Colias croceus chromosome 6, ilColCroc2.1.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Papilionoidea; Pieridae; Coliadinae; Colias.
REFSEQ INFORMATION: The reference sequence is identical to\nHG991964.1.\nAssembly name: ilColCroc2.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2021/02/16.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Colias croceus 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.
COORDINATES: polyA evidence [ECO:0006239]
solute carrier family 35 member E1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
iron-sulfur clusters transporter ABCB7, mitochondrial, transcript variant X1
iron-sulfur clusters transporter ABCB7, mitochondrial, transcript variant X2
iron-sulfur clusters transporter ABCB7, mitochondrial isoform X1
iron-sulfur clusters transporter ABCB7, mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 87% 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 50% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% 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: 11 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
protein vestigial, transcript variant X1
protein vestigial, transcript variant X3
protein vestigial, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
mitotic spindle assembly checkpoint protein MAD2A
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
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: 6 Proteins, and 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
netrin receptor UNC5B-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 7 samples with support for all annotated introns
netrin receptor UNC5B-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 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 34% coverage of the annotated genomic feature by RNAseq alignments
interferon-related developmental regulator 1
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
glucose-induced degradation protein 8-B homolog
spermine synthase, transcript variant X1
spermine synthase, transcript variant X2
eukaryotic translation initiation factor 4E1-like
X-linked retinitis pigmentosa GTPase regulator-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 1 sample with support for all annotated introns
X-linked retinitis pigmentosa GTPase regulator-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 1 sample with support for all annotated introns
X-linked retinitis pigmentosa GTPase regulator-like isoform X1
X-linked retinitis pigmentosa GTPase regulator-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
four and a half LIM domains protein 2, transcript variant X4
four and a half LIM domains protein 2 isoform X4
uncharacterized LOC123692882, transcript variant X2
uncharacterized LOC123692882, transcript variant X1
four and a half LIM domains protein 2, transcript variant X3
LIM domain-containing protein unc-97 isoform X3
four and a half LIM domains protein 2, transcript variant X9
four and a half LIM domains protein 2, transcript variant X8
four and a half LIM domains protein 2, transcript variant X1
four and a half LIM domains protein 2, transcript variant X2
transforming growth factor beta-1-induced transcript 1 protein isoform X2
four and a half LIM domains protein 2, transcript variant X5
four and a half LIM domains protein 2, transcript variant X6
four and a half LIM domains protein 2 isoform X5
four and a half LIM domains protein 2, transcript variant X7
four and a half LIM domains protein 2 isoform X6
four and a half LIM domains protein 2 isoform X7
four and a half LIM domains protein 2, transcript variant X10
four and a half LIM domains protein 2 isoform X8
uracil phosphoribosyltransferase homolog
elongation of very long chain fatty acids protein 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
glutamate synthase [NADH], amyloplastic, 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 13 samples with support for all annotated introns
glutamate synthase [NADH], amyloplastic, 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 4 samples with support for all annotated introns
glutamate synthase [NADH], amyloplastic isoform X2
glutamate synthase [NADH], amyloplastic isoform X1
all trans-polyprenyl-diphosphate synthase PDSS2
DNA N6-methyl adenine demethylase, transcript variant X1
DNA N6-methyl adenine demethylase, transcript variant X2
DNA N6-methyl adenine demethylase isoform X1
DNA N6-methyl adenine demethylase isoform X2
phosphatidate cytidylyltransferase, photoreceptor-specific
rho GTPase-activating protein gacK, transcript variant X2
rho GTPase-activating protein gacK, transcript variant X1
rho GTPase-activating protein gacK isoform X2
rho GTPase-activating protein gacK isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 15% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
pre-rRNA-processing protein TSR1 homolog
protein transport protein Sec61 subunit alpha
ATP-binding cassette sub-family D member 3, transcript variant X1
ATP-binding cassette sub-family D member 3, transcript variant X2
ATP-binding cassette sub-family D member 3 isoform X1
ATP-binding cassette sub-family D member 3 isoform X2
uncharacterized LOC123692441, transcript variant X3
uncharacterized LOC123692441, transcript variant X2
uncharacterized LOC123692441, transcript variant X4
uncharacterized LOC123692441, 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 19 samples with support for all annotated introns
uncharacterized LOC123692784, transcript variant X1
uncharacterized LOC123692784, transcript variant X2
uncharacterized protein LOC123692784 isoform X1
uncharacterized protein LOC123692784 isoform X2
guanine nucleotide-binding protein-like 3 homolog
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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
5'-3' exoribonuclease 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
5'-3' exoribonuclease 1, 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
nuclear transcription factor Y subunit B-3
ATP-binding cassette sub-family G member 5
ATP-binding cassette sub-family G member 8
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
spermatogenesis-associated protein 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
spermatogenesis-associated protein 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
spermatogenesis-associated protein 6 isoform X2
spermatogenesis-associated protein 6 isoform X1
cystinosin homolog, 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 17 samples with support for all annotated introns
cystinosin homolog, transcript variant X3
cystinosin homolog, transcript variant X1
cystinosin homolog, transcript variant X5
cystinosin homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
facilitated trehalose transporter Tret1-2 homolog, transcript variant X3
facilitated trehalose transporter Tret1-2 homolog isoform 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 9 samples with support for all annotated introns
facilitated trehalose transporter Tret1-2 homolog, transcript variant X1
facilitated trehalose transporter Tret1-2 homolog isoform X1
facilitated trehalose transporter Tret1-2 homolog, transcript variant X2
facilitated trehalose transporter Tret1-2 homolog 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 5 samples with support for all annotated introns
facilitated trehalose transporter Tret1-2 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73% coverage of the annotated genomic feature by RNAseq alignments
general odorant-binding protein 70, transcript variant X1
general odorant-binding protein 70 isoform X1
general odorant-binding protein 70, transcript variant X2
general odorant-binding protein 70 isoform X2
calcium uniporter protein, mitochondrial, 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 8 samples with support for all annotated introns
calcium uniporter protein, mitochondrial, transcript variant X1
calcium uniporter protein, mitochondrial isoform X2
calcium uniporter protein, mitochondrial 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 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
V-type proton ATPase 21 kDa proteolipid subunit
protocadherin-like wing polarity protein stan
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
calcyphosin-like protein, transcript variant X1
calcyphosin-like protein, transcript variant X2
calcyphosin-like protein, transcript variant X4
calcyphosin-like protein, transcript variant X5
calcyphosin-like protein, 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 2 samples with support for all annotated introns
27 kDa glycoprotein-like, transcript variant X1
27 kDa glycoprotein-like, transcript variant X2
protein FAM13A-like, transcript variant X2
protein FAM13A-like, transcript variant X3
protein FAM13A-like, transcript variant X4
protein FAM13A-like, transcript variant X7
protein FAM13A-like, transcript variant X6
protein FAM13A-like, transcript variant X5
protein FAM13A-like, transcript variant X1
golgin subfamily A member 6-like protein 7, transcript variant X1
golgin subfamily A member 6-like protein 7, transcript variant X2
golgin subfamily A member 6-like protein 7 isoform X1
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase isoform X2
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase isoform X1
isovaleryl-CoA dehydrogenase, mitochondrial
bifunctional peptidase and arginyl-hydroxylase JMJD5
folliculin-interacting protein 2, transcript variant X1
folliculin-interacting protein 2 isoform X1
folliculin-interacting protein 2, transcript variant X2
folliculin-interacting protein 2, transcript variant X3
folliculin-interacting protein 2 isoform X2
folliculin-interacting protein 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
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
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: 11 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
cytochrome P450 4C1-like, transcript variant X1
cytochrome P450 4C1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
ubiquitin carboxyl-terminal hydrolase-like
GATA-binding factor C-like, transcript variant X3
GATA-binding factor C-like, transcript variant X2
GATA-binding factor C-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
transcription elongation factor 1 homolog, transcript variant X2
transcription elongation factor 1 homolog, transcript variant X1
transcription elongation factor 1 homolog
calcium homeostasis endoplasmic reticulum protein, transcript variant X1
calcium homeostasis endoplasmic reticulum protein isoform X1
calcium homeostasis endoplasmic reticulum protein, transcript variant X2
calcium homeostasis endoplasmic reticulum protein 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 15 samples with support for all annotated introns
bifunctional heparan sulfate N-deacetylase/N-sulfotransferase, transcript variant X1
bifunctional heparan sulfate N-deacetylase/N-sulfotransferase, transcript variant X2
bifunctional heparan sulfate N-deacetylase/N-sulfotransferase
39S ribosomal protein L47, mitochondrial
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
band 7 protein AAEL010189-like, transcript variant X3
band 7 protein AAEL010189-like, transcript variant X5
band 7 protein AAEL010189-like, transcript variant X2
band 7 protein AAEL010189-like, transcript variant X1
band 7 protein AAEL010189-like, transcript variant X4
band 7 protein AGAP004871-like isoform X3
band 7 protein AGAP004871-like isoform X2
band 7 protein AGAP004871-like isoform X5
band 7 protein AGAP004871-like isoform X1
band 7 protein AAEL010189-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
voltage-dependent calcium channel subunit alpha-2/delta-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC123692248, transcript variant X1
uncharacterized protein LOC123692248 isoform X1
uncharacterized LOC123692248, transcript variant X3
uncharacterized LOC123692248, transcript variant X2
uncharacterized protein LOC123692248 isoform X2
DNA-directed RNA polymerase II subunit RPB1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 108 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 121 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: 53 Proteins, and 96% 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: 23 Proteins
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 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 76% 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: 25 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
TBC1 domain family member 5 homolog A-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 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
chromatin modification-related protein MEAF6
osteopetrosis-associated transmembrane protein 1, transcript variant X1
osteopetrosis-associated transmembrane protein 1, transcript variant X2
osteopetrosis-associated transmembrane protein 1 isoform X1
osteopetrosis-associated transmembrane protein 1 isoform X2
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma-like
probable tRNA N6-adenosine threonylcarbamoyltransferase, mitochondrial
protein stunted-like, transcript variant X1
protein stunted-like, transcript variant X2
traB domain-containing protein-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 13 samples with support for all annotated introns
traB domain-containing protein-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
traB domain-containing protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
traB domain-containing protein-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 9 samples with support for all annotated introns
traB domain-containing protein-like isoform X1
traB domain-containing protein-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 6 samples with support for all annotated introns
traB domain-containing protein-like isoform X2
traB domain-containing protein-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 3 samples with support for all annotated introns
traB domain-containing protein-like isoform X3
elongation of very long chain fatty acids protein AAEL008004, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
elongation of very long chain fatty acids protein AAEL008004, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
elongation of very long chain fatty acids protein AAEL008004, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
elongation of very long chain fatty acids protein AAEL008004, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
elongation of very long chain fatty acids protein AAEL008004, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
elongation of very long chain fatty acids protein AAEL008004 isoform X1
elongation of very long chain fatty acids protein AAEL008004 isoform X2
elongation of very long chain fatty acids protein AAEL008004-like, transcript variant X1
elongation of very long chain fatty acids protein AAEL008004-like, transcript variant X2
elongation of very long chain fatty acids protein AAEL008004-like, transcript variant X3
elongation of very long chain fatty acids protein AAEL008004-like
elongation of very long chain fatty acids protein AAEL008004
uncharacterized LOC123692514, transcript variant X2
uncharacterized LOC123692514, transcript variant X1
uncharacterized protein LOC123692514 isoform X2
uncharacterized protein LOC123692514 isoform X1
serine/threonine-protein kinase STK11, transcript variant X1
serine/threonine-protein kinase STK11 isoform X1
serine/threonine-protein kinase STK11, 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 4 samples with support for all annotated introns
serine/threonine-protein kinase STK11 isoform X2
protein yellow-like, transcript variant X2
protein yellow-like, transcript variant X1
putative uncharacterized protein DDB_G0282133, transcript variant X2
putative uncharacterized protein DDB_G0282133, transcript variant X1
putative uncharacterized protein DDB_G0282133 isoform X2
uncharacterized protein LOC123692346 isoform X1
histone-lysine N-methyltransferase 2A-like, transcript variant X2
histone-lysine N-methyltransferase 2A-like, transcript variant X1
histone-lysine N-methyltransferase 2A-like
uncharacterized LOC123692357, transcript variant X2
uncharacterized LOC123692357, transcript variant X1
THUMP domain-containing protein 1 homolog
pancreatic lipase-related protein 2-like
calcium/calmodulin-dependent protein kinase type II alpha chain, transcript variant X1
calcium/calmodulin-dependent protein kinase type II alpha chain, transcript variant X3
calcium/calmodulin-dependent protein kinase type II alpha chain, transcript variant X2
calcium/calmodulin-dependent protein kinase type II alpha chain
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC123692849, transcript variant X1
uncharacterized LOC123692849, 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 3 samples with support for all annotated introns
uncharacterized LOC123692876, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123692876, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123692876, 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 1 sample with support for all annotated introns
uncharacterized LOC123692876, 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 3 samples with support for all annotated introns
uncharacterized LOC123692876, transcript variant X6
uncharacterized LOC123692876, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC123692876, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123692876, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123692876, 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 1 sample with support for all annotated introns
uncharacterized LOC123692876, transcript variant X1
uncharacterized protein LOC123692876 isoform X10
uncharacterized protein LOC123692876 isoform X9
uncharacterized protein LOC123692876 isoform X2
uncharacterized protein LOC123692876 isoform X8
uncharacterized protein LOC123692876 isoform X6
uncharacterized protein LOC123692876 isoform X7
uncharacterized protein LOC123692876 isoform X4
uncharacterized protein LOC123692876 isoform X5
uncharacterized protein LOC123692876 isoform X3
uncharacterized protein LOC123692876 isoform X1
multiple inositol polyphosphate phosphatase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123692341, transcript variant X1
uncharacterized LOC123692341, transcript variant X2
uncharacterized protein LOC123692341 isoform X1
uncharacterized protein LOC123692341 isoform X2
translation initiation factor eIF-2B subunit gamma
pancreatic triacylglycerol lipase-like, transcript variant X1
pancreatic triacylglycerol lipase-like, transcript variant X2
pancreatic triacylglycerol lipase-like, transcript variant X3
pancreatic triacylglycerol lipase-like isoform X1
pancreatic triacylglycerol lipase-like isoform X2
pancreatic triacylglycerol lipase-like isoform X3
39S ribosomal protein L20, mitochondrial
photoreceptor outer segment membrane glycoprotein 2-like
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
succinyl-CoA:3-ketoacid coenzyme A transferase 1, mitochondrial
rhodanese domain-containing protein CG4456-like, transcript variant X1
rhodanese domain-containing protein CG4456-like, transcript variant X2
rhodanese domain-containing protein CG4456-like isoform X2
rhodanese domain-containing protein CG4456-like isoform X1
GPN-loop GTPase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
GPN-loop GTPase 2, transcript variant X2
constitutive coactivator of PPAR-gamma-like protein 1
phosphoribosylformylglycinamidine synthase
glycine dehydrogenase (decarboxylating), mitochondrial
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
UPF0691 protein C9orf116 homolog, transcript variant X2
UPF0691 protein C9orf116 homolog, transcript variant X1
UPF0691 protein C9orf116 homolog isoform X1
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: tRNAscan-SE.
transfer RNA serine (anticodon GGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC123692542, transcript variant X2
uncharacterized LOC123692542, transcript variant X1
uncharacterized protein LOC123692542 isoform X1
uncharacterized protein LOC123692542 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
doublesex- and mab-3-related transcription factor dmd-4
peptidyl-prolyl cis-trans isomerase G-like, transcript variant X2
serine/arginine repetitive matrix protein 1-like isoform X2
peptidyl-prolyl cis-trans isomerase G-like, transcript variant X1
peptidyl-prolyl cis-trans isomerase G-like, transcript variant X3
serine/arginine repetitive matrix protein 1-like isoform X1
serine/arginine repetitive matrix protein 1-like isoform X3
peptidyl-prolyl cis-trans isomerase G-like, transcript variant X4
peptidyl-prolyl cis-trans isomerase G-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
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
protein abrupt-like, transcript variant X1
protein abrupt-like, transcript variant X3
protein abrupt-like, transcript variant X2
broad-complex core protein isoforms 1/2/3/4/5-like 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 5 samples with support for all annotated introns
protein still life, isoform SIF type 1, transcript variant X4
protein still life, isoforms C/SIF type 2 isoform X4
protein still life, isoform SIF type 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein still life, isoform SIF type 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
protein still life, isoform SIF type 1, transcript variant X1
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, including 1 sample with support for all annotated introns
protein still life, isoform SIF type 1 isoform X2
protein still life, isoform SIF type 1 isoform X1
protein still life, isoforms C/SIF type 2 isoform X3
uncharacterized LOC123692378, transcript variant X1
uncharacterized LOC123692378, transcript variant X2
uncharacterized protein LOC123692378 isoform X1
uncharacterized protein LOC123692378 isoform X2
tRNA-dihydrouridine(20a/20b) synthase [NAD(P)+]-like
programmed cell death protein 2, transcript variant X1
programmed cell death protein 2, 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 11 samples with support for all annotated introns
programmed cell death protein 2 isoform X1
programmed cell death protein 2 isoform X2
rapamycin-insensitive companion of mTOR, transcript variant X2
rapamycin-insensitive companion of mTOR, transcript variant X1
rapamycin-insensitive companion of mTOR isoform X2
rapamycin-insensitive companion of mTOR isoform X1
prothoracicotropic hormone-like, transcript variant X3
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 4 samples with support for all annotated introns
prothoracicotropic hormone-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
prothoracicotropic hormone-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 10 samples with support for all annotated introns
prothoracicotropic hormone-like isoform X3
prothoracicotropic hormone-like isoform X2
prothoracicotropic hormone-like isoform X1
zinc finger protein 626-like, transcript variant X2
zinc finger protein 626-like, transcript variant X1
zinc finger protein 626-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
general transcription factor IIE subunit 1, transcript variant X2
general transcription factor IIE subunit 1, transcript variant X1
general transcription factor IIE subunit 1 isoform X2
general transcription factor IIE subunit 1 isoform X1
tyrosine-protein kinase transmembrane receptor Ror2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 130 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
m-AAA protease-interacting protein 1, mitochondrial
lipoamide acyltransferase component of branched-chain alpha-keto acid dehydrogenase complex, mitochondrial
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, 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 8 samples with support for all annotated introns
polyamine-transporting ATPase 13A3-like, transcript variant X2
polyamine-transporting ATPase 13A3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
polyamine-transporting ATPase 13A3-like isoform X2
polyamine-transporting ATPase 13A3-like isoform X1
sodium channel protein Nach-like, transcript variant X2
sodium channel protein Nach-like, transcript variant X3
sodium channel protein Nach-like, transcript variant X1
sodium channel protein Nach-like isoform X2
sodium channel protein Nach-like isoform X1
adenylate kinase 7-like, transcript variant X1
adenylate kinase 7-like, transcript variant X2
band 4.1-like protein 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
band 4.1-like protein 5, 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 20 samples with support for all annotated introns
eukaryotic translation initiation factor 3 subunit G, transcript variant X2
eukaryotic translation initiation factor 3 subunit G, 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 20 samples with support for all annotated introns
eukaryotic translation initiation factor 3 subunit G
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
cytochrome P450 302a1, mitochondrial, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cytochrome P450 302a1, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
larval cuticle protein 65Ag1-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 8 samples with support for all annotated introns
larval cuticle protein 65Ag1-like, transcript variant X1
protein lethal(3)malignant blood neoplasm 1-like, transcript variant X1
protein lethal(3)malignant blood neoplasm 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein lethal(3)malignant blood neoplasm 1-like isoform X1
protein lethal(3)malignant blood neoplasm 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 77% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
endocuticle structural glycoprotein ABD-5-like
endocuticle structural protein SgAbd-6-like
endocuticle structural glycoprotein SgAbd-5-like
endocuticle structural glycoprotein ABD-5-like, transcript variant X3
endocuticle structural glycoprotein ABD-5-like, transcript variant X2
endocuticle structural glycoprotein ABD-5-like isoform X3
endocuticle structural glycoprotein ABD-5-like isoform X2
endocuticle structural glycoprotein ABD-5-like, transcript variant X1
endocuticle structural glycoprotein ABD-5-like isoform X1
endocuticle structural glycoprotein SgAbd-5-like, transcript variant X2
endocuticle structural glycoprotein SgAbd-5-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 13 samples with support for all annotated introns
endocuticle structural glycoprotein SgAbd-5-like isoform X2
larval cuticle protein 16/17-like isoform X1
endocuticle structural glycoprotein SgAbd-2-like
endocuticle structural glycoprotein ABD-4-like
uncharacterized LOC123692291, transcript variant X2
uncharacterized protein LOC123692291 isoform X2
uncharacterized LOC123692291, 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 10 samples with support for all annotated introns
uncharacterized protein LOC123692291 isoform X1
endocuticle structural glycoprotein ABD-4
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
uncharacterized LOC123692295, transcript variant X4
uncharacterized LOC123692295, transcript variant X5
uncharacterized LOC123692295, transcript variant X2
uncharacterized LOC123692295, transcript variant X3
uncharacterized LOC123692295, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
endocuticle structural glycoprotein SgAbd-8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
coiled-coil domain-containing protein 6, transcript variant X4
coiled-coil domain-containing protein 6, transcript variant X3
coiled-coil domain-containing protein 6, transcript variant X2
coiled-coil domain-containing protein 6, transcript variant X1
coiled-coil domain-containing protein 6 isoform X2
coiled-coil domain-containing protein 6 isoform X4
coiled-coil domain-containing protein 6 isoform X3
coiled-coil domain-containing protein 6 isoform X1
uncharacterized LOC123692853, transcript variant X1
uncharacterized LOC123692853, transcript variant X2
uncharacterized LOC123692853, transcript variant X3
uncharacterized protein LOC123692853 isoform X1
uncharacterized protein LOC123692853 isoform X2
uncharacterized protein LOC123692853 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
zinc finger matrin-type protein 2, transcript variant X1
zinc finger matrin-type protein 2, transcript variant X2
zinc finger matrin-type protein 2 isoform X2
zinc finger matrin-type protein 2 isoform X1
uncharacterized LOC123692493, transcript variant X2
uncharacterized LOC123692493, transcript variant X3
uncharacterized LOC123692493, transcript variant X1
uncharacterized protein LOC123692493 isoform X2
uncharacterized protein LOC123692493 isoform X3
uncharacterized protein LOC123692493 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 7-like
serine/threonine-protein kinase Nek8-like
cAMP-specific 3',5'-cyclic phosphodiesterase, isoforms N/G-like, transcript variant X3
cAMP-specific 3',5'-cyclic phosphodiesterase, isoforms N/G-like, transcript variant X2
cAMP-specific 3',5'-cyclic phosphodiesterase, isoforms N/G-like, transcript variant X1
cAMP-specific 3',5'-cyclic phosphodiesterase, isoforms N/G-like, transcript variant X4
cAMP-specific 3',5'-cyclic phosphodiesterase-like isoform X3
cAMP-specific 3',5'-cyclic phosphodiesterase-like isoform X2
cAMP-specific 3',5'-cyclic phosphodiesterase-like isoform X1
cAMP-specific 3',5'-cyclic phosphodiesterase, isoforms N/G-like isoform X4
uncharacterized LOC123692522, transcript variant X1
uncharacterized LOC123692522, transcript variant X2
methionine aminopeptidase 2, transcript variant X1
methionine aminopeptidase 2, transcript variant X2
39S ribosomal protein L55, mitochondrial
choline transporter-like 1, transcript variant X4
choline transporter-like 1, transcript variant X1
choline transporter-like 1, transcript variant X2
choline transporter-like 1, transcript variant X3
choline transporter-like 1, transcript variant X5
ribosome biogenesis protein BRX1 homolog
D-2-hydroxyglutarate dehydrogenase, mitochondrial
polyadenylate-binding protein-interacting protein 1
iron-sulfur cluster assembly 1 homolog, mitochondrial
PDZ and LIM domain protein Zasp, transcript variant X2
PDZ and LIM domain protein Zasp, transcript variant X1
PDZ and LIM domain protein Zasp, transcript variant X3
PDZ and LIM domain protein Zasp, transcript variant X4
PDZ and LIM domain protein Zasp, transcript variant X5
PDZ and LIM domain protein Zasp, transcript variant X6
PDZ and LIM domain protein Zasp isoform X5
PDZ and LIM domain protein Zasp isoform X2
PDZ and LIM domain protein Zasp isoform X4
PDZ and LIM domain protein Zasp isoform X3
PDZ and LIM domain protein Zasp isoform X6
PDZ and LIM domain protein Zasp isoform X1
nucleolar protein dao-5-like, transcript variant X2
nucleolar protein dao-5-like, transcript variant X1
E3 ubiquitin-protein ligase MARCHF8-like
PDZ and LIM domain protein 3, transcript variant X2
PDZ and LIM domain protein 3, transcript variant X3
PDZ and LIM domain protein 3, transcript variant X1
PDZ and LIM domain protein 3, transcript variant X5
PDZ and LIM domain protein 3, transcript variant X4
uncharacterized protein LOC123692911 isoform X2
PDZ and LIM domain protein 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
calcium uptake protein 1 homolog, mitochondrial-like
2-oxoglutarate dehydrogenase, mitochondrial, transcript variant X2
2-oxoglutarate dehydrogenase, mitochondrial, transcript variant X1
2-oxoglutarate dehydrogenase, mitochondrial, transcript variant X3
2-oxoglutarate dehydrogenase, mitochondrial isoform X2
2-oxoglutarate dehydrogenase, mitochondrial isoform X1
2-oxoglutarate dehydrogenase, mitochondrial isoform X3
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
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
uncharacterized LOC123692776, transcript variant X1
uncharacterized LOC123692776, transcript variant X2
uncharacterized protein LOC123692776 isoform X1
uncharacterized protein LOC123692776 isoform X2
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
polypyrimidine tract-binding protein 2, transcript variant X2
polypyrimidine tract-binding protein 2, transcript variant X3
polypyrimidine tract-binding protein 2, transcript variant X1
polypyrimidine tract-binding protein 2 isoform X2
polypyrimidine tract-binding protein 2 isoform X3
polypyrimidine tract-binding protein 2 isoform X1
cytochrome P450 4d2-like, transcript variant X2
cytochrome P450 4d2-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 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 10% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments, including 2 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: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: putative gustatory receptor 28b
rho GTPase-activating protein 39, 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 2 samples with support for all annotated introns
rho GTPase-activating protein 39, 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 2 samples with support for all annotated introns
rho GTPase-activating protein 39, transcript variant X1
rho GTPase-activating protein 39 isoform X2
rho GTPase-activating protein 39 isoform X3
rho GTPase-activating protein 39 isoform X1
uncharacterized protein LOC123692833 isoform X1
uncharacterized LOC123692442, transcript variant X1
uncharacterized LOC123692442, transcript variant X2
uncharacterized LOC123692397, transcript variant X2
uncharacterized LOC123692397, 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 14 samples with support for all annotated introns
poly [ADP-ribose] polymerase-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 16 samples with support for all annotated introns
poly [ADP-ribose] polymerase-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 12 samples with support for all annotated introns
poly [ADP-ribose] polymerase-like isoform X1
poly [ADP-ribose] polymerase-like isoform X2
poly [ADP-ribose] polymerase-like, transcript variant X3
poly [ADP-ribose] polymerase-like isoform 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 10 samples with support for all annotated introns
ceramide phosphoethanolamine synthase-like
SH3 domain-binding glutamic acid-rich protein homolog, transcript variant X1
SH3 domain-binding glutamic acid-rich protein homolog, transcript variant X2
SH3 domain-binding glutamic acid-rich protein homolog isoform X1
SH3 domain-binding glutamic acid-rich protein homolog isoform X2
vacuolar protein sorting-associated protein VTA1 homolog
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
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
dual specificity protein phosphatase Mpk3-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 12 samples with support for all annotated introns
dual specificity protein phosphatase Mpk3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
dual specificity protein phosphatase Mpk3-like isoform X1
dual specificity protein phosphatase Mpk3-like isoform X2
uncharacterized LOC123692896, transcript variant X1
uncharacterized LOC123692896, transcript variant X3
uncharacterized LOC123692896, transcript variant X2
uncharacterized protein LOC123692896 isoform X1
uncharacterized protein LOC123692896 isoform X3
uncharacterized protein LOC123692896 isoform X2
kelch-like ECH-associated protein 1B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
kelch-like ECH-associated protein 1B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
kelch-like ECH-associated protein 1B isoform X1
kelch-like ECH-associated protein 1B isoform X2
putative protein kinase C delta type homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
putative protein kinase C delta type homolog isoform X4
putative protein kinase C delta type homolog, transcript variant X5
putative protein kinase C delta type homolog isoform X5
putative protein kinase C delta type homolog, 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 5 samples with support for all annotated introns
putative protein kinase C delta type homolog, 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 11 samples with support for all annotated introns
putative protein kinase C delta type homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized protein LOC123692895 isoform X1
serine/threonine-protein kinase STE20 isoform X2
serine/threonine-protein kinase BCK1/SLK1/SSP31 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
E3 ubiquitin-protein ligase NRDP1, transcript variant X1
E3 ubiquitin-protein ligase NRDP1, transcript variant X2
E3 ubiquitin-protein ligase NRDP1 isoform X1
E3 ubiquitin-protein ligase NRDP1 isoform X2
proteasome adapter and scaffold protein ECM29
LMBR1 domain-containing protein 2 homolog, transcript variant X2
LMBR1 domain-containing protein 2 homolog, transcript variant X1
LMBR1 domain-containing protein 2 homolog isoform X2
LMBR1 domain-containing protein 2 homolog isoform X1
elongation of very long chain fatty acids protein 7-like, transcript variant X1
elongation of very long chain fatty acids protein 7-like, transcript variant X2
elongation of very long chain fatty acids protein 7-like
elongation of very long chain fatty acids protein 1-like
uncharacterized LOC123692570, transcript variant X1
uncharacterized LOC123692570, transcript variant X2
uncharacterized protein LOC123692570 isoform X1
uncharacterized protein LOC123692570 isoform X2
dual specificity testis-specific protein kinase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC123692772, transcript variant X2
uncharacterized LOC123692772, transcript variant X1
transcription factor cwo, 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 11 samples with support for all annotated introns
transcription factor cwo, 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 13 samples with support for all annotated introns
inactive histone-lysine N-methyltransferase 2E, transcript variant X3
inactive histone-lysine N-methyltransferase 2E, transcript variant X2
inactive histone-lysine N-methyltransferase 2E, transcript variant X4
inactive histone-lysine N-methyltransferase 2E, transcript variant X1
inactive histone-lysine N-methyltransferase 2E isoform X3
inactive histone-lysine N-methyltransferase 2E isoform X1
inactive histone-lysine N-methyltransferase 2E isoform X2
probable rRNA-processing protein EBP2 homolog
signal recognition particle subunit SRP72
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
kinesin-like protein KIF18A, transcript variant X1
kinesin-like protein KIF18A, transcript variant X2
kinesin-like protein KIF18A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
proton-coupled folate transporter-like, transcript variant X6
proton-coupled folate transporter-like, transcript variant X1
proton-coupled folate transporter-like, transcript variant X5
proton-coupled folate transporter-like, transcript variant X2
proton-coupled folate transporter-like, transcript variant X3
proton-coupled folate transporter-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 6 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
leucine-rich repeat-containing protein 74A-like
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
LOW QUALITY PROTEIN: leucine-rich repeat-containing protein 74A-like
tRNA (guanine(37)-N1)-methyltransferase, transcript variant X7
tRNA (guanine(37)-N1)-methyltransferase, transcript variant X1
tRNA (guanine(37)-N1)-methyltransferase, transcript variant X2
tRNA (guanine(37)-N1)-methyltransferase, transcript variant X5
tRNA (guanine(37)-N1)-methyltransferase, transcript variant X6
tRNA (guanine(37)-N1)-methyltransferase, transcript variant X4
tRNA (guanine(37)-N1)-methyltransferase, transcript variant X8
tRNA (guanine(37)-N1)-methyltransferase, transcript variant X9
tRNA (guanine(37)-N1)-methyltransferase isoform X1
tRNA (guanine(37)-N1)-methyltransferase, transcript variant X3
zinc finger and BTB domain-containing protein 42-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 4 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 42-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 4 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 14-like isoform X1
zinc finger and BTB domain-containing protein 42-like isoform X2
E3 ubiquitin-protein ligase Hakai, transcript variant X2
E3 ubiquitin-protein ligase Hakai, transcript variant X1
E3 ubiquitin-protein ligase Hakai isoform X2
E3 ubiquitin-protein ligase Hakai isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
MAP kinase-interacting serine/threonine-protein kinase 1-like
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, including 2 samples with support for all annotated introns
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein ZXDC, transcript variant X2
zinc finger protein ZXDC, transcript variant X1
zinc finger protein ZXDC, transcript variant X3
zinc finger protein ZXDC, transcript variant X4
uncharacterized protein LOC123692792 isoform X2
uncharacterized protein LOC123692792 isoform X1
activating signal cointegrator 1 complex subunit 2 homolog, 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 16 samples with support for all annotated introns
activating signal cointegrator 1 complex subunit 2 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
activating signal cointegrator 1 complex subunit 2 homolog isoform X2
activating signal cointegrator 1 complex subunit 2 homolog 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
cardioacceleratory peptide receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
inducible metalloproteinase inhibitor protein-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 17 samples with support for all annotated introns
uncharacterized LOC123692585, transcript variant X3
uncharacterized LOC123692585, transcript variant X1
uncharacterized LOC123692585, transcript variant X2
uncharacterized protein LOC123692585 isoform X3
uncharacterized protein LOC123692585 isoform X1
uncharacterized protein LOC123692585 isoform X2
elongation of very long chain fatty acids protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 68% coverage of the annotated genomic feature by RNAseq alignments
elongation of very long chain fatty acids protein-like, transcript variant X1
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 2 samples with support for all annotated introns
elongation of very long chain fatty acids protein 7-like isoform X1
elongation of very long chain fatty acids protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
elongation of very long chain fatty acids protein-like, transcript variant X3
elongation of very long chain fatty acids protein-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
elongation of very long chain fatty acids protein-like 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 4 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor-interacting protein 1, transcript variant X1
glutamate receptor-interacting protein 1 isoform X1
glutamate receptor-interacting protein 1, transcript variant X2
glutamate receptor-interacting protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% 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: 9 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123692846, transcript variant X1
uncharacterized LOC123692846, transcript variant X2
uncharacterized protein LOC123692846 isoform X1
uncharacterized protein LOC123692846 isoform X2
uncharacterized LOC123692436, transcript variant X2
uncharacterized LOC123692436, transcript variant X1
uncharacterized protein LOC123692436 isoform X2
uncharacterized protein LOC123692436 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
rap1 GTPase-GDP dissociation stimulator 1-B
uncharacterized protein ZK1073.1, transcript variant X11
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
uncharacterized protein ZK1073.1, transcript variant X12
uncharacterized protein ZK1073.1, transcript variant X4
uncharacterized protein ZK1073.1 isoform X10
uncharacterized protein ZK1073.1 isoform X11
uncharacterized protein ZK1073.1, 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 5 samples with support for all annotated introns
uncharacterized protein ZK1073.1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein ZK1073.1, transcript variant X3
uncharacterized protein ZK1073.1, transcript variant X1
uncharacterized protein ZK1073.1, transcript variant X6
uncharacterized protein ZK1073.1, transcript variant X8
uncharacterized protein ZK1073.1, transcript variant X9
uncharacterized protein ZK1073.1, transcript variant X10
uncharacterized protein ZK1073.1, transcript variant X5
uncharacterized protein ZK1073.1 isoform X1
uncharacterized protein ZK1073.1 isoform X4
uncharacterized protein ZK1073.1 isoform X2
uncharacterized protein ZK1073.1 isoform X6
uncharacterized protein ZK1073.1 isoform X5
uncharacterized protein ZK1073.1 isoform X7
uncharacterized protein ZK1073.1 isoform X8
uncharacterized protein ZK1073.1 isoform X9
uncharacterized protein ZK1073.1 isoform X3
uncharacterized protein ZK1073.1, transcript variant X13
uncharacterized protein ZK1073.1, transcript variant X14
uncharacterized protein ZK1073.1 isoform X12
uncharacterized protein ZK1073.1 isoform X13
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
tubulin alpha-8 chain-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tubulin alpha-8 chain-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 132 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
basic helix-loop-helix neural transcription factor TAP
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized LOC123692509, transcript variant X2
uncharacterized LOC123692509, transcript variant X1
uncharacterized LOC123692509, transcript variant X3
proline-, glutamic acid- and leucine-rich protein 1-like
COORDINATES: nucleotide motif:Rfam:12.0:RF01960
COORDINATES: nucleotide motif:Rfam:12.0:RF00002
COORDINATES: nucleotide motif:Rfam:12.0:RF02543
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, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
formin-like protein 2, transcript variant X2
formin-like protein 2, transcript variant X1
formin-like protein 2, transcript variant X3
uncharacterized protein LOC123692755 isoform X1
proline-, glutamic acid- and leucine-rich protein 1-like 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 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 6 samples with support for all annotated introns
basic proline-rich protein-like, transcript variant X2
basic proline-rich protein-like, transcript variant X1
basic proline-rich protein-like isoform X2
basic proline-rich protein-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC123692546 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA methionine (anticodon CAU); 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: 88% 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: 16 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
radial spoke head protein 3 homolog B, 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
radial spoke head protein 3 homolog B, transcript variant X2
radial spoke head protein 3 homolog B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
40S ribosomal protein S4, transcript variant X1
40S ribosomal protein S4, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: glycogen debranching enzyme
uncharacterized LOC123692361, transcript variant X2
uncharacterized LOC123692361, transcript variant X1