Octopus sinensis linkage group LG9, 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\nCM016867.1.\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.
polyunsaturated fatty acid lipoxygenase ALOX15B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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: 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 4 samples with support for all annotated introns
arachidonate 12-lipoxygenase, 12R-type-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: arachidonate 12-lipoxygenase, 12R-type-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 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: 2 Proteins, and 79% 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 1 sample with support for all annotated introns
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 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 14 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 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
DNA (cytosine-5)-methyltransferase 3B, 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 3 samples with support for all annotated introns
DNA (cytosine-5)-methyltransferase 3B, 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
DNA (cytosine-5)-methyltransferase 3B, transcript variant X8
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
DNA (cytosine-5)-methyltransferase 3B, transcript variant X7
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
DNA (cytosine-5)-methyltransferase 3B, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
DNA (cytosine-5)-methyltransferase 3B, 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 32 samples with support for all annotated introns
DNA (cytosine-5)-methyltransferase 3B isoform X4
DNA (cytosine-5)-methyltransferase 3B, 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 8 samples with support for all annotated introns
DNA (cytosine-5)-methyltransferase 3B, 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 13 samples with support for all annotated introns
DNA (cytosine-5)-methyltransferase 3B isoform X1
DNA (cytosine-5)-methyltransferase 3B isoform X2
DNA (cytosine-5)-methyltransferase 3B isoform X3
tyrosine-protein phosphatase non-receptor type 4, 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 1 sample with support for all annotated introns
tyrosine-protein phosphatase non-receptor type 4, transcript variant X7
tyrosine-protein phosphatase non-receptor type 4, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tyrosine-protein phosphatase non-receptor type 4, transcript variant X8
tyrosine-protein phosphatase non-receptor type 4, transcript variant X4
tyrosine-protein phosphatase non-receptor type 4, 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 14 samples with support for all annotated introns
tyrosine-protein phosphatase non-receptor type 4, 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 15 samples with support for all annotated introns
tyrosine-protein phosphatase non-receptor type 4, transcript variant X1
tyrosine-protein phosphatase non-receptor type 4, 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 25 samples with support for all annotated introns
tyrosine-protein phosphatase non-receptor type 4 isoform X8
tyrosine-protein phosphatase non-receptor type 4 isoform X7
tyrosine-protein phosphatase non-receptor type 4 isoform X3
tyrosine-protein phosphatase non-receptor type 4 isoform X5
tyrosine-protein phosphatase non-receptor type 4 isoform X4
tyrosine-protein phosphatase non-receptor type 4 isoform X2
tyrosine-protein phosphatase non-receptor type 4 isoform X1
tyrosine-protein phosphatase non-receptor type 4 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 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
succinate--hydroxymethylglutarate CoA-transferase
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
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: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 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 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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 41 samples with support for all annotated introns
uncharacterized LOC115215765, transcript variant X1
uncharacterized LOC115215765, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized protein LOC115215765 isoform X1
uncharacterized protein LOC115215765 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 10 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 509 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: 327 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: 81 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: 144 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: 336 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: 514 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: 147 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: 43 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 334 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: 515 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: 214 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 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: 276 Proteins, and 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: 275 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 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: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 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 17 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 11 samples with support for all annotated introns
S-methyl-5'-thioadenosine phosphorylase, 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 36 samples with support for all annotated introns
S-methyl-5'-thioadenosine phosphorylase, 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 46 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 46 samples with support for all annotated introns
eukaryotic translation initiation factor 2 subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
G-protein coupled receptor-associated protein LMBRD2
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 23 samples with support for all annotated introns
microtubule-actin cross-linking factor 1
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: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: microtubule-actin cross-linking factor 1
mitochondrial import inner membrane translocase subunit Tim29
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
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 11 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 21 samples with support for all annotated introns
uncharacterized LOC115215941, 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 20 samples with support for all annotated introns
uncharacterized LOC115215941, 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 21 samples with support for all annotated introns
uncharacterized LOC115215941, transcript variant X4
uncharacterized LOC115215941, 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 24 samples with support for all annotated introns
uncharacterized protein LOC115215941 isoform X2
uncharacterized protein LOC115215941 isoform X3
uncharacterized protein LOC115215941 isoform X1
ubiquitin carboxyl-terminal hydrolase 14
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
kinesin-like protein KIF2A, 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 31 samples with support for all annotated introns
kinesin-like protein KIF2A, 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 41 samples with support for all annotated introns
kinesin-like protein KIF2A, 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 38 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 36 samples with support for all annotated introns
uncharacterized protein C8orf34 homolog, transcript variant X1
uncharacterized protein C8orf34 homolog, transcript variant X2
uncharacterized protein C8orf34 homolog isoform X1
uncharacterized protein C8orf34 homolog isoform X2
60S ribosomal protein L30, 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 39 samples with support for all annotated introns
60S ribosomal protein L30, 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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
putative extracellular sulfatase Sulf-1 homolog, 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
putative extracellular sulfatase Sulf-1 homolog, transcript variant X1
putative extracellular sulfatase Sulf-1 homolog, transcript variant X5
putative extracellular sulfatase Sulf-1 homolog, 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 41 samples with support for all annotated introns
putative extracellular sulfatase Sulf-1 homolog, 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 18 samples with support for all annotated introns
putative extracellular sulfatase Sulf-1 homolog isoform X1
putative extracellular sulfatase Sulf-1 homolog isoform X3
extracellular sulfatase Sulf-1 isoform X2
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
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 20 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 21 samples with support for all annotated introns
monocarboxylate transporter 12, transcript variant X5
monocarboxylate transporter 12, transcript variant X2
monocarboxylate transporter 12, transcript variant X1
monocarboxylate transporter 12, transcript variant X4
monocarboxylate transporter 12, 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 14 samples with support for all annotated introns
uncharacterized protein C19orf44 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized protein C19orf44 homolog isoform X1
uncharacterized protein C19orf44 homolog, 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 protein C19orf44 homolog, transcript variant X3
uncharacterized protein C19orf44 homolog isoform X2
leucine-rich repeat-containing protein 7-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 29 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
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
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
cilia- and flagella-associated protein 251-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
uncharacterized LOC115215778, 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
uncharacterized LOC115215778, 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
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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
transmembrane protein 241, transcript variant X6
transmembrane protein 241, transcript variant X2
transmembrane protein 241, 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 12 samples with support for all annotated introns
transmembrane protein 241, transcript variant X9
transmembrane protein 241, transcript variant X8
transmembrane protein 241, transcript variant X7
transmembrane protein 241, transcript variant X1
transmembrane protein 241, transcript variant X4
transmembrane protein 241, transcript variant X5
transmembrane protein 241, transcript variant X12
transmembrane protein 241, transcript variant X11
transmembrane protein 241, transcript variant X13
transmembrane protein 241, transcript variant X10
transmembrane protein 241, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
adhesion G-protein coupled receptor G6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
adhesion G-protein coupled receptor G6-like, transcript variant X4
adhesion G-protein coupled receptor G6-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
adhesion G-protein coupled receptor G6-like, 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 2 samples with support for all annotated introns
adhesion G-protein coupled receptor G6-like, transcript variant X6
adhesion G-protein coupled receptor G6-like, transcript variant X7
adhesion G-protein coupled receptor G6-like, transcript variant X1
adhesion G-protein coupled receptor G6-like, transcript variant X9
adhesion G-protein coupled receptor G6-like, transcript variant X8
adhesion G-protein coupled receptor G6-like isoform X3
adhesion G-protein coupled receptor G6-like isoform X4
adhesion G-protein coupled receptor G6-like isoform X2
adhesion G-protein coupled receptor G6-like isoform X5
adhesion G-protein coupled receptor G6-like isoform X6
adhesion G-protein coupled receptor G4-like isoform X1
adhesion G-protein coupled receptor G6-like isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 512 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: 233 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA arginine (anticodon UCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
tyrosine-protein phosphatase Lar, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
tyrosine-protein phosphatase Lar, transcript variant X7
uncharacterized LOC118764770, transcript variant X3
uncharacterized LOC118764770, transcript variant X2
uncharacterized LOC118764770, transcript variant X1
uncharacterized LOC118764770, transcript variant X4
tyrosine-protein phosphatase Lar, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
tyrosine-protein phosphatase Lar, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
tyrosine-protein phosphatase Lar, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
tyrosine-protein phosphatase Lar, transcript variant X3
tyrosine-protein phosphatase Lar, transcript variant X8
tyrosine-protein phosphatase Lar, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
tyrosine-protein phosphatase Lar, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase F isoform X1
receptor-type tyrosine-protein phosphatase delta isoform X8
receptor-type tyrosine-protein phosphatase S isoform X10
receptor-type tyrosine-protein phosphatase F isoform X2
receptor-type tyrosine-protein phosphatase F isoform X5
receptor-type tyrosine-protein phosphatase F isoform X6
receptor-type tyrosine-protein phosphatase F isoform X3
receptor-type tyrosine-protein phosphatase F isoform X4
receptor-type tyrosine-protein phosphatase F isoform X7
uncharacterized LOC118764770, transcript variant X5
tyrosine-protein phosphatase Lar, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
tyrosine-protein phosphatase Lar isoform X9
tyrosine-protein phosphatase Lar, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
tyrosine-protein phosphatase Lar isoform X11
uncharacterized LOC115215789, transcript variant X2
uncharacterized LOC115215789, transcript variant X1
transfer RNA leucine (anticodon UAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon UUC); 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: 1 Protein, and 38% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC118764680, transcript variant X1
uncharacterized LOC118764680, transcript variant X2
probable E3 ubiquitin-protein ligase IRF2BPL, 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 7 samples with support for all annotated introns
probable E3 ubiquitin-protein ligase IRF2BPL, 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 43 samples with support for all annotated introns
probable E3 ubiquitin-protein ligase IRF2BPL isoform X1
probable E3 ubiquitin-protein ligase IRF2BPL isoform X2
calcyphosin-like protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
calcyphosin-like protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
calcyphosin-like protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 10, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 10, 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 28 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 10, 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 9 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 10, 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
solute carrier family 2, facilitated glucose transporter member 10 isoform X5
solute carrier family 2, facilitated glucose transporter member 10 isoform X4
solute carrier family 2, facilitated glucose transporter member 10 isoform X1
solute carrier family 2, facilitated glucose transporter member 10 isoform X2
solute carrier family 2, facilitated glucose transporter member 10, transcript variant X3
solute carrier family 2, facilitated glucose transporter member 10 isoform 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 5 samples with support for all annotated introns
uncharacterized LOC115215701, transcript variant X2
uncharacterized LOC115215701, transcript variant X1
uncharacterized LOC115215701, transcript variant X4
uncharacterized LOC115215701, transcript variant X3
uncharacterized LOC115215701, transcript variant X5
uncharacterized protein LOC115215701 isoform X1
uncharacterized protein LOC115215701 isoform X3
uncharacterized protein LOC115215701 isoform X2
uncharacterized protein LOC115215701 isoform 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 46 samples with support for all annotated introns
phosphatidylinositol 5-phosphate 4-kinase type-2 alpha, 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 36 samples with support for all annotated introns
phosphatidylinositol 5-phosphate 4-kinase type-2 alpha, 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 46 samples with support for all annotated introns
phosphatidylinositol 5-phosphate 4-kinase type-2 alpha, 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 22 samples with support for all annotated introns
phosphatidylinositol 5-phosphate 4-kinase type-2 alpha isoform X2
phosphatidylinositol 5-phosphate 4-kinase type-2 alpha isoform X1
phosphatidylinositol 5-phosphate 4-kinase type-2 alpha isoform X3
proteasome subunit beta type-3, transcript variant X1
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 46 samples with support for all annotated introns
proteasome subunit beta type-3 isoform X1
proteasome subunit beta type-3, 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 9 samples with support for all annotated introns
proteasome subunit beta type-3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
growth hormone-regulated TBC protein 1-A-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 40 samples with support for all annotated introns
growth hormone-regulated TBC protein 1-A-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 28 samples with support for all annotated introns
growth hormone-regulated TBC protein 1-A-like isoform X1
growth hormone-regulated TBC protein 1-A-like isoform X2
growth hormone-regulated TBC protein 1-A-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 10 samples with support for all annotated introns
growth hormone-regulated TBC protein 1-A-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC118764774, transcript variant X1
uncharacterized protein LOC118764774 isoform X1
uncharacterized LOC118764774, transcript variant X2
uncharacterized protein LOC118764774 isoform X2
ubiquitin carboxyl-terminal hydrolase 37-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 38 samples with support for all annotated introns
NAD-dependent protein deacetylase sir-2.1-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 8 samples with support for all annotated introns
NAD-dependent protein deacetylase sir-2.1-like, transcript variant X2
NAD-dependent protein deacetylase sir-2.1-like
uncharacterized LOC115215940, transcript variant X3
uncharacterized LOC115215940, transcript variant X1
uncharacterized LOC115215940, transcript variant X2
uncharacterized LOC115215940, transcript variant X4
uncharacterized LOC115215940, transcript variant X5
uncharacterized protein LOC115215940 isoform X1
uncharacterized protein LOC115215940 isoform X2
uncharacterized protein LOC115215940 isoform X3
beta-1,4-galactosyltransferase 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
beta-1,4-galactosyltransferase 3-like, transcript variant X1
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 6 samples with support for all annotated introns
beta-1,4-galactosyltransferase 3-like, 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 8 samples with support for all annotated introns
beta-1,4-galactosyltransferase 4-like isoform X1
beta-1,4-galactosyltransferase 3-like isoform X2
beta-1,3-N-acetylglucosaminyltransferase radical fringe-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
E3 ubiquitin-protein ligase arih1l, 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 44 samples with support for all annotated introns
E3 ubiquitin-protein ligase arih1l, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
E3 ubiquitin-protein ligase arih1l isoform X2
E3 ubiquitin-protein ligase arih1l isoform X1
uncharacterized LOC118764682, transcript variant X1
uncharacterized LOC118764682, transcript variant X2
MOB-like protein phocein, 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 44 samples with support for all annotated introns
MOB-like protein phocein, 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 12 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 32 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
uncharacterized LOC118764778, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC118764778, transcript variant X3
uncharacterized LOC118764778, 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 29 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 40 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 33 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 34 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 35 samples with support for all annotated introns
uncharacterized protein LOC115215681 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 17 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
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
bifunctional peptidase and arginyl-hydroxylase JMJD5
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
sushi domain-containing protein 2-like, transcript variant X2
sushi domain-containing protein 2-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 26 samples with support for all annotated introns
sushi domain-containing protein 2-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 16 samples with support for all annotated introns
sushi domain-containing protein 2-like isoform X2
sushi domain-containing protein 2-like isoform X1
ras-related protein Rab5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
ras-related protein Rab5, 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 9 samples with support for all annotated introns
ras-related protein Rab5, 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 27 samples with support for all annotated introns
ras-related protein Rab5, 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 16 samples with support for all annotated introns
ras-related protein Rab-5B, transcript variant X2
ras-related protein Rab-5B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
EF-hand domain-containing family member B-like
sodium- and chloride-dependent glycine transporter 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
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 26 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
two pore potassium channel protein sup-9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
60S ribosomal protein L7, 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 11 samples with support for all annotated introns
60S ribosomal protein L7, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
60S ribosomal protein L7, 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
60S ribosomal protein L7, transcript variant X7
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 12 samples with support for all annotated introns
60S ribosomal protein L7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
60S ribosomal protein L7, transcript variant X5
60S ribosomal protein L7, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 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 46 samples with support for all annotated introns
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2, transcript variant X2
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2 isoform X1
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2 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 44 samples with support for all annotated introns
NADH dehydrogenase [ubiquinone] flavoprotein 1, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 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: 62% coverage of the annotated genomic feature by RNAseq alignments
tigger transposable element-derived protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC118764791, transcript variant X3
uncharacterized LOC118764791, transcript variant X2
uncharacterized LOC118764791, transcript variant X1
VWFA and cache domain-containing protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
VWFA and cache domain-containing protein 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 24 samples with support for all annotated introns
VWFA and cache domain-containing protein 1-like, 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 30 samples with support for all annotated introns
VWFA and cache domain-containing protein 1-like isoform X1
VWFA and cache domain-containing protein 1-like isoform X2
VWFA and cache domain-containing protein 1-like isoform X3
ras-related protein Rab-23, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ras-related protein Rab-23, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ras-related protein Rab-23, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ras-related protein Rab-23, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
kinesin light chain, transcript variant X2
kinesin light chain, 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 7 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 23 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 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 107 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
cathepsin L1-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 9 samples with support for all annotated introns
cathepsin L1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 115 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 110 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 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 32 samples with support for all annotated introns
ribonuclease P protein subunit p20-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 3 samples with support for all annotated introns
ribonuclease P protein subunit p20-like, transcript variant X1
ribonuclease P protein subunit p20-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
ubiquinol-cytochrome-c reductase complex assembly factor 1, 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 43 samples with support for all annotated introns
ubiquinol-cytochrome-c reductase complex assembly factor 1, transcript variant X1
ubiquinol-cytochrome-c reductase complex assembly factor 1 isoform X2
ubiquinol-cytochrome-c reductase complex assembly factor 1 isoform X1
uncharacterized protein DDB_G0289975, transcript variant X2
uncharacterized protein DDB_G0289975, 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 46 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 8 samples with support for all annotated introns
adrenodoxin-like protein 1, mitochondrial
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
ubiquitin-conjugating enzyme E2 U-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 15 samples with support for all annotated introns
ubiquitin-conjugating enzyme E2 U-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 6 samples with support for all annotated introns
transcription elongation factor B polypeptide 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
somatostatin receptor type 2-like, transcript variant X3
somatostatin receptor type 2-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
somatostatin receptor type 2-like, transcript variant X1
neuropeptide FF receptor 2-like isoform X2
somatostatin receptor type 2-like isoform X1
transmembrane protein 68, 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 13 samples with support for all annotated introns
transmembrane protein 68, 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 38 samples with support for all annotated introns
cerebral cavernous malformations protein 2 homolog, transcript variant X1
cerebral cavernous malformations protein 2 homolog isoform X1
cerebral cavernous malformations protein 2 homolog, transcript variant X2
cerebral cavernous malformations protein 2 homolog isoform X2
sarcoplasmic calcium-binding proteins I, III, and IV-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon UGA); 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 42 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
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 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 35 samples with support for all annotated introns
tRNA (adenine(58)-N(1))-methyltransferase non-catalytic subunit TRM6-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: tRNA (adenine(58)-N(1))-methyltransferase non-catalytic subunit TRM6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
transcription factor MafK, 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 44 samples with support for all annotated introns
transcription factor MafK, 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 43 samples with support for all annotated introns
85/88 kDa calcium-independent phospholipase A2, 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 2 samples with support for all annotated introns
85/88 kDa calcium-independent phospholipase A2, 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 13 samples with support for all annotated introns
85/88 kDa calcium-independent phospholipase A2, 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 31 samples with support for all annotated introns
85/88 kDa calcium-independent phospholipase A2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
85/88 kDa calcium-independent phospholipase A2, 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 7 samples with support for all annotated introns
85/88 kDa calcium-independent phospholipase A2, transcript variant X3
85/88 kDa calcium-independent phospholipase A2 isoform X1
85/88 kDa calcium-independent phospholipase A2 isoform X2
intraflagellar transport protein 56-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
cytosolic carboxypeptidase-like protein 5, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
cytosolic carboxypeptidase-like protein 5, transcript variant X2
cytosolic carboxypeptidase-like protein 5, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cytosolic carboxypeptidase-like protein 5 isoform X2
cytosolic carboxypeptidase-like protein 5, transcript variant X1
cytosolic carboxypeptidase-like protein 5, transcript variant X3
cytosolic carboxypeptidase-like protein 5 isoform X3
cytosolic carboxypeptidase-like protein 5 isoform X1
cytosolic carboxypeptidase-like protein 5 isoform X5
cytosolic carboxypeptidase-like protein 5 isoform X4
cytosolic carboxypeptidase-like protein 5, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cytosolic carboxypeptidase-like protein 5, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
cytosolic carboxypeptidase-like protein 5, transcript variant X8
cytosolic carboxypeptidase-like protein 5, transcript variant X9
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 30 samples with support for all annotated introns
cytosolic carboxypeptidase-like protein 5 isoform X6
uncharacterized LOC115215874, 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 37 samples with support for all annotated introns
uncharacterized LOC115215874, 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
structural maintenance of chromosomes protein 2
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
2-(3-amino-3-carboxypropyl)histidine synthase subunit 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
2-(3-amino-3-carboxypropyl)histidine synthase subunit 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 28 samples with support for all annotated introns
2-(3-amino-3-carboxypropyl)histidine synthase subunit 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
2-(3-amino-3-carboxypropyl)histidine synthase subunit 2 isoform X1
2-(3-amino-3-carboxypropyl)histidine synthase subunit 2 isoform X2
2-(3-amino-3-carboxypropyl)histidine synthase subunit 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 1 sample with support for all annotated introns
2-(3-amino-3-carboxypropyl)histidine synthase subunit 2 isoform X3
2-(3-amino-3-carboxypropyl)histidine synthase subunit 2 isoform X4
UPF0600 protein C5orf51 homolog, transcript variant X2
UPF0600 protein C5orf51 homolog, 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 31 samples with support for all annotated introns
UPF0600 protein C5orf51 homolog, 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 5 samples with support for all annotated introns
UPF0600 protein C5orf51 homolog isoform X2
UPF0600 protein C5orf51 homolog isoform X1
UPF0600 protein C5orf51 homolog isoform X3
FYN-binding protein 1, transcript variant X1
FYN-binding protein 1, transcript variant X2
FYN-binding protein 1, transcript variant X3
FYN-binding protein 1, 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 46 samples with support for all annotated introns
uncharacterized LOC118764809, transcript variant X2
uncharacterized LOC118764809, transcript variant X1
diacylglycerol kinase theta, 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 23 samples with support for all annotated introns
diacylglycerol kinase theta, 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 9 samples with support for all annotated introns
diacylglycerol kinase theta, 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 11 samples with support for all annotated introns
diacylglycerol kinase theta, 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
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
serine/threonine-protein kinase VRK1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins
chitinase domain-containing protein 1, 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 45 samples with support for all annotated introns
chitinase domain-containing protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
uncharacterized LOC115215876, transcript variant X2
uncharacterized LOC115215876, 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 28 samples with support for all annotated introns
phosphatidylinositol-glycan biosynthesis class W protein, 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 19 samples with support for all annotated introns
phosphatidylinositol-glycan biosynthesis class W protein, transcript variant X2
phosphatidylinositol-glycan biosynthesis class W protein, transcript variant X1
phosphatidylinositol-glycan biosynthesis class W protein
eukaryotic translation initiation factor 4E
HEAT repeat-containing protein 1, transcript variant X1
HEAT repeat-containing protein 1, 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 17 samples with support for all annotated introns
HEAT repeat-containing protein 1 isoform X1
HEAT repeat-containing protein 1 isoform X2
28S ribosomal protein S18b, mitochondrial, 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
28S ribosomal protein S18b, mitochondrial isoform X2
28S ribosomal protein S18b, mitochondrial, transcript variant X3
28S ribosomal protein S18b, mitochondrial, transcript variant X1
28S ribosomal protein S18b, mitochondrial isoform X3
28S ribosomal protein S18b, mitochondrial 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 43 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 36 samples with support for all annotated introns
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8B-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 10 samples with support for all annotated introns
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8B-like, 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 27 samples with support for all annotated introns
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8B-like, 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 21 samples with support for all annotated introns
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8B-like isoform X1
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8B-like isoform X2
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8B-like isoform X3
6-pyruvoyl tetrahydrobiopterin synthase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
6-pyruvoyl tetrahydrobiopterin synthase, 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 9 samples with support for all annotated introns
6-pyruvoyl tetrahydrobiopterin synthase, 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 7 samples with support for all annotated introns
6-pyruvoyl tetrahydrobiopterin synthase, 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 40 samples with support for all annotated introns
6-pyruvoyl tetrahydrobiopterin synthase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
cytoplasmic phosphatidylinositol transfer protein 1
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 41 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 46-like, 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 36 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 46-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 46-like, 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 34 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 46-like isoform X3
ubiquitin carboxyl-terminal hydrolase 46-like isoform X2
ubiquitin carboxyl-terminal hydrolase 46-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
protein disulfide-isomerase A4, 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 29 samples with support for all annotated introns
protein disulfide-isomerase A4, 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 44 samples with support for all annotated introns
protein disulfide-isomerase A4 isoform X1
protein disulfide-isomerase A4 isoform X2
HHIP-like protein 1, transcript variant X2
HHIP-like protein 1, transcript variant X1
multidrug resistance-associated protein 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
multidrug resistance-associated protein 5, 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 35 samples with support for all annotated introns
multidrug resistance-associated protein 5 isoform X1
multidrug resistance-associated protein 5 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 32 samples with support for all annotated introns
cyclic AMP-dependent transcription factor ATF-6 alpha
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 45 samples with support for all annotated introns
general transcription factor 3C polypeptide 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
ankyrin repeat domain-containing protein 13C-A
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 44 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 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: 429 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 266 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: 243 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 269 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: 149 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: 198 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 255 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: 140 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: 220 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: 518 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: 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 256 Proteins
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 18 samples with support for all annotated introns
uncharacterized LOC118764817, transcript variant X1
uncharacterized LOC118764817, transcript variant X2
D-amino-acid oxidase-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 11 samples with support for all annotated introns
D-amino-acid oxidase-like, transcript variant X2
D-amino-acid oxidase-like, transcript variant X1
ubiquitin-associated protein 2-like, transcript variant X1
ubiquitin-associated protein 2-like, transcript variant X9
ubiquitin-associated protein 2-like, transcript variant X2
ubiquitin-associated protein 2-like, transcript variant X4
ubiquitin-associated protein 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
ubiquitin-associated protein 2-like, transcript variant X6
ubiquitin-associated protein 2-like, transcript variant X5
ubiquitin-associated protein 2-like, transcript variant X7
ubiquitin-associated protein 2-like, transcript variant X8
ubiquitin-associated protein 2-like isoform X1
ubiquitin-associated protein 2-like isoform X2
ubiquitin-associated protein 2-like isoform X4
ubiquitin-associated protein 2-like isoform X3
ubiquitin-associated protein 2-like isoform X6
ubiquitin-associated protein 2-like isoform X7
ubiquitin-associated protein 2-like isoform X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 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
3-phosphoinositide-dependent protein kinase 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 34 samples with support for all annotated introns
myocardin-related transcription factor B, transcript variant X6
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
myocardin-related transcription factor B, 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 26 samples with support for all annotated introns
myocardin-related transcription factor B, transcript variant X1
myocardin-related transcription factor B, transcript variant X4
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 26 samples with support for all annotated introns
myocardin-related transcription factor B, transcript variant X5
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 27 samples with support for all annotated introns
myocardin-related transcription factor B isoform X1
myocardin-related transcription factor B isoform X3
myocardin-related transcription factor B isoform X4
myocardin-related transcription factor B isoform X5
myocardin-related transcription factor B, 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 40 samples with support for all annotated introns
myocardin-related transcription factor B isoform X2
myocardin-related transcription factor B, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
myocardin-related transcription factor B isoform X6
hybrid signal transduction histidine kinase E-like
LYR motif-containing protein 1, 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
LYR motif-containing 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 38 samples with support for all annotated introns
LYR motif-containing protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 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 43 samples with support for all annotated introns
DCN1-like protein 3, 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 15 samples with support for all annotated introns
DCN1-like protein 3, 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 25 samples with support for all annotated introns
uncharacterized LOC118764822, transcript variant X6
uncharacterized LOC118764822, transcript variant X4
uncharacterized LOC118764822, transcript variant X2
uncharacterized LOC118764822, transcript variant X7
uncharacterized LOC118764822, transcript variant X3
uncharacterized LOC118764822, transcript variant X5
uncharacterized LOC118764822, transcript variant X1
DCN1-like protein 3, 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 44 samples with support for all annotated introns
zinc finger protein 239, transcript variant X2
zinc finger protein 239, transcript variant X1
prolyl 4-hydroxylase subunit alpha-1, transcript variant X2
prolyl 4-hydroxylase subunit alpha-1, transcript variant X1
prolyl 4-hydroxylase subunit alpha-1 isoform X1
prolyl 4-hydroxylase subunit alpha-1 isoform X2
prolyl 4-hydroxylase subunit alpha-2-like, transcript variant X2
prolyl 4-hydroxylase subunit alpha-2-like, transcript variant X1
prolyl 4-hydroxylase subunit alpha-2-like, transcript variant X4
prolyl 4-hydroxylase subunit alpha-2-like, transcript variant X3
prolyl 4-hydroxylase subunit alpha-2-like isoform X2
prolyl 4-hydroxylase subunit alpha-1-like isoform X1
prolyl 4-hydroxylase subunit alpha-3-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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 27 samples with support for all annotated introns
FAST kinase domain-containing protein 5, mitochondrial-like, transcript variant X2
FAST kinase domain-containing protein 5, mitochondrial-like, transcript variant X1
FAST kinase domain-containing protein 5, mitochondrial-like isoform X1
FAST kinase domain-containing protein 5, mitochondrial-like isoform X2
uncharacterized LOC115215501, transcript variant X2
uncharacterized LOC115215501, transcript variant X1
uncharacterized protein LOC115215501 isoform X2
uncharacterized protein LOC115215501 isoform X1
molybdopterin synthase catalytic subunit, 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 17 samples with support for all annotated introns
molybdopterin synthase catalytic subunit, 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 42 samples with support for all annotated introns
molybdopterin synthase catalytic subunit, 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 25 samples with support for all annotated introns
molybdopterin synthase catalytic subunit isoform X2
molybdopterin synthase catalytic subunit isoform X1
oxysterol-binding protein-related protein 6, 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 4 samples with support for all annotated introns
oxysterol-binding protein-related protein 6, transcript variant X9
oxysterol-binding protein-related protein 6, transcript variant X7
oxysterol-binding protein-related protein 6, transcript variant X1
oxysterol-binding protein-related protein 6, transcript variant X2
oxysterol-binding protein-related protein 6, 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 25 samples with support for all annotated introns
oxysterol-binding protein-related protein 6, 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 34 samples with support for all annotated introns
oxysterol-binding protein-related protein 6, 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 36 samples with support for all annotated introns
oxysterol-binding protein-related protein 6 isoform X1
oxysterol-binding protein-related protein 6 isoform X2
oxysterol-binding protein-related protein 6 isoform X7
oxysterol-binding protein-related protein 6 isoform X8
oxysterol-binding protein-related protein 6 isoform X9
oxysterol-binding protein-related protein 6 isoform X4
oxysterol-binding protein-related protein 6 isoform X3
oxysterol-binding protein-related protein 6 isoform X5
oxysterol-binding protein-related protein 6, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
oxysterol-binding protein-related protein 6 isoform X6
intraflagellar transport protein 46 homolog, 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 5 samples with support for all annotated introns
intraflagellar transport protein 46 homolog isoform X1
intraflagellar transport protein 46 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 37 samples with support for all annotated introns
intraflagellar transport protein 46 homolog isoform X2
ubiquitin-like modifier-activating enzyme 6
microtubule-associated protein futsch, 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 41 samples with support for all annotated introns
microtubule-associated protein futsch, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
microtubule-associated protein futsch, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
microtubule-associated protein futsch, 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 13 samples with support for all annotated introns
microtubule-associated protein futsch, transcript variant X7
microtubule-associated protein futsch, transcript variant X4
microtubule-associated protein futsch, transcript variant X2
microtubule-associated protein futsch isoform X1
microtubule-associated protein futsch isoform X5
microtubule-associated protein futsch isoform X6
microtubule-associated protein futsch isoform X3
microtubule-associated protein futsch isoform X7
microtubule-associated protein futsch isoform X4
microtubule-associated protein futsch isoform X2
epidermal growth factor receptor-like, transcript variant X2
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 23 samples with support for all annotated introns
epidermal growth factor receptor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
epidermal growth factor receptor-like isoform X2
epidermal growth factor receptor-like isoform X1
uncharacterized LOC115215930, 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 30 samples with support for all annotated introns
uncharacterized LOC115215930, transcript variant X3
uncharacterized LOC115215930, transcript variant X5
uncharacterized LOC115215930, transcript variant X4
uncharacterized LOC115215930, transcript variant X2
epidermal growth factor receptor, 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 35 samples with support for all annotated introns
epidermal growth factor receptor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
epidermal growth factor receptor isoform X1
epidermal growth factor receptor isoform X2
protein lev-9-like, transcript variant X1
protein lev-9-like, transcript variant X3
protein lev-9-like, transcript variant X4
protein lev-9-like, transcript variant X2
protein lev-9-like, transcript variant X5
protein lev-9-like, transcript variant X7
protein lev-9-like, transcript variant X6
protein lev-9-like, transcript variant X8
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1-like isoform X2
uncharacterized LOC118764827, transcript variant X2
uncharacterized LOC118764827, transcript variant X1
uncharacterized protein LOC118764827 isoform X1
uncharacterized protein LOC118764827 isoform X2
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein 239-like, transcript variant X5
zinc finger protein 239-like, transcript variant X3
zinc finger protein 239-like, transcript variant X4
zinc finger protein 239-like, transcript variant X2
zinc finger protein 239-like, transcript variant X1
uncharacterized LOC115215582, transcript variant X6
uncharacterized LOC115215582, transcript variant X4
uncharacterized LOC115215582, transcript variant X3
uncharacterized LOC115215582, transcript variant X5
uncharacterized LOC115215582, transcript variant X2
uncharacterized LOC115215582, transcript variant X1
uncharacterized LOC115215582, transcript variant X7
carbamoyl-phosphate synthase [ammonia], mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
malignant fibrous histiocytoma-amplified sequence 1 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
malignant fibrous histiocytoma-amplified sequence 1 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
malignant fibrous histiocytoma-amplified sequence 1 homolog
uncharacterized LOC115215747, transcript variant X2
uncharacterized LOC115215747, transcript variant X1
uncharacterized protein LOC115215747 isoform X1
uncharacterized protein LOC115215747 isoform X2
WD repeat-containing protein 47, transcript variant X1
WD repeat-containing protein 47, 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 19 samples with support for all annotated introns
WD repeat-containing protein 47, transcript variant X6
WD repeat-containing protein 47, transcript variant X5
WD repeat-containing protein 47, 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 11 samples with support for all annotated introns
WD repeat-containing protein 47, 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 10 samples with support for all annotated introns
WD repeat-containing protein 47, transcript variant X7
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
WD repeat-containing protein 47, transcript variant X8
WD repeat-containing protein 47, transcript variant X10
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
WD repeat-containing protein 47, transcript variant X9
WD repeat-containing protein 47 isoform X10
WD repeat-containing protein 47 isoform X9
WD repeat-containing protein 47 isoform X7
WD repeat-containing protein 47 isoform X2
WD repeat-containing protein 47 isoform X8
WD repeat-containing protein 47 isoform X6
WD repeat-containing protein 47 isoform X5
WD repeat-containing protein 47 isoform X3
WD repeat-containing protein 47 isoform X4
WD repeat-containing protein 47 isoform X1
selenocysteine-specific elongation factor-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 41 samples with support for all annotated introns
selenocysteine-specific elongation factor-like isoform X1
selenocysteine-specific elongation factor-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 15 samples with support for all annotated introns
selenocysteine-specific elongation factor-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
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
uncharacterized LOC115215828, transcript variant X10
uncharacterized LOC115215828, transcript variant X5
uncharacterized LOC115215828, transcript variant X2
uncharacterized LOC115215828, transcript variant X6
uncharacterized LOC115215828, transcript variant X8
uncharacterized LOC115215828, transcript variant X1
uncharacterized LOC115215828, transcript variant X3
uncharacterized LOC115215828, transcript variant X7
uncharacterized LOC115215828, transcript variant X4
uncharacterized LOC115215828, transcript variant X11
uncharacterized LOC115215828, transcript variant X9
uncharacterized LOC115215897, 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 36 samples with support for all annotated introns
uncharacterized LOC115215897, transcript variant X1
uncharacterized LOC115215897, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC115215897, transcript variant X2
uncharacterized LOC115215869, transcript variant X2
uncharacterized LOC115215869, 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 39 samples with support for all annotated introns
uncharacterized LOC115215869, 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 20 samples with support for all annotated introns
uncharacterized LOC115215869, 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 14 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
uncharacterized LOC118764840, transcript variant X2
uncharacterized LOC118764840, transcript variant X3
uncharacterized LOC118764840, transcript variant X1
zinc finger protein ztf-16-like, transcript variant X4
zinc finger protein ztf-16-like, transcript variant X3
zinc finger protein ztf-16-like, transcript variant X2
zinc finger protein ztf-16-like, transcript variant X1
zinc finger protein ztf-16-like, transcript variant X5
zinc finger protein ztf-16-like isoform X2
zinc finger protein ztf-16-like isoform X1
zinc finger protein ztf-16-like isoform X3
WD repeat-containing protein 48-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 17 samples with support for all annotated introns
WD repeat-containing protein 48-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 37 samples with support for all annotated introns
WD repeat-containing protein 48-like isoform X1
WD repeat-containing protein 48-like isoform X2
solute carrier organic anion transporter family member 5A1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
U5 small nuclear ribonucleoprotein 40 kDa protein
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
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 26 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
solute carrier family 35 member F4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 35 member F4, 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 22 samples with support for all annotated introns
solute carrier family 35 member F4, 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 10 samples with support for all annotated introns
solute carrier family 35 member F4 isoform X2
solute carrier family 35 member F4 isoform X1
ATP-binding cassette sub-family F member 3
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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ras and EF-hand domain-containing protein 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 29 samples with support for all annotated introns
ras and EF-hand domain-containing protein homolog, 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 10 samples with support for all annotated introns
ras and EF-hand domain-containing protein homolog, transcript variant X3
ras and EF-hand domain-containing protein homolog, transcript variant X2
ras and EF-hand domain-containing protein homolog, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ras and EF-hand domain-containing protein homolog, 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 12 samples with support for all annotated introns
ras and EF-hand domain-containing protein homolog, transcript variant X7
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
uncharacterized protein LOC115215937 isoform X1
ras and EF-hand domain-containing protein homolog isoform X4
uncharacterized protein LOC115215937 isoform X3
uncharacterized protein LOC115215937 isoform X2
uncharacterized protein LOC115215937 isoform X7
cation-independent mannose-6-phosphate receptor, transcript variant X2
cation-independent mannose-6-phosphate receptor, 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 21 samples with support for all annotated introns
cation-independent mannose-6-phosphate receptor isoform X2
cation-independent mannose-6-phosphate receptor isoform X1
rho GTPase-activating protein 100F, 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 25 samples with support for all annotated introns
rho GTPase-activating protein 100F isoform X1
rho GTPase-activating protein 100F, 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
rho GTPase-activating protein 100F isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized protein C2orf50 homolog, transcript variant X2
uncharacterized protein C2orf50 homolog, 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 7 samples with support for all annotated introns
uncharacterized protein C2orf50 homolog, transcript variant X1
uncharacterized protein C2orf50 homolog isoform X3
uncharacterized protein C2orf50 homolog isoform X2
uncharacterized protein C2orf50 homolog isoform X1
transcriptional adapter 2-beta-like, 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 39 samples with support for all annotated introns
transcriptional adapter 2-beta-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 5 samples with support for all annotated introns
succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial
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 43 samples with support for all annotated introns
leucine-rich repeat and death domain-containing protein 1-like
general transcription factor II-I repeat domain-containing protein 2-like
chromobox protein homolog 5, transcript variant X2
chromobox protein homolog 5, transcript variant X1
protein GVQW3-like, transcript variant X2
protein GVQW3-like, transcript variant X1
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein 629-like, 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 1 sample with support for all annotated introns
zinc finger protein 629-like, transcript variant X2
zinc finger protein 629-like, transcript variant X1
zinc finger protein 629-like, transcript variant X3
EF-hand domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 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 97% coverage of the annotated genomic feature by RNAseq alignments
clathrin light chain B, 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 30 samples with support for all annotated introns
clathrin light chain B, transcript variant X1
clathrin light chain B, transcript variant X3
clathrin light chain B, transcript variant X5
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 46 samples with support for all annotated introns
clathrin light chain B, 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 43 samples with support for all annotated introns
clathrin light chain B, transcript variant X6
tubulin-specific chaperone cofactor E-like protein, transcript variant X2
tubulin-specific chaperone cofactor E-like protein, transcript variant X1
tubulin-specific chaperone cofactor E-like protein isoform X1
tubulin-specific chaperone cofactor E-like protein isoform X2
U11/U12 small nuclear ribonucleoprotein 25 kDa protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
U11/U12 small nuclear ribonucleoprotein 25 kDa protein, transcript variant X1
U11/U12 small nuclear ribonucleoprotein 25 kDa protein, transcript variant X3
U11/U12 small nuclear ribonucleoprotein 25 kDa protein
DNA-directed RNA polymerase III subunit RPC10
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 46 samples with support for all annotated introns
dual specificity tyrosine-phosphorylation-regulated kinase 4
uncharacterized LOC115215933, transcript variant X1
uncharacterized protein LOC115215933 isoform X1
uncharacterized LOC115215933, transcript variant X2
uncharacterized protein LOC115215933 isoform X2
uncharacterized LOC115215946, transcript variant X1
uncharacterized protein LOC115215946 isoform X1
uncharacterized LOC115215946, transcript variant X2
uncharacterized protein LOC115215946 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC115215614
serine/threonine-protein phosphatase 1 regulatory subunit 10, 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 40 samples with support for all annotated introns
serine/threonine-protein phosphatase 1 regulatory subunit 10, transcript variant X2
serine/threonine-protein phosphatase 1 regulatory subunit 10, transcript variant X5
serine/threonine-protein phosphatase 1 regulatory subunit 10, transcript variant X3
serine/threonine-protein phosphatase 1 regulatory subunit 10, 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 20 samples with support for all annotated introns
serine/threonine-protein phosphatase 1 regulatory subunit 10
uncharacterized LOC115215375, 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 14 samples with support for all annotated introns
uncharacterized LOC115215375, 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 41 samples with support for all annotated introns
uncharacterized protein LOC115215375 isoform X1
uncharacterized LOC115215375, 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 5 samples with support for all annotated introns
uncharacterized protein LOC115215375 isoform X2
uncharacterized LOC115215375, transcript variant X3
uncharacterized LOC115215375, transcript variant X5
uncharacterized protein LOC115215375 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
intraflagellar transport protein 88 homolog, transcript variant X2
intraflagellar transport protein 88 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 27 samples with support for all annotated introns
intraflagellar transport protein 88 homolog
SH3 domain-binding protein 1-like, transcript variant X2
SH3 domain-binding protein 1-like, transcript variant X1
putative ribosome biogenesis protein slx9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
cilia- and flagella-associated protein 65-like
neuronal acetylcholine receptor subunit alpha-3-like, 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 4 samples with support for all annotated introns
neuronal acetylcholine receptor subunit alpha-3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
neuronal acetylcholine receptor subunit alpha-3-like, transcript variant X1
neuronal acetylcholine receptor subunit alpha-3-like, transcript variant X5
neuronal acetylcholine receptor subunit alpha-3-like, transcript variant X4
neuronal acetylcholine receptor subunit alpha-3-like
MAGUK p55 subfamily member 7, transcript variant X8
MAGUK p55 subfamily member 7, transcript variant X5
MAGUK p55 subfamily member 7, transcript variant X1
MAGUK p55 subfamily member 7, transcript variant X3
MAGUK p55 subfamily member 7, transcript variant X9
MAGUK p55 subfamily member 7, transcript variant X7
MAGUK p55 subfamily member 7, transcript variant X6
MAGUK p55 subfamily member 7, transcript variant X4
MAGUK p55 subfamily member 7, transcript variant X10
MAGUK p55 subfamily member 7, transcript variant X13
MAGUK p55 subfamily member 7, transcript variant X2
MAGUK p55 subfamily member 7, transcript variant X11
MAGUK p55 subfamily member 7, transcript variant X12
MAGUK p55 subfamily member 7 isoform X11
MAGUK p55 subfamily member 7 isoform X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
corticotropin-releasing factor receptor 2-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 46 samples with support for all annotated introns
vesicular inhibitory amino acid transporter, transcript variant X2
vesicular inhibitory amino acid transporter, 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 20 samples with support for all annotated introns
vesicular inhibitory amino acid transporter isoform X2
vesicular inhibitory amino acid transporter isoform X1
extracellular signal-regulated kinase 2, 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 27 samples with support for all annotated introns
extracellular signal-regulated kinase 2, 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 9 samples with support for all annotated introns
extracellular signal-regulated kinase 2, transcript variant X3
extracellular signal-regulated kinase 2 isoform X1
extracellular signal-regulated kinase 2 isoform 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
POU domain, class 4, transcription factor 2-like
membrane-bound transcription factor site-2 protease-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cytosolic iron-sulfur assembly component 2A-like
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 44 samples with support for all annotated introns
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC115215680, transcript variant X3
uncharacterized LOC115215680, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC115215680, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC115215680, transcript variant X6
uncharacterized LOC115215680, transcript variant X2
uncharacterized LOC115215680, 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 8 samples with support for all annotated introns
uncharacterized protein LOC115215680 isoform X1
uncharacterized protein LOC115215680 isoform X2
uncharacterized LOC118764868, transcript variant X2
uncharacterized LOC118764868, transcript variant X1
arylacetamide deacetylase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
arylacetamide deacetylase, transcript variant X4
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 28 samples with support for all annotated introns
arylacetamide deacetylase, 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 22 samples with support for all annotated introns
arylacetamide deacetylase, transcript variant X3
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
thiamine transporter 1-like, transcript variant X3
thiamine transporter 1-like, transcript variant X1
thiamine transporter 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 9 samples with support for all annotated introns
histone-lysine N-methyltransferase SETMAR-like
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
uncharacterized LOC118764871, transcript variant X2
uncharacterized LOC118764871, transcript variant X3
uncharacterized LOC118764871, 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 19 samples with support for all annotated introns
adrenocorticotropic hormone receptor-like, 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 1 sample with support for all annotated introns
adrenocorticotropic hormone receptor-like, transcript variant X3
adrenocorticotropic hormone receptor-like, transcript variant X1
adrenocorticotropic hormone receptor-like
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
myb-like protein I, transcript variant X1
myb-like protein I, transcript variant X2
chitinase-3-like protein 1, transcript variant X3
chitinase-3-like protein 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 29 samples with support for all annotated introns
chitinase-3-like protein 1, transcript variant X1
chitinase-3-like protein 1, transcript variant X4
solute carrier family 40 member 1-like, transcript variant X3
solute carrier family 40 member 1-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 6 samples with support for all annotated introns
solute carrier family 40 member 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF126, 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
E3 ubiquitin-protein ligase RNF126, transcript variant X2
E3 ubiquitin-protein ligase RNF126 isoform X1
E3 ubiquitin-protein ligase RNF126 isoform X2
E3 ubiquitin-protein ligase RNF126, transcript variant X3
E3 ubiquitin-protein ligase RNF126, 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 30 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF126 isoform X3
lisH domain-containing protein C1711.05-like
regulator of G-protein signaling 9-binding protein-like
calcium and integrin-binding family member 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC118764882, transcript variant X6
uncharacterized LOC118764882, transcript variant X7
uncharacterized LOC118764882, transcript variant X5
uncharacterized LOC118764882, transcript variant X4
uncharacterized LOC118764882, transcript variant X3
uncharacterized LOC118764882, transcript variant X1
uncharacterized LOC118764882, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC118764883, transcript variant X1
uncharacterized LOC118764883, transcript variant X2
uncharacterized LOC118764885, transcript variant X2
uncharacterized LOC118764885, transcript variant X1
mitogen-activated protein kinase HOG1-like
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
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
histone H1.0-B-like, transcript variant X3
histone H1.0-B-like, transcript variant X4
histone H1.0-B-like, transcript variant X2
histone H1.0-B-like, transcript variant X5
histone H1.0-B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
UDP-glucose:glycoprotein glucosyltransferase 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
LOW QUALITY PROTEIN: UDP-glucose:glycoprotein glucosyltransferase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC115215452, transcript variant X2
uncharacterized LOC115215452, transcript variant X3
uncharacterized LOC115215452, transcript variant X1
uncharacterized protein LOC115215452 isoform X1
uncharacterized protein LOC115215452 isoform X2
uncharacterized protein LOC115215452 isoform X3
uncharacterized LOC115215453, transcript variant X2
uncharacterized LOC115215453, transcript variant X1
uncharacterized LOC115215453, transcript variant X4
uncharacterized LOC115215453, transcript variant X3
uncharacterized protein LOC115215453 isoform X2
uncharacterized protein LOC115215453 isoform X1
uncharacterized protein LOC115215453 isoform X3
cys-loop ligand-gated ion channel-like, transcript variant X3
cys-loop ligand-gated ion channel-like, transcript variant X4
cys-loop ligand-gated ion channel-like, transcript variant X1
cys-loop ligand-gated ion channel-like, transcript variant X5
cys-loop ligand-gated ion channel-like, transcript variant X7
cys-loop ligand-gated ion channel-like, transcript variant X2
cys-loop ligand-gated ion channel-like, transcript variant X6
cys-loop ligand-gated ion channel-like isoform X2
cys-loop ligand-gated ion channel-like isoform X3
cys-loop ligand-gated ion channel-like isoform X5
cys-loop ligand-gated ion channel-like isoform X4
cys-loop ligand-gated ion channel-like isoform X7
cys-loop ligand-gated ion channel-like isoform X1
cys-loop ligand-gated ion channel-like isoform X6
acidic mammalian chitinase, transcript variant X2
acidic mammalian chitinase, transcript variant X1
acidic mammalian chitinase, transcript variant X3
golgin subfamily A member 1, transcript variant X5
golgin subfamily A member 1, 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 28 samples with support for all annotated introns
golgin subfamily A member 1, 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 29 samples with support for all annotated introns
golgin subfamily A member 1, transcript variant X2
golgin subfamily A member 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 42 samples with support for all annotated introns
peptidyl-prolyl cis-trans isomerase FKBP62-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 45 samples with support for all annotated introns
dynein heavy chain 7, axonemal-like, 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 2 samples with support for all annotated introns
dynein heavy chain 7, axonemal-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 2 samples with support for all annotated introns
dynein heavy chain 7, axonemal-like isoform X2
dynein heavy chain 7, axonemal-like isoform X1
organic cation transporter-like protein, transcript variant X2
organic cation transporter-like protein isoform X2
organic cation transporter-like protein, transcript variant X1
organic cation transporter protein-like isoform X1
heparan sulfate glucosamine 3-O-sulfotransferase 5-like, transcript variant X4
heparan sulfate glucosamine 3-O-sulfotransferase 5-like, 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 12 samples with support for all annotated introns
heparan sulfate glucosamine 3-O-sulfotransferase 5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
heparan sulfate glucosamine 3-O-sulfotransferase 5-like, transcript variant X3
heparan sulfate glucosamine 3-O-sulfotransferase 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 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 22 samples with support for all annotated introns
heparan sulfate glucosamine 3-O-sulfotransferase 5-like isoform X1
uncharacterized protein LOC115215914 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
LOW QUALITY PROTEIN: nucleolar protein 58-like
organic cation transporter 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
organic cation transporter protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
PAN2-PAN3 deadenylation complex catalytic subunit Pan2, 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 12 samples with support for all annotated introns
PAN2-PAN3 deadenylation complex catalytic subunit Pan2, 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 14 samples with support for all annotated introns
PAN2-PAN3 deadenylation complex catalytic subunit Pan2, 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 42 samples with support for all annotated introns
PAN2-PAN3 deadenylation complex catalytic subunit Pan2, 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 8 samples with support for all annotated introns
PAN2-PAN3 deadenylation complex catalytic subunit Pan2
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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
LOW QUALITY PROTEIN: DDB1- and CUL4-associated factor 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 85% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein Aster-B-like
uncharacterized protein LOC115215466 isoform X1
uncharacterized protein LOC115215466 isoform X3
methionine--tRNA ligase, mitochondrial, transcript variant X2
methionine--tRNA ligase, mitochondrial isoform X2
methionine--tRNA ligase, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
methionine--tRNA ligase, mitochondrial isoform X1
methionine--tRNA ligase, mitochondrial, 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 35 samples with support for all annotated introns
methionine--tRNA ligase, mitochondrial, transcript variant X4
methionine--tRNA ligase, mitochondrial isoform X3
methionine--tRNA ligase, mitochondrial isoform X4
formin-like protein, transcript variant X1
formin-like protein, transcript variant X2
formin-like protein, transcript variant X3
formin-like protein, transcript variant X4
formin-like protein, transcript variant X5
formin-like protein, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
organic cation transporter protein-like, transcript variant X4
organic cation transporter protein-like, transcript variant X3
organic cation transporter protein-like isoform X3
organic cation transporter protein-like isoform X2
organic cation transporter protein-like isoform X4
telomere-associated protein RIF1-like, transcript variant X7
telomere-associated protein RIF1-like, transcript variant X3
telomere-associated protein RIF1-like, transcript variant X4
telomere-associated protein RIF1-like, transcript variant X6
telomere-associated protein RIF1-like, transcript variant X5
telomere-associated protein RIF1-like, transcript variant X1
telomere-associated protein RIF1-like, transcript variant X2
telomere-associated protein RIF1-like isoform X2
telomere-associated protein RIF1-like isoform X7
telomere-associated protein RIF1-like isoform X3
telomere-associated protein RIF1-like isoform X4
telomere-associated protein RIF1-like isoform X6
telomere-associated protein RIF1-like isoform X5
telomere-associated protein RIF1-like isoform X1
uncharacterized LOC115215378, transcript variant X2
uncharacterized LOC115215378, transcript variant X1
pyridoxal phosphate phosphatase PHOSPHO2
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 42 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
vacuolar protein sorting-associated protein VTA1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 17% coverage of the annotated genomic feature by RNAseq alignments
glucosidase 2 subunit beta, transcript variant X2
glucosidase 2 subunit beta, 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 41 samples with support for all annotated introns
phosphatidylinositol phosphatase PTPRQ, 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 3 samples with support for all annotated introns
phosphatidylinositol phosphatase PTPRQ, transcript variant X3
phosphatidylinositol phosphatase PTPRQ, transcript variant X1
ras-related protein Rab-18A, transcript variant X1
ras-related protein Rab-18A, 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 45 samples with support for all annotated introns
tryptophan 5-hydroxylase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tryptophan 5-hydroxylase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mitochondrial glutamate carrier 1-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 24 samples with support for all annotated introns
mitochondrial glutamate carrier 1-like, transcript variant X2
mitochondrial glutamate carrier 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
ATP synthase subunit beta, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
uncharacterized protein F54F2.9, 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 23 samples with support for all annotated introns
uncharacterized protein F54F2.9, transcript variant X1
DNA-directed RNA polymerase II subunit RPB1
uncharacterized LOC115215841, transcript variant X21
uncharacterized LOC115215841, transcript variant X34
uncharacterized LOC115215841, transcript variant X3
uncharacterized LOC115215841, transcript variant X15
uncharacterized LOC115215841, transcript variant X8
uncharacterized LOC115215841, transcript variant X22
uncharacterized LOC115215841, transcript variant X24
uncharacterized LOC115215841, transcript variant X4
uncharacterized LOC115215841, transcript variant X12
uncharacterized LOC115215841, transcript variant X1
uncharacterized LOC115215841, transcript variant X13
uncharacterized LOC115215841, transcript variant X7
uncharacterized LOC115215841, transcript variant X19
uncharacterized LOC115215841, transcript variant X10
uncharacterized LOC115215841, transcript variant X9
uncharacterized LOC115215841, transcript variant X11
uncharacterized LOC115215841, transcript variant X27
uncharacterized LOC115215841, transcript variant X28
uncharacterized LOC115215841, transcript variant X5
uncharacterized LOC115215841, transcript variant X6
uncharacterized LOC115215841, transcript variant X20
uncharacterized LOC115215841, transcript variant X16
uncharacterized LOC115215841, transcript variant X18
uncharacterized LOC115215841, transcript variant X25
uncharacterized LOC115215841, transcript variant X17
uncharacterized LOC115215841, transcript variant X26
uncharacterized LOC115215841, transcript variant X33
uncharacterized LOC115215841, transcript variant X30
uncharacterized LOC115215841, transcript variant X32
uncharacterized LOC115215841, transcript variant X14
uncharacterized LOC115215841, transcript variant X29
uncharacterized LOC115215841, transcript variant X31
uncharacterized LOC115215841, transcript variant X2
uncharacterized protein LOC115215841 isoform X2
uncharacterized protein LOC115215841 isoform X19
uncharacterized protein LOC115215841 isoform X10
uncharacterized protein LOC115215841 isoform X13
uncharacterized protein LOC115215841 isoform X1
uncharacterized protein LOC115215841 isoform X6
uncharacterized protein LOC115215841 isoform X11
uncharacterized protein LOC115215841 isoform X5
uncharacterized protein LOC115215841 isoform X17
uncharacterized protein LOC115215841 isoform X20
uncharacterized protein LOC115215841 isoform X8
uncharacterized protein LOC115215841 isoform X18
uncharacterized protein LOC115215841 isoform X7
uncharacterized protein LOC115215841 isoform X22
uncharacterized protein LOC115215841 isoform X9
uncharacterized protein LOC115215841 isoform X25
uncharacterized protein LOC115215841 isoform X14
uncharacterized protein LOC115215841 isoform X26
uncharacterized protein LOC115215841 isoform X16
uncharacterized protein LOC115215841 isoform X3
uncharacterized protein LOC115215841 isoform X23
uncharacterized protein LOC115215841 isoform X4
uncharacterized protein LOC115215841 isoform X15
uncharacterized protein LOC115215841 isoform X24
uncharacterized protein LOC115215841 isoform X31
uncharacterized protein LOC115215841 isoform X28
uncharacterized protein LOC115215841 isoform X30
uncharacterized protein LOC115215841 isoform X12
uncharacterized protein LOC115215841 isoform X27
uncharacterized protein LOC115215841 isoform X29
uncharacterized protein LOC115215841 isoform X32
uncharacterized LOC115215841, transcript variant X23
uncharacterized protein LOC115215841 isoform X21
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
organic cation transporter protein, transcript variant X2
organic cation transporter protein, transcript variant X1
organic cation transporter protein isoform X1
organic cation transporter protein isoform 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 5 samples with support for all annotated introns
organic cation transporter protein-like, transcript variant X5
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
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
ADP-ribosylarginine hydrolase Tri1, transcript variant X2
ADP-ribosylarginine hydrolase Tri1, transcript variant X1
ADP-ribosylarginine hydrolase Tri1 isoform X2
ADP-ribosylarginine hydrolase Tri1 isoform X1
lysosome-associated membrane glycoprotein 1, transcript variant X2
lysosome-associated membrane glycoprotein 1, transcript variant X3
lysosome-associated membrane glycoprotein 1, transcript variant X1
lysosome-associated membrane glycoprotein 1 isoform X2
lysosome-associated membrane glycoprotein 1 isoform X3
lysosome-associated membrane glycoprotein 1 isoform X1
ATP-dependent RNA helicase HAS1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
ATP-dependent RNA helicase HAS1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
ATP-dependent RNA helicase HAS1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ATP-dependent RNA helicase HAS1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
ATP-dependent RNA helicase HAS1 isoform X4
ATP-dependent RNA helicase HAS1 isoform X3
ATP-dependent RNA helicase HAS1 isoform X2
ATP-dependent RNA helicase HAS1 isoform X1
golgin subfamily A member 4-like, transcript variant X2
golgin subfamily A member 4-like, transcript variant X1
golgin subfamily A member 4-like, transcript variant X3
golgin subfamily A member 4-like isoform X1
golgin subfamily A member 4-like isoform X2
golgin subfamily A member 4-like isoform X3
beta-1,4-glucuronyltransferase 1-like, transcript variant X4
beta-1,4-glucuronyltransferase 1-like, transcript variant X1
beta-1,4-glucuronyltransferase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
beta-1,4-glucuronyltransferase 1-like, transcript variant X3
survival of motor neuron-related-splicing factor 30
5-formyltetrahydrofolate cyclo-ligase, transcript variant X3
5-formyltetrahydrofolate cyclo-ligase, transcript variant X2
5-formyltetrahydrofolate cyclo-ligase, transcript variant X1
uncharacterized LOC115215478, transcript variant X4
uncharacterized LOC115215478, transcript variant X1
uncharacterized LOC115215478, transcript variant X3
uncharacterized LOC115215478, transcript variant X2
serine/threonine-protein kinase Nek7-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 19 samples with support for all annotated introns
serine/threonine-protein kinase Nek7-like, transcript variant X6
serine/threonine-protein kinase Nek7-like, transcript variant X4
serine/threonine-protein kinase Nek7-like, transcript variant X3
serine/threonine-protein kinase Nek7-like, 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 35 samples with support for all annotated introns
serine/threonine-protein kinase Nek7-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 37 samples with support for all annotated introns
serine/threonine-protein kinase Nek7-like isoform X5
serine/threonine-protein kinase Nek7-like isoform X3
serine/threonine-protein kinase Nek7-like isoform X4
serine/threonine-protein kinase Nek7-like isoform X2
serine/threonine-protein kinase Nek7-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 148 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 414 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: 257 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: 5 Proteins, and 88% 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: 237 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
histone deacetylase 4, 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 3 samples with support for all annotated introns
histone deacetylase 4, transcript variant X3
histone deacetylase 4, transcript variant X2
histone deacetylase 4, transcript variant X4
histone deacetylase 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
leucine-rich repeat-containing protein 15-like, transcript variant X2
leucine-rich repeat-containing protein 15-like, transcript variant X3
leucine-rich repeat-containing protein 15-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 22 samples with support for all annotated introns
leucine-rich repeat-containing protein 15-like isoform X2
leucine-rich repeat-containing protein 15-like isoform X1
leucine-rich repeat-containing protein 15-like isoform X3
splicing factor 3B subunit 1, transcript variant X1
splicing factor 3B subunit 1, 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 38 samples with support for all annotated introns
splicing factor 3B subunit 1, transcript variant X2
DNA-directed RNA polymerase I subunit RPA2, transcript variant X2
DNA-directed RNA polymerase I subunit RPA2, 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 27 samples with support for all annotated introns
DNA-directed RNA polymerase I subunit RPA2 isoform X2
DNA-directed RNA polymerase I subunit RPA2 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, including 18 samples with support for all annotated introns
inositol polyphosphate 5-phosphatase OCRL, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
inositol polyphosphate 5-phosphatase OCRL, transcript variant X1
inositol polyphosphate 5-phosphatase OCRL, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
inositol polyphosphate 5-phosphatase OCRL isoform X2
inositol polyphosphate 5-phosphatase OCRL isoform X1
inositol polyphosphate 5-phosphatase OCRL isoform 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
uncharacterized LOC115215568, transcript variant X2
uncharacterized protein LOC115215568 isoform X2
uncharacterized LOC115215568, transcript variant X1
uncharacterized protein LOC115215568 isoform X1
uncharacterized LOC115215568, transcript variant X3
uncharacterized protein LOC115215568 isoform X3
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC115215539, transcript variant X2
uncharacterized LOC115215539, transcript variant X1
uncharacterized LOC115215539, transcript variant X3
uncharacterized protein LOC115215539 isoform X1
uncharacterized protein LOC115215539 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
tubulin polymerization-promoting protein family member 3, 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 27 samples with support for all annotated introns
tubulin polymerization-promoting protein family member 3, transcript variant X2
tubulin polymerization-promoting protein family member 3, transcript variant X1
tubulin polymerization-promoting protein family member 3 isoform X2
tubulin polymerization-promoting protein family member 3 isoform X1
tubulin polymerization-promoting protein family member 3 isoform 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 44 samples with support for all annotated introns
methyl-accepting chemotaxis protein 2-like
stromal membrane-associated protein 1, transcript variant X1
stromal membrane-associated protein 1, transcript variant X2
stromal membrane-associated protein 1, transcript variant X4
stromal membrane-associated protein 1, transcript variant X3
stromal membrane-associated protein 1 isoform X1
stromal membrane-associated protein 1 isoform X4
stromal membrane-associated protein 1 isoform X2
stromal membrane-associated protein 1 isoform X3
uncharacterized LOC115215651, transcript variant X2
uncharacterized LOC115215651, transcript variant X1
uncharacterized LOC115215651, transcript variant X4
uncharacterized LOC115215651, transcript variant X3
uncharacterized protein LOC115215651 isoform X2
uncharacterized protein LOC115215651 isoform X1
uncharacterized protein LOC115215651 isoform X3
uncharacterized protein LOC115215651 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
RWD domain-containing protein 3, transcript variant X1
RWD domain-containing protein 3, transcript variant X2
RWD domain-containing protein 3, transcript variant X3
RWD domain-containing protein 3 isoform X1
RWD domain-containing protein 3 isoform X2
RWD domain-containing protein 3 isoform X3
YTH domain-containing protein 1, transcript variant X5
YTH domain-containing protein 1, transcript variant X7
YTH domain-containing protein 1, transcript variant X9
YTH domain-containing protein 1, transcript variant X2
YTH domain-containing protein 1, transcript variant X1
YTH domain-containing protein 1, 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 38 samples with support for all annotated introns
YTH domain-containing protein 1, transcript variant X4
YTH domain-containing protein 1, transcript variant X6
YTH domain-containing protein 1, transcript variant X8
YTH domain-containing protein 1, transcript variant X10
YTH domain-containing protein 1 isoform X1
YTH domain-containing protein 1 isoform X2
YTH domain-containing protein 1 isoform X3
YTH domain-containing protein 1 isoform X4
YTH domain-containing protein 1 isoform X8
YTH domain-containing protein 1 isoform X6
YTH domain-containing protein 1 isoform X10
YTH domain-containing protein 1 isoform X5
YTH domain-containing protein 1 isoform X7
YTH domain-containing protein 1 isoform 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 5 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 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 3 samples with support for all annotated introns
DNA-3-methyladenine glycosylase-like, transcript variant X5
DNA-3-methyladenine glycosylase-like, transcript variant X8
DNA-3-methyladenine glycosylase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
DNA-3-methyladenine glycosylase-like, transcript variant X3
DNA-3-methyladenine glycosylase-like, transcript variant X4
DNA-3-methyladenine glycosylase-like, transcript variant X6
DNA-3-methyladenine glycosylase-like, transcript variant X7
DNA-3-methyladenine glycosylase-like, 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 41 samples with support for all annotated introns
DNA-3-methyladenine glycosylase-like isoform X2
DNA-3-methyladenine glycosylase-like isoform X1
inactive rhomboid protein 2-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 29 samples with support for all annotated introns
inactive rhomboid protein 2-like, transcript variant X3
inactive rhomboid protein 2-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 38 samples with support for all annotated introns
WAS/WASL-interacting protein family member 1-like
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 13 samples with support for all annotated introns
SOSS complex subunit C homolog, transcript variant X2
SOSS complex subunit C homolog, transcript variant X1
SOSS complex subunit C homolog isoform X2
sorting nexin-30-like, transcript variant X2
sorting nexin-30-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase NIM1-like, 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 3 samples with support for all annotated introns
serine/threonine-protein kinase par-1-like isoform X1
serine/threonine-protein kinase NIM1-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 27 samples with support for all annotated introns
serine/threonine-protein kinase NIM1-like isoform X2
uncharacterized LOC115215506, transcript variant X3
uncharacterized LOC115215506, transcript variant X1
uncharacterized LOC115215506, 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 31 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 3 samples with support for all annotated introns
guanine nucleotide exchange factor subunit RIC1, 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 39 samples with support for all annotated introns
guanine nucleotide exchange factor subunit RIC1, transcript variant X2
guanine nucleotide exchange factor subunit RIC1 isoform X1
guanine nucleotide exchange factor subunit RIC1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ELAV-like protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ELAV-like protein 2, transcript variant X6
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 23 samples with support for all annotated introns
ELAV-like protein 2, 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 26 samples with support for all annotated introns
ELAV-like protein 2, transcript variant X4
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 26 samples with support for all annotated introns
ELAV-like protein 2, transcript variant X2
ELAV-like protein 2, transcript variant X1
serine/arginine repetitive matrix protein 1-like
caspase activity and apoptosis inhibitor 1, transcript variant X2
caspase activity and apoptosis inhibitor 1, 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
caspase activity and apoptosis inhibitor 1, transcript variant X4
caspase activity and apoptosis inhibitor 1, transcript variant X1
uncharacterized protein LOC115215684 isoform X1
caspase activity and apoptosis inhibitor 1, transcript variant X5
caspase activity and apoptosis inhibitor 1 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
uncharacterized LOC115215499, transcript variant X3
uncharacterized LOC115215499, transcript variant X2
uncharacterized LOC115215499, transcript variant X4
uncharacterized LOC115215499, transcript variant X5
uncharacterized LOC115215499, transcript variant X1
uncharacterized protein LOC115215499 isoform X2
uncharacterized protein LOC115215499 isoform X1