Vulpes lagopus strain Blue_001 chromosome 24, 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\nCM031318.1.\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.
cryptic protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cryptic protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
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; deleted 1 base in 1 codon; substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: probable G-protein coupled receptor 148
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: 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: 10 Proteins
Rho guanine nucleotide exchange factor 4, 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
rho guanine nucleotide exchange factor 4 isoform X1
Rho guanine nucleotide exchange factor 4, 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
rho guanine nucleotide exchange factor 4 isoform X2
family with sequence similarity 168 member B, 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
family with sequence similarity 168 member B, transcript variant X6
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
family with sequence similarity 168 member B, transcript variant X2
family with sequence similarity 168 member B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
family with sequence similarity 168 member B, transcript variant X4
family with sequence similarity 168 member B, transcript variant X5
myelin-associated neurite-outgrowth inhibitor
pleckstrin homology domain containing B2, transcript variant X1
pleckstrin homology domain containing B2, transcript variant X2
pleckstrin homology domain-containing family B member 2 isoform X1
pleckstrin homology domain containing B2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
pleckstrin homology domain-containing family B member 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
UDP-glucose glycoprotein glucosyltransferase 1, transcript variant X2
UDP-glucose glycoprotein glucosyltransferase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
UDP-glucose:glycoprotein glucosyltransferase 1 isoform X2
UDP-glucose:glycoprotein glucosyltransferase 1 isoform X1
Sin3A associated protein 130, 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 4 samples with support for all annotated introns
Sin3A associated protein 130, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Sin3A associated protein 130, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Sin3A associated protein 130, transcript variant X4
histone deacetylase complex subunit SAP130 isoform X1
histone deacetylase complex subunit SAP130 isoform X3
histone deacetylase complex subunit SAP130 isoform X4
histone deacetylase complex subunit SAP130 isoform X2
small nucleolar RNA SNORA62/SNORA6 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00091
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
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
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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit RPB4
WD repeat domain 33, transcript variant X1
WD repeat domain 33, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
WD repeat domain 33, 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 2 samples with support for all annotated introns
WD repeat domain 33, transcript variant X6
WD repeat domain 33, 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 3 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 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: 6 Proteins, and 39% 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
pre-mRNA 3' end processing protein WDR33 isoform X1
pre-mRNA 3' end processing protein WDR33 isoform X2
pre-mRNA 3' end processing protein WDR33 isoform X4
pre-mRNA 3' end processing protein WDR33 isoform X6
pre-mRNA 3' end processing protein WDR33 isoform X5
WD repeat domain 33, 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 3 samples with support for all annotated introns
pre-mRNA 3' end processing protein WDR33 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
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: 18 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 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: LIM and senescent cell antigen-like-containing domain protein 2
uracil nucleotide/cysteinyl leukotriene receptor
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
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
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
interacts with SUPT6H, CTD assembly factor 1, transcript variant X1
interacts with SUPT6H, CTD assembly factor 1, transcript variant X3
interacts with SUPT6H, CTD assembly factor 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
interacts with SUPT6H, CTD assembly factor 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
protein C, inactivator of coagulation factors Va and VIIIa
uncharacterized LOC121482039, transcript variant X1
uncharacterized LOC121482039, transcript variant X2
uncharacterized LOC121482038, transcript variant X3
uncharacterized LOC121482038, transcript variant X2
uncharacterized LOC121482038, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mitogen-activated protein kinase kinase kinase 2, transcript variant X1
mitogen-activated protein kinase kinase kinase 2, 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 3 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 2, transcript variant X2
mitogen-activated protein kinase kinase kinase 2 isoform X1
mitogen-activated protein kinase kinase kinase 2 isoform X2
ERCC excision repair 3, TFIIH core complex helicase subunit, transcript variant X3
ERCC excision repair 3, TFIIH core complex helicase subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ERCC excision repair 3, TFIIH core complex helicase subunit, transcript variant X1
general transcription and DNA repair factor IIH helicase subunit XPB
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
bridging integrator 1, transcript variant X13
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
bridging integrator 1, transcript variant X14
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
bridging integrator 1, transcript variant X15
bridging integrator 1, transcript variant X2
bridging integrator 1, transcript variant X16
bridging integrator 1, transcript variant X4
bridging integrator 1, transcript variant X1
bridging integrator 1, transcript variant X7
bridging integrator 1, transcript variant X8
bridging integrator 1, transcript variant X3
bridging integrator 1, transcript variant X10
bridging integrator 1, transcript variant X5
bridging integrator 1, transcript variant X6
bridging integrator 1, transcript variant X9
bridging integrator 1, transcript variant X12
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
bridging integrator 1, transcript variant X11
myc box-dependent-interacting protein 1 isoform X13
myc box-dependent-interacting protein 1 isoform X14
myc box-dependent-interacting protein 1 isoform X15
myc box-dependent-interacting protein 1 isoform X16
myc box-dependent-interacting protein 1 isoform X1
myc box-dependent-interacting protein 1 isoform X3
myc box-dependent-interacting protein 1 isoform X5
myc box-dependent-interacting protein 1 isoform X6
myc box-dependent-interacting protein 1 isoform X9
myc box-dependent-interacting protein 1 isoform X11
myc box-dependent-interacting protein 1 isoform X2
myc box-dependent-interacting protein 1 isoform X4
myc box-dependent-interacting protein 1 isoform X7
myc box-dependent-interacting protein 1 isoform X8
myc box-dependent-interacting protein 1 isoform X10
myc box-dependent-interacting protein 1 isoform X12
glycophorin C (Gerbich blood group), transcript variant X2
glycophorin C (Gerbich blood group), transcript variant X3
glycophorin C (Gerbich blood group), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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: 12 Proteins
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: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 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: 17 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
contactin associated protein family member 5, transcript variant X1
contactin-associated protein-like 5 isoform X1
contactin associated protein family member 5, transcript variant X3
contactin-associated protein-like 5 isoform X3
contactin associated protein family member 5, transcript variant X2
contactin-associated protein-like 5 isoform X2
uncharacterized LOC121482132, transcript variant X1
uncharacterized LOC121482132, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 13% 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins
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
nucleolar protein interacting with the FHA domain of MKI67
MKI67 FHA domain-interacting nucleolar phosphoprotein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
cytoplasmic linker associated protein 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
cytoplasmic linker associated protein 1, transcript variant X5
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
cytoplasmic linker associated protein 1, 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 1 sample with support for all annotated introns
cytoplasmic linker associated protein 1, transcript variant X4
cytoplasmic linker associated protein 1, transcript variant X6
cytoplasmic linker associated protein 1, transcript variant X7
cytoplasmic linker associated protein 1, transcript variant X8
cytoplasmic linker associated protein 1, transcript variant X10
cytoplasmic linker associated protein 1, transcript variant X9
cytoplasmic linker associated protein 1, transcript variant X3
cytoplasmic linker associated protein 1, transcript variant X11
cytoplasmic linker associated protein 1, transcript variant X12
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00618
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC121482165, transcript variant X1
uncharacterized LOC121482165, 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 3 samples with support for all annotated introns
RAS like proto-oncogene B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
RAS like proto-oncogene B, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
erythrocyte membrane protein band 4.1 like 5, 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 2 samples with support for all annotated introns
erythrocyte membrane protein band 4.1 like 5, 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 2 samples with support for all annotated introns
erythrocyte membrane protein band 4.1 like 5, 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 3 samples with support for all annotated introns
erythrocyte membrane protein band 4.1 like 5, transcript variant X2
erythrocyte membrane protein band 4.1 like 5, transcript variant X3
erythrocyte membrane protein band 4.1 like 5, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
protein tyrosine phosphatase non-receptor type 4, transcript variant X1
protein tyrosine phosphatase non-receptor type 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein tyrosine phosphatase non-receptor type 4, transcript variant X3
tyrosine-protein phosphatase non-receptor type 4 isoform X2
tyrosine-protein phosphatase non-receptor type 4 isoform X1
tyrosine-protein phosphatase non-receptor type 4 isoform X3
cilia and flagella associated protein 221
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
cilia- and flagella-associated protein 221
secretin receptor, 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 3 samples with support for all annotated introns
secretin receptor, transcript variant X2
voltage-dependent calcium channel gamma-like subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
diazepam binding inhibitor, acyl-CoA binding protein
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
chromosome 24 C2orf76 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
chromosome 24 C2orf76 homolog, transcript variant X4
chromosome 24 C2orf76 homolog, transcript variant X1
chromosome 24 C2orf76 homolog, transcript variant X3
UPF0538 protein C2orf76 homolog isoform X1
UPF0538 protein C2orf76 homolog isoform X2
STEAP3 metalloreductase, 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 3 samples with support for all annotated introns
STEAP3 metalloreductase, transcript variant X3
STEAP3 metalloreductase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
STEAP3 metalloreductase, transcript variant X2
STEAP3 metalloreductase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
macrophage receptor with collagenous structure
translation initiation factor IF-2-like, transcript variant X1
translation initiation factor IF-2-like, transcript variant X2
translation initiation factor IF-2-like, transcript variant X3
translation initiation factor IF-2-like, transcript variant X4
translation initiation factor IF-2-like, transcript variant X5
translation initiation factor IF-2-like isoform X2
translation initiation factor IF-2-like isoform X3
translation initiation factor IF-2-like isoform X1
translation initiation factor IF-2-like, transcript variant X6
translation initiation factor IF-2-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
insulin induced gene 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
insulin induced gene 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
insulin induced gene 2, transcript variant X6
insulin induced gene 2, transcript variant X1
insulin induced gene 2, transcript variant X3
insulin induced gene 2, transcript variant X7
insulin induced gene 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
insulin-induced gene 2 protein isoform X2
insulin-induced gene 2 protein isoform X1
insulin-induced gene 2 protein isoform X3
uncharacterized LOC121481929, transcript variant X3
uncharacterized LOC121481929, transcript variant X2
uncharacterized LOC121481929, transcript variant X4
uncharacterized LOC121481929, transcript variant X1
coiled-coil domain containing 93, transcript variant X1
coiled-coil domain containing 93, transcript variant X2
coiled-coil domain containing 93, transcript variant X3
coiled-coil domain containing 93, transcript variant X4
coiled-coil domain-containing protein 93 isoform X1
coiled-coil domain-containing protein 93 isoform X2
coiled-coil domain-containing protein 93 isoform X3
coiled-coil domain-containing protein 93 isoform X4
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
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; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 87% 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; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: 5-hydroxytryptamine receptor 5B-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 5% 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 94% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC121481829, transcript variant X1
uncharacterized LOC121481829, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 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: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC121482170, transcript variant X2
uncharacterized LOC121482170, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00066
G protein-coupled receptor 39, transcript variant X2
G protein-coupled receptor 39, transcript variant X1
G-protein coupled receptor 39 isoform X1
G-protein coupled receptor 39 isoform X2
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
NCK associated protein 5, transcript variant X2
NCK associated protein 5, transcript variant X7
NCK associated protein 5, transcript variant X1
NCK associated protein 5, transcript variant X3
NCK associated protein 5, transcript variant X4
NCK associated protein 5, transcript variant X6
NCK associated protein 5, transcript variant X9
NCK associated protein 5, transcript variant X8
NCK associated protein 5, transcript variant X5
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase, transcript variant X1
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase, transcript variant X4
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase, transcript variant X2
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase, transcript variant X5
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
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase, transcript variant X3
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase A
DNA-directed RNA polymerases I, II, and III subunit RPABC2
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
aminocarboxymuconate semialdehyde decarboxylase, transcript variant X3
aminocarboxymuconate semialdehyde decarboxylase, transcript variant X1
aminocarboxymuconate semialdehyde decarboxylase, transcript variant X2
aminocarboxymuconate semialdehyde decarboxylase, transcript variant X4
2-amino-3-carboxymuconate-6-semialdehyde decarboxylase isoform X1
2-amino-3-carboxymuconate-6-semialdehyde decarboxylase isoform X2
2-amino-3-carboxymuconate-6-semialdehyde decarboxylase isoform X3
2-amino-3-carboxymuconate-6-semialdehyde decarboxylase isoform X4
aminocarboxymuconate semialdehyde decarboxylase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
2-amino-3-carboxymuconate-6-semialdehyde decarboxylase isoform X5
mitogen-activated protein kinase kinase kinase 19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
RAB3 GTPase activating protein catalytic subunit 1, transcript variant X4
RAB3 GTPase activating protein catalytic subunit 1, transcript variant X1
RAB3 GTPase activating protein catalytic subunit 1, 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
RAB3 GTPase activating protein catalytic subunit 1, transcript variant X3
rab3 GTPase-activating protein catalytic subunit isoform X4
rab3 GTPase-activating protein catalytic subunit isoform X1
rab3 GTPase-activating protein catalytic subunit isoform X2
RAB3 GTPase activating protein catalytic subunit 1, transcript variant X5
rab3 GTPase-activating protein catalytic subunit isoform X3
rab3 GTPase-activating protein catalytic subunit isoform X5
zinc finger RANBP2-type containing 3, transcript variant X3
zinc finger RANBP2-type containing 3, transcript variant X2
zinc finger RANBP2-type containing 3, transcript variant X1
DNA annealing helicase and endonuclease ZRANB3
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: 21 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
R3H domain containing 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 1 sample with support for all annotated introns
R3H domain containing 1, transcript variant X8
R3H domain containing 1, transcript variant X1
R3H domain containing 1, transcript variant X7
R3H domain containing 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
R3H domain containing 1, transcript variant X6
R3H domain containing 1, transcript variant X4
R3H domain containing 1, transcript variant X9
R3H domain containing 1, transcript variant X2
R3H domain-containing protein 1 isoform X1
R3H domain-containing protein 1 isoform X3
R3H domain-containing protein 1 isoform X4
R3H domain-containing protein 1 isoform X6
R3H domain-containing protein 1 isoform X2
R3H domain-containing protein 1 isoform X7
R3H domain-containing protein 1 isoform X5
R3H domain-containing protein 1 isoform X8
R3H domain containing 1, transcript variant X10
R3H domain-containing protein 1 isoform X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 73% 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 98% coverage of the annotated genomic feature by RNAseq alignments
minichromosome maintenance complex component 6
COORDINATES: nucleotide motif:Rfam:12.0:RF00581
aspartyl-tRNA synthetase 1, 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
aspartyl-tRNA synthetase 1, transcript variant X2
aspartate--tRNA ligase, cytoplasmic isoform X1
aspartate--tRNA ligase, cytoplasmic isoform X2
thrombospondin type 1 domain containing 7B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 25% coverage of the annotated genomic feature by RNAseq alignments
thrombospondin type-1 domain-containing protein 7B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
histamine N-methyltransferase, transcript variant X1
histamine N-methyltransferase, 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
histamine N-methyltransferase isoform X1
histamine N-methyltransferase isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
speckle type BTB/POZ protein like, transcript variant X2
speckle type BTB/POZ protein like, transcript variant X1
speckle type BTB/POZ protein like, transcript variant X4
speckle type BTB/POZ protein like, transcript variant X5
speckle type BTB/POZ protein like, transcript variant X3
speckle-type POZ protein-like isoform X1
speckle-type POZ protein-like isoform X2
speckle-type POZ protein-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
low-density lipoprotein receptor-related protein 1B
peptidyl-prolyl cis-trans isomerase A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF01210
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: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC121482155, transcript variant X1
uncharacterized LOC121482155, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
glycosyltransferase like domain containing 1, transcript variant X11
glycosyltransferase like domain containing 1, transcript variant X5
glycosyltransferase like domain containing 1, transcript variant X9
glycosyltransferase like domain containing 1, transcript variant X13
glycosyltransferase like domain containing 1, transcript variant X1
glycosyltransferase like domain containing 1, transcript variant X8
glycosyltransferase like domain containing 1, transcript variant X10
glycosyltransferase like domain containing 1, transcript variant X4
glycosyltransferase like domain containing 1, transcript variant X2
glycosyltransferase like domain containing 1, transcript variant X3
glycosyltransferase like domain containing 1, transcript variant X6
glycosyltransferase like domain containing 1, transcript variant X7
glycosyltransferase-like domain-containing protein 1 isoform X1
glycosyltransferase like domain containing 1, transcript variant X12
glycosyltransferase-like domain-containing protein 1 isoform X2
zinc finger E-box binding homeobox 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger E-box binding homeobox 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger E-box binding homeobox 2, transcript variant X4
zinc finger E-box binding homeobox 2, transcript variant X1
zinc finger E-box-binding homeobox 2 isoform X1
zinc finger E-box-binding homeobox 2 isoform X2
uncharacterized LOC121481967, transcript variant X3
uncharacterized LOC121481967, transcript variant X1
uncharacterized LOC121481967, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
translocase of outer mitochondrial membrane 7
mitochondrial import receptor subunit TOM7 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins
origin recognition complex subunit 4, transcript variant X3
origin recognition complex subunit 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
origin recognition complex subunit 4, transcript variant X5
origin recognition complex subunit 4, transcript variant X4
origin recognition complex subunit 4, transcript variant X1
origin recognition complex subunit 4 isoform X3
origin recognition complex subunit 4 isoform X1
origin recognition complex subunit 4 isoform X2
methyl-CpG binding domain protein 5, transcript variant X4
methyl-CpG binding domain protein 5, transcript variant X3
methyl-CpG binding domain protein 5, transcript variant X5
methyl-CpG binding domain protein 5, transcript variant X2
methyl-CpG binding domain protein 5, transcript variant X1
methyl-CpG binding domain protein 5, transcript variant X7
methyl-CpG binding domain protein 5, transcript variant X6
methyl-CpG binding domain protein 5, transcript variant X8
methyl-CpG binding domain protein 5, transcript variant X9
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
methyl-CpG-binding domain protein 5 isoform X1
methyl-CpG-binding domain protein 5 isoform X2
methyl-CpG-binding domain protein 5 isoform X3
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
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
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
LY6/PLAUR domain containing 6B, transcript variant X3
LY6/PLAUR domain containing 6B, transcript variant X2
LY6/PLAUR domain containing 6B, transcript variant X1
LY6/PLAUR domain containing 6B, transcript variant X8
LY6/PLAUR domain containing 6B, transcript variant X7
LY6/PLAUR domain containing 6B, transcript variant X4
LY6/PLAUR domain containing 6B, transcript variant X5
LY6/PLAUR domain containing 6B, transcript variant X6
LY6/PLAUR domain containing 6B, transcript variant X9
LY6/PLAUR domain containing 6B, transcript variant X10
LY6/PLAUR domain containing 6, transcript variant X4
LY6/PLAUR domain containing 6, transcript variant X2
LY6/PLAUR domain containing 6, transcript variant X1
LY6/PLAUR domain containing 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 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: 31 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 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: 5 Proteins
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; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: nuclear RNA export factor 2-like
tumor necrosis factor-inducible gene 6 protein
replication timing regulatory factor 1, transcript variant X1
replication timing regulatory factor 1, transcript variant X3
replication timing regulatory factor 1, transcript variant X2
telomere-associated protein RIF1 isoform X1
telomere-associated protein RIF1 isoform X3
telomere-associated protein RIF1 isoform X2
replication timing regulatory factor 1, transcript variant X4
telomere-associated protein RIF1 isoform X4
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 96% 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 5 bases at 5 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
calcium voltage-gated channel auxiliary subunit beta 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
calcium voltage-gated channel auxiliary subunit beta 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
voltage-dependent L-type calcium channel subunit beta-4 isoform X1
voltage-dependent L-type calcium channel subunit beta-4 isoform X2
signal transducing adaptor molecule 2, 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
signal transducing adaptor molecule 2, transcript variant X1
signal transducing adapter molecule 2 isoform X1
signal transducing adapter molecule 2 isoform X2
pre-mRNA processing factor 40 homolog A, transcript variant X2
pre-mRNA processing factor 40 homolog A, transcript variant X5
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
pre-mRNA processing factor 40 homolog A, transcript variant X4
pre-mRNA processing factor 40 homolog A, transcript variant X3
pre-mRNA processing factor 40 homolog A, transcript variant X1
pre-mRNA-processing factor 40 homolog A isoform X4
pre-mRNA-processing factor 40 homolog A isoform X3
pre-mRNA-processing factor 40 homolog A isoform X2
pre-mRNA-processing factor 40 homolog A isoform X1
ADP ribosylation factor like GTPase 6 interacting protein 6, transcript variant X3
ADP ribosylation factor like GTPase 6 interacting protein 6, transcript variant X4
ADP ribosylation factor like GTPase 6 interacting protein 6, transcript variant X1
ADP ribosylation factor like GTPase 6 interacting protein 6, transcript variant X2
ADP-ribosylation factor-like protein 6-interacting protein 6 isoform X1
ADP-ribosylation factor-like protein 6-interacting protein 6 isoform X2
low density lipoprotein receptor class A domain containing 4, transcript variant X2
low density lipoprotein receptor class A domain containing 4, transcript variant X9
low density lipoprotein receptor class A domain containing 4, transcript variant X3
low density lipoprotein receptor class A domain containing 4, transcript variant X1
low density lipoprotein receptor class A domain containing 4, transcript variant X8
low density lipoprotein receptor class A domain containing 4, transcript variant X4
low density lipoprotein receptor class A domain containing 4, transcript variant X5
low density lipoprotein receptor class A domain containing 4, transcript variant X7
low density lipoprotein receptor class A domain containing 4, transcript variant X6
low-density lipoprotein receptor class A domain-containing protein 4 isoform X1
low-density lipoprotein receptor class A domain-containing protein 4 isoform X2
family with sequence similarity 210 member A
RNA guanine-7 methyltransferase, transcript variant X2
RNA guanine-7 methyltransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 91% 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: 11 Proteins
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
NAD-dependent malic enzyme, mitochondrial isoform X1
NAD-dependent malic enzyme, mitochondrial isoform X2
SMAD family member 4, transcript variant X4
SMAD family member 4, transcript variant X2
SMAD family member 4, transcript variant X1
SMAD family member 4, transcript variant X3
mothers against decapentaplegic homolog 4 isoform X1
mothers against decapentaplegic homolog 4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
RNA-binding E3 ubiquitin-protein ligase MEX3C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
DCC netrin 1 receptor, transcript variant X1
DCC netrin 1 receptor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 127 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
COORDINATES: nucleotide motif:Rfam:12.0:RF00405
DNA polymerase iota, transcript variant X3
DNA polymerase iota, transcript variant X4
DNA polymerase iota, transcript variant X1
DNA polymerase iota, transcript variant X2
DNA polymerase iota, transcript variant X5
DNA polymerase iota, transcript variant X6
StAR related lipid transfer domain containing 6, transcript variant X14
StAR related lipid transfer domain containing 6, transcript variant X10
StAR related lipid transfer domain containing 6, transcript variant X12
StAR related lipid transfer domain containing 6, transcript variant X8
StAR related lipid transfer domain containing 6, transcript variant X13
StAR related lipid transfer domain containing 6, transcript variant X7
StAR related lipid transfer domain containing 6, transcript variant X5
StAR related lipid transfer domain containing 6, transcript variant X9
StAR related lipid transfer domain containing 6, transcript variant X17
StAR related lipid transfer domain containing 6, transcript variant X11
StAR related lipid transfer domain containing 6, transcript variant X2
StAR related lipid transfer domain containing 6, transcript variant X16
StAR related lipid transfer domain containing 6, transcript variant X4
StAR related lipid transfer domain containing 6, transcript variant X15
StAR related lipid transfer domain containing 6, transcript variant X3
StAR related lipid transfer domain containing 6, transcript variant X6
StAR related lipid transfer domain containing 6, transcript variant X1
StAR related lipid transfer domain containing 6, transcript variant X18
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
stAR-related lipid transfer protein 6 isoform X2
stAR-related lipid transfer protein 6 isoform X4
stAR-related lipid transfer protein 6 isoform X3
stAR-related lipid transfer protein 6 isoform X1
stAR-related lipid transfer protein 6 isoform X5
chromosome 24 C18orf54 homolog, transcript variant X1
chromosome 24 C18orf54 homolog, transcript variant X2
lung adenoma susceptibility protein 2 isoform X1
lung adenoma susceptibility protein 2 isoform X2
uncharacterized LOC121482043, transcript variant X1
uncharacterized protein LOC121482043 isoform X1
uncharacterized LOC121482043, transcript variant X2
uncharacterized protein LOC121482043 isoform X2
RAB27B, member RAS oncogene family, transcript variant X4
RAB27B, member RAS oncogene family, transcript variant X3
RAB27B, member RAS oncogene family, transcript variant X1
RAB27B, member RAS oncogene family, transcript variant X2
RAB27B, member RAS oncogene family, transcript variant X5
coiled-coil domain containing 68, transcript variant X2
coiled-coil domain containing 68, transcript variant X4
coiled-coil domain containing 68, transcript variant X1
coiled-coil domain containing 68, transcript variant X3
coiled-coil domain-containing protein 68 isoform X1
coiled-coil domain containing 68, transcript variant X5
coiled-coil domain-containing protein 68 isoform X2
transcription factor 4, transcript variant X21
transcription factor 4, transcript variant X3
transcription factor 4, transcript variant X10
transcription factor 4, transcript variant X11
transcription factor 4, transcript variant X2
transcription factor 4, transcript variant X8
transcription factor 4, transcript variant X9
transcription factor 4, transcript variant X7
transcription factor 4, transcript variant X4
transcription factor 4, transcript variant X5
transcription factor 4, transcript variant X6
transcription factor 4, transcript variant X1
transcription factor 4, transcript variant X12
transcription factor 4, transcript variant X13
transcription factor 4, transcript variant X14
transcription factor 4, transcript variant X16
transcription factor 4, transcript variant X15
transcription factor 4, transcript variant X17
transcription factor 4, transcript variant X20
transcription factor 4, transcript variant X22
transcription factor 4, transcript variant X19
transcription factor 4, transcript variant X18
uncharacterized LOC121482014, transcript variant X1
uncharacterized LOC121482014, transcript variant X2
thioredoxin like 1, transcript variant X1
thioredoxin like 1, transcript variant X2
WD repeat domain 7, transcript variant X6
WD repeat domain 7, transcript variant X7
WD repeat domain 7, transcript variant X1
WD repeat domain 7, transcript variant X2
WD repeat domain 7, transcript variant X3
WD repeat domain 7, transcript variant X4
WD repeat-containing protein 7 isoform X1
WD repeat-containing protein 7 isoform X3
WD repeat-containing protein 7 isoform X5
WD repeat-containing protein 7 isoform X6
WD repeat-containing protein 7 isoform X2
WD repeat domain 7, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 217 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
WD repeat-containing protein 7 isoform X4
uncharacterized LOC121482142, transcript variant X1
uncharacterized LOC121482142, transcript variant X2
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3
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
sia-alpha-2,3-Gal-beta-1,4-GlcNAc-R:alpha 2,8-sialyltransferase
asparaginyl-tRNA synthetase 1, transcript variant X1
asparaginyl-tRNA synthetase 1, transcript variant X2
asparagine--tRNA ligase, cytoplasmic isoform X2
asparagine--tRNA ligase, cytoplasmic isoform X1
ATPase phospholipid transporting 8B1, transcript variant X2
ATPase phospholipid transporting 8B1, transcript variant X1
phospholipid-transporting ATPase IC isoform X1
phospholipid-transporting ATPase IC isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC121482009, transcript variant X1
uncharacterized LOC121482009, transcript variant X2
uncharacterized LOC121482009, transcript variant X3
NEDD4 like E3 ubiquitin protein ligase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
E3 ubiquitin-protein ligase NEDD4-like isoform X2
NEDD4 like E3 ubiquitin protein ligase, transcript variant X1
NEDD4 like E3 ubiquitin protein ligase, transcript variant X5
NEDD4 like E3 ubiquitin protein ligase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NEDD4 like E3 ubiquitin protein ligase, transcript variant X3
E3 ubiquitin-protein ligase NEDD4-like isoform X3
NEDD4 like E3 ubiquitin protein ligase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
E3 ubiquitin-protein ligase NEDD4-like isoform X4
E3 ubiquitin-protein ligase NEDD4-like isoform X1
E3 ubiquitin-protein ligase NEDD4-like isoform X5
uncharacterized LOC121481801, transcript variant X2
uncharacterized LOC121481801, transcript variant X1
uncharacterized LOC121481977, transcript variant X2
uncharacterized LOC121481977, transcript variant X1
uncharacterized LOC121481977, transcript variant X3
MALT1 paracaspase, transcript variant X1
MALT1 paracaspase, transcript variant X2
mucosa-associated lymphoid tissue lymphoma translocation protein 1 isoform X1
mucosa-associated lymphoid tissue lymphoma translocation protein 1 isoform X2
zinc finger protein 532, transcript variant X6
zinc finger protein 532, transcript variant X4
zinc finger protein 532, transcript variant X2
zinc finger protein 532, transcript variant X7
zinc finger protein 532, transcript variant X8
zinc finger protein 532, transcript variant X10
zinc finger protein 532, transcript variant X1
zinc finger protein 532, transcript variant X5
zinc finger protein 532, transcript variant X9
zinc finger protein 532, 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
SEC11 homolog C, signal peptidase complex subunit, transcript variant X1
SEC11 homolog C, signal peptidase complex subunit, transcript variant X2
signal peptidase complex catalytic subunit SEC11C isoform X1
signal peptidase complex catalytic subunit SEC11C isoform X2
SEC11 homolog C, signal peptidase complex subunit, transcript variant X3
gastrin releasing peptide, transcript variant X2
gastrin releasing peptide, transcript variant X1
retina and anterior neural fold homeobox
lectin, mannose binding 1, transcript variant X2
lectin, mannose binding 1, transcript variant X1
collagen and calcium binding EGF domains 1, transcript variant X1
collagen and calcium binding EGF domains 1, transcript variant X2
collagen and calcium-binding EGF domain-containing protein 1 isoform X1
collagen and calcium-binding EGF domain-containing protein 1 isoform X2
collagen and calcium binding EGF domains 1, transcript variant X3
collagen and calcium-binding EGF domain-containing protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
phorbol-12-myristate-13-acetate-induced protein 1
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: 22 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: 22 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: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ring finger protein 152, transcript variant X1
ring finger protein 152, transcript variant X2
phosphatidylinositol glycan anchor biosynthesis class N, transcript variant X5
phosphatidylinositol glycan anchor biosynthesis class N, transcript variant X4
phosphatidylinositol glycan anchor biosynthesis class N, transcript variant X1
phosphatidylinositol glycan anchor biosynthesis class N, transcript variant X2
phosphatidylinositol glycan anchor biosynthesis class N, transcript variant X3
GPI ethanolamine phosphate transferase 1 isoform X2
GPI ethanolamine phosphate transferase 1 isoform X1
GPI ethanolamine phosphate transferase 1 isoform X3
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X5
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X1
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X2
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X3
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X4
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X6
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X7
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 26% 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 58% coverage of the annotated genomic feature by RNAseq alignments
TNF receptor superfamily member 11a, transcript variant X3
tumor necrosis factor receptor superfamily member 11A isoform X3
TNF receptor superfamily member 11a, transcript variant X6
TNF receptor superfamily member 11a, transcript variant X7
TNF receptor superfamily member 11a, transcript variant X9
TNF receptor superfamily member 11a, transcript variant X11
TNF receptor superfamily member 11a, transcript variant X2
TNF receptor superfamily member 11a, transcript variant X1
TNF receptor superfamily member 11a, transcript variant X4
TNF receptor superfamily member 11a, transcript variant X5
tumor necrosis factor receptor superfamily member 11A isoform X1
tumor necrosis factor receptor superfamily member 11A isoform X2
tumor necrosis factor receptor superfamily member 11A isoform X8
TNF receptor superfamily member 11a, transcript variant X8
tumor necrosis factor receptor superfamily member 11A isoform X4
tumor necrosis factor receptor superfamily member 11A isoform X5
tumor necrosis factor receptor superfamily member 11A isoform X6
TNF receptor superfamily member 11a, transcript variant X10
tumor necrosis factor receptor superfamily member 11A isoform X7
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 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: zinc finger CCHC domain-containing protein 2
PH domain and leucine rich repeat protein phosphatase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
PH domain leucine-rich repeat-containing protein phosphatase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
BCL2 apoptosis regulator, transcript variant X1
uncharacterized LOC121481812, transcript variant X2
uncharacterized LOC121481812, transcript variant X3
uncharacterized LOC121481812, transcript variant X1
BCL2 apoptosis regulator, transcript variant X3
BCL2 apoptosis regulator, transcript variant X4
BCL2 apoptosis regulator, transcript variant X2
vacuolar protein sorting-associated protein 4B
serpin family B member 5, transcript variant X1
serpin family B member 5, transcript variant X3
serpin family B member 5, transcript variant X4
serpin family B member 5, transcript variant X2
serpin family B member 5, transcript variant X6
serpin family B member 5, transcript variant X7
serpin family B member 5, transcript variant X5
serpin family B member 5, transcript variant X8
serpin family B member 12, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
serpin family B member 12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
serpin family B member 13, transcript variant X1
serpin family B member 13, transcript variant X2
serpin family B member 13, transcript variant X3
serpin family B member 3, transcript variant X2
serpin family B member 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins
serpin family B member 11, transcript variant X2
serpin family B member 11, transcript variant X1
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
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: 8 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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 2 samples with support for all annotated introns
E2F-associated phosphoprotein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
E2F-associated phosphoprotein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 82% coverage of the annotated genomic feature by RNAseq alignments
E2F-associated phosphoprotein-like isoform X1
E2F-associated phosphoprotein-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
glyceraldehyde-3-phosphate dehydrogenase-like
dermatan sulfate epimerase like, transcript variant X6
dermatan sulfate epimerase like, transcript variant X7
dermatan sulfate epimerase like, transcript variant X5
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
dermatan sulfate epimerase like, transcript variant X2
dermatan sulfate epimerase like, transcript variant X3
dermatan sulfate epimerase like, transcript variant X4
dermatan sulfate epimerase like, transcript variant X1
WAS/WASL-interacting protein family member 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 10 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
thioredoxin related transmembrane protein 3, transcript variant X1
thioredoxin related transmembrane protein 3, transcript variant X2
protein disulfide-isomerase TMX3 isoform X1
protein disulfide-isomerase TMX3 isoform X2
thioredoxin related transmembrane protein 3, transcript variant X3
protein disulfide-isomerase TMX3 isoform X3
coiled-coil domain containing 102B, transcript variant X3
coiled-coil domain containing 102B, transcript variant X1
coiled-coil domain containing 102B, transcript variant X6
coiled-coil domain-containing protein 102B isoform X1
coiled-coil domain-containing protein 102B isoform X3
coiled-coil domain-containing protein 102B isoform X5
coiled-coil domain containing 102B, transcript variant X4
coiled-coil domain containing 102B, transcript variant X2
coiled-coil domain-containing protein 102B isoform X2
coiled-coil domain containing 102B, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 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: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 102B isoform X4
docking protein 6, transcript variant X2
docking protein 6, transcript variant X1
uncharacterized LOC121481936, transcript variant X2
uncharacterized LOC121481936, transcript variant X1
suppressor of cytokine signaling 6, transcript variant X4
suppressor of cytokine signaling 6, transcript variant X8
suppressor of cytokine signaling 6, transcript variant X6
suppressor of cytokine signaling 6, transcript variant X7
suppressor of cytokine signaling 6, transcript variant X9
suppressor of cytokine signaling 6, transcript variant X2
suppressor of cytokine signaling 6, transcript variant X3
suppressor of cytokine signaling 6, transcript variant X1
suppressor of cytokine signaling 6, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 50% 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 40% 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 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: 5 Proteins
cerebellin 2 precursor, transcript variant X2
cerebellin 2 precursor, transcript variant X1
cerebellin 2 precursor, transcript variant X3
cerebellin 2 precursor, transcript variant X6
cerebellin 2 precursor, transcript variant X5
cerebellin 2 precursor, transcript variant X4
neuropilin and tolloid like 1, transcript variant X5
neuropilin and tolloid like 1, transcript variant X2
neuropilin and tolloid like 1, transcript variant X4
neuropilin and tolloid like 1, transcript variant X7
neuropilin and tolloid like 1, transcript variant X8
neuropilin and tolloid like 1, transcript variant X6
neuropilin and tolloid like 1, transcript variant X3
neuropilin and tolloid like 1, transcript variant X1
neuropilin and tolloid-like protein 1 isoform X1
neuropilin and tolloid like 1, transcript variant X9
neuropilin and tolloid-like protein 1 isoform X2
neuropilin and tolloid like 1, transcript variant X10
neuropilin and tolloid like 1, transcript variant X11
neuropilin and tolloid-like protein 1 isoform X3
neuropilin and tolloid-like protein 1 isoform X4
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
translocase of inner mitochondrial membrane 21
mitochondrial import inner membrane translocase subunit Tim21
uncharacterized protein C18orf63 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
carnosine dipeptidase 2, 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, including 4 samples with support for all annotated introns
carnosine dipeptidase 2, transcript variant X2
carnosine dipeptidase 2, transcript variant X3
carnosine dipeptidase 2, transcript variant X4
carnosine dipeptidase 1, transcript variant X1
carnosine dipeptidase 1, transcript variant X2
zinc finger protein 407, transcript variant X1
zinc finger protein 407, transcript variant X2
zinc finger protein 407, transcript variant X3
zinc binding alcohol dehydrogenase domain containing 2, transcript variant X1
zinc binding alcohol dehydrogenase domain containing 2, transcript variant X3
zinc binding alcohol dehydrogenase domain containing 2, transcript variant X2
teashirt zinc finger homeobox 1, transcript variant X2
teashirt zinc finger homeobox 1, transcript variant X1
zinc finger protein 516, transcript variant X30
zinc finger protein 516, transcript variant X33
zinc finger protein 516, transcript variant X32
zinc finger protein 516, transcript variant X35
zinc finger protein 516, transcript variant X28
zinc finger protein 516, transcript variant X31
zinc finger protein 516, transcript variant X36
zinc finger protein 516, transcript variant X29
zinc finger protein 516, transcript variant X34
zinc finger protein 516, transcript variant X27
zinc finger protein 516, transcript variant X5
zinc finger protein 516, transcript variant X11
zinc finger protein 516, transcript variant X17
zinc finger protein 516, transcript variant X1
zinc finger protein 516, transcript variant X19
zinc finger protein 516, transcript variant X23
zinc finger protein 516, transcript variant X24
zinc finger protein 516, transcript variant X12
zinc finger protein 516, transcript variant X7
zinc finger protein 516, transcript variant X14
zinc finger protein 516, transcript variant X9
zinc finger protein 516, transcript variant X4
zinc finger protein 516, transcript variant X15
zinc finger protein 516, transcript variant X18
zinc finger protein 516, transcript variant X16
zinc finger protein 516, transcript variant X10
zinc finger protein 516, transcript variant X3
zinc finger protein 516, transcript variant X8
zinc finger protein 516, transcript variant X2
zinc finger protein 516, transcript variant X22
zinc finger protein 516, transcript variant X21
zinc finger protein 516, transcript variant X6
zinc finger protein 516, transcript variant X13
zinc finger protein 516, transcript variant X20
zinc finger protein 516, transcript variant X26
zinc finger protein 516, transcript variant X25
zinc finger protein 236, transcript variant X2
zinc finger protein 236, transcript variant X13
zinc finger protein 236, transcript variant X1
zinc finger protein 236, transcript variant X6
zinc finger protein 236, transcript variant X5
zinc finger protein 236, transcript variant X3
zinc finger protein 236, transcript variant X4
zinc finger protein 236, transcript variant X7
zinc finger protein 236, transcript variant X8
zinc finger protein 236, transcript variant X10
zinc finger protein 236, transcript variant X9
zinc finger protein 236, transcript variant X12
zinc finger protein 236, transcript variant X11
myelin basic protein, transcript variant X2
myelin basic protein, transcript variant X3
myelin basic protein, transcript variant X1
myelin basic protein, transcript variant X4
COORDINATES: nucleotide motif:Rfam:12.0:RF00156
uncharacterized LOC121482166, transcript variant X1
uncharacterized LOC121482166, transcript variant X4
uncharacterized LOC121482166, transcript variant X3
uncharacterized LOC121482166, transcript variant X2
spalt like transcription factor 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
spalt like transcription factor 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
ATPase phospholipid transporting 9B (putative), transcript variant X1
ATPase phospholipid transporting 9B (putative), transcript variant X3
ATPase phospholipid transporting 9B (putative), transcript variant X2
probable phospholipid-transporting ATPase IIB isoform X1
probable phospholipid-transporting ATPase IIB isoform X3
probable phospholipid-transporting ATPase IIB isoform X2
nuclear factor of activated T cells 1, transcript variant X1
nuclear factor of activated T cells 1, transcript variant X5
nuclear factor of activated T cells 1, transcript variant X3
nuclear factor of activated T cells 1, transcript variant X6
nuclear factor of activated T-cells, cytoplasmic 1 isoform X1
nuclear factor of activated T-cells, cytoplasmic 1 isoform X3
nuclear factor of activated T-cells, cytoplasmic 1 isoform X5
nuclear factor of activated T-cells, cytoplasmic 1 isoform X6
nuclear factor of activated T cells 1, transcript variant X2
nuclear factor of activated T cells 1, transcript variant X4
nuclear factor of activated T-cells, cytoplasmic 1 isoform X2
nuclear factor of activated T-cells, cytoplasmic 1 isoform X4
uncharacterized LOC121481825, transcript variant X2
uncharacterized LOC121481825, transcript variant X1
CTD phosphatase subunit 1, transcript variant X3
CTD phosphatase subunit 1, transcript variant X4
CTD phosphatase subunit 1, transcript variant X1
CTD phosphatase subunit 1, transcript variant X2
RNA polymerase II subunit A C-terminal domain phosphatase isoform X1
RNA polymerase II subunit A C-terminal domain phosphatase isoform X3
RNA polymerase II subunit A C-terminal domain phosphatase isoform X2
potassium voltage-gated channel modifier subfamily G member 2
potassium voltage-gated channel subfamily G member 2
uncharacterized LOC121481843, transcript variant X3
uncharacterized LOC121481843, transcript variant X1
uncharacterized LOC121481843, transcript variant X4
uncharacterized LOC121481843, transcript variant X5
uncharacterized LOC121481843, transcript variant X2
solute carrier family 66 member 2, transcript variant X1
solute carrier family 66 member 2, transcript variant X2
solute carrier family 66 member 2, transcript variant X3
solute carrier family 66 member 2, transcript variant X4
solute carrier family 66 member 2 isoform X2
solute carrier family 66 member 2 isoform X1
solute carrier family 66 member 2 isoform X3
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, including 2 samples with support for all annotated introns
heat shock factor binding protein 1 like 1, transcript variant X1
heat shock factor binding protein 1 like 1, transcript variant X2
heat shock factor-binding protein 1-like protein 1
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
thioredoxin like 4A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
thioredoxin like 4A, transcript variant X2
thioredoxin like 4A, transcript variant X3
putative ribosome-binding factor A, mitochondrial
activity-dependent neuroprotector homeobox protein 2 isoform X1
activity-dependent neuroprotector homeobox protein 2 isoform X2
par-6 family cell polarity regulator gamma