant X1
zinc finger CCCH-type containing 13, transcript variant X2
zinc finger CCCH domain-containing protein 13 isoform X2
zinc finger CCCH domain-containing protein 13 isoform X1
lymphocyte cytosolic protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
lymphocyte cytosolic protein 1, transcript variant X6
lymphocyte cytosolic protein 1, 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 2 samples with support for all annotated introns
lymphocyte cytosolic protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lymphocyte cytosolic protein 1, transcript variant X4
lymphocyte cytosolic protein 1, transcript variant X5
leucine-rich repeat-containing protein 63
uncharacterized LOC121476816, transcript variant X2
uncharacterized LOC121476816, transcript variant X1
rubicon like autophagy enhancer, transcript variant X4
rubicon like autophagy enhancer, transcript variant X2
rubicon like autophagy enhancer, transcript variant X5
rubicon like autophagy enhancer, transcript variant X3
rubicon like autophagy enhancer, transcript variant X1
rubicon like autophagy enhancer, transcript variant X6
rubicon like autophagy enhancer, transcript variant X8
rubicon like autophagy enhancer, transcript variant X7
rubicon like autophagy enhancer, transcript variant X10
rubicon like autophagy enhancer, transcript variant X12
rubicon like autophagy enhancer, transcript variant X9
rubicon like autophagy enhancer, transcript variant X11
protein associated with UVRAG as autophagy enhancer isoform X1
protein associated with UVRAG as autophagy enhancer isoform X2
leucine rich repeats and calponin homology domain containing 1, transcript variant X2
leucine rich repeats and calponin homology domain containing 1, transcript variant X1
leucine rich repeats and calponin homology domain containing 1, transcript variant X3
leucine-rich repeat and calponin homology domain-containing protein 1 isoform X3
leucine-rich repeat and calponin homology domain-containing protein 1 isoform X1
leucine-rich repeat and calponin homology domain-containing protein 1 isoform X2
leucine rich repeats and calponin homology domain containing 1, transcript variant X4
leucine-rich repeat and calponin homology domain-containing protein 1 isoform X4
snRNA-activating protein complex subunit 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
S-formylglutathione hydrolase isoform X1
S-formylglutathione hydrolase isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 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: 44 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
succinate-CoA ligase ADP-forming subunit beta
succinate--CoA ligase [ADP-forming] subunit beta, mitochondrial
nucleotide triphosphate diphosphatase NUDT15
mediator of RNA polymerase II transcription subunit 4
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
RCC1 and BTB domain containing protein 2, transcript variant X3
RCC1 and BTB domain containing protein 2, transcript variant X2
RCC1 and BTB domain containing protein 2, transcript variant X1
RCC1 and BTB domain containing protein 2, transcript variant X4
RCC1 and BTB domain-containing protein 2 isoform X2
RCC1 and BTB domain-containing protein 2 isoform X1
RCC1 and BTB domain-containing protein 2 isoform X3
cysteinyl leukotriene receptor 2, transcript variant X1
cysteinyl leukotriene receptor 2, transcript variant X2
cysteinyl leukotriene receptor 2, transcript variant X4
cysteinyl leukotriene receptor 2, transcript variant X5
cysteinyl leukotriene receptor 2, transcript variant X3
fibronectin type III domain containing 3A, transcript variant X1
fibronectin type III domain containing 3A, transcript variant X2
fibronectin type-III domain-containing protein 3A isoform X1
fibronectin type III domain containing 3A, transcript variant X4
fibronectin type-III domain-containing protein 3A isoform X3
fibronectin type III domain containing 3A, transcript variant X3
fibronectin type-III domain-containing protein 3A isoform X2
developmental pluripotency-associated protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: histone acetyltransferase KAT7-like
cytidine and dCMP deaminase domain containing 1
cytidine and dCMP deaminase domain-containing protein 1
calcium binding protein 39 like, transcript variant X3
calcium binding protein 39 like, transcript variant X2
calcium binding protein 39 like, transcript variant X1
calcium-binding protein 39-like isoform X1
calcium binding protein 39 like, transcript variant X4
calcium-binding protein 39-like isoform X2
histone-lysine N-methyltransferase SETDB2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
RCC1 and BTB domain containing protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
RCC1 and BTB domain containing protein 1, transcript variant X2
RCC1 and BTB domain-containing protein 1
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
tripartite motif containing 13, transcript variant X3
tripartite motif containing 13, transcript variant X2
tripartite motif containing 13, transcript variant X1
E3 ubiquitin-protein ligase TRIM13 isoform X1
E3 ubiquitin-protein ligase TRIM13 isoform X2
glyceraldehyde-3-phosphate dehydrogenase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
ribonuclease H2 subunit B, transcript variant X2
ribonuclease H2 subunit B, transcript variant X1
ribonuclease H2 subunit B, transcript variant X3
guanylate cyclase soluble subunit beta-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 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: 1 Protein, and 55% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein C13orf42 homolog
family with sequence similarity 124 member A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
integrator complex subunit 6, transcript variant X2
integrator complex subunit 6, transcript variant X1
integrator complex subunit 6, transcript variant X3
WD repeat and FYVE domain containing 2, transcript variant X3
WD repeat and FYVE domain containing 2, transcript variant X1
WD repeat and FYVE domain-containing protein 2 isoform X1
WD repeat and FYVE domain-containing protein 2 isoform X3
WD repeat and FYVE domain containing 2, transcript variant X2
WD repeat and FYVE domain-containing protein 2 isoform X2
WD repeat and FYVE domain containing 2, transcript variant X4
WD repeat and FYVE domain-containing protein 2 isoform X4
coiled-coil domain-containing protein 70
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
ATPase copper transporting beta, transcript variant X5
ATPase copper transporting beta, transcript variant X3
ATPase copper transporting beta, transcript variant X6
ATPase copper transporting beta, transcript variant X2
ATPase copper transporting beta, transcript variant X1
ATPase copper transporting beta, transcript variant X4
ALG11 alpha-1,2-mannosyltransferase, transcript variant X2
ALG11 alpha-1,2-mannosyltransferase, transcript variant X1
GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 21% 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 6 bases at 6 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: serine/threonine-protein kinase Nek5