Penaeus chinensis breed Huanghai No. 1 chromosome 26, ASM1920278v2, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Crustacea; Multicrustacea; Malacostraca; Eumalacostraca; Eucarida; Decapoda; Dendrobranchiata; Penaeoidea; Penaeidae; Penaeus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM032951.1.\nAssembly name: ASM1920278v2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Yellow Sea Fisheries Research\nInstitute, Chinese Academy of Fishery Sciences on 2021/07/13. The\noriginal whole-genome shotgun project has the accession\nJAGKSU000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Yellow Sea Fisheries Research Institute,\n Chinese Academy of Fishery Sciences\nAssembly Date :: 2020\nAssembly Method :: FALCON-Unzip v. MAY-2020\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 150.0x\nSequencing Technology :: PacBio Sequel\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Penaeus chinensis Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
conservation base of Haifeng Aquaculture Co., Ltd.
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
vascular endothelial growth factor receptor 1-like
similar to RNA sequence (same species):INSD:GIYE01057199.1
annotated by transcript or proteomic data
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 345 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 345 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
melanoma receptor tyrosine-protein kinase-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 34 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, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 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: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
WSC domain-containing protein 1-like, transcript variant X1
WSC domain-containing protein 1-like, transcript variant X2
WSC domain-containing protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125038861, transcript variant X3
uncharacterized LOC125038861, transcript variant X2
uncharacterized LOC125038861, transcript variant X1
uncharacterized LOC125038861, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC125039093, transcript variant X2
uncharacterized LOC125039093, transcript variant X1
uncharacterized protein LOC125039093 isoform X2
uncharacterized protein LOC125039093 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
fibrous sheath CABYR-binding protein-like
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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tRNA N(3)-methylcytidine methyltransferase METTL2-like
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like
myotubularin-related protein 10-B-like, transcript variant X2
similar to RNA sequence (same species):INSD:GHUY01006982.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 713 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
myotubularin-related protein 10-B-like, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 713 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 602 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
myotubularin-related protein 10-B-like isoform X2
myotubularin-related protein 10-B-like isoform X1
prolow-density lipoprotein receptor-related protein 1-like
similar to RNA sequence (same species):INSD:GIYE01012067.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1455 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 1455 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
WAS/WASL-interacting protein family member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
low-density lipoprotein receptor-related protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125038932, transcript variant X2
uncharacterized LOC125038932, transcript variant X1
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3A-like, transcript variant X1
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3A-like, transcript variant X2
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3A-like
glutamate receptor ionotropic, kainate 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
hematopoietically-expressed homeobox protein HHEX-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
ATP-binding cassette sub-family F member 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 16 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
histone acetyltransferase KAT2A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
histone acetyltransferase KAT2A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
histone acetyltransferase KAT2A-like isoform X2
histone acetyltransferase KAT2A-like 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
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: probable C-mannosyltransferase DPY19L1
MORN repeat-containing protein 4 homolog
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
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: MORN repeat-containing protein 4 homolog
2-iminobutanoate/2-iminopropanoate deaminase-like
retinoic acid receptor RXR-like, transcript variant X2
retinoic acid receptor RXR-like, transcript variant X1
retinoic acid receptor RXR-like isoform X2
retinoic acid receptor RXR-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
vicilin-like seed storage protein At2g18540, transcript variant X5
vicilin-like seed storage protein At2g18540, transcript variant X3
vicilin-like seed storage protein At2g18540 isoform X4
microtubule organizer protein 1-like isoform X2
vicilin-like seed storage protein At2g18540, transcript variant X4
vicilin-like seed storage protein At2g18540, transcript variant X2
vicilin-like seed storage protein At2g18540, transcript variant X1
centrosomal protein of 85 kDa-like isoform X3
centrosomal protein of 85 kDa-like isoform X1
WW domain-containing protein C2F3.14c-like, transcript variant X1
phosphatase and actin regulator 4-B-like isoform X1
WW domain-containing protein C2F3.14c-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
WW domain-containing protein C2F3.14c-like isoform X2
dynein regulatory complex protein 1-like
major facilitator superfamily domain-containing protein 6-like, transcript variant X2
major facilitator superfamily domain-containing protein 6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 6-like
uncharacterized LOC125038916, transcript variant X10
uncharacterized LOC125038916, transcript variant X9
uncharacterized LOC125038916, transcript variant X1
uncharacterized LOC125038916, transcript variant X11
uncharacterized LOC125038916, transcript variant X12
uncharacterized LOC125038916, transcript variant X5
uncharacterized LOC125038916, transcript variant X4
uncharacterized LOC125038916, transcript variant X3
uncharacterized LOC125038916, transcript variant X6
uncharacterized LOC125038916, transcript variant X7
uncharacterized LOC125038916, transcript variant X2
uncharacterized LOC125038916, transcript variant X8
uncharacterized protein LOC125038916 isoform X1
uncharacterized protein LOC125038916 isoform X2
uncharacterized protein LOC125038916 isoform X3
meiotic sister-chromatid recombination protein 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
meiotic sister-chromatid recombination protein 3-like isoform X1
meiotic sister-chromatid recombination protein 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
meiotic sister-chromatid recombination protein 3-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
ubiquitin-fold modifier-conjugating enzyme 1, transcript variant X2
ubiquitin-fold modifier-conjugating enzyme 1, transcript variant X1
ubiquitin-fold modifier-conjugating enzyme 1, transcript variant X3
ubiquitin-fold modifier-conjugating enzyme 1, transcript variant X5
ubiquitin-fold modifier-conjugating enzyme 1, transcript variant X4
ubiquitin-fold modifier-conjugating enzyme 1
proteasomal ubiquitin receptor ADRM1-like, transcript variant X2
proteasomal ubiquitin receptor ADRM1-like, transcript variant X1
proteasomal ubiquitin receptor ADRM1-like isoform X2
proteasomal ubiquitin receptor ADRM1-like isoform X1
condensin complex subunit 1-like, transcript variant X3
condensin complex subunit 1-like, transcript variant X2
condensin complex subunit 1-like, transcript variant X1
condensin complex subunit 1-like isoform X1
condensin complex subunit 1-like isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC125038859
BTB/POZ domain-containing protein 6-like, transcript variant X3
BTB/POZ domain-containing protein 6-like, transcript variant X1
BTB/POZ domain-containing protein 6-like, transcript variant X2
BTB/POZ domain-containing protein 6-like isoform X2
BTB/POZ domain-containing protein 6-like isoform X1
lymphokine-activated killer T-cell-originated protein kinase-like
protein transport protein Sec23A-like, transcript variant X2
protein transport protein Sec23A-like, transcript variant X3
protein transport protein Sec23A-like, transcript variant X1
protein transport protein Sec23A-like isoform X3
protein transport protein Sec23A-like isoform X1
protein transport protein Sec23A-like isoform X2
probable E3 ubiquitin-protein ligase bre1
YY1-associated factor 2-like, transcript variant X1
YY1-associated factor 2-like, transcript variant X4
YY1-associated factor 2-like, transcript variant X3
YY1-associated factor 2-like, transcript variant X2
NADH dehydrogenase [ubiquinone] flavoprotein 1, mitochondrial-like
SCY1-like protein 2, transcript variant X3
SCY1-like protein 2, transcript variant X1
SCY1-like protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
SCY1-like protein 2, transcript variant X2
exosome complex component RRP41-like, transcript variant X1
exosome complex component RRP41-like, transcript variant X2
exosome complex component RRP41-like, transcript variant X3
exosome complex component RRP41-like isoform X1
exosome complex component RRP41-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
rRNA 2'-O-methyltransferase fibrillarin-like
transcription initiation factor TFIID subunit 1-like, transcript variant X4
transcription initiation factor TFIID subunit 1-like, transcript variant X3
transcription initiation factor TFIID subunit 1-like, transcript variant X5
transcription initiation factor TFIID subunit 1-like, transcript variant X1
transcription initiation factor TFIID subunit 1-like, transcript variant X2
transcription initiation factor TFIID subunit 1-like isoform X3
transcription initiation factor TFIID subunit 1-like isoform X2
transcription initiation factor TFIID subunit 1-like isoform X4
transcription initiation factor TFIID subunit 1-like isoform X1
protein transport protein Sec61 subunit alpha-like 1
LOW QUALITY PROTEIN: protein transport protein Sec61 subunit alpha-like 1
uncharacterized LOC125039170, transcript variant X1
uncharacterized LOC125039170, transcript variant X3
uncharacterized LOC125039170, transcript variant X2
tumor protein p73-like, transcript variant X1
tumor protein p73-like, transcript variant X2
tumor protein p73-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
uncharacterized protein LOC125039168 isoform X1
uncharacterized protein LOC125039168 isoform X2
tumor protein p73-like, transcript variant X3
uncharacterized protein LOC125039168 isoform X3
similar to RNA sequence (same species):INSD:GIYE01043439.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 317 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 307 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
WD repeat and FYVE domain-containing protein 3-like, transcript variant X4
WD repeat and FYVE domain-containing protein 3-like, transcript variant X2
WD repeat and FYVE domain-containing protein 3-like, transcript variant X5
WD repeat and FYVE domain-containing protein 3-like, transcript variant X1
WD repeat and FYVE domain-containing protein 3-like, transcript variant X3
WD repeat and FYVE domain-containing protein 3-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
WD repeat and FYVE domain-containing protein 3-like isoform X4
WD repeat and FYVE domain-containing protein 3-like isoform X2
WD repeat and FYVE domain-containing protein 3-like isoform X5
WD repeat and FYVE domain-containing protein 3-like isoform X1
WD repeat and FYVE domain-containing protein 3-like isoform X3
WD repeat and FYVE domain-containing protein 3-like isoform X6
similar to RNA sequence (same species):INSD:GIYE01021013.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 198 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 198 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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 31 samples with support for all annotated introns
46 kDa FK506-binding nuclear protein-like, transcript variant X2
46 kDa FK506-binding nuclear protein-like, transcript variant X1
46 kDa FK506-binding nuclear protein-like isoform X2
46 kDa FK506-binding nuclear protein-like isoform X1
U2 small nuclear ribonucleoprotein A'-like
ribosome quality control complex subunit NEMF-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
ribosome quality control complex subunit NEMF-like, transcript variant X2
ribosome quality control complex subunit NEMF-like isoform X1
ribosome quality control complex subunit NEMF-like isoform X2
uncharacterized LOC125039109, transcript variant X3
uncharacterized LOC125039109, transcript variant X2
uncharacterized LOC125039109, transcript variant X1
cholinesterase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cholinesterase 1-like, transcript variant X3
cholinesterase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
vicilin-like seed storage protein At2g18540
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
regulator of nonsense transcripts 3A-like
uncharacterized histidine-rich protein DDB_G0274557-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 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 6 samples with support for all annotated introns
uncharacterized LOC125039228, transcript variant X1
uncharacterized LOC125039228, transcript variant X2
uncharacterized protein LOC125039228 isoform X1
uncharacterized protein LOC125039228 isoform X2
uncharacterized LOC125038843, transcript variant X1
uncharacterized LOC125038843, transcript variant X2
uncharacterized LOC125038843, transcript variant X6
uncharacterized LOC125038843, transcript variant X3
uncharacterized LOC125038843, transcript variant X4
uncharacterized protein LOC125038843 isoform X1
uncharacterized protein LOC125038843 isoform X2
uncharacterized protein LOC125038843 isoform X6
uncharacterized protein LOC125038843 isoform X3
uncharacterized protein LOC125038843 isoform X4
uncharacterized LOC125038843, transcript variant X5
uncharacterized protein LOC125038843 isoform X5
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00319
ribosomal protein S6 kinase alpha-5-like, transcript variant X3
ribosomal protein S6 kinase alpha-5-like, transcript variant X1
ribosomal protein S6 kinase alpha-5-like, transcript variant X2
ribosomal protein S6 kinase alpha-5-like, transcript variant X4
ribosomal protein S6 kinase alpha-5-like isoform X2
ribosomal protein S6 kinase alpha-5-like isoform X1
ribosomal protein S6 kinase alpha-5-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
aryl hydrocarbon receptor nuclear translocator homolog
similar to RNA sequence (same species):INSD:GHUY01007872.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 272 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 272 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
protein bric-a-brac 1-like, transcript variant X4
protein bric-a-brac 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
protein bric-a-brac 1-like, transcript variant X3
protein bric-a-brac 1-like, transcript variant X5
protein bric-a-brac 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
WD repeat domain-containing protein 83-like
retinal homeobox protein Rx-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
retinal homeobox protein Rx-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cilia- and flagella-associated protein 58-like
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 LOC125038954, transcript variant X2
uncharacterized LOC125038954, transcript variant X1
uncharacterized LOC125038954, 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 30 samples with support for all annotated introns
uncharacterized protein LOC125038954 isoform X1
uncharacterized protein LOC125038954 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
nuclear receptor subfamily 4 group A member 2-like, transcript variant X1
nuclear receptor subfamily 4 group A member 2-like isoform X1
nuclear receptor subfamily 4 group A member 2-like, transcript variant X3
nuclear receptor subfamily 4 group A member 2-like isoform X3
nuclear receptor subfamily 4 group A member 2-like, transcript variant X2
nuclear receptor subfamily 4 group A member 2-like isoform X2
MOB kinase activator-like 1, transcript variant X3
MOB kinase activator-like 1, transcript variant X2
MOB kinase activator-like 1, transcript variant X1
heterogeneous nuclear ribonucleoprotein H3-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein H3-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein H3-like isoform X2
heterogeneous nuclear ribonucleoprotein H3-like isoform X1
heterogeneous nuclear ribonucleoprotein H3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein H3-like isoform X3
apolipoprotein D-like, transcript variant X1
apolipoprotein D-like, transcript variant X2
glycoprotein 3-alpha-L-fucosyltransferase A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
hematopoietic prostaglandin D synthase-like
multidrug resistance-associated protein 1-like, transcript variant X3
multidrug resistance-associated protein 1-like, transcript variant X5
multidrug resistance-associated protein 1-like, transcript variant X4
multidrug resistance-associated protein 1-like, transcript variant X1
multidrug resistance-associated protein 1-like, transcript variant X2
multidrug resistance-associated protein 1-like isoform X3
multidrug resistance-associated protein 1-like isoform X5
multidrug resistance-associated protein 1-like isoform X4
multidrug resistance-associated protein 1-like isoform X1
multidrug resistance-associated protein 1-like isoform X2
ubiquitin-associated domain-containing protein 1-like, transcript variant X2
ubiquitin-associated domain-containing protein 1-like, transcript variant X1
ubiquitin-associated domain-containing protein 1-like isoform X1
ubiquitin-associated domain-containing protein 1-like isoform X2
integrator complex subunit 1-like, transcript variant X1
integrator complex subunit 1-like, transcript variant X2
integrator complex subunit 1-like isoform X1
integrator complex subunit 1-like isoform X2
vesicle-fusing ATPase 1-like, transcript variant X5
vesicle-fusing ATPase 1-like, transcript variant X2
vesicle-fusing ATPase 1-like, transcript variant X3
vesicle-fusing ATPase 1-like, transcript variant X4
vesicle-fusing ATPase 1-like, transcript variant X1
calcium/calmodulin-dependent protein kinase type II alpha chain-like
similar to RNA sequence (same species):INSD:GHUY01000161.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 155 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 155 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC125039086, transcript variant X2
uncharacterized LOC125039086, transcript variant X1
putative leucine-rich repeat-containing protein DDB_G0290503
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
vicilin-like seed storage protein At2g18540 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GIYE01009675.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 147 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 147 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
uncharacterized LOC125038881, transcript variant X2
uncharacterized LOC125038881, transcript variant X1
uncharacterized protein LOC125038881 isoform X1
uncharacterized protein LOC125038881 isoform X2
triokinase/FMN cyclase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
triokinase/FMN cyclase-like, transcript variant X4
triokinase/FMN cyclase-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 11 samples with support for all annotated introns
triokinase/FMN cyclase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
triokinase/FMN cyclase-like, transcript variant X5
angiotensin-converting enzyme-like, transcript variant X2
angiotensin-converting enzyme-like, transcript variant X1
angiotensin-converting enzyme-like isoform X2
angiotensin-converting enzyme-like isoform X1
similar to RNA sequence (same species):INSD:GIYE01040409.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 342 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 278 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
snake venom metalloprotease inhibitor 02D01-like
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, including 5 samples with support for all annotated introns
uncharacterized LOC125039130, transcript variant X1
uncharacterized LOC125039130, transcript variant X4
uncharacterized LOC125039130, transcript variant X2
uncharacterized LOC125039130, transcript variant X3
trithorax group protein osa-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 39 samples with support for all annotated introns
trithorax group protein osa-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
DNA repair protein XRCC1-like, transcript variant X1
DNA repair protein XRCC1-like, transcript variant X2
DNA repair protein XRCC1-like isoform X1
DNA repair protein XRCC1-like isoform X2
charged multivesicular body protein 1a-like
glycogen [starch] synthase-like, transcript variant X1
glycogen [starch] synthase-like, transcript variant X2
glycogen [starch] synthase-like isoform X1
glycogen [starch] synthase-like 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 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 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
DET1- and DDB1-associated protein 1-like
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like protein 1
S-adenosylmethionine decarboxylase proenzyme-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 277-like, transcript variant X1
zinc finger protein 277-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 37 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 30 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
probable 28S ribosomal protein S6, mitochondrial
uncharacterized LOC125039072, transcript variant X6
uncharacterized LOC125039072, transcript variant X4
uncharacterized LOC125039072, transcript variant X5
uncharacterized protein LOC125039072 isoform X4
uncharacterized LOC125039072, transcript variant X3
uncharacterized protein LOC125039072 isoform X3
uncharacterized LOC125039072, transcript variant X1
uncharacterized protein LOC125039072 isoform X1
piggyBac transposable element-derived protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC125039072, transcript variant X2
uncharacterized protein LOC125039072 isoform X2
protein transport protein Sec61 subunit alpha-like 1, transcript variant X2
protein transport protein Sec61 subunit alpha-like 1, transcript variant X1
protein transport protein Sec61 subunit alpha-like 1 isoform X1
protein transport protein Sec61 subunit alpha-like 1 isoform X2
polycomb protein Scm-like, transcript variant X3
polycomb protein Scm-like, transcript variant X1
polycomb protein Scm-like, transcript variant X2
homer protein homolog 2-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 19 samples with support for all annotated introns
homer protein homolog 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
homer protein homolog 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
homer protein homolog 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
homer protein homolog 2-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 23 samples with support for all annotated introns
uncharacterized LOC125039197, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC125039197, transcript variant X2
uncharacterized protein LOC125039197 isoform X1
uncharacterized protein LOC125039197 isoform X2
DNA-directed RNA polymerase I subunit RPA2-like
peroxisomal targeting signal 1 receptor-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
peroxisomal targeting signal 1 receptor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
peroxisomal targeting signal 1 receptor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
peroxisomal targeting signal 1 receptor-like
phosphatidylglycerophosphatase and protein-tyrosine phosphatase 1-like, transcript variant X1
phosphatidylglycerophosphatase and protein-tyrosine phosphatase 1-like, transcript variant X2
phosphatidylglycerophosphatase and protein-tyrosine phosphatase 1-like, transcript variant X3
phosphatidylglycerophosphatase and protein-tyrosine phosphatase 1-like, transcript variant X4
phosphatidylglycerophosphatase and protein-tyrosine phosphatase 1-like isoform X1
phosphatidylglycerophosphatase and protein-tyrosine phosphatase 1-like isoform X2
electron transfer flavoprotein subunit beta-like, transcript variant X3
electron transfer flavoprotein subunit beta-like, transcript variant X2
electron transfer flavoprotein subunit beta-like, transcript variant X1
electron transfer flavoprotein subunit beta-like
adenosine deaminase-like protein, transcript variant X1
adenosine deaminase-like protein, transcript variant X2
adenosine deaminase-like protein, transcript variant X3
adenosine deaminase-like protein isoform X1
adenosine deaminase-like protein isoform X2
calcium uptake protein 1 homolog, mitochondrial-like, transcript variant X2
calcium uptake protein 1 homolog, mitochondrial-like, transcript variant X5
calcium uptake protein 1 homolog, mitochondrial-like, transcript variant X3
calcium uptake protein 1 homolog, mitochondrial-like, transcript variant X1
calcium uptake protein 1 homolog, mitochondrial-like, transcript variant X4
calcium uptake protein 1 homolog, mitochondrial-like isoform X2
calcium uptake protein 1 homolog, mitochondrial-like isoform X4
calcium uptake protein 1 homolog, mitochondrial-like isoform X1
calcium uptake protein 1 homolog, mitochondrial-like isoform X3
upstream activation factor subunit spp27-like, transcript variant X3
upstream activation factor subunit spp27-like, transcript variant X7
upstream activation factor subunit spp27-like, transcript variant X5
upstream activation factor subunit spp27-like, transcript variant X1
upstream activation factor subunit spp27-like, transcript variant X4
upstream activation factor subunit spp27-like, transcript variant X8
upstream activation factor subunit spp27-like, transcript variant X2
upstream activation factor subunit spp27-like, transcript variant X6
upstream activation factor subunit spp27-like isoform X1
upstream activation factor subunit spp27-like isoform X3
upstream activation factor subunit spp27-like isoform X2
upstream activation factor subunit spp27-like isoform X5
upstream activation factor subunit spp27-like isoform X4
upstream activation factor subunit spp27-like isoform X7
upstream activation factor subunit spp27-like isoform X6
upstream activation factor subunit spp27-like isoform X8
upstream activation factor subunit spp27-like, transcript variant X9
upstream activation factor subunit spp27-like isoform X9
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
NACHT domain- and WD repeat-containing protein 1-like
LOW QUALITY PROTEIN: NACHT domain- and WD repeat-containing protein 1-like
B9 domain-containing protein 1-like, transcript variant X1
B9 domain-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GIYE01050238.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 308 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 266 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
dendritic arbor reduction protein 1-like isoform X1
discoidin, CUB and LCCL domain-containing protein 2-like
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: 6 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
attractin-like protein 1, transcript variant X1
attractin-like protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins
potassium channel subfamily K member 13-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69% coverage of the annotated genomic feature by RNAseq alignments
probable leucine--tRNA ligase, mitochondrial
sex-lethal homolog, transcript variant X12
sex-lethal homolog, transcript variant X3
sex-lethal homolog, transcript variant X8
sex-lethal homolog, transcript variant X6
sex-lethal homolog, transcript variant X9
sex-lethal homolog, transcript variant X5
sex-lethal homolog, transcript variant X2
sex-lethal homolog, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
sex-lethal homolog, transcript variant X13
sex-lethal homolog, transcript variant X1
sex-lethal homolog, transcript variant X7
sex-lethal homolog, transcript variant X4
sex-lethal homolog, transcript variant X10
sex-lethal homolog, transcript variant X11
uncharacterized protein KIAA1143 homolog
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
proline-rich receptor-like protein kinase PERK9
uncharacterized LOC125039075, transcript variant X3
uncharacterized LOC125039075, transcript variant X2
uncharacterized LOC125039075, transcript variant X1
uncharacterized protein LOC125039075 isoform X1
uncharacterized protein LOC125039075 isoform X3
uncharacterized protein LOC125039075 isoform X2
similar to RNA sequence (same species):INSD:GHUY01010209.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 425 bases not found in genome assembly; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 425 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
protein arginine N-methyltransferase 5-like
protein phosphatase 1 regulatory subunit 36-like
probable serine carboxypeptidase CPVL, transcript variant X3
probable serine carboxypeptidase CPVL, transcript variant X2
probable serine carboxypeptidase CPVL, transcript variant X5
probable serine carboxypeptidase CPVL, transcript variant X1
probable serine carboxypeptidase CPVL, transcript variant X4
probable serine carboxypeptidase CPVL, transcript variant X6
probable serine carboxypeptidase CPVL isoform X1
probable serine carboxypeptidase CPVL isoform X2
uncharacterized LOC125038856, transcript variant X1
uncharacterized LOC125038856, transcript variant X2
uncharacterized LOC125038856, transcript variant X3
uncharacterized protein LOC125038856 isoform X2
uncharacterized protein LOC125038856 isoform X3
uncharacterized protein LOC125038856 isoform X1
stress-activated protein kinase JNK-like
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 36 samples with support for all annotated introns
programmed cell death 6-interacting protein-like
similar to RNA sequence (same species):INSD:GHUY01000269.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 683 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 642 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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 15 samples with support for all annotated introns
uncharacterized LOC125039135, transcript variant X3
uncharacterized LOC125039135, transcript variant X2
uncharacterized LOC125039135, transcript variant X1
solute carrier family 2, facilitated glucose transporter member 1-like
similar to RNA sequence (same species):INSD:GIYE01022787.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 760 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 468 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
peptidyl-prolyl cis-trans isomerase E-like, transcript variant X2
peptidyl-prolyl cis-trans isomerase E-like, transcript variant X5
peptidyl-prolyl cis-trans isomerase E-like, transcript variant X4
peptidyl-prolyl cis-trans isomerase E-like, transcript variant X1
peptidyl-prolyl cis-trans isomerase E-like, transcript variant X6
uncharacterized protein LOC125038967 isoform X1
uncharacterized protein LOC125038967 isoform X3
peptidyl-prolyl cis-trans isomerase E-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
peptidyl-prolyl cis-trans isomerase E-like isoform X2
NAD(P)H-hydrate epimerase-like, transcript variant X1
NAD(P)H-hydrate epimerase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
facilitated trehalose transporter Tret1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 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, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 2, facilitated glucose transporter member 8-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 8-like, transcript variant X1
solute carrier family 2, facilitated glucose transporter member 8-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 8-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 8-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 4 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 8-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 8-like, transcript variant X7
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
solute carrier family 2, facilitated glucose transporter member 8-like
vacuolar protein sorting-associated protein 18 homolog
venom carboxylesterase-6-like, transcript variant X1
venom carboxylesterase-6-like, transcript variant X2
venom carboxylesterase-6-like isoform X1
venom carboxylesterase-6-like isoform X2
scoloptoxin SSD14-like, transcript variant X7
scoloptoxin SSD14-like, transcript variant X2
scoloptoxin SSD14-like, transcript variant X3
scoloptoxin SSD14-like, transcript variant X1
scoloptoxin SSD14-like, transcript variant X4
scoloptoxin SSD14-like, transcript variant X5
scoloptoxin SSD14-like, transcript variant X6
60S ribosomal protein L27a-like, transcript variant X2
60S ribosomal protein L27a-like, transcript variant X3
60S ribosomal protein L27a-like, transcript variant X1
LOW QUALITY PROTEIN: zinc finger protein 385B-like
gamma-aminobutyric acid receptor subunit beta-like
gamma-aminobutyric acid receptor subunit alpha-1-like
similar to RNA sequence (same species):INSD:GIYE01013905.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 68 bases not found in genome assembly; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 68 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
proline-rich 33 kDa extensin-related protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 26% 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
pollen-specific leucine-rich repeat extensin-like protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
uncharacterized LOC125038947, transcript variant X1
uncharacterized LOC125038947, transcript variant X2
oplophorus-luciferin 2-monooxygenase non-catalytic subunit-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.