Vulpes lagopus strain Blue_001 chromosome 20, 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\nCM031314.1.\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.
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
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
S100 calcium binding protein B, 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
S100 calcium binding protein B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
disco interacting protein 2 homolog A, 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 4 samples with support for all annotated introns
disco interacting protein 2 homolog A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
disco-interacting protein 2 homolog A isoform X2
disco-interacting protein 2 homolog A isoform X1
disco interacting protein 2 homolog A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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
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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein C21orf58 homolog
ybeY metalloendoribonuclease, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ybeY metalloendoribonuclease, transcript variant X3
ybeY metalloendoribonuclease, 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
ybeY metalloendoribonuclease, transcript variant X2
minichromosome maintenance complex component 3 associated protein
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
germinal-center associated nuclear protein
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
spermatogenesis and centriole associated 1 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 1 sample with support for all annotated introns
formimidoyltransferase cyclodeaminase, transcript variant X2
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
formimidoyltransferase cyclodeaminase, 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 4 samples with support for all annotated introns
formimidoyltransferase-cyclodeaminase isoform X2
formimidoyltransferase-cyclodeaminase isoform X1
collagen type VI alpha 2 chain, 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 2 samples with support for all annotated introns
collagen type VI alpha 2 chain, transcript variant X1
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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
poly(rC) binding protein 3, transcript variant X3
poly(rC) binding protein 3, transcript variant X1
poly(rC) binding protein 3, transcript variant X4
poly(rC) binding protein 3, transcript variant X17
poly(rC) binding protein 3, transcript variant X5
poly(rC) binding protein 3, transcript variant X6
poly(rC) binding protein 3, transcript variant X8
poly(rC) binding protein 3, transcript variant X2
poly(rC) binding protein 3, transcript variant X7
poly(rC) binding protein 3, transcript variant X9
poly(rC) binding protein 3, transcript variant X19
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
poly(rC) binding protein 3, transcript variant X16
poly(rC) binding protein 3, transcript variant X18
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
poly(rC) binding protein 3, transcript variant X15
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
poly(rC) binding protein 3, transcript variant X14
poly(rC) binding protein 3, transcript variant X12
poly(rC) binding protein 3, transcript variant X13
poly(rC) binding protein 3, transcript variant X10
poly(rC) binding protein 3, transcript variant X11
poly(rC) binding protein 3, transcript variant X20
solute carrier family 19 member 1, transcript variant X4
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
solute carrier family 19 member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 19 member 1, transcript variant X3
solute carrier family 19 member 1, transcript variant X2
collagen type XVIII alpha 1 chain, transcript variant X8
collagen type XVIII alpha 1 chain, 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 4 samples with support for all annotated introns
collagen type XVIII alpha 1 chain, transcript variant X4
collagen type XVIII alpha 1 chain, transcript variant X3
collagen type XVIII alpha 1 chain, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
collagen type XVIII alpha 1 chain, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
collagen type XVIII alpha 1 chain, transcript variant X6
collagen type XVIII alpha 1 chain, transcript variant X9
collagen type XVIII alpha 1 chain, transcript variant X7
collagen alpha-1(XVIII) chain isoform X8
collagen alpha-1(XVIII) chain isoform X9
collagen alpha-1(XVIII) chain isoform X6
collagen alpha-1(XVIII) chain isoform X5
collagen alpha-1(XVIII) chain isoform X4
collagen alpha-1(XVIII) chain isoform X3
collagen alpha-1(XVIII) chain isoform X2
collagen alpha-1(XVIII) chain isoform X1
collagen alpha-1(XVIII) chain isoform X7
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
GDP-fucose protein O-fucosyltransferase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
adenosine deaminase RNA specific B1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
adenosine deaminase RNA specific B1, transcript variant X1
adenosine deaminase RNA specific B1, transcript variant X3
adenosine deaminase RNA specific B1, transcript variant X2
double-stranded RNA-specific editase 1 isoform X2
double-stranded RNA-specific editase 1 isoform X1
adenosine deaminase RNA specific B1, transcript variant X5
double-stranded RNA-specific editase 1 isoform X3
uncharacterized LOC121479395, transcript variant X2
uncharacterized LOC121479395, transcript variant X1
SLX9 ribosome biogenesis factor, transcript variant X3
SLX9 ribosome biogenesis factor, transcript variant X2
SLX9 ribosome biogenesis factor, transcript variant X1
integrin subunit beta 2, transcript variant X2
integrin subunit beta 2, transcript variant X4
integrin subunit beta 2, transcript variant X3
integrin subunit beta 2, transcript variant X5
integrin subunit beta 2, transcript variant X1
pituitary tumor-transforming gene 1 protein-interacting protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ubiquitin conjugating enzyme E2 G2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ubiquitin conjugating enzyme E2 G2, transcript variant X2
ubiquitin-conjugating enzyme E2 G2 isoform X1
ubiquitin-conjugating enzyme E2 G2 isoform X2
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: 16 Proteins
keratin-associated protein 10-12-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
keratin-associated protein 10-12-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
keratin-associated protein 10-12-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
keratin-associated protein 10-12-like isoform X2
keratin-associated protein 10-7-like isoform X3
keratin-associated protein 10-6-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 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: 6 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: 1 Protein, and 34% coverage of the annotated genomic feature by RNAseq alignments
keratin-associated protein 12-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
keratin-associated protein 12-1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
keratin-associated protein 12-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 75% coverage of the annotated genomic feature by RNAseq alignments
keratin-associated protein 12-3-like isoform X2
keratin-associated protein 12-1-like isoform X3
keratin-associated protein 12-2-like isoform X1
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: 11 Proteins
keratin-associated protein 10-7-like, transcript variant X2
keratin-associated protein 10-7-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
keratin-associated protein 10-7-like isoform X2
keratin-associated protein 10-7-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
keratin-associated protein 10-8-like 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: 6 Proteins
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: keratin-associated protein 10-8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
leucine rich repeat containing 3, 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 2 samples with support for all annotated introns
leucine rich repeat containing 3, transcript variant X1
leucine-rich repeat-containing protein 3
transient receptor potential cation channel subfamily M member 2, 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
transient receptor potential cation channel subfamily M member 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transient receptor potential cation channel subfamily M member 2, transcript variant X1
transient receptor potential cation channel subfamily M member 2, transcript variant X2
transient receptor potential cation channel subfamily M member 2, 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
transient receptor potential cation channel subfamily M member 2, transcript variant X7
transient receptor potential cation channel subfamily M member 2 isoform X2
transient receptor potential cation channel subfamily M member 2 isoform X1
transient receptor potential cation channel subfamily M member 2 isoform X4
COORDINATES: nucleotide motif:Rfam:12.0:RF00285
transient receptor potential cation channel subfamily M member 2, transcript variant X6
transient receptor potential cation channel subfamily M member 2 isoform X3
cilia and flagella associated protein 410, transcript variant X1
cilia and flagella associated protein 410, transcript variant X2
cilia- and flagella-associated protein 410 isoform X1
cilia- and flagella-associated protein 410 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ATP-dependent 6-phosphofructokinase, liver type
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 65% 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 51% coverage of the annotated genomic feature by RNAseq alignments
DNA (cytosine-5)-methyltransferase 3-like
inducible T cell costimulator ligand, transcript variant X1
inducible T cell costimulator ligand, transcript variant X2
glutamine amidotransferase class 1 domain containing 3A, transcript variant X1
glutamine amidotransferase class 1 domain containing 3A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glutamine amidotransferase-like class 1 domain-containing protein 3A, mitochondrial isoform X1
glutamine amidotransferase-like class 1 domain-containing protein 3A, mitochondrial isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 51% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC121479226
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 79% coverage of the annotated genomic feature by RNAseq alignments
trafficking protein particle complex subunit 10, transcript variant X3
trafficking protein particle complex subunit 10, 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 2 samples with support for all annotated introns
trafficking protein particle complex subunit 10, transcript variant X1
trafficking protein particle complex subunit 10 isoform X2
trafficking protein particle complex subunit 10 isoform X1
trafficking protein particle complex subunit 10 isoform X3
1-acylglycerol-3-phosphate O-acyltransferase 3, transcript variant X2
1-acylglycerol-3-phosphate O-acyltransferase 3, 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 3 samples with support for all annotated introns
1-acylglycerol-3-phosphate O-acyltransferase 3, transcript variant X1
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma isoform X2
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma isoform X1
ribosomal RNA processing 1, 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
ribosomal RNA processing protein 1 homolog A isoform X3
ribosomal RNA processing 1, transcript variant X5
ribosomal RNA processing protein 1 homolog A isoform X5
ribosomal RNA processing 1, transcript variant X1
ribosomal RNA processing 1, transcript variant X2
ribosomal RNA processing 1, transcript variant X4
ribosomal RNA processing protein 1 homolog A isoform X1
ribosomal RNA processing protein 1 homolog A isoform X2
ribosomal RNA processing protein 1 homolog A isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% 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 4 samples with support for all annotated introns
ribosomal RNA processing 1B, transcript variant X3
ribosomal RNA processing protein 1 homolog B isoform X3
ribosomal RNA processing 1B, transcript variant X4
ribosomal RNA processing 1B, transcript variant X5
ribosomal RNA processing 1B, transcript variant X2
ribosomal RNA processing 1B, transcript variant X1
ribosomal RNA processing protein 1 homolog B isoform X4
ribosomal RNA processing protein 1 homolog B isoform X2
ribosomal RNA processing protein 1 homolog B isoform X1
ribosomal RNA processing protein 1 homolog B isoform X5
heat shock transcription factor 2 binding protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
salt inducible kinase 1, transcript variant X1
salt inducible kinase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
U2 small nuclear RNA auxiliary factor 1, transcript variant X2
U2 small nuclear RNA auxiliary factor 1, transcript variant X1
splicing factor U2AF 35 kDa subunit isoform X1
splicing factor U2AF 35 kDa subunit isoform X2
cystathionine beta-synthase, transcript variant X2
cystathionine beta-synthase, transcript variant X1
cystathionine beta-synthase-like protein isoform X1
cystathionine beta-synthase, transcript variant X4
cystathionine beta-synthase, transcript variant X3
cystathionine beta-synthase-like protein isoform X2
PBX/knotted 1 homeobox 1, transcript variant X7
PBX/knotted 1 homeobox 1, transcript variant X6
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
PBX/knotted 1 homeobox 1, transcript variant X1
PBX/knotted 1 homeobox 1, transcript variant X3
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 1 sample with support for all annotated introns
PBX/knotted 1 homeobox 1, transcript variant X4
PBX/knotted 1 homeobox 1, transcript variant X5
PBX/knotted 1 homeobox 1, transcript variant X2
NADH:ubiquinone oxidoreductase subunit V3, transcript variant X1
NADH:ubiquinone oxidoreductase subunit V3, transcript variant X2
NADH dehydrogenase [ubiquinone] flavoprotein 3, mitochondrial isoform X2
NADH dehydrogenase [ubiquinone] flavoprotein 3, mitochondrial isoform X1
WD repeat domain 4, transcript variant X1
tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit WDR4 isoform X1
WD repeat domain 4, transcript variant X2
tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit WDR4 isoform X2
phosphodiesterase 9A, transcript variant X4
phosphodiesterase 9A, transcript variant X2
phosphodiesterase 9A, transcript variant X3
phosphodiesterase 9A, transcript variant X1
phosphodiesterase 9A, transcript variant X8
phosphodiesterase 9A, transcript variant X9
phosphodiesterase 9A, transcript variant X5
phosphodiesterase 9A, transcript variant X6
phosphodiesterase 9A, transcript variant X7
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform X1
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform X2
solute carrier family 37 member 1, transcript variant X4
solute carrier family 37 member 1, transcript variant X3
solute carrier family 37 member 1, transcript variant X2
solute carrier family 37 member 1, transcript variant X1
solute carrier family 37 member 1, transcript variant X5
radial spoke head component 1, transcript variant X2
radial spoke head component 1, transcript variant X1
ubiquitin associated and SH3 domain containing A, transcript variant X1
ubiquitin-associated and SH3 domain-containing protein A isoform X1
ubiquitin associated and SH3 domain containing A, transcript variant X2
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
ubiquitin-associated and SH3 domain-containing protein A isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
ATP binding cassette subfamily G member 1, transcript variant X2
ATP binding cassette subfamily G member 1, transcript variant X3
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
ATP binding cassette subfamily G member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ATP-binding cassette sub-family G member 1 isoform X2
ATP-binding cassette sub-family G member 1 isoform X3
ATP-binding cassette sub-family G member 1 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: 8 Proteins, and 67% 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; Derived by automated computational analysis using gene prediction method: Gnomon.
zinc finger and BTB domain containing 21, transcript variant X2
zinc finger and BTB domain containing 21, transcript variant X1
zinc finger and BTB domain containing 21, transcript variant X4
zinc finger and BTB domain containing 21, transcript variant X3
zinc finger and BTB domain-containing protein 21 isoform X1
zinc finger and BTB domain-containing protein 21 isoform X2
C2 calcium dependent 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: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: C2 domain-containing protein 2
PR domain zinc finger protein 15 isoform X1
PR domain zinc finger protein 15 isoform X2
receptor interacting serine/threonine kinase 4
receptor-interacting serine/threonine-protein kinase 4
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
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 36% coverage of the annotated genomic feature by RNAseq alignments
transmembrane serine protease 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane serine protease 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transmembrane serine protease 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transmembrane protease serine 2 isoform X2
transmembrane serine protease 2, transcript variant X3
transmembrane protease serine 2 isoform X3
transmembrane serine protease 2, transcript variant X5
transmembrane serine protease 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane protease serine 2 isoform X1
MX dynamin like GTPase 1, transcript variant X2
MX dynamin like GTPase 1, transcript variant X1
interferon-induced GTP-binding protein Mx1
MX dynamin like GTPase 2, transcript variant X1
MX dynamin like GTPase 2, transcript variant X2
interferon-induced GTP-binding protein Mx2 isoform X2
interferon-induced GTP-binding protein Mx2 isoform X1
FAM3 metabolism regulating signaling molecule B, transcript variant X2
FAM3 metabolism regulating signaling molecule B, transcript variant X1
FAM3 metabolism regulating signaling molecule B, 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 4 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00096
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins
Down syndrome cell adhesion molecule-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
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
immunoglobulin superfamily member 5, transcript variant X3
immunoglobulin superfamily member 5, transcript variant X2
immunoglobulin superfamily member 5, transcript variant X1
immunoglobulin superfamily member 5, transcript variant X5
immunoglobulin superfamily member 5, transcript variant X4
immunoglobulin superfamily member 5 isoform X2
immunoglobulin superfamily member 5 isoform X1
beta-1,3-galactosyltransferase 5, transcript variant X2
beta-1,3-galactosyltransferase 5, transcript variant X1
SH3 domain-binding glutamic acid-rich protein-like
GTP:AMP phosphotransferase AK3, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
GTP:AMP phosphotransferase AK3, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 78% coverage of the annotated genomic feature by RNAseq alignments
GTP:AMP phosphotransferase AK3, mitochondrial-like isoform X1
GTP:AMP phosphotransferase AK3, mitochondrial-like isoform X2
lebercilin LCA5 like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lebercilin LCA5 like, transcript variant X2
lebercilin LCA5 like, transcript variant X3
guided entry of tail-anchored proteins factor 1
high mobility group nucleosome binding domain 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
bromodomain and WD repeat domain containing 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
bromodomain and WD repeat-containing protein 1 isoform X4
bromodomain and WD repeat domain containing 1, transcript variant X2
bromodomain and WD repeat domain containing 1, transcript variant X1
bromodomain and WD repeat domain containing 1, transcript variant X3
bromodomain and WD repeat-containing protein 1 isoform X1
bromodomain and WD repeat-containing protein 1 isoform X2
bromodomain and WD repeat-containing protein 1 isoform X3
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: 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: proteasome assembly chaperone 1
ETS proto-oncogene 2, transcription factor, transcript variant X2
ETS proto-oncogene 2, transcription factor, 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 2 samples with support for all annotated introns
ETS transcription factor ERG, transcript variant X2
transcriptional regulator ERG isoform X2
ETS transcription factor ERG, transcript variant X4
transcriptional regulator ERG isoform X4
ETS transcription factor ERG, transcript variant X1
ETS transcription factor ERG, 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 1 sample with support for all annotated introns
transcriptional regulator ERG isoform X1
transcriptional regulator ERG isoform X3
ETS transcription factor ERG, 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 2 samples with support for all annotated introns
transcriptional regulator ERG isoform X5
potassium inwardly rectifying channel subfamily J member 15, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
potassium inwardly rectifying channel subfamily J member 15, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium inwardly rectifying channel subfamily J member 15, transcript variant X5
potassium inwardly rectifying channel subfamily J member 15, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
potassium inwardly rectifying channel subfamily J member 15, transcript variant X1
potassium inwardly rectifying channel subfamily J member 15, transcript variant X9
potassium inwardly rectifying channel subfamily J member 15, transcript variant X4
potassium inwardly rectifying channel subfamily J member 15, transcript variant X7
potassium inwardly rectifying channel subfamily J member 15, transcript variant X8
ATP-sensitive inward rectifier potassium channel 15
potassium inwardly rectifying channel subfamily J member 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
G protein-activated inward rectifier potassium channel 2 isoform X1
potassium inwardly rectifying channel subfamily J member 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
G protein-activated inward rectifier potassium channel 2 isoform X2
uncharacterized LOC121479531, transcript variant X3
uncharacterized LOC121479531, transcript variant X2
uncharacterized LOC121479531, transcript variant X1
dual specificity tyrosine phosphorylation regulated kinase 1A, 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 1 sample with support for all annotated introns
dual specificity tyrosine phosphorylation regulated kinase 1A, transcript variant X4
dual specificity tyrosine phosphorylation regulated kinase 1A, transcript variant X1
dual specificity tyrosine phosphorylation regulated kinase 1A, transcript variant X3
dual specificity tyrosine phosphorylation regulated kinase 1A, transcript variant X2
dual specificity tyrosine-phosphorylation-regulated kinase 1A isoform X2
dual specificity tyrosine-phosphorylation-regulated kinase 1A isoform X1
dual specificity tyrosine-phosphorylation-regulated kinase 1A isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
VPS26 endosomal protein sorting factor C
vacuolar protein sorting-associated protein 26C
MAPK-interacting and spindle-stabilizing protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tetratricopeptide repeat domain 3, transcript variant X4
tetratricopeptide repeat domain 3, transcript variant X2
tetratricopeptide repeat domain 3, transcript variant X7
tetratricopeptide repeat domain 3, transcript variant X3
tetratricopeptide repeat domain 3, transcript variant X5
tetratricopeptide repeat domain 3, transcript variant X1
tetratricopeptide repeat domain 3, transcript variant X6
E3 ubiquitin-protein ligase TTC3 isoform X2
E3 ubiquitin-protein ligase TTC3 isoform X1
E3 ubiquitin-protein ligase TTC3 isoform X3
phosphatidylinositol glycan anchor biosynthesis class P, transcript variant X3
phosphatidylinositol glycan anchor biosynthesis class P, transcript variant X1
phosphatidylinositol glycan anchor biosynthesis class P, transcript variant X2
phosphatidylinositol N-acetylglucosaminyltransferase subunit P
ripply transcriptional repressor 3, transcript variant X1
ripply transcriptional repressor 3, transcript variant X2
holocarboxylase synthetase, 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
holocarboxylase synthetase, transcript variant X3
holocarboxylase synthetase, transcript variant X4
holocarboxylase synthetase, transcript variant X6
uncharacterized LOC121479303, transcript variant X2
uncharacterized LOC121479303, transcript variant X1
holocarboxylase synthetase, transcript variant X7
holocarboxylase synthetase, transcript variant X8
holocarboxylase synthetase, transcript variant X1
holocarboxylase synthetase, transcript variant X2
collagen alpha-1(I) chain-like, transcript variant X1
collagen alpha-1(I) chain-like, transcript variant X2
collagen alpha-1(I) chain-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
MORC family CW-type zinc finger 3, transcript variant X1
MORC family CW-type zinc finger 3, transcript variant X2
MORC family CW-type zinc finger protein 3 isoform X1
MORC family CW-type zinc finger protein 3 isoform X2
DOP1 leucine zipper like protein B, transcript variant X3
DOP1 leucine zipper like protein B, transcript variant X1
DOP1 leucine zipper like protein B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 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: 29 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: 2 Proteins
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
RUNX family transcription factor 1, transcript variant X2
RUNX family transcription factor 1, transcript variant X1
runt-related transcription factor 1 isoform X1
runt-related transcription factor 1 isoform X2
chloride intracellular channel 6, 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 3 samples with support for all annotated introns
chloride intracellular channel 6, transcript variant X3
chloride intracellular channel 6, transcript variant X2
chloride intracellular channel protein 6 isoform X1
chloride intracellular channel protein 6 isoform X2
chloride intracellular channel protein 6 isoform X3
regulator of calcineurin 1, transcript variant X1
regulator of calcineurin 1, transcript variant X3
regulator of calcineurin 1, transcript variant X4
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
regulator of calcineurin 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
potassium voltage-gated channel subfamily E regulatory subunit 1, transcript variant X2
potassium voltage-gated channel subfamily E regulatory subunit 1, transcript variant X3
potassium voltage-gated channel subfamily E regulatory subunit 1, transcript variant X4
potassium voltage-gated channel subfamily E regulatory subunit 1, transcript variant X1
potassium voltage-gated channel subfamily E member 1
family with sequence similarity 243 member A
small integral membrane protein 11A, transcript variant X1
small integral membrane protein 11A, transcript variant X2
small integral membrane protein 11A, transcript variant X3
potassium voltage-gated channel subfamily E regulatory subunit 2, transcript variant X2
potassium voltage-gated channel subfamily E regulatory subunit 2, transcript variant X3
potassium voltage-gated channel subfamily E regulatory subunit 2, transcript variant X1
potassium voltage-gated channel subfamily E member 2
solute carrier family 5 member 3, transcript variant X2
solute carrier family 5 member 3, 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 3 samples with support for all annotated introns
solute carrier family 5 member 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
ATP synthase peripheral stalk subunit OSCP
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 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: 1 Protein, and 56% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00156
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
crystallin zeta like 1, transcript variant X8
crystallin zeta like 1, transcript variant X3
crystallin zeta like 1, transcript variant X2
crystallin zeta like 1, transcript variant X4
crystallin zeta like 1, transcript variant X1
crystallin zeta like 1, transcript variant X6
crystallin zeta like 1, transcript variant X5
quinone oxidoreductase-like protein 1 isoform X6
quinone oxidoreductase-like protein 1 isoform X1
quinone oxidoreductase-like protein 1 isoform X3
quinone oxidoreductase-like protein 1 isoform X2
quinone oxidoreductase-like protein 1 isoform X4
crystallin zeta like 1, transcript variant X7
quinone oxidoreductase-like protein 1 isoform X5
DNA replication fork stabilization factor DONSON
SON DNA and RNA binding protein, transcript variant X1
SON DNA and RNA binding protein, transcript variant X2
SON DNA and RNA binding protein, transcript variant X3
SON DNA and RNA binding protein, transcript variant X4
SON DNA and RNA binding protein, transcript variant X5
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant X2
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant X1
trifunctional purine biosynthetic protein adenosine-3
DnaJ heat shock protein family (Hsp40) member C28, transcript variant X6
DnaJ heat shock protein family (Hsp40) member C28, transcript variant X2
DnaJ heat shock protein family (Hsp40) member C28, transcript variant X7
DnaJ heat shock protein family (Hsp40) member C28, transcript variant X5
DnaJ heat shock protein family (Hsp40) member C28, transcript variant X4
DnaJ heat shock protein family (Hsp40) member C28, transcript variant X1
DnaJ heat shock protein family (Hsp40) member C28, 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
transmembrane protein 50B, transcript variant X2
dnaJ homolog subfamily C member 28 isoform X3
dnaJ homolog subfamily C member 28 isoform X2
dnaJ homolog subfamily C member 28 isoform X1
transmembrane protein 50B, transcript variant X1
transmembrane protein 50B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 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: 8 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
interferon gamma receptor 2, transcript variant X1
interferon gamma receptor 2, transcript variant X2
interferon alpha and beta receptor subunit 1
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 13% coverage of the annotated genomic feature by RNAseq alignments
interferon alpha and beta receptor subunit 2, transcript variant X2
interferon alpha and beta receptor subunit 2, transcript variant X1
interferon alpha and beta receptor subunit 2, transcript variant X5
interferon alpha and beta receptor subunit 2, transcript variant X3
interferon alpha and beta receptor subunit 2, transcript variant X6
interferon alpha and beta receptor subunit 2, transcript variant X4
interferon alpha/beta receptor 2 isoform X2
interferon alpha/beta receptor 2 isoform X1
activated RNA polymerase II transcriptional coactivator p15-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: activated RNA polymerase II transcriptional coactivator p15-like
chromosome 20 C21orf62 homolog, transcript variant X3
chromosome 20 C21orf62 homolog, transcript variant X2
chromosome 20 C21orf62 homolog, transcript variant X1
uncharacterized protein C21orf62 homolog
cilia and flagella associated protein 298, transcript variant X1
cilia and flagella associated protein 298, transcript variant X2
cilia- and flagella-associated protein 298
39S ribosomal protein L27, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
URB1 ribosome biogenesis homolog, transcript variant X1
nucleolar pre-ribosomal-associated protein 1 isoform X1
URB1 ribosome biogenesis homolog, transcript variant X2
nucleolar pre-ribosomal-associated protein 1 isoform X2
melanocortin 2 receptor accessory protein
melanocortin-2 receptor accessory protein
MIS18 kinetochore protein A, transcript variant X1
MIS18 kinetochore protein A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
hormonally up-regulated Neu-associated kinase, transcript variant X1
hormonally up-regulated Neu-associated kinase, transcript variant X2
hormonally up-regulated Neu-associated kinase, transcript variant X3
hormonally up-regulated neu tumor-associated kinase isoform X1
hormonally up-regulated neu tumor-associated kinase isoform X2
hormonally up-regulated neu tumor-associated kinase isoform X3
SR-related CTD associated factor 4, transcript variant X1
SR-related CTD associated factor 4, transcript variant X2
SR-related and CTD-associated factor 4 isoform X1
SR-related and CTD-associated factor 4 isoform X2
TIAM Rac1 associated GEF 1, transcript variant X2
TIAM Rac1 associated GEF 1, transcript variant X3
TIAM Rac1 associated GEF 1, transcript variant X1
TIAM Rac1 associated GEF 1, transcript variant X6
TIAM Rac1 associated GEF 1, transcript variant X4
TIAM Rac1 associated GEF 1, transcript variant X5
T-lymphoma invasion and metastasis-inducing protein 1 isoform X1
T-lymphoma invasion and metastasis-inducing protein 1 isoform X2
TIAM Rac1 associated GEF 1, transcript variant X7
T-lymphoma invasion and metastasis-inducing protein 1 isoform X3
keratin-associated protein 11-1, transcript variant X1
keratin-associated protein 11-1, 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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
keratin-associated protein 6-2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 40% coverage of the annotated genomic feature by RNAseq alignments
keratin-associated protein 6-2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 49% coverage of the annotated genomic feature by RNAseq alignments
keratin-associated protein 21-1-like isoform X1
keratin-associated protein 6-2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 1 Protein, 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: 3 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: 1 Protein, and 54% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 46% 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 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: 13 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
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 54% 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: keratin-associated protein 23-1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 78% 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
glutamate ionotropic receptor kainate type subunit 1
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
glutamate receptor ionotropic, kainate 1
BTB domain and CNC homolog 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
BTB domain and CNC homolog 1, transcript variant X2
BTB domain and CNC homolog 1, transcript variant X3
BTB domain and CNC homolog 1, transcript variant X4
BTB domain and CNC homolog 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
MAP3K7 C-terminal like, transcript variant X1
MAP3K7 C-terminal like, transcript variant X2
MAP3K7 C-terminal-like protein isoform X1
MAP3K7 C-terminal-like protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
chaperonin containing TCP1 subunit 8, transcript variant X1
chaperonin containing TCP1 subunit 8, transcript variant X2
T-complex protein 1 subunit theta isoform X2
T-complex protein 1 subunit theta isoform X1
ubiquitin specific peptidase 16, transcript variant X3
ubiquitin specific peptidase 16, transcript variant X1
ubiquitin specific peptidase 16, transcript variant X4
ubiquitin specific peptidase 16, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 16 isoform X3
ubiquitin carboxyl-terminal hydrolase 16 isoform X2
ubiquitin carboxyl-terminal hydrolase 16 isoform X1
RWD domain containing 2B, transcript variant X2
RWD domain containing 2B, transcript variant X1
N-6 adenine-specific DNA methyltransferase 1, transcript variant X2
N-6 adenine-specific DNA methyltransferase 1, transcript variant X1
phospholipid scramblase 1-like, transcript variant X2
phospholipid scramblase 1-like, 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
phospholipid scramblase 1-like isoform X1
phospholipid scramblase 1-like isoform 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
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
ADAM metallopeptidase with thrombospondin type 1 motif 5
A disintegrin and metalloproteinase with thrombospondin motifs 5
ADAM metallopeptidase with thrombospondin type 1 motif 1
A disintegrin and metalloproteinase with thrombospondin motifs 1
geranylgeranyl pyrophosphate synthase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
amyloid beta precursor protein, transcript variant X1
amyloid beta precursor protein, transcript variant X2
amyloid beta precursor protein, transcript variant X3
amyloid beta precursor protein, transcript variant X4
amyloid-beta precursor protein isoform X1
amyloid-beta precursor protein isoform X2
amyloid-beta precursor protein isoform X3
amyloid-beta precursor protein isoform X4
GA binding protein transcription factor subunit alpha, transcript variant X8
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
GA binding protein transcription factor subunit alpha, transcript variant X1
GA binding protein transcription factor subunit alpha, transcript variant X10
GA binding protein transcription factor subunit alpha, transcript variant X5
GA binding protein transcription factor subunit alpha, transcript variant X9
GA binding protein transcription factor subunit alpha, transcript variant X6
GA binding protein transcription factor subunit alpha, transcript variant X2
GA binding protein transcription factor subunit alpha, transcript variant X4
GA binding protein transcription factor subunit alpha, transcript variant X3
GA binding protein transcription factor subunit alpha, transcript variant X7
ATP synthase peripheral stalk subunit F6, transcript variant X1
ATP synthase peripheral stalk subunit F6, transcript variant X2
ATP synthase-coupling factor 6, mitochondrial
39S ribosomal protein L39, mitochondrial
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: 5 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
zinc finger Ran-binding domain-containing protein 2-like
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
RING finger and CHY zinc finger domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
neural cell adhesion molecule 2, transcript variant X1
neural cell adhesion molecule 2 isoform X1
neural cell adhesion molecule 2, transcript variant X2
neural cell adhesion molecule 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
four and a half LIM domains protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 38% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
chromosome 20 C21orf91 homolog, transcript variant X1
chromosome 20 C21orf91 homolog, transcript variant X7
chromosome 20 C21orf91 homolog, transcript variant X5
chromosome 20 C21orf91 homolog, transcript variant X8
chromosome 20 C21orf91 homolog, transcript variant X6
chromosome 20 C21orf91 homolog, transcript variant X2
chromosome 20 C21orf91 homolog, transcript variant X3
chromosome 20 C21orf91 homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
BTG anti-proliferation factor 3, transcript variant X5
BTG anti-proliferation factor 3, transcript variant X3
BTG anti-proliferation factor 3, transcript variant X2
BTG anti-proliferation factor 3, transcript variant X1
BTG anti-proliferation factor 3, transcript variant X4
CXADR Ig-like cell adhesion molecule, transcript variant X2
coxsackievirus and adenovirus receptor isoform X2
CXADR Ig-like cell adhesion molecule, transcript variant X1
coxsackievirus and adenovirus receptor isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF01210
uncharacterized LOC121479281, transcript variant X5
uncharacterized LOC121479281, transcript variant X4
uncharacterized LOC121479281, transcript variant X3
uncharacterized LOC121479281, transcript variant X1
uncharacterized LOC121479281, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 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: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin specific peptidase 25, transcript variant X4
ubiquitin specific peptidase 25, 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
ubiquitin specific peptidase 25, transcript variant X3
ubiquitin specific peptidase 25, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 25 isoform X4
ubiquitin carboxyl-terminal hydrolase 25 isoform X2
ubiquitin carboxyl-terminal hydrolase 25 isoform X3
ubiquitin carboxyl-terminal hydrolase 25 isoform X1
small nucleolar RNA SNORA62/SNORA6 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00091
putative uncharacterized protein ENSP00000383407
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SAM domain, SH3 domain and nuclear localization signals 1, transcript variant X2
SAM domain, SH3 domain and nuclear localization signals 1, transcript variant X1
SAM domain-containing protein SAMSN-1 isoform X1
SAM domain-containing protein SAMSN-1 isoform X2
SAM domain, SH3 domain and nuclear localization signals 1, transcript variant X3
SAM domain-containing protein SAMSN-1 isoform X3
heat shock protein family A (Hsp70) member 13
ATP-binding cassette sub-family C member 2-like, transcript variant X1
ATP-binding cassette sub-family C member 2-like, transcript variant X2
ATP-binding cassette sub-family C member 2-like, transcript variant X3
multidrug resistance-associated protein 1-like isoform X1
multidrug resistance-associated protein 1-like isoform X2
ATP-binding cassette sub-family C member 2-like isoform X3
RNA binding motif protein 11, transcript variant X3
RNA binding motif protein 11, transcript variant X2
RNA binding motif protein 11, transcript variant X1
RNA binding motif protein 11, transcript variant X5
RNA binding motif protein 11, transcript variant X4
roundabout guidance receptor 2, transcript variant X4
roundabout guidance receptor 2, transcript variant X1
roundabout guidance receptor 2, transcript variant X2
roundabout guidance receptor 2, transcript variant X3
roundabout guidance receptor 2, transcript variant X9
roundabout guidance receptor 2, transcript variant X8
roundabout guidance receptor 2, transcript variant X14
roundabout guidance receptor 2, transcript variant X7
roundabout guidance receptor 2, transcript variant X13
roundabout guidance receptor 2, transcript variant X6
roundabout guidance receptor 2, transcript variant X12
roundabout guidance receptor 2, transcript variant X11
roundabout guidance receptor 2, transcript variant X10
roundabout guidance receptor 2, transcript variant X15
roundabout guidance receptor 2, transcript variant X16
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
roundabout guidance receptor 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
roundabout guidance receptor 1, transcript variant X1
roundabout guidance receptor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
ras-related C3 botulinum toxin substrate 1-like
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
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; 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
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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC121479375
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins
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
calcium uniporter regulatory subunit MCUb, mitochondrial-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 92% 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: 21 Proteins, and 83% 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 33% 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 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 12 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
vestigial like family member 3, transcript variant X2
vestigial like family member 3, transcript variant X1
vestigial like family member 3, transcript variant X3
transcription cofactor vestigial-like protein 3 isoform X2
transcription cofactor vestigial-like protein 3 isoform X1
charged multivesicular body protein 2B, transcript variant X3
charged multivesicular body protein 2B, transcript variant X1
charged multivesicular body protein 2b isoform X3
charged multivesicular body protein 2b isoform X1
charged multivesicular body protein 2B, transcript variant X2
charged multivesicular body protein 2b isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
pituitary-specific positive transcription factor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: 5-hydroxytryptamine receptor 1F
protein arginine N-methyltransferase 3-like
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
LOW QUALITY PROTEIN: protein arginine N-methyltransferase 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
CGG triplet repeat binding protein 1, transcript variant X2
CGG triplet repeat binding protein 1, transcript variant X1
zinc finger protein 654, transcript variant X1
zinc finger protein 654, transcript variant X3
zinc finger protein 654, transcript variant X2
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