Cotesia glomerata isolate CgM1 linkage group LG9, MPM_Cglom_v2.3, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Hymenoptera; Apocrita; Parasitoida; Ichneumonoidea; Braconidae; Microgastrinae; Cotesia.
A chromosome-level genome assembly of the parasitoid wasp, Cotesia glomerata (Hymenoptera: Braconidae)
Publication Status: Available-Online prior to print
REFSEQ INFORMATION: The reference sequence is identical to\nCM034668.1.\nAssembly name: MPM_Cglom_v2.3\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Milwaukee Public Museum on\n2021/09/24. The original whole-genome shotgun project has the\naccession JAHXZJ000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Milwaukee Public Museum\nAssembly Date :: MAY-2021\nAssembly Method :: Flye v. 2.8.1\nAssembly Name :: MPM_Cglom_v2.3\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 130.0x\nSequencing Technology :: Oxford Nanopore MinION; Illumina HiSeq;\n Hi-C\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Cotesia glomerata 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##
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: 25% coverage of the annotated genomic feature by RNAseq alignments
prion-like-(Q/N-rich) domain-bearing protein 25
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: 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
neurogenic locus notch homolog protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12% coverage of the annotated genomic feature by RNAseq alignments
multiple epidermal growth factor-like domains protein 10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 69% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123271522, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized LOC123271522, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial, transcript variant X1
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial, transcript variant X2
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial
E3 ubiquitin-protein ligase SINAT2-like, transcript variant X1
E3 ubiquitin-protein ligase SINAT2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
neuropathy target esterase sws, transcript variant X1
neuropathy target esterase sws, transcript variant X3
neuropathy target esterase sws, transcript variant X2
neuropathy target esterase sws isoform X1
neuropathy target esterase sws isoform X2
neuropathy target esterase sws isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 11% 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 56% coverage of the annotated genomic feature by RNAseq alignments
folylpolyglutamate synthase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uridine-cytidine kinase-like, transcript variant X3
uridine-cytidine kinase-like, transcript variant X2
uridine-cytidine kinase-like, transcript variant X1
formin-binding protein 1-like, transcript variant X1
formin-binding protein 1-like, transcript variant X5
formin-binding protein 1-like, transcript variant X2
formin-binding protein 1-like, transcript variant X6
formin-binding protein 1-like, transcript variant X3
formin-binding protein 1-like, transcript variant X4
formin-binding protein 1-like, transcript variant X7
formin-binding protein 1-like, transcript variant X8
formin-binding protein 1-like isoform X1
formin-binding protein 1-like isoform X4
formin-binding protein 1-like isoform X5
formin-binding protein 1-like isoform X2
formin-binding protein 1-like isoform X6
formin-binding protein 1-like isoform X3
formin-binding protein 1-like isoform X7
formin-binding protein 1-like isoform X8
leucine-rich repeat protein soc-2, transcript variant X1
leucine-rich repeat protein soc-2, transcript variant X2
leucine-rich repeat protein SHOC-2 isoform X1
leucine-rich repeat protein soc-2 isoform X2
rab GTPase-activating protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
rab GTPase-activating protein 1-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 19 samples with support for all annotated introns
rab GTPase-activating protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
rab GTPase-activating protein 1-like isoform X1
rab GTPase-activating protein 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
slowpoke-binding protein, 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 14 samples with support for all annotated introns
slowpoke-binding protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
transcription factor A, mitochondrial-like
myotubularin-related protein 2, transcript variant X3
myotubularin-related protein 2, transcript variant X2
myotubularin-related protein 2, transcript variant X1
myotubularin-related protein 2 isoform X3
myotubularin-related protein 2 isoform X2
myotubularin-related protein 2 isoform X1
uncharacterized LOC123271352, transcript variant X1
uncharacterized LOC123271352, 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 4 samples with support for all annotated introns
raf homolog serine/threonine-protein kinase Raf
serine/threonine-protein kinase pakG-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 20 samples with support for all annotated introns
serine/threonine-protein kinase pakG-like isoform X1
serine/threonine-protein kinase pakG-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 22 samples with support for all annotated introns
serine/threonine-protein kinase pakG-like isoform X2
peripheral plasma membrane protein CASK-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
nose resistant to fluoxetine protein 6-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 17 samples with support for all annotated introns
nose resistant to fluoxetine protein 6-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 9 samples with support for all annotated introns
nose resistant to fluoxetine protein 6-like isoform X2
nose resistant to fluoxetine protein 6-like isoform X1
nose resistant to fluoxetine protein 6-like, transcript variant X3
nose resistant to fluoxetine protein 6-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
homeobox protein 5-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
homeobox protein 5-like, transcript variant X7
homeobox protein 5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
homeobox protein 5-like, transcript variant X1
homeobox protein 5-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
homeobox protein 5-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
homeobox protein 5-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 11 samples with support for all annotated introns
dual specificity protein kinase splA-like isoform X1
dual specificity protein kinase splA-like isoform X4
dual specificity protein kinase splA-like isoform X3
uncharacterized protein LOC123272139 isoform X5
sodium/potassium-transporting ATPase subunit beta-2-like
sodium/potassium-transporting ATPase subunit beta-2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit beta-2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit beta-2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit beta-2-like isoform X1
sodium/potassium-transporting ATPase subunit beta-like isoform X2
GTPase-activating protein skywalker, transcript variant X4
GTPase-activating protein skywalker, transcript variant X6
GTPase-activating protein skywalker, transcript variant X1
GTPase-activating protein skywalker, transcript variant X7
GTPase-activating protein skywalker, transcript variant X11
GTPase-activating protein skywalker, transcript variant X9
GTPase-activating protein skywalker, transcript variant X8
GTPase-activating protein skywalker, transcript variant X10
GTPase-activating protein skywalker, transcript variant X5
GTPase-activating protein skywalker, transcript variant X2
GTPase-activating protein skywalker, transcript variant X3
GTPase-activating protein skywalker isoform X2
GTPase-activating protein skywalker isoform X1
GTPase-activating protein skywalker isoform X3
GTPase-activating protein skywalker isoform X7
GTPase-activating protein skywalker isoform X5
GTPase-activating protein skywalker isoform X4
GTPase-activating protein skywalker isoform X6
bcl-2-related ovarian killer protein homolog B-like, transcript variant X4
bcl-2-related ovarian killer protein homolog B-like, transcript variant X3
bcl-2-related ovarian killer protein homolog B-like, transcript variant X2
bcl-2-related ovarian killer protein homolog B-like, transcript variant X1
bcl-2-related ovarian killer protein homolog B-like isoform X1
bcl-2-related ovarian killer protein-like isoform X2
intraflagellar transport protein 80 homolog
multiple epidermal growth factor-like domains protein 8, 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 9 samples with support for all annotated introns
multiple epidermal growth factor-like domains protein 8, 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 10 samples with support for all annotated introns
multiple epidermal growth factor-like domains protein 8, 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 16 samples with support for all annotated introns
multiple epidermal growth factor-like domains protein 8 isoform X3
multiple epidermal growth factor-like domains protein 8 isoform X2
multiple epidermal growth factor-like domains protein 8 isoform X1
survival of motor neuron-related-splicing factor 30, transcript variant X1
survival of motor neuron-related-splicing factor 30, transcript variant X2
survival of motor neuron-related-splicing factor 30 isoform X1
survival of motor neuron-related-splicing factor 30 isoform 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 20 samples with support for all annotated introns
Down syndrome cell adhesion molecule-like protein Dscam2
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: 1 Protein
zinc finger protein GLIS3-like, transcript variant X2
zinc finger protein GLIS3-like, transcript variant X1
zinc finger protein GLIS3-like isoform X1
zinc finger protein GLIS3-like isoform X2
deoxynucleotidyltransferase terminal-interacting protein 2
uncharacterized LOC123271693, transcript variant X1
uncharacterized LOC123271693, transcript variant X2
uncharacterized protein LOC123271693 isoform X1
uncharacterized protein LOC123271693 isoform X2
gamma-aminobutyric acid type B receptor subunit 1
mediator of RNA polymerase II transcription subunit 22
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00286
uncharacterized LOC123271695, transcript variant X2
uncharacterized LOC123271695, 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 1 sample with support for all annotated introns
uncharacterized LOC123271695, transcript variant X4
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
uncharacterized LOC123271695, 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 21 samples with support for all annotated introns
uncharacterized protein LOC123271695 isoform X1
uncharacterized protein LOC123271695 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC123271401, 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 15 samples with support for all annotated introns
uncharacterized LOC123271401, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized protein LOC123271401 isoform X1
uncharacterized protein LOC123271401 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ankyrin repeat domain-containing protein 6, 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 15 samples with support for all annotated introns
ankyrin repeat domain-containing protein 6, transcript variant X1
ankyrin repeat domain-containing protein 6 isoform X1
ankyrin repeat domain-containing protein 6 isoform X2
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon UCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
homeobox protein cut-like, transcript variant X8
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
homeobox protein cut-like, transcript variant X3
homeobox protein cut-like, transcript variant X5
homeobox protein cut-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 6 samples with support for all annotated introns
homeobox protein cut-like, transcript variant X1
homeobox protein cut-like, transcript variant X7
homeobox protein cut-like, transcript variant X6
homeobox protein cut-like, transcript variant X4
piggyBac transposable element-derived protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, 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 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 15 samples with support for all annotated introns
uncharacterized protein DDB_G0281025-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 7 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 52% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123271481, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized protein LOC123271481 isoform X2
uncharacterized LOC123271481, transcript variant X2
uncharacterized LOC123271481, transcript variant X1
uncharacterized protein LOC123271481 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 3 samples with support for all annotated introns
platelet-derived growth factor receptor alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58% 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: 75% 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 11 samples with support for all annotated introns
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
ankyrin repeat domain-containing protein 50-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
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
chitooligosaccharidolytic beta-N-acetylglucosaminidase-like
RNA polymerase II-associated factor 1 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
RNA polymerase II-associated factor 1 homolog, 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 8 samples with support for all annotated introns
RNA polymerase II-associated factor 1 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RNA polymerase II-associated factor 1 homolog isoform X1
RNA polymerase II-associated factor 1 homolog isoform X2
RNA polymerase II-associated factor 1 homolog isoform X3
uncharacterized LOC123271636, transcript variant X2
uncharacterized protein LOC123271636 isoform X2
uncharacterized LOC123271636, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC123271636 isoform X1
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
A disintegrin and metalloproteinase with thrombospondin motifs 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51% coverage of the annotated genomic feature by RNAseq alignments
secreted protein C-like, transcript variant X1
secreted protein C-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123272081, transcript variant X2
uncharacterized protein LOC123272081 isoform X2
uncharacterized LOC123272081, transcript variant X1
uncharacterized protein LOC123272081 isoform X1
disintegrin and metalloproteinase domain-containing protein 7-like, transcript variant X1
zinc metalloproteinase/disintegrin VMP-II-like isoform X1
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
disintegrin and metalloproteinase domain-containing protein 7-like, transcript variant X2
disintegrin and metalloproteinase domain-containing protein 7-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
superoxide-generating NADPH oxidase heavy chain subunit C-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 9 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 20 samples with support for all annotated introns
ras-like GTP-binding protein RhoL, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
ras-like GTP-binding protein RhoL, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized LOC123271216, 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 1 sample with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 62% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123271216, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
LARGE xylosyl- and glucuronyltransferase 2-like, transcript variant X2
LARGE xylosyl- and glucuronyltransferase 2-like, transcript variant X1
LARGE xylosyl- and glucuronyltransferase 2-like, transcript variant X3
LARGE xylosyl- and glucuronyltransferase 1-like isoform X1
LARGE xylosyl- and glucuronyltransferase 1-like isoform X2
LARGE xylosyl- and glucuronyltransferase 2-like isoform X3
LARGE xylosyl- and glucuronyltransferase 2-like, transcript variant X4
LARGE xylosyl- and glucuronyltransferase 1-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 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 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
CCR4-NOT transcription complex subunit 7, transcript variant X2
CCR4-NOT transcription complex subunit 7, transcript variant X1
CCR4-NOT transcription complex subunit 7 isoform X2
CCR4-NOT transcription complex subunit 7 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 21 samples with support for all annotated introns
postacrosomal sheath WW domain-binding protein-like
putative uncharacterized protein DDB_G0282133
uncharacterized LOC123271231, transcript variant X1
uncharacterized LOC123271231, transcript variant X2
uncharacterized protein LOC123271231 isoform X1
uncharacterized protein LOC123271231 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
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 9 samples with support for all annotated introns
octopamine receptor beta-2R, transcript variant X2
octopamine receptor beta-2R, transcript variant X1
GATA zinc finger domain-containing protein 8-like, transcript variant X1
GATA zinc finger domain-containing protein 8-like, transcript variant X2
GATA zinc finger domain-containing protein 8-like
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1, transcript variant X2
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1, transcript variant X3
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 isoform X3
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 isoform X1
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 isoform X2
protein scalloped, 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 13 samples with support for all annotated introns
protein scalloped, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
protein scalloped, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
protein scalloped, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
protein scalloped, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
protein scalloped, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein scalloped, 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 11 samples with support for all annotated introns
protein scalloped, transcript variant X4
protein scalloped, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
transcriptional enhancer factor TEF-1 isoform X3
transcriptional enhancer factor TEF-1 isoform X2
transcriptional enhancer factor TEF-1 isoform X1
transcriptional enhancer factor TEF-1 isoform X5
post-GPI attachment to proteins factor 2-like, transcript variant X3
post-GPI attachment to proteins factor 2-like, transcript variant X2
post-GPI attachment to proteins factor 2-like, transcript variant X1
post-GPI attachment to proteins factor 2-like, transcript variant X4
post-GPI attachment to proteins factor 2-like
ras-related protein Rab-11A, transcript variant X1
ras-related protein Rab-11A, transcript variant X2
vacuolar protein sorting-associated protein 72 homolog
AN1-type zinc finger protein 6, transcript variant X1
AN1-type zinc finger protein 6, transcript variant X2
AN1-type zinc finger protein 6, transcript variant X4
AN1-type zinc finger protein 6, transcript variant X3
AN1-type zinc finger protein 6, transcript variant X5
juxtaposed with another zinc finger protein 1, transcript variant X1
juxtaposed with another zinc finger protein 1, transcript variant X2
juxtaposed with another zinc finger protein 1 isoform X2
juxtaposed with another zinc finger protein 1 isoform X1
ATP synthase lipid-binding protein, mitochondrial, transcript variant X1
ATP synthase lipid-binding protein, mitochondrial isoform X1
ATP synthase lipid-binding protein, mitochondrial, transcript variant X2
ATP synthase lipid-binding protein, mitochondrial, transcript variant X3
ATP synthase lipid-binding protein, mitochondrial isoform X2
carboxypeptidase D, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
carboxypeptidase D, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 50% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123271170, transcript variant X3
uncharacterized LOC123271170, transcript variant X2
uncharacterized LOC123271170, transcript variant X1
phospholipid-transporting ATPase ABCA1-like
odorant receptor 13a-like, transcript variant X2
odorant receptor 13a-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
nose resistant to fluoxetine protein 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC123271369, transcript variant X2
uncharacterized LOC123271369, transcript variant X1
uncharacterized protein LOC123271369 isoform X2
uncharacterized protein LOC123271369 isoform X1
zinc finger MYM-type protein 1-like, transcript variant X2
zinc finger MYM-type protein 1-like, transcript variant X1
uncharacterized protein LOC123271507 isoform X2
zinc finger MYM-type protein 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
mushroom body large-type Kenyon cell-specific protein 1, transcript variant X4
mushroom body large-type Kenyon cell-specific protein 1, transcript variant X5
mushroom body large-type Kenyon cell-specific protein 1, transcript variant X3
mushroom body large-type Kenyon cell-specific protein 1, transcript variant X2
mushroom body large-type Kenyon cell-specific protein 1, transcript variant X1
mushroom body large-type Kenyon cell-specific protein 1, transcript variant X6
mushroom body large-type Kenyon cell-specific protein 1 isoform X1
mushroom body large-type Kenyon cell-specific protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 41% coverage of the annotated genomic feature by RNAseq alignments
C-type lectin domain family 4 member M-like
GATA zinc finger domain-containing protein 14-like
uncharacterized LOC123271606, transcript variant X2
uncharacterized LOC123271606, 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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123271288, transcript variant X2
uncharacterized LOC123271288, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC123271280, transcript variant X4
uncharacterized LOC123271280, transcript variant X3
uncharacterized LOC123271280, transcript variant X1
uncharacterized LOC123271280, transcript variant X2
putative ankyrin repeat protein RF_0381, transcript variant X2
putative ankyrin repeat protein RF_0381, 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
putative ankyrin repeat protein RF_0381, transcript variant X4
putative ankyrin repeat protein RF_0381, transcript variant X3
uncharacterized LOC123271290, transcript variant X1
uncharacterized LOC123271290, transcript variant X2
uncharacterized LOC123271290, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68% coverage of the annotated genomic feature by RNAseq alignments
branched-chain-amino-acid aminotransferase, cytosolic, transcript variant X1
branched-chain-amino-acid aminotransferase, cytosolic, transcript variant X4
branched-chain-amino-acid aminotransferase, cytosolic, transcript variant X3
branched-chain-amino-acid aminotransferase, cytosolic, transcript variant X2
branched-chain-amino-acid aminotransferase, cytosolic
uncharacterized LOC123271283, transcript variant X1
uncharacterized LOC123271283, transcript variant X2
uncharacterized protein LOC123271283 isoform X1
uncharacterized protein LOC123271283 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88% coverage of the annotated genomic feature by RNAseq alignments
putative uncharacterized protein DDB_G0282129
similar to RNA sequence (same species):INSD:GDJO01033756.1
annotated by transcript or proteomic data
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 480 bases not found in genome assembly; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 123 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC123271396, transcript variant X1
uncharacterized LOC123271396, transcript variant X2
uncharacterized LOC123271396, transcript variant X3
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 5% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
coiled-coil domain-containing protein R3HCC1L, transcript variant X1
coiled-coil domain-containing protein R3HCC1L isoform X1
coiled-coil domain-containing protein R3HCC1L, transcript variant X2
coiled-coil domain-containing protein R3HCC1L isoform X2
signal recognition particle subunit SRP72
protein fem-1 homolog A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
protein fem-1 homolog A, 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 10 samples with support for all annotated introns
protein fem-1 homolog A, 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
head-specific guanylate cyclase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
head-specific guanylate cyclase, transcript variant X1
head-specific guanylate cyclase, transcript variant X2
uncharacterized LOC123271502, transcript variant X2
uncharacterized LOC123271502, transcript variant X1
probable serine/threonine-protein kinase drkB
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% 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: 3 Proteins, and 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: 71% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized threonine-rich GPI-anchored glycoprotein PJ4664.02-like, transcript variant X1
uncharacterized threonine-rich GPI-anchored glycoprotein PJ4664.02-like, transcript variant X2
uncharacterized threonine-rich GPI-anchored glycoprotein PJ4664.02-like, transcript variant X3
uncharacterized threonine-rich GPI-anchored glycoprotein PJ4664.02-like isoform X2
uncharacterized protein PB18E9.04c-like isoform X3
guanylate cyclase soluble subunit beta-1
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; deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: guanylate cyclase soluble subunit beta-1
ankyrin repeat and SOCS box protein 17, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ankyrin repeat and SOCS box protein 17, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein LOC123271560 isoform X1
ankyrin repeat and SOCS box protein 17 isoform X2
putative uncharacterized protein DDB_G0279653, 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
putative uncharacterized protein DDB_G0279653, 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 20 samples with support for all annotated introns
putative uncharacterized protein DDB_G0279653 isoform X1
putative uncharacterized protein DDB_G0279653 isoform X2
uncharacterized LOC123271557, transcript variant X1
uncharacterized LOC123271557, transcript variant X2
uncharacterized protein LOC123271557 isoform X1
uncharacterized protein LOC123271557 isoform X2
uncharacterized LOC123271558, transcript variant X2
uncharacterized LOC123271558, transcript variant X1
uncharacterized protein LOC123271558 isoform X2
uncharacterized protein LOC123271558 isoform X1
uncharacterized LOC123271558, transcript variant X3
uncharacterized protein LOC123271558 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
similar to RNA sequence (same species):INSD:GDJO01007547.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1008 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 633 bases not found in genome assembly; 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: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123271834, transcript variant X1
uncharacterized LOC123271834, transcript variant X2
uncharacterized LOC123271896, transcript variant X3
uncharacterized LOC123271896, transcript variant X1
uncharacterized LOC123271896, transcript variant X4
uncharacterized LOC123271896, transcript variant X2
uncharacterized protein LOC123271896 isoform X1
uncharacterized protein LOC123271896 isoform X3
uncharacterized protein LOC123271896 isoform X4
uncharacterized protein LOC123271896 isoform X2
growth arrest-specific protein 2-like, transcript variant X4
growth arrest-specific protein 2-like, transcript variant X5
growth arrest-specific protein 2-like, transcript variant X7
growth arrest-specific protein 2-like, transcript variant X6
growth arrest-specific protein 2-like, transcript variant X2
growth arrest-specific protein 2-like, transcript variant X3
growth arrest-specific protein 2-like, transcript variant X8
growth arrest-specific protein 2-like, transcript variant X1
growth arrest-specific protein 2-like, transcript variant X9
growth arrest-specific protein 2-like isoform X3
growth arrest-specific protein 2-like isoform X2
growth arrest-specific protein 2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments
polyphosphoinositide phosphatase, transcript variant X1
polyphosphoinositide phosphatase, transcript variant X2
polyphosphoinositide phosphatase isoform X1
polyphosphoinositide phosphatase isoform X2
N-alpha-acetyltransferase 15, NatA auxiliary subunit
probable serine/threonine-protein kinase DDB_G0275165, transcript variant X2
probable serine/threonine-protein kinase DDB_G0275165, transcript variant X1
probable serine/threonine-protein kinase DDB_G0275165 isoform X1
probable serine/threonine-protein kinase DDB_G0275165 isoform X2
synaptic vesicle glycoprotein 2B-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 7 samples with support for all annotated introns
synaptic vesicle glycoprotein 2B-like, transcript variant X4
synaptic vesicle glycoprotein 2B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
synaptic vesicle glycoprotein 2B-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
synaptic vesicle glycoprotein 2B-like, transcript variant X3
synaptic vesicle glycoprotein 2B-like isoform X4
synaptic vesicle glycoprotein 2B-like isoform X1
synaptic vesicle glycoprotein 2B-like isoform X5
synaptic vesicle glycoprotein 2B-like isoform X2
synaptic vesicle glycoprotein 2B-like isoform X3
G2/mitotic-specific cyclin-B3, transcript variant X1
G2/mitotic-specific cyclin-B3, transcript variant X2
G2/mitotic-specific cyclin-B3 isoform X1
G2/mitotic-specific cyclin-B3, 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 17 samples with support for all annotated introns
G2/mitotic-specific cyclin-B3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 10 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, including 7 samples with support for all annotated introns
uncharacterized LOC123271889, transcript variant X2
uncharacterized LOC123271889, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC123271889, transcript variant X4
uncharacterized LOC123271889, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 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: 98% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GDJO01016392.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 611 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 192 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
rho-related BTB domain-containing protein 1, transcript variant X1
rho-related BTB domain-containing 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 18 samples with support for all annotated introns
rho-related BTB domain-containing protein 1, transcript variant X2
rho-related BTB domain-containing protein 1, 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
rho-related BTB domain-containing protein 1 isoform X1
rho-related BTB domain-containing protein 1 isoform X2
rho-related BTB domain-containing protein 1, 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
rho-related BTB domain-containing protein 1 isoform X3
7-methylguanosine phosphate-specific 5'-nucleotidase-like, transcript variant X2
7-methylguanosine phosphate-specific 5'-nucleotidase-like, transcript variant X3
7-methylguanosine phosphate-specific 5'-nucleotidase-like, transcript variant X1
7-methylguanosine phosphate-specific 5'-nucleotidase-like
muscle-specific protein 20, transcript variant X1
muscle-specific protein 20, 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 12 samples with support for all annotated introns
muscle LIM protein Mlp84B, transcript variant X3
muscle LIM protein Mlp84B, transcript variant X1
muscle LIM protein Mlp84B, transcript variant X2
paired mesoderm homeobox protein 2A-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 1 sample with support for all annotated introns
paired mesoderm homeobox protein 2A-like, transcript variant X2
paired mesoderm homeobox protein 2A-like
39S ribosomal protein L21, mitochondrial, transcript variant X2
39S ribosomal protein L21, mitochondrial, transcript variant X1
39S ribosomal protein L21, mitochondrial
E3 ubiquitin-protein ligase TRIM33-like, transcript variant X3
E3 ubiquitin-protein ligase TRIM33-like, transcript variant X6
E3 ubiquitin-protein ligase TRIM33-like, transcript variant X1
E3 ubiquitin-protein ligase TRIM33-like, transcript variant X4
E3 ubiquitin-protein ligase TRIM33-like, transcript variant X5
E3 ubiquitin-protein ligase TRIM33-like, transcript variant X2
transcription intermediary factor 1-alpha-like isoform X1
transcription intermediary factor 1-alpha-like isoform X2
transcription intermediary factor 1-alpha-like isoform X3
E3 ubiquitin-protein ligase TRIM33-like isoform X4
E3 ubiquitin-protein ligase TRIM33-like isoform X5
RNA cytidine acetyltransferase, transcript variant X1
RNA cytidine acetyltransferase, transcript variant X2
RNA cytidine acetyltransferase isoform X1
RNA cytidine acetyltransferase isoform X2
nuclear fragile X mental retardation-interacting 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 13 samples with support for all annotated introns
nuclear fragile X mental retardation-interacting protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
nuclear fragile X mental retardation-interacting protein 1-like
protein mini spindles, transcript variant X1
protein mini spindles, transcript variant X2
soluble guanylate cyclase 88E, 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 6 samples with support for all annotated introns
soluble guanylate cyclase 88E, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
soluble guanylate cyclase 88E, transcript variant X2
soluble guanylate cyclase 88E, transcript variant X6
soluble guanylate cyclase 88E, 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 7 samples with support for all annotated introns
soluble guanylate cyclase 88E, 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
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
gamma-aminobutyric acid type B receptor subunit 2, transcript variant X2
gamma-aminobutyric acid type B receptor subunit 2, transcript variant X4
gamma-aminobutyric acid type B receptor subunit 2, transcript variant X1
gamma-aminobutyric acid type B receptor subunit 2, transcript variant X3
gamma-aminobutyric acid type B receptor subunit 2 isoform X2
gamma-aminobutyric acid type B receptor subunit 2 isoform X4
gamma-aminobutyric acid type B receptor subunit 2 isoform X1
gamma-aminobutyric acid type B receptor subunit 2 isoform X3
uncharacterized LOC123271871, transcript variant X2
uncharacterized LOC123271871, transcript variant X1
uncharacterized protein LOC123271871 isoform X1
uncharacterized protein LOC123271871 isoform X2
uncharacterized protein DDB_G0275275-like
uncharacterized LOC123271826, transcript variant X1
uncharacterized LOC123271826, transcript variant X2
uncharacterized LOC123271826, transcript variant X3
uncharacterized protein LOC123271826 isoform X1
uncharacterized protein LOC123271826 isoform X2
uncharacterized LOC123271826, transcript variant X4
uncharacterized protein LOC123271826 isoform X3
leukocyte elastase inhibitor, transcript variant X2
leukocyte elastase inhibitor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
serine/threonine-protein kinase Tao, transcript variant X2
serine/threonine-protein kinase Tao, transcript variant X18
serine/threonine-protein kinase Tao, transcript variant X11
serine/threonine-protein kinase Tao, transcript variant X3
serine/threonine-protein kinase Tao, transcript variant X4
serine/threonine-protein kinase Tao, transcript variant X12
serine/threonine-protein kinase Tao, transcript variant X16
serine/threonine-protein kinase Tao, transcript variant X8
serine/threonine-protein kinase Tao, transcript variant X7
serine/threonine-protein kinase Tao, transcript variant X1
serine/threonine-protein kinase Tao, transcript variant X15
serine/threonine-protein kinase Tao, transcript variant X9
serine/threonine-protein kinase Tao, transcript variant X6
serine/threonine-protein kinase Tao, transcript variant X17
serine/threonine-protein kinase Tao, transcript variant X10
serine/threonine-protein kinase Tao, transcript variant X19
serine/threonine-protein kinase Tao, transcript variant X13
serine/threonine-protein kinase Tao, transcript variant X5
serine/threonine-protein kinase Tao, transcript variant X20
serine/threonine-protein kinase Tao, transcript variant X14
serine/threonine-protein kinase Tao isoform X4
serine/threonine-protein kinase Tao isoform X3
serine/threonine-protein kinase Tao isoform X2
serine/threonine-protein kinase Tao isoform X1
homeobox protein Hmx, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
homeobox protein Hmx, 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC123271859, 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 11 samples with support for all annotated introns
uncharacterized LOC123271859, 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 11 samples with support for all annotated introns
uncharacterized LOC123271859, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC123271859, transcript variant X4
uncharacterized LOC123271859, 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 8 samples with support for all annotated introns
uncharacterized LOC123271859, transcript variant X6
uncharacterized protein LOC123271859 isoform X1
uncharacterized protein LOC123271859 isoform X2
uncharacterized protein LOC123271859 isoform X3
uncharacterized protein LOC123271859 isoform X4
uncharacterized protein LOC123271859 isoform X5
uncharacterized protein LOC123271859 isoform X6
uncharacterized LOC123271875, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC123271875, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 32% 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.
LOW QUALITY PROTEIN: uncharacterized protein LOC123272229
uncharacterized LOC123271888, transcript variant X2
uncharacterized LOC123271888, 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 14 samples with support for all annotated introns
uncharacterized LOC123271888, 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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
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
uncharacterized LOC123271892, 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 19 samples with support for all annotated introns
uncharacterized protein LOC123271892 isoform X1
uncharacterized LOC123271892, transcript variant X2
uncharacterized protein LOC123271892 isoform X2
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% 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: 91% coverage of the annotated genomic feature by RNAseq alignments
general odorant-binding protein 56h-like, transcript variant X1
general odorant-binding protein 56h-like, transcript variant X2
general odorant-binding protein 56h-like isoform X1
general odorant-binding protein 56h-like isoform 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67% 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
GATA zinc finger domain-containing protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized LOC123271843, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC123271843, transcript variant X2
uncharacterized LOC123271843, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC123271843, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein LOC123271843 isoform X1
uncharacterized protein LOC123271843 isoform X2
uncharacterized protein LOC123271843 isoform X3
uncharacterized protein LOC123271843 isoform X4
general odorant-binding protein 56h-like, transcript variant X3
general odorant-binding protein 56h-like, transcript variant X4
general odorant-binding protein 56h-like isoform X3
general odorant-binding protein 56h-like isoform X4
general odorant-binding protein 56h-like, transcript variant X6
uncharacterized protein LOC123271923 isoform X6
general odorant-binding protein 56h-like, transcript variant X5
uncharacterized protein LOC123271923 isoform X5
general odorant-binding protein 56d-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
putative aminopeptidase W07G4.4, 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 2 samples with support for all annotated introns
putative aminopeptidase W07G4.4, 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 6 samples with support for all annotated introns
putative aminopeptidase W07G4.4 isoform X1
putative aminopeptidase W07G4.4 isoform X2
sodium-coupled monocarboxylate transporter 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% 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: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dorsal-ventral patterning protein tolloid-like
dorsal-ventral patterning protein tolloid-like, transcript variant X2
dorsal-ventral patterning protein tolloid-like, transcript variant X1
dorsal-ventral patterning protein tolloid-like isoform X2
dorsal-ventral patterning protein tolloid-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
general transcription factor IIH subunit 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
zinc finger BED domain-containing protein 4-like, transcript variant X2
zinc finger BED domain-containing protein 4-like, transcript variant X1
zinc finger BED domain-containing protein 4-like
pyrokinin-1 receptor-like, transcript variant X2
pyrokinin-1 receptor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
adult-specific cuticular protein ACP-20-like
FHF complex subunit HOOK interacting protein 2A-like
DALR anticodon-binding domain-containing protein 3
beta-1,4-glucuronyltransferase 1, transcript variant X2
beta-1,4-glucuronyltransferase 1, transcript variant X1
2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline decarboxylase-like
membrane-bound transcription factor site-2 protease, transcript variant X1
membrane-bound transcription factor site-2 protease, transcript variant X2
membrane-bound transcription factor site-2 protease isoform X1
membrane-bound transcription factor site-2 protease isoform X2
UDP-galactose translocator, transcript variant X1
UDP-galactose translocator, 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 14 samples 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 23 samples with support for all annotated introns
methyl farnesoate epoxidase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
methyl farnesoate epoxidase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
methyl farnesoate epoxidase-like isoform X1
methyl farnesoate epoxidase-like isoform X2
cell wall integrity and stress response component 4-like
putative uncharacterized protein DDB_G0279653, transcript variant X4
putative uncharacterized protein DDB_G0279653, transcript variant X3
putative uncharacterized protein DDB_G0279653 isoform X4
putative uncharacterized protein DDB_G0279653 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 169 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: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized LOC123271272, transcript variant X2
uncharacterized LOC123271272, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
polyadenylate-binding protein-interacting protein 2, transcript variant X1
polyadenylate-binding protein-interacting protein 2, transcript variant X2
polyadenylate-binding protein-interacting protein 2
BCL2/adenovirus E1B 19 kDa protein-interacting protein 3
FHIP family protein GI14169, transcript variant X1
FHIP family protein GI14169, transcript variant X2
FHIP family protein AAEL005291 isoform X1
putative leucine-rich repeat-containing protein DDB_G0290503, transcript variant X3
putative leucine-rich repeat-containing protein DDB_G0290503, transcript variant X5
putative leucine-rich repeat-containing protein DDB_G0290503, transcript variant X4
putative leucine-rich repeat-containing protein DDB_G0290503, transcript variant X6
putative leucine-rich repeat-containing protein DDB_G0290503, transcript variant X2
putative leucine-rich repeat-containing protein DDB_G0290503, transcript variant X7
putative leucine-rich repeat-containing protein DDB_G0290503, transcript variant X8
putative leucine-rich repeat-containing protein DDB_G0290503, transcript variant X1
putative leucine-rich repeat-containing protein DDB_G0290503 isoform X2
putative leucine-rich repeat-containing protein DDB_G0290503 isoform X4
putative leucine-rich repeat-containing protein DDB_G0290503 isoform X1
putative leucine-rich repeat-containing protein DDB_G0290503 isoform X3
putative leucine-rich repeat-containing protein DDB_G0290503 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 484 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
guanine nucleotide-binding protein subunit gamma-1
required for meiotic nuclear division protein 1 homolog, transcript variant X1
required for meiotic nuclear division protein 1 homolog, transcript variant X4
required for meiotic nuclear division protein 1 homolog, transcript variant X6
required for meiotic nuclear division protein 1 homolog, transcript variant X3
required for meiotic nuclear division protein 1 homolog, transcript variant X5
required for meiotic nuclear division protein 1 homolog, transcript variant X7
required for meiotic nuclear division protein 1 homolog, transcript variant X2
required for meiotic nuclear division protein 1 homolog
glutathione synthetase-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 10 samples with support for all annotated introns
glutathione synthetase-like, transcript variant X2
ribonuclease P protein subunit p29, transcript variant X1
ribonuclease P protein subunit p29, transcript variant X2
clathrin heavy chain, transcript variant X2
clathrin heavy chain, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00535
zinc transporter 1, transcript variant X2
zinc transporter 1, transcript variant X3
zinc transporter 1, transcript variant X1
zinc transporter 1, transcript variant X5
zinc transporter 1, transcript variant X4
uncharacterized LOC123272114, transcript variant X1
uncharacterized LOC123272114, transcript variant X2
uncharacterized protein LOC123272114 isoform X1
uncharacterized protein LOC123272114 isoform X2
vascular endothelial growth factor receptor kdr-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 10 samples with support for all annotated introns
vascular endothelial growth factor receptor kdr-like, transcript variant X1
vascular endothelial growth factor receptor kdr-like isoform X1
vascular endothelial growth factor receptor kdr-like isoform X2
uncharacterized LOC123272113, transcript variant X1
uncharacterized LOC123272113, transcript variant X2
uncharacterized protein LOC123272113 isoform X2
uncharacterized protein LOC123272113 isoform X1
uncharacterized LOC123272118, transcript variant X1
uncharacterized LOC123272118, transcript variant X2
uncharacterized protein LOC123272118 isoform X2
uncharacterized protein LOC123272118 isoform X1
uncharacterized LOC123271203, transcript variant X3
uncharacterized protein LOC123271203 isoform X3
uncharacterized LOC123271203, transcript variant X2
uncharacterized LOC123271203, transcript variant X1
uncharacterized protein LOC123271203 isoform X2
uncharacterized protein LOC123271203 isoform X1
tumor necrosis factor receptor superfamily member 14-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
G protein-coupled receptor kinase 2, transcript variant X4
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
G protein-coupled receptor kinase 2, 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 11 samples with support for all annotated introns
G protein-coupled receptor kinase 2, transcript variant X1
G protein-coupled receptor kinase 2, transcript variant X2
Y+L amino acid transporter 2, transcript variant X1
Y+L amino acid transporter 2, transcript variant X3
Y+L amino acid transporter 2, transcript variant X2
large neutral amino acids transporter small subunit 1 isoform X1
dedicator of cytokinesis protein 1, transcript variant X1
dedicator of cytokinesis protein 1, transcript variant X3
dedicator of cytokinesis protein 1, transcript variant X2
dedicator of cytokinesis protein 2 isoform X1
dedicator of cytokinesis protein 1 isoform X3
dedicator of cytokinesis protein 2 isoform X2
dedicator of cytokinesis protein 1, transcript variant X4
dedicator of cytokinesis protein 2 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Fanconi anemia group D2 protein homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Fanconi anemia group D2 protein homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
myb-like protein P, transcript variant X2
myb-like protein P, transcript variant X1
myb-like protein P, transcript variant X3
DEP domain-containing protein DDB_G0279099 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
phospholipase DDHD2, transcript variant X3
phospholipase DDHD2, transcript variant X2
phospholipase DDHD2, transcript variant X1
uncharacterized LOC123271149, transcript variant X3
uncharacterized LOC123271149, transcript variant X2
uncharacterized LOC123271149, 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 12 samples with support for all annotated introns
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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
iron-sulfur cluster assembly scaffold protein IscU
cleavage and polyadenylation specificity factor subunit 6, transcript variant X2
cleavage and polyadenylation specificity factor subunit 6, transcript variant X3
cleavage and polyadenylation specificity factor subunit 6, transcript variant X1
cleavage and polyadenylation specificity factor subunit 6 isoform X2
cleavage and polyadenylation specificity factor subunit 6 isoform X3
cleavage and polyadenylation specificity factor subunit 6 isoform X1
heat shock protein Hsp-12.2, transcript variant X1
heat shock protein Hsp-12.2, transcript variant X2
heat shock protein Hsp-12.2, transcript variant X3
small heat shock protein OV25-2 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 22 samples with support for all annotated introns
speckle-type POZ protein-like, transcript variant X2
speckle-type POZ protein-like, transcript variant X1
SET and MYND domain-containing protein 4-like
SET and MYND domain-containing protein DDB_G0273589-like, transcript variant X2
SET and MYND domain-containing protein DDB_G0273589-like, transcript variant X1
SET and MYND domain-containing protein 4-like isoform X1
SET and MYND domain-containing protein DDB_G0273589-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 16 Proteins
speckle-type POZ protein B-like, transcript variant X4
speckle-type POZ protein B-like, transcript variant X3
speckle-type POZ protein B-like, transcript variant X2
speckle-type POZ protein B-like, transcript variant X1
ABC transporter G family member 23, transcript variant X3
ABC transporter G family member 23, transcript variant X1
ABC transporter G family member 23, transcript variant X2
histone-lysine N-methyltransferase, H3 lysine-79 specific-like
ABC transporter G family member 20-like, transcript variant X4
ABC transporter G family member 20-like, transcript variant X2
ABC transporter G family member 20-like, transcript variant X5
ABC transporter G family member 20-like, transcript variant X1
ABC transporter G family member 20-like, transcript variant X3
ABC transporter G family member 20-like isoform X1
ABC transporter G family member 20-like isoform X2
uncharacterized LOC123271185, transcript variant X2
uncharacterized LOC123271185, transcript variant X1
max dimerization protein 1-like, transcript variant X2
max dimerization protein 1-like, transcript variant X1
max dimerization protein 1-like isoform X1
max dimerization protein 1-like isoform X2
oxygen-dependent coproporphyrinogen-III oxidase
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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
biorientation of chromosomes in cell division protein 1-like 1
probable JmjC domain-containing histone demethylation protein 2C, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
probable JmjC domain-containing histone demethylation protein 2C, 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 4 samples with support for all annotated introns
probable JmjC domain-containing histone demethylation protein 2C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
probable JmjC domain-containing histone demethylation protein 2C, transcript variant X3
probable JmjC domain-containing histone demethylation protein 2C, transcript variant X2
probable JmjC domain-containing histone demethylation protein 2C isoform X1
probable JmjC domain-containing histone demethylation protein 2C isoform X4
uncharacterized protein LOC123271298 isoform X5
probable JmjC domain-containing histone demethylation protein 2C isoform X3
probable JmjC domain-containing histone demethylation protein 2C isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00049
protein GET1-like, transcript variant X2
protein GET1-like, transcript variant X1
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit C-like
E3 ubiquitin-protein ligase MARCHF3-like
1-phosphatidylinositol phosphodiesterase-like
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
fibroblast growth factor receptor homolog 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
fibroblast growth factor receptor homolog 1-like, 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 18 samples with support for all annotated introns
fibroblast growth factor receptor homolog 1-like, 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 10 samples with support for all annotated introns
fibroblast growth factor receptor homolog 1-like isoform X2
fibroblast growth factor receptor homolog 1-like isoform X1
DNA-directed RNA polymerase II subunit RPB2
janus kinase and microtubule-interacting protein 3-like, transcript variant X1
janus kinase and microtubule-interacting protein 3-like, transcript variant X2
janus kinase and microtubule-interacting protein 3-like, transcript variant X3
transfer RNA threonine (anticodon CGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
janus kinase and microtubule-interacting protein 3-like isoform X3
janus kinase and microtubule-interacting protein 3-like isoform X1
uncharacterized protein LOC123271241 isoform X2
U6 snRNA-associated Sm-like protein LSm1
cytoplasmic polyadenylation element-binding protein 2, transcript variant X2
cytoplasmic polyadenylation element-binding protein 2, transcript variant X1
cytoplasmic polyadenylation element-binding protein 2 isoform X2
cytoplasmic polyadenylation element-binding protein 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 160 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
U4/U6 small nuclear ribonucleoprotein Prp3
uncharacterized protein DDB_G0287625, transcript variant X4
uncharacterized protein DDB_G0287625, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized protein DDB_G0287625, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized protein DDB_G0287625, transcript variant X3
uncharacterized protein DDB_G0287625 isoform X1
uncharacterized protein DDB_G0287625 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 3 samples with support for all annotated introns
mitoferrin-1-like, transcript variant X2
mitoferrin-1-like, transcript variant X1
mitoferrin-1-like, transcript variant X3
syntaxin-binding protein 5, transcript variant X2
syntaxin-binding protein 5, transcript variant X3
syntaxin-binding protein 5, transcript variant X6
syntaxin-binding protein 5, transcript variant X4
syntaxin-binding protein 5, transcript variant X5
syntaxin-binding protein 5, transcript variant X1
syntaxin-binding protein 5, transcript variant X7
syntaxin-binding protein 5, transcript variant X8
syntaxin-binding protein 5, transcript variant X10
syntaxin-binding protein 5, transcript variant X12
syntaxin-binding protein 5, transcript variant X11
syntaxin-binding protein 5, transcript variant X9
probable oligoribonuclease, transcript variant X2
probable oligoribonuclease, 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 19 samples with support for all annotated introns
transcription initiation protein SPT3 homolog
uncharacterized LOC123272133, transcript variant X1
uncharacterized protein LOC123272133 isoform X1
uncharacterized LOC123272133, transcript variant X2
uncharacterized protein LOC123272133 isoform X2
zinc finger protein 723-like, transcript variant X1
zinc finger protein 723-like, transcript variant X2
zinc finger protein 723-like, transcript variant X4
zinc finger protein 723-like, transcript variant X3
zinc finger protein 2 homolog isoform X2
uncharacterized LOC123271804, transcript variant X2
uncharacterized LOC123271804, transcript variant X3
uncharacterized LOC123271804, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC123271804, transcript variant X1
uncharacterized protein LOC123271804 isoform X1
uncharacterized LOC123271804, transcript variant X5
uncharacterized protein LOC123271804 isoform X2
uncharacterized LOC123271810, transcript variant X1
uncharacterized protein LOC123271810 isoform X1
uncharacterized LOC123271810, transcript variant X2
uncharacterized protein LOC123271810 isoform X2
uncharacterized LOC123271808, transcript variant X4
uncharacterized LOC123271808, transcript variant X3
uncharacterized protein LOC123271808 isoform X3
uncharacterized LOC123271808, 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 4 samples with support for all annotated introns
uncharacterized LOC123271808, transcript variant X2
uncharacterized protein LOC123271808 isoform X1
uncharacterized protein LOC123271808 isoform X2
uncharacterized protein LOC123271808 isoform X4
tyrosine-protein kinase transmembrane receptor Ror, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
tyrosine-protein kinase transmembrane receptor Ror isoform X1
serine/threonine-protein kinase pakF-like, transcript variant X2
serine/threonine-protein kinase pakF-like, transcript variant X3
serine/threonine-protein kinase pakF-like, transcript variant X4
serine/threonine-protein kinase pakF-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 10 samples with support for all annotated introns
serine/threonine-protein kinase pakF-like, transcript variant X5
serine/threonine-protein kinase pakF-like isoform X1
uncharacterized protein LOC123271807 isoform X3
tyrosine-protein kinase transmembrane receptor Ror, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
tyrosine-protein kinase transmembrane receptor Ror isoform X2
nuclear hormone receptor HR96, transcript variant X3
nuclear hormone receptor HR96, transcript variant X1
nuclear hormone receptor HR96, transcript variant X2
nuclear hormone receptor HR96 isoform X2
nuclear hormone receptor HR96 isoform X1
lymphocyte cytosolic protein 2-like, transcript variant X1
lymphocyte cytosolic protein 2-like, transcript variant X2
lymphocyte cytosolic protein 2-like isoform X1
uncharacterized protein LOC123271461 isoform X2
probable serine/threonine-protein kinase nek3, transcript variant X3
probable serine/threonine-protein kinase nek3, transcript variant X2
probable serine/threonine-protein kinase nek3, transcript variant X1
uncharacterized protein LOC123271456 isoform X2
probable serine/threonine-protein kinase nek3 isoform X3
uncharacterized protein LOC123271456 isoform X1
disintegrin and metalloproteinase domain-containing protein 10-like, transcript variant X1
disintegrin and metalloproteinase domain-containing protein 10-like, transcript variant X2
disintegrin and metalloproteinase domain-containing protein 10-like isoform X1
disintegrin and metalloproteinase domain-containing protein 10-like isoform X2
crossover junction endonuclease EME1, transcript variant X4
crossover junction endonuclease EME1, transcript variant X5
crossover junction endonuclease EME1, transcript variant X1
crossover junction endonuclease EME1, transcript variant X2
crossover junction endonuclease EME1, transcript variant X6
crossover junction endonuclease EME1, transcript variant X3
crossover junction endonuclease EME1 isoform X1
crossover junction endonuclease EME1 isoform X2
KAT8 regulatory NSL complex subunit 3, transcript variant X1
KAT8 regulatory NSL complex subunit 3, transcript variant X2
KAT8 regulatory NSL complex subunit 3 isoform X2
KAT8 regulatory NSL complex subunit 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phospholipid phosphatase 5, transcript variant X1
phospholipid phosphatase 5, transcript variant X2
bromodomain-containing protein DDB_G0280777-like
guanine nucleotide exchange factor for Rab-3A-like, transcript variant X5
guanine nucleotide exchange factor for Rab-3A-like, transcript variant X1
guanine nucleotide exchange factor for Rab-3A-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 18 samples with support for all annotated introns
guanine nucleotide exchange factor for Rab-3A-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
guanine nucleotide exchange factor for Rab-3A-like, transcript variant X3
guanine nucleotide exchange factor for Rab-3A-like isoform X2
guanine nucleotide exchange factor for Rab-3A-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC123272059, 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
uncharacterized LOC123272059, transcript variant X1
centromere protein J, transcript variant X2
centromere protein J, 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 15 samples with support for all annotated introns
protein Skeletor, isoforms B/C, transcript variant X2
protein Skeletor, isoforms B/C, transcript variant X3
protein Skeletor, isoforms B/C, transcript variant X4
protein Skeletor, isoforms B/C, transcript variant X1
protein Skeletor, isoforms B/C isoform X2
protein Skeletor, isoforms B/C isoform X1
uncharacterized LOC123272110, transcript variant X5
uncharacterized LOC123272110, 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 19 samples with support for all annotated introns
uncharacterized LOC123272110, transcript variant X3
uncharacterized LOC123272110, 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 4 samples with support for all annotated introns
uncharacterized protein LOC123272110 isoform X1
uncharacterized LOC123272110, transcript variant X2
uncharacterized protein LOC123272110 isoform X2
uncharacterized protein LOC123272110 isoform X3
THO complex subunit 2, transcript variant X1
THO complex subunit 2, transcript variant X2
UHRF1-binding protein 1-like, transcript variant X1
UHRF1-binding protein 1-like, transcript variant X2
UHRF1-binding protein 1-like, transcript variant X3
MAP kinase-activating death domain protein, transcript variant X1
MAP kinase-activating death domain protein, transcript variant X2
MAP kinase-activating death domain protein isoform X1
MAP kinase-activating death domain protein isoform X2
glutamate [NMDA] receptor subunit 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 12 samples with support for all annotated introns
glutamate [NMDA] receptor subunit 1, transcript variant X1
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 12 samples with support for all annotated introns
glutamate [NMDA] receptor subunit 1 isoform X2
glutamate [NMDA] receptor subunit 1 isoform X1
lysophospholipid acyltransferase 1, transcript variant X1
lysophospholipid acyltransferase 1, transcript variant X2
lysophospholipid acyltransferase 1 isoform X1
lysophospholipid acyltransferase 1, transcript variant X3
lysophospholipid acyltransferase 2 isoform X2
rhomboid-related protein 3, transcript variant X1
rhomboid-related protein 3, transcript variant X2
rhomboid-related protein 3, transcript variant X3
rhomboid-related protein 3, transcript variant X4
uncharacterized LOC123271980, transcript variant X7
uncharacterized LOC123271980, transcript variant X6
uncharacterized LOC123271980, transcript variant X8
uncharacterized LOC123271980, transcript variant X2
uncharacterized LOC123271980, transcript variant X3
uncharacterized LOC123271980, transcript variant X4
uncharacterized LOC123271980, transcript variant X12
uncharacterized LOC123271980, transcript variant X10
uncharacterized LOC123271980, transcript variant X11
uncharacterized LOC123271980, transcript variant X9
uncharacterized LOC123271980, transcript variant X1
uncharacterized LOC123271980, transcript variant X5
uncharacterized protein LOC123271980 isoform X3
uncharacterized protein LOC123271980 isoform X4
uncharacterized protein LOC123271980 isoform X2
uncharacterized protein LOC123271980 isoform X1
uncharacterized protein LOC123271980 isoform X5
zinc finger and BTB domain-containing protein 47
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
uncharacterized LOC123271983, transcript variant X2
uncharacterized LOC123271983, transcript variant X1
39S ribosomal protein L44, mitochondrial
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 22 samples with support for all annotated introns
ankyrin repeat domain-containing protein 13C, transcript variant X2
ankyrin repeat domain-containing protein 13C, transcript variant X1
ankyrin repeat domain-containing protein 13C, transcript variant X3
ankyrin repeat domain-containing protein 13C isoform X2
ankyrin repeat domain-containing protein 13C isoform X1
zinc finger FYVE domain-containing protein 16, transcript variant X1
similar to RNA sequence (same species):INSD:GDJO01028586.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 629 bases not found in genome assembly; 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 21 samples with support for all annotated introns
zinc finger FYVE domain-containing protein 16, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 629 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
zinc finger FYVE domain-containing protein 16, transcript variant X4
zinc finger FYVE domain-containing protein 16, transcript variant X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 629 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 156 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
zinc finger FYVE domain-containing protein 16 isoform X1
zinc finger FYVE domain-containing protein 16 isoform X2
zinc finger FYVE domain-containing protein 16 isoform X3
zinc finger FYVE domain-containing protein 16 isoform X4
similar to RNA sequence (same species):INSD:GDJO01018456.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 415 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 20 bases not found in genome assembly; 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: 8 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123271212, transcript variant X2
uncharacterized LOC123271212, transcript variant X3
uncharacterized LOC123271212, 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 12 samples with support for all annotated introns
uncharacterized protein LOC123271212 isoform X3
uncharacterized protein LOC123271212 isoform X2
uncharacterized protein LOC123271212 isoform X1
C-type lectin domain family 10 member A-like, transcript variant X1
C-type lectin domain family 10 member A-like, transcript variant X2
C-type lectin domain family 10 member A-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
translation factor GUF1 homolog, mitochondrial
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 17 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 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: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
retinol-binding protein pinta-like, transcript variant X2
retinol-binding protein pinta-like, transcript variant X1
growth arrest and DNA damage-inducible proteins-interacting protein 1
bromodomain-containing protein DDB_G0270170-like
attractin-like protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
attractin-like protein 1, transcript variant X2
neurogenic protein mastermind-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 15 samples with support for all annotated introns
neurogenic protein mastermind-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 16 samples with support for all annotated introns
neurogenic protein mastermind-like isoform X1
neurogenic protein mastermind-like isoform X2
uncharacterized LOC123272300, transcript variant X2
uncharacterized LOC123272300, transcript variant X4
uncharacterized LOC123272300, transcript variant X1
uncharacterized LOC123272300, transcript variant X3
neurogenic protein mastermind-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 13 samples with support for all annotated introns
neurogenic protein mastermind-like, transcript variant X4
neurogenic protein mastermind-like isoform X3
neurogenic protein mastermind-like isoform X4
signal recognition particle 54 kDa protein
putative protein FAM10A4, transcript variant X2
putative protein FAM10A4, transcript variant X1
uncharacterized LOC123272104, transcript variant X2
uncharacterized LOC123272104, transcript variant X4
uncharacterized LOC123272104, transcript variant X3
uncharacterized LOC123272104, transcript variant X5
uncharacterized LOC123272104, transcript variant X1
uncharacterized protein LOC123272104 isoform X3
uncharacterized protein LOC123272104 isoform X2
uncharacterized protein LOC123272104 isoform X4
uncharacterized protein LOC123272104 isoform X1
uncharacterized LOC123272096, transcript variant X3
uncharacterized LOC123272096, transcript variant X1
uncharacterized LOC123272096, transcript variant X2
uncharacterized protein LOC123272096 isoform X1
uncharacterized protein LOC123272096 isoform X2
zinc finger matrin-type protein 2-like, transcript variant X2
zinc finger matrin-type protein 2-like isoform X2
zinc finger matrin-type protein 2-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 21 samples with support for all annotated introns
zinc finger matrin-type protein 2-like isoform X1
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit beta, transcript variant X2
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit beta, transcript variant X3
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit beta, transcript variant X1
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit beta, transcript variant X4
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit beta isoform X1
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit beta isoform X3
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit beta isoform X2
homocysteine S-methyltransferase-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
homocysteine S-methyltransferase-like, transcript variant X1
uncharacterized LOC123271407, transcript variant X1
uncharacterized LOC123271407, transcript variant X2
uncharacterized protein LOC123271407 isoform X1
uncharacterized protein LOC123271407 isoform X2
tyrosine-protein phosphatase 69D-like, transcript variant X2
tyrosine-protein phosphatase 69D-like, transcript variant X3
tyrosine-protein phosphatase 69D-like, transcript variant X1
tyrosine-protein phosphatase 69D-like isoform X3
tyrosine-protein phosphatase 69D-like isoform X2
tyrosine-protein phosphatase 69D-like isoform X1
uncharacterized LOC123271167, transcript variant X1
uncharacterized LOC123271167, 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 20 samples with support for all annotated introns
uncharacterized protein LOC123271167 isoform X1
uncharacterized protein LOC123271167 isoform X2
low-density lipoprotein receptor-related protein 6
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 16 samples with support for all annotated introns
probable tubulin polyglutamylase TTLL1, transcript variant X2
probable tubulin polyglutamylase TTLL1, transcript variant X1
39S ribosomal protein L23, mitochondrial
mediator of RNA polymerase II transcription subunit 7, transcript variant X2
mediator of RNA polymerase II transcription subunit 7, transcript variant X3
mediator of RNA polymerase II transcription subunit 7, transcript variant X1
mediator of RNA polymerase II transcription subunit 7, transcript variant X4
mediator of RNA polymerase II transcription subunit 7, transcript variant X5
mediator of RNA polymerase II transcription subunit 7
tyrosine-protein kinase Btk29A, transcript variant X2
tyrosine-protein kinase Btk29A, transcript variant X1
tyrosine-protein kinase Btk29A isoform X1
tyrosine-protein kinase Btk29A isoform X2
tyrosine-protein kinase Btk29A, transcript variant X3
tyrosine-protein kinase Btk29A isoform X3
uncharacterized LOC123271600, transcript variant X2
uncharacterized LOC123271600, transcript variant X1
tyrosine-protein kinase Btk29A, transcript variant X5
tyrosine-protein kinase Btk29A isoform X5
tyrosine-protein kinase Btk29A, transcript variant X4
tyrosine-protein kinase Btk29A isoform X4
tyrosine-protein kinase Btk29A, transcript variant X6
serine/threonine-protein phosphatase PGAM5, mitochondrial-like, transcript variant X3
serine/threonine-protein phosphatase PGAM5, mitochondrial-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 9 samples with support for all annotated introns
tyrosine-protein kinase Btk29A isoform X6
serine/threonine-protein phosphatase PGAM5, mitochondrial-like, transcript variant X2
serine/threonine-protein phosphatase PGAM5, mitochondrial-like
TATA box-binding protein-associated factor RNA polymerase I subunit B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
protein phosphatase PP2A 55 kDa regulatory subunit, transcript variant X2
protein phosphatase PP2A 55 kDa regulatory subunit isoform X2
protein phosphatase PP2A 55 kDa regulatory subunit, transcript variant X1
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B alpha isoform isoform X1
protein phosphatase PP2A 55 kDa regulatory subunit, transcript variant X4
protein phosphatase PP2A 55 kDa regulatory subunit isoform X4
protein phosphatase PP2A 55 kDa regulatory subunit, transcript variant X3
protein phosphatase PP2A 55 kDa regulatory subunit isoform X3
lactosylceramide 4-alpha-galactosyltransferase-like, transcript variant X2
lactosylceramide 4-alpha-galactosyltransferase-like, transcript variant X1
lactosylceramide 4-alpha-galactosyltransferase-like isoform X2
lactosylceramide 4-alpha-galactosyltransferase-like isoform X1
alpha-tocopherol transfer protein-like, transcript variant X1
alpha-tocopherol transfer protein-like, transcript variant X2
alpha-tocopherol transfer protein-like isoform X1
alpha-tocopherol transfer protein-like isoform X2
uncharacterized LOC123271419, transcript variant X1
uncharacterized LOC123271419, transcript variant X2
uncharacterized LOC123271443, transcript variant X2
uncharacterized LOC123271443, transcript variant X1
uncharacterized LOC123271443, transcript variant X3
homeobox protein EMX1-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 8 samples with support for all annotated introns
homeobox protein EMX1-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 19 samples with support for all annotated introns
uncharacterized LOC123271440, transcript variant X1
uncharacterized LOC123271440, transcript variant X3
uncharacterized LOC123271440, transcript variant X2
uncharacterized LOC123271441, transcript variant X1
uncharacterized LOC123271441, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
V-type proton ATPase subunit S1, transcript variant X2
V-type proton ATPase subunit S1, transcript variant X1
glycerol-3-phosphate acyltransferase 1, mitochondrial, transcript variant X2
glycerol-3-phosphate acyltransferase 1, mitochondrial, transcript variant X1
glycerol-3-phosphate acyltransferase 1, mitochondrial, transcript variant X3
glycerol-3-phosphate acyltransferase 1, mitochondrial isoform X1
glycerol-3-phosphate acyltransferase 1, mitochondrial isoform X2
glycerol-3-phosphate acyltransferase 1, mitochondrial isoform X3
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1-like, transcript variant X2
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1-like, transcript variant X1
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1-like, transcript variant X3
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1-like isoform X1
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1-like isoform X2
4-hydroxybutyrate coenzyme A transferase, transcript variant X1
4-hydroxybutyrate coenzyme A transferase, transcript variant X2
4-hydroxybutyrate coenzyme A transferase
brain tumor protein, transcript variant X1
brain tumor protein, transcript variant X2
sterol regulatory element-binding protein 1
ubiquitin carboxyl-terminal hydrolase 46
bifunctional glutamate/proline--tRNA ligase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 413 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
DNA polymerase epsilon catalytic subunit 1
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
bifunctional glutamate/proline--tRNA ligase, transcript variant X3
bifunctional glutamate/proline--tRNA ligase, transcript variant X4
bifunctional glutamate/proline--tRNA ligase, transcript variant X1
bifunctional glutamate/proline--tRNA ligase isoform X2
bifunctional glutamate/proline--tRNA ligase isoform X3
bifunctional glutamate/proline--tRNA ligase isoform X1
glyoxalase domain-containing protein 4, transcript variant X2
glyoxalase domain-containing protein 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC123271653, transcript variant X1
uncharacterized protein LOC123271653 isoform X1
uncharacterized LOC123271653, transcript variant X2
uncharacterized protein LOC123271653 isoform X2
splicing factor 3A subunit 2-like, transcript variant X3
splicing factor 3A subunit 2-like, transcript variant X1
splicing factor 3A subunit 2-like, transcript variant X2
splicing factor 3A subunit 2-like isoform X2
splicing factor 3A subunit 2-like isoform X3
splicing factor 3A subunit 2-like isoform X1
ATP synthase-coupling factor 6, mitochondrial
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
phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform, transcript variant X1
phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform, transcript variant X2
phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform isoform X2
phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
potassium voltage-gated channel subfamily KQT member 1-like, transcript variant X1
potassium voltage-gated channel subfamily KQT member 1-like, transcript variant X4
potassium voltage-gated channel subfamily KQT member 1-like, transcript variant X3
potassium voltage-gated channel subfamily KQT member 1-like, transcript variant X5
potassium voltage-gated channel subfamily KQT member 1-like, transcript variant X8
potassium voltage-gated channel subfamily KQT member 1-like, transcript variant X7
potassium voltage-gated channel subfamily KQT member 1-like, transcript variant X2
potassium voltage-gated channel subfamily KQT member 1-like, transcript variant X6
potassium voltage-gated channel subfamily KQT member 1-like, transcript variant X9
potassium voltage-gated channel subfamily KQT member 1-like isoform X1
potassium voltage-gated channel subfamily KQT member 1-like isoform X4
potassium voltage-gated channel subfamily KQT member 1-like isoform X3
potassium voltage-gated channel subfamily KQT member 1-like isoform X5
potassium voltage-gated channel subfamily KQT member 1-like isoform X8
potassium voltage-gated channel subfamily KQT member 1-like isoform X7
potassium voltage-gated channel subfamily KQT member 1-like isoform X2
potassium voltage-gated channel subfamily KQT member 1-like isoform X9
potassium voltage-gated channel subfamily KQT member 1-like isoform X6
uncharacterized protein DDB_G0283697, transcript variant X1
uncharacterized protein DDB_G0283697, transcript variant X2
uncharacterized protein DDB_G0283697, transcript variant X3
uncharacterized protein DDB_G0283697 isoform X1
uncharacterized protein DDB_G0283697 isoform X2
uncharacterized protein DDB_G0283697 isoform X3
4-hydroxybenzoate polyprenyltransferase, mitochondrial, transcript variant X2
4-hydroxybenzoate polyprenyltransferase, mitochondrial, transcript variant X1
4-hydroxybenzoate polyprenyltransferase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
ubiquitin thioesterase trabid, transcript variant X2
ubiquitin thioesterase trabid, transcript variant X3
ubiquitin thioesterase trabid, transcript variant X1
dihydroxyacetone phosphate acyltransferase
paired box protein Pax-1, transcript variant X1
paired box protein Pax-1, transcript variant X2
hexokinase type 2, transcript variant X1
hexokinase type 2, transcript variant X2
uncharacterized LOC123272128, transcript variant X1
uncharacterized LOC123272128, transcript variant X2
uncharacterized LOC123272128, transcript variant X3
Hermansky-Pudlak syndrome 1 protein homolog
probable sodium/potassium/calcium exchanger CG1090, transcript variant X1
probable sodium/potassium/calcium exchanger CG1090, transcript variant X2
probable sodium/potassium/calcium exchanger CG1090, transcript variant X3
probable sodium/potassium/calcium exchanger CG1090 isoform X1
probable sodium/potassium/calcium exchanger CG1090 isoform X2
uncharacterized LOC123272119, transcript variant X1
uncharacterized LOC123272119, transcript variant X2
uncharacterized protein LOC123272119 isoform X1
uncharacterized protein LOC123272119 isoform X2
myosin regulatory light chain 2, transcript variant X1
myosin regulatory light chain 2, transcript variant X3
myosin regulatory light chain 2 isoform X1
myosin regulatory light chain 2 isoform X3
myosin regulatory light chain 2, transcript variant X2
myosin regulatory light chain 2 isoform X2
probable phospholipid hydroperoxide glutathione peroxidase, transcript variant X3
probable phospholipid hydroperoxide glutathione peroxidase, transcript variant X2
probable phospholipid hydroperoxide glutathione peroxidase, transcript variant X1
probable phospholipid hydroperoxide glutathione peroxidase isoform X1
probable phospholipid hydroperoxide glutathione peroxidase isoform 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 20 samples with support for all annotated introns
piggyBac transposable element-derived protein 4-like
transcriptional activator protein Pur-beta, transcript variant X1
transcriptional activator protein Pur-beta, transcript variant X3
transcriptional activator protein Pur-beta, transcript variant X2
transcriptional activator protein Pur-beta isoform X1
transcriptional activator protein Pur-beta isoform X3
transcriptional activator protein Pur-beta isoform X2
uncharacterized LOC123272046, transcript variant X5
uncharacterized LOC123272046, transcript variant X4
uncharacterized LOC123272046, transcript variant X3
uncharacterized LOC123272046, transcript variant X7
uncharacterized LOC123272046, transcript variant X1
uncharacterized LOC123272046, transcript variant X6
uncharacterized LOC123272046, transcript variant X2
uncharacterized protein LOC123272046 isoform X5
uncharacterized protein LOC123272046 isoform X3
uncharacterized protein LOC123272046 isoform X2
uncharacterized protein LOC123272046 isoform X4
uncharacterized protein LOC123272046 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 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
polycomb protein Scm, transcript variant X2
polycomb protein Scm, transcript variant X1
equilibrative nucleoside transporter 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
equilibrative nucleoside transporter 1 isoform X1
equilibrative nucleoside transporter 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
equilibrative nucleoside transporter 1 isoform X2
C-terminal-binding protein, transcript variant X3
C-terminal-binding protein, transcript variant X1
C-terminal-binding protein, transcript variant X2
protein glass-like, transcript variant X5
protein glass-like, transcript variant X1
protein glass-like, transcript variant X4
protein glass-like, transcript variant X3
protein glass-like, transcript variant X2
protein glass-like, transcript variant X6
protein glass-like, transcript variant X7
ATP-binding cassette sub-family D member, 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, including 5 samples with support for all annotated introns
ATP-binding cassette sub-family D member, transcript variant X1
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, including 22 samples with support for all annotated introns
ATP-binding cassette sub-family D member
osmotic avoidance abnormal protein 3-like, transcript variant X2
osmotic avoidance abnormal protein 3-like, transcript variant X1
osmotic avoidance abnormal protein 3-like, transcript variant X3
osmotic avoidance abnormal protein 3-like isoform X1
osmotic avoidance abnormal protein 3-like isoform X2
cytochrome c oxidase assembly factor 7 homolog
zinc finger protein GLI2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein GLI2-like, transcript variant X1
zinc finger protein GLI2-like isoform X1
zinc finger protein GLI2-like isoform X2
cytoplasmic dynein 2 intermediate chain 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 6, transcript variant X1
major facilitator superfamily domain-containing protein 6, transcript variant X2
major facilitator superfamily domain-containing protein 6 isoform X1
major facilitator superfamily domain-containing protein 6 isoform X2
probable DNA-directed RNA polymerases I and III subunit RPAC2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
actin-binding LIM protein 2, transcript variant X3
actin-binding LIM protein 2, transcript variant X9
actin-binding LIM protein 2, transcript variant X1
actin-binding LIM protein 2, transcript variant X4
actin-binding LIM protein 2, transcript variant X2
actin-binding LIM protein 2, transcript variant X5
actin-binding LIM protein 2, transcript variant X6
actin-binding LIM protein 2, transcript variant X10
actin-binding LIM protein 2, transcript variant X7
actin-binding LIM protein 2, transcript variant X11
actin-binding LIM protein 2, transcript variant X8
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
facilitated trehalose transporter Tret1-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
serine/threonine-protein kinase 32A-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 3 samples with support for all annotated introns
serine/threonine-protein kinase 32A-like, transcript variant X1
serine/threonine-protein kinase 32A-like, transcript variant X7
serine/threonine-protein kinase 32A-like, transcript variant X4
serine/threonine-protein kinase 32A-like, transcript variant X6
serine/threonine-protein kinase 32A-like, transcript variant X3
serine/threonine-protein kinase 32A-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
serine/threonine-protein kinase 32A-like
methenyltetrahydrofolate synthase domain-containing 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
methenyltetrahydrofolate synthase domain-containing protein, transcript variant X2
methenyltetrahydrofolate synthase domain-containing protein isoform X1
methenyltetrahydrofolate synthase domain-containing protein isoform X2
isocitrate dehydrogenase [NAD] subunit beta, mitochondrial
vesicle transport protein SEC20, 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 21 samples with support for all annotated introns
vesicle transport protein SEC20, transcript variant X1
vesicle transport protein SEC20 isoform X1
vesicle transport protein SEC20 isoform X2
phosphoinositide 3-kinase regulatory subunit 4, 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 17 samples with support for all annotated introns
phosphoinositide 3-kinase regulatory subunit 4, transcript variant X1
phosphoinositide 3-kinase regulatory subunit 4 isoform X1
phosphoinositide 3-kinase regulatory subunit 4 isoform X2
insulin-like growth factor-binding protein complex acid labile subunit, 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 2 samples with support for all annotated introns
insulin-like growth factor-binding protein complex acid labile subunit, 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 16 samples with support for all annotated introns
insulin-like growth factor-binding protein complex acid labile subunit isoform 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 17 samples with support for all annotated introns
vacuolar protein sorting-associated protein 51 homolog
nucleolar GTP-binding protein 2, transcript variant X1
nucleolar GTP-binding protein 2, transcript variant X2
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9, transcript variant X2
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9, transcript variant X1
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9
probable protein arginine N-methyltransferase 6
choline/ethanolaminephosphotransferase 1, transcript variant X3
choline/ethanolaminephosphotransferase 1, transcript variant X5
choline/ethanolaminephosphotransferase 1, transcript variant X1
choline/ethanolaminephosphotransferase 1, transcript variant X6
choline/ethanolaminephosphotransferase 1, transcript variant X4
choline/ethanolaminephosphotransferase 1, transcript variant X2
choline/ethanolaminephosphotransferase 1 isoform X2
choline/ethanolaminephosphotransferase 1 isoform X1
choline/ethanolaminephosphotransferase 1 isoform X4
mediator of RNA polymerase II transcription subunit 21, transcript variant X2
mediator of RNA polymerase II transcription subunit 21, 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 23 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 21
histone-lysine N-methyltransferase SETD1, transcript variant X1
histone-lysine N-methyltransferase SETD1, transcript variant X2
histone-lysine N-methyltransferase SETD1, transcript variant X3
histone-lysine N-methyltransferase SETD1
cytochrome b-c1 complex subunit 6, mitochondrial, transcript variant X1
cytochrome b-c1 complex subunit 6, mitochondrial, transcript variant X2
cytochrome b-c1 complex subunit 6, mitochondrial, transcript variant X3
cytochrome b-c1 complex subunit 6, mitochondrial
uncharacterized LOC123271551, transcript variant X1
uncharacterized LOC123271551, 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 21 samples with support for all annotated introns
uncharacterized LOC123271551, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC123271533, transcript variant X2
uncharacterized LOC123271533, transcript variant X1
uncharacterized protein LOC123271533 isoform X1
uncharacterized LOC123271533, transcript variant X3
uncharacterized protein LOC123271533 isoform X2
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84% coverage of the annotated genomic feature by RNAseq alignments
golgin subfamily A member 6-like protein 22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123271534, transcript variant X2
uncharacterized protein LOC123271534 isoform X2
uncharacterized LOC123271534, transcript variant X1
uncharacterized protein LOC123271534 isoform X1
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transcription factor IIIB 90 kDa subunit-like
glucose dehydrogenase [FAD, quinone]-like
glucose dehydrogenase [FAD, quinone], transcript variant X2
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 3 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone], transcript variant X1
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 10 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 17 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone], transcript variant X3
glucose dehydrogenase [FAD, quinone] isoform X1
glucose dehydrogenase [FAD, quinone] isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone]-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 7 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone]-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone]-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone]-like isoform X2
glucose dehydrogenase [FAD, quinone]-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone], transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glucose dehydrogenase [FAD, quinone], transcript variant X4
glucose dehydrogenase [FAD, quinone], transcript variant X5
la-related protein 1, transcript variant X1
la-related protein 1, transcript variant X2
la-related protein 1, transcript variant X4
la-related protein 1, transcript variant X3
heart- and neural crest derivatives-expressed protein 2-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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
DENN domain-containing protein 5B, transcript variant X2
DENN domain-containing protein 5B, transcript variant X1
DENN domain-containing protein 5B, transcript variant X3
DENN domain-containing protein 5B, transcript variant X4
DENN domain-containing protein 5B isoform X2
DENN domain-containing protein 5B isoform X4
DENN domain-containing protein 5B isoform X1
DENN domain-containing protein 5B isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 3 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transcription initiation factor TFIID subunit 9-like
adenylate cyclase type 9, 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 9 samples with support for all annotated introns
adenylate cyclase type 9, 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 13 samples with support for all annotated introns
adenylate cyclase type 9, 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 8 samples with support for all annotated introns
uncharacterized LOC123271589, transcript variant X3
uncharacterized LOC123271589, transcript variant X5
uncharacterized LOC123271589, transcript variant X2
uncharacterized LOC123271589, transcript variant X4
uncharacterized LOC123271589, transcript variant X1
POU domain, class 4, transcription factor 2-like, transcript variant X2
POU domain, class 4, transcription factor 2-like, transcript variant X6
POU domain, class 4, transcription factor 2-like, transcript variant X5
POU domain, class 4, transcription factor 2-like, transcript variant X3
POU domain, class 4, transcription factor 2-like, transcript variant X4
POU domain, class 4, transcription factor 2-like, transcript variant X1
POU domain, class 4, transcription factor 2-like
splicing factor YJU2, transcript variant X2
splicing factor YJU2, transcript variant X1
uncharacterized protein PFB0145c-like, transcript variant X2
uncharacterized protein PFB0145c-like isoform X2
uncharacterized protein PFB0145c-like, transcript variant X1
uncharacterized protein PFB0145c-like isoform X1
uncharacterized LOC123272023, transcript variant X2
uncharacterized LOC123272023, transcript variant X1
uncharacterized protein LOC123272023 isoform X2
uncharacterized protein LOC123272023 isoform X1
E3 ubiquitin-protein ligase Os04g0590900-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
E3 ubiquitin-protein ligase Os04g0590900-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 23 samples with support for all annotated introns
E3 ubiquitin-protein ligase Os04g0590900-like
octopamine receptor beta-3R-like, transcript variant X1
octopamine receptor beta-3R-like, transcript variant X2
tetratricopeptide repeat protein 5-like, transcript variant X2
tetratricopeptide repeat protein 5-like, transcript variant X1
tetratricopeptide repeat protein 5-like isoform X1
tetratricopeptide repeat protein 5-like isoform X2
probable cytochrome P450 301a1, mitochondrial, transcript variant X2
probable cytochrome P450 301a1, mitochondrial, transcript variant X1
probable cytochrome P450 301a1, mitochondrial, transcript variant X3
probable cytochrome P450 301a1, mitochondrial
deaminated glutathione amidase, transcript variant X1
deaminated glutathione amidase, transcript variant X2
deaminated glutathione amidase isoform X1
deaminated glutathione amidase isoform X2
nucleoporin Nup37, transcript variant X1
nucleoporin Nup37, transcript variant X2
oxysterol-binding protein-related protein 8, transcript variant X1
oxysterol-binding protein-related protein 8, transcript variant X2
oxysterol-binding protein-related protein 8, transcript variant X3
oxysterol-binding protein-related protein 8, transcript variant X4
oxysterol-binding protein-related protein 8, transcript variant X6
oxysterol-binding protein-related protein 8, transcript variant X11
oxysterol-binding protein-related protein 8, transcript variant X7
oxysterol-binding protein-related protein 8, transcript variant X8
oxysterol-binding protein-related protein 8, transcript variant X9
oxysterol-binding protein-related protein 8, transcript variant X10
oxysterol-binding protein-related protein 8 isoform X1
oxysterol-binding protein-related protein 8 isoform X3
oxysterol-binding protein-related protein 8 isoform X4
oxysterol-binding protein-related protein 8 isoform X6
oxysterol-binding protein-related protein 8 isoform X7
oxysterol-binding protein-related protein 8 isoform X8
oxysterol-binding protein-related protein 8 isoform X9
oxysterol-binding protein-related protein 8 isoform X10
oxysterol-binding protein-related protein 8 isoform X2
oxysterol-binding protein-related protein 8, transcript variant X5
oxysterol-binding protein-related protein 8 isoform X5
organic cation transporter protein-like, transcript variant X2
organic cation transporter protein-like, transcript variant X1
organic cation transporter protein-like isoform X2
organic cation transporter protein-like isoform X1
mediator of RNA polymerase II transcription subunit 31
fat-like cadherin-related tumor suppressor homolog, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
fat-like cadherin-related tumor suppressor homolog, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
fat-like cadherin-related tumor suppressor homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
fat-like cadherin-related tumor suppressor homolog, transcript variant X2
fat-like cadherin-related tumor suppressor homolog, transcript variant X3
fat-like cadherin-related tumor suppressor homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
fat-like cadherin-related tumor suppressor homolog isoform X6
fat-like cadherin-related tumor suppressor homolog isoform X4
fat-like cadherin-related tumor suppressor homolog isoform X2
fat-like cadherin-related tumor suppressor homolog isoform X3
fat-like cadherin-related tumor suppressor homolog isoform X5
fat-like cadherin-related tumor suppressor homolog isoform X1
heat shock protein 75 kDa, mitochondrial
ankyrin repeat and sterile alpha motif domain-containing protein 1B, transcript variant X7
ankyrin repeat and sterile alpha motif domain-containing protein 1B, transcript variant X6
ankyrin repeat and sterile alpha motif domain-containing protein 1B, transcript variant X5
ankyrin repeat and sterile alpha motif domain-containing protein 1B, transcript variant X3
ankyrin repeat and sterile alpha motif domain-containing protein 1B, transcript variant X2
ankyrin repeat and sterile alpha motif domain-containing protein 1B, transcript variant X4
ankyrin repeat and sterile alpha motif domain-containing protein 1B, transcript variant X1
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X7
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X6
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X5
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X3
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X2
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X4
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X1
transmembrane 7 superfamily member 3-like
paired box protein Pax-6, transcript variant X2
paired box protein Pax-6, transcript variant X1