Chiloscyllium plagiosum isolate BGI_BamShark_2017 chromosome 43, ASM401019v2, whole genome shotgun sequence.
Chiloscyllium plagiosum (whitespotted bambooshark)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Chondrichthyes; Elasmobranchii; Galeomorphii; Galeoidea; Orectolobiformes; Hemiscylliidae; Chiloscyllium.
REFSEQ INFORMATION: The reference sequence is identical to\nCM012998.1.\nAssembly name: ASM401019v2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the BGI on 2019/01/10. The\noriginal whole-genome shotgun project has the accession\nQPFF00000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: BGI\nAssembly Method :: platanus v. 1.2.4; 3ddna v. 170123\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 280.0x\nSequencing Technology :: BGIseq-500\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Chiloscyllium plagiosum Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon.
inositol polyphosphate 1-phosphatase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
inositol polyphosphate 1-phosphatase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
inositol polyphosphate 1-phosphatase-like
poly(A) specific ribonuclease subunit PAN2, transcript variant X3
COORDINATES: polyA evidence [ECO:0006239]
poly(A) specific ribonuclease subunit PAN2, transcript variant X2
poly(A) specific ribonuclease subunit PAN2, transcript variant X1
poly(A) specific ribonuclease subunit PAN2, transcript variant X4
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X2
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X1
poly(A) specific ribonuclease subunit PAN2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
interleukin-23 subunit alpha-like, transcript variant X1
interleukin-23 subunit alpha-like isoform X1
interleukin-23 subunit alpha-like, transcript variant X3
interleukin-23 subunit alpha-like, transcript variant X2
interleukin-23 subunit alpha-like isoform X2
Ts translation elongation factor, mitochondrial
EEF1A lysine methyltransferase 3-like, transcript variant X3
EEF1A lysine methyltransferase 3-like, transcript variant X2
EEF1A lysine methyltransferase 3-like, transcript variant X1
EEF1A lysine methyltransferase 3-like, transcript variant X4
25-hydroxyvitamin D-1 alpha hydroxylase, mitochondrial, transcript variant X2
25-hydroxyvitamin D-1 alpha hydroxylase, mitochondrial, transcript variant X3
25-hydroxyvitamin D-1 alpha hydroxylase, mitochondrial, transcript variant X1
25-hydroxyvitamin D-1 alpha hydroxylase, mitochondrial isoform X3
25-hydroxyvitamin D-1 alpha hydroxylase, mitochondrial isoform X1
25-hydroxyvitamin D-1 alpha hydroxylase, mitochondrial isoform X2
methyltransferase 1, tRNA methylguanosine, 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 22 samples with support for all annotated introns
methyltransferase 1, tRNA methylguanosine, 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 15 samples with support for all annotated introns
tRNA (guanine-N(7)-)-methyltransferase isoform X1
tRNA (guanine-N(7)-)-methyltransferase isoform X2
sodium channel protein type 8 subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 77% coverage of the annotated genomic feature by RNAseq alignments
membrane-associated ring finger (C3HC4) 9
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 5 samples with support for all annotated introns
cyclin-dependent kinase 4, transcript variant X2
cyclin-dependent kinase 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
cyclin-dependent kinase 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
cyclin-dependent kinase 4, transcript variant X5
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 12 samples with support for all annotated introns
cyclin-dependent kinase 4, transcript variant X6
cyclin-dependent kinase 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
cyclin-dependent kinase 4, transcript variant X8
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
cyclin-dependent kinase 4, transcript variant X9
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
cyclin-dependent kinase 4, transcript variant X7
cyclin-dependent kinase 4, transcript variant X10
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1-like isoform X4
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
arf-GAP with GTPase, ANK repeat and PH 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 3 samples with support for all annotated introns
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1-like isoform X1
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1-like isoform X2
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1-like isoform X3
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
zinc finger and BTB domain-containing protein 39, 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 7 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 39, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 39, transcript variant X5
zinc finger and BTB domain-containing protein 39, transcript variant X9
zinc finger and BTB domain-containing protein 39, transcript variant X7
zinc finger and BTB domain-containing protein 39, transcript variant X1
zinc finger and BTB domain-containing protein 39, transcript variant X2
zinc finger and BTB domain-containing protein 39, transcript variant X3
zinc finger and BTB domain-containing protein 39
zinc finger and BTB domain-containing protein 39, transcript variant X8
solute carrier family 11 member 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
solute carrier family 11 member 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
natural resistance-associated macrophage protein 2 isoform X2
natural resistance-associated macrophage protein 2 isoform X3
solute carrier family 11 member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
solute carrier family 11 member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
natural resistance-associated macrophage protein 2 isoform X1
formin-like protein 3, transcript variant X6
formin-like protein 3, transcript variant X5
formin-like protein 3, transcript variant X4
formin-like protein 3, transcript variant X2
formin-like protein 3, transcript variant X1
formin-like protein 3, 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
biogenesis of lysosomal organelles complex-1, subunit 1
biogenesis of lysosome-related organelles complex 1 subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA threonine (anticodon AGU); 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: 7 Proteins
RNA-binding motif, single-stranded-interacting protein 2-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 18 samples with support for all annotated introns
RNA-binding motif, single-stranded-interacting protein 2-like, 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 10 samples with support for all annotated introns
RNA-binding motif, single-stranded-interacting protein 2-like, transcript variant X1
RNA-binding motif, single-stranded-interacting protein 2-like, transcript variant X4
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 18 samples with support for all annotated introns
RNA-binding motif, single-stranded-interacting protein 2-like isoform X5
RNA-binding motif, single-stranded-interacting protein 2-like isoform X1
RNA-binding motif, single-stranded-interacting protein 2-like isoform X4
RNA-binding motif, single-stranded-interacting protein 2-like isoform X2
RNA-binding motif, single-stranded-interacting protein 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
RNA-binding motif, single-stranded-interacting protein 2-like isoform X3
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic-like, transcript variant X2
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic-like, transcript variant X1
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic-like isoform X1
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic-like isoform X2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 1
acid-sensing (proton-gated) ion channel 1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
acid-sensing (proton-gated) ion channel 1b, 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
uncharacterized protein si:ch211-210c8.6
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
PYM homolog 1, exon junction complex associated factor, transcript variant X2
PYM homolog 1, exon junction complex associated factor, transcript variant X3
PYM homolog 1, exon junction complex associated factor, transcript variant X4
PYM homolog 1, exon junction complex associated factor, transcript variant X5
PYM homolog 1, exon junction complex associated factor, transcript variant X1
eukaryotic translation initiation factor 4Ba, transcript variant X1
eukaryotic translation initiation factor 4Ba, transcript variant X3
eukaryotic translation initiation factor 4Ba, transcript variant X2
eukaryotic translation initiation factor 4Ba isoform X1
eukaryotic translation initiation factor 4Ba isoform X3
eukaryotic translation initiation factor 4Ba isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122543304, transcript variant X2
uncharacterized LOC122543304, 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 13 samples with support for all annotated introns
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 5 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 5 samples with support for all annotated introns
uncharacterized LOC122543309, transcript variant X2
uncharacterized LOC122543309, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: tubulin alpha chain-like
limb development membrane protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
GTP-binding protein Rheb-like, transcript variant X1
GTP-binding protein Rheb-like, transcript variant X3
GTP-binding protein Rheb-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 1 sample with support for all annotated introns
GTP-binding protein Rheb-like isoform X1
GTP-binding protein Rheb-like isoform X3
GTP-binding protein Rheb-like isoform X2
lysine (K)-specific methyltransferase 2D, transcript variant X1
lysine (K)-specific methyltransferase 2D, transcript variant X2
lysine (K)-specific methyltransferase 2D, transcript variant X3
lysine (K)-specific methyltransferase 2D, transcript variant X4
histone-lysine N-methyltransferase 2D isoform X1
histone-lysine N-methyltransferase 2D isoform X2
histone-lysine N-methyltransferase 2D isoform X3
histone-lysine N-methyltransferase 2D isoform X4
5'-AMP-activated protein kinase subunit gamma-1, transcript variant X1
5'-AMP-activated protein kinase subunit gamma-1, transcript variant X2
5'-AMP-activated protein kinase subunit gamma-1 isoform X1
5'-AMP-activated protein kinase subunit gamma-1 isoform X2
uncharacterized LOC122543315, transcript variant X2
uncharacterized LOC122543315, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
wingless-type MMTV integration site family, member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
protein Wnt-6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein Wnt-6-like, 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 2 samples with support for all annotated introns
wingless-type MMTV integration site family, member 10b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
ADP-ribosylation factor 3-like, transcript variant X1
ADP-ribosylation factor 3-like, transcript variant X2
FKBP prolyl isomerase 11, transcript variant X1
peptidyl-prolyl cis-trans isomerase FKBP11 isoform X1
FKBP prolyl isomerase 11, transcript variant X2
peptidyl-prolyl cis-trans isomerase FKBP11 isoform X2
coiled-coil domain containing 65, 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 14 samples with support for all annotated introns
coiled-coil domain containing 65, 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 11 samples with support for all annotated introns
coiled-coil domain containing 65, 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 13 samples with support for all annotated introns
coiled-coil domain containing 65, transcript variant X3
coiled-coil domain containing 65, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
neuropeptide FF-amide peptide precursor like
pro-FMRFamide-related neuropeptide FF like
TAR (HIV) RNA binding protein 2, transcript variant X2
TAR (HIV) RNA binding protein 2, transcript variant X1
RISC-loading complex subunit tarbp2 isoform X2
RISC-loading complex subunit tarbp2 isoform X1
pleckstrin homology domain-containing family A member 3-like, 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
pleckstrin homology domain-containing family A member 3-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 12 samples with support for all annotated introns
pleckstrin homology domain-containing family A member 3-like, transcript variant X3
pleckstrin homology domain-containing family A member 3-like, transcript variant X2
pleckstrin homology domain-containing family A member 3-like isoform X1
pleckstrin homology domain-containing family A member 3-like isoform X3
pleckstrin homology domain-containing family A member 3-like isoform X2
pleckstrin homology domain-containing family A member 3-like isoform X4
uncharacterized LOC122543327, transcript variant X2
uncharacterized LOC122543327, transcript variant X1
receptor tyrosine-protein kinase erbB-4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
receptor tyrosine-protein kinase erbB-4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
receptor tyrosine-protein kinase erbB-4-like isoform X1
receptor tyrosine-protein kinase erbB-4-like isoform X2
IKAROS family zinc finger 4, transcript variant X5
IKAROS family zinc finger 4, transcript variant X4
IKAROS family zinc finger 4, transcript variant X3
IKAROS family zinc finger 4, transcript variant X1
IKAROS family zinc finger 4, transcript variant X2
IKAROS family zinc finger 4, transcript variant X6
ribosomal protein S26, transcript variant X1
ribosomal protein S26, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
leucine-rich repeat flightless-interacting protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
leucine-rich repeat flightless-interacting protein 1-like, transcript variant X1
leucine-rich repeat flightless-interacting protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
leucine-rich repeat flightless-interacting protein 1-like isoform X3
leucine-rich repeat flightless-interacting protein 1-like isoform X2
leucine-rich repeat flightless-interacting protein 1-like isoform X1
ras-related protein Rab-5B, transcript variant X2
ras-related protein Rab-5B, transcript variant X1
cyclin-dependent kinase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
cyclin-dependent kinase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
premelanosome protein a, transcript variant X1
premelanosome protein a, transcript variant X2
premelanosome protein a, transcript variant X3
microspherule protein 1, transcript variant X2
microspherule protein 1, transcript variant X1
microspherule protein 1, transcript variant X4
microspherule protein 1, transcript variant X6
microspherule protein 1, transcript variant X5
microspherule protein 1, transcript variant X3
spermatogenesis-associated serine-rich protein 2-like, transcript variant X5
spermatogenesis-associated serine-rich protein 2-like, transcript variant X3
spermatogenesis-associated serine-rich protein 2-like, transcript variant X2
spermatogenesis-associated serine-rich protein 2-like, transcript variant X4
spermatogenesis-associated serine-rich protein 2-like, transcript variant X1
spermatogenesis-associated serine-rich protein 2-like, transcript variant X7
spermatogenesis-associated serine-rich protein 2-like, transcript variant X8
spermatogenesis-associated serine-rich protein 2-like, transcript variant X6
spermatogenesis-associated serine-rich protein 2-like isoform X1
spermatogenesis-associated serine-rich protein 2-like isoform X2
spermatogenesis-associated serine-rich protein 2-like isoform X3
spermatogenesis-associated serine-rich protein 2-like, transcript variant X9
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
spermatogenesis-associated serine-rich protein 2-like isoform X4
DnaJ (Hsp40) homolog, subfamily C, member 22, transcript variant X1
DnaJ (Hsp40) homolog, subfamily C, member 22, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 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 20 samples with support for all annotated introns
zinc finger CCCH domain-containing protein 10-like, transcript variant X17
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
zinc finger CCCH domain-containing protein 10-like, transcript variant X23
zinc finger CCCH domain-containing protein 10-like, transcript variant X21
zinc finger CCCH domain-containing protein 10-like, transcript variant X19
zinc finger CCCH domain-containing protein 10-like, transcript variant X18
zinc finger CCCH domain-containing protein 10-like, transcript variant X20
uncharacterized protein LOC122543347 isoform X3
uncharacterized protein LOC122543347 isoform X5
zinc finger CCCH domain-containing protein 10-like, transcript variant X22
uncharacterized protein LOC122543347 isoform X4
zinc finger CCCH domain-containing protein 10-like, transcript variant X13
zinc finger CCCH domain-containing protein 10-like, transcript variant X16
zinc finger CCCH domain-containing protein 10-like, transcript variant X15
zinc finger CCCH domain-containing protein 10-like, transcript variant X11
zinc finger CCCH domain-containing protein 10-like, transcript variant X12
zinc finger CCCH domain-containing protein 10-like, transcript variant X14
zinc finger CCCH domain-containing protein 10-like isoform X2
zinc finger CCCH domain-containing protein 10-like, transcript variant X8
zinc finger CCCH domain-containing protein 10-like, transcript variant X6
zinc finger CCCH domain-containing protein 10-like, transcript variant X5
zinc finger CCCH domain-containing protein 10-like, transcript variant X1
zinc finger CCCH domain-containing protein 10-like, transcript variant X2
zinc finger CCCH domain-containing protein 10-like, transcript variant X4
zinc finger CCCH domain-containing protein 10-like, transcript variant X10
zinc finger CCCH domain-containing protein 10-like, transcript variant X9
zinc finger CCCH domain-containing protein 10-like, transcript variant X3
zinc finger CCCH domain-containing protein 10-like, transcript variant X7
zinc finger CCCH domain-containing protein 10-like isoform 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 98% 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: 24 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
electroneutral sodium bicarbonate exchanger 1-like, transcript variant X3
electroneutral sodium bicarbonate exchanger 1-like, transcript variant X2
electroneutral sodium bicarbonate exchanger 1-like, transcript variant X1
electroneutral sodium bicarbonate exchanger 1-like isoform X1
electroneutral sodium bicarbonate exchanger 1-like isoform X2
electroneutral sodium bicarbonate exchanger 1-like isoform X3
electroneutral sodium bicarbonate exchanger 1-like, 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 5 samples with support for all annotated introns
electroneutral sodium bicarbonate exchanger 1-like isoform X4
electroneutral sodium bicarbonate exchanger 1-like, 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 4 samples with support for all annotated introns
electroneutral sodium bicarbonate exchanger 1-like isoform X5
TRAF family member-associated NFKB activator, transcript variant X4
TRAF family member-associated NFKB activator, transcript variant X5
TRAF family member-associated NFKB activator, transcript variant X2
TRAF family member-associated NFKB activator, transcript variant X1
TRAF family member-associated NFKB activator, transcript variant X6
TRAF family member-associated NFKB activator, transcript variant X7
TRAF family member-associated NFKB activator, transcript variant X3
TRAF family member-associated NF-kappa-B activator
polypeptide N-acetylgalactosaminyltransferase 6-like, transcript variant X7
polypeptide N-acetylgalactosaminyltransferase 6-like, transcript variant X2
polypeptide N-acetylgalactosaminyltransferase 6-like, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase 6-like, transcript variant X4
polypeptide N-acetylgalactosaminyltransferase 6-like, transcript variant X3
polypeptide N-acetylgalactosaminyltransferase 6-like, transcript variant X6
polypeptide N-acetylgalactosaminyltransferase 6-like, transcript variant X5
polypeptide N-acetylgalactosaminyltransferase 6-like isoform X1
polypeptide N-acetylgalactosaminyltransferase 6-like isoform X2
LETM1 domain containing 1, transcript variant X2
LETM1 domain containing 1, transcript variant X1
LETM1 domain containing 1, transcript variant X3
LETM1 domain-containing protein 1 isoform X2
LETM1 domain-containing protein 1 isoform X1
LETM1 domain-containing protein 1 isoform X3
cysteine/serine-rich nuclear protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cysteine/serine-rich nuclear protein 2-like, 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 3 samples with support for all annotated introns
cysteine/serine-rich nuclear protein 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
cysteine/serine-rich nuclear protein 2-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 5 samples with support for all annotated introns
cysteine/serine-rich nuclear protein 2-like, transcript variant X7
cysteine/serine-rich nuclear protein 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cysteine/serine-rich nuclear protein 2-like, transcript variant X6
cysteine/serine-rich nuclear protein 2-like, 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 5 samples with support for all annotated introns
cysteine/serine-rich nuclear protein 2-like isoform X2
cysteine/serine-rich nuclear protein 2-like isoform X1
cysteine/serine-rich nuclear protein 2-like isoform X3
uncharacterized LOC122543358, transcript variant X1
uncharacterized LOC122543358, transcript variant X2
uncharacterized LOC122543358, transcript variant X5
uncharacterized LOC122543358, transcript variant X3
uncharacterized protein LOC122543358 isoform X1
uncharacterized protein LOC122543358 isoform X2
uncharacterized protein LOC122543358 isoform X5
uncharacterized protein LOC122543358 isoform X3
uncharacterized LOC122543358, transcript variant X4
uncharacterized protein LOC122543358 isoform X4
uncharacterized LOC122543358, transcript variant X6
uncharacterized protein LOC122543358 isoform X6
LIM domain and actin-binding protein 1-like, transcript variant X6
LIM domain and actin-binding protein 1-like, transcript variant X5
LIM domain and actin-binding protein 1-like, transcript variant X3
LIM domain and actin-binding protein 1-like, transcript variant X7
LIM domain and actin-binding protein 1-like, transcript variant X4
LIM domain and actin-binding protein 1-like, transcript variant X2
LIM domain and actin-binding protein 1-like, transcript variant X1
LIM domain and actin-binding protein 1-like, transcript variant X8
LIM domain and actin-binding protein 1-like isoform X3
LIM domain and actin-binding protein 1-like isoform X2
LIM domain and actin-binding protein 1-like isoform X1
LIM domain and actin-binding protein 1-like isoform X4
STE20/SPS1-related proline-alanine-rich protein kinase-like, transcript variant X2
STE20/SPS1-related proline-alanine-rich protein kinase-like isoform X2
STE20/SPS1-related proline-alanine-rich protein kinase-like, transcript variant X1
STE20/SPS1-related proline-alanine-rich protein kinase-like isoform X1
ceramide synthase 6-like, 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 4 samples with support for all annotated introns
ceramide synthase 6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
required for excision 1-B domain-containing protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
cytochrome c oxidase assembly protein COX14 homolog
bromodomain adjacent to zinc finger domain protein 2A-like, 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 1 sample with support for all annotated introns
bromodomain adjacent to zinc finger domain protein 2A-like, transcript variant X2
bromodomain adjacent to zinc finger domain protein 2A-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 3 samples with support for all annotated introns
bromodomain adjacent to zinc finger domain protein 2A-like, transcript variant X1
bromodomain adjacent to zinc finger domain protein 2A-like, transcript variant X7
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
bromodomain adjacent to zinc finger domain protein 2A-like, transcript variant X8
bromodomain adjacent to zinc finger domain protein 2A-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
bromodomain adjacent to zinc finger domain protein 2A-like, transcript variant X10
bromodomain adjacent to zinc finger domain protein 2A-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
bromodomain adjacent to zinc finger domain protein 2A-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
bromodomain adjacent to zinc finger domain protein 2A-like isoform X2
bromodomain adjacent to zinc finger domain protein 2A-like isoform X4
bromodomain adjacent to zinc finger domain protein 2A-like isoform X1
bromodomain adjacent to zinc finger domain protein 2A-like isoform X3
nascent polypeptide associated complex subunit alpha, transcript variant X1
nascent polypeptide associated complex subunit alpha, transcript variant X3
nascent polypeptide associated complex subunit alpha, transcript variant X2
nascent polypeptide associated complex subunit alpha, transcript variant X4
nascent polypeptide-associated complex subunit alpha isoform X4
nascent polypeptide-associated complex subunit alpha isoform X3
nascent polypeptide-associated complex subunit alpha isoform X2
nascent polypeptide-associated complex subunit alpha isoform X1
DNA primase subunit 1, transcript variant X2
DNA primase subunit 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
zinc finger protein 148-like, transcript variant X2
zinc finger protein 148-like, transcript variant X1
zinc finger protein 148-like, transcript variant X4
zinc finger protein 148-like, transcript variant X3
transmembrane protein 106C-like, transcript variant X2
transmembrane protein 106C-like isoform X2
transmembrane protein 106C-like, transcript variant X1
transmembrane protein 106C-like isoform X1
collagen alpha-1(II) chain, transcript variant X1
collagen alpha-1(II) chain, transcript variant X2
cytoplasmic dynein 1 intermediate chain 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain 2-like, transcript variant X3
cytoplasmic dynein 1 intermediate chain 2-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 6 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain 2-like isoform X1
cytoplasmic dynein 1 intermediate chain 2-like isoform X3
cytoplasmic dynein 1 intermediate chain 2-like isoform X2
cytoplasmic dynein 1 intermediate chain 2-like isoform X4
POU class 6 homeobox 1, 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 4 samples with support for all annotated introns
POU class 6 homeobox 1, 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 2 samples with support for all annotated introns
POU class 6 homeobox 1, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
POU class 6 homeobox 1, transcript variant X13
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
POU class 6 homeobox 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
POU class 6 homeobox 1, transcript variant X5
POU class 6 homeobox 1, transcript variant X9
POU class 6 homeobox 1, transcript variant X10
POU class 6 homeobox 1, transcript variant X11
POU class 6 homeobox 1, transcript variant X8
POU class 6 homeobox 1, transcript variant X12
POU class 6 homeobox 1, 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 4 samples with support for all annotated introns
POU class 6 homeobox 1, 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
POU class 6 homeobox 1, transcript variant X4
POU domain, class 6, transcription factor 1 isoform X10
POU domain, class 6, transcription factor 1 isoform X11
POU domain, class 6, transcription factor 1 isoform X1
POU domain, class 6, transcription factor 1 isoform X5
POU domain, class 6, transcription factor 1 isoform X7
POU domain, class 6, transcription factor 1 isoform X8
POU domain, class 6, transcription factor 1 isoform X6
POU domain, class 6, transcription factor 1 isoform X4
POU domain, class 6, transcription factor 1 isoform X9
POU domain, class 6, transcription factor 1 isoform X2
POU domain, class 6, transcription factor 1 isoform X3
transcription factor CP2, transcript variant X1
transcription factor CP2, transcript variant X2
transcription factor CP2, transcript variant X3
sialic acid-binding Ig-like lectin 13 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
SWI/SNF complex subunit SMARCC2-like, transcript variant X1
SWI/SNF complex subunit SMARCC2-like, transcript variant X4
SWI/SNF complex subunit SMARCC2-like, transcript variant X5
SWI/SNF complex subunit SMARCC2-like, transcript variant X2
SWI/SNF complex subunit SMARCC2-like, transcript variant X3
SWI/SNF complex subunit SMARCC2-like isoform X1
SWI/SNF complex subunit SMARCC2-like isoform X4
SWI/SNF complex subunit SMARCC2-like isoform X5
SWI/SNF complex subunit SMARCC2-like isoform X2
SWI/SNF complex subunit SMARCC2-like isoform X3
SWI/SNF complex subunit SMARCC2-like, transcript variant X6
SWI/SNF complex subunit SMARCC2-like isoform X6
myosin light polypeptide 6-like, transcript variant X2
myosin light polypeptide 6-like, transcript variant X1
myosin light polypeptide 6-like isoform X1
myosin light polypeptide 6-like isoform X2
histone acetyltransferase type B catalytic subunit
uncharacterized protein LOC571548 homolog
tumor necrosis factor receptor superfamily member 14-like, transcript variant X1
tumor necrosis factor receptor superfamily member 14-like, transcript variant X2
tumor necrosis factor receptor superfamily member 14-like isoform X2
tumor necrosis factor receptor superfamily member 14-like isoform 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 31 samples with support for all annotated introns
vitamin D3 receptor B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
vitamin D3 receptor B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
vitamin D3 receptor B-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
vitamin D3 receptor B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
elongator acetyltransferase complex subunit 5
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
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 31 samples with support for all annotated introns
rho guanine nucleotide exchange factor 25-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
rho guanine nucleotide exchange factor 25-like, transcript variant X3
rho guanine nucleotide exchange factor 25-like isoform X1
rho guanine nucleotide exchange factor 25-like isoform X3
rho guanine nucleotide exchange factor 25-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
rho guanine nucleotide exchange factor 25-like isoform X2
rho guanine nucleotide exchange factor 25-like, transcript variant X4
rho guanine nucleotide exchange factor 25-like isoform X4
Golgi reassembly-stacking protein 2-like
solute carrier family 26 member 10, transcript variant X1
solute carrier family 26 member 10, transcript variant X2
solute carrier family 26 member 10 isoform X2
solute carrier family 26 member 10 isoform X1
cell wall protein IFF6-like, transcript variant X1
cell wall protein IFF6-like, transcript variant X12
cell wall protein IFF6-like, transcript variant X11
cell wall protein IFF6-like, transcript variant X8
cell wall protein IFF6-like, transcript variant X7
cell wall protein IFF6-like, transcript variant X10
cell wall protein IFF6-like, transcript variant X6
cell wall protein IFF6-like, transcript variant X5
cell wall protein IFF6-like, transcript variant X9
uncharacterized protein LOC122543392 isoform X6
cell wall protein IFF6-like, transcript variant X4
uncharacterized protein LOC122543392 isoform X2
cell wall protein IFF6-like, transcript variant X2
cell wall protein IFF6-like, transcript variant X3
beta-1,4 N-acetylgalactosaminyltransferase 1-like
OS9 endoplasmic reticulum lectin, transcript variant X3
OS9 endoplasmic reticulum lectin, transcript variant X2
OS9 endoplasmic reticulum lectin, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
activin receptor type-1B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
activin receptor type-1B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
activin receptor type-1B-like isoform X1
activin receptor type-1B-like isoform X2
general receptor for phosphoinositides 1-associated scaffold protein-like
nuclear receptor subfamily 4 group A member 1-like
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 13 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein A1-like, transcript variant X4
heterogeneous nuclear ribonucleoprotein A1-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein A1-like, transcript variant X5
heterogeneous nuclear ribonucleoprotein A1-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein A1-like, transcript variant X3
heterogeneous nuclear ribonucleoprotein A1-like isoform X2
heterogeneous nuclear ribonucleoprotein A1-like isoform X4
heterogeneous nuclear ribonucleoprotein A1-like isoform X1
heterogeneous nuclear ribonucleoprotein A1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
natural resistance-associated macrophage protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
insulin-like growth factor-binding protein 5
SPRY domain containing 3, transcript variant X1
SPRY domain containing 3, transcript variant X2
SPRY domain-containing protein 3 isoform X1
SPRY domain-containing protein 3 isoform X2
calcitonin gene-related peptide type 1 receptor-like, transcript variant X2
calcitonin gene-related peptide type 1 receptor-like, transcript variant X1
calcitonin gene-related peptide type 1 receptor-like, transcript variant X4
calcitonin gene-related peptide type 1 receptor-like, transcript variant X3
calcitonin gene-related peptide type 1 receptor-like isoform X2
calcitonin gene-related peptide type 1 receptor-like isoform X1
calcitonin gene-related peptide type 1 receptor-like, transcript variant X5
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon GCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ceramide-1-phosphate transfer protein-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 11 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF167-like, transcript variant X5
E3 ubiquitin-protein ligase RNF167-like, transcript variant X2
E3 ubiquitin-protein ligase RNF167-like, transcript variant X1
E3 ubiquitin-protein ligase RNF167-like, transcript variant X4
E3 ubiquitin-protein ligase RNF167-like, transcript variant X3
E3 ubiquitin-protein ligase RNF167-like isoform X1
E3 ubiquitin-protein ligase RNF167-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83% coverage of the annotated genomic feature by RNAseq alignments
polyunsaturated fatty acid lipoxygenase ALOX8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
cysteinyl leukotriene receptor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cysteinyl leukotriene receptor 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
stress-associated endoplasmic reticulum protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84% coverage of the annotated genomic feature by RNAseq alignments