Electrophorus electricus isolate fEleEle1 chromosome 25, fEleEle1.pri, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Ostariophysi; Gymnotiformes; Gymnotoidei; Gymnotidae; Electrophorus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM023704.1.\nAssembly name: fEleEle1.pri\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Vertebrate Genomes Project on\n2020/06/23. The original whole-genome shotgun project has the\naccession JABVME000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Vertebrate Genomes Project\nAssembly Date :: 17-MAR-2020\nAssembly Method :: FALCON v. 2018.31.08-03.06; FALCON-Unzip\n v. 7.0.1.66975; purge_dups v. v1;\n scaff10x v. 4.1.0; Bionano Solve DLS v.\n 3.4; Salsa HiC v. 2.2; Arrow smrtanalysis\n Pacbio polishing & gap filling v.\n SMRTLink7.0.1; longranger align v. 2.2.2;\n freebayes Illumina polishing v. 1.3.1;\n gEVAL manual curation v. 2020-03-17; VGP\n assembly pipeline individual v. 1.6\nAssembly Name :: fEleEle1.pri\nDiploid :: Principal pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 52.97x\nSequencing Technology :: PacBio Sequel I CLR; llumina NovaSeq;\n Arima Genomics Hi-C; Bionano Genomics DLS\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Electrophorus electricus Annotation\n Release 101\nAnnotation Version :: 101\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.5\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Netherlands: Dejong Marinelife, Rotterdam
Derived by automated computational analysis using gene prediction method: Gnomon.
cytochrome P450 2K1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 142 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cytochrome P450 2K1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ankyrin repeat and SOCS box protein 9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
motile sperm domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC113569371, 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 1 sample with support for all annotated introns
uncharacterized LOC113569371, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
motile sperm 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 8 samples with support for all annotated introns
FA complementation group B, 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 8 samples with support for all annotated introns
FA complementation group B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Fanconi anemia group B protein isoform X1
Fanconi anemia group B protein isoform X2
glycine receptor, alpha 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glycine receptor, alpha 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glycine receptor subunit alpha-2 isoform X2
glycine receptor subunit alpha-2 isoform X1
glycoprotein M6Bb, transcript variant X1
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 9 samples with support for all annotated introns
glycoprotein M6Bb, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
OFD1 centriole and centriolar satellite protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
OFD1 centriole and centriolar satellite protein, transcript variant X1
oral-facial-digital syndrome 1 protein homolog isoform X1
oral-facial-digital syndrome 1 protein homolog isoform X2
OFD1 centriole and centriolar satellite protein, 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 3 samples with support for all annotated introns
oral-facial-digital syndrome 1 protein homolog isoform X3
trafficking protein particle complex 2, transcript variant X3
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 9 samples with support for all annotated introns
trafficking protein particle complex 2, transcript variant X1
trafficking protein particle complex 2, transcript variant X2
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 10 samples with support for all annotated introns
trafficking protein particle complex subunit 2
RAB9A, member RAS oncogene family, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
RAB9A, member RAS oncogene family, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
EGF-like-domain, multiple 6, 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 7 samples with support for all annotated introns
EGF-like-domain, multiple 6, 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
EGF-like-domain, multiple 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
epidermal growth factor-like protein 6 isoform X2
epidermal growth factor-like protein 6 isoform X1
epidermal growth factor-like protein 6 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 11 samples with support for all annotated introns
toll-like receptor 8, transcript variant X4
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
toll-like receptor 8, transcript variant X5
toll-like receptor 8, transcript variant X2
toll-like receptor 8, transcript variant X3
toll-like receptor 8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
FERM and PDZ domain containing 4, 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 2 samples with support for all annotated introns
FERM and PDZ domain containing 4, transcript variant X2
FERM and PDZ domain containing 4, transcript variant X3
FERM and PDZ domain-containing protein 4 isoform X2
FERM and PDZ domain-containing protein 4 isoform X1
FERM and PDZ domain-containing protein 4 isoform X3
rho GTPase-activating protein 6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rho GTPase-activating protein 6-like isoform X1
rho GTPase-activating protein 6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rho GTPase-activating protein 6-like isoform X2
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: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 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: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
E3 ubiquitin-protein ligase Midline-1 isoform X1
E3 ubiquitin-protein ligase Midline-1 isoform X2
component of oligomeric golgi complex 3, 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 8 samples with support for all annotated introns
component of oligomeric golgi complex 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
conserved oligomeric Golgi complex subunit 3 isoform X1
conserved oligomeric Golgi complex subunit 3 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 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, 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; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: endothelin receptor type B
protocadherin-8-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protocadherin-8-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 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: 132 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: 19 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
ribulose-5-phosphate-3-epimerase, 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 8 samples with support for all annotated introns
ribulose-5-phosphate-3-epimerase, transcript variant X1
T-cell surface antigen CD2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
T-cell surface antigen CD2-like, transcript variant X2
T-cell surface antigen CD2-like isoform X1
T-cell surface antigen CD2-like isoform X2
prostaglandin F2 receptor negative regulator-like
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 8 samples with support for all annotated introns
immunoglobulin superfamily member 3, transcript variant X1
immunoglobulin superfamily member 3, 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
immunoglobulin superfamily member 3 isoform X1
immunoglobulin superfamily member 3 isoform 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 5 samples with support for all annotated introns
transcription termination factor, RNA polymerase II, 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 8 samples with support for all annotated introns
transcription termination factor, RNA polymerase II, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transcription termination factor, RNA polymerase II, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transcription termination factor, RNA polymerase II, transcript variant X4
transcription termination factor, RNA polymerase II, transcript variant X5
transcription termination factor, RNA polymerase II, transcript variant X7
transcription termination factor, RNA polymerase II, transcript variant X6
transcription termination factor 2 isoform X1
transcription termination factor 2 isoform X3
transcription termination factor 2 isoform X2
transcription termination factor 2 isoform X4
transcription termination factor 2 isoform X6
transcription termination factor 2 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 6 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 6 bases in 3 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transcription factor CP2-like protein 1
cytoplasmic linker associated protein 1a, 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
cytoplasmic linker associated protein 1a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
cytoplasmic linker associated protein 1a, transcript variant X8
cytoplasmic linker associated protein 1a, transcript variant X3
cytoplasmic linker associated protein 1a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cytoplasmic linker associated protein 1a, transcript variant X7
cytoplasmic linker associated protein 1a, transcript variant X6
cytoplasmic linker associated protein 1a, transcript variant X1
cytoplasmic linker associated protein 1a, transcript variant X10
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
cytoplasmic linker associated protein 1a, transcript variant X9
nucleolar protein interacting with the FHA domain of MKI67
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 9 samples with support for all annotated introns
MKI67 FHA domain-interacting nucleolar phosphoprotein
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF01225
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A
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; deleted 1 base in 1 codon; 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
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; deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A
calcium channel, voltage-dependent, beta 4a subunit, transcript variant X1
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 4 samples with support for all annotated introns
calcium channel, voltage-dependent, beta 4a subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 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, beta 4a subunit, transcript variant X3
voltage-dependent L-type calcium channel subunit beta-4a isoform X1
voltage-dependent L-type calcium channel subunit beta-4a isoform X2
voltage-dependent L-type calcium channel subunit beta-4a isoform X3
signal transducing adaptor molecule (SH3 domain and ITAM motif) 2
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 8 samples with support for all annotated introns
3-hydroxyacyl-CoA dehydratase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
3-hydroxyacyl-CoA dehydratase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 2 isoform X1
very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 2 isoform X2
adenylate cyclase 5, transcript variant X1
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 7 samples with support for all annotated introns
adenylate cyclase 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
adenylate cyclase 5, transcript variant X3
adenylate cyclase 5, transcript variant X4
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
SEC22 homolog A, vesicle trafficking protein
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 10 samples with support for all annotated introns
protein disulfide isomerase family A, member 5, 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 8 samples with support for all annotated introns
protein disulfide isomerase family A, member 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein disulfide-isomerase A5 isoform X1
protein disulfide-isomerase A5 isoform X2
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5Ba, transcript variant X3
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 2 samples with support for all annotated introns
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5Ba, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5Ba, transcript variant X8
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 7 samples with support for all annotated introns
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5Ba, transcript variant X10
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5Ba, transcript variant X6
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
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5Ba, transcript variant X7
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 7 samples with support for all annotated introns
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5Ba, transcript variant X2
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5Ba, 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 4 samples with support for all annotated introns
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5Ba, transcript variant X5
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5Ba, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
solute carrier family 49 member 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
solute carrier family 49 member 4, transcript variant X1
solute carrier family 49 member 4 isoform X2
solute carrier family 49 member 4 isoform X1
hspb associated protein 1, transcript variant X5
hspb associated protein 1, transcript variant X1
hspb associated protein 1, transcript variant X3
hspb associated protein 1, transcript variant X2
hspb associated protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
HSPB1-associated protein 1 homolog isoform X1
HSPB1-associated protein 1 homolog isoform X2
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 8 samples with support for all annotated introns
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 8 samples with support for all annotated introns
ELL associated factor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ELL associated factor 2, transcript variant X1
NAD(P)HX dehydratase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
NAD(P)HX dehydratase, transcript variant X3
NAD(P)HX dehydratase, transcript variant X1
ATP-dependent (S)-NAD(P)H-hydrate dehydratase isoform X3
ATP-dependent (S)-NAD(P)H-hydrate dehydratase isoform X2
ATP-dependent (S)-NAD(P)H-hydrate dehydratase isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
collagen, type IV, alpha 2, transcript variant 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 6 samples with support for all annotated introns
collagen, type IV, alpha 2, transcript variant X4
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 7 samples with support for all annotated introns
collagen, type IV, alpha 2, transcript variant X1
collagen, type IV, alpha 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; 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 8 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: insulin receptor substrate 2
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 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 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TNF superfamily member 13b, 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 7 samples with support for all annotated introns
TNF superfamily member 13b, transcript variant X2
TNF superfamily member 13b, transcript variant X5
TNF superfamily member 13b, transcript variant X3
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 8 samples with support for all annotated introns
tumor necrosis factor ligand superfamily member 13B isoform X4
tumor necrosis factor ligand superfamily member 13B isoform X2
tumor necrosis factor ligand superfamily member 13B isoform X1
TNF superfamily member 13b, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
tumor necrosis factor ligand superfamily member 13B isoform X3
TNF superfamily member 13b, transcript variant X6
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
abhydrolase domain containing 13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
abhydrolase domain containing 13, transcript variant X3
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 6 samples with support for all annotated introns
abhydrolase domain containing 13, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
abhydrolase domain containing 13, 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 4 samples with support for all annotated introns
abhydrolase domain containing 13, transcript variant X4
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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: 25 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: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Na(+)/H(+) exchange regulatory cofactor NHE-RF3
ST6 beta-galactosamide alpha-2,6-sialyltranferase 2a, transcript variant X7
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 4 samples with support for all annotated introns
ST6 beta-galactosamide alpha-2,6-sialyltranferase 2a, transcript variant X9
ST6 beta-galactosamide alpha-2,6-sialyltranferase 2a, 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 8 samples with support for all annotated introns
ST6 beta-galactosamide alpha-2,6-sialyltranferase 2a, transcript variant X1
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
ST6 beta-galactosamide alpha-2,6-sialyltranferase 2a, transcript variant X2
ST6 beta-galactosamide alpha-2,6-sialyltranferase 2a, 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
beta-galactoside alpha-2,6-sialyltransferase 2 isoform X2
beta-galactoside alpha-2,6-sialyltransferase 2 isoform X1
ST6 beta-galactosamide alpha-2,6-sialyltranferase 2a, transcript variant X6
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
ST6 beta-galactosamide alpha-2,6-sialyltranferase 2a, transcript variant X8
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 5 samples with support for all annotated introns
ST6 beta-galactosamide alpha-2,6-sialyltranferase 2a, transcript variant X10
ST6 beta-galactosamide alpha-2,6-sialyltranferase 2a, transcript variant X5
beta-galactoside alpha-2,6-sialyltransferase 2 isoform X3
teleost multiple tissue opsin 2b, transcript variant X1
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 5 samples with support for all annotated introns
teleost multiple tissue opsin 2b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
teleost multiple tissue opsin 2b isoform X2
teleost multiple tissue opsin 2b isoform X1
teleost multiple tissue opsin 2b, transcript variant X3
teleost multiple tissue opsin 2b isoform X3
UDP-glucuronate decarboxylase 1, transcript variant X4
UDP-glucuronate decarboxylase 1, transcript variant X1
UDP-glucuronate decarboxylase 1, transcript variant X3
UDP-glucuronate decarboxylase 1, transcript variant X2
UDP-glucuronic acid decarboxylase 1 isoform X1
UDP-glucuronic acid decarboxylase 1 isoform 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 10 samples with support for all annotated introns
NCK adaptor protein 2a, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NCK adaptor protein 2a, transcript variant X8
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
NCK adaptor protein 2a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
NCK adaptor protein 2a, transcript variant X1
NCK adaptor protein 2a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
NCK adaptor protein 2a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
NCK adaptor protein 2a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
NCK adaptor protein 2a, transcript variant X7
four and a half LIM domains 2a, transcript variant X5
four and a half LIM domains 2a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
four and a half LIM domains 2a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
four and a half LIM domains 2a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
four and a half LIM domains 2a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
four and a half LIM domains protein 2a isoform X1
four and a half LIM domains protein 2a isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
POU class 3 homeobox 3a, transcript variant X2
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 3 samples with support for all annotated introns
POU class 3 homeobox 3a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
POU domain, class 3, transcription factor 3-A isoform X2
POU domain, class 3, transcription factor 3-A isoform X1
major facilitator superfamily domain containing 9, transcript variant X2
major facilitator superfamily domain containing 9, transcript variant X1
major facilitator superfamily domain containing 9, transcript variant X4
major facilitator superfamily domain containing 9, transcript variant X3
major facilitator superfamily domain-containing protein 9
solute carrier family 9 member 2, transcript variant X1
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 1 sample with support for all annotated introns
solute carrier family 9 member 2, transcript variant X2
inositol polyphosphate-4-phosphatase type I Aa, 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
inositol polyphosphate-4-phosphatase type I Aa, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
inositol polyphosphate-4-phosphatase type I Aa, transcript variant X3
inositol polyphosphate-4-phosphatase type I Aa, transcript variant X4
inositol polyphosphate-4-phosphatase type I A isoform X1
inositol polyphosphate-4-phosphatase type I A isoform X2
inositol polyphosphate-4-phosphatase type I A isoform X4
inositol polyphosphate-4-phosphatase type I A isoform X3
uncharacterized protein LOC402865 homolog
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; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 48% 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; deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: pyrimidine-specific ribonucleoside hydrolase RihA
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 11 samples with support for all annotated introns
alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
nascent polypeptide-associated complex subunit alpha, muscle-specific form
MIT, microtubule interacting and transport, domain containing 1, transcript variant X1
MIT, microtubule interacting and transport, domain containing 1, transcript variant X2
MIT, microtubule interacting and transport, domain containing 1, transcript variant X3
MIT, microtubule interacting and transport, domain containing 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
MIT, microtubule interacting and transport, domain containing 1, transcript variant X5
MIT domain-containing protein 1 isoform X2
MIT domain-containing protein 1 isoform X1
MIT domain-containing protein 1 isoform 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 11 samples with support for all annotated introns
39S ribosomal protein L30, mitochondrial
thioredoxin domain containing 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
thioredoxin domain containing 9, transcript variant X2
REV1 DNA directed polymerase, transcript variant X1
REV1 DNA directed polymerase, transcript variant X3
REV1 DNA directed polymerase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
REV1 DNA directed polymerase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 147 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor (GEF) 7a, transcript variant X1
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, including 5 samples with support for all annotated introns
Rho guanine nucleotide exchange factor (GEF) 7a, transcript variant X4
Rho guanine nucleotide exchange factor (GEF) 7a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
rho guanine nucleotide exchange factor 7a isoform X4
rho guanine nucleotide exchange factor 7a isoform X3
rho guanine nucleotide exchange factor 7a isoform X1
Rho guanine nucleotide exchange factor (GEF) 7a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Rho guanine nucleotide exchange factor (GEF) 7a, transcript variant X5
rho guanine nucleotide exchange factor 7a isoform X5
rho guanine nucleotide exchange factor 7a isoform X2
AF4/FMR2 family, member 3, transcript variant X1
AF4/FMR2 family, member 3, transcript variant X5
AF4/FMR2 family, member 3, transcript variant X3
AF4/FMR2 family, member 3, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
AF4/FMR2 family, member 3, transcript variant X4
AF4/FMR2 family, member 3, transcript variant X2
AF4/FMR2 family, member 3, transcript variant X6
serine/arginine repetitive matrix protein 1 isoform X3
M-phase phosphoprotein 8, transcript variant X1
M-phase phosphoprotein 8, transcript variant X2
zinc finger, MYM-type 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger, MYM-type 2, transcript variant X1
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 8 samples with support for all annotated introns
zinc finger, MYM-type 2, transcript variant X3
zinc finger MYM-type protein 2 isoform X1
zinc finger MYM-type protein 2 isoform X3
zinc finger, MYM-type 2, transcript variant X7
zinc finger, MYM-type 2, transcript variant X8
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
zinc finger, MYM-type 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger, MYM-type 2, 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 7 samples with support for all annotated introns
zinc finger, MYM-type 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger MYM-type protein 2 isoform X2
zinc finger MYM-type protein 2 isoform X4
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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: gap junction alpha-3 protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
intraflagellar transport 88 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
intraflagellar transport 88 homolog, transcript variant X2
intraflagellar transport 88 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
intraflagellar transport protein 88 homolog isoform X1
intraflagellar transport protein 88 homolog isoform X2
intraflagellar transport protein 88 homolog isoform X3
uncharacterized LOC113588654, transcript variant X2
uncharacterized LOC113588654, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
histone deacetylase complex subunit SAP18
spindle and kinetochore associated complex subunit 3
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
spindle and kinetochore-associated protein 3
hyperpolarization activated cyclic nucleotide-gated potassium channel 5
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1
uncharacterized LOC118240788, transcript variant X1
uncharacterized LOC118240788, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1-like, transcript variant X4
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1-like isoform X4
uncharacterized LOC118240789, transcript variant X1
uncharacterized LOC118240789, transcript variant X2
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1-like, transcript variant X2
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1-like, transcript variant X1
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1-like isoform X2
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1-like isoform X1
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1-like, transcript variant X3
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1-like isoform X3
poly (ADP-ribose) polymerase family, member 4, transcript variant X2
poly (ADP-ribose) polymerase family, member 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
poly (ADP-ribose) polymerase family, member 4, transcript variant X1
poly (ADP-ribose) polymerase family, member 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
poly (ADP-ribose) polymerase family, member 4, transcript variant X5
poly (ADP-ribose) polymerase family, member 4, transcript variant X6
protein mono-ADP-ribosyltransferase PARP4 isoform X1
protein mono-ADP-ribosyltransferase PARP4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
V-set domain containing T cell activation inhibitor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
V-set domain-containing T-cell activation inhibitor 1
tripartite motif containing 45, transcript variant X2
tripartite motif containing 45, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
tripartite motif-containing protein 45 isoform X2
tripartite motif-containing protein 45 isoform X1
mannosidase, alpha, class 1A, member 2, transcript variant X3
mannosidase, alpha, class 1A, member 2, transcript variant X1
mannosidase, alpha, class 1A, member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mannosyl-oligosaccharide 1,2-alpha-mannosidase IB isoform X2
mannosyl-oligosaccharide 1,2-alpha-mannosidase IB isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ganglioside induced differentiation associated protein 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 8 samples with support for all annotated introns
ganglioside induced differentiation associated protein 2, transcript variant X1
ganglioside-induced differentiation-associated protein 2
WD repeat domain 3, transcript variant X1
WD repeat domain 3, transcript variant X2
WD repeat domain 3, transcript variant X3
WD repeat-containing protein 3 isoform X1
WD repeat-containing protein 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
tryptophanyl tRNA synthetase 2, mitochondrial, transcript variant X2
tryptophanyl tRNA synthetase 2, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
tryptophan--tRNA ligase, mitochondrial isoform X2
tryptophan--tRNA ligase, mitochondrial isoform X1
hydroxyacid oxidase 2 (long chain), 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
hydroxyacid oxidase 2 (long chain), 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 1 sample with support for all annotated introns
hydroxyacid oxidase 2 (long chain), transcript variant X2
kelch-like protein 9, 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 8 samples with support for all annotated introns
kelch-like protein 9, 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 9 samples with support for all annotated introns
hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1, transcript variant X1
hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1, 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
3 beta-hydroxysteroid dehydrogenase/Delta 5-->4-isomerase type 1 isoform X1
3 beta-hydroxysteroid dehydrogenase/Delta 5-->4-isomerase type 1 isoform X2
phospholipase A1 member A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phospholipase A1 member A, transcript variant X1
phospholipase A1 member A, transcript variant X3
popeye domain containing 2, transcript variant X2
popeye domain containing 2, transcript variant X1
cytochrome c oxidase copper chaperone, 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 11 samples with support for all annotated introns
cytochrome c oxidase copper chaperone, transcript variant X1
cytochrome c oxidase copper chaperone, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
protein mono-ADP-ribosyltransferase PARP4-like
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
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: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: R3H domain-containing protein 1-like
RAB3 GTPase activating protein subunit 1, transcript variant X1
RAB3 GTPase activating protein subunit 1, transcript variant X4
RAB3 GTPase activating protein subunit 1, transcript variant X3
RAB3 GTPase activating protein subunit 1, transcript variant X2
rab3 GTPase-activating protein catalytic subunit isoform X4
rab3 GTPase-activating protein catalytic subunit isoform X3
rab3 GTPase-activating protein catalytic subunit isoform X2
rab3 GTPase-activating protein catalytic subunit isoform X1
RAB3 GTPase activating protein subunit 1, transcript variant X6
RAB3 GTPase activating protein subunit 1, transcript variant X5
rab3 GTPase-activating protein catalytic subunit isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
poly(ADP-ribose) polymerase family member 14-related sequence 3
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
protein mono-ADP-ribosyltransferase PARP14
rho-related GTP-binding protein RhoE-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
sterile alpha motif domain-containing protein 9-like
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
LY6/PLAUR domain containing 6, transcript variant X2
LY6/PLAUR domain containing 6, transcript variant X1
LY6/PLAUR domain containing 6B, transcript variant X2
LY6/PLAUR domain containing 6B, transcript variant X1
kinesin family member 5C, transcript variant X1
kinesin family member 5C, transcript variant X2
kinesin family member 5C, transcript variant X3
mitogen-activated protein kinase kinase kinase 19, transcript variant X1
mitogen-activated protein kinase kinase kinase 19 isoform X1
mitogen-activated protein kinase kinase kinase 19, transcript variant X2
mitogen-activated protein kinase kinase kinase 19 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
aminocarboxymuconate semialdehyde decarboxylase
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
2-amino-3-carboxymuconate-6-semialdehyde decarboxylase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85 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: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
contactin associated protein family member 5a
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: 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: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: contactin-associated protein-like 5
glycophorin C (Gerbich blood group), transcript variant X2
glycophorin C (Gerbich blood group), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
NADH:ubiquinone oxidoreductase subunit A10
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 10 samples with support for all annotated introns
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 10, mitochondrial
aryl hydrocarbon receptor-like, 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 2 samples with support for all annotated introns
aryl hydrocarbon receptor-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 6 samples with support for all annotated introns
aryl hydrocarbon receptor-like isoform X1
aryl hydrocarbon receptor-like isoform X2
Fas apoptotic inhibitory molecule a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Fas apoptotic inhibitory molecule a, 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 3 samples with support for all annotated introns
Fas apoptotic inhibitory molecule a, transcript variant X3
poly(ADP-ribose) polymerase family member 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
poly(ADP-ribose) polymerase family member 9, transcript variant X1
protein mono-ADP-ribosyltransferase PARP9
poly(ADP-ribose) polymerase family member 14-related sequence 1
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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 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: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 39 member 10, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
solute carrier family 39 member 10, transcript variant X2
solute carrier family 39 member 10, transcript variant X3
transmembrane protein with EGF-like and two follistatin-like domains 2a
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 5 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 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon CGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
nucleic acid binding protein 1a, transcript variant X1
nucleic acid binding protein 1a, 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 7 samples with support for all annotated introns
formiminotransferase cyclodeaminase N-terminal like 1, transcript variant X5
formiminotransferase cyclodeaminase N-terminal like 1, transcript variant X4
formiminotransferase cyclodeaminase N-terminal like 1, transcript variant X3
formiminotransferase cyclodeaminase N-terminal like 1, transcript variant X2
formiminotransferase cyclodeaminase N-terminal like 1, transcript variant X1
formiminotransferase N-terminal subdomain-containing protein
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 9 samples with support for all annotated introns
serine/threonine kinase 17b (apoptosis-inducing), transcript variant X2
serine/threonine kinase 17b (apoptosis-inducing), transcript variant X1
serine/threonine-protein kinase 17B isoform X2
serine/threonine-protein kinase 17B isoform X1
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
post-GPI attachment to proteins inositol deacylase 1
matrix AAA peptidase interacting protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
m-AAA protease-interacting protein 1, mitochondrial
uncharacterized protein C21orf62 homolog, transcript variant X2
uncharacterized protein C21orf62 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized protein C21orf62 homolog
cytokine receptor family member b1, transcript variant X2
cytokine receptor family member b1, transcript variant X1
cytokine receptor family member b1, transcript variant X3
cytokine receptor family member b1 isoform X1
cytokine receptor family member b1 isoform X2
cytokine receptor family member b1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
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 8 samples with support for all annotated introns
interferon alpha/beta receptor 1-like, transcript variant X1
interferon alpha/beta receptor 1-like, transcript variant X2
interferon alpha/beta receptor 1-like isoform X1
uncharacterized protein LOC113575381 isoform X2
interleukin-1 receptor type 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
interleukin-1 receptor type 1, transcript variant X1
interleukin-1 receptor type 1, transcript variant X3
interleukin-1 receptor type 1, transcript variant X4
interleukin-1 receptor type 1 isoform X1
interleukin-1 receptor type 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X8
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X9
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
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X7
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase kinase 4, 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 7 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X5
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X2
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X4
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X1
mitogen-activated protein kinase kinase kinase kinase 4 isoform X8
mitogen-activated protein kinase kinase kinase kinase 4 isoform X9
mitogen-activated protein kinase kinase kinase kinase 4 isoform X7
mitogen-activated protein kinase kinase kinase kinase 4 isoform X6
mitogen-activated protein kinase kinase kinase kinase 4 isoform X3
mitogen-activated protein kinase kinase kinase kinase 4 isoform X5
mitogen-activated protein kinase kinase kinase kinase 4 isoform X4
glycerol kinase-like, transcript variant X1
glycerol kinase-like, transcript variant X2
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 8 samples with support for all annotated introns
ribosomal RNA processing protein 1 homolog B-like, transcript variant X2
ribosomal RNA processing protein 1 homolog B-like, transcript variant X1
ribosomal RNA processing protein 1 homolog B-like isoform X2
ribosomal RNA processing protein 1 homolog B-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 4, transcript variant X4
mediator of RNA polymerase II transcription subunit 4, transcript variant X1
mediator of RNA polymerase II transcription subunit 4, transcript variant X3
mediator of RNA polymerase II transcription subunit 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
CCR4-NOT transcription complex, subunit 11
CCR4-NOT transcription complex subunit 11
lymphocyte cytosolic protein 1 (L-plastin)
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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 4 isoform X5
ribosomal RNA processing protein 1 homolog A-like
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 11 samples with support for all annotated introns
uncharacterized protein LOC113592174 isoform X2
mediator of RNA polymerase II transcription subunit 4 isoform X3
5-hydroxytryptamine (serotonin) receptor 2A, genome duplicate a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
leucine-rich repeats and calponin homology (CH) domain containing 1, transcript variant X4
leucine-rich repeat and calponin homology domain-containing protein 1 isoform X4
leucine-rich repeats and calponin homology (CH) domain containing 1, transcript variant X2
leucine-rich repeats and calponin homology (CH) domain containing 1, transcript variant X3
leucine-rich repeats and calponin homology (CH) domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
leucine-rich repeat and calponin homology domain-containing protein 1 isoform X2
leucine-rich repeat and calponin homology domain-containing protein 1 isoform X3
leucine-rich repeat and calponin homology domain-containing protein 1 isoform X1
leucine-rich repeats and calponin homology (CH) domain containing 1, transcript variant X5
leucine-rich repeat and calponin homology domain-containing protein 1 isoform X5
leucine-rich repeats and calponin homology (CH) domain containing 1, transcript variant X6
leucine-rich repeats and calponin homology (CH) domain containing 1, transcript variant X7
leucine-rich repeat and calponin homology domain-containing protein 1 isoform X6
protein associated with UVRAG as autophagy enhancer
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
WD repeat and FYVE domain-containing protein 2
integrator complex subunit 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
integrator complex subunit 6, transcript variant X2
integrator complex subunit 6, 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 5 samples with support for all annotated introns
integrator complex subunit 6, transcript variant X5
integrator complex subunit 6, transcript variant X3
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 1 sample with support for all annotated introns
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
uncharacterized protein LOC113585667 isoform X3
uncharacterized protein LOC113585667 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
phospholipase B domain containing 2, transcript variant X2
phospholipase B domain containing 2, transcript variant X1
putative phospholipase B-like 2 isoform X2
putative phospholipase B-like 2 isoform X1
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X7
leucine-rich repeat flightless-interacting protein 2 isoform X7
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X5
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X3
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X4
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X2
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X1
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X6
leucine-rich repeat flightless-interacting protein 1 isoform X5
leucine-rich repeat flightless-interacting protein 1 isoform X3
leucine-rich repeat flightless-interacting protein 1 isoform X4
leucine-rich repeat flightless-interacting protein 1 isoform X2
leucine-rich repeat flightless-interacting protein 1 isoform X1
leucine-rich repeat flightless-interacting protein 1 isoform X6
coiled-coil domain-containing protein 138, transcript variant X1
coiled-coil domain-containing protein 138, transcript variant X2
coiled-coil domain-containing protein 138, transcript variant X4
coiled-coil domain-containing protein 138, transcript variant X3
coiled-coil domain-containing protein 138 isoform X1
coiled-coil domain-containing protein 138 isoform X2
coiled-coil domain-containing protein 138 isoform X4
coiled-coil domain-containing protein 138 isoform X3
ectodysplasin A receptor, transcript variant X2
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 1 sample with support for all annotated introns
ectodysplasin A receptor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tumor necrosis factor receptor superfamily member EDAR isoform X2
tumor necrosis factor receptor superfamily member EDAR isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 94% 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 6 bases in 4 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 6 bases in 4 codons; deleted 1 base in 1 codon; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
sosondowah ankyrin repeat domain family Ca
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: ankyrin repeat domain-containing protein SOWAHC
A kinase (PRKA) anchor protein 17A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
A kinase (PRKA) anchor protein 17A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
dehydrogenase/reductase SDR family member on chromosome X-like, transcript variant X3
dehydrogenase/reductase SDR family member on chromosome X-like, transcript variant X2
dehydrogenase/reductase SDR family member on chromosome X-like, transcript variant X1
dehydrogenase/reductase SDR family member on chromosome X-like isoform X3
dehydrogenase/reductase SDR family member on chromosome X-like isoform X2
dehydrogenase/reductase SDR family member on chromosome X-like isoform X1
uncharacterized protein si:ch211-39i22.1
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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
cAMP-dependent protein kinase catalytic subunit PRKX-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transducin beta like 1 X-linked, transcript variant X3
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 3 samples with support for all annotated introns
transducin beta like 1 X-linked, transcript variant X2
transducin beta like 1 X-linked, transcript variant X1
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 7 samples with support for all annotated introns
F-box-like/WD repeat-containing protein TBL1X isoform X1
F-box-like/WD repeat-containing protein TBL1X isoform X2
uncharacterized protein LOC100141330 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 10 member 2, transcript variant X2
solute carrier family 10 member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
protein O-glucosyltransferase 2, transcript variant X2
protein O-glucosyltransferase 2, transcript variant X1
protein O-glucosyltransferase 2 isoform X2
protein O-glucosyltransferase 2 isoform X1
syntaxin binding protein 5-like, transcript variant X1
syntaxin binding protein 5-like, transcript variant X11
syntaxin binding protein 5-like, transcript variant X10
syntaxin binding protein 5-like, transcript variant X7
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
syntaxin binding protein 5-like, transcript variant X6
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, including 1 sample with support for all annotated introns
syntaxin binding protein 5-like, transcript variant X5
syntaxin binding protein 5-like, transcript variant X9
syntaxin binding protein 5-like, transcript variant X8
syntaxin binding protein 5-like, transcript variant X4
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 1 sample with support for all annotated introns
syntaxin binding protein 5-like, 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 1 sample with support for all annotated introns
syntaxin binding protein 5-like, transcript variant X3
syntaxin-binding protein 5-like isoform X11
syntaxin-binding protein 5-like isoform X10
syntaxin-binding protein 5-like isoform X7
syntaxin-binding protein 5-like isoform X6
syntaxin-binding protein 5-like isoform X5
syntaxin-binding protein 5-like isoform X9
syntaxin-binding protein 5-like isoform X8
syntaxin-binding protein 5-like isoform X4
syntaxin-binding protein 5-like isoform X2
syntaxin-binding protein 5-like isoform X3
syntaxin-binding protein 5-like isoform X1
syntaxin binding protein 5-like, transcript variant X12
syntaxin binding protein 5-like, transcript variant X13
syntaxin-binding protein 5-like isoform X12
syntaxin binding protein 5-like, transcript variant X14
syntaxin-binding protein 5-like isoform X13
general transcription factor IIE, polypeptide 1, alpha
general transcription factor IIE subunit 1
leucine carboxyl methyltransferase 2, transcript variant X3
leucine carboxyl methyltransferase 2, transcript variant X2
leucine carboxyl methyltransferase 2, transcript variant X1
tRNA wybutosine-synthesizing protein 4 isoform X2
tRNA wybutosine-synthesizing protein 4 isoform X1
tRNA wybutosine-synthesizing protein 4 isoform X3
TBCC domain containing 1, transcript variant X2
TBCC domain containing 1, transcript variant X1
TBCC domain containing 1, transcript variant X3
TBCC domain-containing protein 1 isoform X2
TBCC domain-containing protein 1 isoform X1
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 8 samples with support for all annotated introns
debranching RNA lariats 1, transcript variant X1
debranching RNA lariats 1, transcript variant X2
armadillo repeat containing 8, transcript variant X1
armadillo repeat-containing protein 8 isoform X1
armadillo repeat containing 8, transcript variant X2
armadillo repeat-containing protein 8 isoform X2
potassium voltage-gated channel, subfamily H (eag-related), member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium voltage-gated channel subfamily H member 8
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: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
LOW QUALITY PROTEIN: isocitrate dehydrogenase [NADP] cytoplasmic
pleckstrin homology domain containing, family M, member 3
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 8 samples with support for all annotated introns
pleckstrin homology domain-containing family M member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
cAMP responsive element binding protein 1b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cyclic AMP-responsive element-binding protein 1b
cAMP responsive element binding protein 1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC555292 homolog, 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
uncharacterized protein LOC555292 homolog, transcript variant X8
uncharacterized protein LOC555292 homolog, transcript variant X5
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 7 samples with support for all annotated introns
uncharacterized protein LOC555292 homolog, transcript variant X6
uncharacterized protein LOC555292 homolog, transcript variant X4
uncharacterized protein LOC555292 homolog, transcript variant X1
uncharacterized protein LOC555292 homolog, transcript variant X3
putative methyltransferase DDB_G0268948 isoform X2
putative methyltransferase DDB_G0268948 isoform X1
uncharacterized protein LOC555292 homolog, transcript variant X7
putative methyltransferase DDB_G0268948 isoform X3
receptor activity modifying protein 1, transcript variant X1
receptor activity modifying protein 1, transcript variant X3
receptor activity modifying protein 1, transcript variant X2
receptor activity-modifying protein 1 isoform X1
receptor activity-modifying protein 1 isoform X3
receptor activity-modifying protein 1 isoform X2
uncharacterized LOC113567636, transcript variant X2
uncharacterized LOC113567636, transcript variant X1
erythrocyte membrane protein band 4.1 like 5, transcript variant X6
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 7 samples with support for all annotated introns
erythrocyte membrane protein band 4.1 like 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
erythrocyte membrane protein band 4.1 like 5, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
erythrocyte membrane protein band 4.1 like 5, transcript variant X4
erythrocyte membrane protein band 4.1 like 5, transcript variant X2
erythrocyte membrane protein band 4.1 like 5, transcript variant X1
protein tyrosine phosphatase non-receptor type 4a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
protein tyrosine phosphatase non-receptor type 4a, 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 3 samples with support for all annotated introns
protein tyrosine phosphatase non-receptor type 4a, transcript variant X1
protein tyrosine phosphatase non-receptor type 4a, transcript variant X3
tyrosine-protein phosphatase non-receptor type 4 isoform X2
tyrosine-protein phosphatase non-receptor type 4 isoform X1
tyrosine-protein phosphatase non-receptor type 4 isoform X3
tyrosine-protein phosphatase non-receptor type 4 isoform X4
ras-related protein M-Ras, transcript variant X3
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, including 8 samples with support for all annotated introns
ras-related protein M-Ras, transcript variant X7
ras-related protein M-Ras, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 102 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ras-related protein M-Ras, transcript variant X6
ras-related protein M-Ras, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ras-related protein M-Ras, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 102 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ras-related protein M-Ras, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
GLI family zinc finger 2a, 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 4 samples with support for all annotated introns
GLI family zinc finger 2a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
inhibin subunit beta B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
inhibin subunit beta B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ras guanine nucleotide exchange factor F, 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 10 samples with support for all annotated introns
ras guanine nucleotide exchange factor F, transcript variant X3
ras guanine nucleotide exchange factor F, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
ras guanine nucleotide exchange factor F, transcript variant X2
ras guanine nucleotide exchange factor F isoform X1
leucine-zipper-like transcriptional regulator 1 homolog isoform X2
ras guanine nucleotide exchange factor F isoform X3
v-ral simian leukemia viral oncogene homolog Ba (ras related)
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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
low density lipoprotein receptor-related protein 1Bb
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 3 codons; deleted 10 bases in 7 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% 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 4 bases in 3 codons; deleted 10 bases in 7 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: low-density lipoprotein receptor-related protein 1B
ATPase Na+/K+ transporting subunit alpha 1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 271 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ATPase Na+/K+ transporting subunit alpha 1b, transcript variant X1
ATPase Na+/K+ transporting subunit alpha 1b, transcript variant X3
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
ATPase Na+/K+ transporting subunit alpha 1b, transcript variant X4
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 2 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit alpha-1b isoform X1
sodium/potassium-transporting ATPase subunit alpha-1b isoform X2
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; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
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; deleted 1 base in 1 codon; substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein mab-21-like 3
DnaJ (Hsp40) homolog, subfamily C, member 28
potassium voltage-gated channel subfamily E member 1
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
regulator of calcineurin 1a, transcript variant X1
regulator of calcineurin 1a, transcript variant X3
regulator of calcineurin 1a, transcript variant X2
uncharacterized protein LOC792544 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC792544 homolog, transcript variant X1
serine/arginine repetitive matrix protein 2 isoform X2
serine/arginine repetitive matrix protein 2 isoform X1
neural cell adhesion molecule 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
neural cell adhesion molecule 2 isoform X2
neural cell adhesion molecule 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
neural cell adhesion molecule 2, transcript variant X3
neural cell adhesion molecule 2 isoform X1
neural cell adhesion molecule 2 isoform X3
uncharacterized si:dkey-192g7.3, transcript variant X1
uncharacterized si:dkey-192g7.3, transcript variant X2
uncharacterized protein si:dkey-192g7.3 isoform X1
uncharacterized protein si:dkey-192g7.3 isoform X2
amyloid beta (A4) precursor protein b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
amyloid beta (A4) precursor protein b, transcript variant X5
amyloid beta (A4) precursor protein b isoform X2
amyloid beta (A4) precursor protein b isoform X5
amyloid beta (A4) precursor protein b, transcript variant X3
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 8 samples with support for all annotated introns
amyloid beta (A4) precursor protein b, transcript variant X1
amyloid beta (A4) precursor protein b, transcript variant X4
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 8 samples with support for all annotated introns
amyloid beta (A4) precursor protein b isoform X1
amyloid beta (A4) precursor protein b isoform X3
amyloid beta (A4) precursor protein b isoform X4
GA binding protein transcription factor subunit alpha, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
GA binding protein transcription factor subunit alpha, transcript variant X1
GA binding protein transcription factor subunit alpha, transcript variant X2
S-adenosylmethionine-dependent methyltransferase domain-containing protein, transcript variant X1
S-adenosylmethionine-dependent methyltransferase domain-containing protein, transcript variant X2
S-adenosylmethionine-dependent methyltransferase domain-containing protein isoform X1
S-adenosylmethionine-dependent methyltransferase domain-containing protein isoform X2
transcription factor Dp-1, a, transcript variant X3
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
transcription factor Dp-1, a, 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 7 samples with support for all annotated introns
transcription factor Dp-1, a, 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 3 samples with support for all annotated introns
transcription factor Dp-1, a, transcript variant X4
DCN1, defective in cullin neddylation 1, domain containing 2a, transcript variant X4
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 6 samples with support for all annotated introns
DCN1, defective in cullin neddylation 1, domain containing 2a, transcript variant X6
DCN1, defective in cullin neddylation 1, domain containing 2a, transcript variant X5
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 4 samples with support for all annotated introns
DCN1, defective in cullin neddylation 1, domain containing 2a, transcript variant X7
DCN1, defective in cullin neddylation 1, domain containing 2a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
DCN1, defective in cullin neddylation 1, domain containing 2a, transcript variant X2
DCN1, defective in cullin neddylation 1, domain containing 2a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cell division cycle 16 homolog (S. cerevisiae)
UPF3A regulator of nonsense mediated mRNA decay, transcript variant X1
UPF3A regulator of nonsense mediated mRNA decay, transcript variant X2
regulator of nonsense transcripts 3A isoform X1
regulator of nonsense transcripts 3A isoform X2
P2Y receptor family member 8, transcript variant X2
P2Y receptor family member 8, transcript variant X1
P2Y receptor family member 8, transcript variant X3
acetylserotonin O-methyltransferase-like, transcript variant X1
acetylserotonin O-methyltransferase-like, transcript variant X2
probable bifunctional dTTP/UTP pyrophosphatase/methyltransferase protein isoform X1
probable bifunctional dTTP/UTP pyrophosphatase/methyltransferase protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC113567842, transcript variant X1
uncharacterized LOC113567842, transcript variant X3
uncharacterized LOC113567842, transcript variant X2
cytokine receptor-like factor 2 isoform X1
cytokine receptor-like factor 2 isoform X2
cytokine receptor-like factor 2 isoform X3
short stature homeobox, transcript variant X2
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
short stature homeobox protein isoform X2
short stature homeobox, transcript variant X1
short stature homeobox protein isoform X1
protein phosphatase 2, regulatory subunit B'', beta, transcript variant X1
protein phosphatase 2, regulatory subunit B'', beta, transcript variant X2
serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit beta isoform X1
serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit beta isoform X2
protein phosphatase 2, regulatory subunit B'', beta, transcript variant X3
serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit beta isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: cohesin subunit SA-2
uncharacterized protein si:ch211-218d20.15
mediator complex subunit 14, transcript variant X2
mediator complex subunit 14, transcript variant X1
mediator of RNA polymerase II transcription subunit 14 isoform X2
mediator of RNA polymerase II transcription subunit 14 isoform X1
ubiquitin specific peptidase 9, transcript variant X1
ubiquitin specific peptidase 9, transcript variant X3
ubiquitin specific peptidase 9, transcript variant X7
ubiquitin specific peptidase 9, transcript variant X2
ubiquitin specific peptidase 9, transcript variant X8
ubiquitin specific peptidase 9, transcript variant X4
ubiquitin specific peptidase 9, transcript variant X9
ubiquitin specific peptidase 9, transcript variant X5
ubiquitin specific peptidase 9, transcript variant X6
ubiquitin specific peptidase 9, transcript variant X10
ubiquitin specific peptidase 9, transcript variant X11
ubiquitin specific peptidase 9 isoform X1
ubiquitin specific peptidase 9 isoform X3
ubiquitin specific peptidase 9 isoform X7
ubiquitin specific peptidase 9 isoform X2
ubiquitin specific peptidase 9 isoform X8
ubiquitin specific peptidase 9 isoform X4
ubiquitin specific peptidase 9 isoform X9
ubiquitin specific peptidase 9 isoform X5
ubiquitin specific peptidase 9 isoform X6
ubiquitin specific peptidase 9 isoform X10
ubiquitin specific peptidase 9 isoform X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
acid phosphatase 6, lysophosphatidic, transcript variant X1
acid phosphatase 6, lysophosphatidic, transcript variant X4
acid phosphatase 6, lysophosphatidic, transcript variant X5
acid phosphatase 6, lysophosphatidic, transcript variant X2
acid phosphatase 6, lysophosphatidic, transcript variant X3
lysophosphatidic acid phosphatase type 6 isoform X1
lysophosphatidic acid phosphatase type 6 isoform X2
lysophosphatidic acid phosphatase type 6 isoform X3
uncharacterized si:dkey-229b18.3, transcript variant X1
uncharacterized si:dkey-229b18.3, transcript variant X2
uncharacterized protein si:dkey-229b18.3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
chromatin assembly factor 1, subunit B, transcript variant X1
chromatin assembly factor 1, subunit B, transcript variant X2
MORC family CW-type zinc finger protein 3a
MORC family CW-type zinc finger protein 3-like
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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: MORC family CW-type zinc finger protein 3-like
DOP1 leucine zipper like protein B, transcript variant X2
DOP1 leucine zipper like protein B, transcript variant X1
ATP synthase peripheral stalk subunit OSCP, transcript variant X1
ATP synthase peripheral stalk subunit OSCP, transcript variant X2
solute carrier family 5 member 3b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
solute carrier family 5 member 3b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
potassium voltage-gated channel subfamily E member 2-like
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 4 samples with support for all annotated introns
VANGL planar cell polarity protein 1, transcript variant X2
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, including 3 samples with support for all annotated introns
VANGL planar cell polarity protein 1, transcript variant X1
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, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
cyclic nucleotide gated channel subunit alpha 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
cyclic nucleotide-gated cation channel alpha-4
family with sequence similarity 160 member A2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
family with sequence similarity 160 member A2, transcript variant X1
FTS and Hook-interacting protein homolog isoform X2
FTS and Hook-interacting protein homolog isoform X1
ankyrin repeat domain 50-like, transcript variant X2
ankyrin repeat domain 50-like, 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 2 samples with support for all annotated introns
ankyrin repeat domain-containing protein 50
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 36% 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 58% coverage of the annotated genomic feature by RNAseq alignments
glutamine amidotransferase-like class 1 domain-containing protein 3B, mitochondrial
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
glutamine amidotransferase-like class 1 domain-containing protein 3A, mitochondrial
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 9 samples with support for all annotated introns
oligodendrocyte lineage transcription factor 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
excision repair cross-complementation group 1
granzyme B(G,H)-like, transcript variant X3
granzyme B(G,H)-like, transcript variant X2
granzyme B(G,H)-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
RAB, member of RAS oncogene family-like 3
DnaJ heat shock protein family (Hsp40) member B11
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
MOB-like protein phocein, transcript variant X1
MOB-like protein phocein, transcript variant X3
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
MOB-like protein phocein, transcript variant X2
10 kDa heat shock protein, mitochondrial isoform X2
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 10 samples with support for all annotated introns
60 kDa heat shock protein, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
coenzyme Q-binding protein COQ10 homolog B, mitochondrial
splicing factor 3b, subunit 1, transcript variant X1
splicing factor 3b, subunit 1, transcript variant X5
splicing factor 3b, subunit 1, transcript variant X3
splicing factor 3b, subunit 1, transcript variant X4
splicing factor 3b, subunit 1, transcript variant X2
ankyrin repeat domain 44, 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 6 samples with support for all annotated introns
ankyrin repeat domain 44, transcript variant X3
ankyrin repeat domain 44, transcript variant X2
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X1
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X3
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B isoform X2
phosphoinositide kinase, FYVE finger containing, transcript variant X10
phosphoinositide kinase, FYVE finger containing, transcript variant X8
phosphoinositide kinase, FYVE finger containing, transcript variant X4
phosphoinositide kinase, FYVE finger containing, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
phosphoinositide kinase, FYVE finger containing, transcript variant X2
phosphoinositide kinase, FYVE finger containing, transcript variant X9
phosphoinositide kinase, FYVE finger containing, transcript variant X7
phosphoinositide kinase, FYVE finger containing, transcript variant X3
phosphoinositide kinase, FYVE finger containing, transcript variant X5
phosphoinositide kinase, FYVE finger containing, transcript variant X1
phosphoinositide kinase, FYVE finger containing, transcript variant X11
1-phosphatidylinositol 3-phosphate 5-kinase isoform X10
1-phosphatidylinositol 3-phosphate 5-kinase isoform X8
1-phosphatidylinositol 3-phosphate 5-kinase isoform X4
1-phosphatidylinositol 3-phosphate 5-kinase isoform X6
1-phosphatidylinositol 3-phosphate 5-kinase isoform X2
1-phosphatidylinositol 3-phosphate 5-kinase isoform X9
1-phosphatidylinositol 3-phosphate 5-kinase isoform X7
1-phosphatidylinositol 3-phosphate 5-kinase isoform X3
1-phosphatidylinositol 3-phosphate 5-kinase isoform X5
1-phosphatidylinositol 3-phosphate 5-kinase isoform X1
1-phosphatidylinositol 3-phosphate 5-kinase isoform X11
fibroblast growth factor 14, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
fibroblast growth factor 14, transcript variant X3
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 1 sample with support for all annotated introns
fibroblast growth factor 14, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 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 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
LOW QUALITY PROTEIN: integrin beta-like protein 1
uncharacterized LOC118240780, transcript variant X1
uncharacterized LOC118240780, transcript variant X2
sodium leak channel, non-selective, transcript variant X1
sodium leak channel, non-selective, transcript variant X2
sodium leak channel non-selective protein isoform X1
sodium leak channel non-selective protein isoform X2
transmembrane O-mannosyltransferase targeting cadherins 4, transcript variant X1
transmembrane O-mannosyltransferase targeting cadherins 4, transcript variant X4
transmembrane O-mannosyltransferase targeting cadherins 4, transcript variant X2
transmembrane O-mannosyltransferase targeting cadherins 4, transcript variant X3
protein O-mannosyl-transferase TMTC4 isoform X1
protein O-mannosyl-transferase TMTC4 isoform X4
protein O-mannosyl-transferase TMTC4 isoform X2
protein O-mannosyl-transferase TMTC4 isoform X3
zic family member 2 (odd-paired homolog, Drosophila), 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
zic family member 2 (odd-paired homolog, Drosophila), a, transcript variant X1
uncharacterized LOC113572084, transcript variant X1
uncharacterized LOC113572084, transcript variant X2
zic family member 5 (odd-paired homolog, Drosophila)
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 9 samples with support for all annotated introns
uncharacterized protein LOC798560 homolog
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 9 samples with support for all annotated introns
G protein-coupled receptor 18, transcript variant X2
G protein-coupled receptor 18, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Kruppel-like factor 12b, 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 3 samples with support for all annotated introns
Kruppel-like factor 12b, 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 6 samples with support for all annotated introns
Kruppel-like factor 12b, transcript variant X2
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
TBC1 domain family, member 4, transcript variant X2
TBC1 domain family, member 4, transcript variant X1
TBC1 domain family, member 4, transcript variant X3
TBC1 domain family, member 4, transcript variant X5
TBC1 domain family, member 4, transcript variant X4
COMM domain containing 6, transcript variant X1
COMM domain containing 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
COMM domain-containing protein 6 isoform X1
COMM domain-containing protein 6 isoform X2
lysosomal associated membrane protein 1b
lysosome-associated membrane glycoprotein 1b
POU class 2 homeobox 1b, transcript variant X4
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, including 1 sample with support for all annotated introns
POU class 2 homeobox 1b, transcript variant X3
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 1 sample with support for all annotated introns
POU class 2 homeobox 1b, transcript variant X6
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
POU class 2 homeobox 1b, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
POU class 2 homeobox 1b, transcript variant X7
POU class 2 homeobox 1b, transcript variant X2
POU class 2 homeobox 1b, transcript variant X1
POU domain, class 2, transcription factor 1b isoform X6
POU domain, class 2, transcription factor 1b isoform X5
POU domain, class 2, transcription factor 1b isoform X4
POU domain, class 2, transcription factor 1b isoform X7
POU domain, class 2, transcription factor 1b isoform X3
POU domain, class 2, transcription factor 1b isoform X2
POU domain, class 2, transcription factor 1b isoform X1
glycoprotein A33 (transmembrane), paralog b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
immunoglobulin-like domain containing receptor 2, transcript variant X1
immunoglobulin-like domain containing receptor 2, transcript variant X3
immunoglobulin-like domain containing receptor 2, transcript variant X2
immunoglobulin-like domain-containing receptor 2 isoform X1
immunoglobulin-like domain-containing receptor 2 isoform X3
immunoglobulin-like domain-containing receptor 2 isoform X2
immunoglobulin-like domain containing receptor 2, transcript variant X4
immunoglobulin-like domain-containing receptor 2 isoform X4
immunoglobulin-like domain containing receptor 1b
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; deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 5 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 3 bases in 2 codons; deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: immunoglobulin-like domain-containing receptor 1b
malic enzyme 3, NADP(+)-dependent, mitochondrial
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: 7 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 8 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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: NADP-dependent malic enzyme, mitochondrial
neurexophilin and PC-esterase domain family, member 3, transcript variant X2
neurexophilin and PC-esterase domain family, member 3, transcript variant X1
ddb1 and cul4 associated factor 6, transcript variant X1
ddb1 and cul4 associated factor 6, transcript variant X2
ddb1 and cul4 associated factor 6, transcript variant X3
ddb1 and cul4 associated factor 6, transcript variant X4
DDB1- and CUL4-associated factor 6 isoform X1
DDB1- and CUL4-associated factor 6 isoform X2
DDB1- and CUL4-associated factor 6 isoform X3
DDB1- and CUL4-associated factor 6 isoform X4
ddb1 and cul4 associated factor 6, transcript variant X5
ddb1 and cul4 associated factor 6, transcript variant X6
ddb1 and cul4 associated factor 6, transcript variant X7
DDB1- and CUL4-associated factor 6 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 1 base in 1 codon; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: coagulation factor VIII-like
solute carrier family 35 member A5, transcript variant X1
solute carrier family 35 member A5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
solute carrier family 35 member A5, transcript variant X4
solute carrier family 35 member A5, transcript variant X2
solute carrier family 35 member A5, transcript variant X5
probable UDP-sugar transporter protein SLC35A5
coiled-coil domain-containing protein 80
lysine (K)-specific demethylase 6A, transcript variant X2
lysine (K)-specific demethylase 6A, transcript variant X4
lysine (K)-specific demethylase 6A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
lysine (K)-specific demethylase 6A, transcript variant X5
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 7 samples with support for all annotated introns
lysine (K)-specific demethylase 6A, transcript variant X3
lysine-specific demethylase 6A isoform X5
lysine-specific demethylase 6A isoform X2
lysine-specific demethylase 6A isoform X4
lysine-specific demethylase 6A isoform X3
lysine-specific demethylase 6A isoform X1
FUN14 domain containing 1, transcript variant X1
FUN14 domain containing 1, transcript variant X2
FUN14 domain-containing protein 1 isoform X1
FUN14 domain-containing protein 1 isoform X2
EF-hand domain (C-terminal) containing 2, transcript variant X1
EF-hand domain (C-terminal) containing 2, transcript variant X2
EF-hand domain-containing family member C2 isoform X1
EF-hand domain-containing family member C2 isoform X2
seminal vesicle major clotting proteins, transcript variant X1
seminal vesicle major clotting proteins, transcript variant X2
seminal vesicle major clotting proteins isoform X2
seminal vesicle major clotting proteins isoform X1
monoamine oxidase, 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 4 samples with support for all annotated introns
monoamine oxidase, 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
amine oxidase [flavin-containing] isoform X1
amine oxidase [flavin-containing] isoform X2
calcium/calmodulin-dependent serine protein kinase a, transcript variant X3
calcium/calmodulin-dependent serine protein kinase a, transcript variant X11
calcium/calmodulin-dependent serine protein kinase a, transcript variant X1
calcium/calmodulin-dependent serine protein kinase a, transcript variant X5
calcium/calmodulin-dependent serine protein kinase a, transcript variant X9
calcium/calmodulin-dependent serine protein kinase a, transcript variant X2
calcium/calmodulin-dependent serine protein kinase a, transcript variant X14
calcium/calmodulin-dependent serine protein kinase a, transcript variant X17
calcium/calmodulin-dependent serine protein kinase a, transcript variant X13
calcium/calmodulin-dependent serine protein kinase a, transcript variant X6
calcium/calmodulin-dependent serine protein kinase a, transcript variant X10
calcium/calmodulin-dependent serine protein kinase a, transcript variant X4
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 5 samples with support for all annotated introns
calcium/calmodulin-dependent serine protein kinase a, transcript variant X8
calcium/calmodulin-dependent serine protein kinase a, transcript variant X12
calcium/calmodulin-dependent serine protein kinase a, transcript variant X15
peripheral plasma membrane protein CASK isoform X1
peripheral plasma membrane protein CASK isoform X3
peripheral plasma membrane protein CASK isoform X5
peripheral plasma membrane protein CASK isoform X9
peripheral plasma membrane protein CASK isoform X13
peripheral plasma membrane protein CASK isoform X2
peripheral plasma membrane protein CASK isoform X6
peripheral plasma membrane protein CASK isoform X10
peripheral plasma membrane protein CASK isoform X11
peripheral plasma membrane protein CASK isoform X14
peripheral plasma membrane protein CASK isoform X4
peripheral plasma membrane protein CASK isoform X8
peripheral plasma membrane protein CASK isoform X17
peripheral plasma membrane protein CASK isoform X12
peripheral plasma membrane protein CASK isoform X15
calcium/calmodulin-dependent serine protein kinase a, transcript variant X7
peripheral plasma membrane protein CASK isoform X7
calcium/calmodulin-dependent serine protein kinase a, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
probable G-protein coupled receptor 34, transcript variant X2
probable G-protein coupled receptor 34, transcript variant X1
probable G-protein coupled receptor 34 isoform X2
probable G-protein coupled receptor 34 isoform X1
peripheral plasma membrane protein CASK isoform X16
DEAD-box helicase 3 X-linked a, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
DEAD-box helicase 3 X-linked a, transcript variant X6
DEAD-box helicase 3 X-linked a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
DEAD-box helicase 3 X-linked a, transcript variant X4
DEAD-box helicase 3 X-linked a, transcript variant X3
DEAD-box helicase 3 X-linked a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
DEAD-box helicase 3 X-linked a, transcript variant X1
DEAD-box helicase 3 X-linked a isoform X7
DEAD-box helicase 3 X-linked a isoform X6
DEAD-box helicase 3 X-linked a isoform X5
DEAD-box helicase 3 X-linked a isoform X4
DEAD-box helicase 3 X-linked a isoform X3
DEAD-box helicase 3 X-linked a isoform X2
DEAD-box helicase 3 X-linked a isoform X1
E3 ubiquitin-protein ligase TRIM7-like, transcript variant X4
uncharacterized protein LOC113574314 isoform X4
E3 ubiquitin-protein ligase TRIM7-like, transcript variant X3
E3 ubiquitin-protein ligase TRIM7-like, transcript variant X1
E3 ubiquitin-protein ligase TRIM7-like, transcript variant X2
E3 ubiquitin-protein ligase TRIM39-like isoform X2
E3 ubiquitin-protein ligase TRIM7-like isoform X3
E3 ubiquitin-protein ligase TRIM7-like isoform X1
uncharacterized LOC113574363, transcript variant X2
uncharacterized LOC113574363, transcript variant X3
uncharacterized LOC113574363, transcript variant X4
uncharacterized LOC113574363, transcript variant X1
interleukin 1 receptor accessory protein-like 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
interleukin 1 receptor accessory protein-like 1a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
interleukin-1 receptor accessory protein-like 1-A isoform X2
interleukin-1 receptor accessory protein-like 1-A isoform X1
cms1 ribosomal small subunit homolog, transcript variant X1
cms1 ribosomal small subunit homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
discoidin, CUB and LCCL domain containing 2, transcript variant X1
discoidin, CUB and LCCL domain containing 2, transcript variant X2
discoidin, CUB and LCCL domain-containing protein 2 isoform X2
discoidin, CUB and LCCL domain-containing protein 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
trafficking from ER to golgi regulator, 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 10 samples with support for all annotated introns
trafficking from ER to golgi regulator, transcript variant X3
trafficking from ER to golgi regulator, transcript variant X2
target of Nesh-SH3, transcript variant X3
target of Nesh-SH3, transcript variant X2
target of Nesh-SH3, transcript variant X1
fibronectin type III domain-containing protein 1 isoform X3
SUMO specific peptidase 7, transcript variant X1
SUMO specific peptidase 7, transcript variant X3
SUMO specific peptidase 7, transcript variant X2
cyclic AMP receptor-like protein A, transcript variant X1
cyclic AMP receptor-like protein A, transcript variant X2
cyclic AMP receptor-like protein A isoform X1
cyclic AMP receptor-like protein A isoform 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
ornithine carbamoyltransferase, mitochondrial
sushi-repeat containing protein X-linked, transcript variant X1
sushi-repeat containing protein X-linked, transcript variant X2
sushi repeat-containing protein SRPX isoform X1
sushi repeat-containing protein SRPX isoform X2
sushi-repeat containing protein X-linked, transcript variant X4
sushi-repeat containing protein X-linked, transcript variant X3
sushi repeat-containing protein SRPX isoform X3
sushi repeat-containing protein SRPX isoform X4
uncharacterized LOC113590768, transcript variant X1
uncharacterized LOC113590768, transcript variant X3
uncharacterized LOC113590768, transcript variant X5
uncharacterized LOC113590768, transcript variant X2
uncharacterized LOC113590768, transcript variant X4
uncharacterized protein LOC113590768 isoform X1
uncharacterized protein LOC113590768 isoform X2
uncharacterized protein LOC113590768 isoform X3
NADP-dependent malic enzyme, mitochondrial-like, transcript variant X1
NADP-dependent malic enzyme, mitochondrial-like, transcript variant X2
NADP-dependent malic enzyme, mitochondrial-like
sushi repeat-containing protein SRPX-like
synaptotagmin-like 5, transcript variant X3
synaptotagmin-like 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
synaptotagmin-like 5, transcript variant X1
ankyrin repeat and SOCS box containing 11
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: 12 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: ankyrin repeat and SOCS box protein 11
phosphatidylinositol glycan anchor biosynthesis, class A, transcript variant X1
phosphatidylinositol glycan anchor biosynthesis, class A, transcript variant X2
phosphatidylinositol N-acetylglucosaminyltransferase subunit A
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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ribonuclease H2, subunit B, transcript variant X2
ribonuclease H2, subunit B, transcript variant X1
tripartite motif containing 13, transcript variant X2
tripartite motif containing 13, 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 4 samples with support for all annotated introns
tripartite motif containing 13, transcript variant X1
SPRY domain containing 7b, transcript variant X2
SPRY domain containing 7b, transcript variant X1
SPRY domain-containing protein 7b isoform X1
SPRY domain-containing protein 7b 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: 46 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
LOW QUALITY PROTEIN: importin subunit alpha-4-like
cyclin-dependent kinase 5 activator 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
rho guanine nucleotide exchange factor 11-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: polyadenylate-binding protein 1A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 29-like, transcript variant X5
ubiquitin carboxyl-terminal hydrolase 29-like, transcript variant X6
ubiquitin carboxyl-terminal hydrolase 29-like, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 29-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 29-like, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 29-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 29-like isoform X1
ubiquitin carboxyl-terminal hydrolase 29-like isoform X2
homeodomain-interacting protein kinase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 30% 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 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 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: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq 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: homeodomain-interacting protein kinase 1-like
homeodomain-interacting protein kinase 1-like, transcript variant X1
homeodomain-interacting protein kinase 1-like, transcript variant X2
TOG array regulator of axonemal microtubules protein 1-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: 3 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: 2-oxoglutarate receptor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
heparan-sulfate 6-O-sulfotransferase 3-B
UDP-glucose glycoprotein glucosyltransferase 2, transcript variant X1
UDP-glucose glycoprotein glucosyltransferase 2, transcript variant X3
UDP-glucose glycoprotein glucosyltransferase 2, transcript variant X2
UDP-glucose glycoprotein glucosyltransferase 2, transcript variant X4
UDP-glucose:glycoprotein glucosyltransferase 2 isoform X1
UDP-glucose:glycoprotein glucosyltransferase 2 isoform X3
UDP-glucose:glycoprotein glucosyltransferase 2 isoform X2
UDP-glucose:glycoprotein glucosyltransferase 2 isoform X4
DnaJ (Hsp40) homolog, subfamily C, member 3a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
mcf.2 cell line derived transforming sequence-like b, 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
mcf.2 cell line derived transforming sequence-like b, transcript variant X2
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
guanine nucleotide exchange factor DBS isoform X1
guanine nucleotide exchange factor DBS isoform X2
mcf.2 cell line derived transforming sequence-like b, transcript variant X3
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
guanine nucleotide exchange factor DBS isoform X3
mcf.2 cell line derived transforming sequence-like b, transcript variant X4
guanine nucleotide exchange factor DBS isoform X4
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
LOW QUALITY PROTEIN: interferon-induced protein 44-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC113582429, transcript variant X1
uncharacterized LOC113582429, transcript variant X2
glycosyltransferase-like domain containing 1, transcript variant X3
glycosyltransferase-like domain containing 1, transcript variant X4
glycosyltransferase-like domain containing 1, transcript variant X1
glycosyltransferase-like domain containing 1, transcript variant X2
glycosyltransferase-like domain-containing protein 1 isoform X2
glycosyltransferase-like domain-containing protein 1 isoform X1
zinc finger E-box binding homeobox 2a, transcript variant X1
zinc finger E-box binding homeobox 2a, transcript variant X2
zinc finger E-box-binding homeobox 2a isoform X2
zinc finger E-box-binding homeobox 2a isoform X1
activin A receptor type 2Aa, transcript variant X1
activin A receptor type 2Aa, transcript variant X2
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 6 samples with support for all annotated introns
activin A receptor type 2Aa, transcript variant X3
activin A receptor type 2Aa, transcript variant X4
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 6 samples with support for all annotated introns
enhancer of polycomb homolog 2 (Drosophila), transcript variant X1
enhancer of polycomb homolog 2 (Drosophila), transcript variant X2
enhancer of polycomb homolog 2 (Drosophila), transcript variant X3
enhancer of polycomb homolog 2 isoform X1
enhancer of polycomb homolog 2 isoform X2
enhancer of polycomb homolog 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 35% coverage of the annotated genomic feature by RNAseq alignments
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% 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: 39 Proteins, and 43% 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 53% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns