Plutella xylostella chromosome 12, ilPluXylo3.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Yponomeutoidea; Plutellidae; Plutella.
REFSEQ INFORMATION: The reference sequence is identical to\nOW026561.1.\nAssembly name: ilPluXylo3.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2022/03/10. The original whole-genome shotgun project has the\naccession CAKNZZ000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Plutella xylostella Annotation\n Release 103\nAnnotation Version :: 103\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: 59% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized LOC119693146, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
uncharacterized LOC119693146, 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 43 samples with support for all annotated introns
uncharacterized protein LOC119693146 isoform X2
uncharacterized protein LOC119693146 isoform X1
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 58 samples with support for all annotated introns
uncharacterized LOC125489262, transcript variant X2
uncharacterized LOC125489262, transcript variant X1
POU domain, class 3, transcription factor 4 isoform X3
POU domain, class 3, transcription factor 4 isoform X2
POU domain, class 3, transcription factor 4 isoform X1
POU domain, class 3, transcription factor 4 isoform X5
POU domain, class 3, transcription factor 4 isoform X4
uncharacterized LOC105394052, transcript variant X3
uncharacterized protein LOC105394052 isoform X3
uncharacterized LOC105394052, transcript variant X1
uncharacterized LOC105394052, transcript variant X2
uncharacterized protein LOC105394052 isoform X1
uncharacterized protein LOC105394052 isoform X2
uncharacterized protein K02A2.6-like, transcript variant X2
uncharacterized protein K02A2.6-like, transcript variant X3
uncharacterized protein K02A2.6-like, transcript variant X1
uncharacterized protein K02A2.6-like, transcript variant X4
uncharacterized protein LOC105389039 isoform X2
uncharacterized protein LOC105389039 isoform X3
uncharacterized protein K02A2.6-like isoform X1
probable serine/threonine-protein kinase DDB_G0278845
3-oxoacyl-[acyl-carrier-protein] reductase FabG
fork head domain transcription factor slp2
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
putative E3 ubiquitin-protein ligase UBR7
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 85 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 83 samples with support for all annotated introns
60S ribosomal protein L44; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309095.1
annotated by transcript or proteomic data
The RefSeq transcript has 2 substitutions, 3 non-frameshifting indels compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
apoptosis-resistant E3 ubiquitin protein ligase 1, transcript variant X3
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
apoptosis-resistant E3 ubiquitin protein ligase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
apoptosis-resistant E3 ubiquitin protein ligase 1 isoform X3
apoptosis-resistant E3 ubiquitin protein ligase 1 isoform X1
apoptosis-resistant E3 ubiquitin protein ligase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
apoptosis-resistant E3 ubiquitin protein ligase 1 isoform X2
embryonic polarity protein dorsal, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 75 samples with support for all annotated introns
embryonic polarity protein dorsal, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 74 samples with support for all annotated introns
embryonic polarity protein dorsal isoform X2
embryonic polarity protein dorsal, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 68 samples with support for all annotated introns
embryonic polarity protein dorsal, transcript variant X4
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 68 samples with support for all annotated introns
embryonic polarity protein dorsal, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 56 samples with support for all annotated introns
embryonic polarity protein dorsal, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
embryonic polarity protein dorsal isoform X4
embryonic polarity protein dorsal isoform X5
embryonic polarity protein dorsal isoform X1
embryonic polarity protein dorsal isoform X3
signal-induced proliferation-associated 1-like protein 1, transcript variant X1
signal-induced proliferation-associated 1-like protein 1 isoform X1
signal-induced proliferation-associated 1-like protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
signal-induced proliferation-associated 1-like protein 1 isoform X2
signal-induced proliferation-associated 1-like protein 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 14 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 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protease serine 9, transcript variant X1
transmembrane protease serine 9, transcript variant X2
transmembrane protease serine 9, transcript variant X3
transmembrane protease serine 9 isoform X1
transmembrane protease serine 9 isoform X2
transmembrane protease serine 9 isoform X3
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamine (anticodon UUG); 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
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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
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
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
39S ribosomal protein L38, mitochondrial
hsc70-interacting protein, transcript variant X1
hsc70-interacting protein, transcript variant X2
uncharacterized LOC105389939, transcript variant X5
uncharacterized LOC105389939, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized LOC105389939, 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 33 samples with support for all annotated introns
uncharacterized LOC105389939, 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 46 samples with support for all annotated introns
uncharacterized LOC105389939, 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 48 samples with support for all annotated introns
uncharacterized protein LOC105389939 isoform X1
uncharacterized protein LOC105389939 isoform X2
uncharacterized protein LOC105389939 isoform X4
uncharacterized protein LOC105389939 isoform X3
uncharacterized protein LOC105389939 isoform X5
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 80 samples with support for all annotated introns
excitatory amino acid transporter, 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 15 samples with support for all annotated introns
excitatory amino acid transporter, 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 4 samples with support for all annotated introns
excitatory amino acid transporter, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
excitatory amino acid transporter, 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 23 samples with support for all annotated introns
excitatory amino acid transporter isoform X3
excitatory amino acid transporter isoform X2
excitatory amino acid transporter isoform X1
excitatory amino acid transporter isoform X4
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
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
putative fatty acyl-CoA reductase CG5065
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
gamma-aminobutyric acid type B receptor subunit 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
probable ATP-dependent RNA helicase DDX28
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 61 samples with support for all annotated introns
carnitine O-palmitoyltransferase 2, mitochondrial
ATP-binding cassette sub-family G member 1, transcript variant X1
ATP-binding cassette sub-family G member 1, transcript variant X2
ATP-binding cassette sub-family G member 4 isoform X1
ATP-binding cassette sub-family G member 1 isoform X2
ATP-binding cassette subfamily G member 4
ATP-binding cassette sub-family G member 1-like, transcript variant X2
ATP-binding cassette sub-family G member 1-like, transcript variant X1
ATP-binding cassette sub-family G member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 56% 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 15 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 16 samples with support for all annotated introns
androgen-dependent TFPI-regulating protein
inactive pancreatic lipase-related protein 1, transcript variant X2
inactive pancreatic lipase-related protein 1 isoform X2
inactive pancreatic lipase-related protein 1, transcript variant X1
inactive pancreatic lipase-related protein 1 isoform X1
cytosolic 10-formyltetrahydrofolate dehydrogenase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 72 samples with support for all annotated introns
DDB1- and CUL4-associated factor 8, 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 63 samples with support for all annotated introns
DDB1- and CUL4-associated factor 8, transcript variant X2
DDB1- and CUL4-associated factor 8, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
DDB1- and CUL4-associated factor 8 isoform X3
DDB1- and CUL4-associated factor 8 isoform X1
DDB1- and CUL4-associated factor 8 isoform X2
ribosomal L1 domain-containing protein CG13096-like
neutral ceramidase, transcript variant X1
neutral ceramidase, transcript variant X2
triokinase/FMN cyclase, transcript variant X2
triokinase/FMN cyclase, transcript variant X1
STE20-related kinase adapter protein alpha
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 64 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 66% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125489260, transcript variant X2
uncharacterized LOC125489260, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 73 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 3 samples with support for all annotated introns
activating signal cointegrator 1 complex subunit 2 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 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 73 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 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 88% 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 31 samples with support for all annotated introns
sodium-dependent nutrient amino acid transporter 1, transcript variant X2
sodium-dependent nutrient amino acid transporter 1, transcript variant X1
sodium-dependent nutrient amino acid transporter 1 isoform X2
sodium-dependent nutrient amino acid transporter 1 isoform X1
CUGBP Elav-like family member 1, transcript variant X7
CUGBP Elav-like family member 1, transcript variant X9
CUGBP Elav-like family member 1, transcript variant X4
CUGBP Elav-like family member 1, transcript variant X1
CUGBP Elav-like family member 1, transcript variant X3
CUGBP Elav-like family member 1, transcript variant X6
CUGBP Elav-like family member 1, transcript variant X8
CUGBP Elav-like family member 1 isoform X1
CUGBP Elav-like family member 1 isoform X6
CUGBP Elav-like family member 1-A isoform X8
CUGBP Elav-like family member 1 isoform X4
CUGBP Elav-like family member 1 isoform X3
CUGBP Elav-like family member 1 isoform X7
CUGBP Elav-like family member 1 isoform X9
CUGBP Elav-like family member 1, transcript variant X13
CUGBP Elav-like family member 1, transcript variant X2
CUGBP Elav-like family member 1 isoform X13
CUGBP Elav-like family member 2 isoform X2
CUGBP Elav-like family member 1, transcript variant X5
CUGBP Elav-like family member 1, transcript variant X10
CUGBP Elav-like family member 1, transcript variant X12
CUGBP Elav-like family member 1 isoform X5
CUGBP Elav-like family member 1 isoform X10
CUGBP Elav-like family member 1-A isoform X12
CUGBP Elav-like family member 1, transcript variant X11
CUGBP Elav-like family member 1, transcript variant X14
CUGBP Elav-like family member 1 isoform X11
CUGBP Elav-like family member 2 isoform X14
endoplasmic reticulum lectin 1, transcript variant X2
endoplasmic reticulum lectin 1, transcript variant X1
endoplasmic reticulum lectin 1 isoform X2
endoplasmic reticulum lectin 1 isoform X1
phosphatidylinositol 3-kinase regulatory subunit gamma
serine/arginine-rich splicing factor 3, transcript variant X2
serine/arginine-rich splicing factor 3, transcript variant X1
serine/arginine-rich splicing factor 3 isoform X2
serine/arginine-rich splicing factor 7 isoform X1
serine/arginine-rich splicing factor 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
juvenile hormone acid O-methyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 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 62 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
dachshund homolog 1, transcript variant X7
dachshund homolog 1, transcript variant X10
dachshund homolog 1, transcript variant X9
dachshund homolog 1, transcript variant X6
dachshund homolog 1, transcript variant X2
dachshund homolog 1, transcript variant X8
dachshund homolog 1, transcript variant X4
dachshund homolog 1, transcript variant X5
dachshund homolog 1, transcript variant X3
dachshund homolog 1, transcript variant X1
dachshund homolog 1, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
phosphoinositide 3-kinase adapter 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 35 samples with support for all annotated introns
T-cell activation inhibitor, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
protein decapentaplegic, transcript variant X2
protein decapentaplegic, transcript variant X1
39S ribosomal protein L46, mitochondrial
60S ribosomal protein L9, transcript variant X1
60S ribosomal protein L9, transcript variant X2
disks large 1 tumor suppressor protein, transcript variant X2
disks large 1 tumor suppressor protein, transcript variant X3
disks large 1 tumor suppressor protein, transcript variant X1
disks large 1 tumor suppressor protein, transcript variant X4
disks large 1 tumor suppressor protein, transcript variant X5
disks large 1 tumor suppressor protein, transcript variant X6
disks large 1 tumor suppressor protein isoform X2
disks large 1 tumor suppressor protein isoform X3
disks large 1 tumor suppressor protein isoform X4
disks large 1 tumor suppressor protein isoform X1
disks large 1 tumor suppressor protein isoform X5
disks large 1 tumor suppressor protein isoform X6
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: 25 Proteins, and 89% 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: deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: odorant receptor 85c-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
calcium/calmodulin-dependent protein kinase type 1
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 75 samples with support for all annotated introns
chitin deacetylase 1, transcript variant X1
chitin deacetylase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105394985, transcript variant X1
uncharacterized protein LOC105394985 isoform X1
uncharacterized LOC105394985, 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 11 samples with support for all annotated introns
uncharacterized protein LOC105394985 isoform X2
transport and Golgi organization protein 1
cytochrome c oxidase assembly protein COX20, mitochondrial
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 77% coverage of the annotated genomic feature by RNAseq alignments
cysteine and histidine-rich domain-containing protein morgana
WD repeat and FYVE domain-containing protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105384200, 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 25 samples with support for all annotated introns
uncharacterized LOC105384200, 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 38 samples with support for all annotated introns
uncharacterized protein LOC105384200 isoform X1
uncharacterized protein LOC105384200 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 67 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 71 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64% coverage of the annotated genomic feature by RNAseq alignments, including 64 samples with support for all annotated introns
uncharacterized LOC105380288, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC105380288, transcript variant X3
uncharacterized LOC105380288, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized protein LOC105380288 isoform X1
uncharacterized protein LOC105380288 isoform X3
uncharacterized protein LOC105380288 isoform X2
uncharacterized LOC105380288, transcript variant X4
uncharacterized protein LOC105380288 isoform X4
progestin and adipoQ receptor family member 3
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
pituitary homeobox homolog Ptx1, transcript variant X1
pituitary homeobox homolog Ptx1, transcript variant X2
pituitary homeobox homolog Ptx1, transcript variant X3
uncharacterized LOC105397196, transcript variant X1
uncharacterized LOC105397196, transcript variant X3
uncharacterized LOC105397196, transcript variant X2
uncharacterized protein LOC105397196 isoform X1
uncharacterized protein LOC105397196 isoform X3
uncharacterized protein LOC105397196 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
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 53 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 15
putative uncharacterized protein DDB_G0282133
sodium/hydrogen exchanger 9B2, transcript variant X1
sodium/hydrogen exchanger 9B2, transcript variant X2
sodium/hydrogen exchanger 9B2 isoform X1
sodium/hydrogen exchanger 9B2 isoform X2
acyl-CoA Delta-9 desaturase, transcript variant X2
acyl-CoA Delta-9 desaturase, transcript variant X1
breast cancer type 1 susceptibility protein homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
ATP synthase subunit delta, mitochondrial
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X13
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X14
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X16
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X18
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X1
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X2
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X10
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X9
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X11
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X6
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X7
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X15
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X12
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X4
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X8
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X3
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X5
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X35
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X33
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X19
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X20
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X32
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X34
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X27
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X30
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X22
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X36
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X21
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X17
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X25
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X23
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X26
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X24
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X28
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X29
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X31
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X50
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X44
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X41
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X46
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X42
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X49
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X48
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X47
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X43
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X37
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X40
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X45
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X39
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X38
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X13
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X14
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X16
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X18
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X1
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X2
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X10
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X9
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X11
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X6
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X7
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X15
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X12
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X4
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X8
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X3
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X5
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X35
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X33
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X19
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X20
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X32
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X34
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X27
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X30
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X22
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X36
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X21
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X17
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X25
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X23
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X26
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X24
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X28
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X29
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X31
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X37
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 78 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 77 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 70 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
PR domain zinc finger protein 10, transcript variant X2
PR domain zinc finger protein 10, transcript variant X1
PR domain zinc finger protein 10 isoform X2
PR domain zinc finger protein 10 isoform X1
protein cornichon, transcript variant X2
protein cornichon, transcript variant X1
mesoderm induction early response protein 1
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 85 samples with support for all annotated introns
cGMP-dependent 3',5'-cyclic phosphodiesterase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 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: 6 Proteins
TBC1 domain family member 15, transcript variant X1
TBC1 domain family member 15, 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 31 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
electron transfer flavoprotein regulatory factor 1
cilia- and flagella-associated protein 44
histone H2A-beta, sperm-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
histone H2A-beta, sperm-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 8
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
carotenoid isomerooxygenase, 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
carotenoid isomerooxygenase, transcript variant X3
carotenoid isomerooxygenase, transcript variant X1
VWFA and cache domain-containing protein CG16868
zinc finger protein 182, transcript variant X1
zinc finger protein 182, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
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: uncharacterized protein LOC105381275
juvenile hormone esterase, transcript variant X1
juvenile hormone esterase, transcript variant X2
splicing factor U2af 38 kDa subunit, transcript variant X2
splicing factor U2af 38 kDa subunit, transcript variant X1
splicing factor U2af 38 kDa subunit isoform X2
splicing factor U2af 38 kDa subunit isoform X1
multidrug resistance-associated protein 1, transcript variant X2
multidrug resistance-associated protein 1, transcript variant X4
multidrug resistance-associated protein 1, transcript variant X1
multidrug resistance-associated protein 1, transcript variant X3
multidrug resistance-associated protein 1 isoform X2
multidrug resistance-associated protein 1 isoform X1
multidrug resistance-associated protein 1 isoform X4
multidrug resistance-associated protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
NADH dehydrogenase [ubiquinone] 1 subunit C2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
protein-L-isoaspartate(D-aspartate) O-methyltransferase, transcript variant X3
protein-L-isoaspartate(D-aspartate) O-methyltransferase isoform X3
protein-L-isoaspartate(D-aspartate) O-methyltransferase, transcript variant X2
protein-L-isoaspartate(D-aspartate) O-methyltransferase isoform X2
protein-L-isoaspartate(D-aspartate) O-methyltransferase, transcript variant X1
protein-L-isoaspartate(D-aspartate) O-methyltransferase isoform X1
neuroendocrine protein 7B2, transcript variant X2
neuroendocrine protein 7B2, 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
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
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 85 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 84% 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: MAP7 domain-containing protein 1
uncharacterized LOC105383245, transcript variant X2
uncharacterized LOC105383245, transcript variant X1
uncharacterized protein LOC105383245 isoform X2
uncharacterized protein LOC105383245 isoform X1
RNA polymerase II transcriptional coactivator
tubulin-specific chaperone C, transcript variant X1
tubulin-specific chaperone C, transcript variant X2
L-2-hydroxyglutarate dehydrogenase, mitochondrial
microtubule-associated protein futsch, transcript variant X1
microtubule-associated protein futsch isoform X1
post-GPI attachment to proteins factor 2
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 81 samples with support for all annotated introns
microtubule-associated protein futsch, transcript variant X2
microtubule-associated protein futsch isoform X2
medium-chain acyl-CoA ligase ACSF2, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 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: 1 EST, and 88% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105383292, transcript variant X2
uncharacterized LOC105383292, transcript variant X1
uncharacterized protein LOC105383292 isoform X1
uncharacterized protein LOC105383292 isoform X2
uncharacterized LOC105383292, transcript variant X3
uncharacterized protein LOC105383292 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich PPR motif-containing protein, mitochondrial
ATP-binding cassette sub-family G member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125489242, transcript variant X2
uncharacterized LOC125489242, transcript variant X3
uncharacterized LOC125489242, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
uncharacterized LOC125489282, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC125489282, 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 LOC125489282, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized protein LOC125489282 isoform X1
uncharacterized protein LOC125489282 isoform X2
uncharacterized protein LOC125489282 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
probable protein S-acyltransferase 23, 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 27 samples with support for all annotated introns
probable protein S-acyltransferase 23, 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 50 samples with support for all annotated introns
probable protein S-acyltransferase 23 isoform X1
probable protein S-acyltransferase 23 isoform X2
proton-coupled amino acid transporter-like protein pathetic
5'-AMP-activated protein kinase subunit beta-1, transcript variant X1
5'-AMP-activated protein kinase subunit beta-1, transcript variant X2
5'-AMP-activated protein kinase subunit beta-1 isoform X1
5'-AMP-activated protein kinase subunit beta-1 isoform X2
transmembrane protein 87A, transcript variant X1
transmembrane protein 87A, transcript variant X2
protein argonaute-2, transcript variant X1
protein argonaute-2, transcript variant X3
protein argonaute-2, transcript variant X2
protein argonaute-2, transcript variant X4
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
START domain-containing protein 10, transcript variant X2
START domain-containing protein 10, transcript variant X1
START domain-containing protein 10 isoform X2
START domain-containing protein 10 isoform X1
calponin homology domain-containing protein DDB_G0272472
uncharacterized protein KIAA1143 homolog
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 69 samples with support for all annotated introns
putative glycine-rich cell wall structural protein 1
mitochondrial import receptor subunit TOM70
uncharacterized LOC105382805, transcript variant X1
uncharacterized protein LOC105382805 isoform X1
uncharacterized LOC105382805, transcript variant X2
uncharacterized protein LOC105382805 isoform X2
coiled-coil domain-containing protein 97
ATP-binding cassette sub-family C member 10
LOW QUALITY PROTEIN: ATP-binding cassette sub-family C member 10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 70 samples with support for all annotated introns
uridine phosphorylase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uridine phosphorylase 1, 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 19 samples with support for all annotated introns
polycystic kidney disease protein 1-like 3
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 74 samples with support for all annotated introns
coiled-coil domain-containing protein 170
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
rab3 GTPase-activating protein regulatory subunit
uncharacterized LOC105393847, transcript variant X3
uncharacterized LOC105393847, transcript variant X2
uncharacterized LOC105393847, transcript variant X1
uncharacterized protein LOC105393847 isoform X3
uncharacterized protein LOC105393847 isoform X2
uncharacterized protein LOC105393847 isoform X1
UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase
vacuolar protein sorting-associated protein 54
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
cytoplasmic dynein 2 light intermediate chain 1, transcript variant X1
cytoplasmic dynein 2 light intermediate chain 1, transcript variant X2
cytoplasmic dynein 2 light intermediate chain 1 isoform X1
cytoplasmic dynein 2 light intermediate chain 1 isoform X2
ribonucleoside-diphosphate reductase large subunit
ATP-dependent RNA helicase me31b, transcript variant X1
ATP-dependent RNA helicase me31b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 74% 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 69% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 3 subunit K
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 17
protein bark beetle, transcript variant X1
protein bark beetle, transcript variant X2
ATP-binding cassette sub-family G member 1 isoform X1
uncharacterized LOC105384986, transcript variant X2
uncharacterized LOC105384986, transcript variant X1
uncharacterized protein LOC105384986 isoform X1
uncharacterized protein LOC105384986 isoform X2
polypeptide N-acetylgalactosaminyltransferase 2, transcript variant X2
polypeptide N-acetylgalactosaminyltransferase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 2 isoform X2
polypeptide N-acetylgalactosaminyltransferase 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
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
A-kinase anchor protein 200, transcript variant X3
A-kinase anchor protein 200, transcript variant X4
A-kinase anchor protein 200, transcript variant X1
A-kinase anchor protein 200, transcript variant X2
DNA replication complex GINS protein PSF1
uncharacterized LOC105380138, transcript variant X3
uncharacterized LOC105380138, transcript variant X2
uncharacterized LOC105380138, transcript variant X1
uncharacterized protein LOC105380138 isoform X3
uncharacterized protein LOC105380138 isoform X2
uncharacterized protein LOC105380138 isoform X1
uncharacterized LOC119694103, transcript variant X5
uncharacterized LOC119694103, transcript variant X4
uncharacterized LOC119694103, transcript variant X3
uncharacterized LOC119694103, transcript variant X2
uncharacterized LOC119694103, transcript variant X1
succinate dehydrogenase cytochrome b560 subunit, mitochondrial
GRIP and coiled-coil domain-containing protein 1, transcript variant X1
GRIP and coiled-coil domain-containing protein 1, 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 31 samples with support for all annotated introns
GRIP and coiled-coil domain-containing protein 1 isoform X1
GRIP and coiled-coil domain-containing protein 1 isoform X2
retinoblastoma-binding protein 5 homolog
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 14 samples with support for all annotated introns
CUGBP Elav-like family member 3, transcript variant X4
CUGBP Elav-like family member 3, transcript variant X3
CUGBP Elav-like family member 3, transcript variant X2
CUGBP Elav-like family member 3, transcript variant X1
CUGBP Elav-like family member 3, transcript variant X5
CUGBP Elav-like family member 3-B isoform X4
CUGBP Elav-like family member 3-B isoform X3
CUGBP Elav-like family member 3 isoform X2
CUGBP Elav-like family member 3-B isoform X1
CUGBP Elav-like family member 4 isoform X5
chitooligosaccharidolytic beta-N-acetylglucosaminidase, transcript variant X2
chitooligosaccharidolytic beta-N-acetylglucosaminidase, transcript variant X1
chitooligosaccharidolytic beta-N-acetylglucosaminidase isoform X1
chitooligosaccharidolytic beta-N-acetylglucosaminidase
chitooligosaccharidolytic beta-N-acetylglucosaminidase, transcript variant X5
chitooligosaccharidolytic beta-N-acetylglucosaminidase, transcript variant X4
chitooligosaccharidolytic beta-N-acetylglucosaminidase, transcript variant X3
chitooligosaccharidolytic beta-N-acetylglucosaminidase isoform X4
chitooligosaccharidolytic beta-N-acetylglucosaminidase isoform X3
chitooligosaccharidolytic beta-N-acetylglucosaminidase isoform X2
transcription initiation factor IIE subunit beta
spermidine synthase, transcript variant X1
spermidine synthase, transcript variant X3
spermidine synthase, transcript variant X2
phospholipid-transporting ATPase IF, 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 56 samples with support for all annotated introns
phospholipid-transporting ATPase IF isoform X1
phospholipid-transporting ATPase IF, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
phospholipid-transporting ATPase IF isoform X2
alpha-aminoadipic semialdehyde synthase, mitochondrial, transcript variant X1
alpha-aminoadipic semialdehyde synthase, mitochondrial, transcript variant X2
alpha-aminoadipic semialdehyde synthase, mitochondrial isoform X1
alpha-aminoadipic semialdehyde synthase, mitochondrial isoform X2
kelch-like protein 10, transcript variant X1
kelch-like protein 10, transcript variant X2
kelch-like protein 10, transcript variant X3
kelch-like protein 10, transcript variant X4
kelch-like protein 10, transcript variant X6
kelch-like protein 10, transcript variant X5
kelch-like protein 10, transcript variant X7
mitochondrial basic amino acids transporter
uncharacterized LOC119691211, 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 30 samples with support for all annotated introns
uncharacterized LOC119691211, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC119691211, 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 46 samples with support for all annotated introns
uncharacterized protein LOC119691211 isoform X1
uncharacterized protein LOC119691211 isoform X2
uncharacterized protein LOC119691211 isoform X3
pyrokinin-1 receptor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 59 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
pyrokinin-1 receptor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
bifunctional endo-1,4-beta-xylanase XylA
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 34 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glutamyl aminopeptidase, transcript variant X1
glutamyl aminopeptidase, transcript variant X2
E3 ubiquitin-protein ligase TRIM9, 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 6 samples with support for all annotated introns
E3 ubiquitin-protein ligase TRIM9, 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 37 samples with support for all annotated introns
E3 ubiquitin-protein ligase TRIM9 isoform X2
E3 ubiquitin-protein ligase TRIM9 isoform X1
RNA-binding protein 42, 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 73 samples with support for all annotated introns
RNA-binding protein 42, 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 65 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 97% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 85C-B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
anaphase-promoting complex subunit 11, transcript variant X1
uncharacterized protein DDB_G0284459 isoform X1
anaphase-promoting complex subunit 11, 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 85 samples with support for all annotated introns
anaphase-promoting complex subunit 11 isoform X2
alpha,alpha-trehalose-phosphate synthase [UDP-forming]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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: 187 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
acyl-CoA Delta-9 desaturase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 187 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: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
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 40 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 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: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat-containing protein 40
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
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: 1 Protein, and 55% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
sodium-dependent nutrient amino acid transporter 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
WD repeat-containing and planar cell polarity effector protein fritz
ubiquitin-60S ribosomal protein L40; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305519.1
The RefSeq transcript has 7 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001292448.1
The RefSeq protein has 3 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
cytochrome c oxidase subunit 7A2, mitochondrial
polyphosphoinositide phosphatase, 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 18 samples with support for all annotated introns
polyphosphoinositide phosphatase, 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 22 samples with support for all annotated introns
polyphosphoinositide phosphatase isoform X2
polyphosphoinositide phosphatase isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 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 25 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 23 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 99% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
DNA methyltransferase 1-associated protein 1
retinoid-inducible serine carboxypeptidase-like
uncharacterized LOC125488555, transcript variant X3
uncharacterized LOC125488555, transcript variant X1
uncharacterized LOC125488555, transcript variant X2
facilitated trehalose transporter Tret1, 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 23 samples with support for all annotated introns
facilitated trehalose transporter Tret1, 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 41 samples with support for all annotated introns
facilitated trehalose transporter Tret1 isoform X1
facilitated trehalose transporter Tret1 isoform X2
glycine-rich cell wall structural protein 1.8, transcript variant X1
glycine-rich cell wall structural protein 1.8, transcript variant X2
glycine-rich cell wall structural protein 1.8 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 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: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 58 samples with support for all annotated introns
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
tyrosine-protein kinase transmembrane receptor Ror
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 56 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 45 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
myosin-2 essential light chain, transcript variant X2
myosin-2 essential light chain, transcript variant X4
myosin-2 essential light chain, transcript variant X1
myosin-2 essential light chain, transcript variant X3
myosin-2 essential light chain isoform X4
myosin-2 essential light chain isoform X2
myosin-2 essential light chain isoform X3
myosin-2 essential light chain isoform X1
protein phosphatase 1 regulatory subunit 14B, transcript variant X1
protein phosphatase 1 regulatory subunit 14B, transcript variant X2
protein phosphatase 1 regulatory subunit 14B isoform X1
protein phosphatase 1 regulatory subunit 14B isoform X2
uncharacterized LOC119694051, transcript variant X1
uncharacterized LOC119694051, transcript variant X2
uncharacterized LOC119694051, transcript variant X3
uncharacterized protein LOC119694051 isoform X1
uncharacterized protein LOC119694051 isoform X2
uncharacterized protein LOC119694051 isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 52 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: blastoderm-specific protein 25D
solute carrier family 52, riboflavin transporter, member 3, 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 48 samples with support for all annotated introns
solute carrier family 52, riboflavin transporter, member 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
solute carrier family 52, riboflavin transporter, member 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 66 samples with support for all annotated introns
solute carrier family 52, riboflavin transporter, member 3 isoform X2
solute carrier family 52, riboflavin transporter, member 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
solute carrier family 52, riboflavin transporter, member 3 isoform X1
neuronal acetylcholine receptor subunit beta-4-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 93% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
trafficking protein particle complex subunit 4
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, including 68 samples with support for all annotated introns
28S ribosomal protein S21, mitochondrial
WD repeat-containing protein on Y chromosome
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
LOW QUALITY PROTEIN: WD repeat-containing protein on Y chromosome
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
plasminogen activator inhibitor 1-like, transcript variant X2
plasminogen activator inhibitor 1-like, transcript variant X1
transcription factor AP-4, transcript variant X1
transcription factor AP-4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 139 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 52 samples with support for all annotated introns
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: 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: 5 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat-containing protein 24
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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 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 64 samples with support for all annotated introns
probable E3 ubiquitin-protein ligase bre1
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 21 samples with support for all annotated introns
cleft lip and palate transmembrane protein 1 homolog
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 44 samples with support for all annotated introns
saccharopine dehydrogenase-like oxidoreductase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase classes I and II
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 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: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
hydrolethalus syndrome protein 1 homolog
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 2 samples with support for all annotated introns
counting factor associated protein D-like