Equus asinus breed Dezhou chromosome Y, ASM1607732v2, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Laurasiatheria; Perissodactyla; Equidae; Equus.
Donkey genomes provide new insights into domestication and selection for coat color
REFSEQ INFORMATION: The reference sequence is identical to\nCM027721.2.\nAssembly name: ASM1607732v2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Dairy Cattle Research Center,\nShandong Academy of Agricultural Sciences on 2021/10/14. The\noriginal whole-genome shotgun project has the accession\nJADWZW000000000.2.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Dairy Cattle Research Center, Shandong\n Academy of Agricultural Sciences\nAssembly Method :: SOAPdenovo v. 2.04.4; DBG2OLC v. 1;\n 3D-DNA v. 170123\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 211.0x\nSequencing Technology :: Illumina HiSeq; PacBio Sequel; Hi-C\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Equus asinus Annotation Release 101\nAnnotation Version :: 101\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
uncharacterized LOC123282829, 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 5 samples with support for all annotated introns
uncharacterized LOC123282829, transcript variant X2
RALBP1 associated Eps domain containing 2, transcript variant X7
COORDINATES: polyA evidence [ECO:0006239]
RALBP1 associated Eps domain containing 2, transcript variant X6
RALBP1 associated Eps domain containing 2, transcript variant X5
RALBP1 associated Eps domain containing 2, transcript variant X14
RALBP1 associated Eps domain containing 2, transcript variant X10
RALBP1 associated Eps domain containing 2, transcript variant X15
RALBP1 associated Eps domain containing 2, transcript variant X2
RALBP1 associated Eps domain containing 2, transcript variant X3
RALBP1 associated Eps domain containing 2, transcript variant X9
RALBP1 associated Eps domain containing 2, transcript variant X4
RALBP1 associated Eps domain containing 2, transcript variant X1
RALBP1 associated Eps domain containing 2, transcript variant X8
RALBP1 associated Eps domain containing 2, transcript variant X19
RALBP1 associated Eps domain containing 2, transcript variant X20
RALBP1 associated Eps domain containing 2, transcript variant X21
ralBP1-associated Eps domain-containing protein 2 isoform X5
ralBP1-associated Eps domain-containing protein 2 isoform X12
ralBP1-associated Eps domain-containing protein 2 isoform X2
ralBP1-associated Eps domain-containing protein 2 isoform X8
ralBP1-associated Eps domain-containing protein 2 isoform X3
ralBP1-associated Eps domain-containing protein 2 isoform X11
ralBP1-associated Eps domain-containing protein 2 isoform X7
ralBP1-associated Eps domain-containing protein 2 isoform X4
ralBP1-associated Eps domain-containing protein 2 isoform X1
ralBP1-associated Eps domain-containing protein 2 isoform X6
ralBP1-associated Eps domain-containing protein 2 isoform X15
RALBP1 associated Eps domain containing 2, transcript variant X18
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
ralBP1-associated Eps domain-containing protein 2 isoform X14
RALBP1 associated Eps domain containing 2, transcript variant X12
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
ralBP1-associated Eps domain-containing protein 2 isoform X10
RALBP1 associated Eps domain containing 2, transcript variant X17
RALBP1 associated Eps domain containing 2, transcript variant X16
ralBP1-associated Eps domain-containing protein 2 isoform X13
RALBP1 associated Eps domain containing 2, transcript variant X13
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
RALBP1 associated Eps domain containing 2, transcript variant X11
ralBP1-associated Eps domain-containing protein 2 isoform X9
RB binding protein 7, chromatin remodeling factor, transcript variant X2
RB binding protein 7, chromatin remodeling factor, transcript variant X1
RB binding protein 7, chromatin remodeling factor, transcript variant X3
histone-binding protein RBBP7 isoform X1
histone-binding protein RBBP7 isoform X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 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: 3 mRNAs, 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 63 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
S100 calcium binding protein G, transcript variant X1
S100 calcium binding protein G, transcript variant X2
uncharacterized LOC123282807, transcript variant X4
uncharacterized LOC123282807, 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
uncharacterized LOC123282807, transcript variant X1
uncharacterized LOC123282807, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
adaptor related protein complex 1 subunit sigma 2, transcript variant X1
adaptor related protein complex 1 subunit sigma 2, transcript variant X4
adaptor related protein complex 1 subunit sigma 2, transcript variant X5
adaptor related protein complex 1 subunit sigma 2, transcript variant X6
adaptor related protein complex 1 subunit sigma 2, transcript variant X2
adaptor related protein complex 1 subunit sigma 2, transcript variant X8
adaptor related protein complex 1 subunit sigma 2, transcript variant X9
adaptor related protein complex 1 subunit sigma 2, transcript variant X3
adaptor related protein complex 1 subunit sigma 2, transcript variant X7
zinc finger CCCH-type, RNA binding motif and serine/arginine rich 2
U2 small nuclear ribonucleoprotein auxiliary factor 35 kDa subunit-related protein 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
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: carbonic anhydrase 5B, mitochondrial
uncharacterized LOC106828086, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 3 ESTs, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC106828086, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 ESTs, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC106828086, transcript variant X7
uncharacterized LOC106828086, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 ESTs, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
uncharacterized LOC106828086, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 3 ESTs, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC106828086, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 ESTs, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC106828086, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 ESTs, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC106828086, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 3 ESTs, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
uncharacterized LOC106828086, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
uncharacterized LOC106828086, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC106828086, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC106828086, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
collectrin, amino acid transport regulator, transcript variant X2
collectrin, amino acid transport regulator, transcript variant X3
collectrin, amino acid transport regulator, transcript variant X1
angiotensin converting enzyme 2, transcript variant X1
angiotensin-converting enzyme 2 isoform X1
angiotensin converting enzyme 2, transcript variant X2
angiotensin-converting enzyme 2 isoform X2
BMX non-receptor tyrosine kinase, transcript variant X1
BMX non-receptor tyrosine kinase, transcript variant X2
cytoplasmic tyrosine-protein kinase BMX isoform X2
cytoplasmic tyrosine-protein kinase BMX isoform X1
vascular endothelial growth factor D, transcript variant X1
vascular endothelial growth factor D isoform X1
vascular endothelial growth factor D, transcript variant X2
vascular endothelial growth factor D isoform X2
phosphatidylinositol glycan anchor biosynthesis class A, transcript variant X1
phosphatidylinositol glycan anchor biosynthesis class A, transcript variant X3
phosphatidylinositol N-acetylglucosaminyltransferase subunit A isoform X2
phosphatidylinositol glycan anchor biosynthesis class A, transcript variant X2
phosphatidylinositol N-acetylglucosaminyltransferase subunit A isoform X1
ankyrin repeat and SOCS box containing 11, transcript variant X2
ankyrin repeat and SOCS box containing 11, transcript variant X1
ankyrin repeat and SOCS box protein 11 isoform X1
ankyrin repeat and SOCS box protein 11 isoform X2
ankyrin repeat and SOCS box containing 11, transcript variant X4
ankyrin repeat and SOCS box containing 11, transcript variant X3
ankyrin repeat and SOCS box protein 11 isoform X3
ankyrin repeat and SOCS box protein 11 isoform X4
ankyrin repeat and SOCS box containing 9, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ankyrin repeat and SOCS box containing 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
ankyrin repeat and SOCS box containing 9, 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 9 samples with support for all annotated introns
ankyrin repeat and SOCS box containing 9, transcript variant X6
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 14 samples with support for all annotated introns
ankyrin repeat and SOCS box containing 9, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ankyrin repeat and SOCS box protein 9 isoform X1
ankyrin repeat and SOCS box protein 9 isoform X3
ankyrin repeat and SOCS box containing 9, 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 9 samples with support for all annotated introns
ankyrin repeat and SOCS box protein 9 isoform X2
motile sperm domain-containing protein 2
FA complementation group B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
FA complementation group B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
FA complementation group B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
FA complementation group B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Fanconi anemia group B protein isoform X1
Fanconi anemia group B protein isoform X2
glycine receptor alpha 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
glycine receptor alpha 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
glycine receptor alpha 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glycine receptor subunit alpha-2 isoform X2
glycine receptor subunit alpha-2 isoform X1
glycine receptor subunit alpha-2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC123282809, transcript variant X1
uncharacterized LOC123282809, 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
gem nuclear organelle associated protein 8, transcript variant X2
gem nuclear organelle associated protein 8, transcript variant X5
gem nuclear organelle associated protein 8, transcript variant X1
gem nuclear organelle associated protein 8, transcript variant X7
gem nuclear organelle associated protein 8, transcript variant X3
gem nuclear organelle associated protein 8, transcript variant X6
gem nuclear organelle associated protein 8, transcript variant X4
holocytochrome c-type synthase, transcript variant X3
holocytochrome c-type synthase, transcript variant X1
holocytochrome c-type synthase, transcript variant X2
Rho GTPase activating protein 6, transcript variant X2
Rho GTPase activating protein 6, transcript variant X1
Rho GTPase activating protein 6, transcript variant X6
Rho GTPase activating protein 6, transcript variant X4
Rho GTPase activating protein 6, transcript variant X3
Rho GTPase activating protein 6, transcript variant X5
rho GTPase-activating protein 6 isoform X2
rho GTPase-activating protein 6 isoform X1
rho GTPase-activating protein 6 isoform X4
rho GTPase-activating protein 6 isoform X3
rho GTPase-activating protein 6 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 21 Proteins
MSL complex subunit 3, transcript variant X2
MSL complex subunit 3, transcript variant X1
male-specific lethal 3 homolog isoform X1
male-specific lethal 3 homolog isoform X2
MSL complex subunit 3, transcript variant X3
MSL complex subunit 3, transcript variant X4
male-specific lethal 3 homolog isoform X3
FERM and PDZ domain containing 4, transcript variant X2
FERM and PDZ domain containing 4, transcript variant X3
FERM and PDZ domain containing 4, transcript variant X1
FERM and PDZ domain containing 4, transcript variant X4
FERM and PDZ domain containing 4, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
FERM and PDZ domain-containing protein 4 isoform X1
FERM and PDZ domain-containing protein 4 isoform X5
FERM and PDZ domain-containing protein 4 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
FERM and PDZ domain containing 4, transcript variant X5
FERM and PDZ domain-containing protein 4 isoform X3
uncharacterized LOC123282801, transcript variant X2
uncharacterized LOC123282801, transcript variant X1
uncharacterized LOC123282801, transcript variant X3
FERM and PDZ domain containing 4, transcript variant X6
FERM and PDZ domain containing 4, transcript variant X7
FERM and PDZ domain-containing protein 4 isoform X4
uncharacterized LOC123282818, transcript variant X2
uncharacterized LOC123282818, transcript variant X1
phosphoribosyl pyrophosphate synthetase 2
toll like receptor 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
toll like receptor 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
toll like receptor 7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
toll like receptor 8, transcript variant X1
toll like receptor 8, transcript variant X5
toll like receptor 8, transcript variant X3
toll like receptor 8, transcript variant X7
toll like receptor 8, transcript variant X8
toll like receptor 8, transcript variant X9
toll like receptor 8, transcript variant X10
toll like receptor 8, transcript variant X6
toll like receptor 8, transcript variant X2
toll like receptor 8, transcript variant X4
uncharacterized LOC123282822, transcript variant X2
uncharacterized LOC123282822, 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 7 samples with support for all annotated introns
uncharacterized LOC123282810, transcript variant X1
uncharacterized LOC123282810, transcript variant X2
uncharacterized LOC123282810, transcript variant X3
uncharacterized LOC123282810, transcript variant X5
uncharacterized LOC123282810, transcript variant X4
uncharacterized LOC106825820, transcript variant X1
uncharacterized LOC106825820, transcript variant X2
uncharacterized LOC106825820, transcript variant X3
uncharacterized LOC106825820, transcript variant X4
uncharacterized LOC106825820, transcript variant X5
uncharacterized LOC123282811, transcript variant X1
uncharacterized LOC123282811, transcript variant X2
uncharacterized LOC123282827, transcript variant X1
uncharacterized LOC123282827, transcript variant X3
uncharacterized LOC123282827, transcript variant X6
uncharacterized LOC123282827, transcript variant X8
uncharacterized LOC123282827, transcript variant X2
uncharacterized LOC123282827, transcript variant X5
uncharacterized LOC123282827, transcript variant X7
uncharacterized LOC123282827, transcript variant X4
EGF like domain multiple 6, transcript variant X3
EGF like domain multiple 6, transcript variant X1
EGF like domain multiple 6, transcript variant X2
epidermal growth factor-like protein 6 isoform X1
epidermal growth factor-like protein 6 isoform X2
epidermal growth factor-like protein 6 isoform X3
transcription elongation factor A N-terminal and central domain containing
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 75 samples with support for all annotated introns
RAB9A, member RAS oncogene family, transcript variant X2
transcription elongation factor A N-terminal and central domain-containing protein
RAB9A, member RAS oncogene family, transcript variant X1
RAB9A, member RAS oncogene family, transcript variant X3
trafficking protein particle complex subunit 2
OFD1 centriole and centriolar satellite protein, transcript variant X1
oral-facial-digital syndrome 1 protein isoform X1
OFD1 centriole and centriolar satellite protein, transcript variant X3
OFD1 centriole and centriolar satellite protein, transcript variant X2
oral-facial-digital syndrome 1 protein isoform X2
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
LOW QUALITY PROTEIN: 40S ribosomal protein S3a-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
probable ubiquitin carboxyl-terminal hydrolase FAF-X
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 4 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 mRNA, 24 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
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 38 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: heat shock 70 kDa protein 1-like
lysine-specific demethylase 6A-like, transcript variant X3
lysine-specific demethylase 6A-like, transcript variant X4
lysine-specific demethylase 6A-like, transcript variant X1
lysine-specific demethylase 6A-like, transcript variant X2
lysine-specific demethylase 6A-like, transcript variant X5
lysine-specific demethylase 6A-like, transcript variant X6
lysine-specific demethylase 6A-like isoform X3
lysine-specific demethylase 6A-like isoform X4
lysine-specific demethylase 6A-like isoform X1
lysine-specific demethylase 6A-like isoform X5
lysine-specific demethylase 6A-like isoform X6
lysine-specific demethylase 6A-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 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: 1 Protein, and 52% 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 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons; substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein Shroom2-like
F-box-like/WD repeat-containing protein TBL1X, transcript variant X2
F-box-like/WD repeat-containing protein TBL1X, transcript variant X5
F-box-like/WD repeat-containing protein TBL1X, transcript variant X3
F-box-like/WD repeat-containing protein TBL1X, transcript variant X4
F-box-like/WD repeat-containing protein TBL1X, transcript variant X1
F-box-like/WD repeat-containing protein TBL1X isoform X2
F-box-like/WD repeat-containing protein TBL1X isoform X1
F-box-like/WD repeat-containing protein TBL1X isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 87% coverage of the annotated genomic feature by RNAseq alignments
neuronal membrane glycoprotein M6-b isoform X6
neuronal membrane glycoprotein M6-b isoform X1
neuronal membrane glycoprotein M6-b isoform X4
neuronal membrane glycoprotein M6-b isoform X2
neuronal membrane glycoprotein M6-b isoform X5
neuronal membrane glycoprotein M6-b isoform X3
oral-facial-digital syndrome 1 protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
uncharacterized LOC106843059, 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 19 samples with support for all annotated introns
uncharacterized LOC106843059, 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 14 samples with support for all annotated introns
uncharacterized LOC106843059, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 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 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 2 subunit 3, Y-linked-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
zinc finger X-chromosomal protein, transcript variant X2
zinc finger X-chromosomal protein, transcript variant X3
zinc finger X-chromosomal protein, transcript variant X4
zinc finger X-chromosomal protein, transcript variant X9
zinc finger X-chromosomal protein, transcript variant X6
zinc finger X-chromosomal protein, transcript variant X7
zinc finger X-chromosomal protein, transcript variant X1
zinc finger X-chromosomal protein, transcript variant X5
zinc finger X-chromosomal protein, transcript variant X8
zinc finger X-chromosomal protein isoform X1
zinc finger X-chromosomal protein isoform X2
zinc finger X-chromosomal protein, transcript variant X10
zinc finger X-chromosomal protein isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 1A, Y-chromosomal-like, transcript variant X9
eukaryotic translation initiation factor 1A, Y-chromosomal-like, transcript variant X8
eukaryotic translation initiation factor 1A, Y-chromosomal-like, transcript variant X10
eukaryotic translation initiation factor 1A, Y-chromosomal-like, transcript variant X4
eukaryotic translation initiation factor 1A, Y-chromosomal-like, transcript variant X5
eukaryotic translation initiation factor 1A, Y-chromosomal-like, transcript variant X2
eukaryotic translation initiation factor 1A, Y-chromosomal-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
eukaryotic translation initiation factor 1A, Y-chromosomal-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
eukaryotic translation initiation factor 1A, Y-chromosomal-like, transcript variant X11
eukaryotic translation initiation factor 1A, Y-chromosomal-like, transcript variant X3
eukaryotic translation initiation factor 1A, Y-chromosomal-like, transcript variant X1
eukaryotic translation initiation factor 1A, Y-chromosomal-like
heat shock transcription factor, Y-linked-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
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: heat shock transcription factor, Y-linked-like
gamma-taxilin-like, transcript variant X2
gamma-taxilin-like, transcript variant X5
gamma-taxilin-like, transcript variant X4
gamma-taxilin-like, transcript variant X8
gamma-taxilin-like, transcript variant X6
gamma-taxilin-like, transcript variant X7
gamma-taxilin-like, transcript variant X1
gamma-taxilin-like, transcript variant X9
gamma-taxilin-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: lysine-specific demethylase 5D
V-type proton ATPase 16 kDa proteolipid subunit-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
RNA-binding motif protein, X chromosome-like, transcript variant X1
RNA-binding motif protein, X chromosome-like, transcript variant X2
RNA-binding motif protein, X chromosome-like
testis-specific Y-encoded protein 3-like
LOW QUALITY PROTEIN: testis-specific Y-encoded protein 3-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.