Leguminivora glycinivorella isolate SPB_JAAS2020 chromosome 14, LegGlyc_1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Tortricoidea; Tortricidae; Olethreutinae; Grapholitini; Leguminivora.
REFSEQ INFORMATION: The reference sequence is identical to\nCM041134.1.\nAssembly name: LegGlyc_1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the USDA-ARS on 2022/04/22. The\noriginal whole-genome shotgun project has the accession\nJAKXMO000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: USDA-ARS\nAssembly Date :: 08-OCT-2021\nAssembly Method :: NextDeNovo v. 2.5.0\nAssembly Name :: LegGlyc_1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 85.48x\nSequencing Technology :: Oxford Nanopore GridION\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Leguminivora glycinivorella\n Annotation Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
sodium-independent sulfate anion transporter, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
sodium-independent sulfate anion transporter, transcript variant X2
sodium-independent sulfate anion transporter
pyridoxal-dependent decarboxylase domain-containing protein 1, 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 2 samples with support for all annotated introns
pyridoxal-dependent decarboxylase domain-containing protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
pyridoxal-dependent decarboxylase domain-containing protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X3
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X2
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X1
NADH-ubiquinone oxidoreductase subunit 8-like
cytochrome P450 9e2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cytochrome P450 9e2-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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
glutaconyl-CoA decarboxylase subunit gamma-like
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
uncharacterized LOC125233240, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC125233240, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC125233240, transcript variant X13
uncharacterized LOC125233240, transcript variant X10
uncharacterized protein LOC125233240 isoform X9
uncharacterized protein LOC125233240 isoform X7
uncharacterized protein LOC125233240 isoform X10
uncharacterized LOC125233240, transcript variant X4
uncharacterized LOC125233240, transcript variant X14
uncharacterized LOC125233240, transcript variant X5
uncharacterized protein LOC125233240 isoform X11
uncharacterized protein LOC125233240 isoform X4
uncharacterized LOC125233240, transcript variant X3
uncharacterized LOC125233240, transcript variant X2
uncharacterized LOC125233240, transcript variant X7
uncharacterized protein LOC125233240 isoform X2
uncharacterized LOC125233240, transcript variant X1
uncharacterized LOC125233240, transcript variant X8
uncharacterized LOC125233240, transcript variant X6
uncharacterized LOC125233240, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC125233240 isoform X1
uncharacterized protein LOC125233240 isoform X6
uncharacterized protein LOC125233240 isoform X8
uncharacterized protein LOC125233240 isoform X3
uncharacterized protein LOC125233240 isoform X5
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon CGC); 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: 82% 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium-independent sulfate anion transporter-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sodium-independent sulfate anion transporter-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sodium-independent sulfate anion transporter-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
sodium-independent sulfate anion transporter-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
sodium-independent sulfate anion transporter-like isoform X2
sodium-independent sulfate anion transporter-like isoform X1
sodium-independent sulfate anion transporter-like isoform X3
senecionine N-oxygenase, transcript variant X1
senecionine N-oxygenase, transcript variant X3
senecionine N-oxygenase, 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 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: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC125233469
uncharacterized LOC125233541, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125233541, transcript variant X3
uncharacterized LOC125233541, transcript variant X1
uncharacterized protein LOC125233541 isoform X1
uncharacterized LOC125233541, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized protein LOC125233541 isoform 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125233202, transcript variant X2
uncharacterized LOC125233202, transcript variant X3
uncharacterized LOC125233202, transcript variant X1
uncharacterized LOC125233201, transcript variant X2
uncharacterized LOC125233201, transcript variant X1
uncharacterized LOC125233201, transcript variant X3
uncharacterized protein LOC125233201 isoform X1
uncharacterized protein LOC125233201 isoform X2
cilia- and flagella-associated protein 52, transcript variant X2
cilia- and flagella-associated protein 52, transcript variant X1
cilia- and flagella-associated protein 52 isoform X2
cilia- and flagella-associated protein 52 isoform X1
baculoviral IAP repeat-containing protein 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
monocarboxylate transporter 14-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
monocarboxylate transporter 14-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125233369, transcript variant X2
uncharacterized LOC125233369, transcript variant X1
uncharacterized LOC125233369, transcript variant X3
uncharacterized LOC125233369, transcript variant X4
uncharacterized protein LOC125233369 isoform X1
uncharacterized protein LOC125233369 isoform X2
uncharacterized protein LOC125233369 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 283 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA alanine (anticodon GGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125233582, transcript variant X2
uncharacterized LOC125233582, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized protein LOC125233582 isoform X2
uncharacterized protein LOC125233582 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
lactosylceramide 4-alpha-galactosyltransferase-like
uncharacterized protein K02A2.6-like, transcript variant X1
uncharacterized protein K02A2.6-like, transcript variant X3
uncharacterized protein K02A2.6-like, transcript variant X2
uncharacterized protein LOC125233694 isoform X2
uncharacterized protein K02A2.6-like isoform X1
uncharacterized protein LOC125233694 isoform X3
uncharacterized LOC125233124, 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 7 samples with support for all annotated introns
uncharacterized protein LOC125233124 isoform X2
uncharacterized LOC125233124, 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 13 samples with support for all annotated introns
uncharacterized protein LOC125233124 isoform X1
WD repeat domain phosphoinositide-interacting protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
WD repeat domain phosphoinositide-interacting protein 2, transcript variant X2
WD repeat domain phosphoinositide-interacting protein 2, transcript variant X3
WD repeat domain phosphoinositide-interacting protein 2, transcript variant X4
WD repeat domain phosphoinositide-interacting protein 2 isoform X1
WD repeat domain phosphoinositide-interacting protein 2 isoform X2
WD repeat domain phosphoinositide-interacting protein 2 isoform X3
WD repeat domain phosphoinositide-interacting protein 2 isoform X4
nuclear protein localization protein 4 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
sodium-independent sulfate anion transporter-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
prominin-like protein, transcript variant X1
prominin-like protein, transcript variant X3
prominin-like protein, transcript variant X2
prominin-like protein, transcript variant X4
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA proline (anticodon AGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ETS-related transcription factor Elf-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
transfer RNA threonine (anticodon GGU); 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: 418 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125233664, transcript variant X7
uncharacterized LOC125233664, transcript variant X2
uncharacterized LOC125233664, transcript variant X3
uncharacterized LOC125233664, transcript variant X6
uncharacterized LOC125233664, transcript variant X4
uncharacterized LOC125233664, transcript variant X1
uncharacterized LOC125233664, transcript variant X5
uncharacterized protein LOC125233664 isoform X1
uncharacterized protein LOC125233664 isoform X2
uncharacterized protein LOC125233664 isoform X3
cytochrome P450 6B2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cytochrome P450 6B2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 99% 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: 6 Proteins
pheromone-processing carboxypeptidase KEX1-like
uncharacterized LOC125233358, transcript variant X1
uncharacterized LOC125233358, transcript variant X2
uncharacterized protein LOC125233358 isoform X1
uncharacterized protein LOC125233358 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 1 sample with support for all annotated introns
uncharacterized LOC125233079, transcript variant X1
uncharacterized LOC125233079, transcript variant X2
uncharacterized LOC125233623, transcript variant X1
uncharacterized protein LOC125233623 isoform X1
uncharacterized LOC125233623, transcript variant X2
uncharacterized protein LOC125233623 isoform X2
arp2/3 complex-activating protein rickA-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65% coverage of the annotated genomic feature by RNAseq alignments
probable 3-hydroxyisobutyrate dehydrogenase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
protein tweety-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein tweety-like, transcript variant X2
protein tweety-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transfer RNA serine (anticodon GGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cytosolic Fe-S cluster assembly factor NUBP2 homolog
sulfide:quinone oxidoreductase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat-containing protein let-4-like
short-chain specific acyl-CoA dehydrogenase, mitochondrial-like, transcript variant X1
short-chain specific acyl-CoA dehydrogenase, mitochondrial-like, transcript variant X2
short-chain specific acyl-CoA dehydrogenase, mitochondrial-like isoform X2
short-chain specific acyl-CoA dehydrogenase, mitochondrial-like isoform X1
vacuolar protein sorting-associated protein 18 homolog, 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 12 samples with support for all annotated introns
vacuolar protein sorting-associated protein 18 homolog, 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 7 samples with support for all annotated introns
vacuolar protein sorting-associated protein 18 homolog isoform X1
vacuolar protein sorting-associated protein 18 homolog isoform X2
BAG domain-containing protein Samui-like, transcript variant X3
BAG domain-containing protein Samui-like, transcript variant X2
BAG domain-containing protein Samui-like, transcript variant X1
BAG domain-containing protein Samui-like isoform X3
BAG domain-containing protein Samui-like isoform X2
BAG domain-containing protein Samui-like isoform X1
uncharacterized LOC125233193, transcript variant X1
uncharacterized protein LOC125233193 isoform X1
uncharacterized LOC125233193, transcript variant X3
uncharacterized protein LOC125233193 isoform X3
uncharacterized LOC125233193, transcript variant X2
uncharacterized protein LOC125233193 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 9 samples with support for all annotated introns
39S ribosomal protein L12, mitochondrial
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% 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 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
TATA-binding protein-associated factor 172
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; 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 7 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: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: TATA-binding protein-associated factor 172
uncharacterized LOC125233277, 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 2 samples with support for all annotated introns
uncharacterized LOC125233277, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
developmentally-regulated GTP-binding protein 2, 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 13 samples with support for all annotated introns
developmentally-regulated GTP-binding protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
developmentally-regulated GTP-binding protein 2 isoform X2
developmentally-regulated GTP-binding protein 2 isoform X1
probable RNA-binding protein 46, transcript variant X1
probable RNA-binding protein 46, transcript variant X3
probable RNA-binding protein 46 isoform X2
probable RNA-binding protein 46, transcript variant X2
probable RNA-binding protein 46, transcript variant X4
probable RNA-binding protein 46 isoform X1
probable RNA-binding protein 46 isoform X3
paternally-expressed gene 3 protein-like
unconventional myosin-XV-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
unconventional myosin-XV-like, transcript variant X2
unconventional myosin-XV-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 10 samples with support for all annotated introns
unconventional myosin-XV-like isoform X3
unconventional myosin-XV-like isoform X2
unconventional myosin-XV-like isoform X1
leucine-rich repeat extensin-like protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon CGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
putative mediator of RNA polymerase II transcription subunit 12
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: 7 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
LOW QUALITY PROTEIN: E3 ubiquitin-protein ligase RING1
60S ribosomal protein L22-like, transcript variant X1
60S ribosomal protein L22-like, 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
LOW QUALITY PROTEIN: exocyst complex component 6
probable aconitate hydratase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
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
LOW QUALITY PROTEIN: adenylosuccinate lyase
uncharacterized LOC125233413, transcript variant X1
uncharacterized LOC125233413, transcript variant X2
uncharacterized protein LOC125233413 isoform X1
uncharacterized protein LOC125233413 isoform X2
hydroxysteroid dehydrogenase-like protein 2, transcript variant X2
hydroxysteroid dehydrogenase-like protein 2, transcript variant X1
hydroxysteroid dehydrogenase-like protein 2 isoform X2
hydroxysteroid dehydrogenase-like protein 2 isoform X1
uncharacterized LOC125233675, transcript variant X2
uncharacterized LOC125233675, transcript variant X1
uncharacterized protein LOC125233675 isoform X2
uncharacterized protein LOC125233675 isoform X1
uncharacterized LOC125233675, transcript variant X3
uncharacterized protein LOC125233675 isoform X3
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125233680, transcript variant X1
uncharacterized LOC125233680, transcript variant X3
uncharacterized LOC125233680, transcript variant X2
uncharacterized protein LOC125233680 isoform X1
uncharacterized protein LOC125233680 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 3 subunit B
multiple inositol polyphosphate phosphatase 1-like
DNA-directed RNA polymerase III subunit RPC5
LOW QUALITY PROTEIN: DNA-directed RNA polymerase III subunit RPC5
alpha-(1,3)-fucosyltransferase 10, transcript variant X3
alpha-(1,3)-fucosyltransferase 10, 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 1 sample with support for all annotated introns
alpha-(1,3)-fucosyltransferase 10, transcript variant X2
uncharacterized protein LOC125233168 isoform X2
alpha-(1,3)-fucosyltransferase 10 isoform X1
dihydropyrimidine dehydrogenase [NADP(+)]
ras-related C3 botulinum toxin substrate 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC125233160, transcript variant X2
uncharacterized LOC125233160, transcript variant X1
uncharacterized LOC125233141, transcript variant X1
uncharacterized LOC125233141, transcript variant X4
uncharacterized LOC125233141, transcript variant X2
uncharacterized LOC125233141, transcript variant X3
uncharacterized protein LOC125233141 isoform X2
uncharacterized protein LOC125233141 isoform X1
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
proton-coupled amino acid transporter-like protein pathetic, transcript variant X1
proton-coupled amino acid transporter-like protein pathetic, transcript variant X3
proton-coupled amino acid transporter-like protein pathetic, transcript variant X2
proton-coupled amino acid transporter-like protein pathetic isoform X1
proton-coupled amino acid transporter-like protein pathetic isoform X3
proton-coupled amino acid transporter-like protein pathetic isoform X2
tRNA-splicing endonuclease subunit Sen54
heparan sulfate glucosamine 3-O-sulfotransferase 3A1
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
LOW QUALITY PROTEIN: luc7-like protein 3
small cysteine and glycine repeat-containing protein 10-like
uncharacterized LOC125233359, transcript variant X3
uncharacterized LOC125233359, 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 5 samples with support for all annotated introns
uncharacterized LOC125233359, transcript variant X1
uncharacterized protein LOC125233359 isoform X3
uncharacterized protein LOC125233359 isoform X2
uncharacterized protein LOC125233359 isoform X1
uncharacterized LOC125233198, transcript variant X2
uncharacterized protein LOC125233198 isoform X2
uncharacterized LOC125233198, transcript variant X1
uncharacterized protein LOC125233198 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
voltage-dependent T-type calcium channel subunit alpha-1G
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex-like
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: 1 Protein, 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: 15 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: 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
mitochondrial glycine transporter B-like, transcript variant X2
mitochondrial glycine transporter B-like isoform X2
mitochondrial glycine transporter B-like, transcript variant X1
mitochondrial glycine transporter B-like isoform X1
mitochondrial glycine transporter B-like, transcript variant X4
mitochondrial glycine transporter-like isoform X4
mitochondrial glycine transporter B-like, transcript variant X3
mitochondrial glycine transporter B-like isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC125233303, transcript variant X1
uncharacterized LOC125233303, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein CLEC16A homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
prostaglandin reductase 1-like, transcript variant X1
prostaglandin reductase 1-like, transcript variant X2
histone-binding protein N1/N2, transcript variant X1
histone-binding protein N1/N2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
small subunit processome component 20 homolog
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 1 base in 1 codon; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: small subunit processome component 20 homolog
hydroxyacylglutathione hydrolase, mitochondrial, transcript variant X1
hydroxyacylglutathione hydrolase, mitochondrial isoform X1
hydroxyacylglutathione hydrolase, mitochondrial, transcript variant X2
hydroxyacylglutathione hydrolase, mitochondrial isoform X2
zinc finger protein 271-like, transcript variant X2
zinc finger protein 271-like, transcript variant X3
zinc finger protein 271-like, transcript variant X7
zinc finger protein 271-like, transcript variant X5
zinc finger protein 271-like, transcript variant X6
zinc finger protein 271-like, transcript variant X4
zinc finger protein 271-like, transcript variant X9
zinc finger protein 271-like, transcript variant X8
zinc finger protein 271-like, transcript variant X1
extracellular serine/threonine protein CG31145-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125233463, transcript variant X3
uncharacterized protein LOC125233463 isoform X3
uncharacterized LOC125233463, transcript variant X2
uncharacterized LOC125233463, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized protein LOC125233463 isoform X2
uncharacterized protein LOC125233463 isoform X1
uncharacterized LOC125233463, transcript variant X5
uncharacterized LOC125233463, transcript variant X4
uncharacterized protein LOC125233463 isoform X5
uncharacterized protein LOC125233463 isoform X4
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
uncharacterized LOC125233460, transcript variant X2
uncharacterized LOC125233460, transcript variant X3
uncharacterized LOC125233460, transcript variant X1
uncharacterized protein LOC125233460 isoform X1
uncharacterized protein LOC125233460 isoform X2
glucose-induced degradation protein 4 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
tyrosine-protein phosphatase non-receptor type 23
probable 28S ribosomal protein S23, mitochondrial
major facilitator superfamily domain-containing protein 10, transcript variant X2
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
major facilitator superfamily domain-containing protein 10, transcript variant X1
major facilitator superfamily domain-containing protein 10 isoform X2
major facilitator superfamily domain-containing protein 10 isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: DNA topoisomerase 3-alpha
rRNA methyltransferase 2, mitochondrial-like
serine hydroxymethyltransferase, transcript variant X2
serine hydroxymethyltransferase, transcript variant X1
serine hydroxymethyltransferase, transcript variant X3
serine hydroxymethyltransferase isoform X2
serine hydroxymethyltransferase isoform X1
serine hydroxymethyltransferase isoform X3
serine hydroxymethyltransferase, transcript variant X4
serine hydroxymethyltransferase 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 4 samples with support for all annotated introns
zinc finger CCCH domain-containing protein 10-like
probable isoaspartyl peptidase/L-asparaginase CG7860
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial, transcript variant X1
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial isoform X1
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial, 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 10 samples with support for all annotated introns
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial isoform X2
rhomboid-related protein 3, transcript variant X1
rhomboid-related protein 3, transcript variant X2
rhomboid-related protein 3, transcript variant X3
spermatogenesis-associated protein 20, 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
spermatogenesis-associated protein 20, transcript variant X2
spermatogenesis-associated protein 20 isoform X1
spermatogenesis-associated protein 20 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125233589, transcript variant X1
uncharacterized LOC125233589, transcript variant X2
hemolymph lipopolysaccharide-binding 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 6 samples with support for all annotated introns
hemolymph lipopolysaccharide-binding protein-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 8 samples with support for all annotated introns
hemolymph lipopolysaccharide-binding protein-like isoform X2
C-type mannose receptor 2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72% coverage of the annotated genomic feature by RNAseq alignments
hemolymph lipopolysaccharide-binding protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
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: 78% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC125233184, transcript variant X2
uncharacterized LOC125233184, transcript variant X1
transfer RNA threonine (anticodon CGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
C-type mannose receptor 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
C-type mannose receptor 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein LOC125233380 isoform X2
uncharacterized LOC125233480, transcript variant X2
uncharacterized LOC125233480, 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 9 samples with support for all annotated introns
oxidized purine nucleoside triphosphate hydrolase-like
uncharacterized LOC125233074, transcript variant X1
uncharacterized LOC125233074, transcript variant X2
uncharacterized LOC125233074, transcript variant X3
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 5 samples with support for all annotated introns
peptidyl-tRNA hydrolase ICT1, 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 3 samples with support for all annotated introns
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
organic cation/carnitine transporter 7-like
Usher syndrome type-1G protein homolog, transcript variant X1
Usher syndrome type-1G protein homolog, transcript variant X2
Usher syndrome type-1G protein homolog isoform X1
Usher syndrome type-1G protein homolog isoform X2
uncharacterized LOC125233221, transcript variant X2
uncharacterized LOC125233221, transcript variant X1
uncharacterized protein LOC125233221 isoform X1
uncharacterized protein LOC125233221 isoform X2
zinc-type alcohol dehydrogenase-like protein SE_1777
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
zinc-type alcohol dehydrogenase-like protein SERP1785
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
(E3-independent) E2 ubiquitin-conjugating enzyme, transcript variant X8
(E3-independent) E2 ubiquitin-conjugating enzyme, transcript variant X1
(E3-independent) E2 ubiquitin-conjugating enzyme, transcript variant X2
(E3-independent) E2 ubiquitin-conjugating enzyme, transcript variant X6
(E3-independent) E2 ubiquitin-conjugating enzyme, transcript variant X7
(E3-independent) E2 ubiquitin-conjugating enzyme, transcript variant X3
(E3-independent) E2 ubiquitin-conjugating enzyme, transcript variant X5
(E3-independent) E2 ubiquitin-conjugating enzyme, transcript variant X4
(E3-independent) E2 ubiquitin-conjugating enzyme isoform X1
(E3-independent) E2 ubiquitin-conjugating enzyme isoform X2
(E3-independent) E2 ubiquitin-conjugating enzyme isoform X6
(E3-independent) E2 ubiquitin-conjugating enzyme isoform X7
(E3-independent) E2 ubiquitin-conjugating enzyme isoform X3
(E3-independent) E2 ubiquitin-conjugating enzyme isoform X8
(E3-independent) E2 ubiquitin-conjugating enzyme isoform X4
(E3-independent) E2 ubiquitin-conjugating enzyme isoform X5
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: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
hemoglobin-2-like, transcript variant X1
hemoglobin-2-like, 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: 49 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein LOC125233546
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: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein K02A2.6-like
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 2 samples with support for all annotated introns
facilitated trehalose transporter Tret1-like
eukaryotic translation initiation factor 3 subunit D
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
signal recognition particle subunit SRP68
E3 ubiquitin-protein ligase ZNF598, transcript variant X3
E3 ubiquitin-protein ligase ZNF598 isoform X2
E3 ubiquitin-protein ligase ZNF598, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
E3 ubiquitin-protein ligase ZNF598, 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 10 samples with support for all annotated introns
E3 ubiquitin-protein ligase ZNF598 isoform X1
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X2
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X1
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X3
phosphoribosyl pyrophosphate synthase-associated protein 2 isoform X1
phosphoribosyl pyrophosphate synthase-associated protein 2 isoform X2
UNC93-like protein MFSD11, transcript variant X1
UNC93-like protein MFSD11, 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 9 samples with support for all annotated introns
transmembrane protein 70 homolog, mitochondrial
testis-expressed protein 2, transcript variant X2
testis-expressed protein 2, transcript variant X1
testis-expressed protein 2, transcript variant X4
testis-expressed protein 2, transcript variant X3
serine/threonine-protein kinase/endoribonuclease IRE1
ankyrin repeat domain-containing protein 27-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
H/ACA ribonucleoprotein complex subunit 1-like
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X2
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X2
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X1
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin carboxyl-terminal hydrolase 7-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 7-like, transcript variant X5
ubiquitin carboxyl-terminal hydrolase 7-like, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 7-like, transcript variant X7
ubiquitin carboxyl-terminal hydrolase 7-like, transcript variant X6
ubiquitin carboxyl-terminal hydrolase 7-like, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 7-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 7-like isoform X1
ubiquitin carboxyl-terminal hydrolase 7-like isoform X3
ubiquitin carboxyl-terminal hydrolase 7-like isoform X2
ubiquitin carboxyl-terminal hydrolase 7-like isoform X5
ubiquitin carboxyl-terminal hydrolase 7-like isoform X4
uncharacterized LOC125233451, transcript variant X1
uncharacterized LOC125233451, transcript variant X2
uncharacterized protein LOC125233451 isoform X1
uncharacterized protein LOC125233451 isoform X2
ubiquitin carboxyl-terminal hydrolase 7, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 7, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 7, transcript variant X6
ubiquitin carboxyl-terminal hydrolase 7, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 7, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 7, transcript variant X5
ubiquitin carboxyl-terminal hydrolase 7, transcript variant X7
ubiquitin carboxyl-terminal hydrolase 7 isoform X5
ubiquitin carboxyl-terminal hydrolase 7 isoform X4
ubiquitin carboxyl-terminal hydrolase 7 isoform X3
ubiquitin carboxyl-terminal hydrolase 7 isoform X2
ubiquitin carboxyl-terminal hydrolase 7 isoform X1
ubiquitin carboxyl-terminal hydrolase 7 isoform X6
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
uncharacterized LOC125233559, transcript variant X2
uncharacterized LOC125233559, transcript variant X1
uncharacterized LOC125233559, transcript variant X3
uncharacterized protein LOC125233559 isoform X1
uncharacterized protein LOC125233559 isoform X2
mitochondrial uncoupling protein 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
mitochondrial uncoupling protein 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
mitochondrial uncoupling protein 4, transcript variant X1
mitochondrial uncoupling protein 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
mitochondrial uncoupling protein 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
mitochondrial uncoupling protein 4 isoform X1
mitochondrial uncoupling protein 4, transcript variant X6
mitochondrial uncoupling protein 4 isoform 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 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
inactive rhomboid protein 1, transcript variant X1
inactive rhomboid protein 1, transcript variant X2
uncharacterized LOC125233119, transcript variant X1
uncharacterized LOC125233119, transcript variant X2
putative inorganic phosphate cotransporter, transcript variant X2
putative inorganic phosphate cotransporter, transcript variant X1
putative inorganic phosphate cotransporter
putative inorganic phosphate cotransporter isoform X1
putative inorganic phosphate cotransporter isoform X2
putative inorganic phosphate cotransporter, transcript variant X3
putative inorganic phosphate cotransporter isoform X3
putative inorganic phosphate cotransporter, transcript variant X4
putative inorganic phosphate cotransporter isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
coiled-coil domain-containing protein 96
uncharacterized LOC125233192, transcript variant X2
uncharacterized LOC125233192, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
protein I'm not dead yet-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein I'm not dead yet-like, transcript variant X2
protein I'm not dead yet-like isoform X1
protein I'm not dead yet-like isoform X2
voltage-dependent calcium channel gamma-4 subunit, transcript variant X1
voltage-dependent calcium channel gamma-4 subunit, transcript variant X2
voltage-dependent calcium channel gamma-4 subunit isoform X1
voltage-dependent calcium channel gamma-4 subunit isoform X2
ATP synthase subunit O, mitochondrial-like
protein yellow-like, transcript variant X2
protein yellow-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC125233127, transcript variant X2
uncharacterized LOC125233127, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 31
phospholipid-transporting ATPase ABCA1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phospholipid-transporting ATPase ABCA1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phospholipid-transporting ATPase ABCA1-like, transcript variant X4
phospholipid-transporting ATPase ABCA1-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phospholipid-transporting ATPase ABCA1-like, transcript variant X1
phospholipid-transporting ATPase ABCA1-like, transcript variant X6
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
phospholipid-transporting ATPase ABCA1-like, transcript variant X5
phospholipid-transporting ATPase ABCA3-like isoform X1
phospholipid-transporting ATPase ABCA1-like isoform X3
phospholipid-transporting ATPase ABCA3-like isoform X2
phospholipid-transporting ATPase ABCA1-like isoform X4
phospholipid-transporting ATPase ABCA3-like, transcript variant X2
phospholipid-transporting ATPase ABCA3-like, transcript variant X1
phospholipid-transporting ATPase ABCA3-like
DNA-directed RNA polymerase I subunit RPA43
dual specificity mitogen-activated protein kinase kinase 4-like
mitochondrial dicarboxylate carrier, 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 3 samples with support for all annotated introns
mitochondrial dicarboxylate carrier, transcript variant X4
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 8 samples with support for all annotated introns
mitochondrial dicarboxylate carrier, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mitochondrial dicarboxylate carrier isoform X2
uncharacterized LOC125233444, transcript variant X2
uncharacterized LOC125233444, transcript variant X1
uncharacterized LOC125233444, transcript variant X4
uncharacterized LOC125233444, transcript variant X3
uncharacterized protein LOC125233444 isoform X1
uncharacterized protein LOC125233444 isoform X2
mitochondrial dicarboxylate carrier, 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 13 samples with support for all annotated introns
mitochondrial dicarboxylate carrier isoform X1
diacylglycerol kinase epsilon, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
diacylglycerol kinase epsilon, transcript variant X2
diacylglycerol kinase epsilon isoform X1
diacylglycerol kinase epsilon isoform X2
26S proteasome non-ATPase regulatory subunit 10-like
LOW QUALITY PROTEIN: 26S proteasome non-ATPase regulatory subunit 10-like
lysophospholipid acyltransferase 6, transcript variant X1
lysophospholipid acyltransferase 6, transcript variant X3
lysophospholipid acyltransferase 6, transcript variant X2
lysophospholipid acyltransferase 6, transcript variant X4
lysophospholipid acyltransferase 6 isoform X1
lysophospholipid acyltransferase 6 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
eukaryotic peptide chain release factor GTP-binding subunit ERF3A, transcript variant X1
eukaryotic peptide chain release factor GTP-binding subunit ERF3A, transcript variant X3
eukaryotic peptide chain release factor GTP-binding subunit ERF3A, transcript variant X2
eukaryotic peptide chain release factor GTP-binding subunit ERF3A, transcript variant X4
eukaryotic peptide chain release factor GTP-binding subunit ERF3A, transcript variant X5
eukaryotic peptide chain release factor GTP-binding subunit ERF3A isoform X4
eukaryotic peptide chain release factor GTP-binding subunit ERF3A isoform X3
eukaryotic peptide chain release factor GTP-binding subunit ERF3A isoform X2
eukaryotic peptide chain release factor GTP-binding subunit ERF3A isoform X1
eukaryotic peptide chain release factor GTP-binding subunit ERF3A isoform X5
sodium-dependent nutrient amino acid transporter 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
sodium-dependent nutrient amino acid transporter 1-like, transcript variant X1
sodium-dependent nutrient amino acid transporter 1-like, transcript variant X2
sodium-dependent nutrient amino acid transporter 1-like isoform X1
sodium-dependent nutrient amino acid transporter 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
carboxypeptidase B-like, transcript variant X2
carboxypeptidase B-like, transcript variant X3
carboxypeptidase B-like, transcript variant X4
carboxypeptidase B-like, transcript variant X1
carboxypeptidase B-like, transcript variant X5
zinc carboxypeptidase A 1-like isoform X4
nuclear distribution protein nudE-like 1
phosphatidylinositol N-acetylglucosaminyltransferase subunit Q, transcript variant X1
phosphatidylinositol N-acetylglucosaminyltransferase subunit Q, transcript variant X2
phosphatidylinositol N-acetylglucosaminyltransferase subunit Q isoform X2
phosphatidylinositol N-acetylglucosaminyltransferase subunit Q isoform X1
putative RNA-binding protein Luc7-like 2, transcript variant X1
putative RNA-binding protein Luc7-like 2 isoform X1
putative RNA-binding protein Luc7-like 2, transcript variant X2
putative RNA-binding protein Luc7-like 2, transcript variant X3
putative RNA-binding protein Luc7-like 2 isoform X2
putative RNA-binding protein Luc7-like 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dynein intermediate chain 3, ciliary-like
28 kDa heat- and acid-stable phosphoprotein
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: 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125233335, transcript variant X1
uncharacterized LOC125233335, transcript variant X2
uncharacterized protein LOC125233335 isoform X1
uncharacterized protein LOC125233335 isoform X2
uncharacterized LOC125233334, transcript variant X2
uncharacterized LOC125233334, transcript variant X1
dual specificity mitogen-activated protein kinase kinase 6
transmembrane protein 94, transcript variant X3
transmembrane protein 94, transcript variant X2
transmembrane protein 94, transcript variant X1
WASH complex subunit 1-like, transcript variant X2
WASH complex subunit 1-like, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC125233660
ribonuclease Z, mitochondrial, transcript variant X2
ribonuclease Z, mitochondrial, transcript variant X1
ribonuclease Z, mitochondrial, transcript variant X3
ribonuclease Z, mitochondrial, transcript variant X4
ribonuclease Z, mitochondrial, transcript variant X5
ribonuclease Z, mitochondrial isoform X2
ribonuclease Z, mitochondrial isoform X1
ribonuclease Z, mitochondrial isoform X3
ribonuclease Z, mitochondrial isoform X4
ribonuclease Z, mitochondrial isoform X5
26S proteasome non-ATPase regulatory subunit 4
LOW QUALITY PROTEIN: 26S proteasome non-ATPase regulatory subunit 4
putative ATP synthase subunit f, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
mesencephalic astrocyte-derived neurotrophic factor 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 4 samples with support for all annotated introns
leucine-rich repeat and death domain-containing protein 1-like
cancer-related nucleoside-triphosphatase homolog
probable enoyl-CoA hydratase, mitochondrial, transcript variant X2
probable enoyl-CoA hydratase, mitochondrial isoform X2
probable enoyl-CoA hydratase, mitochondrial, transcript variant X1
enoyl-CoA hydratase, mitochondrial isoform X1
uncharacterized LOC125233443, transcript variant X1
uncharacterized protein LOC125233443 isoform X1
uncharacterized LOC125233443, transcript variant X2
uncharacterized protein LOC125233443 isoform X2
uncharacterized LOC125233443, transcript variant X3
uncharacterized protein LOC125233443 isoform X3
diphthine methyltransferase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
diphthine methyltransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
diphthine methyltransferase, transcript variant X2
serine/arginine repetitive matrix protein 1, transcript variant X4
serine/arginine repetitive matrix protein 1, transcript variant X2
serine/arginine repetitive matrix protein 1, transcript variant X3
serine/arginine repetitive matrix protein 1, transcript variant X1
serine/arginine repetitive matrix protein 1 isoform X4
serine/arginine repetitive matrix protein 1 isoform X2
uncharacterized protein CG5098 isoform X3
serine/arginine repetitive matrix protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
acylamino-acid-releasing enzyme-like, transcript variant X1
acylamino-acid-releasing enzyme-like, transcript variant X2
acylamino-acid-releasing enzyme-like isoform X1
acylamino-acid-releasing enzyme-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
glucose dehydrogenase [FAD, quinone]-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
geranylgeranyl transferase type-2 subunit beta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like
uncharacterized oxidoreductase TM_0325-like
oxidoreductase-like domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 67% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125233057, transcript variant X2
uncharacterized LOC125233057, transcript variant X1
uncharacterized protein LOC125233057 isoform X2
uncharacterized protein LOC125233057 isoform X1
transfer RNA aspartic acid (anticodon AUC); 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: 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide-binding protein subunit gamma-e, transcript variant X3
guanine nucleotide-binding protein subunit gamma-e, transcript variant X2
guanine nucleotide-binding protein subunit gamma-e, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
guanine nucleotide-binding protein subunit gamma-e
ecdysone oxidase-like, transcript variant X1
ecdysone oxidase-like, transcript variant X2
ecdysone oxidase-like, transcript variant X4
ecdysone oxidase-like, transcript variant X3
ecdysone oxidase-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 5 samples with support for all annotated introns
ecdysone oxidase-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125233178, transcript variant X1
uncharacterized LOC125233178, transcript variant X2
uncharacterized protein LOC125233178 isoform X2
uncharacterized protein LOC125233178 isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: luciferin sulfotransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 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 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 46% coverage of the annotated genomic feature by RNAseq alignments
myosin heavy chain, non-muscle, transcript variant X2
myosin heavy chain, non-muscle isoform X2
myosin heavy chain, non-muscle, transcript variant X1
myosin heavy chain, non-muscle isoform X1
probable low-specificity L-threonine aldolase 2, transcript variant X1
probable low-specificity L-threonine aldolase 2 isoform X1
probable low-specificity L-threonine aldolase 2, transcript variant X2
probable low-specificity L-threonine aldolase 2 isoform X2
beta-1,3-galactosyltransferase brn-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gastrula zinc finger protein XlCGF58.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
zinc finger protein 853-like, transcript variant X3
zinc finger protein 853-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
zinc finger protein 853-like, transcript variant X2
zinc finger protein 853-like, transcript variant X4
uncharacterized LOC125233654, transcript variant X2
uncharacterized LOC125233654, transcript variant X1
uncharacterized protein LOC125233654 isoform X2
uncharacterized protein LOC125233654 isoform X1
klaroid protein-like, transcript variant X1
klaroid protein-like, transcript variant X2
Fanconi anemia group I protein homolog, transcript variant X1
Fanconi anemia group I protein homolog isoform X1
Fanconi anemia group I protein homolog, transcript variant X2
Fanconi anemia group I protein homolog isoform X2
zinc finger protein 69 homolog B-like, transcript variant X2
zinc finger protein 69 homolog B-like, transcript variant X1
zinc finger protein 69 homolog B-like isoform X2
zinc finger protein 700-like, transcript variant X2
zinc finger protein 700-like, transcript variant X3
zinc finger protein 700-like, transcript variant X1
zinc finger protein 501-like, transcript variant X1
zinc finger protein 501-like, transcript variant X2
thrombospondin type-1 domain-containing protein 7A-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: thrombospondin type-1 domain-containing protein 7A-like
uncharacterized LOC125233316, transcript variant X3
uncharacterized LOC125233316, transcript variant X1
uncharacterized LOC125233316, transcript variant X2
uncharacterized protein LOC125233316 isoform X2
uncharacterized protein LOC125233316 isoform X1
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
methylglutaconyl-CoA hydratase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC125233402, transcript variant X1
uncharacterized LOC125233402, transcript variant X2
uncharacterized LOC125233402, transcript variant X5
uncharacterized LOC125233402, transcript variant X7
uncharacterized LOC125233402, transcript variant X6
uncharacterized LOC125233402, transcript variant X4
uncharacterized LOC125233402, transcript variant X3
uncharacterized protein LOC125233402 isoform X1
uncharacterized protein LOC125233402 isoform X2
uncharacterized protein LOC125233402 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 4 samples with support for all annotated introns
serine/arginine-rich splicing factor 2, transcript variant X1
serine/arginine-rich splicing factor 2, transcript variant X2
serine/arginine-rich splicing factor 2, transcript variant X3
serine/arginine-rich splicing factor 2 isoform X1
serine/arginine-rich splicing factor 2 isoform X2
U3 small nucleolar RNA-interacting protein 2
ribosome biogenesis regulatory protein homolog
DNA fragmentation factor subunit beta, transcript variant X2
DNA fragmentation factor subunit beta, transcript variant X1
DNA fragmentation factor subunit beta isoform X1
DNA fragmentation factor subunit beta isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
alpha-(1,3)-fucosyltransferase 7-like, transcript variant X1
alpha-(1,3)-fucosyltransferase 7-like isoform X1
alpha-(1,3)-fucosyltransferase 7-like, transcript variant X2
alpha-(1,3)-fucosyltransferase 7-like isoform X2
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase FUT5-like
polyglutamylase complex subunit TTLL1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
outer dynein arm-docking complex subunit 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
transcription initiation factor TFIID subunit 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons
LOW QUALITY PROTEIN: transcription initiation factor TFIID subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125233158, transcript variant X1
uncharacterized LOC125233158, transcript variant X2
uncharacterized protein LOC125233158 isoform X1
uncharacterized protein LOC125233158 isoform X2
evolutionarily conserved signaling intermediate in Toll pathway, mitochondrial
nuclear pore complex protein Nup214-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nuclear pore complex protein Nup214-like, transcript variant X1
nuclear pore complex protein Nup214-like isoform X2
nuclear pore complex protein Nup214-like isoform X1
D-beta-hydroxybutyrate dehydrogenase, mitochondrial
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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
brain-specific angiogenesis inhibitor 1-associated protein 2, transcript variant X5
brain-specific angiogenesis inhibitor 1-associated protein 2, transcript variant X4
brain-specific angiogenesis inhibitor 1-associated protein 2, transcript variant X1
brain-specific angiogenesis inhibitor 1-associated protein 2, transcript variant X2
brain-specific angiogenesis inhibitor 1-associated protein 2, transcript variant X3
brain-specific angiogenesis inhibitor 1-associated protein 2 isoform X2
uncharacterized protein LOC125233499 isoform X1
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
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 65% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC125233501
eukaryotic translation initiation factor 3 subunit A-like
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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
UDP-N-acetylglucosamine transferase subunit ALG14 homolog
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
LOW QUALITY PROTEIN: GPI inositol-deacylase
serine-threonine kinase receptor-associated protein, transcript variant X1
serine-threonine kinase receptor-associated protein, transcript variant X2
serine-threonine kinase receptor-associated protein isoform X2
serine-threonine kinase receptor-associated protein isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 10 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: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC125233212
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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125233650, transcript variant X1
uncharacterized LOC125233650, transcript variant X2
uncharacterized protein LOC125233650 isoform X1
uncharacterized protein LOC125233650 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 65% 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 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: dynein axonemal heavy chain 3-like
GSK3-beta interaction protein-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 1 sample with support for all annotated introns
GSK3-beta interaction protein-like, transcript variant X3
GSK3-beta interaction protein-like, transcript variant X1
GSK3-beta interaction protein-like, transcript variant X2
uncharacterized protein LOC125233348 isoform X2
uncharacterized protein LOC125233348 isoform X1
GSK3-beta interaction protein-like isoform X3
LOW QUALITY PROTEIN: forkhead box protein K1
ubiquitin carboxyl-terminal hydrolase nonstop, transcript variant X2
ubiquitin carboxyl-terminal hydrolase nonstop isoform X2
ubiquitin carboxyl-terminal hydrolase nonstop, transcript variant X1
ubiquitin carboxyl-terminal hydrolase nonstop isoform X1
uncharacterized protein K02A2.6-like isoform X2
uncharacterized protein LOC125233154 isoform X3
LOW QUALITY PROTEIN: protein yellow-like
G protein-activated inward rectifier potassium channel 3-like, transcript variant X2
G protein-activated inward rectifier potassium channel 3-like, transcript variant X5
G protein-activated inward rectifier potassium channel 3-like, transcript variant X1
G protein-activated inward rectifier potassium channel 3-like, transcript variant X3
G protein-activated inward rectifier potassium channel 3-like, transcript variant X4
inward rectifier potassium channel 2-like isoform X1
ATP-sensitive inward rectifier potassium channel 12-like isoform X3
inward rectifier potassium channel 2-like isoform X2
uncharacterized protein LOC125233398 isoform X5
inward rectifier potassium channel 2-like isoform X4
G protein-activated inward rectifier potassium channel 3-like, transcript variant X6
G protein-activated inward rectifier potassium channel 3-like, transcript variant X7
G protein-activated inward rectifier potassium channel 3-like isoform X6
G protein-activated inward rectifier potassium channel 3-like isoform X7
G protein-activated inward rectifier potassium channel 3-like isoform X1
G protein-activated inward rectifier potassium channel 3-like isoform X3
G protein-activated inward rectifier potassium channel 3-like isoform X2
G protein-activated inward rectifier potassium channel 3-like, transcript variant X8
G protein-activated inward rectifier potassium channel 3-like isoform X4
G protein-activated inward rectifier potassium channel 3-like isoform X5
uncharacterized LOC125233602, transcript variant X2
uncharacterized LOC125233602, transcript variant X1
hepatocyte growth factor-regulated tyrosine kinase substrate-like