Plutella xylostella chromosome 25, 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\nOW026573.1.\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: 54% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: polyA evidence [ECO:0006239]
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 67 samples with support for all annotated introns
paired box protein Pax-1, transcript variant X1
paired box protein Pax-1, transcript variant X2
high affinity copper uptake protein 1, transcript variant X3
high affinity copper uptake protein 1, transcript variant X1
high affinity copper uptake protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 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 100% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and SCAN domain-containing protein 10, 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 46 samples with support for all annotated introns
zinc finger and SCAN domain-containing protein 10, transcript variant X1
zinc finger and SCAN domain-containing protein 10 isoform X2
zinc finger and BTB domain-containing protein 49 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 79 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 28 samples with support for all annotated introns
RNA-binding protein Pasilla, transcript variant X1
RNA-binding protein Pasilla, transcript variant X4
RNA-binding protein Pasilla, transcript variant X2
RNA-binding protein Pasilla, transcript variant X5
RNA-binding protein Pasilla, transcript variant X3
RNA-binding protein Pasilla, transcript variant X6
putative inactive tyrosine-protein kinase Wsck
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: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
hippocampus abundant transcript 1 protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments
integrator complex subunit 1, transcript variant X2
integrator complex subunit 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
peptidyl-prolyl cis-trans isomerase FKBP62
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 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: 2 ESTs, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
ATP synthase-coupling factor 6, mitochondrial, transcript variant X1
ATP synthase-coupling factor 6, mitochondrial, transcript variant X2
ATP synthase-coupling factor 6, mitochondrial
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 59 samples with support for all annotated introns
ribosome-releasing factor 2, mitochondrial, transcript variant X1
ribosome-releasing factor 2, mitochondrial, transcript variant X2
ribosome-releasing factor 2, mitochondrial isoform X1
ribosome-releasing factor 2, mitochondrial isoform X2
5'-3' exoribonuclease 2 homolog, transcript variant X1
5'-3' exoribonuclease 2 homolog, transcript variant X4
5'-3' exoribonuclease 2 homolog, transcript variant X2
5'-3' exoribonuclease 2 homolog, transcript variant X3
5'-3' exoribonuclease 2 homolog isoform X1
5'-3' exoribonuclease 2 homolog isoform X4
5'-3' exoribonuclease 2 homolog isoform X2
5'-3' exoribonuclease 2 homolog isoform X3
homeobox protein Nkx-2.1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
homeobox protein Nkx-2.1, 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 14 samples with support for all annotated introns
nose resistant to fluoxetine protein 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83% coverage of the annotated genomic feature by RNAseq alignments
DNA-directed RNA polymerase III subunit RPC1
bromodomain adjacent to zinc finger domain protein 1A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
nose resistant to fluoxetine protein 6, transcript variant X1
nose resistant to fluoxetine protein 6, transcript variant X2
nose resistant to fluoxetine protein 6 isoform X1
nose resistant to fluoxetine protein 6 isoform X2
uncharacterized LOC105393335, transcript variant X1
uncharacterized LOC105393335, transcript variant X2
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
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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein RRP5 homolog
flavin reductase (NADPH), transcript variant X1
flavin reductase (NADPH), transcript variant X2
ribosome quality control complex subunit NEMF homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 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 98% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
all trans-polyprenyl-diphosphate synthase PDSS2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
homeobox protein homothorax, transcript variant X6
homeobox protein homothorax, transcript variant X4
homeobox protein homothorax, transcript variant X3
homeobox protein homothorax, transcript variant X1
homeobox protein homothorax, transcript variant X5
homeobox protein homothorax, 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 68 samples with support for all annotated introns
phosphatidylglycerophosphatase and protein-tyrosine phosphatase 1
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 70 samples with support for all annotated introns
succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial, transcript variant X2
succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial isoform X2
succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial, transcript variant X1
succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial isoform X1
26S proteasome regulatory subunit 6A-B, transcript variant X2
26S proteasome regulatory subunit 6A-B, transcript variant X1
26S proteasome regulatory subunit 6A-B isoform X2
26S proteasome regulatory subunit 6A-B isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
general transcription factor II-I repeat domain-containing protein 2A-like
RNA-binding protein 4.1, transcript variant X2
RNA-binding protein 4.1, transcript variant X1
probable ATP-dependent RNA helicase DHX35
neurofilament heavy polypeptide, transcript variant X2
neurofilament heavy polypeptide, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 61 samples with support for all annotated introns
transcription termination factor 2, 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 11 samples with support for all annotated introns
transcription termination factor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
transcription termination factor 2 isoform X2
transcription termination factor 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
protein sel-1 homolog 1, transcript variant X1
protein sel-1 homolog 1, transcript variant X2
protein sel-1 homolog 1, transcript variant X3
molybdopterin synthase catalytic subunit, 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 22 samples with support for all annotated introns
molybdopterin synthase catalytic subunit, 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 65 samples with support for all annotated introns
molybdopterin synthase catalytic subunit isoform X1
molybdopterin synthase catalytic subunit isoform X2
molybdopterin synthase sulfur carrier subunit-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 80 samples with support for all annotated introns
molybdopterin synthase sulfur carrier subunit-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 63 samples with support for all annotated introns
molybdopterin synthase sulfur carrier subunit-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 81 samples with support for all annotated introns
molybdopterin synthase sulfur carrier subunit-like
intraflagellar transport protein 46 homolog
cell growth regulator with RING finger domain protein 1
cyclin-dependent kinase-like 4, transcript variant X1
cyclin-dependent kinase-like 4, transcript variant X2
cyclin-dependent kinase-like 4 isoform X1
cyclin-dependent kinase-like 4 isoform X2
cyclin-dependent kinase-like 4, transcript variant X3
cyclin-dependent kinase-like 4, transcript variant X4
cyclin-dependent kinase-like 4 isoform X3
cyclin-dependent kinase-like 4 isoform X4
polyribonucleotide nucleotidyltransferase 1, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
sodium/calcium exchanger 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
sodium/calcium exchanger 2, 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 14 samples with support for all annotated introns
sodium/calcium exchanger 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
sodium/calcium exchanger 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 94% 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: 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: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
carboxypeptidase B, transcript variant X2
carboxypeptidase B, transcript variant X1
carboxypeptidase B, transcript variant X3
uncharacterized LOC105386067, transcript variant X1
uncharacterized LOC105386067, 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 44 samples with support for all annotated introns
serine/threonine-protein phosphatase 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309144.1
annotated by transcript or proteomic data
The RefSeq transcript has 42 substitutions and aligns at 84% coverage compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001296073.1
The RefSeq protein has 4 substitutions compared to this genomic sequence; 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: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
post-GPI attachment to proteins factor 6
FERM domain-containing protein 8, transcript variant X1
FERM domain-containing protein 8, transcript variant X2
FERM domain-containing protein 8 isoform X1
FERM domain-containing protein 8 isoform X2
protein transport protein Sec23A, transcript variant X2
protein transport protein Sec23A, transcript variant X1
protein transport protein Sec23A isoform X2
protein transport protein Sec23A isoform X1
metastasis-associated protein MTA3, transcript variant X2
metastasis-associated protein MTA3, transcript variant X4
metastasis-associated protein MTA3, transcript variant X3
metastasis-associated protein MTA3, transcript variant X1
metastasis-associated protein MTA3, transcript variant X5
metastasis-associated protein MTA3, transcript variant X6
metastasis-associated protein MTA3 isoform X2
metastasis-associated protein MTA3 isoform X1
metastasis-associated protein MTA3 isoform X5
metastasis-associated protein MTA3 isoform X6
metastasis-associated protein MTA3 isoform X4
metastasis-associated protein MTA3 isoform X3
splicing factor 3B subunit 2, transcript variant X1
splicing factor 3B subunit 2, transcript variant X2
splicing factor 3B subunit 2, transcript variant X4
splicing factor 3B subunit 2, transcript variant X3
electron transfer flavoprotein subunit beta, transcript variant X1
electron transfer flavoprotein subunit beta, transcript variant X2
electron transfer flavoprotein subunit beta
DDB1- and CUL4-associated factor 10 homolog, transcript variant X3
DDB1- and CUL4-associated factor 10 homolog, transcript variant X2
DDB1- and CUL4-associated factor 10 homolog, transcript variant X1
DDB1- and CUL4-associated factor 10 isoform X2
DDB1- and CUL4-associated factor 10 homolog isoform X3
DDB1- and CUL4-associated factor 10 isoform X1
DNA polymerase epsilon catalytic subunit 1
uncharacterized LOC105394901, transcript variant X4
uncharacterized LOC105394901, transcript variant X3
uncharacterized LOC105394901, transcript variant X2
uncharacterized LOC105394901, transcript variant X1
uncharacterized protein LOC105394901 isoform X2
uncharacterized protein LOC105394901 isoform X1
uncharacterized protein LOC105394901 isoform X3
ras-related protein Rab-8A, transcript variant X1
ras-related protein Rab-8A, transcript variant X2
DNA-directed RNA polymerase II subunit RPB7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
lysM and putative peptidoglycan-binding domain-containing protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
lysM and putative peptidoglycan-binding domain-containing protein 2, 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 67 samples with support for all annotated introns
lysM and putative peptidoglycan-binding domain-containing protein 2 isoform X2
lysM and putative peptidoglycan-binding domain-containing protein 2 isoform X1
3-oxoacyl-[acyl-carrier-protein] reductase FabG
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
5-hydroxytryptamine receptor 1A-alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
G-protein coupled receptor 12, 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 41 samples with support for all annotated introns
5-hydroxytryptamine receptor 1A-alpha isoform X2
G-protein coupled receptor 12, 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 16 samples with support for all annotated introns
G-protein coupled receptor 12, 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 43 samples with support for all annotated introns
G-protein coupled receptor 12 isoform X3
5-hydroxytryptamine receptor 1A isoform X1
39S ribosomal protein L40, mitochondrial
uncharacterized LOC105380803, 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 44 samples with support for all annotated introns
uncharacterized LOC105380803, 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 30 samples with support for all annotated introns
uncharacterized protein LOC105380803 isoform X2
uncharacterized protein LOC105380803 isoform X1
uncharacterized LOC105380803, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
uncharacterized protein LOC105380803 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
uncharacterized LOC105385854, transcript variant X1
uncharacterized LOC105385854, transcript variant X2
uncharacterized protein LOC105385854 isoform X1
uncharacterized protein LOC105385854 isoform X2
uncharacterized LOC105385854, transcript variant X3
uncharacterized protein LOC105385854 isoform X3
uncharacterized LOC105385854, transcript variant X5
uncharacterized protein LOC105385854 isoform X5
uncharacterized LOC105385854, transcript variant X4
uncharacterized protein LOC105385854 isoform X4
tubulin--tyrosine ligase-like protein 12
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 84 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B, transcript variant X1
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B, transcript variant X2
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B isoform X1
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B isoform X2
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
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 74 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 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: 1 Protein, and 83% coverage of the annotated genomic feature by RNAseq alignments
isopentenyl-diphosphate Delta-isomerase 1, 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 83 samples with support for all annotated introns
isopentenyl-diphosphate Delta-isomerase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 66 samples with support for all annotated introns
isopentenyl-diphosphate Delta-isomerase 1
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 20 samples with support for all annotated introns
RDS/peripherin-like protein xRDS35 isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: L-threonine ammonia-lyase
DNA-directed RNA polymerase II subunit RPB3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
probable pterin-4-alpha-carbinolamine dehydratase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 77 samples with support for all annotated introns
L-threonine ammonia-lyase, transcript variant X2
L-threonine ammonia-lyase, transcript variant X1
probable pterin-4-alpha-carbinolamine dehydratase, transcript variant X1
probable pterin-4-alpha-carbinolamine dehydratase
CCA tRNA nucleotidyltransferase 1, mitochondrial
signal recognition particle 54 kDa protein
presenilin homolog, transcript variant X1
presenilin homolog, transcript variant X2
adipocyte plasma membrane-associated protein, transcript variant X2
adipocyte plasma membrane-associated protein, transcript variant X1
adipocyte plasma membrane-associated protein isoform X1
adipocyte plasma membrane-associated protein isoform X2
transmembrane emp24 domain-containing protein 5
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 8
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
DNA-directed RNA polymerases I and III subunit RPAC1
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 85 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
3'(2'),5'-bisphosphate nucleotidase 1, transcript variant X1
3'(2'),5'-bisphosphate nucleotidase 1, transcript variant X2
3'(2'),5'-bisphosphate nucleotidase 1 isoform X1
3'(2'),5'-bisphosphate nucleotidase 1 isoform X2
putative transmembrane protein INAFM2, transcript variant X1
putative transmembrane protein INAFM2 isoform X1
putative transmembrane protein INAFM2, transcript variant X2
putative transmembrane protein INAFM2 isoform X2
U3 small nucleolar RNA-associated protein 25 homolog
protein farnesyltransferase subunit beta
mediator of RNA polymerase II transcription subunit 6
probable DNA-directed RNA polymerase III subunit RPC6
putative OPA3-like protein CG13603, transcript variant X2
putative OPA3-like protein CG13603, transcript variant X1
putative OPA3-like protein CG13603 isoform X2
putative OPA3-like protein CG13603 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
uncharacterized LOC105382368, transcript variant X1
uncharacterized LOC105382368, transcript variant X2
uncharacterized protein LOC105382368 isoform X2
uncharacterized protein LOC105382368 isoform X1
dimethyladenosine transferase 2, mitochondrial
uncharacterized LOC105382366, 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 37 samples with support for all annotated introns
uncharacterized LOC105382366, 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 72 samples with support for all annotated introns
uncharacterized protein LOC105382366 isoform X2
uncharacterized protein LOC105382366 isoform X1
ribosome-binding protein 1, transcript variant X1
ribosome-binding protein 1, transcript variant X9
ribosome-binding protein 1, transcript variant X2
ribosome-binding protein 1, transcript variant X5
ribosome-binding protein 1, transcript variant X6
ribosome-binding protein 1, transcript variant X7
ribosome-binding protein 1, transcript variant X8
ribosome-binding protein 1, transcript variant X4
ribosome-binding protein 1, transcript variant X3
lipopolysaccharide-induced tumor necrosis factor-alpha factor homolog
nuclear-pore anchor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
nuclear-pore anchor, transcript variant X2
serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit epsilon isoform
rap guanine nucleotide exchange factor 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 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 14 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 99% coverage of the annotated genomic feature by RNAseq alignments
AT-rich interactive domain-containing protein 4A, transcript variant X1
AT-rich interactive domain-containing protein 4A, 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 2 samples with support for all annotated introns
AT-rich interactive domain-containing protein 4A isoform X1
AT-rich interactive domain-containing protein 4A isoform X2
39S ribosomal protein L37, mitochondrial
ETS-like protein pointed, transcript variant X2
ETS-like protein pointed, transcript variant X1
ETS-like protein pointed, transcript variant X4
ETS-like protein pointed, transcript variant X3
testis-specific serine/threonine-protein kinase 2
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 2 samples with support for all annotated introns
putative nuclease HARBI1, 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 34 samples with support for all annotated introns
putative nuclease HARBI1, 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 71 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
Down syndrome cell adhesion molecule-like protein Dscam2
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
transcriptional adapter 2B, transcript variant X4
transcriptional adapter 2B, transcript variant X3
transcriptional adapter 2B, transcript variant X2
transcriptional adapter 2B, transcript variant X1
transcriptional adapter 2B, transcript variant X6
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 38 samples with support for all annotated introns
transcriptional adapter 2B, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
probable ATP-dependent RNA helicase spindle-E
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
C-1-tetrahydrofolate synthase, cytoplasmic
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
probable G-protein coupled receptor Mth-like 3
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 69 samples with support for all annotated introns
probable G-protein coupled receptor Mth-like 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
synaptosomal-associated protein 25, 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 76 samples with support for all annotated introns
synaptosomal-associated protein 25, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 samples with support for all annotated introns
synaptosomal-associated protein 25 isoform X2
synaptosomal-associated protein 25 isoform X1
synaptosomal-associated protein 25, transcript variant X4
synaptosomal-associated protein 25, transcript variant X3
synaptosomal-associated protein 25 isoform X3
synaptosomal-associated protein 25 isoform X4
uncharacterized protein C14orf119, transcript variant X2
uncharacterized protein C14orf119, transcript variant X1
uncharacterized protein C14orf119 isoform X1
uncharacterized protein C14orf119 isoform X2
CLIP domain-containing serine protease HP8, transcript variant X2
CLIP domain-containing serine protease HP8 isoform X2
CLIP domain-containing serine protease HP8, transcript variant X3
CLIP domain-containing serine protease HP8, transcript variant X1
CLIP domain-containing serine protease HP8 isoform X1
CLIP domain-containing serine protease HP8 isoform X3
CLIP domain-containing serine protease HP8
ubiquinone biosynthesis monooxygenase COQ6, mitochondrial
transient receptor potential channel pyrexia
uncharacterized LOC125490549, transcript variant X1
uncharacterized LOC125490549, transcript variant X2
uncharacterized protein LOC125490549 isoform X1
uncharacterized protein LOC125490549 isoform X2
uncharacterized LOC119691127, transcript variant X3
uncharacterized LOC119691127, transcript variant X2
uncharacterized LOC119691127, transcript variant X1
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like, transcript variant X1
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like, transcript variant X3
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like, transcript variant X4
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like isoform X1
uncharacterized protein LOC125488557 isoform X2
uncharacterized protein LOC125488557 isoform X3
uncharacterized protein LOC125488557 isoform X4
uncharacterized protein LOC125488557 isoform X5
uncharacterized LOC119691128, transcript variant X1
uncharacterized LOC119691128, transcript variant X2
phosphatidylinositol N-acetylglucosaminyltransferase subunit H
cilia- and flagella-associated protein 36
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
serine/threonine-protein phosphatase 4 regulatory subunit 3, transcript variant X6
serine/threonine-protein phosphatase 4 regulatory subunit 3, transcript variant X7
serine/threonine-protein phosphatase 4 regulatory subunit 3, transcript variant X1
serine/threonine-protein phosphatase 4 regulatory subunit 3, transcript variant X5
serine/threonine-protein phosphatase 4 regulatory subunit 3, transcript variant X3
serine/threonine-protein phosphatase 4 regulatory subunit 3, transcript variant X2
serine/threonine-protein phosphatase 4 regulatory subunit 3, transcript variant X4
serine/threonine-protein phosphatase 4 regulatory subunit 3 isoform X2
serine/threonine-protein phosphatase 4 regulatory subunit 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and SCAN domain-containing protein 26
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
senecionine N-oxygenase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 69 samples with support for all annotated introns
senecionine N-oxygenase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 79 samples with support for all annotated introns
senecionine N-oxygenase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 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 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
transcription initiation factor IIA subunit 2
proteasome activator complex subunit 4, transcript variant X4
proteasome activator complex subunit 4, transcript variant X2
proteasome activator complex subunit 4, transcript variant X3
proteasome activator complex subunit 4, transcript variant X1
proteasome activator complex subunit 4 isoform X4
proteasome activator complex subunit 4 isoform X2
proteasome activator complex subunit 4 isoform X3
proteasome activator complex subunit 4 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
neural cell adhesion molecule 1, transcript variant X2
neural cell adhesion molecule 1, transcript variant X1
neural cell adhesion molecule 1, transcript variant X3
neural cell adhesion molecule 1, transcript variant X4
39S ribosomal protein L11, mitochondrial
N-terminal kinase-like protein, transcript variant X1
N-terminal kinase-like protein, transcript variant X2
N-terminal kinase-like protein isoform X1
N-terminal kinase-like protein isoform X2
probable glucosamine 6-phosphate N-acetyltransferase, 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 45 samples with support for all annotated introns
probable glucosamine 6-phosphate N-acetyltransferase, transcript variant X1
probable glucosamine 6-phosphate N-acetyltransferase isoform X1
probable glucosamine 6-phosphate N-acetyltransferase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 81 samples with support for all annotated introns
probable glucosamine 6-phosphate N-acetyltransferase isoform X2
complex I intermediate-associated protein 30, mitochondrial
transforming acidic coiled-coil-containing protein 3
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 79 samples with support for all annotated introns
probable cardiolipin synthase (CMP-forming)
zinc finger FYVE domain-containing protein 26 homolog
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
signal recognition particle 14 kDa protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
trafficking protein particle complex subunit 6b
single-strand selective monofunctional uracil DNA glycosylase
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 72 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 78 samples with support for all annotated introns
elongation of very long chain fatty acids protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 19 Proteins, and 100% 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: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 81 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 29 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 47 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 12A
probable Rho GTPase-activating protein CG5521
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
H/ACA ribonucleoprotein complex subunit 3
protein UBASH3A homolog, transcript variant X1
protein UBASH3A homolog, transcript variant X2
dol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase
ubiquitin carboxyl-terminal hydrolase puf
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
RNA helicase Mov10l1, transcript variant X1
RNA helicase Mov10l1, transcript variant X2
dihydroxyacetone phosphate acyltransferase
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 65 samples with support for all annotated introns
uncharacterized LOC125490577, 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 76 samples with support for all annotated introns
uncharacterized LOC125490577, 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 55 samples with support for all annotated introns
uncharacterized LOC125490577, 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 26 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit alpha, transcript variant X6
sodium/potassium-transporting ATPase subunit alpha, transcript variant X11
sodium/potassium-transporting ATPase subunit alpha, transcript variant X3
sodium/potassium-transporting ATPase subunit alpha, transcript variant X2
sodium/potassium-transporting ATPase subunit alpha, transcript variant X1
sodium/potassium-transporting ATPase subunit alpha, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit alpha, transcript variant X7
sodium/potassium-transporting ATPase subunit alpha isoform X3
sodium/potassium-transporting ATPase subunit alpha isoform X2
sodium/potassium-transporting ATPase subunit alpha isoform X1
sodium/potassium-transporting ATPase subunit alpha isoform X7
sodium/potassium-transporting ATPase subunit alpha, transcript variant X5
sodium/potassium-transporting ATPase subunit alpha, transcript variant X4
sodium/potassium-transporting ATPase subunit alpha, transcript variant X10
sodium/potassium-transporting ATPase subunit alpha, transcript variant X9
sodium/potassium-transporting ATPase subunit alpha, transcript variant X8
sodium/potassium-transporting ATPase subunit alpha isoform X5
sodium/potassium-transporting ATPase subunit alpha isoform X4
sodium/potassium-transporting ATPase subunit alpha isoform X6
sodium/potassium-transporting ATPase subunit alpha isoform X10
sodium/potassium-transporting ATPase subunit alpha isoform X9
sodium/potassium-transporting ATPase subunit alpha isoform X8
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
transcription factor kayak, transcript variant X2
transcription factor kayak, transcript variant X3
transcription factor kayak, transcript variant X1
transcription factor IIIB 90 kDa subunit
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 36 samples with support for all annotated introns
BTB/POZ domain-containing protein 6-B, transcript variant X1
BTB/POZ domain-containing protein 6-B, transcript variant X2
BTB/POZ domain-containing protein 6-B isoform X1
BTB/POZ domain-containing protein 6-B isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
baculoviral IAP repeat-containing protein 6, transcript variant X1
baculoviral IAP repeat-containing protein 6, transcript variant X2
baculoviral IAP repeat-containing protein 6 isoform X1
baculoviral IAP repeat-containing protein 6 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 32 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 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 54 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 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 15 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 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
conserved oligomeric Golgi complex subunit 2, transcript variant X2
conserved oligomeric Golgi complex subunit 2, transcript variant X1
conserved oligomeric Golgi complex subunit 2 isoform X1
conserved oligomeric Golgi complex subunit 2 isoform X2
protein phosphatase 1 regulatory subunit 21, transcript variant X1
protein phosphatase 1 regulatory subunit 21, transcript variant X2
protein phosphatase 1 regulatory subunit 21 isoform X1
protein phosphatase 1 regulatory subunit 21 isoform X2
serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit gamma isoform, transcript variant X3
serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit gamma isoform, transcript variant X2
serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit gamma isoform, transcript variant X1
serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit gamma isoform isoform X3
serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit gamma isoform isoform X2
serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit gamma isoform isoform X1
neurogenic locus notch homolog protein 1
ribosomal RNA processing protein 36 homolog
bifunctional glutamate/proline--tRNA ligase, transcript variant X2
bifunctional glutamate/proline--tRNA ligase, transcript variant X3
bifunctional glutamate/proline--tRNA ligase, transcript variant X1
bifunctional glutamate/proline--tRNA ligase, transcript variant X4
bifunctional glutamate/proline--tRNA ligase isoform X2
bifunctional glutamate/proline--tRNA ligase isoform X3
bifunctional glutamate/proline--tRNA ligase isoform X1
bifunctional glutamate/proline--tRNA ligase isoform X4
uncharacterized LOC105393187, 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 5 samples with support for all annotated introns
uncharacterized LOC105393187, transcript variant X1
uncharacterized protein LOC105393187 isoform X1
uncharacterized protein LOC105393187 isoform X2
two pore potassium channel protein sup-9
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 32 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 70% coverage of the annotated genomic feature by RNAseq alignments
protein doublesex, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
protein doublesex, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
protein doublesex, transcript variant X4
protein doublesex, transcript variant X3
protein doublesex, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
homeobox protein prospero, transcript variant X2
homeobox protein prospero, transcript variant X1
homeobox protein prospero, transcript variant X3
fibroin heavy chain, transcript variant X1
fibroin heavy chain, transcript variant X2
dihydrolipoyllysine-residue succinyltransferase component of 2-oxoglutarate dehydrogenase complex, mitochondrial
NAD-dependent protein deacetylase sirtuin-2
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 59 samples with support for all annotated introns
unc-112-related protein, transcript variant X3
unc-112-related protein, transcript variant X4
unc-112-related protein, transcript variant X1
unc-112-related protein, transcript variant X2
ATP-dependent Clp protease proteolytic subunit
neuroendocrine convertase 2, transcript variant X1
neuroendocrine convertase 2, 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 23 samples with support for all annotated introns
putative epidermal cell surface receptor
chromosome-associated kinesin KIF4, transcript variant X4
chromosome-associated kinesin KIF4, transcript variant X6
chromosome-associated kinesin KIF4, transcript variant X3
chromosome-associated kinesin KIF4, transcript variant X7
chromosome-associated kinesin KIF4, transcript variant X5
chromosome-associated kinesin KIF4 isoform X4
chromosome-associated kinesin KIF4 isoform X3
chromosome-associated kinesin KIF4, transcript variant X2
chromosome-associated kinesin KIF4, transcript variant X1
chromosome-associated kinesin KIF4 isoform X2
chromosome-associated kinesin KIF4 isoform X1
uncharacterized LOC105392168, 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 64 samples with support for all annotated introns
uncharacterized protein LOC105392168 isoform X1
uncharacterized LOC105392168, 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 protein LOC105392168 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 samples with support for all annotated introns
uridine diphosphate glucose pyrophosphatase NUDT14, transcript variant X2
uridine diphosphate glucose pyrophosphatase NUDT14, transcript variant X1
uridine diphosphate glucose pyrophosphatase NUDT14 isoform X1
uridine diphosphate glucose pyrophosphatase NUDT14 isoform X2
zinc finger protein 569, transcript variant X3
zinc finger protein 569, transcript variant X1
zinc finger protein 569, transcript variant X4
zinc finger protein 569, transcript variant X6
zinc finger protein 62 homolog isoform X1
zinc finger protein 569, transcript variant X2
zinc finger protein 569, transcript variant X5
zinc finger protein 62 homolog isoform X2
zinc finger protein Xfin, transcript variant X5
zinc finger protein Xfin, transcript variant X7
zinc finger protein Xfin, transcript variant X4
zinc finger protein Xfin, transcript variant X6
zinc finger protein Xfin, transcript variant X2
zinc finger protein Xfin, transcript variant X3
zinc finger protein Xfin, transcript variant X1
PR domain zinc finger protein 5 isoform X4
zinc finger and SCAN domain-containing protein 31 isoform X3
zinc finger and SCAN domain-containing protein 2 isoform X1
zinc finger and SCAN domain-containing protein 2 isoform X6
zinc finger protein 724, transcript variant X5
PR domain zinc finger protein 15 isoform X5
zinc finger protein 724, transcript variant X1
zinc finger protein 724, transcript variant X3
zinc finger protein 724, transcript variant X2
zinc finger protein 724, transcript variant X7
zinc finger protein 724, transcript variant X4
PR domain zinc finger protein 15 isoform X1
PR domain zinc finger protein 15 isoform X3
PR domain zinc finger protein 15 isoform X2
PR domain zinc finger protein 15 isoform X4
zinc finger protein 724, transcript variant X6
uncharacterized LOC105381016, transcript variant X1
uncharacterized LOC105381016, transcript variant X2
uncharacterized LOC105386543, transcript variant X1
uncharacterized LOC105386543, transcript variant X2
uncharacterized LOC119693723, transcript variant X2
uncharacterized LOC119693723, transcript variant X1
uncharacterized protein LOC119693723 isoform X1
uncharacterized protein LOC119693723 isoform X2
uncharacterized LOC125488538, transcript variant X1
uncharacterized LOC125488538, transcript variant X2
uncharacterized protein LOC125488538 isoform X2
uncharacterized protein LOC125488538 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105382359, transcript variant X2
uncharacterized LOC105382359, transcript variant X1
uncharacterized LOC125490554, transcript variant X1
uncharacterized LOC125490554, transcript variant X2
uncharacterized protein LOC125490554 isoform X2
uncharacterized protein LOC125490554 isoform X1
probable cleavage and polyadenylation specificity factor subunit 2
steroid hormone receptor ERR1, transcript variant X5
steroid hormone receptor ERR1, transcript variant X4
steroid hormone receptor ERR1, transcript variant X2
steroid hormone receptor ERR1, transcript variant X3
steroid hormone receptor ERR1, transcript variant X1
steroid hormone receptor ERR1, transcript variant X6
steroid hormone receptor ERR1, transcript variant X7
steroid hormone receptor ERR1 isoform X4
steroid hormone receptor ERR1 isoform X3
steroid hormone receptor ERR1 isoform X2
steroid hormone receptor ERR1 isoform X1
steroid hormone receptor ERR1 isoform X5
steroid hormone receptor ERR1 isoform X7
steroid hormone receptor ERR1 isoform X6
transmembrane emp24 domain-containing protein bai
protein anoxia up-regulated, 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 85 samples with support for all annotated introns
protein anoxia up-regulated, transcript variant X2
uncharacterized protein CG45078 isoform X1
probable maleylacetoacetate isomerase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
probable maleylacetoacetate isomerase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
probable maleylacetoacetate isomerase 2 isoform X2
probable maleylacetoacetate isomerase 2 isoform X1
phosphofurin acidic cluster sorting protein 1, 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 16 samples with support for all annotated introns
phosphofurin acidic cluster sorting protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
phosphofurin acidic cluster sorting protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
phosphofurin acidic cluster sorting protein 1, transcript variant X4
phosphofurin acidic cluster sorting protein 2 isoform X1
phosphofurin acidic cluster sorting protein 2 isoform X2
phosphofurin acidic cluster sorting protein 1 isoform X3
phosphofurin acidic cluster sorting protein 2 isoform X4
serine/arginine repetitive matrix protein 1, transcript variant X9
serine/arginine repetitive matrix protein 1, transcript variant X8
serine/arginine repetitive matrix protein 1, transcript variant X7
serine/arginine repetitive matrix protein 1, transcript variant X6
serine/arginine repetitive matrix protein 1, transcript variant X5
serine/arginine repetitive matrix protein 1, transcript variant X4
serine/arginine repetitive matrix protein 1, transcript variant X3
serine/arginine repetitive matrix protein 1, transcript variant X2
serine/arginine repetitive matrix protein 1, transcript variant X1
serine/arginine repetitive matrix protein 1 isoform X9
uncharacterized protein LOC105382741 isoform X8
uncharacterized protein LOC105382741 isoform X7
uncharacterized protein LOC105382741 isoform X6
serine/arginine repetitive matrix protein 1 isoform X5
serine/arginine repetitive matrix protein 1 isoform X4
uncharacterized protein LOC105382741 isoform X3
serine/arginine repetitive matrix protein 1 isoform X2
uncharacterized protein LOC105382741 isoform X1
uncharacterized LOC105391207, 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 9 samples with support for all annotated introns
uncharacterized LOC105391207, transcript variant X1
uncharacterized protein LOC105391207 isoform X2
uncharacterized protein LOC105391207 isoform X1
uncharacterized LOC119692485, transcript variant X5
uncharacterized LOC119692485, transcript variant X4
uncharacterized LOC119692485, transcript variant X3
uncharacterized LOC119692485, transcript variant X1
uncharacterized LOC119692485, transcript variant X2
uncharacterized protein LOC119692485 isoform X1
uncharacterized protein LOC119692485 isoform X2
uncharacterized protein LOC119692485 isoform X3
uncharacterized protein LOC119692485 isoform X4
uncharacterized protein LOC119692485 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 61 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 51 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 17 samples with support for all annotated introns
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 23 samples with support for all annotated introns
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 58 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 59 samples with support for all annotated introns
uncharacterized LOC105384842, transcript variant X4
uncharacterized protein LOC105384842 isoform X4
uncharacterized LOC105384842, transcript variant X2
uncharacterized LOC105384842, transcript variant X1
uncharacterized protein LOC105384842 isoform X1
uncharacterized protein LOC105384842 isoform X2
uncharacterized LOC105384842, transcript variant X3
uncharacterized protein LOC105384842 isoform X3
protein phosphatase 1B; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001320021.1
The RefSeq transcript has 20 substitutions 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 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
protein preli-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
protein preli-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 78 samples with support for all annotated introns
protein preli-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 61 samples with support for all annotated introns
protein preli-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63% 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 13 samples with support for all annotated introns
probable metabolite transport protein CsbC, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
probable metabolite transport protein CsbC, transcript variant X2
probable metabolite transport protein CsbC, transcript variant X1
probable metabolite transport protein CsbC
structural maintenance of chromosomes protein 2
uncharacterized LOC119691041, transcript variant X1
uncharacterized LOC119691041, transcript variant X3
uncharacterized LOC119691041, transcript variant X2