Pieris napi chromosome 18, ilPieNapi1.2, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Papilionoidea; Pieridae; Pierinae; Pieris.
REFSEQ INFORMATION: The reference sequence is identical to\nFR997712.1.\nAssembly name: ilPieNapi1.2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2022/01/30. The original whole-genome shotgun project has the\naccession CAJQFT000000000.2.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Pieris napi Annotation Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: polyA evidence [ECO:0006239]
bromodomain and WD repeat-containing protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
bromodomain and WD repeat-containing protein 3, 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 2 samples with support for all annotated introns
bromodomain and WD repeat-containing protein 3, transcript variant X3
bromodomain and WD repeat-containing protein 3 isoform X2
bromodomain and WD repeat-containing protein 3 isoform X1
bromodomain and WD repeat-containing protein 3 isoform X3
E3 ubiquitin-protein ligase COP1-like, transcript variant X2
E3 ubiquitin-protein ligase COP1-like, transcript variant X1
CLIP domain-containing serine protease HP8-like, transcript variant X1
CLIP domain-containing serine protease HP8-like, transcript variant X2
CLIP domain-containing serine protease HP8-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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 69 samples with support for all annotated introns
pyridoxal phosphate phosphatase PHOSPHO2-like
ovochymase-2-like, transcript variant X2
ovochymase-2-like, transcript variant X1
gastrula zinc finger protein XlCGF49.1-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 147 samples with support for all annotated introns
putative Dol-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-Dol alpha-1,2-glucosyltransferase, transcript variant X2
putative Dol-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-Dol alpha-1,2-glucosyltransferase, transcript variant X1
putative Dol-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-Dol alpha-1,2-glucosyltransferase isoform X1
putative Dol-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-Dol alpha-1,2-glucosyltransferase isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
RNA-binding protein Musashi homolog Rbp6, 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 125 samples with support for all annotated introns
RNA-binding protein Musashi homolog Rbp6 isoform X1
RNA-binding protein Musashi homolog Rbp6, 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 9 samples with support for all annotated introns
RNA-binding protein Musashi homolog Rbp6 isoform X2
probable proline--tRNA ligase, mitochondrial
uncharacterized protein PF3D7_1120000-like, transcript variant X3
uncharacterized protein PF3D7_1120000-like, transcript variant X2
uncharacterized protein PF3D7_1120000-like, transcript variant X1
uncharacterized protein PF3D7_1120000-like isoform X1
zinc finger protein 723-like, transcript variant X2
zinc finger protein 723-like, transcript variant X1
RE1-silencing transcription factor B-like, transcript variant X2
RE1-silencing transcription factor B-like, transcript variant X3
RE1-silencing transcription factor B-like, transcript variant X1
RE1-silencing transcription factor B-like
gamma-interferon-inducible lysosomal thiol reductase-like, transcript variant X2
gamma-interferon-inducible lysosomal thiol reductase-like, transcript variant X1
gamma-interferon-inducible lysosomal thiol reductase-like, transcript variant X3
gamma-interferon-inducible lysosomal thiol reductase-like isoform X1
gamma-interferon-inducible lysosomal thiol reductase-like isoform X2
putative pre-mRNA-splicing factor ATP-dependent RNA helicase PRP1
uncharacterized LOC125058251, 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 62 samples with support for all annotated introns
uncharacterized LOC125058251, 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 43 samples with support for all annotated introns
uncharacterized LOC125058251, 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 84 samples with support for all annotated introns
serine/arginine repetitive matrix protein 1, transcript variant X3
serine/arginine repetitive matrix protein 1, transcript variant X1
serine/arginine repetitive matrix protein 1, transcript variant X2
serine/arginine repetitive matrix protein 1 isoform X2
serine/arginine repetitive matrix protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
protein phosphatase 1 regulatory subunit 3C
serine protease snake-like, transcript variant X2
serine protease snake-like, transcript variant X1
uncharacterized LOC125058183, transcript variant X1
uncharacterized LOC125058183, transcript variant X2
uncharacterized LOC125058181, transcript variant X1
uncharacterized LOC125058181, transcript variant X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
spliceosome-associated protein CWC27 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase epsilon-1-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 2 samples with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase epsilon-1-like, transcript variant X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase epsilon-1-like isoform X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase epsilon-1-like isoform X1
uncharacterized LOC125058561, transcript variant X2
uncharacterized LOC125058561, transcript variant X1
uncharacterized protein LOC125058561 isoform X1
uncharacterized protein LOC125058561 isoform X2
glutamate receptor ionotropic, kainate 2
complex I assembly factor ACAD9, mitochondrial
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
glutamate receptor ionotropic, kainate glr-3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
single-stranded DNA-binding protein 3, 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 145 samples with support for all annotated introns
single-stranded DNA-binding protein 3 isoform X1
single-stranded DNA-binding protein 3, 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 37 samples with support for all annotated introns
single-stranded DNA-binding protein 3 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00545
uncharacterized LOC125058661, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125058661, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC125058661 isoform X1
uncharacterized protein LOC125058661 isoform X2
zinc finger protein 614-like, transcript variant X1
zinc finger protein 614-like, transcript variant X2
DNA/RNA-binding protein KIN17, transcript variant X2
DNA/RNA-binding protein KIN17, transcript variant X1
DNA/RNA-binding protein KIN17 isoform X2
DNA/RNA-binding protein KIN17 isoform 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 98 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
poly [ADP-ribose] polymerase tankyrase, transcript variant X2
poly [ADP-ribose] polymerase tankyrase, transcript variant X1
poly [ADP-ribose] polymerase tankyrase isoform X2
poly [ADP-ribose] polymerase tankyrase isoform X1
serine/threonine-protein kinase 10, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
serine/threonine-protein kinase 10, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 54 samples with support for all annotated introns
serine/threonine-protein kinase 10, transcript variant X3
serine/threonine-protein kinase 10 isoform X3
serine/threonine-protein kinase 10 isoform X1
serine/threonine-protein kinase 10 isoform X2
interleukin enhancer-binding factor 2 homolog
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
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 169 samples with support for all annotated introns
putative U5 small nuclear ribonucleoprotein 200 kDa helicase
mediator of RNA polymerase II transcription subunit 28
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: 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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
uncharacterized protein DDB_G0286299-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 12 samples with support for all annotated introns
dipeptidyl peptidase 9, transcript variant X1
dipeptidyl peptidase 9, transcript variant X2
ferritin, chloroplastic, transcript variant X1
ferritin, chloroplastic, transcript variant X2
luciferin 4-monooxygenase-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 11 samples with support for all annotated introns
luciferin 4-monooxygenase-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 47 samples with support for all annotated introns
gastrula zinc finger protein XlCGF26.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA serine (anticodon CGA); 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, and 100% coverage of the annotated genomic feature by RNAseq alignments
gastrula zinc finger protein XlCGF26.1-like, transcript variant X4
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 60 samples with support for all annotated introns
gastrula zinc finger protein XlCGF26.1-like, 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 41 samples with support for all annotated introns
gastrula zinc finger protein XlCGF26.1-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 26 samples with support for all annotated introns
transcriptional repressor CTCF-like isoform X9
gastrula zinc finger protein XlCGF26.1-like, transcript variant X3
gastrula zinc finger protein XlCGF26.1-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 56 samples with support for all annotated introns
gastrula zinc finger protein XlCGF26.1-like, 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 140 samples with support for all annotated introns
gastrula zinc finger protein XlCGF26.1-like isoform X7
gastrula zinc finger protein XlCGF26.1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
gastrula zinc finger protein XlCGF26.1-like, transcript variant X8
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 75 samples with support for all annotated introns
gastrula zinc finger protein XlCGF26.1-like, transcript variant X5
gastrula zinc finger protein XlCGF26.1-like, transcript variant X11
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
uncharacterized protein LOC125058745 isoform X11
gastrula zinc finger protein XlCGF26.1-like, transcript variant X10
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 128 samples with support for all annotated introns
zinc finger protein 888-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 9 samples with support for all annotated introns
zinc finger protein 888-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 97 samples with support for all annotated introns
PR domain zinc finger protein 5-like, transcript variant X1
PR domain zinc finger protein 5-like isoform X1
PR domain zinc finger protein 5-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 29 samples with support for all annotated introns
uncharacterized protein LOC125058747 isoform 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 162 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 80 samples with support for all annotated introns
gastrula zinc finger protein XlCGF26.1-like 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
eukaryotic peptide chain release factor subunit 1, transcript variant X2
eukaryotic peptide chain release factor subunit 1 isoform X2
eukaryotic peptide chain release factor subunit 1, transcript variant X1
eukaryotic peptide chain release factor subunit 1 isoform X1
uncharacterized LOC125058608, transcript variant X1
uncharacterized LOC125058608, transcript variant X3
uncharacterized LOC125058608, transcript variant X4
uncharacterized LOC125058608, transcript variant X2
piggyBac transposable element-derived protein 4-like
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 119 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 2 samples with support for all annotated introns
putative nuclease HARBI1, transcript variant X2
putative nuclease HARBI1, transcript variant X1
uncharacterized protein LOC125058919 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 1 Protein, 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 74 samples with support for all annotated introns
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
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-like, transcript variant X1
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-like, transcript variant X2
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 107 samples with support for all annotated introns
protein ALP1-like, transcript variant X2
protein ALP1-like, transcript variant X1
uncharacterized protein LOC125058451 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 74 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
uncharacterized protein LOC125058452 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 161 samples with support for all annotated introns
uncharacterized LOC125058648, transcript variant X2
uncharacterized LOC125058648, transcript variant X1
dihydrolipoyllysine-residue succinyltransferase component of 2-oxoglutarate dehydrogenase complex, mitochondrial-like, transcript variant X2
dihydrolipoyllysine-residue succinyltransferase component of 2-oxoglutarate dehydrogenase complex, mitochondrial-like, transcript variant X1
dihydrolipoyllysine-residue succinyltransferase component of 2-oxoglutarate dehydrogenase complex, mitochondrial-like
uncharacterized LOC125058326, 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 41 samples with support for all annotated introns
uncharacterized LOC125058326, 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 76 samples with support for all annotated introns
uncharacterized LOC125058326, 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 22 samples with support for all annotated introns
uncharacterized protein LOC125058326 isoform X2
uncharacterized protein LOC125058326 isoform X1
uncharacterized protein LOC125058326 isoform X3
zinc finger protein OZF-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 13 samples with support for all annotated introns
zinc finger protein OZF-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 153 samples with support for all annotated introns
H/ACA ribonucleoprotein complex subunit 4
DNA-directed RNA polymerases I, II, and III subunit RPABC3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
EP300-interacting inhibitor of differentiation 3-like
coiled-coil domain-containing protein 186, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
coiled-coil domain-containing protein 186, 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 31 samples with support for all annotated introns
coiled-coil domain-containing protein 186, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
coiled-coil domain-containing protein 186, 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 32 samples with support for all annotated introns
coiled-coil domain-containing protein 186, 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 69 samples with support for all annotated introns
coiled-coil domain-containing protein 186 isoform X5
coiled-coil domain-containing protein 186 isoform X4
coiled-coil domain-containing protein 186 isoform X3
coiled-coil domain-containing protein 186 isoform X1
coiled-coil domain-containing protein 186 isoform X2
peptidyl-prolyl cis-trans isomerase E-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin-associated domain-containing protein 1
uncharacterized LOC125058462, transcript variant X2
uncharacterized LOC125058462, transcript variant X1
uncharacterized LOC125058462, transcript variant X3
uncharacterized protein LOC125058462 isoform X2
uncharacterized protein LOC125058462 isoform X1
uncharacterized protein LOC125058462 isoform X3
transcription initiation factor TFIID subunit 10-like, transcript variant X3
transcription initiation factor TFIID subunit 10-like, transcript variant X1
transcription initiation factor TFIID subunit 10-like, transcript variant X2
transcription initiation factor TFIID subunit 10-like
phosphate carrier protein, mitochondrial-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 9 samples with support for all annotated introns
uncharacterized LOC125058486, 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 77 samples with support for all annotated introns
uncharacterized LOC125058486, 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 121 samples with support for all annotated introns
uncharacterized LOC125058473, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
uncharacterized LOC125058473, transcript variant X2
uncharacterized LOC125058473, 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 8 samples with support for all annotated introns
uncharacterized LOC125058473, 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 11 samples with support for all annotated introns
uncharacterized LOC125058473, transcript variant X5
uncharacterized protein LOC125058473 isoform X1
uncharacterized protein LOC125058473 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 64 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 18 samples with support for all annotated introns
phenoloxidase-activating factor 2-like, transcript variant X3
phenoloxidase-activating factor 2-like isoform X3
phenoloxidase-activating factor 2-like, transcript variant X2
phenoloxidase-activating factor 2-like, transcript variant X1
phenoloxidase-activating factor 2-like isoform X1
phenoloxidase-activating factor 2-like 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 21 samples with support for all annotated introns
phenoloxidase-activating factor 2-like, transcript variant X4
phenoloxidase-activating factor 2-like, 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 45 samples with support for all annotated introns
phenoloxidase-activating factor 2-like isoform X4
phenoloxidase-activating factor 2-like isoform X6
phenoloxidase-activating factor 2-like, transcript variant X5
phenoloxidase-activating factor 2-like isoform X5
uncharacterized LOC125058310, transcript variant X2
uncharacterized LOC125058310, transcript variant X1
uncharacterized protein LOC125058310 isoform X2
uncharacterized protein LOC125058310 isoform X1
uncharacterized protein DDB_G0290685-like
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 105 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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
ATP-citrate synthase, transcript variant X1
ATP-citrate synthase, 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 81 samples with support for all annotated introns
zinc finger protein 728-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 99 samples with support for all annotated introns
zinc finger protein 728-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 107 samples with support for all annotated introns
zinc finger protein 728-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 14 samples with support for all annotated introns
uncharacterized protein LOC125058293 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 652-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 93 samples with support for all annotated introns
zinc finger protein 652-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 140 samples with support for all annotated introns
zinc finger protein interacting with ribonucleoprotein K-like isoform X2
zinc finger protein 652-like, transcript variant X4
zinc finger protein 652-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 83 samples with support for all annotated introns
zinc finger protein 652-B-like isoform X5
zinc finger protein 652-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 149 samples with support for all annotated introns
uncharacterized serine-rich protein C215.13-like
uncharacterized LOC125058392, transcript variant X2
uncharacterized protein LOC125058392 isoform X2
uncharacterized LOC125058392, transcript variant X1
uncharacterized protein LOC125058392 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 62 samples with support for all annotated introns
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-like isoform X2
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-like isoform X1
uncharacterized LOC125058404, transcript variant X2
uncharacterized LOC125058404, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 62 samples with support for all annotated introns
myosin tail region-interacting protein MTI1-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 47 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 165 samples with support for all annotated introns
uncharacterized LOC125058411, transcript variant X1
uncharacterized LOC125058411, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 31 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 82 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 63 samples with support for all annotated introns
piggyBac transposable element-derived protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
piggyBac transposable element-derived protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76% coverage of the annotated genomic feature by RNAseq alignments
gastrula zinc finger protein XlCGF8.2DB-like
zinc finger protein 729-like, transcript variant X9
zinc finger protein 729-like, transcript variant X8
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 69 samples with support for all annotated introns
zinc finger protein 729-like, 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 25 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 41-like isoform X5
zinc finger protein 729-like, transcript variant X4
zinc finger protein 729-like, 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 66 samples with support for all annotated introns
zinc finger protein 729-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 8 samples with support for all annotated introns
zinc finger protein 729-like, transcript variant X1
zinc finger protein 729-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 33 samples with support for all annotated introns
zinc finger protein 729-like, transcript variant X7
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 48 samples with support for all annotated introns
uncharacterized LOC125058406, transcript variant X1
uncharacterized LOC125058406, transcript variant X2
uncharacterized LOC125058366, 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 46 samples with support for all annotated introns
uncharacterized LOC125058366, 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 126 samples with support for all annotated introns
uncharacterized protein LOC125058366 isoform X2
uncharacterized protein LOC125058366 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 31 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 104 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
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% 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 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: putative nuclease HARBI1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 73% coverage of the annotated genomic feature by RNAseq alignments
golgin subfamily A member 6-like protein 7
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 116 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 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 130 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 49 samples with support for all annotated introns
F-box/WD repeat-containing protein 11, 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 150 samples with support for all annotated introns
F-box/WD repeat-containing protein 11, 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 149 samples with support for all annotated introns
F-box/WD repeat-containing protein 11 isoform X1
F-box/WD repeat-containing protein 11 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, including 13 samples with support for all annotated introns
uncharacterized LOC125058729, transcript variant X1
uncharacterized LOC125058729, 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 105 samples with support for all annotated introns
uncharacterized LOC125058830, transcript variant X2
uncharacterized LOC125058830, transcript variant X1
uncharacterized LOC125058461, transcript variant X1
uncharacterized LOC125058461, 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 127 samples with support for all annotated introns
cytochrome c oxidase assembly factor 4 homolog, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 52 samples with support for all annotated introns
methyltransferase-like protein 17, mitochondrial
translocon-associated protein subunit delta
LIM domain-binding protein 2, transcript variant X2
LIM domain-binding protein 2, transcript variant X1
LIM domain-binding protein 2, transcript variant X4
LIM domain-binding protein 2, transcript variant X5
LIM domain-binding protein 2, transcript variant X3
LIM domain-binding protein 2, transcript variant X7
LIM domain-binding protein 2, transcript variant X6
LIM domain-binding protein 2, 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 7 samples with support for all annotated introns
uncharacterized LOC125058826, 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 5 samples with support for all annotated introns
uncharacterized LOC125058826, 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 5 samples with support for all annotated introns
uncharacterized LOC125058826, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC125058826 isoform X2
uncharacterized protein LOC125058826 isoform 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 43 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 95 samples with support for all annotated introns
conserved oligomeric Golgi complex subunit 7, transcript variant X2
conserved oligomeric Golgi complex subunit 7, transcript variant X1
conserved oligomeric Golgi complex subunit 7 isoform X2
conserved oligomeric Golgi complex subunit 7 isoform X1
uncharacterized LOC125058614, transcript variant X2
uncharacterized LOC125058614, 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 67 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 168 samples with support for all annotated introns
apical junction molecule, transcript variant X8
apical junction molecule, transcript variant X1
apical junction molecule, transcript variant X3
apical junction molecule, 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 38 samples with support for all annotated introns
apical junction molecule, 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 54 samples with support for all annotated introns
apical junction molecule, transcript variant X6
apical junction molecule, 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 58 samples with support for all annotated introns
apical junction molecule, transcript variant X2
CAP-Gly domain-containing linker protein 1 isoform X1
CAP-Gly domain-containing linker protein 1 isoform X2
CAP-Gly domain-containing linker protein 1 isoform X3
UDP-glucosyltransferase 2-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 17 samples with support for all annotated introns
UDP-glucosyltransferase 2-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 54 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 108 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
UDP-glucosyltransferase 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
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
39S ribosomal protein L43, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 169 samples with support for all annotated introns
cilia- and flagella-associated protein 91-like
uncharacterized LOC125058273, 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 76 samples with support for all annotated introns
uncharacterized LOC125058273, 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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 169 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 97% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin ligase BIG BROTHER-related-like
zinc finger protein 423-like, transcript variant X2
zinc finger protein 423-like, transcript variant X3
zinc finger protein 423-like, transcript variant X1
thioredoxin-related transmembrane protein 2 homolog
uncharacterized LOC125058782, transcript variant X1
uncharacterized LOC125058782, 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 129 samples with support for all annotated introns
uncharacterized LOC125058783, transcript variant X1
uncharacterized LOC125058783, transcript variant X2
uncharacterized LOC125058261, transcript variant X2
uncharacterized protein LOC125058261 isoform X2
uncharacterized LOC125058261, transcript variant X1
uncharacterized LOC125058261, transcript variant X3
uncharacterized LOC125058261, transcript variant X5
uncharacterized LOC125058261, transcript variant X6
uncharacterized protein LOC125058261 isoform X1
uncharacterized protein LOC125058261 isoform X3
uncharacterized protein LOC125058261 isoform X5
uncharacterized protein LOC125058261 isoform X6
uncharacterized LOC125058261, transcript variant X4
uncharacterized protein LOC125058261 isoform X4
uncharacterized LOC125058261, transcript variant X7
uncharacterized protein LOC125058261 isoform X7
uncharacterized LOC125058926, transcript variant X2
uncharacterized LOC125058926, transcript variant X3
uncharacterized LOC125058926, transcript variant X1
uncharacterized protein LOC125058926 isoform X2
uncharacterized protein LOC125058926 isoform X1
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transmembrane emp24 domain-containing protein 5-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 93 samples with support for all annotated introns
transmembrane emp24 domain-containing protein 5-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
transmembrane emp24 domain-containing protein 5-like, transcript variant X1
transmembrane emp24 domain-containing protein 5-like, transcript variant X2
transmembrane emp24 domain-containing protein 5-like
double-stranded RNA-specific editase Adar, transcript variant X1
double-stranded RNA-specific editase Adar, transcript variant X2
double-stranded RNA-specific editase Adar, transcript variant X3
double-stranded RNA-specific editase Adar isoform X1
double-stranded RNA-specific editase Adar isoform X2
double-stranded RNA-specific editase Adar isoform X3
pancreatic lipase-related protein 2-like, 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 8 samples with support for all annotated introns
pancreatic lipase-related protein 2-like, transcript variant X2
pancreatic lipase-related protein 2-like isoform X2
pancreatic lipase-related protein 2-like isoform X1
GDP-fucose protein O-fucosyltransferase 2
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
aldo-keto reductase family 1 member B1-like, transcript variant X2
aldo-keto reductase family 1 member B1-like isoform X2
aldo-keto reductase family 1 member B1-like, transcript variant X1
aldo-keto reductase family 1 member B1-like isoform X1
glycerol-3-phosphate acyltransferase 3, 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 133 samples with support for all annotated introns
glycerol-3-phosphate acyltransferase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
glycerol-3-phosphate acyltransferase 3 isoform X1
glycerol-3-phosphate acyltransferase 3 isoform X2
gastrula zinc finger protein XlCGF67.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 122 samples with support for all annotated introns
zinc finger protein 62 homolog, transcript variant X5
zinc finger protein 62 homolog, 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 19 samples with support for all annotated introns
zinc finger protein 62 homolog, transcript variant X3
zinc finger protein 62 homolog, transcript variant X1
zinc finger protein 62 homolog, transcript variant X4
zinc finger protein 62 homolog, transcript variant X7
zinc finger protein 62 homolog isoform X4
zinc finger protein 62 homolog, transcript variant X2
spectrin beta chain, non-erythrocytic 1, transcript variant X5
spectrin beta chain, non-erythrocytic 1, transcript variant X7
spectrin beta chain, non-erythrocytic 1, transcript variant X2
spectrin beta chain, non-erythrocytic 1, transcript variant X3
spectrin beta chain, non-erythrocytic 1, transcript variant X6
spectrin beta chain, non-erythrocytic 1, transcript variant X4
spectrin beta chain, non-erythrocytic 1, transcript variant X1
spectrin beta chain, non-erythrocytic 1 isoform X6
spectrin beta chain, non-erythrocytic 1 isoform X2
spectrin beta chain, non-erythrocytic 1 isoform X5
spectrin beta chain, non-erythrocytic 1 isoform X3
spectrin beta chain, non-erythrocytic 1 isoform X1
spectrin beta chain, non-erythrocytic 1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat serine/threonine-protein kinase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125058565, transcript variant X3
uncharacterized LOC125058565, transcript variant X2
uncharacterized LOC125058565, transcript variant X1
uncharacterized protein LOC125058565 isoform X3
uncharacterized protein LOC125058565 isoform X2
uncharacterized protein LOC125058565 isoform 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 74 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 96% coverage of the annotated genomic feature by RNAseq alignments
protein hu-li tai shao, transcript variant X2
protein hu-li tai shao, transcript variant X3
protein hu-li tai shao, transcript variant X1
protein hu-li tai shao, transcript variant X6
protein hu-li tai shao, transcript variant X5
protein hu-li tai shao, 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
uncharacterized LOC125058636, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC125058636, 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 32 samples with support for all annotated introns
uncharacterized LOC125058636, 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 62 samples with support for all annotated introns
uncharacterized protein LOC125058636 isoform X2
uncharacterized protein LOC125058636 isoform X1
AT-rich interactive domain-containing protein 5B-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 108 samples with support for all annotated introns
AT-rich interactive domain-containing protein 5B-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 47 samples with support for all annotated introns
AT-rich interactive domain-containing protein 5B-like isoform X1
AT-rich interactive domain-containing protein 5B-like isoform X2
U4/U6 small nuclear ribonucleoprotein Prp3
probable serine/threonine-protein kinase clkA, transcript variant X2
probable serine/threonine-protein kinase clkA, transcript variant X3
probable serine/threonine-protein kinase clkA, 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 167 samples with support for all annotated introns
GATA zinc finger domain-containing protein 14-like isoform X2
probable serine/threonine-protein kinase clkA isoform X3
GATA zinc finger domain-containing protein 14-like isoform X1
U4/U6 small nuclear ribonucleoprotein Prp4
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
segment polarity protein dishevelled homolog DVL-3
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 79 samples with support for all annotated introns
3-oxoacyl-[acyl-carrier-protein] reductase FabG-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
uncharacterized LOC125058646, 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 152 samples with support for all annotated introns
uncharacterized LOC125058646, 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
uncharacterized LOC125058812, transcript variant X1
uncharacterized LOC125058812, transcript variant X3
uncharacterized LOC125058812, transcript variant X2
uncharacterized protein LOC125058812 isoform X3
uncharacterized protein LOC125058812 isoform X2
uncharacterized protein LOC125058812 isoform X1
cytoplasmic dynein 2 intermediate chain 2-like
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 18 samples with support for all annotated introns
basic salivary proline-rich protein 2-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 167 samples with support for all annotated introns
transcription elongation regulator 1-like
uncharacterized LOC125058817, transcript variant X1
uncharacterized protein LOC125058817 isoform X1
uncharacterized LOC125058817, transcript variant X2
uncharacterized protein LOC125058817 isoform X2
glutenin, high molecular weight subunit 12-like
aldo-keto reductase family 1 member B1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 166 samples with support for all annotated introns
uncharacterized LOC125058836, transcript variant X1
uncharacterized LOC125058836, transcript variant X2
uncharacterized LOC125058836, transcript variant X3
protein neuralized, transcript variant X3
protein neuralized, transcript variant X2
protein neuralized, transcript variant X1
glycerophosphodiester phosphodiesterase 1, transcript variant X1
glycerophosphodiester phosphodiesterase 1, transcript variant X4
glycerophosphodiester phosphodiesterase 1 isoform X1
glycerophosphodiester phosphodiesterase 1 isoform X4
glycerophosphodiester phosphodiesterase 1, transcript variant X2
glycerophosphodiester phosphodiesterase 1 isoform X2
glycerophosphodiester phosphodiesterase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glycerophosphodiester phosphodiesterase 1 isoform X3
kinesin-like protein KIF18A, transcript variant X3
uncharacterized protein LOC125058198 isoform X2
kinesin-like protein KIF18A, transcript variant X2
kinesin-like protein KIF18A, 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 37 samples with support for all annotated introns
uncharacterized LOC125058190, transcript variant X6
uncharacterized LOC125058190, transcript variant X5
uncharacterized LOC125058190, transcript variant X3
uncharacterized LOC125058190, transcript variant X4
uncharacterized LOC125058190, transcript variant X7
uncharacterized protein LOC125058190 isoform X4
uncharacterized protein LOC125058190 isoform X3
uncharacterized LOC125058190, transcript variant X8
uncharacterized LOC125058190, transcript variant X10
uncharacterized protein LOC125058190 isoform X5
uncharacterized protein LOC125058190 isoform X7
uncharacterized LOC125058190, 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 99 samples with support for all annotated introns
uncharacterized LOC125058190, transcript variant X11
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 108 samples with support for all annotated introns
uncharacterized protein LOC125058190 isoform X6
uncharacterized protein LOC125058190 isoform X8
uncharacterized LOC125058190, transcript variant X1
uncharacterized LOC125058190, transcript variant X2
uncharacterized protein LOC125058190 isoform X2
uncharacterized protein LOC125058190 isoform X1
uncharacterized LOC125058228, transcript variant X3
uncharacterized LOC125058228, transcript variant X2
uncharacterized LOC125058228, transcript variant X1
uncharacterized LOC125058213, transcript variant X2
uncharacterized LOC125058213, transcript variant X1
myb/SANT-like DNA-binding domain-containing protein 3, transcript variant X1
myb/SANT-like DNA-binding domain-containing protein 3, transcript variant X2
myb/SANT-like DNA-binding domain-containing protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 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: 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 91 samples with support for all annotated introns
uncharacterized LOC125058230, transcript variant X2
uncharacterized LOC125058230, transcript variant X1
protein ANTAGONIST OF LIKE HETEROCHROMATIN 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 73 samples with support for all annotated introns
uncharacterized LOC125058229, transcript variant X1
uncharacterized LOC125058229, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 91 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
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
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: signaling mucin MSB2-like
uncharacterized protein LOC125058210 isoform X2
zinc finger BED domain-containing protein 4-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 26 samples with support for all annotated introns
uncharacterized LOC125058233, transcript variant X1
uncharacterized LOC125058233, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 33% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% 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: 1 Protein, and 35% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125058247, transcript variant X2
uncharacterized LOC125058247, 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 94 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 39 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 22 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 96% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC125058187
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: 2 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC125058895
uncharacterized LOC125058787, transcript variant X1
uncharacterized LOC125058787, 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 44 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 114 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 168 samples with support for all annotated introns
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
tetratricopeptide repeat protein 1, transcript variant X3
tetratricopeptide repeat protein 1, transcript variant X4
tetratricopeptide repeat protein 1, transcript variant X2
tetratricopeptide repeat protein 1, transcript variant X1
tetratricopeptide repeat protein 1 isoform X1
tetratricopeptide repeat protein 1 isoform X2
tetratricopeptide repeat protein 1 isoform X3
tetratricopeptide repeat protein 1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
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 45% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125058252, transcript variant X2
uncharacterized LOC125058252, 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 58 samples with support for all annotated introns
uncharacterized protein LOC125058252 isoform X2
uncharacterized protein LOC125058252 isoform X1
chymotrypsin-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
chymotrypsin-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 88 samples with support for all annotated introns
uncharacterized LOC125058744, transcript variant X1
uncharacterized LOC125058744, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized protein LOC125058567 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 75 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 97% coverage of the annotated genomic feature by RNAseq alignments, including 62 samples with support for all annotated introns
uncharacterized LOC125058548, 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 97 samples with support for all annotated introns
uncharacterized LOC125058548, transcript variant X2
uncharacterized LOC125058547, transcript variant X1
uncharacterized LOC125058547, transcript variant X2
uncharacterized LOC125058575, transcript variant X2
uncharacterized LOC125058575, 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 10 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 10 samples with support for all annotated introns
uncharacterized protein LOC125058577 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 59 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
modular serine protease-like, transcript variant X2
modular serine protease-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 159 samples with support for all annotated introns
BRCA1-associated RING domain protein 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 153 samples with support for all annotated introns
probable small nuclear ribonucleoprotein Sm D1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
eukaryotic translation initiation factor eIF1
dynactin subunit 1, transcript variant X1
dynactin subunit 1, transcript variant X2
dynactin subunit 1, transcript variant X5
dynactin subunit 1, transcript variant X3
dynactin subunit 1, transcript variant X4
dynactin subunit 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 5 samples with support for all annotated introns
serine hydrolase-like protein, transcript variant X2
serine hydrolase-like protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
serine hydrolase-like protein, transcript variant X1
serine hydrolase-like protein isoform X1
serine hydrolase-like protein isoform X2
serine hydrolase-like protein isoform X3
serine hydrolase-like protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
serine hydrolase-like protein 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 116 samples with support for all annotated introns
serine hydrolase-like protein 2 isoform X2
serine hydrolase-like protein 2 isoform 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 169 samples with support for all annotated introns
pantothenate kinase 3, transcript variant X3
pantothenate kinase 3, transcript variant X2
pantothenate kinase 3, transcript variant X1
charged multivesicular body protein 7, 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 39 samples with support for all annotated introns
charged multivesicular body protein 7, 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 59 samples with support for all annotated introns
charged multivesicular body protein 7, 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 58 samples with support for all annotated introns
charged multivesicular body protein 7 isoform X1
charged multivesicular body protein 7 isoform X2
charged multivesicular body protein 7 isoform X3
endocuticle structural glycoprotein SgAbd-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
uncharacterized LOC125058743, transcript variant X2
uncharacterized LOC125058743, 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 38 samples with support for all annotated introns
uncharacterized LOC125058318, transcript variant X1
uncharacterized LOC125058318, transcript variant X2
uncharacterized protein LOC125058318 isoform X2
uncharacterized protein LOC125058318 isoform X1
MATH and LRR domain-containing protein PFE0570w-like
uncharacterized LOC125058564, transcript variant X2
uncharacterized LOC125058564, transcript variant X1
uncharacterized protein LOC125058564 isoform X2
uncharacterized protein LOC125058564 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125058655, transcript variant X1
uncharacterized LOC125058655, transcript variant X2
uncharacterized protein LOC125058656 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
uncharacterized LOC125058829, 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 41 samples with support for all annotated introns
uncharacterized LOC125058829, transcript variant X1
putative nuclease HARBI1, 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 52 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 78 samples with support for all annotated introns
myb/SANT-like DNA-binding domain-containing protein 3 isoform X2
myb/SANT-like DNA-binding domain-containing protein 3 isoform 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 82% coverage of the annotated genomic feature by RNAseq alignments
hepatitis A virus cellular receptor 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125058832, transcript variant X2
uncharacterized LOC125058832, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF02543
COORDINATES: nucleotide motif:Rfam:12.0:RF01960
COORDINATES: nucleotide motif:Rfam:12.0:RF00002
uncharacterized LOC125058776, transcript variant X2
uncharacterized LOC125058776, transcript variant X4
uncharacterized LOC125058776, transcript variant X3
uncharacterized LOC125058776, transcript variant X1
uncharacterized LOC125058673, transcript variant X1
uncharacterized protein LOC125058673 isoform X1
uncharacterized LOC125058673, transcript variant X2
facilitated trehalose transporter Tret1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized protein LOC125058673 isoform X2
serine/threonine-protein kinase VRK1-like
voltage-gated potassium channel subunit beta-2-like, transcript variant X1
voltage-gated potassium channel subunit beta-2-like, transcript variant X2
voltage-gated potassium channel subunit beta-2-like, transcript variant X4
voltage-gated potassium channel subunit beta-2-like, transcript variant X3
voltage-gated potassium channel subunit beta-2-like, 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 25 samples with support for all annotated introns
voltage-gated potassium channel subunit beta-2-like isoform X1
voltage-gated potassium channel subunit beta-2-like isoform X2
voltage-gated potassium channel subunit beta-2-like isoform X3
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 12 bases at 12 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized LOC125058705, transcript variant X1
uncharacterized LOC125058705, transcript variant X2
NADH-ubiquinone oxidoreductase chain 5-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 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: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: NADH-ubiquinone oxidoreductase chain 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 138 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 125 samples with support for all annotated introns
28S ribosomal protein S31, mitochondrial-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 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; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: 28S ribosomal protein S31, mitochondrial-like
tumor necrosis factor ligand superfamily member 13-like, transcript variant X1
tumor necrosis factor ligand superfamily member 13-like, transcript variant X2
tumor necrosis factor ligand superfamily member 13-like, transcript variant X8
uncharacterized protein LOC125058687 isoform X2
uncharacterized protein LOC125058687 isoform X1
tumor necrosis factor ligand superfamily member 13-like isoform X5
tumor necrosis factor ligand superfamily member 13-like, 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 34 samples with support for all annotated introns
tumor necrosis factor ligand superfamily member 13-like, 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 37 samples with support for all annotated introns
uncharacterized protein LOC125058687 isoform X4
uncharacterized protein LOC125058687 isoform X3
uncharacterized LOC125058710, transcript variant X2
uncharacterized LOC125058710, transcript variant X1
uncharacterized LOC125058710, transcript variant X3
uncharacterized protein LOC125058710 isoform X1
uncharacterized protein LOC125058710 isoform X2
transmembrane emp24 domain-containing protein 3-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transmembrane emp24 domain-containing protein 3-like
tumor necrosis factor ligand superfamily member 13-like, transcript variant X7
tumor necrosis factor ligand superfamily member 13-like, transcript variant X3
tumor necrosis factor ligand superfamily member 13-like, transcript variant X4
transmembrane and coiled-coil domains protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125058679, transcript variant X2
uncharacterized LOC125058679, transcript variant X1
uncharacterized LOC125058679, transcript variant X3
uncharacterized protein LOC125058679 isoform X2
uncharacterized protein LOC125058679 isoform X1
uncharacterized protein LOC125058679 isoform X3
uncharacterized LOC125058690, transcript variant X3
uncharacterized LOC125058690, 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 15 samples with support for all annotated introns
uncharacterized LOC125058690, transcript variant X1
uncharacterized LOC125058690, transcript variant X2
uncharacterized LOC125058690, transcript variant X5
uncharacterized LOC125058690, 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 16 samples with support for all annotated introns
uncharacterized LOC125058690, 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 29 samples with support for all annotated introns
uncharacterized protein LOC125058690 isoform X1
uncharacterized protein LOC125058690 isoform X2
uncharacterized protein LOC125058690 isoform X6
uncharacterized protein LOC125058690 isoform X7
uncharacterized protein LOC125058690 isoform X3
uncharacterized protein LOC125058690 isoform X4
uncharacterized protein LOC125058690 isoform X5
uncharacterized protein K02A2.6-like, transcript variant X4
uncharacterized protein K02A2.6-like, transcript variant X1
uncharacterized protein K02A2.6-like, transcript variant X2
uncharacterized protein K02A2.6-like isoform X1
uncharacterized protein K02A2.6-like isoform X2
uncharacterized protein LOC125058675 isoform X4
uncharacterized protein K02A2.6-like, transcript variant X3
uncharacterized protein K02A2.6-like isoform X3
uncharacterized LOC125058717, transcript variant X3
uncharacterized LOC125058717, transcript variant X2
uncharacterized LOC125058717, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 53% coverage of the annotated genomic feature by RNAseq alignments
glucose-6-phosphatase 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, including 18 samples with support for all annotated introns
glucose-6-phosphatase 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 25 samples with support for all annotated introns
glucose-6-phosphatase 2-like, transcript variant X3
glucose-6-phosphatase catalytic subunit 1-like isoform X3
voltage-gated potassium channel subunit beta-2-like
uncharacterized LOC125058802, transcript variant X5
uncharacterized LOC125058802, transcript variant X8
uncharacterized LOC125058802, transcript variant X3
uncharacterized LOC125058802, transcript variant X7
uncharacterized LOC125058802, transcript variant X4
uncharacterized LOC125058802, transcript variant X2
uncharacterized LOC125058802, transcript variant X6
uncharacterized LOC125058802, transcript variant X9
uncharacterized LOC125058802, transcript variant X1
uncharacterized LOC125058803, transcript variant X2
uncharacterized LOC125058803, transcript variant X1
uncharacterized LOC125058804, transcript variant X2
uncharacterized LOC125058804, 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