Arvicola amphibius chromosome 18, mArvAmp1.2, whole genome shotgun sequence.
Arvicola amphibius (Eurasian water vole)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Cricetidae; Arvicolinae; Arvicola.
REFSEQ INFORMATION: The reference sequence is identical to\nLR862398.1.\nAssembly name: mArvAmp1.2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Wellcome Sanger Institute on\n2021/05/15. The original whole-genome shotgun project has the\naccession CAJEUG000000000.2.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Arvicola amphibius Annotation\n 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: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF02543
Derived by automated computational analysis using gene prediction method: Gnomon.
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 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: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: polyadenylate-binding protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, 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: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
laminin subunit alpha-1-like, transcript variant X5
laminin subunit alpha-1-like, transcript variant X4
laminin subunit alpha-1-like, transcript variant X1
laminin subunit alpha-1-like, transcript variant X2
laminin subunit alpha-1-like, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
calcium voltage-gated channel auxiliary subunit alpha2delta 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
calcium voltage-gated channel auxiliary subunit alpha2delta 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
voltage-dependent calcium channel subunit alpha-2/delta-1 isoform X2
voltage-dependent calcium channel subunit alpha-2/delta-1 isoform X1
hepatocyte growth factor, transcript variant X1
hepatocyte growth factor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
cadherin EGF LAG seven-pass G-type receptor 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 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: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins
guanine nucleotide-binding protein G(t) subunit alpha-3
guanine nucleotide-binding protein G(i) subunit alpha-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
G protein subunit alpha i1, transcript variant X1
G protein subunit alpha i1, transcript variant X2
guanine nucleotide-binding protein G(i) subunit alpha-1 isoform X1
guanine nucleotide-binding protein G(i) subunit alpha-1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
LOW QUALITY PROTEIN: catechol O-methyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins
membrane associated guanylate kinase, WW and PDZ domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
membrane associated guanylate kinase, WW and PDZ domain containing 2, transcript variant X2
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 isoform X1
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 isoform X2
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: 14 Proteins
putative homeodomain transcription factor 2, transcript variant X3
putative homeodomain transcription factor 2, transcript variant X1
putative homeodomain transcription factor 2, transcript variant X2
putative homeodomain transcription factor 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
putative homeodomain transcription factor 2, transcript variant X7
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 6 samples with support for all annotated introns
putative homeodomain transcription factor 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
putative homeodomain transcription factor 2, transcript variant X6
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
protein tyrosine phosphatase non-receptor type 12, transcript variant X2
protein tyrosine phosphatase non-receptor type 12, transcript variant X1
protein tyrosine phosphatase non-receptor type 12, transcript variant X3
tyrosine-protein phosphatase non-receptor type 12 isoform X2
tyrosine-protein phosphatase non-receptor type 12 isoform X1
tyrosine-protein phosphatase non-receptor type 12 isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00561
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 146
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 6 samples with support for all annotated introns
family with sequence similarity 185 member A, 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 6 samples with support for all annotated introns
family with sequence similarity 185 member A, 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 5 samples with support for all annotated introns
F-box and leucine rich repeat protein 13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leucine-rich repeat-containing protein 17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
N-acyl phosphatidylethanolamine phospholipase D, transcript variant X1
N-acyl phosphatidylethanolamine phospholipase D, transcript variant X2
N-acyl phosphatidylethanolamine phospholipase D, transcript variant X3
N-acyl phosphatidylethanolamine phospholipase D, transcript variant X4
N-acyl-phosphatidylethanolamine-hydrolyzing phospholipase D isoform X2
N-acyl-phosphatidylethanolamine-hydrolyzing phospholipase D isoform X1
peptidase, mitochondrial processing subunit beta
mitochondrial-processing peptidase subunit beta
DnaJ heat shock protein family (Hsp40) member C2
solute carrier family 26 member 5, transcript variant X4
solute carrier family 26 member 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
solute carrier family 26 member 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins
solute carrier family 26 member 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
LHFPL tetraspan subfamily member 3 protein
lysine methyltransferase 2E (inactive), transcript variant X3
lysine methyltransferase 2E (inactive), transcript variant X4
lysine methyltransferase 2E (inactive), transcript variant X1
lysine methyltransferase 2E (inactive), transcript variant X2
inactive histone-lysine N-methyltransferase 2E isoform X1
inactive histone-lysine N-methyltransferase 2E isoform X2
inactive histone-lysine N-methyltransferase 2E isoform X3
SRSF protein kinase 2, transcript variant X6
SRSF protein kinase 2, transcript variant X2
SRSF protein kinase 2, transcript variant X5
SRSF protein kinase 2, transcript variant X4
SRSF protein kinase 2, transcript variant X1
SRSF protein kinase 2, transcript variant X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 3 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 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: pseudouridylate synthase 7 homolog
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 11 bases in 8 codons; 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: inserted 2 bases in 2 codons; deleted 11 bases in 8 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: RAD50-interacting protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
zinc finger protein 431-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
zinc finger protein 431-like, transcript variant X1
zinc finger protein 431-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
YES proto-oncogene 1, Src family tyrosine kinase, transcript variant X3
YES proto-oncogene 1, Src family tyrosine kinase, transcript variant X1
YES proto-oncogene 1, Src family tyrosine kinase, transcript variant X2
adenylate cyclase activating polypeptide 1
pituitary adenylate cyclase-activating polypeptide
multiple epidermal growth factor-like domains protein 9
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 50% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: multiple epidermal growth factor-like domains protein 9
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC119803791, 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 5 samples with support for all annotated introns
uncharacterized LOC119803791, transcript variant X1
uncharacterized LOC119803791, 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 LOC119803791, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
thymidylate synthetase, transcript variant X5
thymidylate synthetase, transcript variant X2
thymidylate synthetase, transcript variant X1
thymidylate synthetase, transcript variant X3
thymidylate synthetase, transcript variant X4
thymidylate synthetase, transcript variant X6
uncharacterized LOC119804015, transcript variant X3
uncharacterized LOC119804015, transcript variant X2
uncharacterized LOC119804015, transcript variant X1
A-kinase anchoring protein 9, transcript variant X6
A-kinase anchoring protein 9, transcript variant X4
A-kinase anchoring protein 9, transcript variant X3
A-kinase anchoring protein 9, transcript variant X7
A-kinase anchoring protein 9, transcript variant X5
A-kinase anchoring protein 9, transcript variant X2
A-kinase anchoring protein 9, transcript variant X1
mitochondrial transcription termination factor 1, transcript variant X4
mitochondrial transcription termination factor 1, transcript variant X7
mitochondrial transcription termination factor 1, transcript variant X9
mitochondrial transcription termination factor 1, transcript variant X1
mitochondrial transcription termination factor 1, transcript variant X2
mitochondrial transcription termination factor 1, transcript variant X5
mitochondrial transcription termination factor 1, transcript variant X3
mitochondrial transcription termination factor 1, transcript variant X6
mitochondrial transcription termination factor 1, transcript variant X8
transcription termination factor 1, mitochondrial isoform X2
transcription termination factor 1, mitochondrial isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
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 6 samples with support for all annotated introns
GTP binding protein 10, transcript variant X1
GTP binding protein 10, transcript variant X2
family with sequence similarity 237 member B
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
cilia and flagella associated protein 69, transcript variant X2
cilia and flagella associated protein 69, transcript variant X1
cilia and flagella associated protein 69, transcript variant X4
cilia and flagella associated protein 69, transcript variant X3
cilia and flagella associated protein 69, transcript variant X5
cilia- and flagella-associated protein 69 isoform X2
cilia- and flagella-associated protein 69 isoform X1
cilia- and flagella-associated protein 69 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 25% 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
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: 2 Proteins
LOW QUALITY PROTEIN: proline-rich protein 23A3-like
ADAM metallopeptidase domain 22, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
ADAM metallopeptidase domain 22, transcript variant X15
ADAM metallopeptidase domain 22, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
ADAM metallopeptidase domain 22, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
ADAM metallopeptidase domain 22, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
ADAM metallopeptidase domain 22, transcript variant X6
ADAM metallopeptidase domain 22, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
ADAM metallopeptidase domain 22, transcript variant X11
ADAM metallopeptidase domain 22, transcript variant X7
ADAM metallopeptidase domain 22, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
ADAM metallopeptidase domain 22, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
ADAM metallopeptidase domain 22, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
ADAM metallopeptidase domain 22, transcript variant X1
ADAM metallopeptidase domain 22, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 24% coverage of the annotated genomic feature by RNAseq alignments
ADAM metallopeptidase domain 22, transcript variant X12
ADAM metallopeptidase domain 22, transcript variant X3
disintegrin and metalloproteinase domain-containing protein 22 isoform X14
disintegrin and metalloproteinase domain-containing protein 22 isoform X15
disintegrin and metalloproteinase domain-containing protein 22 isoform X9
disintegrin and metalloproteinase domain-containing protein 22 isoform X10
disintegrin and metalloproteinase domain-containing protein 22 isoform X2
disintegrin and metalloproteinase domain-containing protein 22 isoform X6
disintegrin and metalloproteinase domain-containing protein 22 isoform X13
disintegrin and metalloproteinase domain-containing protein 22 isoform X11
disintegrin and metalloproteinase domain-containing protein 22 isoform X7
disintegrin and metalloproteinase domain-containing protein 22 isoform X8
disintegrin and metalloproteinase domain-containing protein 22 isoform X4
disintegrin and metalloproteinase domain-containing protein 22 isoform X5
disintegrin and metalloproteinase domain-containing protein 22 isoform X1
disintegrin and metalloproteinase domain-containing protein 22 isoform X16
disintegrin and metalloproteinase domain-containing protein 22 isoform X12
disintegrin and metalloproteinase domain-containing protein 22 isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00423
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
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
RUN domain containing 3B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
RUN domain containing 3B, transcript variant X1
RUN domain-containing protein 3B isoform X2
RUN domain-containing protein 3B isoform X1
multidrug resistance protein 2, transcript variant X1
multidrug resistance protein 2 isoform X1
multidrug resistance protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
multidrug resistance protein 2 isoform X3
multidrug resistance protein 2, transcript variant X2
multidrug resistance protein 2 isoform X2
phosphatidylcholine translocator ABCB4, transcript variant X3
phosphatidylcholine translocator ABCB4, transcript variant X1
phosphatidylcholine translocator ABCB4, transcript variant X4
phosphatidylcholine translocator ABCB4, transcript variant X2
phosphatidylcholine translocator ABCB4 isoform X1
phosphatidylcholine translocator ABCB4 isoform X2
phosphatidylcholine translocator ABCB4, transcript variant X5
phosphatidylcholine translocator ABCB4 isoform X3
carnitine O-octanoyltransferase, transcript variant X1
carnitine O-octanoyltransferase, transcript variant X2
carnitine O-octanoyltransferase, transcript variant X3
peroxisomal carnitine O-octanoyltransferase isoform X1
peroxisomal carnitine O-octanoyltransferase isoform X2
transmembrane protein 243, transcript variant X1
transmembrane protein 243, transcript variant X2
transmembrane protein 243, transcript variant X3
cyclin D binding myb like transcription factor 1, transcript variant X2
cyclin D binding myb like transcription factor 1, transcript variant X1
cyclin-D-binding Myb-like transcription factor 1 isoform X2
cyclin-D-binding Myb-like transcription factor 1 isoform X1
endosome-lysosome associated apoptosis and autophagy regulator family member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
endosome/lysosome-associated apoptosis and autophagy regulator family member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: mortality factor 4-like protein 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 4 codons; deleted 11 bases in 9 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 82% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 4 codons; deleted 11 bases in 9 codons; substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
branched-chain-amino-acid aminotransferase, mitochondrial-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: branched-chain-amino-acid aminotransferase, mitochondrial-like
methyltransferase 4, N6-adenosine, transcript variant X9
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
methyltransferase 4, N6-adenosine, transcript variant X1
methyltransferase 4, N6-adenosine, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
N(6)-adenine-specific methyltransferase METTL4 isoform X4
N(6)-adenine-specific methyltransferase METTL4 isoform X1
methyltransferase 4, N6-adenosine, transcript variant X4
methyltransferase 4, N6-adenosine, transcript variant X3
N(6)-adenine-specific methyltransferase METTL4 isoform X3
N(6)-adenine-specific methyltransferase METTL4 isoform X2
methyltransferase 4, N6-adenosine, transcript variant X7
methyltransferase 4, N6-adenosine, transcript variant X8
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
methyltransferase 4, N6-adenosine, transcript variant X5
methyltransferase 4, N6-adenosine, transcript variant X6
NDC80 kinetochore complex component, transcript variant X1
NDC80 kinetochore complex component, transcript variant X2
structural maintenance of chromosomes flexible hinge domain containing 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 4 bases in 3 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: structural maintenance of chromosomes flexible hinge domain-containing protein 1
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
phosphatidate phosphatase LPIN2 isoform X2
phosphatidate phosphatase LPIN2 isoform X1
phosphatidate phosphatase LPIN2 isoform X3
uncharacterized LOC119803851, transcript variant X2
uncharacterized LOC119803851, transcript variant X1
uncharacterized LOC119803851, transcript variant X3
myosin regulatory light polypeptide 9, transcript variant X2
myosin regulatory light polypeptide 9, transcript variant X1
uncharacterized LOC119803830, transcript variant X2
uncharacterized LOC119803830, transcript variant X1
uncharacterized LOC119803830, transcript variant X3
TGFB induced factor homeobox 1, transcript variant X1
TGFB induced factor homeobox 1, transcript variant X3
TGFB induced factor homeobox 1, transcript variant X4
TGFB induced factor homeobox 1, transcript variant X2
DLG associated protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
DLG associated protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
DLG associated protein 1, transcript variant X1
disks large-associated protein 1 isoform X2
disks large-associated protein 1 isoform X3
disks large-associated protein 1 isoform X1
DLG associated protein 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
DLG associated protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
disks large-associated protein 1 isoform X7
disks large-associated protein 1 isoform X4
DLG associated protein 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
DLG associated protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
DLG associated protein 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
disks large-associated protein 1 isoform X6
disks large-associated protein 1 isoform X5
disks large-associated protein 1 isoform X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins
zinc finger and BTB domain containing 14, transcript variant X2
zinc finger and BTB domain containing 14, transcript variant X3
zinc finger and BTB domain containing 14, transcript variant X4
zinc finger and BTB domain containing 14, transcript variant X1
zinc finger and BTB domain-containing protein 14
erythrocyte membrane protein band 4.1 like 3, transcript variant X2
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
erythrocyte membrane protein band 4.1 like 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Rho GTPase activating protein 28, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rho GTPase-activating protein 28 isoform X1
Rho GTPase activating protein 28, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Rho GTPase activating protein 28, transcript variant X2
Rho GTPase activating protein 28, transcript variant X4
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
39S ribosomal protein L42, mitochondrial
rho GTPase-activating protein 28 isoform X2
microtubule crosslinking factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
microtubule cross-linking factor 1 isoform X1
microtubule crosslinking factor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
microtubule crosslinking factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
microtubule cross-linking factor 1 isoform X3
microtubule cross-linking factor 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
protein tyrosine phosphatase receptor type M
receptor-type tyrosine-protein phosphatase mu
leucine-rich repeat-containing protein 30
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
structural maintenance of chromosomes flexible hinge domain-containing protein 1-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 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, and 14% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein-lysine methyltransferase METTL21C
tripeptidyl peptidase 2, transcript variant X2
tripeptidyl peptidase 2, transcript variant X1
tripeptidyl peptidase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
coiled-coil domain-containing protein 168
testis expressed 30, transcript variant X1
testis expressed 30, transcript variant X2
basic, immunoglobulin-like variable motif containing, transcript variant X3
basic, immunoglobulin-like variable motif containing, transcript variant X2
basic, immunoglobulin-like variable motif containing, transcript variant X4
basic, immunoglobulin-like variable motif containing, transcript variant X1
basic immunoglobulin-like variable motif-containing protein isoform X1
basic immunoglobulin-like variable motif-containing protein isoform X2
ERCC excision repair 5, endonuclease, transcript variant X2
DNA repair protein complementing XP-G cells isoform X2
ERCC excision repair 5, endonuclease, transcript variant X1
DNA repair protein complementing XP-G cells isoform X1
protein-lysine methyltransferase METTL21E
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
GULP PTB domain containing engulfment adaptor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
GULP PTB domain containing engulfment adaptor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins
PTB domain-containing engulfment adapter protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC119803833, transcript variant X1
uncharacterized LOC119803833, transcript variant X4
uncharacterized LOC119803833, transcript variant X2
uncharacterized LOC119803833, transcript variant X5
uncharacterized LOC119803833, transcript variant X7
uncharacterized LOC119803833, transcript variant X3
uncharacterized LOC119803833, transcript variant X6
uncharacterized LOC119803833, transcript variant X8
uncharacterized LOC119803833, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ASNSD1 upstream open reading frame protein
asparagine synthetase domain containing 1
asparagine synthetase domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
ankyrin and armadillo repeat-containing protein
O-sialoglycoprotein endopeptidase like 1, transcript variant X2
O-sialoglycoprotein endopeptidase like 1, transcript variant X1
probable tRNA N6-adenosine threonylcarbamoyltransferase, mitochondrial isoform X2
probable tRNA N6-adenosine threonylcarbamoyltransferase, mitochondrial isoform X1
PMS1 homolog 1, mismatch repair system component, transcript variant X1
PMS1 homolog 1, mismatch repair system component, transcript variant X7
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
PMS1 homolog 1, mismatch repair system component, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
PMS1 homolog 1, mismatch repair system component, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PMS1 homolog 1, mismatch repair system component, transcript variant X2
PMS1 homolog 1, mismatch repair system component, transcript variant X3
PMS1 homolog 1, mismatch repair system component, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins
3-hydroxyisobutyryl-CoA hydrolase, mitochondrial
inositol polyphosphate-1-phosphatase, transcript variant X1
inositol polyphosphate-1-phosphatase, transcript variant X3
inositol polyphosphate-1-phosphatase, transcript variant X2
major facilitator superfamily domain containing 6
major facilitator superfamily domain-containing protein 6
nuclear envelope integral membrane protein 2, 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 6 samples with support for all annotated introns
nuclear envelope integral membrane protein 2, transcript variant X1
nuclear envelope integral membrane protein 2 isoform X2
nuclear envelope integral membrane protein 2 isoform X1
NGFI-A binding protein 1, transcript variant X1
NGFI-A binding protein 1, transcript variant X3
NGFI-A binding protein 1, transcript variant X2
glutaminase kidney isoform, mitochondrial
signal transducer and activator of transcription 1, transcript variant X1
signal transducer and activator of transcription 1, transcript variant X2
signal transducer and activator of transcription 1-alpha/beta
signal transducer and activator of transcription 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
nucleic acid binding protein 1, 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 5 samples with support for all annotated introns
nucleic acid binding protein 1, transcript variant X2
nucleic acid binding protein 1, transcript variant X3
transmembrane protein with EGF like and two follistatin like domains 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 34% 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 95% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 12% 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; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 39 member 10, 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 6 samples with support for all annotated introns
solute carrier family 39 member 10, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2, transcript variant X1
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2, transcript variant X2
E3 ubiquitin-protein ligase HECW2 isoform X1
E3 ubiquitin-protein ligase HECW2 isoform X2
coiled-coil domain containing 150, transcript variant X3
coiled-coil domain-containing protein 150 isoform X3
coiled-coil domain containing 150, transcript variant X1
coiled-coil domain-containing protein 150 isoform X1
coiled-coil domain containing 150, transcript variant X2
coiled-coil domain-containing protein 150 isoform X2
general transcription factor IIIC subunit 3, transcript variant X2
general transcription factor IIIC subunit 3, transcript variant X1
general transcription factor 3C polypeptide 3 isoform X2
general transcription factor 3C polypeptide 3 isoform X1
post-GPI attachment to proteins inositol deacylase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
post-GPI attachment to proteins inositol deacylase 1, transcript variant X2
ankyrin repeat domain 44, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ankyrin repeat domain 44, transcript variant X1
ankyrin repeat domain 44, transcript variant X2
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X3
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X1
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X2
splicing factor 3b subunit 1, transcript variant X1
splicing factor 3b subunit 1, transcript variant X2
coenzyme Q-binding protein COQ10 homolog B, mitochondrial
heat shock protein family D (Hsp60) member 1
60 kDa heat shock protein, mitochondrial
MOB-like protein phocein, transcript variant X5
MOB-like protein phocein, transcript variant X4
10 kDa heat shock protein, mitochondrial isoform X4
MOB-like protein phocein, transcript variant X1
MOB-like protein phocein, transcript variant X2
MOB-like protein phocein, transcript variant X3
methionyl-tRNA synthetase 2, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
heat shock transcription factor, Y-linked-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
matrix AAA peptidase interacting protein 1
m-AAA protease-interacting protein 1, mitochondrial
spermatogenesis associated serine rich 2 like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
spermatogenesis associated serine rich 2 like, transcript variant X5
spermatogenesis associated serine rich 2 like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
spermatogenesis associated serine rich 2 like, 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 2 samples with support for all annotated introns
spermatogenesis associated serine rich 2 like, transcript variant X4
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
potassium channel tetramerization domain containing 18, transcript variant X1
potassium channel tetramerization domain containing 18, transcript variant X4
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
potassium channel tetramerization domain containing 18, transcript variant X2
potassium channel tetramerization domain containing 18, transcript variant X3
BTB/POZ domain-containing protein KCTD18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: aldehyde oxidase 1-like
aldehyde oxidase 4, transcript variant X1
aldehyde oxidase 4, transcript variant X2
aldehyde oxidase 4, transcript variant X3
basic leucine zipper and W2 domains 1, transcript variant X1
basic leucine zipper and W2 domain-containing protein 1 isoform X1
basic leucine zipper and W2 domains 1, transcript variant X2
basic leucine zipper and W2 domain-containing protein 1 isoform X2
CDC like kinase 1, transcript variant X1
CDC like kinase 1, transcript variant X2
dual specificity protein kinase CLK1 isoform X1
dual specificity protein kinase CLK1 isoform X2
peptidyl-prolyl cis-trans isomerase-like 3
NGG1 interacting factor 3 like 1, transcript variant X2
NGG1 interacting factor 3 like 1, transcript variant X1
origin recognition complex subunit 2, transcript variant X5
origin recognition complex subunit 2, transcript variant X4
origin recognition complex subunit 2, transcript variant X1
origin recognition complex subunit 2, transcript variant X3
origin recognition complex subunit 2, transcript variant X2
family with sequence similarity 126 member B, transcript variant X5
family with sequence similarity 126 member B, transcript variant X1
family with sequence similarity 126 member B, transcript variant X4
family with sequence similarity 126 member B, transcript variant X3
family with sequence similarity 126 member B, transcript variant X2
NADH:ubiquinone oxidoreductase subunit B3
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 3
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; 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 3 bases in 3 codons; deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: CASP8 and FADD-like apoptosis regulator
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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 6 samples with support for all annotated introns
flagellum associated containing coiled-coil domains 1
flagellum-associated coiled-coil domain-containing protein 1
trafficking kinesin protein 2, transcript variant X2
trafficking kinesin protein 2, transcript variant X1
STE20 related adaptor beta, transcript variant X1
STE20-related kinase adapter protein beta isoform X1
STE20 related adaptor beta, transcript variant X2
STE20-related kinase adapter protein beta isoform X2
C2 calcium dependent domain containing 6
C2 calcium-dependent domain-containing protein 6
transmembrane protein 237, transcript variant X1
transmembrane protein 237, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X2
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X4
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X6
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X1
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X3
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X5
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X7
cyclin dependent kinase 15, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
cyclin dependent kinase 15, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC119803939, transcript variant X2
uncharacterized LOC119803939, transcript variant X1
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
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: 4 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein KIAA2012 homolog
NOP58 ribonucleoprotein, transcript variant X1
NOP58 ribonucleoprotein, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00575
COORDINATES: nucleotide motif:Rfam:12.0:RF01192
COORDINATES: nucleotide motif:Rfam:12.0:RF01182
bone morphogenetic protein receptor type 2
bone morphogenetic protein receptor type-2
family with sequence similarity 117 member B
islet cell autoantigen 1 like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
islet cell autoantigen 1 like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
islet cell autoantigen 1-like protein isoform X1
islet cell autoantigen 1-like protein isoform X2
WD repeat domain 12, transcript variant X1
WD repeat domain 12, transcript variant X2
calcium responsive transcription factor, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
calcium responsive transcription factor, transcript variant X2
calcium responsive transcription factor, transcript variant X1
calcium responsive transcription factor, transcript variant X3
calcium-responsive transcription factor isoform X4
calcium-responsive transcription factor isoform X2
calcium-responsive transcription factor isoform X1
calcium-responsive transcription factor isoform X3
signal-regulatory protein beta-1-like, transcript variant X2
signal-regulatory protein beta-1-like, transcript variant X1
signal-regulatory protein beta-1-like, transcript variant X3
tyrosine-protein phosphatase non-receptor type substrate 1-like isoform X2
signal-regulatory protein beta-1-like isoform X1
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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns