Plectropomus leopardus isolate mb chromosome 22, YSFRI_Pleo_2.0, whole genome shotgun sequence.
Plectropomus leopardus (leopard coralgrouper)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Neoteleostei; Acanthomorphata; Eupercaria; Perciformes; Serranoidei; Serranidae; Epinephelinae; Epinephelini; Plectropomus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM018429.2.\nAssembly name: YSFRI_Pleo_2.0\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Yellow Sea Fisheries Research\nInstitute, Chinese Academy of Fishery Sciences on 2020/05/27. The\noriginal whole-genome shotgun project has the accession\nVJNF00000000.2.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Yellow Sea Fisheries Research Institute,\n Chinese Academy of Fishery Sciences\nAssembly Method :: Supernova v. 1.2.4\nAssembly Name :: YSFRI_Pleo_2.0\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 381.0x\nSequencing Technology :: PacBio\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Plectropomus leopardus Annotation\n Release 100\nAnnotation Version :: 100\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.
zinc finger CCCH-type antiviral protein 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger CCCH-type antiviral protein 1-like, 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 3 samples with support for all annotated introns
zinc finger CCCH-type antiviral protein 1-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 3 samples with support for all annotated introns
zinc finger CCCH-type antiviral protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger CCCH-type antiviral protein 1-like isoform X1
zinc finger CCCH-type antiviral protein 1-like isoform X4
zinc finger CCCH-type antiviral protein 1-like isoform X2
zinc finger CCCH-type antiviral protein 1-like isoform X3
zinc finger CCCH-type antiviral protein 1-like, transcript variant X5
zinc finger CCCH-type antiviral protein 1-like isoform X5
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: UPF0606 protein KIAA1549-like
COORDINATES: polyA evidence [ECO:0006239]
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: putative transporter SVOPL
protein-methionine sulfoxide oxidase mical3a-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein-methionine sulfoxide oxidase mical3a-like, transcript variant X1
protein-methionine sulfoxide oxidase mical3a-like, transcript variant X3
protein-methionine sulfoxide oxidase mical3a-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein-methionine sulfoxide oxidase mical3a-like isoform X2
protein-methionine sulfoxide oxidase mical3a-like isoform X1
protein-methionine sulfoxide oxidase mical3a-like isoform X3
protein-methionine sulfoxide oxidase mical3a-like isoform X4
GRIP and coiled-coil domain containing 1, transcript variant X1
GRIP and coiled-coil domain containing 1, transcript variant X3
GRIP and coiled-coil domain containing 1, transcript variant X2
GRIP and coiled-coil domain-containing protein 1 isoform X1
GRIP and coiled-coil domain-containing protein 1 isoform X2
DENN/MADD domain containing 6B, transcript variant X2
DENN/MADD domain containing 6B, transcript variant X1
DENN/MADD domain containing 6B, 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 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 60% coverage of the annotated genomic feature by RNAseq alignments
interferon regulatory factor 5-like, transcript variant X1
interferon regulatory factor 5-like, transcript variant X2
interferon regulatory factor 5-like isoform X1
interferon regulatory factor 5-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
interferon regulatory factor 5-like isoform X2
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: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: interferon regulatory factor 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 57% coverage of the annotated genomic feature by RNAseq alignments
opsin 1 (cone pigments), short-wave-sensitive 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1010 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily D member 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons
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.
non-SMC condensin II complex, subunit H2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
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 99% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: E3 ubiquitin-protein ligase Mdm2
solute carrier family 35 member E3, transcript variant X3
solute carrier family 35 member E3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
solute carrier family 35 member E3, transcript variant X2
UPF2 regulator of nonsense mediated mRNA decay
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: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: regulator of nonsense transcripts 2
proline-rich protein 36, transcript variant X1
proline-rich protein 36, transcript variant X2
transmembrane protein 243, mitochondrial b, transcript variant X2
transmembrane protein 243, mitochondrial b, transcript variant X1
meiosis expressed gene 1 protein homolog
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: 11 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: meiosis expressed gene 1 protein homolog
DNA cross-link repair 1C, PSO2 homolog (S. cerevisiae), 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
DNA cross-link repair 1C, PSO2 homolog (S. cerevisiae), 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 3 samples with support for all annotated introns
overexpressed in colon carcinoma 1 protein-like
laminin subunit beta-1-like, transcript variant X2
laminin subunit beta-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ATP synthase subunit gamma, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
inter-alpha-trypsin inhibitor heavy chain 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
inter-alpha-trypsin inhibitor heavy chain H2
inter-alpha-trypsin inhibitor heavy chain 5
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: inter-alpha-trypsin inhibitor heavy chain H5
transmembrane protein 110, 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
transmembrane protein 110, like, transcript variant X3
transmembrane protein 110, like, transcript variant X1
transmembrane protein 110, like isoform X1
transmembrane protein 110, like isoform X2
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: 7 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: scm-like with four MBT domains protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
TBC1 domain family, member 30, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TBC1 domain family, member 30, 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
TBC1 domain family, member 30, 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 1 sample with support for all annotated introns
TBC1 domain family, member 30, transcript variant X1
glucosamine (N-acetyl)-6-sulfatase a, transcript variant X1
glucosamine (N-acetyl)-6-sulfatase a, transcript variant X2
N-acetylglucosamine-6-sulfatase isoform X1
N-acetylglucosamine-6-sulfatase isoform X2
uncharacterized protein LOC570908 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC570908 homolog, transcript variant X3
uncharacterized protein LOC570908 homolog, transcript variant X1
adipocyte plasma membrane-associated protein
cugbp, Elav-like family member 2, transcript variant X5
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 1 sample with support for all annotated introns
cugbp, Elav-like family member 2, transcript variant X2
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
cugbp, Elav-like family member 2, transcript variant 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 1 sample with support for all annotated introns
cugbp, Elav-like family member 2, transcript variant X3
cugbp, Elav-like family member 2, transcript variant X4
CUGBP Elav-like family member 2 isoform X2
CUGBP Elav-like family member 2 isoform X1
CUGBP Elav-like family member 2 isoform X3
CUGBP Elav-like family member 2 isoform X4
CUGBP Elav-like family member 2 isoform X5
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 5 bases in 4 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 5 bases in 4 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transcription factor GATA-3
protein tyrosine phosphatase receptor type O
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 93% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: receptor-type tyrosine-protein phosphatase O
ATP-binding cassette sub-family C member 9-like
enoyl-CoA hydratase domain-containing protein 3, mitochondrial
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
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: 31 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: serine/threonine-protein kinase TBK1
low density lipoprotein receptor-related protein 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
low-density lipoprotein receptor-related protein 6
uncharacterized protein C11orf98 homolog
parathyroid hormone-like hormone a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
parathyroid hormone-like hormone a, transcript variant X1
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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: 60S ribosomal protein L18a
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00263
exportin, tRNA (nuclear export receptor for tRNAs)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments, including 3 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
shaker-related potassium channel tsha2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 101 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily A member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 103 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
potassium voltage-gated channel subfamily A member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 77% coverage of the annotated genomic feature by RNAseq alignments
chaperonin containing TCP1, subunit 2 (beta)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 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: 18 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
SH3 and multiple ankyrin repeat domains 3b
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: SH3 and multiple ankyrin repeat domains protein 3
leucine-rich repeat-containing G-protein coupled receptor 5-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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 2 bases in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: leucine-rich repeat-containing G-protein coupled receptor 5-like
LSM8 homolog, U6 small nuclear RNA associated
glutamate receptor interacting protein 1, transcript variant X2
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
glutamate receptor interacting protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutamate receptor interacting protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor interacting protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glutamate receptor-interacting protein 1 isoform X2
glutamate receptor-interacting protein 1 isoform X3
glutamate receptor-interacting protein 1 isoform X1
glutamate receptor-interacting protein 1 isoform X4
cullin-associated NEDD8-dissociated protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 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: 10 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: 1 Protein, and 83% 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 98% 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: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dual specificity tyrosine-phosphorylation-regulated kinase 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: F-box only protein 15-like
uncharacterized LOC121961488, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC121961488, transcript variant X1
uncharacterized LOC121961488, 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 1 sample with support for all annotated introns
nuclear factor 7, ovary-like, transcript variant X1
nuclear factor 7, ovary-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 3 samples with support for all annotated introns
uncharacterized LOC121961493, transcript variant X3
uncharacterized LOC121961493, transcript variant X2
uncharacterized LOC121961493, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
thyrotropin-releasing hormone-degrading ectoenzyme-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 Proteins, and 89% 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: 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: 75 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SLIT-ROBO Rho GTPase-activating protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 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: inserted 1 base in 1 codon; deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: KICSTOR subunit 2-like
transmembrane and coiled-coil domain family 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane and coiled-coil domain family 3, transcript variant X2
transmembrane and coiled-coil domain protein 3 isoform X1
transmembrane and coiled-coil domain protein 3 isoform X2
NADH:ubiquinone oxidoreductase subunit A12
LOW QUALITY PROTEIN: NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
vezatin, adherens junctions transmembrane protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
vezatin, adherens junctions transmembrane protein, transcript variant X2
endosome/lysosome-associated apoptosis and autophagy regulator family member 2-like, transcript variant X2
endosome/lysosome-associated apoptosis and autophagy regulator family member 2-like, transcript variant X1
endosome/lysosome-associated apoptosis and autophagy regulator family member 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
integrin alpha FG-GAP repeat containing 2
achaete-scute family bHLH transcription factor 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 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: 69 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 81% 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: 115 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: 7 Proteins
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, including 3 samples with support for all annotated introns
ankyrin repeat and BTB/POZ domain-containing protein BTBD11-A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 99 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transcription termination factor 2, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 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: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 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: 27 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: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein phosphatase 1, regulatory subunit 12A, transcript variant X11
protein phosphatase 1, regulatory subunit 12A, transcript variant X10
protein phosphatase 1, regulatory subunit 12A, transcript variant X3
protein phosphatase 1, regulatory subunit 12A, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein phosphatase 1 regulatory subunit 12A isoform X10
protein phosphatase 1 regulatory subunit 12A isoform X9
protein phosphatase 1 regulatory subunit 12A isoform X3
protein phosphatase 1, regulatory subunit 12A, 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
protein phosphatase 1, regulatory subunit 12A, transcript variant X9
protein phosphatase 1, regulatory subunit 12A, transcript variant X1
protein phosphatase 1, regulatory subunit 12A, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein phosphatase 1, regulatory subunit 12A, transcript variant X4
protein phosphatase 1, regulatory subunit 12A, transcript variant X8
protein phosphatase 1 regulatory subunit 12A isoform X6
protein phosphatase 1 regulatory subunit 12A isoform X2
protein phosphatase 1 regulatory subunit 12A isoform X4
protein phosphatase 1 regulatory subunit 12A isoform X8
protein phosphatase 1 regulatory subunit 12A isoform X7
protein phosphatase 1 regulatory subunit 12A isoform X1
protein phosphatase 1, regulatory subunit 12A, transcript variant X6
protein phosphatase 1 regulatory subunit 12A isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
lin-7 homolog A (C. elegans), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lin-7 homolog A (C. elegans), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
lin-7 homolog A (C. elegans), 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
acyl-CoA synthetase short chain family member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
acyl-CoA synthetase short-chain family member 3, mitochondrial
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
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: 34 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: cystine/glutamate transporter
RAD9-HUS1-RAD1 interacting nuclear orphan 1
RAD9, HUS1, RAD1-interacting nuclear orphan protein 1
TUB like protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
TUB like protein 3, transcript variant X1
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 1 sample with support for all annotated introns
TUB like protein 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein mono-ADP-ribosyltransferase TIPARP-like, transcript variant X1
protein mono-ADP-ribosyltransferase TIPARP-like, transcript variant X2
protein mono-ADP-ribosyltransferase TIPARP-like isoform X1
protein mono-ADP-ribosyltransferase TIPARP-like isoform X2
E3 ubiquitin-protein ligase TRIM35-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
E3 ubiquitin-protein ligase TRIM35-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
E3 ubiquitin-protein ligase TRIM35-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 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: 16 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 1
guanine nucleotide-binding protein G(i) subunit alpha-1
membrane associated guanylate kinase, WW and PDZ domain containing 2a, transcript variant X1
membrane associated guanylate kinase, WW and PDZ domain containing 2a, transcript variant X2
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2a isoform X1
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2a isoform X2
endoplasmic reticulum-Golgi intermediate compartment protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
lysine (K)-specific demethylase 7Aa, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
lysine (K)-specific demethylase 7Aa, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lysine-specific demethylase 7A isoform X1
lysine-specific demethylase 7A isoform X2
NADH:ubiquinone oxidoreductase subunit B2
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 2, mitochondrial
lysine (K)-specific methyltransferase 2E, transcript variant X1
lysine (K)-specific methyltransferase 2E, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
lysine (K)-specific methyltransferase 2E, transcript variant X2
lysine (K)-specific methyltransferase 2E, transcript variant X3
lysine (K)-specific methyltransferase 2E, transcript variant X6
lysine (K)-specific methyltransferase 2E, transcript variant X4
inactive histone-lysine N-methyltransferase 2E isoform X1
inactive histone-lysine N-methyltransferase 2E isoform X3
inactive histone-lysine N-methyltransferase 2E isoform X5
inactive histone-lysine N-methyltransferase 2E isoform X6
inactive histone-lysine N-methyltransferase 2E isoform X2
inactive histone-lysine N-methyltransferase 2E isoform X4
TP53 induced glycolysis regulatory phosphatase b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
peroxisomal biogenesis factor 26, transcript variant X2
peroxisomal biogenesis factor 26, transcript variant X1
peroxisome assembly protein 26 isoform X2
peroxisome assembly protein 26 isoform X1
LLP homolog, long-term synaptic facilitation factor
hematopoietic cell-specific Lyn substrate 1
LOW QUALITY PROTEIN: src substrate protein p85-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins
LOW QUALITY PROTEIN: guanylyl cyclase-activating protein 1
origin recognition complex, subunit 5, transcript variant X1
origin recognition complex, subunit 5, transcript variant X2
origin recognition complex, subunit 5, transcript variant X3
origin recognition complex subunit 5 isoform X1
origin recognition complex subunit 5 isoform X2
LHFPL tetraspan subfamily member 3, transcript variant X2
LHFPL tetraspan subfamily member 3, transcript variant X1
LHFPL tetraspan subfamily member 3 protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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: 30 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
probable polypeptide N-acetylgalactosaminyltransferase 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 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: 14 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
proline-, glutamic acid- and leucine-rich protein 1-like
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transcription factor Spi-C-like, transcript variant X1
transcription factor Spi-C-like, transcript variant X2
transcription factor Spi-C-like isoform X1
transcription factor Spi-C-like isoform X2
LOW QUALITY PROTEIN: myosin-binding protein C, slow-type
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
N-acetylglucosamine-1-phosphate transferase subunits alpha and beta
N-acetylglucosamine-1-phosphotransferase subunits alpha/beta
DNA-damage regulated autophagy modulator 1, transcript variant X1
DNA-damage regulated autophagy modulator 1, transcript variant X2
DNA damage-regulated autophagy modulator protein 1 isoform X2
DNA damage-regulated autophagy modulator protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
DEF6 guanine nucleotide exchange factor c
malonyl CoA:ACP acyltransferase (mitochondrial)
LOW QUALITY PROTEIN: malonyl-CoA-acyl carrier protein transacylase, mitochondrial
tubulin tyrosine ligase-like family, member 1
protein kinase C and casein kinase substrate in neurons 2, transcript variant X1
protein kinase C and casein kinase substrate in neurons 2, transcript variant X3
protein kinase C and casein kinase substrate in neurons 2, transcript variant X2
protein kinase C and casein kinase substrate in neurons 2, transcript variant X4
protein kinase C and casein kinase substrate in neurons protein 2 isoform X1
protein kinase C and casein kinase substrate in neurons protein 2 isoform X3
protein kinase C and casein kinase substrate in neurons protein 2 isoform X2
protein kinase C and casein kinase substrate in neurons protein 2 isoform X4
ADP-ribosylation factor GTPase activating protein 3, transcript variant X2
ADP-ribosylation factor GTPase activating protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ADP-ribosylation factor GTPase-activating protein 3 isoform X2
ADP-ribosylation factor GTPase-activating protein 3 isoform X1
IKBKB interacting protein, transcript variant X2
IKBKB interacting protein, transcript variant X1
inhibitor of nuclear factor kappa-B kinase-interacting protein isoform X2
inhibitor of nuclear factor kappa-B kinase-interacting protein isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: UHRF1-binding protein 1-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
ankyrin repeat and sterile alpha motif domain-containing protein 1B-like
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
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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ankyrin repeat and sterile alpha motif domain-containing protein 1B-like
apoptotic peptidase activating factor 1, transcript variant X2
apoptotic peptidase activating factor 1, transcript variant X1
apoptotic protease-activating factor 1 isoform X2
apoptotic protease-activating factor 1 isoform X1
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase 9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SCY1 like pseudokinase 2, transcript variant X1
SCY1 like pseudokinase 2, transcript variant X2
uncharacterized protein LOC557230 homolog, transcript variant X2
uncharacterized protein LOC557230 homolog, transcript variant X1
uncharacterized protein si:ch211-244b2.3 isoform X2
uncharacterized protein si:ch211-244b2.3 isoform X1
uncharacterized protein LOC541512 homolog
uncharacterized protein si:ch211-244b2.4
uncharacterized protein LOC568385 homolog
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 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: 14 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
B-cell translocation gene 1, anti-proliferative
FAM3 metabolism regulating signaling molecule C
IMP (inosine 5'-monophosphate) dehydrogenase 1b, transcript variant X1
IMP (inosine 5'-monophosphate) dehydrogenase 1b, transcript variant X2
inosine-5'-monophosphate dehydrogenase 1b isoform X1
inosine-5'-monophosphate dehydrogenase 1b isoform X2
proline rich transmembrane protein 4b, transcript variant X3
proline rich transmembrane protein 4b, transcript variant X2
proline rich transmembrane protein 4b, transcript variant X1
staphylococcal nuclease and tudor domain containing 1
staphylococcal nuclease domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
leucine-rich repeat-containing protein 4
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: 13 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, alpha 2/delta subunit 1a, transcript variant X3
calcium channel, voltage-dependent, alpha 2/delta subunit 1a, transcript variant X2
calcium channel, voltage-dependent, alpha 2/delta subunit 1a, transcript variant X1
voltage-dependent calcium channel subunit alpha-2/delta-1a isoform X3
voltage-dependent calcium channel subunit alpha-2/delta-1a isoform X2
voltage-dependent calcium channel subunit alpha-2/delta-1a isoform X1
piccolo presynaptic cytomatrix protein a
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
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3Aa
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
protein arginine N-methyltransferase 8-B
calcium release activated channel regulator 2Ab, transcript variant X2
calcium release activated channel regulator 2Ab, transcript variant X1
EF-hand calcium-binding domain-containing protein 4B isoform X2
EF-hand calcium-binding domain-containing protein 4B isoform X1
calcium release activated channel regulator 2Ab, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
thyroid transcription factor 1-associated protein 26 homolog
methyltransferase like 25, transcript variant X1
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, including 2 samples with support for all annotated introns
methyltransferase like 25, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
methyltransferase-like protein 25 isoform X1
methyltransferase-like protein 25 isoform X2
transmembrane O-mannosyltransferase targeting cadherins 2a
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: 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: protein O-mannosyl-transferase TMTC2
protein mono-ADP-ribosyltransferase PARP11
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
protein mono-ADP-ribosyltransferase PARP11-like
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: 17 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein mono-ADP-ribosyltransferase PARP11-like
sodium- and chloride-dependent GABA transporter 2-like, transcript variant X2
sodium- and chloride-dependent GABA transporter 2-like, transcript variant X3
sodium- and chloride-dependent GABA transporter 2-like, transcript variant X1
sodium- and chloride-dependent GABA transporter 2-like isoform X1
sodium- and chloride-dependent GABA transporter 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
IQ motif and SEC7 domain-containing protein 3-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: IQ motif and SEC7 domain-containing protein 3-like
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1
alpha-N-acetylneuraminide alpha-2,8-sialyltransferase
ATPase plasma membrane Ca2+ transporting 1a, transcript variant X1
ATPase plasma membrane Ca2+ transporting 1a, transcript variant X2
plasma membrane calcium-transporting ATPase 1a isoform X1
plasma membrane calcium-transporting ATPase 1a isoform X2
mesoderm specific transcript, transcript variant X1
mesoderm specific transcript, transcript variant X2
mesoderm-specific transcript homolog 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeats and guanylate kinase domain containing, transcript variant X2
leucine-rich repeats and guanylate kinase domain containing, transcript variant X1
leucine-rich repeat and guanylate kinase domain-containing protein isoform X2
leucine-rich repeat and guanylate kinase domain-containing protein isoform X1
coiled-coil-helix-coiled-coil-helix domain containing 3a
nuclear respiratory factor 1, transcript variant X2
nuclear respiratory factor 1, transcript variant X1
ubiquitin-conjugating enzyme E2H (UBC8 homolog, yeast)
cation/H+ exchanger protein 1, transcript variant X2
cation/H+ exchanger protein 1, transcript variant X1
cation/H+ exchanger protein 1 isoform X2
cation/H+ exchanger protein 1 isoform 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
voltage-dependent L-type calcium channel subunit alpha-1C-like
LOW QUALITY PROTEIN: voltage-dependent L-type calcium channel subunit alpha-1C-like
calcium channel, voltage-dependent, alpha 2/delta subunit 4a
voltage-dependent calcium channel subunit alpha-2/delta-4
leucine-rich repeats and transmembrane domains 2a
leucine-rich repeat and transmembrane domain-containing protein 2
cleavage and polyadenylation specificity factor subunit 6-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; deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cleavage and polyadenylation specificity factor subunit 6-like
N-acyl-phosphatidylethanolamine-hydrolyzing phospholipase D-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 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 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: serine/threonine-protein kinase WNK1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
E3 ubiquitin/ISG15 ligase TRIM25-like, transcript variant X2
E3 ubiquitin/ISG15 ligase TRIM25-like, transcript variant X1
ELKS/Rab6-interacting/CAST family member 1-like, transcript variant X1
ELKS/Rab6-interacting/CAST family member 1-like, transcript variant X2
ELKS/Rab6-interacting/CAST family member 1-like, transcript variant X3
ELKS/Rab6-interacting/CAST family member 1-like, transcript variant X4
ELKS/Rab6-interacting/CAST family member 1-like isoform X1
ELKS/Rab6-interacting/CAST family member 1-like isoform X2
ELKS/Rab6-interacting/CAST family member 1-like isoform X3
ELKS/Rab6-interacting/CAST family member 1-like isoform X4
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
wingless-type MMTV integration site family, member 5b
F-box and leucine-rich repeat protein 14b
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
putative homeodomain transcription factor 2, transcript variant X3
putative homeodomain transcription factor 2, transcript variant X1
putative homeodomain transcription factor 2, 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
putative homeodomain transcription factor 2 isoform X2
putative homeodomain transcription factor 2 isoform X3
putative homeodomain transcription factor 2 isoform X1
transmembrane protein 60-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane protein 60-like, transcript variant X1
transmembrane protein 60-like isoform X1
transmembrane protein 60-like isoform X2
protein tyrosine phosphatase non-receptor type 12, transcript variant X3
protein tyrosine phosphatase non-receptor type 12, transcript variant X1
protein tyrosine phosphatase non-receptor type 12, transcript variant X2
tyrosine-protein phosphatase non-receptor type 12 isoform X3
tyrosine-protein phosphatase non-receptor type 12 isoform X1
tyrosine-protein phosphatase non-receptor type 12 isoform X2
uncharacterized protein LOC503753 homolog, transcript variant X2
uncharacterized protein LOC503753 homolog, transcript variant X1
uncharacterized protein zgc:113263 isoform X2
uncharacterized protein zgc:113263 isoform X1
zinc finger protein 557-like, transcript variant X1
zinc finger protein 557-like, transcript variant X2
zinc finger protein 557-like, transcript variant X3
zinc finger protein 1 homolog isoform X1
uncharacterized protein LOC121961642 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ATP23 metallopeptidase and ATP synthase assembly factor homolog
mitochondrial inner membrane protease ATP23 homolog
leucine-rich repeats and immunoglobulin-like domains 3
leucine-rich repeats and immunoglobulin-like domains protein 3
uncharacterized protein LOC561188 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 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: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: transcription factor ETV6-like
uncharacterized protein LOC553517 homolog, transcript variant X1
uncharacterized protein LOC553517 homolog, transcript variant X2
protein mono-ADP-ribosyltransferase PARP12 isoform X1
protein mono-ADP-ribosyltransferase PARP12 isoform X2
RAS-like, estrogen-regulated, growth inhibitor
ras-related and estrogen-regulated growth inhibitor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100 Proteins
patatin-like phospholipase domain containing 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
calcium-independent phospholipase A2-gamma
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: neuronal cell adhesion molecule a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
PDZ domain-containing RING finger protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger CCHC-type and RNA binding motif 1
zinc finger CCHC-type and RNA-binding motif-containing protein 1
prickle homolog 1b, transcript variant X2
prickle homolog 1b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
pseudouridylate synthase 7 homolog-like protein
leucine-rich repeat-containing protein 17
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
coiled-coil domain-containing protein 146
gamma-secretase activating protein, transcript variant X2
gamma-secretase activating protein, transcript variant X1
gamma-secretase-activating protein isoform X2
gamma-secretase-activating protein isoform X1
nicotinamide phosphoribosyltransferase 1
synaptophysin-like 1, transcript variant X2
synaptophysin-like 1, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger protein 800b
uncharacterized LOC121961083, transcript variant X2
uncharacterized LOC121961083, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 96% 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: 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 88% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
WASP like actin nucleation promoting factor b
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
LOW QUALITY PROTEIN: WASP like actin nucleation promoting factor b
ankyrin repeat and SOCS box containing 15b
uncharacterized protein LOC121961390 isoform X2
high affinity choline transporter 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
nudix (nucleoside diphosphate linked moiety X)-type motif 4b
diphosphoinositol polyphosphate phosphohydrolase NUDT4B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ras association domain-containing protein 8b
peroxisomal N(1)-acetyl-spermine/spermidine oxidase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
FYVE, RhoGEF and PH domain-containing protein 4-like
UTP20 small subunit processome component
small subunit processome component 20 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
sodium-coupled monocarboxylate transporter 1
LYR motif containing 5a, transcript variant X1
LYR motif containing 5a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
lymphoid-restricted membrane protein, transcript variant X3
lymphoid-restricted membrane protein, transcript variant X2
lymphoid-restricted membrane protein, transcript variant X1
inositol 1,4,5-triphosphate receptor associated 2 isoform X3
inositol 1,4,5-triphosphate receptor associated 2 isoform X2
inositol 1,4,5-triphosphate receptor associated 2 isoform X1
branched chain amino-acid transaminase 1, cytosolic
branched-chain-amino-acid aminotransferase, cytosolic
SRY-box transcription factor 5, transcript variant X1
SRY-box transcription factor 5, transcript variant X2
SRY-box transcription factor 5, transcript variant X6
SRY-box transcription factor 5, transcript variant X7
SRY-box transcription factor 5, transcript variant X3
SRY-box transcription factor 5, transcript variant X5
SRY-box transcription factor 5, transcript variant X8
SRY-box transcription factor 5, transcript variant X4
SRY-box transcription factor 5, transcript variant X9
ethanolamine kinase 1, transcript variant X2
ethanolamine kinase 1, transcript variant X1
pyridine nucleotide-disulphide oxidoreductase domain 1, transcript variant X2
pyridine nucleotide-disulphide oxidoreductase domain 1, transcript variant X1
pyridine nucleotide-disulfide oxidoreductase domain-containing protein 1 isoform X2
pyridine nucleotide-disulfide oxidoreductase domain-containing protein 1 isoform X1
pyridine nucleotide-disulphide oxidoreductase domain 1, transcript variant X3
pyridine nucleotide-disulfide oxidoreductase domain-containing protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
solute carrier organic anion transporter family member 1C1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: solute carrier organic anion transporter family member 1C1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 91% 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: 79% coverage of the annotated genomic feature by RNAseq alignments
ATP-binding cassette sub-family D member 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
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: 22 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: kinesin-like protein KIF21A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dol-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-Dol alpha-1,2-glucosyltransferase
tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase
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 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: mitochondrial tRNA-specific 2-thiouridylase 1
cadherin EGF LAG seven-pass G-type receptor 1a
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: cadherin EGF LAG seven-pass G-type receptor 1
GRAM domain containing 4a, transcript variant X1
GRAM domain containing 4a, transcript variant X3
GRAM domain containing 4a, transcript variant X2
GRAM domain containing 4a, transcript variant X4
GRAM domain-containing protein 4 isoform X1
GRAM domain-containing protein 4 isoform X3
GRAM domain-containing protein 4 isoform X2
GRAM domain-containing protein 4 isoform X4
GRAM domain containing 4a, transcript variant X5
GRAM domain-containing protein 4 isoform X5
TBC1 domain family, member 22a, transcript variant X2
TBC1 domain family, member 22a, transcript variant X1
TBC1 domain family member 22A isoform X2
TBC1 domain family member 22A isoform X1
TAFA chemokine like family member 5a, 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
chemokine-like protein TAFA-5a isoform X2
TAFA chemokine like family member 5a, transcript variant X1
chemokine-like protein TAFA-5a isoform X1
bromodomain containing 1a, transcript variant X1
bromodomain containing 1a, transcript variant X2
bromodomain-containing protein 1 isoform X2
bromodomain-containing protein 1 isoform X1
zinc finger BED domain-containing protein 4
dol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase
cysteine-rich with EGF-like domain protein 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: protein phosphatase 1H-like
ubiquitin carboxyl-terminal hydrolase 15-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 15-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 15-like isoform X2
ubiquitin carboxyl-terminal hydrolase 15-like isoform X1
sodium- and chloride-dependent GABA transporter 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 148 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
aldo-keto reductase family 1 member D1-like
tripartite motif containing 24, transcript variant X1
tripartite motif containing 24, transcript variant X3
tripartite motif containing 24, transcript variant X2
tripartite motif containing 24, transcript variant X4
transcription intermediary factor 1-alpha isoform X1
transcription intermediary factor 1-alpha isoform X3
transcription intermediary factor 1-alpha isoform X2
transcription intermediary factor 1-alpha isoform X4
wingless-type MMTV integration site family, member 7Ba
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 109 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
peroxisome proliferator-activated receptor alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 120 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cysteine rich DPF motif domain containing 1
cysteine-rich DPF motif domain-containing protein 1
cyclin-dependent kinase inhibitor 1D, transcript variant X1
cyclin-dependent kinase inhibitor 1D, transcript variant X2
cyclin-dependent kinase inhibitor 1D isoform X1
cyclin-dependent kinase inhibitor 1D isoform X2
suppressor APC domain-containing protein 1
adenosylhomocysteinase like 2b, transcript variant X1
adenosylhomocysteinase like 2b isoform X1
adenosylhomocysteinase like 2b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
adenosylhomocysteinase like 2b isoform X2
striatin interacting protein 2, transcript variant X1
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, including 2 samples with support for all annotated introns
striatin interacting protein 2, transcript variant X2
striatin interacting protein 2, transcript variant X3
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
striatin-interacting protein 1 homolog isoform X1
striatin-interacting protein 1 homolog isoform X2
striatin-interacting protein 1 homolog isoform X3
MORN repeat containing 2, transcript variant X2
MORN repeat containing 2, 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
MORN repeat-containing protein 2 isoform X1
MORN repeat-containing protein 2 isoform X2
DEAH (Asp-Glu-Ala-Asp/His) box polypeptide 57, transcript variant X2
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, including 1 sample with support for all annotated introns
DEAH (Asp-Glu-Ala-Asp/His) box polypeptide 57, transcript variant X1
putative ATP-dependent RNA helicase DHX57
dynamin-1-like protein, transcript variant X1
dynamin-1-like protein, transcript variant X2
dynamin-1-like protein, transcript variant X3
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 2 samples with support for all annotated introns
dynamin-1-like protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dedicator of cytokinesis 4b, transcript variant X3
dedicator of cytokinesis 4b, transcript variant X4
dedicator of cytokinesis 4b, transcript variant X1
dedicator of cytokinesis 4b, transcript variant X2
dedicator of cytokinesis protein 4b isoform X3
dedicator of cytokinesis protein 4b isoform X4
dedicator of cytokinesis protein 4b isoform X2
dedicator of cytokinesis protein 4b isoform X1
interferon-related developmental regulator 1
G protein-coupled receptor 85, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
G protein-coupled receptor 85, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
G protein-coupled receptor 85, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
G protein-coupled receptor 85, transcript variant X3
protein phosphatase 1, regulatory subunit 3Aa
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
myoD family inhibitor domain-containing protein
transcription factor EC, transcript variant X3
transcription factor EC, transcript variant X2
transcription factor EC, transcript variant X1
transcription factor EC, transcript variant X6
transcription factor EC, transcript variant X5
transcription factor EC, transcript variant X4
transcription factor EC, transcript variant X7
aldo-keto reductase family 1 member B1-like
aldo-keto reductase family 1 member B15-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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 2 bases in 1 codon; 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, including 1 sample with support for all annotated introns
centrosomal protein 83, transcript variant X1
centrosomal protein 83, transcript variant X3
centrosomal protein 83, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
upper zone of growth plate and cartilage matrix associated a
minichromosome maintenance 10 replication initiation factor, transcript variant X2
minichromosome maintenance 10 replication initiation factor, transcript variant X1
coiled-coil domain-containing protein 3a
calcium/calmodulin-dependent protein kinase 1Da
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: calcium/calmodulin-dependent protein kinase type 1D
cell division cycle 123 homolog (S. cerevisiae)
nudix (nucleoside diphosphate linked moiety X)-type motif 5, transcript variant X2
nudix (nucleoside diphosphate linked moiety X)-type motif 5, transcript variant X1
F-box DNA helicase 1, transcript variant X1
F-box DNA helicase 1, transcript variant X2
interleukin 15 receptor subunit alpha, transcript variant X3
interleukin 15 receptor subunit alpha, transcript variant X1
interleukin 15 receptor subunit alpha, transcript variant X2
interleukin 15 receptor subunit alpha, transcript variant X4
interleukin-15 receptor subunit alpha isoform X4
interleukin-15 receptor subunit alpha isoform X3
interleukin-15 receptor subunit alpha isoform X2
interleukin-15 receptor subunit alpha isoform X1
RNA binding motif protein 17, transcript variant X2
RNA binding motif protein 17, transcript variant X3
RNA binding motif protein 17, transcript variant X4
RNA binding motif protein 17, transcript variant X1
6-phosphofructo-2-kinase/fructose-2, 6-biphosphatase 3, transcript variant X1
6-phosphofructo-2-kinase/fructose-2, 6-biphosphatase 3, transcript variant X3
6-phosphofructo-2-kinase/fructose-2, 6-biphosphatase 3, transcript variant X2
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 3 isoform X2
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 3 isoform X1
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 3 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform-like
LOW QUALITY PROTEIN: phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform-like
HMG box-containing protein 1-like, transcript variant X3
HMG box-containing protein 1-like, transcript variant X1
HMG box-containing protein 1-like, transcript variant X2
HMG box-containing protein 1-like isoform X1
HMG box-containing protein 1-like isoform X2
HMG box-containing protein 1-like isoform X3
protein tyrosine phosphatase receptor type Z1b
receptor-type tyrosine-protein phosphatase zeta
cytochrome c oxidase assembly factor 6 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC793007 homolog
aryl hydrocarbon receptor nuclear translocator-like protein 2, transcript variant X4
aryl hydrocarbon receptor nuclear translocator-like protein 2, transcript variant X3
aryl hydrocarbon receptor nuclear translocator-like protein 2, transcript variant X2
aryl hydrocarbon receptor nuclear translocator-like protein 2, transcript variant X1
aryl hydrocarbon receptor nuclear translocator-like protein 2 isoform X4
aryl hydrocarbon receptor nuclear translocator-like protein 2 isoform X3
aryl hydrocarbon receptor nuclear translocator-like protein 2 isoform X2
aryl hydrocarbon receptor nuclear translocator-like protein 2 isoform X1
mediator of RNA polymerase II transcription subunit 21
FGFR1 oncogene partner 2, transcript variant X2
FGFR1 oncogene partner 2 homolog isoform X2
FGFR1 oncogene partner 2, transcript variant X1
FGFR1 oncogene partner 2 homolog isoform X1
growth arrest-specific 2 like 3, transcript variant X1
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, including 2 samples with support for all annotated introns
growth arrest-specific 2 like 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: transmembrane 7 superfamily member 3
AT rich interactive domain 2 (ARID, RFX-like)
AT-rich interactive domain-containing protein 2
SR-related CTD-associated factor 11, transcript variant X1
SR-related CTD-associated factor 11, transcript variant X2
sodium-coupled neutral amino acid transporter 2
sodium-coupled neutral amino acid transporter 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NXPE family member 3-like, transcript variant X2
NXPE family member 3-like, transcript variant X1
NXPE family member 3-like, transcript variant X3
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 3 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 64% coverage of the annotated genomic feature by RNAseq alignments
APEX nuclease (multifunctional DNA repair enzyme) 1, transcript variant X2
DNA-(apurinic or apyrimidinic site) endonuclease isoform X2
APEX nuclease (multifunctional DNA repair enzyme) 1, transcript variant X1
DNA-(apurinic or apyrimidinic site) endonuclease isoform X1
probable tRNA N6-adenosine threonylcarbamoyltransferase
uncharacterized protein LOC558894 homolog
uncharacterized protein si:ch211-214j24.10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
cysteine and glycine-rich protein 2, transcript variant X2
cysteine and glycine-rich protein 2, transcript variant X3
cysteine and glycine-rich protein 2, transcript variant X1
zinc finger DHHC-type palmitoyltransferase 17
oxysterol binding protein-like 8, transcript variant X1
oxysterol binding protein-like 8, transcript variant X3
oxysterol binding protein-like 8, transcript variant X2
oxysterol binding protein-like 8, transcript variant X6
oxysterol-binding protein-related protein 8 isoform X1
oxysterol-binding protein-related protein 8 isoform X2
oxysterol binding protein-like 8, transcript variant X5
oxysterol binding protein-like 8, transcript variant X8
oxysterol binding protein-like 8, transcript variant X7
oxysterol-binding protein-related protein 8 isoform X4
oxysterol binding protein-like 8, transcript variant X9
oxysterol binding protein-like 8, transcript variant X4
oxysterol-binding protein-related protein 8 isoform X3
oxysterol-binding protein-related protein 8 isoform X5
nucleosome assembly protein 1-like 1, transcript variant X3
nucleosome assembly protein 1-like 1, transcript variant X1
nucleosome assembly protein 1-like 1, transcript variant X2
nucleosome assembly protein 1-like 1 isoform X1
nucleosome assembly protein 1-like 1 isoform X2
nucleosome assembly protein 1-like 1 isoform X3
pleckstrin homology-like domain, family A, member 1, transcript variant X3
pleckstrin homology-like domain, family A, member 1, transcript variant X2
pleckstrin homology-like domain, family A, member 1, transcript variant X1
pleckstrin homology-like domain family A member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 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: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
KRR1 small subunit processome component homolog
cytidine monophospho-N-acetylneuraminic acid hydroxylase
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 71% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: cytidine monophosphate-N-acetylneuraminic acid hydroxylase
coiled-coil domain containing 107, transcript variant X1
coiled-coil domain containing 107, transcript variant X2
coiled-coil domain-containing protein 107 isoform X1
coiled-coil domain-containing protein 107 isoform X2
potassium voltage-gated channel, Shaw-related subfamily, member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
potassium voltage-gated channel, Shaw-related subfamily, member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
potassium voltage-gated channel, Shaw-related subfamily, member 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
potassium voltage-gated channel subfamily C member 2 isoform X2
potassium voltage-gated channel subfamily C member 2 isoform X1
phosphorylated adaptor for RNA export, transcript variant X1
phosphorylated adaptor for RNA export, transcript variant X2
phosphorylated adapter RNA export protein
mitochondrial-processing peptidase subunit beta-like
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, including 3 samples with support for all annotated introns
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, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 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: 15 Proteins
Cbl proto-oncogene-like 1, E3 ubiquitin protein ligase, transcript variant X2
Cbl proto-oncogene-like 1, E3 ubiquitin protein ligase, transcript variant X3
Cbl proto-oncogene-like 1, E3 ubiquitin protein ligase, transcript variant X1
E3 ubiquitin-protein ligase Hakai isoform X2
E3 ubiquitin-protein ligase Hakai isoform X3
E3 ubiquitin-protein ligase Hakai isoform X1
protein phosphatase 6, regulatory subunit 2a, transcript variant X1
protein phosphatase 6, regulatory subunit 2a, transcript variant X2
serine/threonine-protein phosphatase 6 regulatory subunit 2a isoform X1
serine/threonine-protein phosphatase 6 regulatory subunit 2a isoform X2
SET binding factor 1, transcript variant X4
SET binding factor 1, transcript variant X2
SET binding factor 1, transcript variant X3
SET binding factor 1, transcript variant X1
myotubularin-related protein 5 isoform X4
myotubularin-related protein 5 isoform X2
myotubularin-related protein 5 isoform X3
myotubularin-related protein 5 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glycosyltransferase 8 domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
glycosyltransferase 8 domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ankyrin repeat domain-containing protein 16
rab GDP dissociation inhibitor beta-like
ankyrin repeat and SOCS box containing 13a, tandem duplicate 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and SOCS box protein 13a.1
ankyrin repeat and SOCS box protein 13-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
neuroepithelial cell transforming 1, transcript variant X1
neuroepithelial cell transforming 1, transcript variant X2
neuroepithelial cell-transforming gene 1 protein isoform X1
neuroepithelial cell-transforming gene 1 protein isoform X2
RecQ helicase-like, transcript variant X1
ATP-dependent DNA helicase Q1 isoform X1
RecQ helicase-like, transcript variant X3
ATP-dependent DNA helicase Q1 isoform X3
RecQ helicase-like, transcript variant X2
ATP-dependent DNA helicase Q1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
lactate dehydrogenase Ba, transcript variant X1
lactate dehydrogenase Ba, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 3 bases in 2 codons
LOW QUALITY PROTEIN: solute carrier family 25 member 3a
COORDINATES: nucleotide motif:Rfam:12.0:RF00563
serine/threonine kinase receptor associated protein
serine-threonine kinase receptor-associated protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
LARGE xylosyl- and glucuronyltransferase 1, transcript variant X2
LARGE xylosyl- and glucuronyltransferase 1, transcript variant X1
LARGE xylosyl- and glucuronyltransferase 1
B-Raf proto-oncogene, serine/threonine kinase, transcript variant X4
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 3 samples with support for all annotated introns
B-Raf proto-oncogene, serine/threonine kinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
B-Raf proto-oncogene, serine/threonine kinase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
B-Raf proto-oncogene, serine/threonine kinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine-protein kinase B-raf isoform X4
serine/threonine-protein kinase B-raf isoform X2
serine/threonine-protein kinase B-raf isoform X3
serine/threonine-protein kinase B-raf isoform X1
28S ribosomal protein S33, mitochondrial
CCR4-NOT transcription complex, subunit 4b
CCR4-NOT transcription complex subunit 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
makorin, ring finger protein, 1, transcript variant X1
makorin, ring finger protein, 1, transcript variant X2
probable E3 ubiquitin-protein ligase makorin-1 isoform X1
probable E3 ubiquitin-protein ligase makorin-1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
interleukin 17 receptor A1a, transcript variant X2
interleukin 17 receptor A1a, transcript variant X1
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: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: ras-related and estrogen-regulated growth inhibitor-like protein
Rho guanine nucleotide exchange factor (GEF) 39, transcript variant X2
Rho guanine nucleotide exchange factor (GEF) 39, transcript variant X1
rho guanine nucleotide exchange factor 39 isoform X2
rho guanine nucleotide exchange factor 39 isoform X1
LIM domain only 3, transcript variant X1
LIM domain only 3, transcript variant X2
LIM domain only 3, transcript variant X3
LIM domain only 3, transcript variant X4
microsomal glutathione S-transferase 1-like
deoxyribose-phosphate aldolase (putative)
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
methionine sulfoxide reductase B3, transcript variant X2
methionine sulfoxide reductase B3, transcript variant X1
methionine sulfoxide reductase B3, transcript variant X3
methionine-R-sulfoxide reductase B3 isoform X1
methionine-R-sulfoxide reductase B3 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 3 bases in 2 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: inner nuclear membrane protein Man1
transmembrane BAX inhibitor motif containing 4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: beta-2-microglobulin-like
interleukin-1 receptor-associated kinase 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: heat shock 70 kDa protein 14-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 72% 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: 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: RAD50-interacting protein 1-like
DENN domain-containing protein 5B-like, transcript variant X6
DENN domain-containing protein 5B-like, transcript variant X3
DENN domain-containing protein 5B-like, transcript variant X5
DENN domain-containing protein 5B-like, transcript variant X4
DENN domain-containing protein 5B-like, transcript variant X2
DENN domain-containing protein 5B-like, transcript variant X1
DENN domain-containing protein 5B-like isoform X6
DENN domain-containing protein 5B-like isoform X3
DENN domain-containing protein 5B-like isoform X5
DENN domain-containing protein 5B-like isoform X4
DENN domain-containing protein 5B-like isoform X2
DENN domain-containing protein 5B-like isoform X1
uncharacterized LOC121961207, transcript variant X6
uncharacterized LOC121961207, transcript variant X4
uncharacterized LOC121961207, transcript variant X2
uncharacterized LOC121961207, transcript variant X3
uncharacterized LOC121961207, transcript variant X5
uncharacterized LOC121961207, transcript variant X7
uncharacterized LOC121961207, transcript variant X1
uncharacterized protein LOC121961207 isoform X4
uncharacterized protein LOC121961207 isoform X3
uncharacterized protein LOC121961207 isoform X2
uncharacterized protein LOC121961207 isoform X1
uncharacterized protein LOC121961207 isoform X5
tubulin tyrosine ligase-like family, member 12
tubulin--tyrosine ligase-like protein 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
patatin-like phospholipase domain containing 3
LOW QUALITY PROTEIN: patatin-like phospholipase domain containing 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 62% coverage of the annotated genomic feature by RNAseq alignments
EF-hand calcium-binding domain-containing protein 6
metallophosphoesterase domain containing 1, transcript variant X1
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
metallophosphoesterase domain containing 1, transcript variant X2
metallophosphoesterase domain-containing protein 1
signal peptide, CUB domain, EGF-like 1, transcript variant X2
signal peptide, CUB domain, EGF-like 1, transcript variant X1
signal peptide, CUB and EGF-like domain-containing protein 1 isoform X2
signal peptide, CUB and EGF-like domain-containing protein 1 isoform X1
sorting and assembly machinery component 50 homolog, like
sorting and assembly machinery component 50 homolog B
aldehyde dehydrogenase 1 family, member L2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: mitochondrial 10-formyltetrahydrofolate dehydrogenase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
deleted in malignant brain tumors 1 protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 69% coverage of the annotated genomic feature by RNAseq alignments
caprin family member 2, transcript variant X1
caprin family member 2, transcript variant X2
transmembrane O-mannosyltransferase targeting cadherins 1
conserved oligomeric Golgi complex subunit 5-like
LOW QUALITY PROTEIN: conserved oligomeric Golgi complex subunit 5-like
NADH:ubiquinone oxidoreductase subunit A5
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 5
pleckstrin homology domain-containing family A member 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
muskelin 1, intracellular mediator containing kelch motifs, transcript variant X1
muskelin 1, intracellular mediator containing kelch motifs, transcript variant X2
nuclear transcription factor Y, beta a, transcript variant X1
nuclear transcription factor Y, beta a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 33% coverage of the annotated genomic feature by RNAseq alignments
carbohydrate (chondroitin 4) sulfotransferase 11
solute carrier family 41 member 2b, transcript variant X2
solute carrier family 41 member 2b, transcript variant X1
uncharacterized protein C12orf45 homolog