Helicoverpa zea isolate HzStark_Cry1AcR chromosome 28, ilHelZeax1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Noctuoidea; Noctuidae; Heliothinae; Helicoverpa.
REFSEQ INFORMATION: The reference sequence is identical to\nCM040230.1.\nAssembly name: ilHelZeax1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the United States Department of\nAgriculture on 2022/03/18. The original whole-genome shotgun\nproject has the accession JAKYJW000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: United States Department of Agriculture\nAssembly Date :: 31-DEC-2021\nAssembly Method :: FALCON v. 1.8.1; FALCON-Unzip v. 1.3.7;\n purge_dups v. 1.2.5; bwa-mem v. 2.2.1;\n Juicebox v. 1.11.08; Arrow gcpp v. 2.0.2;\n FreeBayes v. 1.0.2; Merqury v. 1.1\nAssembly Name :: ilHelZeax1.1\nDiploid :: Principal Pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 144x\nSequencing Technology :: PacBio Sequel II CLR; Illumina NovaSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Helicoverpa zea 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##
laboratory colony at USDA ARS Southern Insect Management Unit, Stoneville, MS
USDA-ARS Genetics and Sustainability Agricultural Research Unit, Starkville, MS, USA
Derived by automated computational analysis using gene prediction method: Gnomon.
COORDINATES: polyA evidence [ECO:0006239]
sorting and assembly machinery component 50 homolog A-like, transcript variant X1
sorting and assembly machinery component 50 homolog A-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 8 samples with support for all annotated introns
sorting and assembly machinery component 50 homolog A-like, transcript variant X2
sorting and assembly machinery component 50 homolog A-like isoform X1
sorting and assembly machinery component 50 homolog A-like isoform X2
sorting and assembly machinery component 50 homolog A-like isoform X3
putative fatty acyl-CoA reductase CG5065, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
putative fatty acyl-CoA reductase CG5065, 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 4 samples with support for all annotated introns
putative fatty acyl-CoA reductase CG5065 isoform X2
putative fatty acyl-CoA reductase CG5065, 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 6 samples with support for all annotated introns
putative fatty acyl-CoA reductase CG5065, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
putative fatty acyl-CoA reductase CG5065, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
putative fatty acyl-CoA reductase CG5065 isoform X1
putative fatty acyl-CoA reductase CG5065 isoform X3
uncharacterized LOC124643874, transcript variant X2
uncharacterized LOC124643874, transcript variant X3
uncharacterized LOC124643874, transcript variant X1
uncharacterized protein LOC124643874 isoform X2
uncharacterized protein LOC124643874 isoform X3
uncharacterized protein LOC124643874 isoform X1
adenosine 5'-monophosphoramidase HINT1-like
putative fatty acyl-CoA reductase CG5065
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 57% 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
SID1 transmembrane family member 1-like, transcript variant X1
SID1 transmembrane family member 1-like isoform X1
SID1 transmembrane family member 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
SID1 transmembrane family member 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ribosomal RNA processing protein 1 homolog
general transcription factor II-I repeat domain-containing protein 2B-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 7 samples with support for all annotated introns
general transcription factor II-I repeat domain-containing protein 2B-like, transcript variant X2
general transcription factor II-I repeat domain-containing protein 2B-like isoform X1
general transcription factor II-I repeat domain-containing protein 2B-like isoform X2
transmembrane protein 183, transcript variant X3
transmembrane protein 183, transcript variant X1
transmembrane protein 183, 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 24 samples with support for all annotated introns
zinc finger protein 501-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
zinc finger protein 501-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 3 samples with support for all annotated introns
zinc finger protein 501-like, transcript variant X2
uncharacterized protein LOC124643726 isoform X2
gastrula zinc finger protein XlCGF57.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC124643665, transcript variant X1
uncharacterized LOC124643665, transcript variant X2
uncharacterized protein LOC124643665 isoform X1
uncharacterized protein LOC124643665 isoform X2
extracellular serine/threonine protein kinase four-jointed
uncharacterized LOC124643761, transcript variant X2
uncharacterized LOC124643761, transcript variant X1
uncharacterized protein LOC124643761 isoform X2
uncharacterized protein LOC124643761 isoform X1
BLOC-1-related complex subunit 5, transcript variant X2
BLOC-1-related complex subunit 5, transcript variant X1
ubiquitin-fold modifier-conjugating enzyme 1
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 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 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC124643786
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 6% 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 2% coverage of the annotated genomic feature by RNAseq alignments
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: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC124643822, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC124643822, transcript variant X2
uncharacterized protein LOC124643822 isoform X1
uncharacterized protein LOC124643822 isoform X2
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 81% 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 55% coverage of the annotated genomic feature by RNAseq alignments
NADH-ubiquinone oxidoreductase 49 kDa subunit, transcript variant X2
NADH-ubiquinone oxidoreductase 49 kDa subunit, transcript variant X1
NADH-ubiquinone oxidoreductase 49 kDa subunit isoform X2
NADH-ubiquinone oxidoreductase 49 kDa subunit isoform X1
U6 snRNA-associated Sm-like protein LSm2
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
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ankyrin repeat domain-containing protein 50
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 31% 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
uncharacterized LOC124643621, 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 10 samples with support for all annotated introns
uncharacterized LOC124643621, 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 13 samples with support for all annotated introns
uncharacterized protein LOC124643621 isoform X1
uncharacterized protein LOC124643621 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat neuronal protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
scavenger receptor class B member 1-like
protein diaphanous, transcript variant X2
protein diaphanous, transcript variant X10
protein diaphanous, transcript variant X8
protein diaphanous, transcript variant X1
protein diaphanous, transcript variant X6
protein diaphanous, transcript variant X3
protein diaphanous, transcript variant X4
protein diaphanous, transcript variant X7
protein diaphanous, transcript variant X5
protein diaphanous, transcript variant X9
43 kDa receptor-associated protein of the synapse homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
CUE domain-containing protein 2, transcript variant X2
CUE domain-containing protein 2 isoform X2
CUE domain-containing protein 2, transcript variant X1
uncharacterized protein LOC124643806 isoform X1
isocitrate dehydrogenase [NAD] subunit gamma, mitochondrial-like
transcriptional repressor protein YY1-like, transcript variant X1
transcriptional repressor protein YY1-like, transcript variant X3
transcriptional repressor protein YY1-like, transcript variant X2
transcriptional repressor protein YY1-like, transcript variant X4
transcriptional repressor protein YY1-like, transcript variant X6
transcriptional repressor protein YY1-like, transcript variant X5
transcriptional repressor protein YY1-like isoform X1
transcriptional repressor protein YY1-like isoform X3
transcriptional repressor protein YY1-like isoform X2
transcriptional repressor protein YY1-like isoform X4
transcriptional repressor protein YY1-like isoform X6
transcriptional repressor protein YY1-like isoform X5
2-iminobutanoate/2-iminopropanoate deaminase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
putative uncharacterized protein DDB_G0282133
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: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
histone-lysine N-methyltransferase SETDB1-A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
histone-lysine N-methyltransferase SETDB1-A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
histone-lysine N-methyltransferase SETDB1-A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
histone-lysine N-methyltransferase SETDB1-A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
histone-lysine N-methyltransferase SETDB1-A isoform X4
histone-lysine N-methyltransferase SETDB1-A isoform X2
histone-lysine N-methyltransferase SETDB1-A isoform X3
histone-lysine N-methyltransferase SETDB1-A isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124643853, transcript variant X4
uncharacterized LOC124643853, transcript variant X2
uncharacterized LOC124643853, transcript variant X5
uncharacterized LOC124643853, transcript variant X3
uncharacterized LOC124643853, transcript variant X6
uncharacterized LOC124643853, transcript variant X7
uncharacterized LOC124643853, transcript variant X1
uncharacterized protein LOC124643853 isoform X1
uncharacterized protein LOC124643853 isoform X3
uncharacterized protein LOC124643853 isoform X4
uncharacterized protein LOC124643853 isoform X2
uncharacterized LOC124643873, 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
uncharacterized LOC124643873, transcript variant X2
uncharacterized protein LOC124643873 isoform X1
uncharacterized protein LOC124643873 isoform X2
uncharacterized LOC124643749, transcript variant X1
uncharacterized LOC124643749, transcript variant X3
uncharacterized LOC124643749, transcript variant X2
uncharacterized protein LOC124643749 isoform X3
uncharacterized protein LOC124643749 isoform X2
uncharacterized protein LOC124643749 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 18% coverage of the annotated genomic feature by RNAseq alignments
cilia- and flagella-associated protein 44-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
mitogen-activated protein kinase-binding protein 1, transcript variant X3
mitogen-activated protein kinase-binding protein 1, transcript variant X5
mitogen-activated protein kinase-binding protein 1, transcript variant X1
mitogen-activated protein kinase-binding protein 1, transcript variant X4
mitogen-activated protein kinase-binding protein 1, transcript variant X6
mitogen-activated protein kinase-binding protein 1 isoform X1
mitogen-activated protein kinase-binding protein 1 isoform X5
mitogen-activated protein kinase-binding protein 1 isoform X4
mitogen-activated protein kinase-binding protein 1 isoform X6
mitogen-activated protein kinase-binding protein 1 isoform X3
mitogen-activated protein kinase-binding protein 1, transcript variant X2
mitogen-activated protein kinase-binding protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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 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 21 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 95% coverage of the annotated genomic feature by RNAseq alignments
nitrilase and fragile histidine triad fusion protein NitFhit, transcript variant X1
nitrilase and fragile histidine triad fusion protein NitFhit isoform X1
nitrilase and fragile histidine triad fusion protein NitFhit, transcript variant X2
nitrilase and fragile histidine triad fusion protein NitFhit isoform X2
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: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124643715, 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 27 samples with support for all annotated introns
uncharacterized LOC124643715, 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 21 samples with support for all annotated introns
uncharacterized LOC124643715, 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 19 samples with support for all annotated introns
uncharacterized LOC124643715, transcript variant X4
uncharacterized protein LOC124643715 isoform X1
uncharacterized protein LOC124643715 isoform X2
uncharacterized protein LOC124643715 isoform X3
MAP kinase-activated protein kinase 2, transcript variant X1
MAP kinase-activated protein kinase 2, transcript variant X2
MAP kinase-activated protein kinase 2 isoform X1
MAP kinase-activated protein kinase 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
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
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
TBC1 domain family member 1, transcript variant X1
TBC1 domain family member 1, transcript variant X2
TBC1 domain family member 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
IQ and AAA domain-containing protein 1-like
uncharacterized LOC124643696, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC124643696, 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 1 sample with support for all annotated introns
uncharacterized LOC124643696, transcript variant X1
uncharacterized LOC124643696, transcript variant X3
uncharacterized protein LOC124643696 isoform X3
uncharacterized protein LOC124643696 isoform X2
uncharacterized protein LOC124643696 isoform X1
uncharacterized protein LOC124643696 isoform X4
acetyl-CoA carboxylase, transcript variant X1
acetyl-CoA carboxylase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124643614, transcript variant X2
uncharacterized LOC124643614, transcript variant X1
uncharacterized protein LOC124643614 isoform X1
uncharacterized protein LOC124643614 isoform X2
probable multidrug resistance-associated protein lethal(2)03659, transcript variant X2
probable multidrug resistance-associated protein lethal(2)03659, transcript variant X3
probable multidrug resistance-associated protein lethal(2)03659, transcript variant X1
probable multidrug resistance-associated protein lethal(2)03659, transcript variant X4
probable multidrug resistance-associated protein lethal(2)03659 isoform X2
probable multidrug resistance-associated protein lethal(2)03659 isoform X3
probable multidrug resistance-associated protein lethal(2)03659 isoform X1
probable multidrug resistance-associated protein lethal(2)03659 isoform X4
probable multidrug resistance-associated protein lethal(2)03659, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
probable multidrug resistance-associated protein lethal(2)03659 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
juvenile hormone esterase-like, transcript variant X1
juvenile hormone esterase-like, transcript variant X3
juvenile hormone esterase-like isoform X1
juvenile hormone esterase-like, transcript variant X2
juvenile hormone esterase-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
esterase FE4-like, transcript variant X1
esterase FE4-like, transcript variant X2
type-2 histone deacetylase 1, transcript variant X1
type-2 histone deacetylase 1, transcript variant X3
type-2 histone deacetylase 1, transcript variant X2
type-2 histone deacetylase 1, transcript variant X4
uncharacterized protein LOC124643764 isoform X1
uncharacterized protein LOC124643764 isoform X2
dynein axonemal intermediate chain 7 homolog
toll-like receptor 13, transcript variant X1
toll-like receptor 13, transcript variant X3
toll-like receptor 13, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA arginine (anticodon UCG); 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: 6 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
fatty acyl-CoA reductase wat-like, transcript variant X2
fatty acyl-CoA reductase wat-like, transcript variant X1
vacuolar protein sorting-associated protein 37A
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 27 samples with support for all annotated introns
putative fatty acyl-CoA reductase CG8306
uncharacterized LOC124643720, transcript variant X4
uncharacterized LOC124643720, transcript variant X2
uncharacterized LOC124643720, transcript variant X1
uncharacterized LOC124643720, transcript variant X3
uncharacterized protein LOC124643720 isoform X4
uncharacterized protein LOC124643720 isoform X2
uncharacterized protein LOC124643720 isoform X3
uncharacterized protein LOC124643720 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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
arginine-hydroxylase NDUFAF5, mitochondrial
tigger transposable element-derived protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
gastrula zinc finger protein XlCGF17.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 17% 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 90% coverage of the annotated genomic feature by RNAseq alignments
carcinine transporter-like, transcript variant X2
carcinine transporter-like, transcript variant X3
carcinine transporter-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
breast cancer type 2 susceptibility protein
oocyte zinc finger protein XlCOF7.1-like
uncharacterized protein C1orf198 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 8% 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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
scavenger receptor class B member 1, transcript variant X1
scavenger receptor class B member 1, transcript variant X2
scavenger receptor class B member 1, transcript variant X3
scavenger receptor class B member 1 isoform X1
scavenger receptor class B member 1 isoform X2
uncharacterized LOC124643605, transcript variant X1
uncharacterized LOC124643605, transcript variant X2
uncharacterized protein LOC124643605 isoform X1
uncharacterized protein LOC124643605 isoform X2
choline/ethanolamine kinase, transcript variant X2
choline/ethanolamine kinase, transcript variant X3
choline/ethanolamine kinase, transcript variant X1
acidic fibroblast growth factor intracellular-binding protein
sorting and assembly machinery component 50 homolog B-like
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 3
multidrug resistance protein homolog 49-like
protein bric-a-brac 2-like, transcript variant X6
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
protein bric-a-brac 2-like, transcript variant X5
longitudinals lacking protein, isoforms H/M/V-like isoform X2
protein bric-a-brac 2-like, transcript variant X7
protein bric-a-brac 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
protein bric-a-brac 2-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 24 samples with support for all annotated introns
protein bric-a-brac 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
protein bric-a-brac 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC124643882 isoform X1
uncharacterized LOC124643738, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized LOC124643738, 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 7 samples with support for all annotated introns
uncharacterized LOC124643692, transcript variant X2
uncharacterized LOC124643692, transcript variant X1
26S proteasome non-ATPase regulatory subunit 13, transcript variant X2
26S proteasome non-ATPase regulatory subunit 13, transcript variant X3
26S proteasome non-ATPase regulatory subunit 13, transcript variant X1
26S proteasome non-ATPase regulatory subunit 13
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
uncharacterized LOC124643676, transcript variant X2
uncharacterized LOC124643676, transcript variant X1
uncharacterized protein LOC124643676 isoform X1
uncharacterized protein LOC124643676 isoform X2
ets DNA-binding protein pokkuri, transcript variant X2
ets DNA-binding protein pokkuri, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC124643683, transcript variant X1
uncharacterized LOC124643683, transcript variant X2
uncharacterized protein LOC124643683 isoform X1
uncharacterized protein LOC124643683 isoform X2
copper-transporting ATPase 1, transcript variant X5
copper-transporting ATPase 1, transcript variant X1
copper-transporting ATPase 1, transcript variant X4
copper-transporting ATPase 1, transcript variant X6
copper-transporting ATPase 1, transcript variant X8
copper-transporting ATPase 1, transcript variant X2
copper-transporting ATPase 1, transcript variant X7
copper-transporting ATPase 1, 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 24 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 98% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns