Diprion similis isolate iyDipSimi1 chromosome 9, iyDipSimi1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Hymenoptera; Tenthredinoidea; Diprionidae; Diprioninae; Diprion.
REFSEQ INFORMATION: The reference sequence is identical to\nCM037727.1.\nAssembly name: iyDipSimi1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the United States Department of\nAgriculture on 2021/12/10. The original whole-genome shotgun\nproject has the accession JAJNQI000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: United States Department of Agriculture\nAssembly Date :: 17-NOV-2021\nAssembly Method :: HiFiASM v. 0.16.1-r375; Juicebox Assembly\n Toolkit v. 1.11\nAssembly Name :: iyDipSimi1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 100.0x\nSequencing Technology :: PacBio Sequel; Illumina NovaSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Diprion similis Annotation Release\n 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##
Catherine Linnen, University of Kentucky
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 8 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
mediator of DNA damage checkpoint protein 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 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 55% 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 4% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
small ubiquitin-related modifier-like, transcript variant X1
small ubiquitin-related modifier-like, transcript variant X2
small ubiquitin-related modifier-like isoform X1
small ubiquitin-related modifier-like isoform X2
E3 ubiquitin-protein ligase Ubr3, transcript variant X2
E3 ubiquitin-protein ligase Ubr3, transcript variant X1
E3 ubiquitin-protein ligase Ubr3 isoform X2
E3 ubiquitin-protein ligase Ubr3 isoform X1
uncharacterized LOC124410410, transcript variant X1
uncharacterized protein LOC124410410 isoform X1
uncharacterized LOC124410410, transcript variant X4
uncharacterized LOC124410410, transcript variant X3
uncharacterized LOC124410410, transcript variant X2
uncharacterized LOC124410410, transcript variant X5
uncharacterized protein LOC124410410 isoform X2
uncharacterized protein LOC124410410 isoform X3
DNA topoisomerase 2, transcript variant X1
DNA topoisomerase 2, transcript variant X2
DNA topoisomerase 2, transcript variant X4
DNA topoisomerase 2, transcript variant X3
serine/threonine-protein kinase tousled-like 2, transcript variant X3
serine/threonine-protein kinase tousled-like 2, transcript variant X2
serine/threonine-protein kinase tousled-like 2, transcript variant X1
serine/threonine-protein kinase tousled-like 2, transcript variant X10
serine/threonine-protein kinase tousled-like 2, transcript variant X7
serine/threonine-protein kinase tousled-like 2, transcript variant X5
serine/threonine-protein kinase tousled-like 2, transcript variant X4
serine/threonine-protein kinase tousled-like 2, transcript variant X9
serine/threonine-protein kinase tousled-like 2, transcript variant X8
serine/threonine-protein kinase tousled-like 2, transcript variant X6
serine/threonine-protein kinase tousled-like 2 isoform X2
serine/threonine-protein kinase tousled-like 2 isoform X3
serine/threonine-protein kinase tousled-like 2 isoform X1
serine/threonine-protein kinase tousled-like 2 isoform X5
serine/threonine-protein kinase tousled-like 2 isoform X4
serine/threonine-protein kinase tousled-like 2 isoform X6
serine/threonine-protein kinase tousled-like 2 isoform X7
late secretory pathway protein AVL9 homolog
VPS35 endosomal protein-sorting factor-like
4-aminobutyrate aminotransferase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
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
39S ribosomal protein L50, mitochondrial
mediator of RNA polymerase II transcription subunit 13-like, transcript variant X1
mediator of RNA polymerase II transcription subunit 13-like, transcript variant X2
mediator of RNA polymerase II transcription subunit 13 isoform X1
mediator of RNA polymerase II transcription subunit 13-like isoform X2
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, transcript variant X3
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, transcript variant X2
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, transcript variant X4
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like, transcript variant X1
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like isoform X2
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1-like isoform X1
SUZ domain-containing protein 1-like, transcript variant X3
SUZ domain-containing protein 1-like, transcript variant X1
SUZ domain-containing protein 1-like, transcript variant X2
SUZ domain-containing protein 1-like isoform X1
SUZ domain-containing protein 1-like isoform X2
SUZ domain-containing protein 1-like isoform X3
aminoacyl tRNA synthase complex-interacting multifunctional protein 2, transcript variant X2
aminoacyl tRNA synthase complex-interacting multifunctional protein 2, transcript variant X1
aminoacyl tRNA synthase complex-interacting multifunctional protein 2 isoform X2
probable aminoacyl tRNA synthase complex-interacting multifunctional protein 2 isoform X1
nucleosome-remodeling factor subunit NURF301, 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 13 samples with support for all annotated introns
nucleosome-remodeling factor subunit NURF301, transcript variant X3
nucleosome-remodeling factor subunit NURF301, transcript variant X2
nucleosome-remodeling factor subunit NURF301, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
nucleosome-remodeling factor subunit NURF301, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
nucleosome-remodeling factor subunit NURF301, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
nucleosome-remodeling factor subunit NURF301, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
nucleosome-remodeling factor subunit NURF301 isoform X1
nucleosome-remodeling factor subunit NURF301 isoform X3
nucleosome-remodeling factor subunit NURF301 isoform X2
nucleosome-remodeling factor subunit NURF301 isoform X6
nucleosome-remodeling factor subunit NURF301 isoform X5
nucleosome-remodeling factor subunit NURF301 isoform X7
nucleosome-remodeling factor subunit NURF301 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 40 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 79 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF25, transcript variant X2
E3 ubiquitin-protein ligase RNF25, transcript variant X1
E3 ubiquitin-protein ligase RNF25 isoform X2
E3 ubiquitin-protein ligase RNF25 isoform X1
zinc finger protein 436-like, transcript variant X2
zinc finger protein 436-like, transcript variant X3
zinc finger protein 436-like, transcript variant X1
zinc finger protein 436-like, transcript variant X4
zinc finger protein 436-like, transcript variant X5
zinc finger protein 436-like, transcript variant X6
zinc finger protein 436-like, transcript variant X7
lissencephaly-1 homolog, transcript variant X3
lissencephaly-1 homolog, transcript variant X1
lissencephaly-1 homolog, transcript variant X2
zinc finger and BTB domain-containing protein 11-like, transcript variant X1
zinc finger and BTB domain-containing protein 11-like, transcript variant X2
uncharacterized protein LOC124410545 isoform X1
zinc finger and BTB domain-containing protein 11-like isoform X2
NEDD4-binding protein 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NEDD4-binding protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NEDD4-binding protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NEDD4-binding protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 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 7 samples with support for all annotated introns
putative phospholipase B-like lamina ancestor, transcript variant X3
putative phospholipase B-like lamina ancestor, transcript variant X2
putative phospholipase B-like lamina ancestor, transcript variant X1
putative phospholipase B-like lamina ancestor isoform X3
putative phospholipase B-like lamina ancestor isoform X2
putative phospholipase B-like lamina ancestor isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
active breakpoint cluster region-related protein
armadillo repeat-containing protein 5, transcript variant X1
armadillo repeat-containing protein 5, transcript variant X2
armadillo repeat-containing protein 5 isoform X1
uncharacterized protein LOC124410547 isoform X2
density-regulated protein homolog, transcript variant X1
density-regulated protein homolog isoform X1
density-regulated protein homolog, transcript variant X2
density-regulated protein homolog isoform X2
DNA-directed RNA polymerase III subunit RPC9
serine/threonine-protein kinase unc-51, transcript variant X2
serine/threonine-protein kinase unc-51, transcript variant X1
serine/threonine-protein kinase unc-51 isoform X2
serine/threonine-protein kinase unc-51 isoform X1
trafficking protein particle complex subunit 11, 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 8 samples with support for all annotated introns
trafficking protein particle complex subunit 11, 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 8 samples with support for all annotated introns
trafficking protein particle complex subunit 11, 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 4 samples with support for all annotated introns
trafficking protein particle complex subunit 11
TNF receptor-associated factor 4, transcript variant X2
TNF receptor-associated factor 4, transcript variant X3
TNF receptor-associated factor 4, transcript variant X1
TNF receptor-associated factor 4 isoform X3
TNF receptor-associated factor 4 isoform X1
TNF receptor-associated factor 4 isoform X2
ionotropic receptor 21a-like, transcript variant X2
ionotropic receptor 21a-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 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 13 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 72% coverage of the annotated genomic feature by RNAseq alignments
beta-1,3-glucosyltransferase, transcript variant X2
beta-1,3-glucosyltransferase, transcript variant X1
fatty acid-binding protein, adipocyte-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
B-cell CLL/lymphoma 7 protein family member A
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: B-cell CLL/lymphoma 7 protein family member A
thioredoxin reductase 1, mitochondrial, transcript variant X1
thioredoxin reductase 2, mitochondrial isoform X1
thioredoxin reductase 1, mitochondrial, transcript variant X3
thioredoxin reductase 1, mitochondrial isoform X3
thioredoxin reductase 1, mitochondrial, transcript variant X2
thioredoxin reductase 1, mitochondrial isoform X2
matrix metalloproteinase-2-like, transcript variant X1
matrix metalloproteinase-2-like, transcript variant X2
matrix metalloproteinase-24-like isoform X2
matrix metalloproteinase-2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cilia- and flagella-associated protein 251-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 79% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase TRIM37-like, transcript variant X4
E3 ubiquitin-protein ligase TRIM37-like, transcript variant X2
E3 ubiquitin-protein ligase TRIM37-like, transcript variant X1
E3 ubiquitin-protein ligase TRIM37-like, transcript variant X3
E3 ubiquitin-protein ligase TRIM37-like isoform X2
E3 ubiquitin-protein ligase TRIM37-like isoform X3
E3 ubiquitin-protein ligase TRIM37-like isoform X1
E3 ubiquitin-protein ligase TRIM37-like isoform X4
F-box only protein 21-like, transcript variant X1
F-box only protein 21-like, transcript variant X2
translation initiation factor IF-2, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
probable Rho GTPase-activating protein CG5521, transcript variant X1
probable Rho GTPase-activating protein CG5521, transcript variant X3
probable Rho GTPase-activating protein CG5521, transcript variant X2
probable Rho GTPase-activating protein CG5521, transcript variant X6
probable Rho GTPase-activating protein CG5521, transcript variant X4
probable Rho GTPase-activating protein CG5521 isoform X3
probable Rho GTPase-activating protein CG5521 isoform X2
probable Rho GTPase-activating protein CG5521 isoform X6
probable Rho GTPase-activating protein CG5521 isoform X4
probable Rho GTPase-activating protein CG5521 isoform X1
probable Rho GTPase-activating protein CG5521, 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 2 samples with support for all annotated introns
probable Rho GTPase-activating protein CG5521 isoform X5
probable Rho GTPase-activating protein CG5521, transcript variant X7
probable Rho GTPase-activating protein CG5521 isoform X7
protein sine oculis-like, 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 9 samples with support for all annotated introns
protein sine oculis-like, 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 12 samples with support for all annotated introns
uncharacterized LOC124410549, transcript variant X1
uncharacterized LOC124410549, transcript variant X3
uncharacterized LOC124410549, transcript variant X2
uncharacterized protein LOC124410549 isoform X1
uncharacterized protein LOC124410549 isoform X2
uncharacterized LOC124410220, 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 22 samples with support for all annotated introns
uncharacterized LOC124410220, 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 22 samples with support for all annotated introns
uncharacterized protein LOC124410220 isoform X1
uncharacterized protein LOC124410220 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
proline hydroxylase buaE-like, transcript variant X1
proline hydroxylase buaE-like, transcript variant X2
uncharacterized protein DDB_G0290301-like
UDP-glycosyltransferase UGT5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
UDP-glycosyltransferase UGT5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
UDP-glycosyltransferase UGT5-like isoform X2
UDP-glycosyltransferase UGT5-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 21 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 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
arrestin domain-containing protein 2-like
probable ATP-dependent RNA helicase spindle-E
G protein pathway suppressor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 60 samples with support for all annotated introns
G protein pathway suppressor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 56 samples with support for all annotated introns
G protein pathway suppressor 2 isoform X2
G protein pathway suppressor 2 isoform X1
centromere protein L-like, transcript variant X1
centromere protein L-like, transcript variant X3
centromere protein L-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 81 samples with support for all annotated introns
uncharacterized protein LOC124410274 isoform X4
uncharacterized LOC124410276, transcript variant X2
uncharacterized LOC124410276, transcript variant X1
uncharacterized protein LOC124410276 isoform X2
uncharacterized protein LOC124410276 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
inositol polyphosphate 5-phosphatase K-like, transcript variant X1
inositol polyphosphate 5-phosphatase K-like isoform X1
inositol polyphosphate 5-phosphatase K-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
inositol polyphosphate 5-phosphatase K-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 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 54 samples with support for all annotated introns
ovarian-specific serine/threonine-protein kinase Lok
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
succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
trifunctional purine biosynthetic protein adenosine-3
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 4 samples with support for all annotated introns
cyclic AMP-responsive element-binding protein 1, transcript variant X12
cyclic AMP-responsive element-binding protein 1, transcript variant X10
cyclic AMP-responsive element-binding protein 1, transcript variant X4
cyclic AMP-responsive element-binding protein 1, transcript variant X11
cyclic AMP-responsive element-binding protein 1, transcript variant X2
cyclic AMP-responsive element-binding protein 1, transcript variant X9
cyclic AMP-responsive element-binding protein 1, transcript variant X7
cyclic AMP-responsive element-binding protein 1, transcript variant X3
cyclic AMP-responsive element-binding protein 1, transcript variant X1
cyclic AMP-responsive element-binding protein 1, transcript variant X14
cyclic AMP-responsive element-binding protein 1, transcript variant X6
cyclic AMP-responsive element-binding protein 1, transcript variant X13
cyclic AMP-responsive element-binding protein 1, transcript variant X5
cyclic AMP-responsive element-binding protein 1, transcript variant X8
cAMP-responsive element modulator isoform X12
cAMP-responsive element modulator isoform X11
cyclic AMP-responsive element-binding protein 1 isoform X6
cyclic AMP-responsive element-binding protein 1 isoform X4
cyclic AMP-responsive element-binding protein 1 isoform X8
cyclic AMP response element-binding protein B isoform X10
cyclic AMP-responsive element-binding protein 1 isoform X3
cyclic AMP-responsive element-binding protein 1 isoform X7
cyclic AMP-responsive element-binding protein 1 isoform X5
cyclic AMP response element-binding protein B isoform X9
cyclic AMP-responsive element-binding protein 1 isoform X2
cyclic AMP-responsive element-binding protein 1 isoform X1
uncharacterized LOC124410654, 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 28 samples with support for all annotated introns
lanC-like protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
lanC-like protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC124410654, transcript variant X2
uncharacterized LOC124410654, transcript variant X1
uncharacterized protein LOC124410654 isoform X1
uncharacterized protein LOC124410654 isoform X2
very-long-chain 3-oxoacyl-CoA reductase-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
phosphatidylinositol-glycan biosynthesis class X protein
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 60 samples with support for all annotated introns
uncharacterized LOC124410714, transcript variant X2
uncharacterized protein LOC124410714 isoform X2
uncharacterized LOC124410714, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC124410714, transcript variant X1
uncharacterized protein LOC124410714 isoform X1
uncharacterized protein LOC124410714 isoform X3
probable nuclear transport factor 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 2 samples with support for all annotated introns
probable nuclear transport factor 2 isoform X1
4-hydroxyphenylpyruvate dioxygenase, transcript variant X2
4-hydroxyphenylpyruvate dioxygenase, transcript variant X1
4-hydroxyphenylpyruvate dioxygenase isoform X1
4-hydroxyphenylpyruvate dioxygenase isoform X2
probable nuclear transport factor 2, transcript variant X2
probable nuclear transport factor 2, transcript variant X3
probable nuclear transport factor 2 isoform X2
probable nuclear transport factor 2 isoform X3
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
ribosome biogenesis protein WDR12 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
protein alan shepard, transcript variant X9
protein alan shepard, transcript variant X8
protein alan shepard, transcript variant X19
protein alan shepard, transcript variant X18
protein alan shepard, transcript variant X17
protein alan shepard, transcript variant X7
protein alan shepard, transcript variant X1
protein alan shepard, transcript variant X2
protein alan shepard, transcript variant X4
protein alan shepard, transcript variant X12
protein alan shepard, transcript variant X16
protein alan shepard, transcript variant X13
protein alan shepard, transcript variant X10
protein alan shepard, transcript variant X11
protein alan shepard, transcript variant X6
protein alan shepard, transcript variant X3
protein alan shepard, transcript variant X5
protein alan shepard, transcript variant X14
protein alan shepard, transcript variant X15
NADH-quinone oxidoreductase subunit B 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 87% coverage of the annotated genomic feature by RNAseq alignments
transcriptional repressor p66-beta, transcript variant X5
transcriptional repressor p66-beta, transcript variant X7
transcriptional repressor p66-beta, transcript variant X4
transcriptional repressor p66-beta, transcript variant X1
transcriptional repressor p66-beta, transcript variant X6
transcriptional repressor p66-beta, transcript variant X2
transcriptional repressor p66-beta, transcript variant X3
transcriptional repressor p66-beta isoform X3
transcriptional repressor p66-beta isoform X4
transcriptional repressor p66-beta isoform X2
transcriptional repressor p66-beta 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 28 samples with support for all annotated introns
uncharacterized LOC124410469, transcript variant X2
uncharacterized LOC124410469, transcript variant X1
uncharacterized LOC124410468, transcript variant X1
uncharacterized LOC124410468, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
multiple C2 and transmembrane domain-containing protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
multiple C2 and transmembrane domain-containing protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
multiple C2 and transmembrane domain-containing protein, 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 6 samples with support for all annotated introns
multiple C2 and transmembrane domain-containing protein, transcript variant X1
multiple C2 and transmembrane domain-containing protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
multiple C2 and transmembrane domain-containing protein isoform X4
multiple C2 and transmembrane domain-containing protein isoform X2
multiple C2 and transmembrane domain-containing protein isoform X3
multiple C2 and transmembrane domain-containing protein isoform X1
multiple C2 and transmembrane domain-containing protein isoform X5
uncharacterized LOC124410200, 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 8 samples with support for all annotated introns
uncharacterized LOC124410200, transcript variant X1
uncharacterized protein LOC124410200 isoform X2
uncharacterized protein LOC124410200 isoform X1
glycine-rich cell wall structural protein-like
uncharacterized LOC124410219, 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 16 samples with support for all annotated introns
uncharacterized LOC124410219, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
cohesin subunit SA-1, transcript variant X6
cohesin subunit SA-1, transcript variant X4
cohesin subunit SA-1, transcript variant X5
cohesin subunit SA-1, transcript variant X1
cohesin subunit SA-1, transcript variant X2
cohesin subunit SA-1, transcript variant X3
cohesin subunit SA-1, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cohesin subunit SA-1, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cohesin subunit SA-1, transcript variant X8
cohesin subunit SA-1, transcript variant X7
uncharacterized LOC124410210, transcript variant X1
uncharacterized LOC124410210, transcript variant X2
uncharacterized protein LOC124410210 isoform X1
uncharacterized protein LOC124410210 isoform X2
epidermal growth factor receptor substrate 15-like 1, transcript variant X2
epidermal growth factor receptor substrate 15-like 1, transcript variant X1
epidermal growth factor receptor substrate 15-like 1 isoform X2
epidermal growth factor receptor substrate 15-like 1 isoform X1
epidermal growth factor receptor substrate 15-like 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
epidermal growth factor receptor substrate 15-like 1 isoform X4
epidermal growth factor receptor substrate 15-like 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
epidermal growth factor receptor substrate 15-like 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
probable cytosolic Fe-S cluster assembly factor CPIJ010948
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 57 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 10, transcript variant X2
CCR4-NOT transcription complex subunit 10, transcript variant X1
CCR4-NOT transcription complex subunit 10, transcript variant X3
CCR4-NOT transcription complex subunit 10
uncharacterized protein PB18E9.04c isoform X1
uncharacterized protein PB18E9.04c isoform X2
pregnancy zone protein-like, transcript variant X2
pregnancy zone protein-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 2 samples with support for all annotated introns
uncharacterized LOC124410665, transcript variant X1
uncharacterized LOC124410665, transcript variant X2
uncharacterized protein LOC124410665 isoform X1
uncharacterized protein LOC124410665 isoform X2
GPI ethanolamine phosphate transferase 3, transcript variant X2
GPI ethanolamine phosphate transferase 3, transcript variant X1
GPI ethanolamine phosphate transferase 3
collagen and calcium-binding EGF domain-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
collagen and calcium-binding EGF domain-containing protein 1-like, transcript variant X1
collagen and calcium-binding EGF domain-containing protein 1-like isoform X1
collagen and calcium-binding EGF domain-containing protein 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
transmembrane and coiled-coil domain-containing protein 4-like, transcript variant X2
transmembrane and coiled-coil domain-containing protein 4-like, transcript variant X1
transmembrane and coiled-coil domain-containing protein 4-like isoform X2
transmembrane and coiled-coil domain-containing protein 4-like isoform X1
uncharacterized LOC124410679, transcript variant X1
uncharacterized LOC124410679, transcript variant X2
putative leucine-rich repeat-containing protein DDB_G0290503, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
putative leucine-rich repeat-containing protein DDB_G0290503, transcript variant X2
putative leucine-rich repeat-containing protein DDB_G0290503, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
putative leucine-rich repeat-containing protein DDB_G0290503 isoform X3
putative leucine-rich repeat-containing protein DDB_G0290503 isoform X2
putative leucine-rich repeat-containing protein DDB_G0290503 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein yellow-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
protein yellow-like, transcript variant X2
BUB3-interacting and GLEBS motif-containing protein ZNF207-like, transcript variant X1
BUB3-interacting and GLEBS motif-containing protein ZNF207-like, transcript variant X2
BUB3-interacting and GLEBS motif-containing protein ZNF207-like, transcript variant X4
BUB3-interacting and GLEBS motif-containing protein ZNF207-like, transcript variant X3
BUB3-interacting and GLEBS motif-containing protein ZNF207-like isoform X2
BUB3-interacting and GLEBS motif-containing protein ZNF207-like isoform X3
BUB3-interacting and GLEBS motif-containing protein ZNF207-like isoform X1
structural maintenance of chromosomes protein 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
structural maintenance of chromosomes protein 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
structural maintenance of chromosomes protein 4, transcript variant X2
structural maintenance of chromosomes protein 4
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC124410689, transcript variant X1
uncharacterized LOC124410689, transcript variant X2
uncharacterized protein LOC124410689 isoform X1
uncharacterized protein LOC124410689 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dynein regulatory complex subunit 2-like
differentially expressed in FDCP 6 homolog
U6 small nuclear RNA (adenine-(43)-N(6))-methyltransferase, 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 7 samples with support for all annotated introns
U6 small nuclear RNA (adenine-(43)-N(6))-methyltransferase, transcript variant X3
U6 small nuclear RNA (adenine-(43)-N(6))-methyltransferase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
U6 small nuclear RNA (adenine-(43)-N(6))-methyltransferase, 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 9 samples with support for all annotated introns
U6 small nuclear RNA (adenine-(43)-N(6))-methyltransferase, 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 20 samples with support for all annotated introns
U6 small nuclear RNA (adenine-(43)-N(6))-methyltransferase isoform X1
U6 small nuclear RNA (adenine-(43)-N(6))-methyltransferase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
RNA N6-adenosine-methyltransferase METTL16 isoform X2
clustered mitochondria protein homolog, transcript variant X2
clustered mitochondria protein homolog, transcript variant X1
clustered mitochondria protein homolog isoform X2
clustered mitochondria protein homolog isoform X1
mRNA export factor Gle1, transcript variant X1
mRNA export factor Gle1, transcript variant X2
zinc finger HIT domain-containing protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
transfer RNA serine (anticodon GCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC124410295, transcript variant X3
uncharacterized LOC124410295, transcript variant X2
uncharacterized LOC124410295, transcript variant X1
uncharacterized protein LOC124410295 isoform X3
uncharacterized protein LOC124410295 isoform X2
uncharacterized protein LOC124410295 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
breast cancer type 1 susceptibility protein homolog, transcript variant X2
breast cancer type 1 susceptibility protein homolog, transcript variant X1
breast cancer type 1 susceptibility protein homolog isoform X2
breast cancer type 1 susceptibility protein homolog isoform X1
zinc finger CCCH domain-containing protein 13-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
dihydropyrimidine dehydrogenase [NADP(+)]
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 71 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 240 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA glycine (anticodon UCC); 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: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial potassium channel ATP-binding subunit, transcript variant X1
mitochondrial potassium channel ATP-binding subunit, transcript variant X2
mitochondrial potassium channel ATP-binding subunit isoform X1
mitochondrial potassium channel ATP-binding subunit isoform X2
pneumococcal serine-rich repeat protein-like
sodium- and chloride-dependent GABA transporter 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sodium- and chloride-dependent GABA transporter 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 10 samples with support for all annotated introns
sodium- and chloride-dependent GABA transporter 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
troponin C, isoallergen Bla g 6.0101-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
troponin C, isoallergen Bla g 6.0101-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 48% 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 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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
calcium-transporting ATPase sarcoplasmic/endoplasmic reticulum type, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 72 samples with support for all annotated introns
calcium-transporting ATPase sarcoplasmic/endoplasmic reticulum type, transcript variant X3
calcium-transporting ATPase sarcoplasmic/endoplasmic reticulum type, transcript variant X1
calcium-transporting ATPase sarcoplasmic/endoplasmic reticulum type isoform X2
calcium-transporting ATPase sarcoplasmic/endoplasmic reticulum type isoform X3
calcium-transporting ATPase sarcoplasmic/endoplasmic reticulum type isoform X1
uncharacterized LOC124410701, transcript variant X1
uncharacterized LOC124410701, transcript variant X2
uncharacterized protein LOC124410701 isoform X1
uncharacterized protein LOC124410701 isoform X2
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, including 3 samples with support for all annotated introns
uncharacterized LOC124410593, transcript variant X2
meiosis-specific nuclear structural protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124410593, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 58 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 67 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon UAA); 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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC124410329, transcript variant X1
uncharacterized LOC124410329, 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
uncharacterized LOC124410329, transcript variant X4
uncharacterized LOC124410329, transcript variant X6
uncharacterized LOC124410329, 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 3 samples with support for all annotated introns
uncharacterized LOC124410329, transcript variant X3
uncharacterized protein LOC124410329 isoform X1
uncharacterized protein LOC124410329 isoform X2
uncharacterized protein LOC124410329 isoform X4
uncharacterized protein LOC124410329 isoform X5
uncharacterized protein LOC124410329 isoform X6
uncharacterized protein LOC124410329 isoform X3
CD63 antigen-like, transcript variant X1
CD63 antigen-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 20 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 91% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124410699, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC124410699, 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 1 sample with support for all annotated introns
uncharacterized LOC124410699, transcript variant X4
uncharacterized LOC124410699, 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 1 sample with support for all annotated introns
uncharacterized protein LOC124410699 isoform X1
uncharacterized protein LOC124410699 isoform X3
uncharacterized protein LOC124410699 isoform X2
group 3 secretory phospholipase A2-like, transcript variant X2
group 3 secretory phospholipase A2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
group 3 secretory phospholipase A2-like isoform X2
group 3 secretory phospholipase A2-like isoform X1
leucine-rich repeat-containing protein 15-like, transcript variant X1
leucine-rich repeat-containing protein 15-like, transcript variant X2
leucine-rich repeat-containing protein 15-like
uncharacterized LOC124410651, 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
uncharacterized LOC124410651, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
tetratricopeptide repeat protein 37, transcript variant X1
tetratricopeptide repeat protein 37, transcript variant X2
tetratricopeptide repeat protein 37 isoform X1
tetratricopeptide repeat protein 37 isoform X2
tetratricopeptide repeat protein 37, transcript variant X3
tetratricopeptide repeat protein 37 isoform X3
pentatricopeptide repeat-containing protein 2, mitochondrial-like
E3 ubiquitin-protein ligase TRIM71-like, transcript variant X1
E3 ubiquitin-protein ligase TRIM71-like, transcript variant X3
E3 ubiquitin-protein ligase TRIM71-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
retinoblastoma-like protein 1, transcript variant X2
retinoblastoma-like protein 1, transcript variant X1
retinoblastoma-like protein 1 isoform X2
retinoblastoma-like protein 1 isoform X1
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X1
(Lyso)-N-acylphosphatidylethanolamine lipase, transcript variant X2
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X1
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X2
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
synaptic vesicle membrane protein VAT-1 homolog-like
guanine nucleotide exchange factor subunit Rich
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 41 samples with support for all annotated introns
protein lingerer-like, transcript variant X2
protein lingerer-like, transcript variant X3
protein lingerer-like, transcript variant X4
protein lingerer-like, transcript variant X6
protein lingerer-like, transcript variant X5
protein lingerer-like, transcript variant X7
protein lingerer-like, transcript variant X1
probable 28S ribosomal protein S16, mitochondrial
transfer RNA isoleucine (anticodon UAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC124410461, transcript variant X1
zinc finger protein 90-like, transcript variant X2
uncharacterized LOC124410461, transcript variant X3
uncharacterized LOC124410461, transcript variant X2
zinc finger protein 90-like, transcript variant X1
peptidyl-prolyl cis-trans isomerase FKBP8-like, transcript variant X1
peptidyl-prolyl cis-trans isomerase FKBP8-like, transcript variant X2
peptidyl-prolyl cis-trans isomerase FKBP8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 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 38% coverage of the annotated genomic feature by RNAseq alignments
60S ribosomal protein L10, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
probable enoyl-CoA hydratase, mitochondrial, transcript variant X2
probable enoyl-CoA hydratase, mitochondrial, transcript variant X1
probable enoyl-CoA hydratase, mitochondrial isoform X2
uncharacterized protein LOC124410614 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
GTP-binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 54 samples with support for all annotated introns
GTP-binding protein 1, 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 13 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 9
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 84 samples with support for all annotated introns
60S ribosomal protein L10, transcript variant X1
E3 ubiquitin ligase Rnf157, transcript variant X1
E3 ubiquitin ligase Rnf157, transcript variant X2
probable E3 ubiquitin-protein ligase MGRN1 isoform X1
protein FAM117B-like, transcript variant X1
protein FAM117B-like, transcript variant X2
tripartite motif-containing protein 2-like, transcript variant X2
tripartite motif-containing protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tripartite motif-containing protein 2-like, transcript variant X3
tripartite motif-containing protein 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
tripartite motif-containing protein 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
tripartite motif-containing protein 2-like isoform X2
tripartite motif-containing protein 2-like isoform X1
tripartite motif-containing protein 2-like isoform X3
tripartite motif-containing protein 2-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
alkaline phosphatase-like, transcript variant X2
alkaline phosphatase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 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 11 samples with support for all annotated introns
28S ribosomal protein S21, mitochondrial
uncharacterized LOC124410294, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC124410294, transcript variant X2
uncharacterized LOC124410294, transcript variant X4
uncharacterized LOC124410294, transcript variant X1
uncharacterized protein LOC124410294 isoform X3
uncharacterized protein LOC124410294 isoform X2
uncharacterized protein LOC124410294 isoform X4
uncharacterized protein LOC124410294 isoform X1
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
lipid droplet-associated hydrolase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
lipid droplet-associated hydrolase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
lipid droplet-associated hydrolase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
probable 28S ribosomal protein S23, mitochondrial
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
facilitated trehalose transporter Tret1-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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
facilitated trehalose transporter Tret1-2 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: facilitated trehalose transporter Tret1-like
facilitated trehalose transporter Tret1-2 homolog, transcript variant X1
facilitated trehalose transporter Tret1-2 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
facilitated trehalose transporter Tret1-2 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
facilitated trehalose transporter Tret1-2 homolog, transcript variant X4
facilitated trehalose transporter Tret1-2 homolog isoform X2
facilitated trehalose transporter Tret1-2 homolog 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 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
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 63 samples with support for all annotated introns
putative inorganic phosphate cotransporter, transcript variant X2
putative inorganic phosphate cotransporter, transcript variant X1
putative inorganic phosphate cotransporter isoform X2
putative inorganic phosphate cotransporter isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 154 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
BMP-binding endothelial regulator protein, 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
BMP-binding endothelial regulator protein, transcript variant X2
BMP-binding endothelial regulator protein
doublesex- and mab-3-related transcription factor A2
thioredoxin domain-containing protein 12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein mono-ADP-ribosyltransferase PARP14-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 3% coverage of the annotated genomic feature by RNAseq alignments
protein mono-ADP-ribosyltransferase TIPARP-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
protein mono-ADP-ribosyltransferase TIPARP-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 75 samples with support for all annotated introns
protein mono-ADP-ribosyltransferase TIPARP-like
uncharacterized LOC124410237, transcript variant X4
uncharacterized LOC124410237, transcript variant X2
uncharacterized LOC124410237, transcript variant X3
uncharacterized LOC124410237, transcript variant X1
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA proline (anticodon AGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
inhibitor of nuclear factor kappa-B kinase subunit epsilon
leucine-rich repeat serine/threonine-protein kinase 1
oxidized purine nucleoside triphosphate hydrolase-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: oxidized purine nucleoside triphosphate hydrolase-like
poly(A)-specific ribonuclease PARN-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 29 samples with support for all annotated introns
poly(A)-specific ribonuclease PARN-like isoform X2
poly(A)-specific ribonuclease PARN-like, transcript variant X1
poly(A)-specific ribonuclease PARN-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein dimmed-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 18 samples with support for all annotated introns
transfer RNA serine (anticodon CGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
protein dimmed-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
protein dimmed-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 26 samples with support for all annotated introns
protein dimmed-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC124410373, transcript variant X1
uncharacterized LOC124410373, transcript variant X2
RING finger and CHY zinc finger domain-containing protein 1
PX domain-containing protein kinase-like protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
PX domain-containing protein kinase-like protein, transcript variant X1
PX domain-containing protein kinase-like protein isoform X1
PX domain-containing protein kinase-like protein isoform X2
PX domain-containing protein kinase-like protein, transcript variant X3
PX domain-containing protein kinase-like protein isoform X3
protein prickle-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
protein prickle-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
protein prickle-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein prickle-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC124410271, transcript variant X5
uncharacterized LOC124410271, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC124410271, transcript variant X7
uncharacterized LOC124410271, transcript variant X1
uncharacterized LOC124410271, transcript variant X2
uncharacterized LOC124410271, transcript variant X3
uncharacterized LOC124410271, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC124410271, transcript variant X8
uncharacterized protein LOC124410271 isoform X1
uncharacterized protein LOC124410271 isoform X2
uncharacterized protein LOC124410271 isoform X3
uncharacterized protein LOC124410271 isoform X5
uncharacterized protein LOC124410271 isoform X6
uncharacterized protein LOC124410271 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
peptide-N(4)-(N-acetyl-beta- glucosaminyl)asparagine amidase
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
endoplasmic reticulum metallopeptidase 1-like, transcript variant X2
endoplasmic reticulum metallopeptidase 1-like, transcript variant X1
endoplasmic reticulum metallopeptidase 1-like, transcript variant X3
endoplasmic reticulum metallopeptidase 1-like isoform X2
endoplasmic reticulum metallopeptidase 1-like isoform X1
endoplasmic reticulum metallopeptidase 1-like isoform X3
elongation factor Tu, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
ATP synthase subunit alpha, mitochondrial
guanine nucleotide-binding protein subunit beta-5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 14
tyrosine-protein kinase Src42A, transcript variant X1
tyrosine-protein kinase Src42A, transcript variant X2
BAG family molecular chaperone regulator 2
receptor expression-enhancing protein 5-like, transcript variant X1
receptor expression-enhancing protein 5-like isoform X1
receptor expression-enhancing protein 5-like, transcript variant X2
receptor expression-enhancing protein 5-like isoform X2
armadillo repeat-containing protein gudu, transcript variant X2
armadillo repeat-containing protein gudu, transcript variant X1
armadillo repeat-containing protein gudu isoform X2
armadillo repeat-containing protein gudu isoform X1
uncharacterized LOC124410338, transcript variant X1
uncharacterized LOC124410338, 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 54 samples with support for all annotated introns
28S ribosomal protein S33, mitochondrial
phosphomannomutase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
phosphomannomutase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 56 samples with support for all annotated introns
phosphomannomutase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
methylglutaconyl-CoA hydratase, mitochondrial
protein bfr2-like, 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 22 samples with support for all annotated introns
protein bfr2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
MATH and LRR domain-containing protein PFE0570w-like isoform X1
regulatory-associated protein of mTOR, transcript variant X5
regulatory-associated protein of mTOR, transcript variant X1
regulatory-associated protein of mTOR, transcript variant X4
regulatory-associated protein of mTOR, transcript variant X3
regulatory-associated protein of mTOR, transcript variant X2
regulatory-associated protein of mTOR, transcript variant X6
regulatory-associated protein of mTOR isoform X5
regulatory-associated protein of mTOR isoform X4
regulatory-associated protein of mTOR isoform X3
regulatory-associated protein of mTOR isoform X2
regulatory-associated protein of mTOR isoform X1
regulatory-associated protein of mTOR isoform X6
sodium-independent sulfate anion transporter-like, transcript variant X2
sodium-independent sulfate anion transporter-like, 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 6 samples with support for all annotated introns
sodium-independent sulfate anion transporter-like isoform X2
sodium-independent sulfate anion transporter-like isoform X1
uncharacterized LOC124410437, transcript variant X2
uncharacterized LOC124410437, transcript variant X1
uncharacterized LOC124410437, transcript variant X4
uncharacterized LOC124410437, transcript variant X3
uncharacterized protein LOC124410437 isoform X2
uncharacterized protein LOC124410437 isoform X4
uncharacterized protein LOC124410437 isoform X1
uncharacterized protein LOC124410437 isoform X3
nuclear protein localization protein 4 homolog, transcript variant X3
nuclear protein localization protein 4 homolog, transcript variant X1
nuclear protein localization protein 4 homolog, transcript variant X2
nuclear protein localization protein 4 homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
nuclear protein localization protein 4 homolog, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 54 samples with support for all annotated introns
nuclear protein localization protein 4 homolog isoform X1
nuclear protein localization protein 4 homolog isoform X2
nuclear protein localization protein 4 homolog isoform X3
nuclear protein localization protein 4 homolog isoform X4
nuclear protein localization protein 4 homolog isoform X5
uncharacterized LOC124410436, transcript variant X2
uncharacterized LOC124410436, transcript variant X3
uncharacterized LOC124410436, transcript variant X1
uncharacterized protein LOC124410436 isoform X1
uncharacterized protein LOC124410436 isoform X2
uncharacterized protein LOC124410436 isoform X3
E3 ubiquitin-protein ligase COP1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
E3 ubiquitin-protein ligase COP1-like, transcript variant X2
cuticle protein 21-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
cuticle protein 21-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
larval cuticle protein A3A-like, transcript variant X4
larval cuticle protein A3A-like, transcript variant X3
larval cuticle protein A3A-like, transcript variant X1
larval cuticle protein A3A-like, transcript variant X2
larval cuticle protein A3A-like isoform X4
larval cuticle protein A3A-like isoform X3
larval cuticle protein A3A-like isoform X1
larval cuticle protein A3A-like isoform X2
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, including 14 samples with support for all annotated introns
larval cuticle protein A3A-like, transcript variant X5
larval cuticle protein A3A-like isoform X5
larval cuticle protein A2B-like isoform X2
larval cuticle protein A2B-like isoform X1
larval cuticle protein A2B-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 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 23 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit RPB1-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 20 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 98% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein OZF-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 50 samples with support for all annotated introns
zinc finger protein OZF-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
cyclin-dependent kinase 12, transcript variant X6
cyclin-dependent kinase 12, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
cyclin-dependent kinase 12, transcript variant X3
cyclin-dependent kinase 12, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
cyclin-dependent kinase 12, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
cyclin-dependent kinase 12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
cyclin-dependent kinase 12, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase N2, transcript variant X4
receptor-type tyrosine-protein phosphatase N2, transcript variant X1
receptor-type tyrosine-protein phosphatase N2, transcript variant X3
receptor-type tyrosine-protein phosphatase N2, transcript variant X2
receptor-type tyrosine-protein phosphatase N2 isoform X4
receptor-type tyrosine-protein phosphatase N2 isoform X3
receptor-type tyrosine-protein phosphatase N2 isoform X2
receptor-type tyrosine-protein phosphatase N2 isoform X1
uncharacterized LOC124410390, transcript variant X1
uncharacterized LOC124410390, transcript variant X3
uncharacterized protein LOC124410390 isoform X1
uncharacterized LOC124410390, 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 55 samples with support for all annotated introns
uncharacterized protein LOC124410390 isoform X2
60S ribosomal protein L27, transcript variant X1
60S ribosomal protein L27, transcript variant X3
60S ribosomal protein L27, 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 65 samples with support for all annotated introns
inositol hexakisphosphate kinase 1, transcript variant X1
inositol hexakisphosphate kinase 1 isoform X1
inositol hexakisphosphate kinase 1, transcript variant X4
inositol hexakisphosphate kinase 1, transcript variant X2
inositol hexakisphosphate kinase 1, transcript variant X3
uncharacterized protein LOC124410511 isoform X2
huntingtin-interacting protein 1, transcript variant X2
huntingtin-interacting protein 1, transcript variant X3
huntingtin-interacting protein 1, transcript variant X1
huntingtin-interacting protein 1, transcript variant X4
huntingtin-interacting protein 1 isoform X2
huntingtin-interacting protein 1 isoform X1
huntingtin-interacting protein 1 isoform X3
vascular endothelial growth factor receptor kdr-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
glucose dehydrogenase [FAD, quinone]-like, transcript variant X2
glucose dehydrogenase [FAD, quinone]-like, transcript variant X3
glucose dehydrogenase [FAD, quinone]-like, transcript variant X1
glucose dehydrogenase [FAD, quinone]-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
histone H3.3-like, transcript variant X1
histone H3.3-like, transcript variant X2
histone H3-like centromeric protein CSE4 isoform X2
NAD(+) hydrolase sarm1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
NAD(+) hydrolase sarm1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
NAD(+) hydrolase sarm1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
NAD(+) hydrolase sarm1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
NAD(+) hydrolase sarm1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
NAD(+) hydrolase sarm1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
NAD(+) hydrolase sarm1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
macrophage colony-stimulating factor 1 receptor 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
vascular endothelial growth factor receptor 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 50% 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 58% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 28% 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: glucose dehydrogenase [FAD, quinone]-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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: 8 Proteins, and 80% 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: 10 Proteins, and 74% 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 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NFX1-type zinc finger-containing protein 1-like, transcript variant X1
NFX1-type zinc finger-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
NFX1-type zinc finger-containing protein 1-like
uncharacterized WD repeat-containing protein alr2800-like
protein phosphatase Slingshot homolog 2, transcript variant X4
protein phosphatase Slingshot homolog 2, transcript variant X3
protein phosphatase Slingshot homolog 2, transcript variant X2
protein phosphatase Slingshot homolog 2, transcript variant X1
protein phosphatase Slingshot homolog 2, transcript variant X5
protein phosphatase Slingshot homolog 2, transcript variant X6
protein phosphatase Slingshot homolog 2, transcript variant X8
protein phosphatase Slingshot homolog 2, transcript variant X7
protein phosphatase Slingshot homolog 2 isoform X4
protein phosphatase Slingshot homolog 2 isoform X3
protein phosphatase Slingshot homolog 2 isoform X2
protein phosphatase Slingshot homolog 2 isoform X1
protein phosphatase Slingshot homolog 2 isoform X5
protein phosphatase Slingshot homolog 2 isoform X6
protein phosphatase Slingshot homolog 2 isoform X8
protein phosphatase Slingshot homolog 2 isoform X7
corrinoid adenosyltransferase-like, transcript variant X2
corrinoid adenosyltransferase-like, transcript variant X1
corrinoid adenosyltransferase-like isoform X2
corrinoid adenosyltransferase-like isoform X1
leucine-rich repeat protein soc-2 homolog, transcript variant X2
leucine-rich repeat protein soc-2 homolog, transcript variant X1
leucine-rich repeat protein soc-2 homolog isoform X1
leucine-rich repeat protein soc-2 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
decapping and exoribonuclease protein-like
p53 and DNA damage-regulated protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
p53 and DNA damage-regulated protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
p53 and DNA damage-regulated protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
p53 and DNA damage-regulated protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 84 samples with support for all annotated introns
p53 and DNA damage-regulated protein 1 isoform X2
p53 and DNA damage-regulated protein 1 isoform X3
p53 and DNA damage-regulated protein 1 isoform X1
p53 and DNA damage-regulated protein 1 isoform X4
G patch domain and ankyrin repeat-containing protein 1 homolog
tectonin beta-propeller repeat-containing protein, transcript variant X6
tectonin beta-propeller repeat-containing protein, transcript variant X1
tectonin beta-propeller repeat-containing protein, transcript variant X2
tectonin beta-propeller repeat-containing protein, transcript variant X4
tectonin beta-propeller repeat-containing protein, transcript variant X3
tectonin beta-propeller repeat-containing protein isoform X1
tectonin beta-propeller repeat-containing protein isoform X2
tectonin beta-propeller repeat-containing protein isoform X4
tectonin beta-propeller repeat-containing protein, transcript variant X5
tectonin beta-propeller repeat-containing protein isoform X3
cationic amino acid transporter 3, transcript variant X2
cationic amino acid transporter 3, transcript variant X1
general transcription factor IIH subunit 2, transcript variant X2
general transcription factor IIH subunit 2, transcript variant X3
general transcription factor IIH subunit 2, transcript variant X1
general transcription factor IIH subunit 2
serine-rich adhesin for platelets isoform X1
serine-rich adhesin for platelets isoform X2
serine-rich adhesin for platelets isoform X4
tRNA (cytosine(72)-C(5))-methyltransferase NSUN6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tRNA (cytosine(72)-C(5))-methyltransferase NSUN6, transcript variant X1
tRNA (cytosine(72)-C(5))-methyltransferase NSUN6 isoform X2
tRNA (cytosine(72)-C(5))-methyltransferase NSUN6 isoform X1
ADP-ribosylation factor 1, transcript variant X1
ADP-ribosylation factor 1, 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 15 samples with support for all annotated introns
alanine--glyoxylate aminotransferase, transcript variant X1
alanine--glyoxylate aminotransferase, transcript variant X2
alanine--glyoxylate aminotransferase, transcript variant X3
rho guanine nucleotide exchange factor 10-like, transcript variant X1
rho guanine nucleotide exchange factor 10-like, transcript variant X2
rho guanine nucleotide exchange factor 10-like protein isoform X1
rho guanine nucleotide exchange factor 10-like protein isoform X2
transcription elongation factor SPT5-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 14 samples with support for all annotated introns
transcription elongation factor SPT5-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 15 samples with support for all annotated introns
transcription elongation factor SPT5-like, 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 22 samples with support for all annotated introns
transcription elongation factor SPT5-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 57 samples with support for all annotated introns
transcription elongation factor SPT5-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 60 samples with support for all annotated introns
transcription elongation factor SPT5-like isoform X5
transcription elongation factor SPT5-like isoform X2
transcription elongation factor SPT5-like isoform X4
transcription elongation factor SPT5-like isoform X3
transcription elongation factor SPT5-like isoform X1
rho guanine nucleotide exchange factor 10-like, transcript variant X3
rho guanine nucleotide exchange factor 10-like isoform X3
transmembrane protein 47, transcript variant X3
transmembrane protein 47, transcript variant X2
transmembrane protein 47, transcript variant X4
transmembrane protein 47, transcript variant X1
zinc finger protein 845, transcript variant X2
zinc finger protein 845, transcript variant X1
ester hydrolase C11orf54 homolog, transcript variant X2
ester hydrolase C11orf54 homolog, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 43% 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: uncharacterized protein LOC124410164
inositol-trisphosphate 3-kinase homolog, transcript variant X2
inositol-trisphosphate 3-kinase homolog, transcript variant X1
inositol-trisphosphate 3-kinase homolog, transcript variant X3
inositol-trisphosphate 3-kinase homolog isoform X1
inositol-trisphosphate 3-kinase homolog isoform X3
inositol-trisphosphate 3-kinase homolog isoform X2
pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16, transcript variant X1
pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16, 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 21 samples with support for all annotated introns
pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 isoform X1
pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 isoform X2
pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16, transcript variant X3
pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16, transcript variant X4
pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 isoform X3
pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
mitochondrial import receptor subunit TOM22 homolog
protein flightless-1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 479 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
protein flightless-1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 479 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
ADP-ribosylation factor-binding protein GGA1, transcript variant X1
ADP-ribosylation factor-binding protein GGA1, transcript variant X2
ADP-ribosylation factor-binding protein GGA1 isoform X1
ADP-ribosylation factor-binding protein GGA1 isoform X2
target of rapamycin complex subunit lst8, transcript variant X1
target of rapamycin complex subunit lst8, transcript variant X2
target of rapamycin complex subunit lst8 isoform X1
target of rapamycin complex subunit lst8 isoform X2
E3 ubiquitin-protein ligase rififylin, transcript variant X1
E3 ubiquitin-protein ligase rififylin, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
E3 ubiquitin-protein ligase rififylin, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
E3 ubiquitin-protein ligase rififylin isoform X2
E3 ubiquitin-protein ligase rififylin isoform X1
LOW QUALITY PROTEIN: uncharacterized protein LOC124410642
RING-type E3 ubiquitin-protein ligase PPIL2
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 39 samples with support for all annotated introns
ubiquitin-conjugating enzyme E2-24 kDa, transcript variant X1
ubiquitin-conjugating enzyme E2-24 kDa, transcript variant X4
ubiquitin-conjugating enzyme E2-24 kDa, transcript variant X3
ubiquitin-conjugating enzyme E2-24 kDa, transcript variant X5
ubiquitin-conjugating enzyme E2-24 kDa, transcript variant X2
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
alpha-ketoglutarate-dependent dioxygenase alkB homolog 4, transcript variant X2
alpha-ketoglutarate-dependent dioxygenase alkB homolog 4, transcript variant X1
alpha-ketoglutarate-dependent dioxygenase alkB homolog 4 isoform X2
alpha-ketoglutarate-dependent dioxygenase alkB homolog 4 isoform X1
serine/threonine-protein kinase NLK, transcript variant X1
serine/threonine-protein kinase NLK, transcript variant X2
serine/threonine-protein kinase NLK, transcript variant X3
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: 27 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: peptidoglycan recognition protein-like
trafficking kinesin-binding protein milt, transcript variant X1
trafficking kinesin-binding protein milt, transcript variant X3
trafficking kinesin-binding protein milt, transcript variant X2
trafficking kinesin-binding protein milt, transcript variant X7
trafficking kinesin-binding protein milt, transcript variant X5
trafficking kinesin-binding protein milt, transcript variant X6
trafficking kinesin-binding protein milt, transcript variant X4
trafficking kinesin-binding protein milt isoform X1
trafficking kinesin-binding protein milt isoform X3
trafficking kinesin-binding protein milt isoform X2
trafficking kinesin-binding protein milt isoform X4
trafficking kinesin-binding protein milt isoform X5
protein bric-a-brac 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein bric-a-brac 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
protein bric-a-brac 2-like, transcript variant X1
zinc finger and BTB domain-containing protein 17-like isoform X2
zinc finger and BTB domain-containing protein 14-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
guanine nucleotide-binding protein subunit alpha homolog, transcript variant X2
guanine nucleotide-binding protein subunit alpha homolog, transcript variant X1
guanine nucleotide-binding protein subunit alpha homolog, transcript variant X3
guanine nucleotide-binding protein subunit alpha homolog, transcript variant X4
guanine nucleotide-binding protein subunit alpha homolog
protein MTO1 homolog, mitochondrial, transcript variant X1
protein MTO1 homolog, mitochondrial isoform X1
protein MTO1 homolog, mitochondrial, transcript variant X2
protein MTO1 homolog, mitochondrial isoform X2
probable G-protein coupled receptor Mth-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 83% 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 95% coverage of the annotated genomic feature by RNAseq alignments
glucose dehydrogenase [FAD, quinone]-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone]-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
protein rhomboid-like, transcript variant X2
protein rhomboid-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 11 samples with support for all annotated introns
myeloid differentiation primary response protein MyD88, transcript variant X1
myeloid differentiation primary response protein MyD88 isoform X1
myeloid differentiation primary response protein MyD88, 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 3 samples with support for all annotated introns
myeloid differentiation primary response protein MyD88 isoform X2
telomerase-binding protein EST1A-like, transcript variant X2
telomerase-binding protein EST1A-like, transcript variant X4
telomerase-binding protein EST1A-like, transcript variant X5
telomerase-binding protein EST1A-like, transcript variant X3
telomerase-binding protein EST1A-like, transcript variant X1
telomerase-binding protein EST1A-like isoform X3
telomerase-binding protein EST1A-like isoform X4
telomerase-binding protein EST1A-like isoform X2
telomerase-binding protein EST1A-like isoform X1
uncharacterized LOC124410191, transcript variant X2
uncharacterized LOC124410191, 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 33 samples with support for all annotated introns
uncharacterized protein LOC124410191 isoform X1
uncharacterized protein LOC124410191 isoform X2
mpv17-like protein, transcript variant X2
mpv17-like protein, transcript variant X1
transcription factor E2F4-like, transcript variant X1
transcription factor E2F4-like, transcript variant X2
transcription factor E2F4-like isoform X1
transcription factor E2F4-like isoform X2
uncharacterized LOC124410341, transcript variant X4
uncharacterized LOC124410341, transcript variant X1
uncharacterized LOC124410341, transcript variant X3
uncharacterized LOC124410341, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
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, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF01960
COORDINATES: nucleotide motif:Rfam:12.0:RF00002