Clupea harengus chromosome 26, Ch_v2.0.2, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Clupei; Clupeiformes; Clupeoidei; Clupeidae; Clupea.
REFSEQ INFORMATION: The reference sequence is identical to\nLR535882.1.\nAssembly name: Ch_v2.0.2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the UPPSALA UNIVERISTY on\n2019/04/16. The original whole-genome shotgun project has the\naccession CAADHV000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Clupea harengus Annotation Release\n 102\nAnnotation Version :: 102\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.
COORDINATES: polyA evidence [ECO:0006239]
glutamate receptor ionotropic, NMDA 2D-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
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: 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein kinase C, beta a
voltage-dependent calcium channel gamma-2 subunit
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
uncharacterized protein LOC678514 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide binding protein (G protein), gamma 13a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-13a
CTF18, chromosome transmission fidelity factor 18 homolog (S. cerevisiae)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
chromosome transmission fidelity protein 18 homolog
endoplasmic reticulum to nucleus signaling 2
serine/threonine-protein kinase/endoribonuclease IRE1
polo-like kinase 1 (Drosophila), transcript variant X1
serine/threonine-protein kinase PLK1 isoform X1
polo-like kinase 1 (Drosophila), 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 7 samples with support for all annotated introns
serine/threonine-protein kinase PLK1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
NADH:ubiquinone oxidoreductase subunit AB1a, transcript variant X1
NADH:ubiquinone oxidoreductase subunit AB1a, transcript variant X2
NADH:ubiquinone oxidoreductase subunit AB1a isoform X1
NADH:ubiquinone oxidoreductase subunit AB1a isoform X2
interferon alpha-inducible protein 27-like protein 2A
uncharacterized protein si:ch211-14k19.8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
F-box and leucine-rich repeat protein 18
lipopolysaccharide-induced tumor necrosis factor-alpha factor homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
cell death-inducing p53-target protein 1 homolog
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
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 13 samples with support for all annotated introns
mitochondrial elongation factor 2, transcript variant X3
mitochondrial elongation factor 2, transcript variant X2
mitochondrial elongation factor 2, transcript variant X1
Smith-Magenis syndrome chromosome region, candidate 8b, 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 3 samples with support for all annotated introns
Smith-Magenis syndrome chromosome region, candidate 8b, transcript variant X1
guanine nucleotide exchange protein smcr8b isoform X2
guanine nucleotide exchange protein smcr8b isoform X1
uncharacterized protein LOC503706 homolog, transcript variant X2
uncharacterized protein LOC503706 homolog, transcript variant X1
uncharacterized protein LOC503706 homolog, transcript variant X3
uncharacterized protein LOC503706 homolog, transcript variant X4
uncharacterized protein zgc:112980 isoform X2
uncharacterized protein zgc:112980 isoform X1
uncharacterized protein zgc:112980 isoform X3
uncharacterized protein zgc:112980 isoform X4
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
uncharacterized LOC122128889, transcript variant X4
uncharacterized LOC122128889, 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 LOC122128889, transcript variant X3
uncharacterized protein LOC122128889 isoform X1
uncharacterized protein LOC122128889 isoform X3
uncharacterized protein LOC122128889 isoform X4
uncharacterized LOC122128889, 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 7 samples with support for all annotated introns
uncharacterized protein LOC122128889 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 4 samples with support for all annotated introns
zinc finger protein 135-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
zinc finger protein 135-like, 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 1 sample with support for all annotated introns
post-glycosylphosphatidylinositol attachment to proteins 6, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
post-glycosylphosphatidylinositol attachment to proteins 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
post-glycosylphosphatidylinositol attachment to proteins 6, transcript variant X2
post-glycosylphosphatidylinositol attachment to proteins 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
post-GPI attachment to proteins factor 6 isoform X3
post-GPI attachment to proteins factor 6 isoform X2
post-GPI attachment to proteins factor 6 isoform X1
post-GPI attachment to proteins factor 6 isoform X4
NLR family CARD domain-containing protein 3-like, transcript variant X1
NLR family CARD domain-containing protein 3-like, transcript variant X3
NLR family CARD domain-containing protein 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
NLR family CARD domain-containing protein 3-like
NACHT, LRR and PYD domains-containing protein 6-like
piggyBac transposable element-derived protein 4-like
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: 73% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ras-associating and dilute domain-containing protein
uncharacterized LOC116219820, transcript variant X1
uncharacterized LOC116219820, transcript variant X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00271
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 56% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC116219819, transcript variant X2
uncharacterized LOC116219819, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
extracellular leucine-rich repeat and fibronectin type III domain containing 1b
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 88% 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 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
mitotic spindle assembly checkpoint protein MAD1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
chromosome 26 C7orf26 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
chromosome 26 C7orf26 homolog, 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 12 samples with support for all annotated introns
chromosome 26 C7orf26 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized protein C7orf26 homolog isoform X1
uncharacterized protein C7orf26 homolog isoform X2
phosphomannomutase 2, transcript variant X3
phosphomannomutase 2, transcript variant X2
phosphomannomutase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
mitotic spindle assembly checkpoint protein MAD1
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
serine/threonine-protein kinase/endoribonuclease IRE1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 84% 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 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: homeobox protein unc-4 homolog
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 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: 20 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 70-like, transcript variant X7
zinc finger protein 70-like, transcript variant X3
zinc finger protein 70-like, transcript variant X8
zinc finger protein 70-like, transcript variant X10
zinc finger protein 70-like, transcript variant X6
zinc finger protein 70-like, transcript variant X4
zinc finger protein 70-like, transcript variant X5
zinc finger protein 70-like, transcript variant X9
zinc finger protein 70-like, transcript variant X1
zinc finger protein 70-like, transcript variant X11
zinc finger protein 70-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 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: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 239-like, transcript variant X2
zinc finger protein 239-like, 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 8 samples with support for all annotated introns
zinc finger protein 436-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
zinc finger protein 436-like, transcript variant X1
gastrula zinc finger protein XlCGF57.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
gastrula zinc finger protein XlCGF57.1-like, transcript variant X3
gastrula zinc finger protein XlCGF57.1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
zinc finger protein 2 homolog isoform X3
gastrula zinc finger protein XlCGF57.1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 2 homolog isoform X2
gastrula zinc finger protein XlCGF57.1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
gastrula zinc finger protein XlCGF57.1-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
gastrula zinc finger protein XlCGF7.1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: gastrula zinc finger protein XlCGF7.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 16% 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 7% coverage of the annotated genomic feature by RNAseq alignments
NACHT, LRR and PYD domains-containing protein 12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, 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 38% 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 6% 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 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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: 3 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
butyrophilin subfamily 1 member A1-like, transcript variant X1
butyrophilin subfamily 1 member A1-like, transcript variant X3
butyrophilin subfamily 1 member A1-like, transcript variant X2
butyrophilin subfamily 1 member A1-like isoform X1
butyrophilin subfamily 1 member A1-like isoform X3
butyrophilin subfamily 1 member A1-like isoform 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 10 samples with support for all annotated introns
MIS18 kinetochore protein A, transcript variant X5
MIS18 kinetochore protein A, transcript variant X6
MIS18 kinetochore protein A, transcript variant X3
MIS18 kinetochore protein A, transcript variant X2
MIS18 kinetochore protein A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
MIS18 kinetochore protein A, 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein 271-like, transcript variant X2
zinc finger protein 271-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 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: 29 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger protein OZF-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 573 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: 3 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 4% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 658B-like isoform X1
uncharacterized LOC116219823, transcript variant X1
uncharacterized LOC116219823, transcript variant X2
autophagy related 4D, cysteine peptidase a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
autophagy related 4D, cysteine peptidase a, 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
autophagy related 4D, cysteine peptidase a, 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 12 samples with support for all annotated introns
coiled-coil domain-containing protein 106-like
piggyBac transposable element-derived protein 4-like, transcript variant X1
piggyBac transposable element-derived protein 4-like, transcript variant X2
piggyBac transposable element-derived protein 4-like isoform X2
piggyBac transposable element-derived protein 4-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 116 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
gastrula zinc finger protein XlCGF57.1-like isoform X1
zinc finger protein 708-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein 708-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 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: 70 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: 70 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: 70 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
THAP domain-containing protein 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
zinc finger MYM-type protein 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 177 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: 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
gastrula zinc finger protein XlCGF57.1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 206 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
gastrula zinc finger protein XlCGF57.1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 208 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
gastrula zinc finger protein XlCGF57.1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 206 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
histone-lysine N-methyltransferase PRDM9-like isoform X2
histone-lysine N-methyltransferase PRDM9-like isoform X4
gastrula zinc finger protein XlCGF57.1-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 107 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: 109 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
gastrula zinc finger protein XlCGF57.1-like isoform X6
histone-lysine N-methyltransferase PRDM9-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
mitogen-activated protein kinase kinase 7, transcript variant X1
mitogen-activated protein kinase kinase 7, transcript variant X2
dual specificity mitogen-activated protein kinase kinase 7 isoform X2
dual specificity mitogen-activated protein kinase kinase 7 isoform X1
serine/threonine-protein kinase N1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
serine/threonine-protein kinase N1-like, transcript variant X1
serine/threonine-protein kinase N1-like isoform X2
serine/threonine-protein kinase N1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC116219803, transcript variant X3
uncharacterized LOC116219803, transcript variant X1
uncharacterized LOC116219803, transcript variant X2
uncharacterized protein LOC116219803 isoform X2
uncharacterized protein LOC116219803 isoform X3
uncharacterized protein LOC116219803 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
NACHT, LRR and PYD domains-containing protein 3-like, 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
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X3
NACHT, LRR and PYD domains-containing protein 3-like isoform X1
NACHT, LRR and PYD domains-containing protein 3-like isoform X3
serine/threonine-protein kinase pakH-like
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X2
NACHT, LRR and PYD domains-containing protein 3-like isoform X2
histone-lysine N-methyltransferase PRDM9-like
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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 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 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: 6 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC116219772, transcript variant X1
uncharacterized LOC116219772, transcript variant X2
uncharacterized protein LOC116219772 isoform X1
uncharacterized protein LOC116219772 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 189 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: 62 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
gastrula zinc finger protein XlCGF49.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% 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 62% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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 53% coverage of the annotated genomic feature by RNAseq alignments
probable serine/threonine-protein kinase SIK1B
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: 1 Protein, and 53% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 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: 7 Proteins, and 94% 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 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 147 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 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: 4 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
microtubule-associated serine/threonine-protein kinase 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: microtubule-associated serine/threonine-protein kinase 1-like
ethanolamine-phosphate cytidylyltransferase-like
N-sulfoglucosamine sulfohydrolase (sulfamidase)
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 13 samples with support for all annotated introns
sodium-independent sulfate anion transporter
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
heterogeneous nuclear ribonucleoprotein L-like
serine/arginine-rich splicing factor 7, transcript variant X2
serine/arginine-rich splicing factor 7, transcript variant X1
serine/arginine-rich splicing factor 7 isoform X2
serine/arginine-rich splicing factor 7 isoform X1
gem (nuclear organelle) associated protein 6
son of sevenless homolog 1, transcript variant X1
son of sevenless homolog 1, transcript variant X2
mitogen-activated protein kinase kinase kinase kinase 3-like, transcript variant X2
mitogen-activated protein kinase kinase kinase kinase 3-like, transcript variant X3
mitogen-activated protein kinase kinase kinase kinase 3-like, transcript variant X1
mitogen-activated protein kinase kinase kinase kinase 3-like isoform X2
mitogen-activated protein kinase kinase kinase kinase 3-like isoform X3
mitogen-activated protein kinase kinase kinase kinase 3-like isoform 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 6 samples with support for all annotated introns
YJU2 splicing factor homolog B, 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 11 samples with support for all annotated introns
YJU2 splicing factor homolog B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
YJU2 splicing factor homolog B, transcript variant X1
coiled-coil domain-containing protein 130 homolog isoform X2
coiled-coil domain-containing protein 130 homolog isoform X1
coiled-coil domain-containing protein 130 homolog isoform X3
suppressor of cytokine signaling 7, transcript variant X1
suppressor of cytokine signaling 7, transcript variant X2
suppressor of cytokine signaling 7 isoform X2
suppressor of cytokine signaling 7 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
39S ribosomal protein L45, mitochondrial
chromosome 26 C6orf120 homolog, transcript variant X1
chromosome 26 C6orf120 homolog, transcript variant X2
structural maintenance of chromosomes protein 3
max interactor 1, dimerization protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
max interactor 1, dimerization protein, transcript variant X2
X-prolyl aminopeptidase (aminopeptidase P) 1, soluble, transcript variant X2
X-prolyl aminopeptidase (aminopeptidase P) 1, soluble, transcript variant X1
chemokine (C-X-C motif) ligand 12b (stromal cell-derived factor 1)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
platelet-derived growth factor subunit A-like
DnaJ heat shock protein family (Hsp40) member A3b, transcript variant X2
DnaJ heat shock protein family (Hsp40) member A3b, transcript variant X1
dnaJ heat shock protein family (Hsp40) member A3b isoform X2
dnaJ heat shock protein family (Hsp40) member A3b isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 372 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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: 664 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 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 86% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein DDB_G0271670-like
ladderlectin-like, transcript variant X3
ladderlectin-like, transcript variant X1
ladderlectin-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
transcription factor AP-4, transcript variant X1
transcription factor AP-4, transcript variant X3
transcription factor AP-4, transcript variant X2
transcription factor AP-4, transcript variant X4
transcription factor AP-4, transcript variant X6
transcription factor AP-4, transcript variant X5
transcription factor AP-4, transcript variant X7
adenylate cyclase 9, transcript variant X2
adenylate cyclase 9, transcript variant X1
CREB binding protein a, transcript variant X1
CREB binding protein a, transcript variant X2
CREB binding protein a, transcript variant X5
CREB binding protein a, transcript variant X3
CREB binding protein a, transcript variant X4
SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae)
structure-specific endonuclease subunit SLX4
MAPK regulated corepressor interacting protein 2
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 10 samples with support for all annotated introns
glycerophosphodiester phosphodiesterase 1
NACHT, LRR and PYD domains-containing protein 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
4-aminobutyrate aminotransferase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
tumor necrosis factor receptor superfamily member 14-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% coverage of the annotated genomic feature by RNAseq alignments
SEC14-like protein 1, transcript variant X3
SEC14-like protein 1, transcript variant X1
SEC14-like protein 1, transcript variant X5
SEC14-like protein 1, transcript variant X4
SEC14-like protein 1, transcript variant X6
SEC14-like protein 1, transcript variant X2
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B, transcript variant X2
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B, transcript variant X1
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B isoform X1
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
phosphoribosyl pyrophosphate synthase-associated protein 1, transcript variant X2
phosphoribosyl pyrophosphate synthase-associated protein 1, transcript variant X1
phosphoribosyl pyrophosphate synthase-associated protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
(E3-independent) E2 ubiquitin-conjugating enzyme UBE2O
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 5 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 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: sphingosine kinase 1
(E3-independent) E2 ubiquitin-conjugating enzyme UBE2O-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
inactive rhomboid protein 2, transcript variant X3
inactive rhomboid protein 2, transcript variant X1
inactive rhomboid protein 2, transcript variant X2
peroxisomal acyl-coenzyme A oxidase 1, transcript variant X3
peroxisomal acyl-coenzyme A oxidase 1, transcript variant X1
peroxisomal acyl-coenzyme A oxidase 1, transcript variant X2
peroxisomal acyl-coenzyme A oxidase 1 isoform X1
peroxisomal acyl-coenzyme A oxidase 1 isoform X2
TEN1 subunit of CST complex, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TEN1 subunit of CST complex, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
signal recognition particle subunit SRP68
polymerase (DNA directed), gamma 2, accessory subunit
DNA polymerase subunit gamma-2, mitochondrial
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, including 5 samples with support for all annotated introns
peroxisomal acyl-coenzyme A oxidase 1-like, transcript variant X2
peroxisomal acyl-coenzyme A oxidase 1-like, transcript variant X1
peroxisomal acyl-coenzyme A oxidase 1-like, transcript variant X3
peroxisomal acyl-coenzyme A oxidase 1-like isoform X2
peroxisomal acyl-coenzyme A oxidase 1-like isoform X1
peroxisomal acyl-coenzyme A oxidase 1-like, transcript variant X4
peroxisomal acyl-coenzyme A oxidase 1-like isoform 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 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 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: signal recognition particle subunit SRP68
probable ATP-dependent RNA helicase DDX5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase SMURF2, transcript variant X3
E3 ubiquitin-protein ligase SMURF2, transcript variant X1
E3 ubiquitin-protein ligase SMURF2, transcript variant X4
E3 ubiquitin-protein ligase SMURF2, transcript variant X5
E3 ubiquitin-protein ligase SMURF2, transcript variant X2
E3 ubiquitin-protein ligase SMURF2, transcript variant X6
E3 ubiquitin-protein ligase SMURF2 isoform X6
E3 ubiquitin-protein ligase SMURF2 isoform X5
E3 ubiquitin-protein ligase SMURF2 isoform X4
E3 ubiquitin-protein ligase SMURF2 isoform X2
E3 ubiquitin-protein ligase SMURF2 isoform X3
E3 ubiquitin-protein ligase SMURF2 isoform X1
transfer RNA arginine (anticodon CCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
nucleosome-remodeling factor subunit BPTF
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: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: nucleosome-remodeling factor subunit BPTF
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
phosphatidylinositol transfer protein cytoplasmic 1, transcript variant X1
cytoplasmic phosphatidylinositol transfer protein 1 isoform X1
phosphatidylinositol transfer protein cytoplasmic 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
cytoplasmic phosphatidylinositol transfer protein 1 isoform X2
testis-expressed protein 2, transcript variant X3
testis-expressed protein 2, transcript variant X2
testis-expressed protein 2, transcript variant X1
myeloid-associated differentiation marker homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
beta-2-glycoprotein 1-like, transcript variant X2
beta-2-glycoprotein 1-like, transcript variant X1
protein kinase C, alpha, a, transcript variant X1
protein kinase C, alpha, a, transcript variant X2
calcium channel, voltage-dependent, gamma subunit 5a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
calcium channel, voltage-dependent, gamma subunit 5a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
calcium channel, voltage-dependent, gamma subunit 5a isoform X1
calcium channel, voltage-dependent, gamma subunit 5a isoform X2
voltage-dependent calcium channel gamma-4 subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
calcium channel, voltage-dependent, gamma subunit 1a
26S proteasome non-ATPase regulatory subunit 12
protein phosphatase 1, regulatory subunit 12C
protein phosphatase 1 regulatory subunit 12C
uncharacterized LOC116219868, transcript variant X2
uncharacterized LOC116219868, transcript variant X1
adhesion G protein-coupled receptor E1-like, transcript variant X1
adhesion G protein-coupled receptor E1-like, transcript variant X2
adhesion G protein-coupled receptor E1-like isoform X1
adhesion G protein-coupled receptor E1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
golgi-associated, gamma adaptin ear containing, ARF binding protein 1
ADP-ribosylation factor-binding protein GGA1
DEAD-box helicase 17, transcript variant X1
DEAD-box helicase 17, transcript variant X2
probable ATP-dependent RNA helicase DDX17 isoform X2
probable ATP-dependent RNA helicase DDX17 isoform X1
protein N-terminal asparagine amidohydrolase
GTPase IMAP family member 4-like, transcript variant X3
GTPase IMAP family member 4-like, transcript variant X1
GTPase IMAP family member 4-like, transcript variant X5
GTPase IMAP family member 4-like, transcript variant X2
GTPase IMAP family member 4-like, transcript variant X4
GTPase IMAP family member 9-like isoform X1
GTPase IMAP family member 4-like isoform X3
GTPase IMAP family member 9-like isoform X2
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X2
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X3
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X1
NACHT, LRR and PYD domains-containing protein 12-like isoform X2
NACHT, LRR and PYD domains-containing protein 12-like isoform X1
meiosis regulator and mRNA stability factor 1, transcript variant X5
meiosis regulator and mRNA stability factor 1, transcript variant X4
meiosis regulator and mRNA stability factor 1, transcript variant X2
meiosis regulator and mRNA stability factor 1, transcript variant X1
meiosis regulator and mRNA stability factor 1, transcript variant X6
meiosis regulator and mRNA stability factor 1, transcript variant X3
meiosis regulator and mRNA stability factor 1 isoform X4
meiosis regulator and mRNA stability factor 1 isoform X3
meiosis regulator and mRNA stability factor 1 isoform X2
meiosis regulator and mRNA stability factor 1 isoform X1
transcription activator BRG1, transcript variant X1
transcription activator BRG1, transcript variant X3
transcription activator BRG1, transcript variant X2
transcription activator BRG1, transcript variant X4
adaptor related protein complex 1 subunit mu 2
cyclin-dependent kinase inhibitor 2D (p19, inhibits CDK4)
volume-regulated anion channel subunit LRRC8C, transcript variant X2
volume-regulated anion channel subunit LRRC8C, transcript variant X1
volume-regulated anion channel subunit LRRC8C
kelch-like ECH-associated protein 1b, transcript variant X2
kelch-like ECH-associated protein 1b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
zinc finger GATA like protein 1, transcript variant X1
zinc finger GATA like protein 1, transcript variant X2
GATA-type zinc finger protein 1 isoform X1
GATA-type zinc finger protein 1 isoform X2
LYL1 basic helix-loop-helix family member
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
HMG box-containing protein 4-like, transcript variant X1
HMG box-containing protein 4-like, transcript variant X2
heme oxygenase-like, transcript variant X1
heme oxygenase-like, transcript variant X2
target of Myb protein 1-like, transcript variant X1
target of Myb protein 1-like, transcript variant X2
target of Myb protein 1-like, transcript variant X3
bone gamma-carboxyglutamate (gla) protein, like
endoplasmic reticulum resident protein 27
retinal cone rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RNA binding protein fox-1 homolog 2-like
T-cell acute lymphocytic leukemia protein 1 homolog
endoplasmic reticulum resident protein 27-like
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
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; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: endoplasmic reticulum resident protein 27-like
RNA binding fox-1 homolog 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RNA binding fox-1 homolog 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
RNA binding fox-1 homolog 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RNA binding protein fox-1 homolog 2 isoform X2
RNA binding protein fox-1 homolog 2 isoform X1
RNA binding protein fox-1 homolog 2 isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; 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
LOW QUALITY PROTEIN: uncharacterized protein LOC116219889
uncharacterized LOC105893544, transcript variant X2
uncharacterized LOC105893544, transcript variant X1
uncharacterized protein LOC105893544 isoform X1
uncharacterized protein LOC105893544 isoform X2
cyclic AMP-dependent transcription factor ATF-4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC116219864, transcript variant X2
uncharacterized LOC116219864, transcript variant X1
uncharacterized LOC116219864, transcript variant X3
uncharacterized protein LOC116219864 isoform X2
uncharacterized protein LOC116219864 isoform X3
uncharacterized protein LOC116219864 isoform X1
uncharacterized LOC116219857, transcript variant X2
uncharacterized LOC116219857, transcript variant X1
uncharacterized protein LOC116219857 isoform X2
uncharacterized protein LOC116219857 isoform X1
3-mercaptopyruvate sulfurtransferase, transcript variant X2
3-mercaptopyruvate sulfurtransferase, transcript variant X1
3-mercaptopyruvate sulfurtransferase isoform X1
3-mercaptopyruvate sulfurtransferase isoform X2
uncharacterized LOC116219759, transcript variant X1
uncharacterized LOC116219759, transcript variant X2
uncharacterized LOC116219759, transcript variant X3
uncharacterized LOC116219759, transcript variant X4
mitochondrial sodium/calcium exchanger protein-like, transcript variant X1
mitochondrial sodium/calcium exchanger protein-like, transcript variant X2
mitochondrial sodium/calcium exchanger protein-like isoform X1
mitochondrial sodium/calcium exchanger protein-like isoform 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 3 samples with support for all annotated introns
complement C1q tumor necrosis factor-related protein 1
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase b
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 9 samples with support for all annotated introns
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase
TGF-beta activated kinase 1/MAP3K7 binding protein 1, transcript variant X1
TGF-beta activated kinase 1/MAP3K7 binding protein 1, transcript variant X2
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 isoform X2
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 isoform X1
integrin alpha-L-like, transcript variant X2
integrin alpha-L-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
zinc finger CCCH domain-containing protein 6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
zinc finger CCCH domain-containing protein 6-like, transcript variant X1
zinc finger CCCH domain-containing protein 6-like isoform X1
zinc finger CCCH domain-containing protein 6-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105905692, transcript variant X2
uncharacterized LOC105905692, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
nicotinate-nucleotide pyrophosphorylase [carboxylating], transcript variant X1
nicotinate-nucleotide pyrophosphorylase [carboxylating], transcript variant X2
nicotinate-nucleotide pyrophosphorylase [carboxylating]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
ATP-sensitive inward rectifier potassium channel 12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger and BTB domain containing 45
zinc finger and BTB domain-containing protein 45
uncharacterized LOC116219871, transcript variant X1
uncharacterized LOC116219871, transcript variant X2
mitochondrial sodium/calcium exchanger protein
acyl-CoA dehydrogenase family member 11-like
cartilage intermediate layer protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
probable E3 ubiquitin-protein ligase HERC6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 49% 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 94% coverage of the annotated genomic feature by RNAseq alignments
regulatory associated protein of MTOR, complex 1, transcript variant X3
regulatory associated protein of MTOR, complex 1, transcript variant X4
regulatory associated protein of MTOR, complex 1, transcript variant X1
regulatory associated protein of MTOR, complex 1, transcript variant X2
regulatory-associated protein of mTOR isoform X1
regulatory-associated protein of mTOR isoform X2
regulatory-associated protein of mTOR isoform X3
regulatory-associated protein of mTOR isoform X4
platelet and endothelial cell adhesion molecule 1b, transcript variant X2
platelet and endothelial cell adhesion molecule 1b, transcript variant X1
platelet and endothelial cell adhesion molecule 1b, transcript variant X4
platelet and endothelial cell adhesion molecule 1b, transcript variant X3
platelet and endothelial cell adhesion molecule 1b, transcript variant X5
platelet endothelial cell adhesion molecule isoform X1
platelet endothelial cell adhesion molecule isoform X2
platelet endothelial cell adhesion molecule isoform X3
platelet endothelial cell adhesion molecule isoform X4
protein phosphatase 1, regulatory subunit 27b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 27b
APC11 anaphase promoting complex subunit 11 homolog (yeast), transcript variant X1
APC11 anaphase promoting complex subunit 11 homolog (yeast), transcript variant X2
NFX1-type zinc finger-containing protein 1-like, transcript variant X1
NFX1-type zinc finger-containing protein 1-like, transcript variant X2
NFX1-type zinc finger-containing protein 1-like isoform X1
NFX1-type zinc finger-containing protein 1-like isoform X2
ras homolog family member T1, transcript variant X2
ras homolog family member T1, transcript variant X1
arf-GAP with dual PH domain-containing protein 2-like
transcription elongation factor, mitochondrial
ATPase family AAA domain containing 5b, 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 1 sample with support for all annotated introns
ATPase family AAA domain containing 5b, transcript variant X1
ATPase family AAA domain containing 5b, transcript variant X3
ATPase family AAA domain-containing protein 5b isoform X2
ATPase family AAA domain-containing protein 5b isoform X1
ATPase family AAA domain-containing protein 5b isoform X3
SUZ12 polycomb repressive complex 2 subunit b, transcript variant X2
SUZ12 polycomb repressive complex 2 subunit b, transcript variant X1
U3 small nucleolar RNA-associated protein 6 homolog
RAB11 family interacting protein 4 (class II) b, transcript variant X1
RAB11 family interacting protein 4 (class II) b, transcript variant X2
RAB11 family interacting protein 4 (class II) b, transcript variant X3
RAB11 family interacting protein 4 (class II) b, transcript variant X4
RAB11 family interacting protein 4 (class II) b, transcript variant X5
RAB11 family interacting protein 4 (class II) b, transcript variant X6
rab11 family-interacting protein 4B isoform X2
rab11 family-interacting protein 4B isoform X3
rab11 family-interacting protein 4B isoform X1
rab11 family-interacting protein 4B isoform X4
rab11 family-interacting protein 4B isoform X5
rab11 family-interacting protein 4B isoform X6
tripartite motif containing 25, transcript variant X2
tripartite motif containing 25, transcript variant X1
tripartite motif containing 25, transcript variant X3
E3 ubiquitin/ISG15 ligase TRIM25 isoform X1
E3 ubiquitin/ISG15 ligase TRIM25 isoform X2
E3 ubiquitin/ISG15 ligase TRIM25 isoform 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 9 samples with support for all annotated introns
chromosome 26 C17orf67 homolog, transcript variant X2
chromosome 26 C17orf67 homolog, transcript variant X1
chromosome 26 C17orf67 homolog, transcript variant X3
uncharacterized protein C17orf67 homolog isoform X2
uncharacterized protein C17orf67 homolog isoform X1
uncharacterized protein C17orf67 homolog isoform X3
E3 SUMO-protein ligase CBX4, transcript variant X2
E3 SUMO-protein ligase CBX4, transcript variant X1
caspase recruitment domain-containing protein 14-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 77% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 40
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 2 samples with support for all annotated introns
caspase recruitment domain-containing protein 14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 40-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% 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: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
trinucleotide repeat-containing gene 6C protein-like
neuronal-specific septin-3-like isoform X2
neuronal-specific septin-3-like isoform X1
uncharacterized LOC116219906, transcript variant X2
uncharacterized LOC116219906, transcript variant X1
uncharacterized protein LOC116219906 isoform X2
uncharacterized protein LOC116219906 isoform X1
CD276 antigen-like, transcript variant X1
CD276 antigen-like, transcript variant X2
V-set domain-containing T-cell activation inhibitor 1-like isoform X1
CD276 antigen-like, transcript variant X4
CD276 antigen-like, transcript variant X3
V-set domain-containing T-cell activation inhibitor 1-like isoform X3
N-acetyllactosaminide alpha-1,3-galactosyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Jupiter microtubule associated homolog 1a
golgi associated, gamma adaptin ear containing, ARF binding protein 3a
ADP-ribosylation factor-binding protein GGA3a
MIF4G domain containing a, transcript variant X1
MIF4G domain containing a, transcript variant X2
growth factor receptor-bound protein 2-like
growth factor receptor-bound protein 2-like, transcript variant X2
growth factor receptor-bound protein 2-like, transcript variant X1
growth factor receptor-bound protein 2-like isoform X2
growth factor receptor-bound protein 2-like isoform X1
melanin-concentrating hormone receptor 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
melanin-concentrating hormone receptor 1
ubiquitin carboxyl-terminal hydrolase 43a
cilia and flagella associated protein 52
cilia- and flagella-associated protein 52
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 58% coverage of the annotated genomic feature by RNAseq alignments
phosphoinositide-3-kinase, regulatory subunit 5, 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 5 samples with support for all annotated introns
phosphoinositide-3-kinase, regulatory subunit 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phosphoinositide-3-kinase, regulatory subunit 5, transcript variant X3
phosphoinositide-3-kinase, regulatory subunit 5, transcript variant X4
phosphoinositide-3-kinase, regulatory subunit 5, transcript variant X5
phosphoinositide 3-kinase regulatory subunit 5
phosphoinositide 3-kinase regulatory subunit 6, transcript variant X1
phosphoinositide 3-kinase regulatory subunit 6, transcript variant X2
phosphoinositide 3-kinase regulatory subunit 6
phosphoinositide-3-kinase, regulatory subunit 6a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
myosin, heavy chain 10, non-muscle, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
myosin, heavy chain 10, non-muscle, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phospholipid phosphatase-related protein type 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
myosin, heavy chain 9a, non-muscle, transcript variant X1
myosin, heavy chain 9a, non-muscle, transcript variant X2
mitochondrial glycine transporter B, transcript variant X1
mitochondrial glycine transporter B, transcript variant X2
mitochondrial glycine transporter B isoform X2
mitochondrial glycine transporter B isoform X1
small nucleolar RNA SNORA62/SNORA6 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00091
mitochondrial glycine transporter B-like, transcript variant X1
mitochondrial glycine transporter B-like, transcript variant X2
mitochondrial glycine transporter B-like isoform X2
mitochondrial glycine transporter B-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
phospholipid phosphatase-related protein type 5
mitotic interactor and substrate of PLK1
uncharacterized LOC116219904, transcript variant X2
uncharacterized LOC116219904, transcript variant X1
uncharacterized protein LOC116219904 isoform X2
uncharacterized protein LOC116219904 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
nuclear factor, interleukin 3 regulated, member 3, transcript variant X1
nuclear factor, interleukin 3 regulated, member 3, transcript variant X2
nuclear factor, interleukin 3 regulated, member 3
nuclear factor, interleukin 3 regulated, member 5
ral guanine nucleotide dissociation stimulator-like 3a
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
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; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ral guanine nucleotide dissociation stimulator-like 1
outer dynein arm docking complex subunit 3
coiled-coil domain-containing protein 151
solute carrier family 44 member 2, transcript variant X3
choline transporter-like protein 2 isoform X3
solute carrier family 44 member 2, transcript variant X1
solute carrier family 44 member 2, transcript variant X2
choline transporter-like protein 2 isoform X1
choline transporter-like protein 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tartrate-resistant acid phosphatase type 5a
interleukin enhancer binding factor 3a, transcript variant X3
interleukin enhancer binding factor 3a, transcript variant X2
interleukin enhancer binding factor 3a, transcript variant X1
interleukin enhancer-binding factor 3a isoform X3
interleukin enhancer-binding factor 3a isoform X2
interleukin enhancer-binding factor 3a isoform X1
prostaglandin E receptor 1a (subtype EP1)
WIZ zinc finger a, transcript variant X1
WIZ zinc finger a, transcript variant X3
WIZ zinc finger a, transcript variant X2
RAS protein activator like 3, transcript variant X1
RAS protein activator like 3, transcript variant X2
disabled homolog 2-interacting protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
nuclear distribution protein nudE homolog 1-like
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 8 samples with support for all annotated introns
myosin, heavy chain 11a, smooth muscle, transcript variant X2
myosin, heavy chain 11a, smooth muscle, transcript variant X1
myosin, heavy chain 11a, smooth muscle, transcript variant X3
ATP-binding cassette, sub-family C (CFTR/MRP), member 6a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
multidrug resistance-associated protein 1
coenzyme Q7 homolog, ubiquinone (yeast), transcript variant X2
5-demethoxyubiquinone hydroxylase, mitochondrial isoform X2
coenzyme Q7 homolog, ubiquinone (yeast), transcript variant X1
5-demethoxyubiquinone hydroxylase, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
ADP-ribosylation factor-like protein 6-interacting protein 1, transcript variant X1
ADP-ribosylation factor-like protein 6-interacting protein 1, transcript variant X2
ADP-ribosylation factor-like protein 6-interacting protein 1 isoform X1
ADP-ribosylation factor-like protein 6-interacting protein 1 isoform X2
lengsin, lens protein with glutamine synthetase domain
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
HYLS1 centriolar and ciliogenesis associated, transcript variant X2
hydrolethalus syndrome protein 1 isoform X2
HYLS1 centriolar and ciliogenesis associated, transcript variant X1
uncharacterized protein hyls1 isoform X1
programmed cell death 4b, transcript variant X1
programmed cell death 4b, transcript variant X2
programmed cell death 4b, transcript variant X3
SHOC2 leucine rich repeat scaffold protein, transcript variant X4
SHOC2 leucine rich repeat scaffold protein, transcript variant X1
SHOC2 leucine rich repeat scaffold protein, transcript variant X3
SHOC2 leucine rich repeat scaffold protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
leucine-rich repeat protein SHOC-2 isoform X1
leucine-rich repeat protein SHOC-2 isoform X2
BUB3-interacting and GLEBS motif-containing protein ZNF207b
SUN domain-containing protein 2-like, transcript variant X4
SUN domain-containing protein 2-like, transcript variant X2
SUN domain-containing protein 2-like, transcript variant X3
SUN domain-containing protein 2-like, transcript variant X1
SUN domain-containing protein 2-like isoform X2
SUN domain-containing protein 2-like isoform X1
mediator of RNA polymerase II transcription subunit 1.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
LOW QUALITY PROTEIN: mediator of RNA polymerase II transcription subunit 1.1
cytokine receptor common subunit beta-like
BAR/IMD domain containing adaptor protein 2 like 2b
brain-specific angiogenesis inhibitor 1-associated protein 2-like protein 2
phospholipase A2, group VI (cytosolic, calcium-independent)
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 7 samples with support for all annotated introns
85/88 kDa calcium-independent phospholipase A2
family with sequence similarity 20 member C, like, transcript variant X1
family with sequence similarity 20 member C, like, transcript variant X2
extracellular serine/threonine protein kinase FAM20C isoform X1
extracellular serine/threonine protein kinase FAM20C isoform X2
protein transport protein Sec16B-like, transcript variant X1
protein transport protein Sec16B-like, transcript variant X2
NLR family CARD domain-containing protein 3-like, transcript variant X4
NLR family CARD domain-containing protein 3-like isoform X1
NLR family CARD domain-containing protein 3-like isoform X3
NLR family CARD domain-containing protein 3-like isoform X4
NACHT, LRR and PYD domains-containing protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
NLR family CARD domain-containing protein 3-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DDB1 and CUL4 associated factor 15, transcript variant X2
DDB1 and CUL4 associated factor 15, transcript variant X1
DDB1 and CUL4 associated factor 15, transcript variant X3
DDB1- and CUL4-associated factor 15 isoform X1
DDB1- and CUL4-associated factor 15 isoform X2
DDB1- and CUL4-associated factor 15 isoform X3
regulatory factor X, 1b (influences HLA class II expression), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
regulatory factor X, 1b (influences HLA class II expression), transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 89% 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Na(+)/H(+) exchange regulatory cofactor NHE-RF2
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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
TSC complex subunit 2, transcript variant X1
TSC complex subunit 2, transcript variant X2
somatostatin receptor type 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
somatostatin receptor type 5, transcript variant X1
somatostatin receptor type 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
G protein-coupled receptor, class C, group 5, member Bb
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 13 samples with support for all annotated introns
uncharacterized protein DDB_G0283697-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol 4-kinase type 2 alpha
phosphatidylinositol 4-kinase type 2-alpha
arginine vasopressin induced 1, transcript variant X2
arginine vasopressin induced 1, transcript variant X1
zinc finger, FYVE domain containing 27, transcript variant X1
zinc finger, FYVE domain containing 27, transcript variant X2
zinc finger, FYVE domain containing 27, transcript variant X3
zinc finger, FYVE domain containing 27, transcript variant X4
zinc finger, FYVE domain containing 27, transcript variant X5
zinc finger, FYVE domain containing 27, transcript variant X7
zinc finger, FYVE domain containing 27, transcript variant X6
zinc finger, FYVE domain containing 27, transcript variant X8
zinc finger, FYVE domain containing 27, transcript variant X9
zinc finger, FYVE domain containing 27, transcript variant X10
golgin subfamily A member 7B-like, 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
golgin subfamily A member 7B-like, transcript variant X2
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 5 samples with support for all annotated introns
golgin subfamily A member 7B-like isoform X2
golgin subfamily A member 7B-like isoform X1
B-cell receptor CD22-like, transcript variant X1
B-cell receptor CD22-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
inactive C-alpha-formylglycine-generating enzyme 2
chaperonin containing TCP1, subunit 6A (zeta 1)
VPS54 subunit of GARP complex, transcript variant X4
VPS54 subunit of GARP complex, transcript variant X3
VPS54 subunit of GARP complex, transcript variant X2
VPS54 subunit of GARP complex, transcript variant X1
vacuolar protein sorting-associated protein 54 isoform X4
vacuolar protein sorting-associated protein 54 isoform X3
vacuolar protein sorting-associated protein 54 isoform X2
vacuolar protein sorting-associated protein 54 isoform X1
pellino E3 ubiquitin protein ligase 1a, 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 4 samples with support for all annotated introns
pellino E3 ubiquitin protein ligase 1a, transcript variant X2
E3 ubiquitin-protein ligase pellino homolog 1
proliferation associated nuclear element
single-pass membrane protein with aspartate-rich tail 1b
centriole, cilia and spindle-associated protein a
centriole, cilia and spindle-associated protein
actin alpha 1, skeletal muscle a; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309834.1
annotated by transcript or proteomic data
The RefSeq transcript has 5 substitutions, 1 non-frameshifting indel and aligns at 99% coverage compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: BestRefSeq.
phosphatidylinositol glycan anchor biosynthesis, class L
N-acetylglucosaminyl-phosphatidylinositol de-N-acetylase
heme-binding protein soul4, transcript variant X1
heme-binding protein soul4, transcript variant X4
heme-binding protein soul4, transcript variant X3
heme-binding protein soul4, transcript variant X2
protein tyrosine kinase 7a, transcript variant X1
protein tyrosine kinase 7a, transcript variant X2
inactive tyrosine-protein kinase 7a isoform X1
inactive tyrosine-protein kinase 7a isoform X2
MAP/microtubule affinity-regulating kinase 1, transcript variant X1
MAP/microtubule affinity-regulating kinase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
serine/threonine-protein kinase MARK1 isoform X1
serine/threonine-protein kinase MARK1 isoform X2
Tnf receptor-associated factor 5, transcript variant X4
Tnf receptor-associated factor 5, transcript variant X2
Tnf receptor-associated factor 5, transcript variant X1
Tnf receptor-associated factor 5, transcript variant X3
TNF receptor-associated factor 5 isoform X1
TNF receptor-associated factor 5 isoform X2
potassium voltage-gated channel, subfamily H (eag-related), member 1b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily H member 1b
uncharacterized LOC116219861, transcript variant X1
uncharacterized LOC116219861, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 86% 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 2 bases in 1 codon
LOW QUALITY PROTEIN: tau-tubulin kinase 1
myelin and lymphocyte protein-like, transcript variant X2
post-GPI attachment to proteins GalNAc transferase 4
myelin and lymphocyte protein-like isoform X2
myelin and lymphocyte protein-like, transcript variant X1
myelin and lymphocyte protein-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns