Leguminivora glycinivorella isolate SPB_JAAS2020 chromosome 8, LegGlyc_1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Tortricoidea; Tortricidae; Olethreutinae; Grapholitini; Leguminivora.
REFSEQ INFORMATION: The reference sequence is identical to\nCM041128.1.\nAssembly name: LegGlyc_1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the USDA-ARS on 2022/04/22. The\noriginal whole-genome shotgun project has the accession\nJAKXMO000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: USDA-ARS\nAssembly Date :: 08-OCT-2021\nAssembly Method :: NextDeNovo v. 2.5.0\nAssembly Name :: LegGlyc_1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 85.48x\nSequencing Technology :: Oxford Nanopore GridION\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Leguminivora glycinivorella\n Annotation Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
mediator of RNA polymerase II transcription subunit 7
COORDINATES: polyA evidence [ECO:0006239]
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: mediator of RNA polymerase II transcription subunit 7
uncharacterized LOC125229224, transcript variant X2
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 1 sample with support for all annotated introns
uncharacterized LOC125229224, 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 12 samples with support for all annotated introns
uncharacterized transmembrane protein DDB_G0289901-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 37% 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: 34 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
putative fatty acyl-CoA reductase CG5065
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tyrosine-protein kinase Btk29A, 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 2 samples with support for all annotated introns
tyrosine-protein kinase Btk29A, transcript variant X2
tyrosine-protein kinase Btk29A, transcript variant X9
tyrosine-protein kinase Btk29A isoform X1
tyrosine-protein kinase Btk29A isoform X8
tyrosine-protein kinase Btk29A isoform X2
tyrosine-protein kinase Btk29A, 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 4 samples with support for all annotated introns
uncharacterized protein LOC125229234 isoform X3
tyrosine-protein kinase Btk29A, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tyrosine-protein kinase Btk29A, transcript variant X4
uncharacterized protein LOC125229234 isoform X4
tyrosine-protein kinase Btk29A, transcript variant X6
uncharacterized protein LOC125229234 isoform X5
tyrosine-protein kinase Btk29A, transcript variant X8
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 protein LOC125229234 isoform X7
tyrosine-protein kinase Btk29A, transcript variant X7
uncharacterized protein LOC125229234 isoform X6
CRAL-TRIO domain-containing protein C3H8.02
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
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: 2 Proteins, 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: 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: 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon CGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
beta-1,4-mannosyltransferase egh, transcript variant X2
beta-1,4-mannosyltransferase egh isoform X2
beta-1,4-mannosyltransferase egh, 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
beta-1,4-mannosyltransferase egh isoform X3
beta-1,4-mannosyltransferase egh, transcript variant X1
beta-1,4-mannosyltransferase egh isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: 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.
single-stranded DNA-binding protein, mitochondrial
gamma-tubulin complex component 2 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential cation channel protein painless
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 13 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: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transient receptor potential cation channel protein painless
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: dynamin-1-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
circadian clock-controlled protein daywake-like
TWiK family of potassium channels protein 9, 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 9 samples with support for all annotated introns
TWiK family of potassium channels protein 9, transcript variant X1
TWiK family of potassium channels protein 9, transcript variant X4
TWiK family of potassium channels protein 9, transcript variant X2
TWiK family of potassium channels protein 9
cAMP-dependent protein kinase catalytic subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 114 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
cAMP-dependent protein kinase catalytic subunit gamma-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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89% coverage of the annotated genomic feature by RNAseq alignments
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
LOW QUALITY PROTEIN: cytochrome P450 4g15-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 13 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 71% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125228866, transcript variant X1
uncharacterized LOC125228866, transcript variant X2
transcriptional regulator ovo-like, transcript variant X1
transcriptional regulator ovo-like, transcript variant X2
transcriptional regulator ovo-like, transcript variant X3
transcriptional regulator ovo-like isoform X2
transcriptional regulator ovo-like isoform X1
transcriptional regulator ovo-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
vacuolar ATPase assembly integral membrane protein VMA21 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 13 samples with support for all annotated introns
vacuolar protein-sorting-associated protein 36
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
histidine--tRNA ligase, cytoplasmic, transcript variant X1
histidine--tRNA ligase, cytoplasmic, transcript variant X4
histidine--tRNA ligase, cytoplasmic, transcript variant X2
histidine--tRNA ligase, cytoplasmic, transcript variant X3
histidine--tRNA ligase, cytoplasmic isoform X1
histidine--tRNA ligase, cytoplasmic isoform X3
histidine--tRNA ligase, cytoplasmic isoform X2
transfer RNA tyrosine (anticodon GUA); 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: 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125228754, transcript variant X2
uncharacterized LOC125228754, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: LIM domain only protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
malate dehydrogenase, mitochondrial-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: malate dehydrogenase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; 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: inserted 1 base in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: apoptosis inhibitor 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline decarboxylase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
proline-rich extensin-like protein EPR1, transcript variant X1
proline-rich extensin-like protein EPR1, transcript variant X6
proline-rich extensin-like protein EPR1, transcript variant X3
adhesive plaque matrix protein isoform X1
adhesive plaque matrix protein isoform X3
proline-rich extensin-like protein EPR1, transcript variant X2
adhesive plaque matrix protein isoform X2
proline-rich extensin-like protein EPR1, transcript variant X4
adhesive plaque matrix protein isoform X4
proline-rich extensin-like protein EPR1, transcript variant X5
proline-rich extensin-like protein EPR1, transcript variant X7
adhesive plaque matrix protein isoform X5
proline-rich extensin-like protein EPR1, transcript variant X8
proline-rich extensin-like protein EPR1 isoform X6
vascular endothelial growth factor receptor 1, 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 2 samples with support for all annotated introns
vascular endothelial growth factor receptor 1, 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 5 samples with support for all annotated introns
vascular endothelial growth factor receptor 1, transcript variant X2
vascular endothelial growth factor receptor 1, 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 1 sample with support for all annotated introns
vascular endothelial growth factor receptor 1, 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 3 samples with support for all annotated introns
vascular endothelial growth factor receptor 1, transcript variant X5
vascular endothelial growth factor receptor 1 isoform X1
vascular endothelial growth factor receptor 1 isoform X4
vascular endothelial growth factor receptor 1 isoform X2
vascular endothelial growth factor receptor 1 isoform X3
vascular endothelial growth factor receptor 1 isoform X6
vascular endothelial growth factor receptor 1 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
cytochrome P450 4d2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
cytochrome P450 4d2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 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 7 samples with support for all annotated introns
insulin-like growth factor-binding protein complex acid labile subunit
N-acetylglucosamine-6-phosphate deacetylase
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
LOW QUALITY PROTEIN: N-acetylglucosamine-6-phosphate deacetylase
LOW QUALITY PROTEIN: brain tumor protein-like
signal recognition particle 9 kDa protein
transcription factor SPT20 homolog-like 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: transcription factor SPT20 homolog-like 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: probable Ufm1-specific protease 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125228456, transcript variant X2
uncharacterized LOC125228456, transcript variant X1
uncharacterized protein LOC125228456 isoform X1
uncharacterized protein LOC125228456 isoform X2
LOW QUALITY PROTEIN: uncharacterized protein LOC125228662
uncharacterized LOC125228455, transcript variant X2
uncharacterized LOC125228455, 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 5 samples with support for all annotated introns
uncharacterized protein LOC125228455 isoform X2
uncharacterized protein LOC125228455 isoform X1
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
bombyxin-related peptide A-like, transcript variant X2
bombyxin-related peptide A-like, transcript variant X6
bombyxin-related peptide A-like, transcript variant X1
bombyxin-related peptide A-like, transcript variant X3
bombyxin-related peptide A-like, transcript variant X7
bombyxin-related peptide A-like, transcript variant X5
bombyxin-related peptide A-like, transcript variant X4
insulin-like growth factor I, juvenile form isoform X2
uncharacterized protein LOC125228966 isoform X3
uncharacterized protein LOC125228966 isoform X1
uncharacterized protein LOC125228966 isoform X5
uncharacterized protein LOC125228966 isoform X4
bombyxin-related peptide A-like isoform X7
bombyxin-related peptide A-like isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ras-related and estrogen-regulated growth inhibitor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
MAP kinase-activating death domain protein
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
uncharacterized LOC125228935, transcript variant X1
uncharacterized LOC125228935, transcript variant X2
uncharacterized protein LOC125228935 isoform X1
uncharacterized protein LOC125228935 isoform X2
uncharacterized LOC125228524, 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 5 samples with support for all annotated introns
uncharacterized LOC125228524, transcript variant X2
LOW QUALITY PROTEIN: THO complex subunit 2
probable 28S ribosomal protein S6, mitochondrial
translation initiation factor eIF-2B subunit epsilon
LOW QUALITY PROTEIN: translation initiation factor eIF-2B subunit epsilon
uncharacterized LOC125228623, transcript variant X1
uncharacterized LOC125228623, transcript variant X2
uncharacterized LOC125228623, transcript variant X3
uncharacterized LOC125228623, transcript variant X5
uncharacterized protein LOC125228623 isoform X2
uncharacterized protein LOC125228623 isoform X1
uncharacterized protein LOC125228623 isoform X4
uncharacterized LOC125228623, transcript variant X4
uncharacterized protein LOC125228623 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
paired mesoderm homeobox protein 2B-like
muscle LIM protein 1, transcript variant X1
muscle LIM protein 1, transcript variant X5
muscle LIM protein 1, transcript variant X3
muscle LIM protein 1, transcript variant X4
muscle LIM protein 1, transcript variant X2
DNA repair protein complementing XP-C cells homolog
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
ankyrin repeat, SAM and basic leucine zipper domain-containing protein 1
vesicle-associated membrane protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 36-like, transcript variant X2
protein phosphatase 1 regulatory subunit 36-like, transcript variant X1
protein phosphatase 1 regulatory subunit 36-like isoform X2
protein phosphatase 1 regulatory subunit 36-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
palmitoyltransferase Hip14, transcript variant X1
palmitoyltransferase Hip14, 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 12 samples with support for all annotated introns
uncharacterized LOC125228950, transcript variant X5
uncharacterized LOC125228950, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125228950, transcript variant X1
uncharacterized LOC125228950, transcript variant X7
uncharacterized protein LOC125228950 isoform X6
uncharacterized protein LOC125228950 isoform X1
uncharacterized LOC125228950, transcript variant X6
uncharacterized protein LOC125228950 isoform X10
uncharacterized protein LOC125228950 isoform X5
uncharacterized LOC125228950, transcript variant X3
uncharacterized LOC125228950, transcript variant X9
uncharacterized protein LOC125228950 isoform X8
uncharacterized protein LOC125228950 isoform X3
uncharacterized LOC125228950, transcript variant X8
uncharacterized LOC125228950, transcript variant X2
uncharacterized protein LOC125228950 isoform X7
uncharacterized protein LOC125228950 isoform X2
uncharacterized LOC125228950, transcript variant X4
uncharacterized LOC125228950, transcript variant X10
uncharacterized protein LOC125228950 isoform X9
uncharacterized protein LOC125228950 isoform X4
eukaryotic translation initiation factor 4 gamma 2, 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 12 samples with support for all annotated introns
eukaryotic translation initiation factor 4 gamma 2, 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 12 samples with support for all annotated introns
eukaryotic translation initiation factor 4 gamma 2 isoform X1
eukaryotic translation initiation factor 4 gamma 2 isoform X2
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
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: tyrosine-protein phosphatase 10D-like
uncharacterized LOC125228944, transcript variant X1
uncharacterized LOC125228944, transcript variant X2
uncharacterized protein LOC125228944 isoform X1
uncharacterized protein LOC125228944 isoform X2
double-strand break repair protein MRE11
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
RISC-loading complex subunit TARBP2-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 12 samples with support for all annotated introns
RISC-loading complex subunit TARBP2-like, transcript variant X2
RISC-loading complex subunit TARBP2-like isoform X2
RISC-loading complex subunit TARBP2-like isoform X1
transient receptor potential-gamma protein-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: transient receptor potential-gamma protein-like
caseinolytic peptidase B protein homolog, transcript variant X2
caseinolytic peptidase B protein homolog, transcript variant X1
caseinolytic peptidase B protein homolog isoform X2
caseinolytic peptidase B protein homolog isoform X1
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like
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
uncharacterized protein KIAA0930 homolog
phosphatidylcholine:ceramide cholinephosphotransferase 2-like, transcript variant X1
phosphatidylcholine:ceramide cholinephosphotransferase 2-like, transcript variant X3
phosphatidylcholine:ceramide cholinephosphotransferase 2-like, transcript variant X2
phosphatidylcholine:ceramide cholinephosphotransferase 2-like, transcript variant X4
phosphatidylcholine:ceramide cholinephosphotransferase 2-like isoform X1
phosphatidylcholine:ceramide cholinephosphotransferase 2-like isoform X2
probable cytochrome P450 6a21, transcript variant X1
probable cytochrome P450 6a21, transcript variant X2
probable cytochrome P450 6a21 isoform X2
probable phospholipid-transporting ATPase IA, transcript variant X2
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 4 samples with support for all annotated introns
probable phospholipid-transporting ATPase IA, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
probable phospholipid-transporting ATPase IA isoform X2
probable phospholipid-transporting ATPase IA isoform X5
probable phospholipid-transporting ATPase IA, transcript variant X3
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
probable phospholipid-transporting ATPase IA, transcript variant X1
probable phospholipid-transporting ATPase IA, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
probable phospholipid-transporting ATPase IA isoform X3
probable phospholipid-transporting ATPase IA isoform X1
probable phospholipid-transporting ATPase IA isoform X4
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125228991, transcript variant X2
uncharacterized LOC125228991, transcript variant X1
cholinephosphotransferase 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cholinephosphotransferase 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
cholinephosphotransferase 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
cholinephosphotransferase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
cholinephosphotransferase 1, transcript variant X2
cholinephosphotransferase 1, 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
ankyrin repeat and BTB/POZ domain-containing protein 2
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
NADH-cytochrome b5 reductase 2, transcript variant X2
NADH-cytochrome b5 reductase 2, transcript variant X1
NADH-cytochrome b5 reductase 2 isoform X2
NADH-cytochrome b5 reductase 2 isoform X1
proton-coupled amino acid transporter-like protein pathetic, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
proton-coupled amino acid transporter-like protein pathetic, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
proton-coupled amino acid transporter-like protein pathetic, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
proton-coupled amino acid transporter-like protein pathetic, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
proton-coupled amino acid transporter-like protein pathetic isoform X3
proton-coupled amino acid transporter-like protein CG1139 isoform X1
proton-coupled amino acid transporter-like protein CG1139 isoform X2
proton-coupled amino acid transporter-like protein pathetic isoform X4
proton-coupled amino acid transporter-like protein pathetic
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
proton-coupled amino acid transporter-like protein pathetic isoform X1
proton-coupled amino acid transporter-like protein pathetic isoform X2
transfer RNA alanine (anticodon GGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 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: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transfer RNA threonine (anticodon CGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 7-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 7-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 7-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 12 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 7-like isoform X1
CCR4-NOT transcription complex subunit 7-like isoform X2
chromatin-remodeling complex ATPase chain Iswi
uncharacterized LOC125228696, transcript variant X1
uncharacterized LOC125228696, transcript variant X3
uncharacterized LOC125228696, transcript variant X2
sodium- and chloride-dependent glycine transporter 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: sodium- and chloride-dependent glycine transporter 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
heat shock 70 kDa protein 4, transcript variant X1
heat shock 70 kDa protein 4, 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 13 samples with support for all annotated introns
RNA polymerase II subunit A C-terminal domain phosphatase SSU72
39S ribosomal protein L22, mitochondrial
LOW QUALITY PROTEIN: 39S ribosomal protein L22, mitochondrial
UDP-N-acetylglucosamine transporter, 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 11 samples with support for all annotated introns
UDP-N-acetylglucosamine transporter, 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
UDP-N-acetylglucosamine transporter, 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 3 samples with support for all annotated introns
UDP-N-acetylglucosamine transporter, transcript variant X6
UDP-N-acetylglucosamine transporter, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
UDP-N-acetylglucosamine transporter, 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 7 samples with support for all annotated introns
UDP-N-acetylglucosamine transporter isoform X3
UDP-N-acetylglucosamine transporter isoform X1
UDP-N-acetylglucosamine transporter isoform X4
UDP-N-acetylglucosamine transporter isoform X2
UDP-N-acetylglucosamine transporter isoform X5
coiled-coil domain-containing protein 22 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized oxidoreductase YrbE-like
zeta-sarcoglycan-like, transcript variant X1
zeta-sarcoglycan-like, transcript variant X3
zeta-sarcoglycan-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125228503, transcript variant X2
uncharacterized LOC125228503, transcript variant X1
proton channel OtopLc-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 9 samples with support for all annotated introns
proton channel OtopLc-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 7 samples with support for all annotated introns
proton channel OtopLc-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 8 samples with support for all annotated introns
histone-lysine N-methyltransferase Suv4-20
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
CASP-like protein 4U1, transcript variant X2
CASP-like protein 4U1, transcript variant X3
CASP-like protein 4U1, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; 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: inserted 3 bases in 3 codons; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cytoplasmic dynein 2 heavy chain 1
succinate dehydrogenase assembly factor 2-B, mitochondrial-like
branched-chain-amino-acid aminotransferase, cytosolic
intraflagellar transport protein 88 homolog, transcript variant X2
intraflagellar transport protein 88 homolog, transcript variant X1
intraflagellar transport protein 88 homolog isoform X2
intraflagellar transport protein 88 homolog isoform X1
uncharacterized LOC125228939, transcript variant X1
uncharacterized LOC125228939, 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 13 samples with support for all annotated introns
uncharacterized protein LOC125228939 isoform X2
uncharacterized protein LOC125228939 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
eukaryotic translation initiation factor 3 subunit M
heat shock protein 75 kDa, mitochondrial
LOW QUALITY PROTEIN: heat shock protein 75 kDa, mitochondrial
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 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
saccharopine dehydrogenase-like oxidoreductase
myosin heavy chain, clone 203, transcript variant X2
myosin heavy chain, clone 203 isoform X2
myosin heavy chain, clone 203, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9, mitochondrial
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
H/ACA ribonucleoprotein complex subunit GAR1-like
uncharacterized LOC125228508, transcript variant X1
uncharacterized LOC125228508, transcript variant X2
uncharacterized LOC125228508, transcript variant X3
uncharacterized protein LOC125228508 isoform X1
uncharacterized protein LOC125228508 isoform X2
uncharacterized protein LOC125228508 isoform X3
coiled-coil domain-containing protein 186-like
myosin heavy chain, non-muscle-like, transcript variant X1
myosin heavy chain, non-muscle-like, transcript variant X4
myosin heavy chain, non-muscle-like, transcript variant X5
myosin heavy chain, non-muscle-like, transcript variant X2
myosin heavy chain, non-muscle-like, transcript variant X3
myosin heavy chain, cardiac muscle isoform-like isoform X4
myosin heavy chain, non-muscle-like isoform X3
uncharacterized LOC125229075, transcript variant X1
uncharacterized LOC125229075, transcript variant X2
uncharacterized protein LOC125229075 isoform X1
uncharacterized protein LOC125229075 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 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 11 samples with support for all annotated introns
splicing factor YJU2, 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 1 sample with support for all annotated introns
splicing factor YJU2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
39S ribosomal protein L28, mitochondrial
probable phosphorylase b kinase regulatory subunit alpha, transcript variant X2
probable phosphorylase b kinase regulatory subunit alpha, transcript variant X1
probable phosphorylase b kinase regulatory subunit alpha, 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 10 samples with support for all annotated introns
probable phosphorylase b kinase regulatory subunit alpha, transcript variant X6
probable phosphorylase b kinase regulatory subunit alpha, 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 2 samples with support for all annotated introns
probable phosphorylase b kinase regulatory subunit alpha, transcript variant X5
probable phosphorylase b kinase regulatory subunit alpha isoform X5
probable phosphorylase b kinase regulatory subunit alpha isoform X3
probable phosphorylase b kinase regulatory subunit alpha isoform X4
probable phosphorylase b kinase regulatory subunit alpha isoform X1
probable phosphorylase b kinase regulatory subunit alpha isoform X6
probable phosphorylase b kinase regulatory subunit alpha isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: adenylate cyclase type 9
gamma-aminobutyric acid receptor alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit beta-like
low-density lipoprotein receptor-related protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
pyridine nucleotide-disulfide oxidoreductase domain-containing protein 1
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
proton channel OtopLc, transcript variant X2
proton channel OtopLc, transcript variant X3
proton channel OtopLc, transcript variant X1
proton channel OtopLc, transcript variant X6
proton channel OtopLc, transcript variant X7
proton channel OtopLc, transcript variant X11
proton channel OtopLc, transcript variant X8
proton channel OtopLc, transcript variant X5
proton channel OtopLc, transcript variant X4
proton channel OtopLc, transcript variant X9
proton channel OtopLc, transcript variant X10
uncharacterized LOC125229044, transcript variant X2
uncharacterized LOC125229044, transcript variant X3
uncharacterized LOC125229044, transcript variant X1
uncharacterized protein LOC125229044 isoform X1
uncharacterized protein LOC125229044 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
glucose dehydrogenase [FAD, quinone]-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
anther-specific proline-rich protein APG-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
lipopolysaccharide-induced tumor necrosis factor-alpha factor homolog
lipopolysaccharide-induced tumor necrosis factor-alpha factor-like
lipopolysaccharide-induced tumor necrosis factor-alpha factor homolog, 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 4 samples with support for all annotated introns
lipopolysaccharide-induced tumor necrosis factor-alpha factor homolog, 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 8 samples with support for all annotated introns
lipopolysaccharide-induced tumor necrosis factor-alpha factor homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
lipopolysaccharide-induced tumor necrosis factor-alpha factor homolog isoform X3
lipopolysaccharide-induced tumor necrosis factor-alpha factor homolog isoform X2
lipopolysaccharide-induced tumor necrosis factor-alpha factor homolog isoform X1
39S ribosomal protein L27, mitochondrial
membrane-associated progesterone receptor component 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
iduronate 2-sulfatase, 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 4 samples with support for all annotated introns
iduronate 2-sulfatase, transcript variant X2
uncharacterized LOC125228918, transcript variant X2
uncharacterized LOC125228918, transcript variant X1
uncharacterized LOC125228918, transcript variant X3
uncharacterized protein LOC125228918 isoform X1
uncharacterized LOC125228918, transcript variant X4
uncharacterized protein LOC125228918 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC125228528, transcript variant X1
uncharacterized LOC125228528, transcript variant X2
uncharacterized LOC125228528, transcript variant X4
uncharacterized LOC125228528, transcript variant X3
nose resistant to fluoxetine protein 6-like
nose resistant to fluoxetine protein 6-like, transcript variant X1
nose resistant to fluoxetine protein 6-like isoform X1
nose resistant to fluoxetine protein 6-like, transcript variant X2
nose resistant to fluoxetine protein 6-like isoform X2
uncharacterized LOC125228970, transcript variant X2
uncharacterized LOC125228970, transcript variant X1
uncharacterized protein LOC125228970 isoform X1
uncharacterized protein LOC125228970 isoform X2
lipase member H-B-like, transcript variant X2
lipase member H-B-like, transcript variant X1
endothelial lipase-like, transcript variant X1
endothelial lipase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53% 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 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125229195, transcript variant X2
uncharacterized LOC125229195, transcript variant X1
uncharacterized protein LOC125229195 isoform X2
uncharacterized protein LOC125229195 isoform X1
uncharacterized LOC125229190, transcript variant X2
uncharacterized LOC125229190, transcript variant X1
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125228563, 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 8 samples with support for all annotated introns
uncharacterized LOC125228563, transcript variant X2
uncharacterized LOC125228563, transcript variant X3
uncharacterized protein LOC125228563 isoform X1
uncharacterized protein LOC125228563 isoform X2
uncharacterized protein LOC125228563 isoform X3
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
DNA-binding protein D-ETS-4-like, transcript variant X2
DNA-binding protein D-ETS-4-like isoform X2
DNA-binding protein D-ETS-4-like, transcript variant X1
DNA-binding protein D-ETS-4-like isoform X1
DNA-binding protein D-ETS-4-like, transcript variant X3
DNA-binding protein D-ETS-4-like, transcript variant X4
DNA-binding protein D-ETS-4-like isoform X3
DNA-binding protein D-ETS-4-like isoform X4
facilitated trehalose transporter Tret1-like
ADP-ribosylation factor-like protein 1, 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 7 samples with support for all annotated introns
ADP-ribosylation factor-like protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
ADP-ribosylation factor-like protein 1 isoform X1
ADP-ribosylation factor-like protein 1 isoform X2
1-acylglycerol-3-phosphate O-acyltransferase Pnpla3-like, transcript variant X3
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 13 samples with support for all annotated introns
1-acylglycerol-3-phosphate O-acyltransferase Pnpla3-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 11 samples with support for all annotated introns
1-acylglycerol-3-phosphate O-acyltransferase Pnpla3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
1-acylglycerol-3-phosphate O-acyltransferase Pnpla3-like isoform X3
1-acylglycerol-3-phosphate O-acyltransferase Pnpla3-like isoform X1
1-acylglycerol-3-phosphate O-acyltransferase Pnpla3-like isoform X2
nitric oxide synthase-interacting protein homolog
ubiquitin carboxyl-terminal hydrolase 46, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 46, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 46 isoform X2
ubiquitin carboxyl-terminal hydrolase 46 isoform X1
facilitated trehalose transporter Tret1-like, transcript variant X3
facilitated trehalose transporter Tret1-like, transcript variant X4
facilitated trehalose transporter Tret1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
facilitated trehalose transporter Tret1-like, transcript variant X2
facilitated trehalose transporter Tret1-like isoform X4
facilitated trehalose transporter Tret1-like isoform X1
facilitated trehalose transporter Tret1-like isoform X3
facilitated trehalose transporter Tret1-like isoform X2
uncharacterized LOC125229006, transcript variant X2
uncharacterized LOC125229006, transcript variant X3
uncharacterized LOC125229006, 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 LOC125229208, transcript variant X2
uncharacterized LOC125229208, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon GGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
low-density lipoprotein receptor-related protein 6
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 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
LOW QUALITY PROTEIN: low-density lipoprotein receptor-related protein 6
dolichyl-phosphate beta-glucosyltransferase
programmed cell death protein 6, transcript variant X2
programmed cell death protein 6 isoform X2
programmed cell death protein 6, transcript variant X1
programmed cell death protein 6, transcript variant X3
programmed cell death protein 6 isoform X1
programmed cell death protein 6 isoform X3
uncharacterized LOC125228639, transcript variant X1
uncharacterized protein LOC125228639 isoform X1
uncharacterized LOC125228639, transcript variant X2
uncharacterized protein LOC125228639 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
7-methylguanosine phosphate-specific 5'-nucleotidase, transcript variant X3
7-methylguanosine phosphate-specific 5'-nucleotidase, transcript variant X2
7-methylguanosine phosphate-specific 5'-nucleotidase, transcript variant X1
7-methylguanosine phosphate-specific 5'-nucleotidase
phospholipid-transporting ATPase VA, 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 9 samples with support for all annotated introns
phospholipid-transporting ATPase VA, 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
phospholipid-transporting ATPase VB isoform X2
phospholipid-transporting ATPase VA isoform X1
protein kinase C-binding protein NELL1-like
uncharacterized LOC125229036, transcript variant X2
uncharacterized LOC125229036, transcript variant X1
uncharacterized protein LOC125229036 isoform X2
uncharacterized protein LOC125229036 isoform X1
peptidyl-prolyl cis-trans isomerase E-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: peptidyl-prolyl cis-trans isomerase E-like
tetraspanin-4-like, transcript variant X1
tetraspanin-4-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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC125229187, transcript variant X2
uncharacterized LOC125229187, transcript variant X1
uncharacterized protein LOC125229187 isoform X1
uncharacterized protein LOC125229187 isoform X2
DNA-(apurinic or apyrimidinic site) endonuclease
rab proteins geranylgeranyltransferase component A 1
putative uncharacterized protein DDB_G0279653
CD151 antigen-like, transcript variant X4
CD151 antigen-like, transcript variant X5
CD151 antigen-like, transcript variant X7
CD151 antigen-like, transcript variant X1
CD151 antigen-like, transcript variant X3
CD151 antigen-like, transcript variant X2
CD151 antigen-like, transcript variant X6
CD151 antigen-like, transcript variant X8
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
LOW QUALITY PROTEIN: sorting nexin lst-4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55% coverage of the annotated genomic feature by RNAseq alignments
post-GPI attachment to proteins factor 2-like
transcriptional enhancer factor TEF-1, transcript variant X1
transcriptional enhancer factor TEF-1, transcript variant X2
transcriptional enhancer factor TEF-1 isoform X1
transcriptional enhancer factor TEF-1, transcript variant X3
transcriptional enhancer factor TEF-1, transcript variant X4
transcriptional enhancer factor TEF-1 isoform X3
transcriptional enhancer factor TEF-1 isoform X4
mitochondrial inner membrane protease subunit 1
zinc transporter 1, 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 7 samples with support for all annotated introns
zinc transporter 1, transcript variant X1
zinc/cadmium resistance protein isoform X1
glutamate receptor ionotropic, delta-2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutamate receptor ionotropic, delta-2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glutamate receptor ionotropic, delta-2 isoform X2
glutamate receptor ionotropic, delta-2 isoform X1
histone deacetylase complex subunit SAP30 homolog
high mobility group protein DSP1-like, transcript variant X4
high mobility group protein DSP1-like, transcript variant X1
high mobility group protein DSP1-like isoform X1
high mobility group protein DSP1-like, transcript variant X3
high mobility group protein DSP1-like isoform X3
high mobility group protein DSP1-like, transcript variant X2
high mobility group protein DSP1-like isoform X2
high mobility group protein DSP1-like isoform X4
protein O-mannosyl-transferase Tmtc3, transcript variant X1
protein O-mannosyl-transferase Tmtc3, transcript variant X2
protein O-mannosyl-transferase Tmtc3 isoform X1
protein O-mannosyl-transferase Tmtc3 isoform X2
uncharacterized LOC125229157, transcript variant X2
uncharacterized LOC125229157, transcript variant X1
uncharacterized protein LOC125229157 isoform X2
uncharacterized protein LOC125229157 isoform X1
uncharacterized LOC125229159, transcript variant X1
uncharacterized LOC125229159, transcript variant X2
FGFR1 oncogene partner 2 homolog, 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 5 samples with support for all annotated introns
FGFR1 oncogene partner 2 homolog, transcript variant X1
protein bric-a-brac 2, transcript variant X2
protein bric-a-brac 2, transcript variant X1
sterol regulatory element-binding protein 1, transcript variant X1
sterol regulatory element-binding protein 1, transcript variant X2
sterol regulatory element-binding protein 1, transcript variant X3
sterol regulatory element-binding protein 1 isoform X1
sterol regulatory element-binding protein 1 isoform X2
sterol regulatory element-binding protein 1 isoform X3
uncharacterized LOC125228738, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC125228738, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
carbonic anhydrase-related protein 10-like
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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
acyl-CoA Delta(11) desaturase-like, transcript variant X2
acyl-CoA Delta(11) desaturase-like, transcript variant X1
serine/threonine-protein phosphatase rdgC, transcript variant X2
serine/threonine-protein phosphatase rdgC, transcript variant X1
serine/threonine-protein phosphatase rdgC isoform X2
serine/threonine-protein phosphatase rdgC isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 80% coverage of the annotated genomic feature by RNAseq alignments
protein PTCD3 homolog, mitochondrial, transcript variant X1
protein PTCD3 homolog, mitochondrial, transcript variant X2
protein PTCD3 homolog, mitochondrial isoform X1
protein PTCD3 homolog, mitochondrial isoform X2
probable GPI-anchored adhesin-like protein PGA55
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125228531, transcript variant X1
uncharacterized protein LOC125228531 isoform X1
uncharacterized LOC125228531, transcript variant X2
uncharacterized protein LOC125228531 isoform X2
uncharacterized LOC125228533, transcript variant X3
uncharacterized LOC125228533, transcript variant X1
uncharacterized LOC125228533, transcript variant X2
uncharacterized protein LOC125228533 isoform X2
uncharacterized protein LOC125228533 isoform X1
uncharacterized protein LOC125228533 isoform X3
transmembrane protein 41 homolog, transcript variant X1
transmembrane protein 41 homolog, transcript variant X2
transmembrane protein 41 homolog isoform X2
transmembrane protein 41 homolog isoform X1
tumor necrosis factor receptor superfamily member wengen, transcript variant X2
tumor necrosis factor receptor superfamily member wengen, transcript variant X1
tumor necrosis factor receptor superfamily member wengen isoform X1
tumor necrosis factor receptor superfamily member wengen isoform X2
ER degradation-enhancing alpha-mannosidase-like protein 2
testis-specific serine/threonine-protein kinase 3-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 1 sample with support for all annotated introns
testis-specific serine/threonine-protein kinase 3-like, transcript variant X1
testis-specific serine/threonine-protein kinase 3-like
testis-specific serine/threonine-protein kinase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins
testis-specific serine/threonine-protein kinase 3-like, transcript variant X4
testis-specific serine/threonine-protein kinase 3-like, transcript variant X3
testis-specific serine/threonine-protein kinase 3-like isoform X2
testis-specific serine/threonine-protein kinase 3-like isoform X1
testis-specific serine/threonine-protein kinase 3-like, transcript variant X5
testis-specific serine/threonine-protein kinase 6-like isoform X3
testis-specific serine/threonine-protein kinase 3-like isoform X4
uncharacterized protein LOC125228977 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
gastrula zinc finger protein XlCGF8.2DB-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
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; 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
solute carrier family 22 member 3-like, transcript variant X6
solute carrier family 22 member 3-like, transcript variant X3
solute carrier family 22 member 3-like, transcript variant X4
solute carrier family 22 member 3-like, transcript variant X1
solute carrier family 22 member 3-like, transcript variant X2
solute carrier family 22 member 3-like, transcript variant X5
solute carrier family 22 member 3-like isoform X1
solute carrier family 22 member 3-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 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: 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein O-mannosyl-transferase TMTC1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 69% coverage of the annotated genomic feature by RNAseq alignments
bombyxin A-3 homolog, transcript variant X3
bombyxin A-3 homolog, transcript variant X2
bombyxin A-3 homolog, transcript variant X1
V-type proton ATPase 16 kDa proteolipid subunit c
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 127 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: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
growth arrest and DNA damage-inducible proteins-interacting protein 1
clathrin light chain, transcript variant X1
clathrin light chain, transcript variant X2
phosphatidylinositol N-acetylglucosaminyltransferase subunit A
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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
LOW QUALITY PROTEIN: phosphatidylinositol N-acetylglucosaminyltransferase subunit A
alkylated DNA repair protein alkB homolog 8-like
LOW QUALITY PROTEIN: alkylated DNA repair protein alkB homolog 8-like
LOW QUALITY PROTEIN: TBC1 domain family member 19
tyrosine-protein phosphatase non-receptor type 11
arylsulfatase I-like, transcript variant X1
arylsulfatase I-like, transcript variant X3
arylsulfatase I-like, transcript variant X4
arylsulfatase I-like, transcript variant X5
arylsulfatase I-like, transcript variant X6
arylsulfatase I-like, transcript variant X7
arylsulfatase I-like, transcript variant X2
N-acetylgalactosaminyltransferase 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized protein K02A2.6-like, transcript variant X2
uncharacterized protein K02A2.6-like, transcript variant X1
uncharacterized protein K02A2.6-like isoform X1
uncharacterized protein LOC125228561 isoform X2
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: 13 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: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
cytochrome P450 6B6-like, transcript variant X3
cytochrome P450 6B6-like, transcript variant X2
cytochrome P450 6B6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC125228795, transcript variant X1
uncharacterized LOC125228795, transcript variant X2
uncharacterized protein LOC125228795 isoform X1
uncharacterized protein LOC125228795 isoform X2
proton-coupled amino acid transporter-like protein CG1139
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cholecystokinin receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; 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
LOW QUALITY PROTEIN: proton-coupled amino acid transporter-like protein pathetic
elongation of very long chain fatty acids protein 4-like
MORN repeat-containing protein 4 homolog
general transcription factor II-I repeat domain-containing protein 2-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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: sensory neuron membrane protein 2-like
uncharacterized LOC125229062, transcript variant X1
uncharacterized LOC125229062, transcript variant X2
uncharacterized protein LOC125229062 isoform X1
uncharacterized protein LOC125229062 isoform X2
uncharacterized LOC125228922, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC125228922 isoform X2
uncharacterized LOC125228922, transcript variant X1
uncharacterized LOC125228922, 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 1 sample with support for all annotated introns
uncharacterized protein LOC125228922 isoform X1
uncharacterized protein LOC125228922 isoform X3
carbohydrate sulfotransferase 4-like, transcript variant X2
carbohydrate sulfotransferase 4-like, transcript variant X1
carbohydrate sulfotransferase 4-like isoform X1
carbohydrate sulfotransferase 4-like isoform X2
histone-lysine N-methyltransferase SETMAR-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125228593, transcript variant X1
uncharacterized LOC125228593, transcript variant X4
uncharacterized LOC125228593, transcript variant X5
uncharacterized LOC125228593, transcript variant X3
uncharacterized LOC125228593, transcript variant X2
uncharacterized protein LOC125228593 isoform X1
uncharacterized protein LOC125228593 isoform X2
uncharacterized protein LOC125228593 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 85% 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: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
SH3 and multiple ankyrin repeat domains protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
probable arginine--tRNA ligase, mitochondrial
dehydrodolichyl diphosphate synthase complex subunit DHDDS
RNA transcription, translation and transport factor protein
mitochondrial import inner membrane translocase subunit Tim8
probable DNA-directed RNA polymerases I and III subunit RPAC2, transcript variant X1
probable DNA-directed RNA polymerases I and III subunit RPAC2, transcript variant X2
probable DNA-directed RNA polymerases I and III subunit RPAC2 isoform X1
probable DNA-directed RNA polymerases I and III subunit RPAC2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
carboxypeptidase Q-like, transcript variant X3
carboxypeptidase Q-like, transcript variant X1
carboxypeptidase Q-like, transcript variant X2
uncharacterized LOC125229205, 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 8 samples with support for all annotated introns
uncharacterized LOC125229205, transcript variant X2
uncharacterized protein LOC125229205 isoform X1
uncharacterized protein LOC125229205 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125228869, transcript variant X1
uncharacterized LOC125228869, transcript variant X2
uncharacterized LOC125228869, transcript variant X3
uncharacterized LOC125228869, transcript variant X4
uncharacterized protein LOC125228869 isoform X1
uncharacterized protein LOC125228869 isoform X2
uncharacterized protein LOC125228869 isoform X3
uncharacterized protein LOC125228869 isoform X4
uncharacterized LOC125228872, transcript variant X1
uncharacterized LOC125228872, transcript variant X2
uncharacterized protein LOC125228872 isoform X2
uncharacterized protein LOC125228872 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC125228976, transcript variant X1
uncharacterized LOC125228976, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: acetylcholinesterase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
acetylcholinesterase-like, transcript variant X1
acetylcholinesterase-like, transcript variant X2
acetylcholinesterase-like, transcript variant X3
acetylcholinesterase-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
fat-like cadherin-related tumor suppressor homolog
probable U3 small nucleolar RNA-associated protein 11
neprilysin-4-like, transcript variant X2
neprilysin-4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
zinc finger matrin-type protein CG9776-like
protein transport protein Sec61 subunit gamma
uncharacterized LOC125228557, transcript variant X2
uncharacterized LOC125228557, transcript variant X1
uncharacterized protein LOC125228557 isoform X2
uncharacterized protein LOC125228557 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC125228913, transcript variant X1
uncharacterized LOC125228913, transcript variant X2
uncharacterized protein LOC125228913 isoform X1
uncharacterized protein LOC125228913 isoform X2
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X2
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X3
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X4
basement membrane-specific heparan sulfate proteoglycan core protein-like, transcript variant X1
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X2
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X3
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X4
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X1
transfer RNA aspartic acid (anticodon AUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ATP-dependent RNA helicase SUV3 homolog, mitochondrial
eukaryotic translation initiation factor 5B, transcript variant X1
eukaryotic translation initiation factor 5B, transcript variant X2
eukaryotic translation initiation factor 5B isoform X1
eukaryotic translation initiation factor 5B isoform X2
uncharacterized LOC125229227, transcript variant X1
uncharacterized LOC125229227, transcript variant X2
uncharacterized protein LOC125229227 isoform X2
uncharacterized protein LOC125229227 isoform X1
protein sprouty homolog 4, transcript variant X2
protein sprouty homolog 4, transcript variant X1
protein sprouty homolog 4, transcript variant X3
retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit delta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha, 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 3 samples with support for all annotated introns
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha, 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 1 sample with support for all annotated introns
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha, transcript variant X3
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha, transcript variant X5
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha, transcript variant X1
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha, transcript variant X6
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha isoform X1
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha isoform X2
heparan-alpha-glucosaminide N-acetyltransferase, transcript variant X1
heparan-alpha-glucosaminide N-acetyltransferase, transcript variant X2
heparan-alpha-glucosaminide N-acetyltransferase isoform X1
heparan-alpha-glucosaminide N-acetyltransferase isoform X2
cyclic AMP response element-binding protein A, transcript variant X2
cyclic AMP response element-binding protein A isoform X2
cyclic AMP response element-binding protein A, transcript variant X1
uncharacterized protein LOC125228887 isoform X1
piggyBac transposable element-derived protein 3-like
transfer RNA arginine (anticodon GCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
TBC domain-containing protein kinase-like protein
biorientation of chromosomes in cell division protein 1-like 1, transcript variant X3
biorientation of chromosomes in cell division protein 1-like 1, transcript variant X2
biorientation of chromosomes in cell division protein 1-like 1, transcript variant X1
biorientation of chromosomes in cell division protein 1-like 1, transcript variant X4
biorientation of chromosomes in cell division protein 1-like 1 isoform X1
biorientation of chromosomes in cell division protein 1-like 1 isoform X2
synaptotagmin-5-like, transcript variant X1
synaptotagmin-5-like, transcript variant X2
venom dipeptidyl peptidase 4-like, transcript variant X1
venom dipeptidyl peptidase 4-like, transcript variant X2
venom dipeptidyl peptidase 4-like isoform X1
venom dipeptidyl peptidase 4-like, transcript variant X3
venom dipeptidyl peptidase 4-like isoform X2
venom dipeptidyl peptidase 4-like, transcript variant X4
venom dipeptidyl peptidase 4-like isoform X3
cytochrome P450 CYP12A2-like, transcript variant X2
cytochrome P450 CYP12A2-like, transcript variant X1
trimethyllysine dioxygenase, mitochondrial
probable cytochrome P450 301a1, mitochondrial
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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: cytochrome P450 CYP12A2-like
uncharacterized mitochondrial protein AtMg00820-like
LOW QUALITY PROTEIN: seminal metalloprotease 1-like
uncharacterized LOC125229255, transcript variant X1
uncharacterized LOC125229255, transcript variant X2
uncharacterized protein LOC125229255 isoform X1
uncharacterized protein LOC125229255 isoform X2
seminal metalloprotease 1-like, transcript variant X1
seminal metalloprotease 1-like isoform X1
seminal metalloprotease 1-like, transcript variant X2
seminal metalloprotease 1-like isoform X2
zinc finger BED domain-containing protein 4-like