Octopus sinensis linkage group LG13, ASM634580v1, whole genome shotgun sequence.
Octopus sinensis (East Asian common octopus)
Eukaryota; Metazoa; Spiralia; Lophotrochozoa; Mollusca; Cephalopoda; Coleoidea; Octopodiformes; Octopoda; Incirrata; Octopodidae; Octopus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM016871.1.\nAssembly name: ASM634580v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Yellow Sea Fisheries Research\nInstitute, Chinese Academy of Fishery Sciences on 2019/06/14. The\noriginal whole-genome shotgun project has the accession\nVCDQ00000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Yellow Sea Fisheries Research Institute,\n Chinese Academy of Fishery Sciences\nAssembly Method :: CANU v. 1.5; Wtdbg v. 1.1.006\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 285.0x\nSequencing Technology :: PacBio; Illumina\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Octopus sinensis Annotation Release\n 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##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC118765732, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC118765732, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized protein LOC118765732 isoform X2
uncharacterized protein LOC118765732 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 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 3 samples with support for all annotated introns
uncharacterized LOC115218432, 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 18 samples with support for all annotated introns
uncharacterized LOC115218432, 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 22 samples with support for all annotated introns
uncharacterized protein LOC115218432 isoform X1
uncharacterized protein LOC115218432 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
uncharacterized LOC118765736, 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 2 samples with support for all annotated introns
uncharacterized LOC118765736, 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 6 samples with support for all annotated introns
uncharacterized LOC115218238, transcript variant X8
uncharacterized LOC115218238, transcript variant X7
uncharacterized LOC115218238, transcript variant X6
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
uncharacterized LOC115218238, transcript variant X9
uncharacterized LOC115218238, transcript variant X5
uncharacterized LOC115218238, transcript variant X4
uncharacterized LOC115218238, transcript variant X3
uncharacterized LOC115218238, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC115218238, 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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
nuclear factor related to kappa-B-binding protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
nuclear factor related to kappa-B-binding protein, 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 14 samples with support for all annotated introns
nuclear factor related to kappa-B-binding protein isoform X1
nuclear factor related to kappa-B-binding protein isoform X2
uncharacterized LOC118765740, transcript variant X2
uncharacterized LOC118765740, transcript variant X1
eukaryotic translation initiation factor 3 subunit F
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 46 samples with support for all annotated introns
transcription termination factor 2, 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 6 samples with support for all annotated introns
transcription termination factor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transcription termination factor 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transcription termination factor 2 isoform X1
transcription termination factor 2 isoform X2
transcription termination factor 2 isoform X3
neuroblast differentiation-associated protein AHNAK, transcript variant X31
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
neuroblast differentiation-associated protein AHNAK, transcript variant X26
neuroblast differentiation-associated protein AHNAK, transcript variant X20
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 16 samples with support for all annotated introns
neuroblast differentiation-associated protein AHNAK, transcript variant X21
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 13 samples with support for all annotated introns
neuroblast differentiation-associated protein AHNAK, transcript variant X15
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
neuroblast differentiation-associated protein AHNAK, transcript variant X8
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 15 samples with support for all annotated introns
neuroblast differentiation-associated protein AHNAK, transcript variant X17
neuroblast differentiation-associated protein AHNAK, transcript variant X10
neuroblast differentiation-associated protein AHNAK, transcript variant X6
neuroblast differentiation-associated protein AHNAK, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
neuroblast differentiation-associated protein AHNAK, transcript variant X11
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
neuroblast differentiation-associated protein AHNAK, transcript variant X12
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 7 samples with support for all annotated introns
neuroblast differentiation-associated protein AHNAK, transcript variant X7
neuroblast differentiation-associated protein AHNAK, transcript variant X9
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 14 samples with support for all annotated introns
neuroblast differentiation-associated protein AHNAK, transcript variant X5
neuroblast differentiation-associated protein AHNAK, transcript variant X4
neuroblast differentiation-associated protein AHNAK, transcript variant X13
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 28 samples with support for all annotated introns
neuroblast differentiation-associated protein AHNAK, transcript variant X3
neuroblast differentiation-associated protein AHNAK, transcript variant X30
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 16 samples with support for all annotated introns
neuroblast differentiation-associated protein AHNAK, transcript variant X14
neuroblast differentiation-associated protein AHNAK, transcript variant X1
neuroblast differentiation-associated protein AHNAK, transcript variant X37
neuroblast differentiation-associated protein AHNAK, transcript variant X36
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
neuroblast differentiation-associated protein AHNAK, transcript variant X35
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 33 samples with support for all annotated introns
neuroblast differentiation-associated protein AHNAK, transcript variant X33
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 18 samples with support for all annotated introns
neuroblast differentiation-associated protein AHNAK, transcript variant X25
neuroblast differentiation-associated protein AHNAK, transcript variant X24
neuroblast differentiation-associated protein AHNAK, transcript variant X34
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 34 samples with support for all annotated introns
neuroblast differentiation-associated protein AHNAK, transcript variant X27
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 29 samples with support for all annotated introns
neuroblast differentiation-associated protein AHNAK, transcript variant X32
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
neuroblast differentiation-associated protein AHNAK, transcript variant X28
neuroblast differentiation-associated protein AHNAK, transcript variant X29
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
neuroblast differentiation-associated protein AHNAK, transcript variant X22
neuroblast differentiation-associated protein AHNAK, transcript variant X23
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 12 samples with support for all annotated introns
neuroblast differentiation-associated protein AHNAK, transcript variant X19
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 30 samples with support for all annotated introns
neuroblast differentiation-associated protein AHNAK, transcript variant X18
neuroblast differentiation-associated protein AHNAK, transcript variant X2
neuroblast differentiation-associated protein AHNAK, transcript variant X39
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 16 samples with support for all annotated introns
neuroblast differentiation-associated protein AHNAK, transcript variant X38
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
uncharacterized protein LOC115218249 isoform X36
uncharacterized protein LOC115218249 isoform X35
neuroblast differentiation-associated protein AHNAK isoform X30
uncharacterized protein LOC115218249 isoform X25
uncharacterized protein LOC115218249 isoform X19
uncharacterized protein LOC115218249 isoform X34
uncharacterized protein LOC115218249 isoform X32
neuroblast differentiation-associated protein AHNAK isoform X24
uncharacterized protein LOC115218249 isoform X20
neuroblast differentiation-associated protein AHNAK isoform X23
uncharacterized protein LOC115218249 isoform X14
neuroblast differentiation-associated protein AHNAK isoform X7
uncharacterized protein LOC115218249 isoform X33
uncharacterized protein LOC115218249 isoform X26
uncharacterized protein LOC115218249 isoform X31
uncharacterized protein LOC115218249 isoform X16
uncharacterized protein LOC115218249 isoform X9
neuroblast differentiation-associated protein AHNAK isoform X5
uncharacterized protein LOC115218249 isoform X27
uncharacterized protein LOC115218249 isoform X15
neuroblast differentiation-associated protein AHNAK isoform X10
uncharacterized protein LOC115218249 isoform X28
uncharacterized protein LOC115218249 isoform X11
neuroblast differentiation-associated protein AHNAK isoform X6
uncharacterized protein LOC115218249 isoform X21
uncharacterized protein LOC115218249 isoform X8
neuroblast differentiation-associated protein AHNAK isoform X4
uncharacterized protein LOC115218249 isoform X22
uncharacterized protein LOC115218249 isoform X18
neuroblast differentiation-associated protein AHNAK isoform X3
uncharacterized protein LOC115218249 isoform X12
uncharacterized protein LOC115218249 isoform X2
neuroblast differentiation-associated protein AHNAK isoform X29
uncharacterized protein LOC115218249 isoform X13
uncharacterized protein LOC115218249 isoform X17
uncharacterized protein LOC115218249 isoform X1
neuroblast differentiation-associated protein AHNAK isoform X37
neuroblast differentiation-associated protein AHNAK isoform X38
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
uncharacterized LOC118765697, transcript variant X1
uncharacterized LOC118765697, transcript variant X2
histone-lysine N-methyltransferase SETMAR-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
zinc finger BED domain-containing protein 5-like
uncharacterized LOC115218400, transcript variant X1
uncharacterized LOC115218400, 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 34 samples with support for all annotated introns
uncharacterized LOC115218400, transcript variant X3
uncharacterized LOC115218351, 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 39 samples with support for all annotated introns
uncharacterized LOC115218351, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC115218351, 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 10 samples with support for all annotated introns
cytochrome c oxidase assembly factor 7 homolog
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 44 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 45 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
NADH-cytochrome b5 reductase-like, 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 9 samples with support for all annotated introns
NADH-cytochrome b5 reductase-like, 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 21 samples with support for all annotated introns
NADH-cytochrome b5 reductase-like, transcript variant X3
homeobox-containing protein 1-like, 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 4 samples with support for all annotated introns
homeobox-containing protein 1-like, 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 5 samples with support for all annotated introns
homeobox-containing protein 1-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 7 samples with support for all annotated introns
homeobox-containing protein 1-like isoform X1
homeobox-containing protein 1-like isoform X3
homeobox-containing protein 1-like isoform X2
uncharacterized LOC115218375, 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
uncharacterized LOC115218375, 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 14 samples with support for all annotated introns
uncharacterized protein LOC115218375 isoform X1
uncharacterized protein LOC115218375 isoform X2
microtubule-associated protein RP/EB family member 1-like
uncharacterized LOC115218644, 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 4 samples with support for all annotated introns
uncharacterized LOC115218644, 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 16 samples with support for all annotated introns
uncharacterized protein LOC115218644 isoform X1
uncharacterized protein LOC115218644 isoform X2
synaptojanin-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
synaptojanin-1-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 26 samples with support for all annotated introns
elongation of very long chain fatty acids protein 4
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 41 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 94% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115218230, transcript variant X2
uncharacterized LOC115218230, transcript variant X1
melatonin receptor type 1B-like, transcript variant X2
melatonin receptor type 1B-like, transcript variant X1
very-long-chain 3-oxoacyl-CoA reductase-B
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 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC118765758, transcript variant X2
uncharacterized LOC118765758, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
ATP-dependent DNA helicase DDX11-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
ATP-dependent DNA helicase DDX11-like, 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 3 samples with support for all annotated introns
ATP-dependent DNA helicase DDX11-like isoform X1
ATP-dependent DNA helicase DDX11-like isoform X2
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
neurogenic locus protein delta-like, 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 15 samples with support for all annotated introns
neurogenic locus protein delta-like, 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 16 samples with support for all annotated introns
neurogenic locus protein delta-like, transcript variant X3
neurogenic locus protein delta-like isoform X2
neurogenic locus protein delta-like isoform X1
neurogenic locus protein delta-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
DNA excision repair protein ERCC-1-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 5 samples with support for all annotated introns
DNA excision repair protein ERCC-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
DNA excision repair protein ERCC-1-like isoform X2
DNA excision repair protein ERCC-1-like isoform X1
phosphoglycerate kinase 1, 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 46 samples with support for all annotated introns
phosphoglycerate kinase 1, transcript variant X1
probable phosphoglycerate kinase isoform X1
phosphoglycerate kinase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 2-like
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 33 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 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 24 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 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 27 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 2 isoform X2
glutamate receptor ionotropic, kainate 2 isoform X1
uncharacterized LOC115218353, 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 44 samples with support for all annotated introns
uncharacterized protein LOC115218353 isoform X1
zinc finger CCHC domain-containing protein 7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115218353, transcript variant X2
uncharacterized LOC115218353, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
uncharacterized protein LOC115218353 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
probable phospholipid-transporting ATPase VB, transcript variant X1
probable phospholipid-transporting ATPase VB, 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 18 samples with support for all annotated introns
probable phospholipid-transporting ATPase VB isoform X1
probable phospholipid-transporting ATPase VB isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9, mitochondrial
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 46 samples with support for all annotated introns
axonemal 84 kDa protein-like, transcript variant X3
axonemal 84 kDa protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
axonemal 84 kDa protein-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 11 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 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 37 samples with support for all annotated introns
zinc finger protein 433-like, 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 39 samples with support for all annotated introns
zinc finger protein 433-like, transcript variant X1
zinc finger protein 433-like, 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 6 samples with support for all annotated introns
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
kremen protein 1-like, transcript variant X2
kremen protein 1-like, transcript variant X1
kremen protein 1-like, transcript variant X3
WSC domain-containing protein ARB_07867, transcript variant X2
WSC domain-containing protein ARB_07867, transcript variant X1
WSC domain-containing protein ARB_07867, transcript variant X3
WSC domain-containing protein ARB_07867, transcript variant X4
WSC domain-containing protein ARB_07867 isoform X1
WSC domain-containing protein ARB_07867 isoform X2
polyprenol reductase, transcript variant X5
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 15 samples with support for all annotated introns
polyprenol reductase, 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 29 samples with support for all annotated introns
polyprenol reductase, 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 18 samples with support for all annotated introns
polyprenol reductase, 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 44 samples with support for all annotated introns
polyprenol reductase, transcript variant X2
dual specificity protein phosphatase 23, 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 35 samples with support for all annotated introns
dual specificity protein phosphatase 23, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
dual specificity protein phosphatase 23, 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 36 samples with support for all annotated introns
dual specificity protein phosphatase 23, transcript variant X4
dual specificity protein phosphatase 23 isoform X3
dual specificity protein phosphatase CDC14B isoform X1
dual specificity protein phosphatase CDC14B isoform X2
serine/threonine-protein kinase pakB isoform X4
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
molybdenum cofactor biosynthesis protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
molybdenum cofactor biosynthesis protein 1, transcript variant X2
molybdenum cofactor biosynthesis protein 1 isoform X1
molybdenum cofactor biosynthesis protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
molybdenum cofactor biosynthesis protein 1 isoform X2
uncharacterized LOC115218622, 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 25 samples with support for all annotated introns
uncharacterized LOC115218622, transcript variant X1
uncharacterized protein LOC115218622 isoform X1
uncharacterized protein LOC115218622 isoform X2
coiled-coil domain-containing protein 24-like, transcript variant X1
coiled-coil domain-containing protein 24-like, transcript variant X2
coiled-coil domain-containing protein 24-like isoform X1
coiled-coil domain-containing protein 24-like 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 41 samples with support for all annotated introns
phospholipid phosphatase 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
phospholipid phosphatase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
phospholipid phosphatase 1-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
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 45 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 88% coverage of the annotated genomic feature by RNAseq alignments
neurocalcin homolog, transcript variant X5
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 10 samples with support for all annotated introns
neurocalcin homolog, transcript variant X4
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 42 samples with support for all annotated introns
neurocalcin homolog, 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 26 samples with support for all annotated introns
neurocalcin homolog, 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 46 samples with support for all annotated introns
neurocalcin homolog, transcript variant X2
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 39 samples with support for all annotated introns
UDP-N-acetylglucosamine/UDP-glucose/GDP-mannose transporter, transcript variant X4
UDP-N-acetylglucosamine/UDP-glucose/GDP-mannose transporter, 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 15 samples with support for all annotated introns
UDP-N-acetylglucosamine/UDP-glucose/GDP-mannose transporter, transcript variant X3
UDP-N-acetylglucosamine/UDP-glucose/GDP-mannose transporter, transcript variant X1
UDP-N-acetylglucosamine/UDP-glucose/GDP-mannose transporter isoform X2
UDP-N-acetylglucosamine/UDP-glucose/GDP-mannose transporter isoform X1
E3 ubiquitin-protein ligase TRIM56-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
E3 ubiquitin-protein ligase TRIM56-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
E3 ubiquitin-protein ligase TRIM56-like, 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 42 samples with support for all annotated introns
elongation of very long chain fatty acids protein AAEL008004, transcript variant X2
elongation of very long chain fatty acids protein AAEL008004, 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 36 samples with support for all annotated introns
elongation of very long chain fatty acids protein AAEL008004
zinc metalloproteinase-disintegrin-like atrase-B, transcript variant X1
zinc metalloproteinase-disintegrin-like atrase-B isoform X1
zinc metalloproteinase-disintegrin-like atrase-B, transcript variant X2
zinc metalloproteinase-disintegrin-like atrase-B isoform X2
transient receptor potential-gamma protein-like, 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 8 samples with support for all annotated introns
transient receptor potential-gamma protein-like, transcript variant X3
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 10 samples with support for all annotated introns
transient receptor potential-gamma protein-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 11 samples with support for all annotated introns
transient receptor potential-gamma protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
transient receptor potential-gamma protein-like isoform X1
transient receptor potential-gamma protein-like isoform X3
transient receptor potential-gamma protein-like isoform X2
protein FAM47E-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
protein FAM47E-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
medium-chain acyl-CoA ligase ACSF2, mitochondrial, 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 13 samples with support for all annotated introns
medium-chain acyl-CoA ligase ACSF2, mitochondrial, transcript variant X3
medium-chain acyl-CoA ligase ACSF2, mitochondrial, 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 13 samples with support for all annotated introns
medium-chain acyl-CoA ligase ACSF2, mitochondrial, 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 26 samples with support for all annotated introns
medium-chain acyl-CoA ligase ACSF2, mitochondrial isoform X2
medium-chain acyl-CoA ligase ACSF2, mitochondrial isoform X1
E3 ubiquitin-protein ligase RNF170, transcript variant X1
E3 ubiquitin-protein ligase RNF170, 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 27 samples with support for all annotated introns
protein Hook homolog 3, 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 40 samples with support for all annotated introns
protein Hook homolog 3, 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 45 samples with support for all annotated introns
protein Hook homolog 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
protein Hook homolog 3, transcript variant X4
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 21 samples with support for all annotated introns
transfer RNA glycine (anticodon ACC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
replication protein A 32 kDa subunit, 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 18 samples with support for all annotated introns
replication protein A 32 kDa subunit, transcript variant X2
replication protein A 32 kDa subunit isoform X1
replication protein A 32 kDa subunit isoform X2
polyadenylate-binding protein-interacting protein 1
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 46 samples with support for all annotated introns
very low-density lipoprotein receptor, 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 17 samples with support for all annotated introns
very low-density lipoprotein receptor, 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 34 samples with support for all annotated introns
very low-density lipoprotein receptor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
very low-density lipoprotein receptor isoform X2
very low-density lipoprotein receptor isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments
receptor-type tyrosine-protein phosphatase T-like, transcript variant X1
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 19 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase T-like, transcript variant X2
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 23 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase T-like isoform X2
receptor-type tyrosine-protein phosphatase U-like isoform X1
DDB1- and CUL4-associated factor 17, 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 32 samples with support for all annotated introns
DDB1- and CUL4-associated factor 17, transcript variant X6
DDB1- and CUL4-associated factor 17, transcript variant 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 29 samples with support for all annotated introns
DDB1- and CUL4-associated factor 17, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
DDB1- and CUL4-associated factor 17, transcript variant X4
DDB1- and CUL4-associated factor 17 isoform X1
DDB1- and CUL4-associated factor 17 isoform X6
DDB1- and CUL4-associated factor 17 isoform X5
DDB1- and CUL4-associated factor 17 isoform X2
DDB1- and CUL4-associated factor 17 isoform X4
DDB1- and CUL4-associated factor 17, transcript variant X3
DDB1- and CUL4-associated factor 17 isoform X3
coiled-coil domain-containing protein 22 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
coiled-coil domain-containing protein 22 homolog, transcript variant X2
coiled-coil domain-containing protein 22 homolog
serine/threonine-protein kinase STK11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
serine/threonine-protein kinase STK11, 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 12 samples with support for all annotated introns
serine/threonine-protein kinase STK11, transcript variant X3
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 39 samples with support for all annotated introns
serine/threonine-protein kinase STK11 isoform X1
serine/threonine-protein kinase STK11 isoform X2
serine/threonine-protein kinase STK11 isoform X3
asparagine synthetase domain-containing protein 1, transcript variant X2
asparagine synthetase domain-containing protein 1, transcript variant X6
asparagine synthetase domain-containing protein 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 8 samples with support for all annotated introns
asparagine synthetase domain-containing protein 1, transcript variant X5
asparagine synthetase domain-containing protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
asparagine synthetase domain-containing protein 1, transcript variant X3
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
asparagine synthetase domain-containing protein 1 isoform X2
asparagine synthetase domain-containing protein 1 isoform X5
asparagine synthetase domain-containing protein 1 isoform X4
asparagine synthetase domain-containing protein 1 isoform X1
asparagine synthetase domain-containing protein 1 isoform X3
asparagine synthetase domain-containing protein 1 isoform X6
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 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 99% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
NF-X1-type zinc finger protein NFXL1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein OZF-like, transcript variant X2
zinc finger protein OZF-like, transcript variant X1
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
uncharacterized LOC115218449, transcript variant X1
uncharacterized LOC115218449, transcript variant X2
uncharacterized protein LOC115218449 isoform X1
uncharacterized protein LOC115218449 isoform X2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 5, transcript variant X9
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 34 samples with support for all annotated introns
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily 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 45 samples with support for all annotated introns
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 5, transcript variant X7
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 5, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 5, transcript variant X8
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 34 samples with support for all annotated introns
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 5, transcript variant X6
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 5, transcript variant X4
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 5, transcript variant X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 5 isoform X9
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 5 isoform X8
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 5 isoform X6
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 5 isoform X7
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 5 isoform X5
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 5 isoform X3
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 5 isoform X4
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 5 isoform X2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 5 isoform X1
DNA primase large subunit, 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
DNA primase large subunit, 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 21 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC115218674, transcript variant X2
uncharacterized LOC115218674, transcript variant X1
uncharacterized LOC115218537, transcript variant X2
uncharacterized LOC115218537, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115218436, transcript variant X2
uncharacterized LOC115218436, transcript variant X1
uncharacterized protein LOC115218436 isoform X1
uncharacterized protein LOC115218436 isoform X2
uncharacterized LOC115218502, 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 28 samples with support for all annotated introns
uncharacterized LOC115218502, transcript variant X1
uncharacterized protein LOC115218502 isoform X1
uncharacterized protein LOC115218502 isoform X2
uncharacterized LOC115218383, transcript variant X2
uncharacterized LOC115218383, transcript variant X1
uncharacterized protein LOC115218383 isoform X1
uncharacterized protein LOC115218383 isoform X2
uncharacterized LOC115218502, transcript variant X3
uncharacterized protein LOC115218502 isoform X3
uncharacterized LOC115218660, 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 33 samples with support for all annotated introns
uncharacterized LOC115218660, transcript variant X1
uncharacterized protein LOC115218660 isoform X1
uncharacterized protein LOC115218660 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
heat shock protein 75 kDa, mitochondrial
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 44 samples with support for all annotated introns
periodic tryptophan protein 2 homolog, transcript variant X3
V-type proton ATPase 16 kDa proteolipid subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
periodic tryptophan protein 2 homolog, 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 43 samples with support for all annotated introns
periodic tryptophan protein 2 homolog isoform X2
periodic tryptophan protein 2 homolog, 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 10 samples with support for all annotated introns
periodic tryptophan protein 2 homolog isoform X1
U3 small nucleolar RNA-associated protein 6 homolog
probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase, 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
probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase, transcript variant X2
probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase isoform X2
probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase isoform X3
probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase isoform X1
NEDD4-binding protein 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 23 samples with support for all annotated introns
NEDD4-binding protein 2, transcript variant X2
uncharacterized protein LOC115218429 isoform X2
uncharacterized protein LOC115218429 isoform X1
NEDD4-binding protein 2, transcript variant X3
uncharacterized LOC118765779, transcript variant X1
uncharacterized LOC118765779, transcript variant X2
coiled-coil domain-containing protein 138-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 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: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 32 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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC115218574
transmembrane protein 185B-like, 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 26 samples with support for all annotated introns
transmembrane protein 185B-like, transcript variant X1
transmembrane protein 185B-like isoform X2
transmembrane protein 185B-like isoform X1
ankyrin repeat domain-containing protein 46
DNA-directed RNA polymerase I subunit RPA49
disks large-associated protein 5, transcript variant X30
disks large-associated protein 5, transcript variant X27
disks large-associated protein 5, transcript variant X32
disks large-associated protein 5, transcript variant X29
disks large-associated protein 5, transcript variant X23
disks large-associated protein 5, transcript variant X19
disks large-associated protein 5, transcript variant X13
disks large-associated protein 5, transcript variant X21
disks large-associated protein 5, transcript variant X28
disks large-associated protein 5, transcript variant X8
disks large-associated protein 5, transcript variant X2
disks large-associated protein 5, transcript variant X18
disks large-associated protein 5, transcript variant X15
disks large-associated protein 5, transcript variant X7
disks large-associated protein 5, transcript variant X22
disks large-associated protein 5, transcript variant X16
disks large-associated protein 5, transcript variant X9
disks large-associated protein 5, transcript variant X17
disks large-associated protein 5, transcript variant X10
disks large-associated protein 5, transcript variant X25
disks large-associated protein 5, transcript variant X11
disks large-associated protein 5, transcript variant X31
disks large-associated protein 5, transcript variant X26
disks large-associated protein 5, transcript variant X24
disks large-associated protein 5, transcript variant X14
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
disks large-associated protein 5, transcript variant X20
disks large-associated protein 5, transcript variant X5
disks large-associated protein 5, transcript variant X1
disks large-associated protein 5, transcript variant X6
disks large-associated protein 5, transcript variant X3
disks large-associated protein 5, transcript variant X12
disks large-associated protein 5, transcript variant X4
disks large-associated protein 5 isoform X30
disks large-associated protein 5 isoform X27
disks large-associated protein 5 isoform X32
disks large-associated protein 5 isoform X29
disks large-associated protein 5 isoform X23
neurofilament heavy polypeptide isoform X19
neurofilament heavy polypeptide isoform X13
neurofilament heavy polypeptide isoform X21
disks large-associated protein 5 isoform X28
neurofilament heavy polypeptide isoform X8
uncharacterized protein LOC115218498 isoform X2
neurofilament heavy polypeptide isoform X18
neurofilament heavy polypeptide isoform X15
uncharacterized protein LOC115218498 isoform X7
disks large-associated protein 4 isoform X22
neurofilament heavy polypeptide isoform X16
uncharacterized protein LOC115218498 isoform X9
neurofilament heavy polypeptide isoform X17
uncharacterized protein LOC115218498 isoform X10
disks large-associated protein 5 isoform X25
neurofilament heavy polypeptide isoform X11
disks large-associated protein 5 isoform X31
disks large-associated protein 5 isoform X26
disks large-associated protein 5 isoform X24
disks large-associated protein 4 isoform X14
disks large-associated protein 4 isoform X20
neurofilament heavy polypeptide isoform X5
neurofilament heavy polypeptide isoform X1
neurofilament heavy polypeptide isoform X6
neurofilament heavy polypeptide isoform X3
neurofilament heavy polypeptide isoform X12
neurofilament heavy polypeptide isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
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 2 samples with support for all annotated introns
organic cation transporter protein, transcript variant X3
organic cation transporter protein, transcript variant X2
organic cation transporter protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
solute carrier family 22 member 4 isoform X2
organic cation transporter protein 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
organic cation transporter protein, transcript variant X4
organic cation transporter protein isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
organic cation transporter protein, transcript variant X5
organic cation transporter protein isoform X2
organic cation transporter protein isoform X4
organic cation transporter protein, transcript variant X6
organic cation transporter protein isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 1 Protein, and 85% 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: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
protocadherin-11 X-linked, transcript variant X11
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 5 samples with support for all annotated introns
protocadherin-11 X-linked, transcript variant X5
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
protocadherin-11 X-linked, transcript variant X10
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
protocadherin-11 X-linked, transcript variant X6
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 4 samples with support for all annotated introns
protocadherin-11 X-linked, 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
protocadherin-11 X-linked, transcript variant X3
protocadherin-11 X-linked, transcript variant X4
protocadherin-11 X-linked, transcript variant X2
protocadherin-11 X-linked, transcript variant X8
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
protocadherin-11 X-linked, transcript variant X9
protocadherin-11 X-linked, transcript variant X13
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 7 samples with support for all annotated introns
protocadherin-11 X-linked, transcript variant X12
protocadherin-11 X-linked, transcript variant X7
uncharacterized LOC118765782, transcript variant X1
uncharacterized LOC118765782, transcript variant X2
uncharacterized LOC118765783, transcript variant X2
uncharacterized LOC118765783, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
uncharacterized LOC118765786, transcript variant X1
uncharacterized LOC118765786, transcript variant X2
uncharacterized LOC115218265, transcript variant X1
uncharacterized LOC115218265, 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 20 samples with support for all annotated introns
uncharacterized protein LOC115218265 isoform X2
uncharacterized protein LOC115218265 isoform X1
centrosomal protein of 135 kDa-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 13 samples with support for all annotated introns
centrosomal protein of 135 kDa-like, transcript variant X3
centrosomal protein of 135 kDa-like isoform X1
testis-specific gene 10 protein-like isoform X2
centrosomal protein of 135 kDa-like, 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 10 samples with support for all annotated introns
DNA repair and recombination protein RAD54-like
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
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
F-box/LRR-repeat protein 12, transcript variant X1
F-box/LRR-repeat protein 12, transcript variant X2
dimethyladenosine transferase 1, mitochondrial
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
coiled-coil domain-containing protein 169-like, transcript variant X2
coiled-coil domain-containing protein 169-like, transcript variant X1
coiled-coil domain-containing protein 169-like isoform X2
coiled-coil domain-containing protein 169-like isoform X1
rho GTPase-activating protein 7, 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 34 samples with support for all annotated introns
rho GTPase-activating protein 7, 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 24 samples with support for all annotated introns
rho GTPase-activating protein 7, 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 41 samples with support for all annotated introns
rho GTPase-activating protein 7, 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 16 samples with support for all annotated introns
rho GTPase-activating protein 7 isoform X1
rho GTPase-activating protein 7 isoform X4
rho GTPase-activating protein 7 isoform X2
rho GTPase-activating protein 7 isoform 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 46 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 14 samples with support for all annotated introns
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
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 42 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized LOC115218615, 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 33 samples with support for all annotated introns
uncharacterized LOC115218615, transcript variant X2
uncharacterized LOC115218648, transcript variant X1
uncharacterized LOC115218648, transcript variant X2
uncharacterized protein LOC115218648 isoform X2
uncharacterized protein LOC115218648 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
uncharacterized LOC115218518, 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 40 samples with support for all annotated introns
uncharacterized LOC115218518, transcript variant X2
uncharacterized protein LOC115218518 isoform X1
uncharacterized protein LOC115218518 isoform X2
L-aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase-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 28 samples with support for all annotated introns
L-aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase-like, 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 8 samples with support for all annotated introns
L-aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
L-aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase-like isoform X1
L-aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase-like, transcript variant X3
L-aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase-like isoform X2
piggyBac transposable element-derived protein 5-like
transcription initiation factor TFIID subunit 1, 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 23 samples with support for all annotated introns
transcription initiation factor TFIID subunit 1, transcript variant X1
transcription initiation factor TFIID subunit 1, transcript variant X3
transcription initiation factor TFIID subunit 1, transcript variant X2
transcription initiation factor TFIID subunit 1 isoform X2
transcription initiation factor TFIID subunit 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
post-GPI attachment to proteins factor 2-like, 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 25 samples with support for all annotated introns
post-GPI attachment to proteins factor 2-like isoform X2
post-GPI attachment to proteins factor 2-like, 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 33 samples with support for all annotated introns
post-GPI attachment to proteins factor 2-like, 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 2 samples with support for all annotated introns
post-GPI attachment to proteins factor 2-like, 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 4 samples with support for all annotated introns
post-GPI attachment to proteins factor 2-like isoform X1
post-GPI attachment to proteins factor 2-like isoform X4
post-GPI attachment to proteins factor 2-like isoform X3
mitochondrial ornithine transporter 1, 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 41 samples with support for all annotated introns
mitochondrial ornithine transporter 1, transcript variant X4
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 23 samples with support for all annotated introns
mitochondrial ornithine transporter 1, transcript variant X2
mitochondrial ornithine transporter 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
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 45 samples with support for all annotated introns
general transcription factor IIH subunit 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, including 43 samples with support for all annotated introns
uridine-cytidine kinase-like 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uridine-cytidine kinase-like 1, transcript variant X2
uridine-cytidine kinase-like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uridine-cytidine kinase-like 1 isoform X1
uridine-cytidine kinase-like 1 isoform X2
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like, transcript variant X2
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like, transcript variant X1
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like isoform X1
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like isoform X2
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase
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 40 samples with support for all annotated introns
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like
glycine receptor subunit alpha-3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glycine receptor subunit alpha-3-like, 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
glycine receptor subunit alpha-3-like, transcript variant X1
glycine receptor subunit alpha-3-like, transcript variant X4
glycine receptor subunit alpha-3-like isoform X2
glycine receptor subunit alpha-3-like isoform X1
CENPB DNA-binding domain-containing protein 1-like, transcript variant X3
CENPB DNA-binding domain-containing protein 1-like, transcript variant X2
CENPB DNA-binding domain-containing protein 1-like, transcript variant X1
CENPB DNA-binding domain-containing protein 1-like
ATPase family protein 2 homolog, transcript variant X1
ATPase family protein 2 homolog, 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 21 samples with support for all annotated introns
ATPase family protein 2 homolog isoform X1
ATPase family protein 2 homolog isoform X2
RNA-binding protein 26, transcript variant X2
RNA-binding protein 26, transcript variant X3
RNA-binding protein 26, 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 37 samples with support for all annotated introns
uncharacterized LOC118765800, transcript variant X1
uncharacterized LOC118765800, transcript variant X3
uncharacterized LOC118765800, transcript variant X2
uncharacterized LOC118765800, transcript variant X4
uncharacterized LOC118765800, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cadherin-related tumor suppressor-like
vascular endothelial growth factor D, transcript variant X2
vascular endothelial growth factor D, transcript variant X1
mediator of RNA polymerase II transcription subunit 16-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
branched-chain-amino-acid aminotransferase, cytosolic, 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 38 samples with support for all annotated introns
branched-chain-amino-acid aminotransferase, cytosolic, 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 30 samples with support for all annotated introns
branched-chain-amino-acid aminotransferase, cytosolic isoform X1
branched-chain-amino-acid aminotransferase, cytosolic isoform X2
alkylated DNA repair protein alkB homolog 8, 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 38 samples with support for all annotated introns
alkylated DNA repair protein alkB homolog 8, transcript variant X2
alkylated DNA repair protein alkB homolog 8, transcript variant X3
alkylated DNA repair protein alkB homolog 8, transcript variant X4
alkylated DNA repair protein alkB homolog 8 isoform X1
alkylated DNA repair protein alkB homolog 8 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
GRB2-associated-binding protein 2, transcript variant X2
GRB2-associated-binding protein 2, transcript variant X1
GRB2-associated-binding protein 2 isoform X1
GRB2-associated-binding protein 2 isoform X2
GRB2-associated-binding protein 2, 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 17 samples with support for all annotated introns
GRB2-associated-binding protein 2, transcript variant X3
uncharacterized protein LOC115218412 isoform X3
transmembrane protein 144-like, transcript variant X3
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 18 samples with support for all annotated introns
transmembrane protein 144-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 15 samples with support for all annotated introns
transmembrane protein 144-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
transmembrane protein 144-like isoform X3
transmembrane protein 144-like isoform X1
transmembrane protein 144-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
inositol hexakisphosphate kinase 1, 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 36 samples with support for all annotated introns
inositol hexakisphosphate kinase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
glutamate receptor ionotropic, NMDA 3A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
glutamate receptor ionotropic, NMDA 3A-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 19 samples with support for all annotated introns
glutamate receptor ionotropic, NMDA 3A-like isoform X1
glutamate receptor ionotropic, NMDA 3A-like isoform X2
uncharacterized LOC115218653, transcript variant X1
uncharacterized LOC115218653, transcript variant X2
GATA zinc finger domain-containing protein 14-like
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
inverted formin-2, transcript variant X1
inverted formin-2, transcript variant X4
inverted formin-2, transcript variant X3
inverted formin-2, transcript variant X2
pre-mRNA 3'-end-processing factor FIP1, 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 42 samples with support for all annotated introns
pre-mRNA 3'-end-processing factor FIP1, transcript variant X1
pre-mRNA 3'-end-processing factor FIP1, transcript variant X4
pre-mRNA 3'-end-processing factor FIP1, transcript variant X3
pre-mRNA 3'-end-processing factor FIP1 isoform X4
pre-mRNA 3'-end-processing factor FIP1 isoform X3
pre-mRNA 3'-end-processing factor FIP1 isoform X2
pre-mRNA 3'-end-processing factor FIP1 isoform X1
translation initiation factor IF-3, mitochondrial
cGMP-dependent 3',5'-cyclic phosphodiesterase-like, transcript variant X1
cGMP-dependent 3',5'-cyclic phosphodiesterase-like, 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 1 sample with support for all annotated introns
cGMP-dependent 3',5'-cyclic phosphodiesterase-like, transcript variant X3
cGMP-dependent 3',5'-cyclic phosphodiesterase-like isoform X1
cGMP-dependent 3',5'-cyclic phosphodiesterase-like isoform X2
uncharacterized LOC115218538, 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 26 samples with support for all annotated introns
uncharacterized LOC115218538, transcript variant X1
uncharacterized protein LOC115218538 isoform X2
uncharacterized protein LOC115218538 isoform X1
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
E3 ubiquitin-protein ligase MYCBP2, 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 25 samples with support for all annotated introns
E3 ubiquitin-protein ligase MYCBP2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
E3 ubiquitin-protein ligase MYCBP2, 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 27 samples with support for all annotated introns
E3 ubiquitin-protein ligase MYCBP2, transcript variant X4
E3 ubiquitin-protein ligase MYCBP2, transcript variant X3
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 23 samples with support for all annotated introns
E3 ubiquitin-protein ligase MYCBP2, 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 21 samples with support for all annotated introns
E3 ubiquitin-protein ligase MYCBP2, transcript variant X6
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 22 samples with support for all annotated introns
E3 ubiquitin-protein ligase MYCBP2 isoform X7
E3 ubiquitin-protein ligase MYCBP2 isoform X5
E3 ubiquitin-protein ligase MYCBP2 isoform X2
E3 ubiquitin-protein ligase MYCBP2 isoform X4
E3 ubiquitin-protein ligase MYCBP2 isoform X3
E3 ubiquitin-protein ligase MYCBP2 isoform X1
E3 ubiquitin-protein ligase MYCBP2 isoform X6
uncharacterized LOC115218647, transcript variant X1
uncharacterized LOC115218647, transcript variant X2
uncharacterized LOC115218299, transcript variant X2
uncharacterized LOC115218299, transcript variant X1
uncharacterized protein LOC115218299 isoform X1
uncharacterized protein LOC115218299 isoform X2
zinc finger protein 239-like, transcript variant X4
zinc finger protein 239-like, transcript variant X2
zinc finger protein 239-like, transcript variant X3
zinc finger protein 239-like, transcript variant X1
zinc finger protein 239-like, transcript variant X5
zinc finger protein 239-like, transcript variant X6
fatty acid hydroxylase domain-containing protein 2, transcript variant X3
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 34 samples with support for all annotated introns
fatty acid hydroxylase domain-containing protein 2, transcript variant X4
fatty acid hydroxylase domain-containing protein 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 28 samples with support for all annotated introns
fatty acid hydroxylase domain-containing protein 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, including 33 samples with support for all annotated introns
fatty acid hydroxylase domain-containing protein 2
fucose-1-phosphate guanylyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
myotubularin-related protein 6, 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 45 samples with support for all annotated introns
myotubularin-related protein 6, 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 31 samples with support for all annotated introns
myotubularin-related protein 6, 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 37 samples with support for all annotated introns
myotubularin-related protein 6 isoform X3
myotubularin-related protein 8 isoform X1
myotubularin-related protein 8 isoform X2
myotubularin-related protein 6, transcript variant X4
myotubularin-related protein 8 isoform X4
nucleoporin p58/p45, 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 1 sample with support for all annotated introns
nucleoporin p58/p45, transcript variant X4
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
nucleoporin p58/p45, transcript variant X2
nucleoporin p58/p45, transcript variant X5
nucleoporin p58/p45, transcript variant X7
nucleoporin p58/p45, transcript variant X8
nucleoporin p58/p45, transcript variant X6
nucleoporin p58/p45, 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 27 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
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 45 samples with support for all annotated introns
uncharacterized LOC115218667, transcript variant X3
uncharacterized LOC115218667, transcript variant X1
uncharacterized LOC115218667, transcript variant X2
cilia- and flagella-associated protein 97-like, transcript variant X1
cilia- and flagella-associated protein 97-like, transcript variant X2
cilia- and flagella-associated protein 97-like isoform X2
cilia- and flagella-associated protein 97-like isoform X1
cilia- and flagella-associated protein 97-like, transcript variant X3
cilia- and flagella-associated protein 97-like isoform X3
probable cysteine--tRNA ligase, mitochondrial, transcript variant X6
probable cysteine--tRNA ligase, mitochondrial, transcript variant X5
probable cysteine--tRNA ligase, mitochondrial, 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 24 samples with support for all annotated introns
probable cysteine--tRNA ligase, mitochondrial, transcript variant X8
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 23 samples with support for all annotated introns
probable cysteine--tRNA ligase, mitochondrial, 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 29 samples with support for all annotated introns
probable cysteine--tRNA ligase, mitochondrial, transcript variant X4
probable cysteine--tRNA ligase, mitochondrial, transcript variant X3
probable cysteine--tRNA ligase, mitochondrial, transcript variant X7
probable cysteine--tRNA ligase, mitochondrial isoform X2
probable cysteine--tRNA ligase, mitochondrial isoform X1
inhibitor of growth protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
inhibitor of growth protein 1 isoform X1
inhibitor of growth protein 1, 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 12 samples with support for all annotated introns
inhibitor of growth protein 1 isoform X2
uncharacterized oxidoreductase SSP0419-like
linear gramicidin synthase subunit D, transcript variant X3
linear gramicidin synthase subunit D, 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 28 samples with support for all annotated introns
linear gramicidin synthase subunit D, 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 26 samples with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1, 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 17 samples with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1, transcript variant X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1, 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 27 samples with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1, transcript variant X3
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1 isoform X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1 isoform X4
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1 isoform X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1 isoform X3
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase, transcript variant X5
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
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase, transcript variant X4
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase isoform X5
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase isoform X4
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase, transcript variant X3
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 31 samples with support for all annotated introns
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase, 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 35 samples with support for all annotated introns
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase isoform X3
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase isoform X2
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase, transcript variant X1
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase isoform 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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31% 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
vascular endothelial growth factor receptor 1, transcript variant X1
vascular endothelial growth factor receptor 1, 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 30 samples with support for all annotated introns
vascular endothelial growth factor receptor 1, transcript variant X3
vascular endothelial growth factor receptor 1, transcript variant X4
vascular endothelial growth factor receptor 1, transcript variant X5
vascular endothelial growth factor receptor 1, transcript variant X6
vascular endothelial growth factor receptor 1 isoform X1
vascular endothelial growth factor receptor 1 isoform X2
vascular endothelial growth factor receptor 1 isoform X3
vascular endothelial growth factor receptor 1 isoform X4
vascular endothelial growth factor receptor 1 isoform X5
vascular endothelial growth factor receptor 1 isoform X6
mediator of RNA polymerase II transcription subunit 7
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 46 samples with support for all annotated introns
Bardet-Biedl syndrome 7 protein homolog, transcript variant X2
Bardet-Biedl syndrome 7 protein 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 19 samples with support for all annotated introns
Bardet-Biedl syndrome 7 protein homolog isoform X2
Bardet-Biedl syndrome 7 protein homolog isoform X1
DNA-binding protein SMUBP-2, transcript variant X2
DNA-binding protein SMUBP-2, 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 9 samples with support for all annotated introns
DNA-binding protein SMUBP-2, 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 23 samples with support for all annotated introns
DNA-binding protein SMUBP-2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ras-related protein Rab-30, 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 17 samples with support for all annotated introns
ras-related protein Rab-30, 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 41 samples with support for all annotated introns
ras-related protein Rab-30, 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 38 samples with support for all annotated introns
ras-related protein Rab-30, 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 10 samples with support for all annotated introns
pre-mRNA cleavage complex 2 protein Pcf11, transcript variant X5
pre-mRNA cleavage complex 2 protein Pcf11, transcript variant X4
pre-mRNA cleavage complex 2 protein Pcf11, transcript variant X2
pre-mRNA cleavage complex 2 protein Pcf11, transcript variant X1
pre-mRNA cleavage complex 2 protein Pcf11, transcript variant X3
pre-mRNA cleavage complex 2 protein Pcf11 isoform X1
pre-mRNA cleavage complex 2 protein Pcf11 isoform X2
pre-mRNA cleavage complex 2 protein Pcf11 isoform X3
pre-mRNA cleavage complex 2 protein Pcf11 isoform X4
pre-mRNA cleavage complex 2 protein Pcf11 isoform X5
putative Ras-related protein Rab-33, 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 12 samples with support for all annotated introns
putative Ras-related protein Rab-33, 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 14 samples with support for all annotated introns
N-alpha-acetyltransferase 15, NatA auxiliary subunit
armadillo repeat-containing protein 3-like, transcript variant X1
armadillo repeat-containing protein 3-like, 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 8 samples with support for all annotated introns
armadillo repeat-containing protein 3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
armadillo repeat-containing protein 3-like isoform X1
armadillo repeat-containing protein 3-like isoform X2
ATP synthase mitochondrial F1 complex assembly factor 1, transcript variant X3
ATP synthase mitochondrial F1 complex assembly factor 1, transcript variant X2
ATP synthase mitochondrial F1 complex assembly factor 1, transcript variant X4
ATP synthase mitochondrial F1 complex assembly factor 1, transcript variant X1
ATP synthase mitochondrial F1 complex assembly factor 1
sodium bicarbonate transporter-like protein 11, 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 1 sample with support for all annotated introns
sodium bicarbonate transporter-like protein 11, 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 27 samples with support for all annotated introns
sodium bicarbonate transporter-like protein 11, 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 15 samples with support for all annotated introns
sodium bicarbonate transporter-like protein 11 isoform X1
sodium bicarbonate transporter-like protein 11 isoform X2
protein SGT1 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 31 samples with support for all annotated introns
protein SGT1 homolog, 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 35 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
putative uncharacterized protein DDB_G0272516
polyadenylate-binding protein 1-A, transcript variant X1
polyadenylate-binding protein 1-A, transcript variant X2
polyadenylate-binding protein 1-A, transcript variant X4
polyadenylate-binding protein 1-A, transcript variant X3
polyadenylate-binding protein, cytoplasmic and nuclear isoform X1
polyadenylate-binding protein 1-A isoform X2
polyadenylate-binding protein 1-A, transcript variant X5
polyadenylate-binding protein, cytoplasmic and nuclear isoform X3
protein tumorous imaginal discs, mitochondrial, 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 45 samples with support for all annotated introns
protein tumorous imaginal discs, mitochondrial, transcript variant X1
protein tumorous imaginal discs, mitochondrial isoform X2
protein tumorous imaginal discs, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
protocadherin Fat 1, 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 2 samples with support for all annotated introns
protocadherin Fat 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protocadherin Fat 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
protocadherin Fat 1, transcript variant X5
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 24 samples with support for all annotated introns
protocadherin Fat 1, transcript variant X7
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 29 samples with support for all annotated introns
protocadherin Fat 1, transcript variant X8
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 12 samples with support for all annotated introns
protocadherin Fat 1, transcript variant X9
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 21 samples with support for all annotated introns
protocadherin Fat 1, transcript variant X4
protocadherin Fat 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
protocadherin Fat 1, transcript variant X10
protocadherin Fat 1, transcript variant X12
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 15 samples with support for all annotated introns
protocadherin Fat 1, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
protocadherin Fat 1, transcript variant X13
protocadherin Fat 1, transcript variant X16
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 17 samples with support for all annotated introns
protocadherin Fat 1, transcript variant X20
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 19 samples with support for all annotated introns
protocadherin Fat 1, transcript variant X14
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 14 samples with support for all annotated introns
protocadherin Fat 1, transcript variant X18
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 20 samples with support for all annotated introns
protocadherin Fat 1, transcript variant X19
protocadherin Fat 1, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
protocadherin Fat 1, transcript variant X15
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 25 samples with support for all annotated introns
magnesium transporter NIPA2, 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 44 samples with support for all annotated introns
magnesium transporter NIPA2, 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 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
sodium-dependent glucose transporter 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
sodium-dependent glucose transporter 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 9 samples with support for all annotated introns
uncharacterized LOC118765724, transcript variant X6
uncharacterized LOC118765724, transcript variant X2
uncharacterized LOC118765724, transcript variant X3
uncharacterized LOC118765724, transcript variant X5
uncharacterized LOC118765724, transcript variant X1
uncharacterized LOC118765724, transcript variant X4
serine-aspartate repeat-containing protein I-like
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC115218424, transcript variant X2
uncharacterized protein LOC115218424 isoform X2
uncharacterized LOC115218424, transcript variant X1
uncharacterized LOC115218424, transcript variant X3
uncharacterized LOC115218424, transcript variant X4
uncharacterized protein LOC115218424 isoform X1
uncharacterized protein LOC115218424 isoform X3
uncharacterized protein LOC115218424 isoform X4
beta-1,3-galactosyltransferase 2, 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 26 samples with support for all annotated introns
beta-1,3-galactosyltransferase 2, 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 8 samples with support for all annotated introns
beta-1,3-galactosyltransferase 2, 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 30 samples with support for all annotated introns
NTF2-related export protein 2, transcript variant X2
NTF2-related export protein 2 isoform X2
NTF2-related export protein 2, 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 38 samples with support for all annotated introns
uncharacterized LOC115218231, 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 24 samples with support for all annotated introns
uncharacterized protein LOC115218231 isoform X1
uncharacterized LOC115218231, transcript variant X2
uncharacterized protein LOC115218231 isoform X2
uncharacterized LOC115218231, transcript variant X3
uncharacterized protein LOC115218231 isoform X3
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
uncharacterized LOC118765834, transcript variant X4
uncharacterized LOC118765834, transcript variant X5
uncharacterized LOC118765834, transcript variant X3
uncharacterized LOC118765834, transcript variant X6
uncharacterized LOC118765834, transcript variant X2
uncharacterized LOC118765834, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
mesoderm induction early response protein 1, transcript variant X6
mesoderm induction early response protein 1, 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 34 samples with support for all annotated introns
mesoderm induction early response protein 1, transcript variant X4
mesoderm induction early response protein 1, transcript variant X2
mesoderm induction early response protein 1, transcript variant X3
mesoderm induction early response protein 1, 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 37 samples with support for all annotated introns
mesoderm induction early response protein 1 isoform X6
mesoderm induction early response protein 1 isoform X1
mesoderm induction early response protein 1 isoform X4
mesoderm induction early response protein 1 isoform X2
mesoderm induction early response protein 1 isoform X3
mesoderm induction early response protein 1 isoform X5
probable global transcription activator SNF2L2, transcript variant X7
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 17 samples with support for all annotated introns
probable global transcription activator SNF2L2, transcript variant X1
probable global transcription activator SNF2L2, transcript variant X6
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 14 samples with support for all annotated introns
probable global transcription activator SNF2L2, transcript variant X5
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 44 samples with support for all annotated introns
probable global transcription activator SNF2L2, transcript variant X4
probable global transcription activator SNF2L2, transcript variant X2
probable global transcription activator SNF2L2 isoform X6
probable global transcription activator SNF2L2 isoform X1
probable global transcription activator SNF2L2 isoform X5
probable global transcription activator SNF2L2 isoform X4
probable global transcription activator SNF2L2 isoform X3
probable global transcription activator SNF2L2, transcript variant X3
probable global transcription activator SNF2L2 isoform X2
12 kDa FK506-binding protein-like, 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 31 samples with support for all annotated introns
12 kDa FK506-binding protein-like, 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 46 samples with support for all annotated introns
12 kDa FK506-binding protein-like isoform X2
12 kDa FK506-binding protein-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
CDK5 and ABL1 enzyme substrate 1-like, transcript variant X1
CDK5 and ABL1 enzyme substrate 1-like, transcript variant X6
CDK5 and ABL1 enzyme substrate 1-like, transcript variant X3
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
CDK5 and ABL1 enzyme substrate 1-like, 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
CDK5 and ABL1 enzyme substrate 1-like, transcript variant X7
CDK5 and ABL1 enzyme substrate 1-like, transcript variant X5
CDK5 and ABL1 enzyme substrate 1-like, transcript variant X4
CDK5 and ABL1 enzyme substrate 1-like, transcript variant X8
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 22 samples with support for all annotated introns
CDK5 and ABL1 enzyme substrate 1-like isoform X8
CDK5 and ABL1 enzyme substrate 1-like isoform X6
CDK5 and ABL1 enzyme substrate 1-like isoform X3
CDK5 and ABL1 enzyme substrate 2-like isoform X7
CDK5 and ABL1 enzyme substrate 1-like isoform X2
CDK5 and ABL1 enzyme substrate 2-like isoform X5
CDK5 and ABL1 enzyme substrate 1-like isoform X4
uncharacterized protein LOC115218474 isoform X1
E3 ubiquitin-protein ligase MIB1, 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 43 samples with support for all annotated introns
E3 ubiquitin-protein ligase MIB1, transcript variant X2
E3 ubiquitin-protein ligase MIB1 isoform X1
E3 ubiquitin-protein ligase MIB1 isoform X2
nuclear pore complex protein Nup153, 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 42 samples with support for all annotated introns
nuclear pore complex protein Nup153, transcript variant X2
nuclear pore complex protein Nup153 isoform X2
nuclear pore complex protein Nup153 isoform X1
uncharacterized LOC115218611, transcript variant X3
uncharacterized LOC115218611, transcript variant X2
uncharacterized LOC115218611, transcript variant X1
uncharacterized LOC115218611, transcript variant X4
uncharacterized protein LOC115218611 isoform X1
uncharacterized protein LOC115218611 isoform X3
uncharacterized protein LOC115218611 isoform X2
uncharacterized protein LOC115218611 isoform X4
uncharacterized LOC115218611, transcript variant X5
uncharacterized protein LOC115218611 isoform X5
uncharacterized LOC115218515, transcript variant X2
uncharacterized LOC115218515, transcript variant X1
uncharacterized LOC115218515, transcript variant X4
uncharacterized LOC115218515, transcript variant X3
uncharacterized LOC115218515, transcript variant X5
uncharacterized protein LOC115218515 isoform X1
uncharacterized protein LOC115218515 isoform X3
uncharacterized protein LOC115218515 isoform X2
uncharacterized protein LOC115218515 isoform X4
proton channel OtopLc, 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 6 samples with support for all annotated introns
proton channel OtopLc, transcript variant X2
proton channel OtopLc, transcript variant X4
proton channel OtopLc, 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 8 samples with support for all annotated introns
kinase D-interacting substrate of 220 kDa
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 42 samples with support for all annotated introns
transcriptional regulator ATRX, 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 9 samples with support for all annotated introns
transcriptional regulator ATRX, 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 17 samples with support for all annotated introns
transcriptional regulator ATRX, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
transcriptional regulator ATRX isoform X1
transcriptional regulator ATRX isoform X2
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 18 samples with support for all annotated introns
tigger transposable element-derived protein 1-like
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial, transcript variant X2
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial, 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 37 samples with support for all annotated introns
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial isoform X1
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial isoform X2
sister chromatid cohesion protein PDS5 homolog B, transcript variant X3
sister chromatid cohesion protein PDS5 homolog B, 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 42 samples with support for all annotated introns
sister chromatid cohesion protein PDS5 homolog B, transcript variant X4
sister chromatid cohesion protein PDS5 homolog B, transcript variant X2
sister chromatid cohesion protein PDS5 homolog B isoform X2
sister chromatid cohesion protein PDS5 homolog B isoform X1
sister chromatid cohesion protein PDS5 homolog B isoform X3
transcription initiation factor TFIID subunit 7
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 46 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
platelet-derived growth factor subunit A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
platelet-derived growth factor subunit A, transcript variant X2
platelet-derived growth factor subunit A isoform X1
uncharacterized protein LOC115218435 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 229 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
motile sperm domain-containing protein 2, transcript variant X4
motile sperm domain-containing protein 2, transcript variant X3
motile sperm domain-containing protein 2, transcript variant X1
motile sperm domain-containing protein 2, 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 41 samples with support for all annotated introns
motile sperm domain-containing protein 2 isoform X4
motile sperm domain-containing protein 2 isoform X3
motile sperm domain-containing protein 2 isoform X1
motile sperm domain-containing protein 2 isoform X2
tripartite motif-containing protein 2-like, transcript variant X1
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 20 samples with support for all annotated introns
tripartite motif-containing protein 2-like, transcript variant X4
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 31 samples with support for all annotated introns
tripartite motif-containing protein 2-like, transcript variant X3
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 4 samples with support for all annotated introns
tripartite motif-containing protein 2-like, transcript variant X2
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 19 samples with support for all annotated introns
tripartite motif-containing protein 2-like isoform X1
tripartite motif-containing protein 2-like isoform X3
tripartite motif-containing protein 2-like isoform X2
tripartite motif-containing protein 2-like isoform 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 42 samples with support for all annotated introns
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 24 samples with support for all annotated introns
zinc finger protein 271-like, transcript variant X2
zinc finger protein 271-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
zinc finger protein 271-like, transcript variant X3
zinc finger protein 98-like, transcript variant X2
zinc finger protein 98-like, transcript variant X1
zinc finger protein 98-like, transcript variant X3
zinc finger protein 492-like, transcript variant X3
zinc finger protein 492-like, transcript variant X2
zinc finger protein 492-like, transcript variant X1
zinc finger protein 675-like, transcript variant X2
zinc finger protein 675-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
zinc finger protein 675-like, transcript variant X3
organic cation transporter protein-like, transcript variant X1
organic cation transporter protein-like, transcript variant X2
organic cation transporter protein-like, transcript variant X3
organic cation transporter protein-like, transcript variant X4
organic cation transporter protein-like isoform X1
organic cation transporter protein-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 29% coverage of the annotated genomic feature by RNAseq alignments
organic cation transporter protein-like isoform X4
organic cation transporter protein-like isoform X3
organic cation transporter protein-like, transcript variant X6
organic cation transporter protein-like, transcript variant X5
nucleolar protein dao-5, transcript variant X3
nucleolar protein dao-5, transcript variant X7
nucleolar protein dao-5, transcript variant X6
nucleolar protein dao-5, transcript variant X5
nucleolar protein dao-5, transcript variant X2
nucleolar protein dao-5, transcript variant X4
nucleolar protein dao-5, transcript variant X1
nucleolar protein dao-5, transcript variant X10
nucleolar protein dao-5, transcript variant X9
nucleolar protein dao-5, transcript variant X8
muscle M-line assembly protein unc-89 isoform X3
muscle M-line assembly protein unc-89 isoform X10
muscle M-line assembly protein unc-89 isoform X7
muscle M-line assembly protein unc-89 isoform X6
muscle M-line assembly protein unc-89 isoform X9
muscle M-line assembly protein unc-89 isoform X8
muscle M-line assembly protein unc-89 isoform 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 36 samples with support for all annotated introns
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 46 samples with support for all annotated introns
capping protein inhibiting regulator of actin dynamics, transcript variant X1
capping protein inhibiting regulator of actin dynamics, transcript variant X2
capping protein inhibiting regulator of actin dynamics isoform X1
capping protein inhibiting regulator of actin dynamics isoform X2
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
POU domain, class 4, transcription factor 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115218420, transcript variant X1
uncharacterized LOC115218420, transcript variant X4
uncharacterized LOC115218420, transcript variant X3
uncharacterized LOC115218420, transcript variant X2
uncharacterized protein LOC115218420 isoform X2
uncharacterized protein LOC115218420 isoform X1
small ubiquitin-related modifier 3, 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 46 samples with support for all annotated introns
small ubiquitin-related modifier 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
small ubiquitin-related modifier 3, transcript variant X2
small ubiquitin-related modifier 3-like isoform X1
small ubiquitin-related modifier 3 isoform X2
rho guanine nucleotide exchange factor 17
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 44 samples with support for all annotated introns
myotubularin-related protein 2, transcript variant X2
myotubularin-related protein 2, 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 44 samples with support for all annotated introns
myotubularin-related protein 2 isoform X1
myotubularin-related protein 2 isoform X2
myotubularin-related protein 2, transcript variant X3
myotubularin-related protein 2 isoform X3
myotubularin-related protein 2, 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 42 samples with support for all annotated introns
myotubularin-related protein 2 isoform X4
DBF4-type zinc finger-containing protein 2 homolog, transcript variant X3
DBF4-type zinc finger-containing protein 2 homolog isoform X2
DBF4-type zinc finger-containing protein 2 homolog, transcript variant X2
DBF4-type zinc finger-containing protein 2 homolog, transcript variant X1
DBF4-type zinc finger-containing protein 2 homolog isoform 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 5 samples with support for all annotated introns
transmembrane protein KIAA1109 homolog, transcript variant X13
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 20 samples with support for all annotated introns
transmembrane protein KIAA1109 homolog, transcript variant X10
transmembrane protein KIAA1109 homolog, transcript variant X7
transmembrane protein KIAA1109 homolog, transcript variant X4
transmembrane protein KIAA1109 homolog, transcript variant X8
transmembrane protein KIAA1109 homolog, 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 14 samples with support for all annotated introns
transmembrane protein KIAA1109 homolog, transcript variant X5
transmembrane protein KIAA1109 homolog, transcript variant X2
transmembrane protein KIAA1109 homolog, transcript variant X3
transmembrane protein KIAA1109 homolog, transcript variant X12
transmembrane protein KIAA1109 homolog, transcript variant X1
transmembrane protein KIAA1109 homolog, transcript variant X11
transmembrane protein KIAA1109 homolog, transcript variant X9
transmembrane protein KIAA1109 isoform X13
transmembrane protein KIAA1109 homolog isoform X10
transmembrane protein KIAA1109 homolog isoform X7
transmembrane protein KIAA1109 homolog isoform X4
transmembrane protein KIAA1109 homolog isoform X8
transmembrane protein KIAA1109 homolog isoform X6
transmembrane protein KIAA1109 homolog isoform X5
transmembrane protein KIAA1109 homolog isoform X2
transmembrane protein KIAA1109 homolog isoform X3
transmembrane protein KIAA1109 isoform X12
transmembrane protein KIAA1109 homolog isoform X1
transmembrane protein KIAA1109 isoform X11
transmembrane protein KIAA1109 isoform X9
cytoplasmic FMR1-interacting protein, 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 33 samples with support for all annotated introns
cytoplasmic FMR1-interacting protein, transcript variant X1
cytoplasmic FMR1-interacting protein, 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 29 samples with support for all annotated introns
cytoplasmic FMR1-interacting protein, transcript variant X4
cytoplasmic FMR1-interacting protein, transcript variant X5
WD repeat-containing protein 55, 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 26 samples with support for all annotated introns
WD repeat-containing protein 55, 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 43 samples with support for all annotated introns
post-GPI attachment to proteins factor 2-like
putative zinc finger protein 66, transcript variant X3
putative zinc finger protein 66, transcript variant X2
putative zinc finger protein 66, transcript variant X1
putative zinc finger protein 66 isoform X2
zinc finger protein 62-like, transcript variant X1
zinc finger protein 62-like, transcript variant X4
zinc finger protein 62-like, transcript variant X2
zinc finger protein 62-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 2 homolog, transcript variant X2
zinc finger protein 2 homolog, transcript variant X1
zinc finger protein 2 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
sulfate transporter, 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 27 samples with support for all annotated introns
sulfate transporter, 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 21 samples with support for all annotated introns
sulfate transporter, transcript variant X4
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 13 samples with support for all annotated introns
sulfate transporter, transcript variant X6
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 15 samples with support for all annotated introns
sulfate transporter, 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 32 samples with support for all annotated introns
sulfate transporter, transcript variant X5
tumor suppressor candidate 3, transcript variant X4
tumor suppressor candidate 3, transcript variant X2
tumor suppressor candidate 3, transcript variant X3
tumor suppressor candidate 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
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
zinc finger protein 726-like, transcript variant X3
zinc finger protein 726-like, transcript variant X1
zinc finger protein 726-like, transcript variant X2