Pieris rapae chromosome 20, ilPieRapa1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Papilionoidea; Pieridae; Pierinae; Pieris.
REFSEQ INFORMATION: The reference sequence is identical to\nLR990602.1.\nAssembly name: ilPieRapa1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Wellcome Sanger Institute on\n2021/01/28. The original whole-genome shotgun project has the\naccession CAJHWY000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Pieris rapae Annotation Release 101\nAnnotation Version :: 101\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.
DNA repair protein complementing XP-A cells homolog, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
DNA repair protein complementing XP-A cells homolog, transcript variant X2
DNA repair protein complementing XP-A cells homolog, transcript variant X4
DNA repair protein complementing XP-A cells homolog, transcript variant X3
DNA repair protein complementing XP-A cells homolog isoform X1
DNA repair protein complementing XP-A cells homolog isoform X2
probable malonyl-CoA-acyl carrier protein transacylase, mitochondrial
very long-chain specific acyl-CoA dehydrogenase, mitochondrial, 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 60 samples with support for all annotated introns
very long-chain specific acyl-CoA dehydrogenase, mitochondrial, 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 33 samples with support for all annotated introns
very long-chain specific acyl-CoA dehydrogenase, mitochondrial, 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 47 samples with support for all annotated introns
very long-chain specific acyl-CoA dehydrogenase, mitochondrial, 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 101 samples with support for all annotated introns
very long-chain specific acyl-CoA dehydrogenase, mitochondrial, transcript variant X5
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X2
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 100 samples with support for all annotated introns
zwei Ig domain protein zig-8, transcript variant X6
zwei Ig domain protein zig-8, transcript variant X5
zwei Ig domain protein zig-8, transcript variant X4
zwei Ig domain protein zig-8, transcript variant X3
zwei Ig domain protein zig-8, transcript variant X2
zwei Ig domain protein zig-8, transcript variant X1
phospholipid scramblase 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 4 samples with support for all annotated introns
phospholipid scramblase 1, 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 3 samples with support for all annotated introns
phospholipid scramblase 1, transcript variant X2
phospholipid scramblase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC110996059, transcript variant X7
uncharacterized LOC110996059, transcript variant X1
uncharacterized LOC110996059, transcript variant X3
uncharacterized LOC110996059, transcript variant X2
uncharacterized LOC110996059, transcript variant X8
uncharacterized LOC110996059, transcript variant X4
uncharacterized LOC110996059, transcript variant X10
uncharacterized LOC110996059, transcript variant X5
uncharacterized LOC110996059, transcript variant X9
uncharacterized protein LOC110996059 isoform X1
uncharacterized protein LOC110996059 isoform X3
uncharacterized protein LOC110996059 isoform X2
uncharacterized protein LOC110996059 isoform X7
uncharacterized protein LOC110996059 isoform X8
uncharacterized protein LOC110996059 isoform X4
uncharacterized protein LOC110996059 isoform X9
uncharacterized protein LOC110996059 isoform X5
uncharacterized LOC110996059, transcript variant X6
uncharacterized protein LOC110996059 isoform X6
calcium and integrin-binding family member 3, transcript variant X1
calcium and integrin-binding family member 3, transcript variant X2
calcium and integrin-binding family member 3 isoform X1
calcium and integrin-binding family member 3 isoform X2
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, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
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: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
G1/S-specific cyclin-E, transcript variant X1
G1/S-specific cyclin-E, transcript variant X2
structural maintenance of chromosomes protein 6
COP9 signalosome complex subunit 2, transcript variant X1
COP9 signalosome complex subunit 2, transcript variant X3
COP9 signalosome complex subunit 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88% coverage of the annotated genomic feature by RNAseq alignments
ribonucleoside-diphosphate reductase subunit M2, transcript variant X1
ribonucleoside-diphosphate reductase subunit M2, transcript variant X2
ribonucleoside-diphosphate reductase subunit M2 isoform X1
ribonucleoside-diphosphate reductase subunit M2 isoform X2
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 2, transcript variant X2
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 2, transcript variant X1
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 2 isoform X2
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 2 isoform X1
28S ribosomal protein S29, mitochondrial
neuroblastoma-amplified sequence, 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 16 samples with support for all annotated introns
neuroblastoma-amplified sequence, 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 18 samples with support for all annotated introns
neuroblastoma-amplified sequence isoform X2
neuroblastoma-amplified sequence isoform X1
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
unconventional prefoldin RPB5 interactor, transcript variant X1
unconventional prefoldin RPB5 interactor, transcript variant X2
unconventional prefoldin RPB5 interactor isoform X1
unconventional prefoldin RPB5 interactor isoform X2
28S ribosomal protein S11, mitochondrial
coiled-coil domain-containing protein 124
2-(3-amino-3-carboxypropyl)histidine synthase subunit 2
14 kDa phosphohistidine phosphatase-like, transcript variant X2
14 kDa phosphohistidine phosphatase-like, transcript variant X1
14 kDa phosphohistidine phosphatase-like isoform X1
14 kDa phosphohistidine phosphatase-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 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 51 samples with support for all annotated introns
rho GTPase-activating protein conundrum, transcript variant X1
rho GTPase-activating protein conundrum isoform X1
rho GTPase-activating protein conundrum, transcript variant X2
rho GTPase-activating protein conundrum isoform X2
rho GTPase-activating protein conundrum, transcript variant X4
rho GTPase-activating protein conundrum isoform X4
rho GTPase-activating protein conundrum, transcript variant X3
rho GTPase-activating protein conundrum isoform X3
uncharacterized LOC110994984, transcript variant X1
uncharacterized LOC110994984, transcript variant X2
uncharacterized LOC110994984, transcript variant X4
uncharacterized protein LOC110994984 isoform X1
uncharacterized protein LOC110994984 isoform X2
uncharacterized protein LOC110994984 isoform X3
uncharacterized LOC110994984, transcript variant X3
uncharacterized LOC110994987, 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 1 sample with support for all annotated introns
uncharacterized LOC110994987, 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 2 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
uncharacterized MFS-type transporter C09D4.1, transcript variant X2
uncharacterized MFS-type transporter C09D4.1, transcript variant X3
uncharacterized MFS-type transporter C09D4.1, transcript variant X1
uncharacterized MFS-type transporter C09D4.1 isoform X1
uncharacterized MFS-type transporter C09D4.1, transcript variant X4
uncharacterized MFS-type transporter C09D4.1 isoform X2
uncharacterized MFS-type transporter C09D4.1
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 23 samples with support for all annotated introns
uncharacterized LOC110994965, 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 4 samples with support for all annotated introns
uncharacterized LOC110994965, 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 5 samples with support for all annotated introns
uncharacterized LOC110994965, transcript variant X2
uncharacterized LOC110994965, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC110994965 isoform X1
uncharacterized protein LOC110994965 isoform X3
uncharacterized protein LOC110994965 isoform X2
uncharacterized protein LOC110994965 isoform X4
uncharacterized LOC110994965, 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 4 samples with support for all annotated introns
uncharacterized LOC110994965, transcript variant X5
uncharacterized protein LOC110994965 isoform X6
uncharacterized protein LOC110994965 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
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 8 samples with support for all annotated introns
uncharacterized protein LOC110994995 isoform X11
vacuolar protein-sorting-associated protein 25
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
solute carrier organic anion transporter family member 4A1, 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 16 samples with support for all annotated introns
solute carrier organic anion transporter family member 4A1, 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 8 samples with support for all annotated introns
solute carrier organic anion transporter family member 4A1 isoform X1
solute carrier organic anion transporter family member 4A1 isoform X2
dynein assembly factor with WDR repeat domains 1
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: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ubiquitin-like modifier-activating enzyme 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 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: 2 Proteins, and 2% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC111000830, transcript variant X3
uncharacterized LOC111000830, transcript variant X1
uncharacterized LOC111000830, transcript variant X2
uncharacterized protein LOC111000830 isoform X3
uncharacterized protein LOC111000830 isoform X1
uncharacterized protein LOC111000830 isoform X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
bromodomain-containing protein 7, 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 21 samples with support for all annotated introns
bromodomain-containing protein 7, 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 21 samples with support for all annotated introns
bromodomain-containing protein 7 isoform X1
bromodomain-containing protein 7 isoform X2
hairy/enhancer-of-split related with YRPW motif protein
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 5 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 36 samples with support for all annotated introns
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
serine/threonine-protein kinase 3, transcript variant X3
serine/threonine-protein kinase 3, transcript variant X1
serine/threonine-protein kinase 3, transcript variant X2
serine/threonine-protein kinase 3 isoform X3
serine/threonine-protein kinase 4 isoform X1
serine/threonine-protein kinase 3 isoform X2
cilia- and flagella-associated protein 20
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 112 samples with support for all annotated introns
17-beta-hydroxysteroid dehydrogenase 13, transcript variant X3
17-beta-hydroxysteroid dehydrogenase 13, transcript variant X2
17-beta-hydroxysteroid dehydrogenase 13, transcript variant X1
17-beta-hydroxysteroid dehydrogenase 13 isoform X1
17-beta-hydroxysteroid dehydrogenase 13 isoform X2
BLOC-1-related complex subunit 8 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 111 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 18 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 21 samples with support for all annotated introns
heterogeneous nuclear ribonucleoproteins A1 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 8 samples with support for all annotated introns
glycine-rich cell wall structural protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
solute carrier organic anion transporter family member 74D, transcript variant X4
solute carrier organic anion transporter family member 74D, transcript variant X3
solute carrier organic anion transporter family member 74D, transcript variant X1
solute carrier organic anion transporter family member 74D, transcript variant X5
solute carrier organic anion transporter family member 74D, transcript variant X2
solute carrier organic anion transporter family member 74D isoform X1
solute carrier organic anion transporter family member 74D isoform X2
solute carrier organic anion transporter family member 74D isoform X3
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 1
translation initiation factor eIF-2B subunit delta
oocyte zinc finger protein XlCOF6.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
probable peroxisomal acyl-coenzyme A oxidase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
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 115 samples with support for all annotated introns
pneumococcal serine-rich repeat protein-like
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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: 4 Proteins, 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 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: 13 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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ras-related protein Rab-32, transcript variant X8
ras-related protein Rab-32, transcript variant X5
ras-related protein Rab-32, transcript variant X4
ras-related protein Rab-32, transcript variant X1
ras-related protein Rab-32, transcript variant X2
ras-related protein Rab-32, transcript variant X7
ras-related protein Rab-32, transcript variant X3
ras-related protein Rab-32, transcript variant X6
uncharacterized protein LOC110993121 isoform X1
mitochondrial folate transporter/carrier
mitochondrial-processing peptidase subunit beta
conserved oligomeric Golgi complex subunit 3
protein bunched, class 1/class 3/D/E isoforms, transcript variant X2
protein bunched, class 1/class 3/D/E isoforms, transcript variant X1
protein bunched, class 1/class 3/D/E isoforms, transcript variant X4
protein bunched, class 1/class 3/D/E isoforms, transcript variant X3
protein bunched, class 2/F/G isoform isoform X2
protein bunched, class 2/F/G isoform isoform X1
protein bunched, class 1/class 3/D/E isoforms isoform X4
protein bunched, class 1/class 3/D/E isoforms isoform X3
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
apolipoprotein D-like, transcript variant X1
apolipoprotein D-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
transcription factor Ken, transcript variant X2
transcription factor Ken, transcript variant X1
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
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
peptidylglycine alpha-hydroxylating monooxygenase
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 19 samples with support for all annotated introns
myocyte-specific enhancer factor 2, transcript variant X1
myocyte-specific enhancer factor 2, transcript variant X2
myocyte-specific enhancer factor 2, transcript variant X3
myocyte-specific enhancer factor 2, transcript variant X4
myocyte-specific enhancer factor 2, transcript variant X6
myocyte-specific enhancer factor 2, transcript variant X5
myocyte-specific enhancer factor 2 isoform X1
myocyte-specific enhancer factor 2 isoform X6
myocyte-specific enhancer factor 2 isoform X2
myocyte-specific enhancer factor 2 isoform X3
myocyte-specific enhancer factor 2 isoform X4
myocyte-specific enhancer factor 2 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC110993132 isoform X5
uncharacterized protein LOC110993132 isoform X4
PAS domain-containing serine/threonine-protein kinase, 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 3 samples with support for all annotated introns
PAS domain-containing serine/threonine-protein kinase isoform X1
PAS domain-containing serine/threonine-protein kinase, transcript variant X2
PAS domain-containing serine/threonine-protein kinase isoform X2
double-stranded RNA-binding protein Staufen homolog 2, transcript variant X2
double-stranded RNA-binding protein Staufen homolog 2, transcript variant X3
double-stranded RNA-binding protein Staufen homolog 2, transcript variant X1
double-stranded RNA-binding protein Staufen homolog 2 isoform X2
double-stranded RNA-binding protein Staufen homolog 2 isoform X3
double-stranded RNA-binding protein Staufen homolog 2 isoform 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 115 samples with support for all annotated introns
guanine nucleotide exchange factor DBS, transcript variant X1
guanine nucleotide exchange factor DBS, transcript variant X4
guanine nucleotide exchange factor DBS, transcript variant X3
guanine nucleotide exchange factor DBS, transcript variant X2
guanine nucleotide exchange factor DBS isoform X1
guanine nucleotide exchange factor DBS isoform X4
guanine nucleotide exchange factor DBS isoform X3
guanine nucleotide exchange factor DBS isoform X2
guanine nucleotide exchange factor DBS, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
guanine nucleotide exchange factor DBS, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
guanine nucleotide exchange factor DBS isoform X5
flocculation protein FLO11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
flocculation protein FLO11, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
flocculation protein FLO11, transcript variant X6
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 25 samples with support for all annotated introns
flocculation protein FLO11, 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 20 samples with support for all annotated introns
flocculation protein FLO11, transcript variant X4
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 18 samples with support for all annotated introns
flocculation protein FLO11, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
general transcriptional corepressor trfA isoform X4
uncharacterized protein LOC111000962 isoform X3
uncharacterized protein LOC111000962 isoform X2
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC111000960, transcript variant X4
uncharacterized LOC111000960, transcript variant X3
uncharacterized LOC111000960, transcript variant X2
uncharacterized LOC111000960, transcript variant X1
uncharacterized protein LOC111000960 isoform X4
uncharacterized protein LOC111000960 isoform X3
uncharacterized protein LOC111000960 isoform X2
uncharacterized protein LOC111000960 isoform 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 3 samples with support for all annotated introns
uncharacterized protein LOC111000961 isoform X4
uncharacterized protein LOC111000961 isoform X5
uncharacterized protein LOC111000961 isoform X3
uncharacterized protein LOC111000961 isoform X2
uncharacterized protein LOC111000961 isoform X1
kinesin-like protein KIF13A, transcript variant X9
kinesin-like protein KIF13A, transcript variant X7
kinesin-like protein KIF13A, transcript variant X4
kinesin-like protein KIF13A, transcript variant X3
kinesin-like protein KIF13A, transcript variant X6
kinesin-like protein KIF13A, transcript variant X2
kinesin-like protein KIF13A, transcript variant X8
kinesin-like protein KIF13A, transcript variant X5
kinesin-like protein KIF13A, transcript variant X1
protein tyrosine phosphatase type IVA 3, transcript variant X1
protein tyrosine phosphatase type IVA 3, transcript variant X2
protein tyrosine phosphatase type IVA 3, transcript variant X3
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 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC110996027, transcript variant X2
uncharacterized LOC110996027, transcript variant X3
uncharacterized LOC110996027, transcript variant X1
uncharacterized protein LOC110996027 isoform X1
uncharacterized protein LOC110996027 isoform X2
uncharacterized protein LOC110996027 isoform X3
28S ribosomal protein S31, mitochondrial
uncharacterized LOC110996037, transcript variant X1
uncharacterized LOC110996037, transcript variant X2
uncharacterized protein LOC110996037 isoform X1
uncharacterized protein LOC110996037 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 8 samples with support for all annotated introns
pancreatic triacylglycerol lipase-like, transcript variant X1
pancreatic triacylglycerol lipase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 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 15 samples with support for all annotated introns
39S ribosomal protein L38, mitochondrial
putative uncharacterized protein DDB_G0282499, transcript variant X3
putative uncharacterized protein DDB_G0282499 isoform X3
putative uncharacterized protein DDB_G0282499, transcript variant X1
putative uncharacterized protein DDB_G0282499, transcript variant X2
putative uncharacterized protein DDB_G0282499, transcript variant X5
putative uncharacterized protein DDB_G0282499, transcript variant X4
putative uncharacterized protein DDB_G0282499, transcript variant X7
putative uncharacterized protein DDB_G0282499, transcript variant X6
putative uncharacterized protein DDB_G0282499 isoform X1
putative uncharacterized protein DDB_G0282499 isoform X4
GATA zinc finger domain-containing protein 14 isoform X7
GATA zinc finger domain-containing protein 14 isoform X6
putative uncharacterized protein DDB_G0282499 isoform X2
putative uncharacterized protein DDB_G0282499 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cilia- and flagella-associated protein 44, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cilia- and flagella-associated protein 44 isoform X1
cilia- and flagella-associated protein 44, transcript variant X2
cilia- and flagella-associated protein 44 isoform X2
signal-induced proliferation-associated 1-like protein 2
uncharacterized LOC110998728, transcript variant X3
uncharacterized LOC110998728, transcript variant X1
uncharacterized protein LOC110998728 isoform X1
uncharacterized protein LOC110998728 isoform X3
uncharacterized LOC110998728, transcript variant X2
uncharacterized protein LOC110998728 isoform X2
uncharacterized LOC110998728, transcript variant X4
uncharacterized protein LOC110998728 isoform X4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: putative nuclease HARBI1
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X16
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X19
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X8
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X9
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X1
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X11
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X3
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X12
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X2
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X14
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X4
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X15
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 1 sample with support for all annotated introns
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X13
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X20
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
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X21
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
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X10
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X6
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X20
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X22
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X18
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X17
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X16
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X19
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X8
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X9
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X1
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X11
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X3
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X12
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X2
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X14
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X4
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X15
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X5
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X13
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X21
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X10
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X6
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X7
uncharacterized LOC123690051, transcript variant X1
uncharacterized LOC123690051, transcript variant X2
ATP synthase subunit delta, mitochondrial
uncharacterized LOC110995488, transcript variant X1
uncharacterized LOC110995488, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
acyl-CoA Delta-9 desaturase, transcript variant X1
acyl-CoA Delta-9 desaturase, transcript variant X2
probable protein S-acyltransferase 23, transcript variant X2
probable protein S-acyltransferase 23, transcript variant X1
probable protein S-acyltransferase 23 isoform X2
probable protein S-acyltransferase 23 isoform X1
proton-coupled amino acid transporter-like protein pathetic
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 Proteins, and 66% 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: 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82% 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 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 6 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
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
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: Down syndrome cell adhesion molecule-like protein Dscam2
atrial natriuretic peptide-converting enzyme-like
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
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
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 94 samples with support for all annotated introns
mitotic spindle assembly checkpoint protein MAD2B-like
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
neuronal acetylcholine receptor subunit alpha-7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neuronal acetylcholine receptor subunit alpha-7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neuronal acetylcholine receptor subunit alpha-7, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
neuronal acetylcholine receptor subunit alpha-7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neuronal acetylcholine receptor subunit alpha-7, transcript variant X5
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
neuronal acetylcholine receptor subunit alpha-7 isoform X3
neuronal acetylcholine receptor subunit alpha-7 isoform X1
neuronal acetylcholine receptor subunit alpha-7 isoform X4
neuronal acetylcholine receptor subunit alpha-7 isoform X2
neuronal acetylcholine receptor subunit alpha-7 isoform X5
mediator of RNA polymerase II transcription subunit 27
RCC1-like G exchanging factor-like protein
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 49 samples with support for all annotated introns
centromere/kinetochore protein zw10 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 113 samples with support for all annotated introns
translocon-associated protein subunit beta
scm-like with four MBT domains 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 3 samples with support for all annotated introns
scm-like with four MBT domains 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 12 samples with support for all annotated introns
scm-like with four MBT domains 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 13 samples with support for all annotated introns
scm-like with four MBT domains protein 1
5-demethoxyubiquinone hydroxylase, mitochondrial
DNA-binding protein Ewg, 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 9 samples with support for all annotated introns
DNA-binding protein Ewg, transcript variant X1
DNA-binding protein Ewg, transcript variant X3
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 9 samples with support for all annotated introns
DNA-binding protein Ewg, 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
cytochrome c oxidase subunit 5A, mitochondrial
bifunctional arginine demethylase and lysyl-hydroxylase PSR
guanine nucleotide-binding protein G(f) subunit alpha, transcript variant X1
guanine nucleotide-binding protein G(f) subunit alpha, transcript variant X2
guanine nucleotide-binding protein G(f) subunit alpha isoform X1
guanine nucleotide-binding protein G(f) subunit alpha isoform X2
kinesin-like protein Klp10A, 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 9 samples with support for all annotated introns
kinesin-like protein Klp10A, transcript variant X1
kinesin-like protein Klp10A, transcript variant X2
kinesin-like protein Klp10A, transcript variant X5
kinesin-like protein Klp10A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
zinc transporter 2, transcript variant X2
zinc transporter 2, transcript variant X1
zinc transporter 2, transcript variant X3
protein lethal(2)essential for life-like
probable G-protein coupled receptor CG31760
neuronal acetylcholine receptor subunit beta-2-like
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
cilia- and flagella-associated protein 57-like
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 9 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 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
17-beta-hydroxysteroid dehydrogenase 13-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 5 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 34 samples with support for all annotated introns
oxysterol-binding protein-related protein 1, transcript variant X1
oxysterol-binding protein-related protein 1, transcript variant X2
oxysterol-binding protein-related protein 1 isoform X1
oxysterol-binding protein-related protein 1, transcript variant X3
oxysterol-binding protein-related protein 1, transcript variant X4
oxysterol-binding protein-related protein 1, transcript variant X5
oxysterol-binding protein-related protein 1 isoform X2
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
epidermal retinol dehydrogenase 2, transcript variant X2
epidermal retinol dehydrogenase 2 isoform X2
epidermal retinol dehydrogenase 2, transcript variant X1
epidermal retinol dehydrogenase 2 isoform X1
EF-hand calcium-binding domain-containing protein 1, transcript variant X1
EF-hand calcium-binding 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 1 sample with support for all annotated introns
EF-hand calcium-binding domain-containing protein 1 isoform X1
EF-hand calcium-binding domain-containing protein 1 isoform X2
uncharacterized LOC111000978, 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 22 samples with support for all annotated introns
uncharacterized LOC111000978, 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 16 samples with support for all annotated introns
uncharacterized LOC111000978, transcript variant X3
1,2-dihydroxy-3-keto-5-methylthiopentene dioxygenase
chromatin accessibility complex 16kD protein
uncharacterized LOC111001865, transcript variant X2
uncharacterized LOC111001865, transcript variant X3
uncharacterized LOC111001865, transcript variant X1
uncharacterized LOC123690070, 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 8 samples with support for all annotated introns
uncharacterized LOC123690070, transcript variant X1
uncharacterized protein LOC123690070 isoform X1
uncharacterized protein LOC123690070 isoform X2
peptidyl-alpha-hydroxyglycine alpha-amidating lyase 1, 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 29 samples with support for all annotated introns
peptidyl-alpha-hydroxyglycine alpha-amidating lyase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
peptidyl-alpha-hydroxyglycine alpha-amidating lyase 1, 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 27 samples with support for all annotated introns
peptidyl-alpha-hydroxyglycine alpha-amidating lyase 1 isoform X1
peptidyl-alpha-hydroxyglycine alpha-amidating lyase 1 isoform X2
peptidyl-alpha-hydroxyglycine alpha-amidating lyase 1 isoform X3
methyltransferase-like protein 25B, 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 30 samples with support for all annotated introns
methyltransferase-like protein 25B, transcript variant X2
methyltransferase-like protein 25B isoform X1
methyltransferase-like protein 25B isoform X2
methyltransferase-like protein 25B, transcript variant X3
methyltransferase-like protein 25B isoform X3
histone deacetylase 6, transcript variant X1
histone deacetylase 6, 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 22 samples with support for all annotated introns
mitochondrial intermediate peptidase, transcript variant X1
mitochondrial intermediate peptidase, transcript variant X2
neurogenic protein big brain, transcript variant X1
neurogenic protein big brain, transcript variant X2
ras-related protein Rab6, transcript variant X1
ras-related protein Rab6, transcript variant X2
U2 snRNP-associated SURP motif-containing protein
kinesin-like protein KIF21A, transcript variant X2
kinesin-like protein KIF21A, transcript variant X1
kinesin-like protein KIF21A, transcript variant X3
protein limb expression 1 homolog, transcript variant X1
protein limb expression 1 homolog, transcript variant X2
protein limb expression 1 homolog isoform X1
protein limb expression 1 homolog isoform X2
uncharacterized LOC110995739, transcript variant X2
uncharacterized LOC110995739, transcript variant X1
acyl-coenzyme A diphosphatase NUDT19-like
STE20/SPS1-related proline-alanine-rich protein kinase
FERM domain-containing protein 5, transcript variant X1
FERM domain-containing protein 5, transcript variant X2
FERM domain-containing protein 5 isoform X2
FERM domain-containing protein 5 isoform X1
LOW QUALITY PROTEIN: uncharacterized protein LOC110995561
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 20 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 98% coverage of the annotated genomic feature by RNAseq alignments
mannose-1-phosphate guanyltransferase alpha-A
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 86 samples with support for all annotated introns
facilitated trehalose transporter Tret1-like
solute carrier family 2, facilitated glucose transporter member 8, transcript variant X1
solute carrier family 2, facilitated glucose transporter member 8, transcript variant X2
solute carrier family 2, facilitated glucose transporter member 8
sister chromatid cohesion protein PDS5 homolog B-B
retinaldehyde-binding protein 1, transcript variant X2
retinaldehyde-binding protein 1, transcript variant X1
retinaldehyde-binding protein 1 isoform X1
retinaldehyde-binding protein 1 isoform X2
transcription factor AP-2-epsilon, 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 2 samples with support for all annotated introns
transcription factor AP-2-epsilon, 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 3 samples with support for all annotated introns
transcription factor AP-2-epsilon isoform X3
transcription factor AP-2-epsilon isoform X2
transcription factor AP-2-epsilon, transcript variant X1
transcription factor AP-2-epsilon isoform X1
zinc finger MYND domain-containing protein 10
dual specificity protein phosphatase CDC14C, transcript variant X2
dual specificity protein phosphatase CDC14C, transcript variant X1
dual specificity protein phosphatase CDC14C isoform X1
dual specificity protein phosphatase CDC14C isoform X2
N6-adenosine-methyltransferase subunit METTL3
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9-like
DNA polymerase interacting tetratricopeptide repeat-containing, protein of 47 kDa, transcript variant X1
DNA polymerase interacting tetratricopeptide repeat-containing, protein of 47 kDa isoform X1
DNA polymerase interacting tetratricopeptide repeat-containing, protein of 47 kDa, transcript variant X2
DNA polymerase interacting tetratricopeptide repeat-containing, protein of 47 kDa isoform X2
vesicular inhibitory amino acid transporter
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
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 10 samples with support for all annotated introns
glutamate--cysteine ligase regulatory subunit
A disintegrin and metalloproteinase with thrombospondin motifs 16, transcript variant X6
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
A disintegrin and metalloproteinase with thrombospondin motifs 16, transcript variant X5
A disintegrin and metalloproteinase with thrombospondin motifs 16, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 16, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 16, 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 10 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 16, transcript variant X3
A disintegrin and metalloproteinase with thrombospondin motifs 16 isoform X4
A disintegrin and metalloproteinase with thrombospondin motifs 16 isoform X3
A disintegrin and metalloproteinase with thrombospondin motifs 1 isoform X1
A disintegrin and metalloproteinase with thrombospondin motifs 1 isoform X2
ubiquitin carboxyl-terminal hydrolase 20
focal adhesion kinase 1, transcript variant X7
focal adhesion kinase 1, transcript variant X5
focal adhesion kinase 1, transcript variant X4
focal adhesion kinase 1, transcript variant X6
focal adhesion kinase 1, transcript variant X2
focal adhesion kinase 1, transcript variant X3
focal adhesion kinase 1, transcript variant X1
focal adhesion kinase 1, transcript variant X9
focal adhesion kinase 1, transcript variant X8
40S ribosomal protein S7, transcript variant X1
40S ribosomal protein S7, transcript variant X3
40S ribosomal protein S7, transcript variant X2
UDP-glucose 4-epimerase, transcript variant X3
UDP-glucose 4-epimerase, transcript variant X4
UDP-glucose 4-epimerase, transcript variant X2
UDP-glucose 4-epimerase, transcript variant X1
uncharacterized LOC110995980, transcript variant X2
uncharacterized LOC110995980, transcript variant X1
uncharacterized protein LOC110995980 isoform X1
uncharacterized protein LOC110995980 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC111002034, transcript variant X1
uncharacterized LOC111002034, transcript variant X2
uncharacterized protein LOC111002034 isoform X1
uncharacterized protein LOC111002034 isoform X2
transmembrane protein 165, transcript variant X1
transmembrane protein 165, transcript variant X3
transmembrane protein 165, transcript variant X4
transmembrane protein 165, transcript variant X2
exosome complex component MTR3, transcript variant X1
exosome complex component MTR3, transcript variant X2
exosome complex component MTR3 isoform X1
exosome complex component MTR3 isoform X2
disintegrin and metalloproteinase domain-containing protein 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dystrobrevin beta, transcript variant X1
dystrobrevin beta, 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 34 samples with support for all annotated introns
long-chain fatty acid transport protein 1, transcript variant X2
long-chain fatty acid transport protein 1, transcript variant X1
long-chain fatty acid transport protein 1
facilitated trehalose transporter Tret1-like, transcript variant X1
facilitated trehalose transporter Tret1-like, transcript variant X2
facilitated trehalose transporter Tret1-like, transcript variant X3
facilitated trehalose transporter Tret1-like isoform X1
facilitated trehalose transporter Tret1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 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 11 samples with support for all annotated introns
serine protease inhibitor dipetalogastin
transfer RNA isoleucine (anticodon UAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
facilitated trehalose transporter Tret1-like, transcript variant X4
facilitated trehalose transporter Tret1-like, transcript variant X6
facilitated trehalose transporter Tret1-like, transcript variant X5
facilitated trehalose transporter Tret1-like, transcript variant X7
uncharacterized LOC110999900, transcript variant X4
uncharacterized LOC110999900, transcript variant X2
uncharacterized LOC110999900, transcript variant X3
uncharacterized LOC110999900, transcript variant X1
uncharacterized protein LOC110999900 isoform X4
uncharacterized protein LOC110999900 isoform X2
uncharacterized protein LOC110999900 isoform X3
uncharacterized protein LOC110999900 isoform X1
guanine nucleotide exchange factor MSS4 homolog, transcript variant X2
guanine nucleotide exchange factor MSS4 homolog, transcript variant X3
guanine nucleotide exchange factor MSS4 homolog, transcript variant X1
guanine nucleotide exchange factor MSS4 homolog
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 5 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 2
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 3 samples with support for all annotated introns
protein CASC3-like, transcript variant X2
protein CASC3-like, transcript variant X1
tubulointerstitial nephritis antigen-like
coiled-coil-helix-coiled-coil-helix domain-containing protein 7
dual specificity protein phosphatase 23, transcript variant X1
dual specificity protein phosphatase 23, transcript variant X2
dual specificity protein phosphatase 23 isoform X1
dual specificity protein phosphatase 23 isoform X2
dual specificity protein phosphatase 23-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
26S proteasome non-ATPase regulatory subunit 9
uncharacterized protein LOC110999013 isoform X16
uncharacterized protein LOC110999013 isoform X10
uncharacterized protein LOC110999013 isoform X11
uncharacterized protein LOC110999013 isoform X14
uncharacterized protein LOC110999013 isoform X3
uncharacterized protein LOC110999013 isoform X5
uncharacterized protein LOC110999013 isoform X27
microtubule-actin cross-linking factor 1 isoform X25
microtubule-actin cross-linking factor 1 isoform X24
microtubule-actin cross-linking factor 1 isoform X23
uncharacterized protein LOC110999013 isoform X2
uncharacterized protein LOC110999013 isoform X17
uncharacterized protein LOC110999013 isoform X13
uncharacterized protein LOC110999013 isoform X15
uncharacterized protein LOC110999013 isoform X7
uncharacterized protein LOC110999013 isoform X4
uncharacterized protein LOC110999013 isoform X9
uncharacterized protein LOC110999013 isoform X21
uncharacterized protein LOC110999013 isoform X19
uncharacterized protein LOC110999013 isoform X6
uncharacterized protein LOC110999013 isoform X20
uncharacterized protein LOC110999013 isoform X18
uncharacterized protein LOC110999013 isoform X12
uncharacterized protein LOC110999013 isoform X1
uncharacterized protein LOC110999013 isoform X8
uncharacterized protein LOC110999013 isoform X22
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein Cep89 homolog, 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 11 samples with support for all annotated introns
protein Cep89 homolog, transcript variant X2
sporulation-specific protein 15 isoform X1
venom serine protease, transcript variant X2
venom serine protease, transcript variant X1
transfer RNA cysteine (anticodon GCA); 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: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
tRNA (cytosine(34)-C(5))-methyltransferase
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
facilitated trehalose transporter Tret1-like isoform X3
serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit gamma-like
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 22 samples with support for all annotated introns
influenza virus NS1A-binding protein homolog B
sugar transporter ERD6-like 12, transcript variant X1
sugar transporter ERD6-like 12, transcript variant X2
inactive dipeptidyl peptidase 10, transcript variant X2
inactive dipeptidyl peptidase 10 isoform X2
proteoglycan 4-like, transcript variant X8
proteoglycan 4-like, transcript variant X6
proteoglycan 4-like, transcript variant X10
proteoglycan 4-like, transcript variant X3
proteoglycan 4-like, transcript variant X7
proteoglycan 4-like, transcript variant X4
proteoglycan 4-like, transcript variant X9
proteoglycan 4-like, transcript variant X5
proteoglycan 4-like, transcript variant X2
proteoglycan 4-like, transcript variant X1
inactive dipeptidyl peptidase 10, transcript variant X1
inactive dipeptidyl peptidase 10 isoform X1
cytochrome c oxidase subunit 4 isoform 1, mitochondrial
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
cytochrome c oxidase subunit 4 isoform 1, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cytochrome c oxidase subunit 4 isoform 1, mitochondrial-like, transcript variant X1
cytochrome c oxidase subunit 4 isoform 1, mitochondrial-like isoform X2
cytochrome c oxidase subunit 4 isoform 1, mitochondrial-like isoform 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 10 samples with support for all annotated introns
three-prime repair exonuclease 1, transcript variant X2
three-prime repair exonuclease 1, transcript variant X1
biorientation of chromosomes in cell division protein 1-like 1, transcript variant X2
biorientation of chromosomes in cell division protein 1-like 1, transcript variant X1
biorientation of chromosomes in cell division protein 1-like 1, transcript variant X3
biorientation of chromosomes in cell division protein 1-like 1
protein EFR3 homolog cmp44E, transcript variant X2
protein EFR3 homolog cmp44E, transcript variant X1
protein EFR3 homolog cmp44E, transcript variant X5
protein EFR3 homolog cmp44E, transcript variant X3
protein EFR3 homolog cmp44E, transcript variant X4
reticulon-4-interacting protein 1, mitochondrial
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 95 samples with support for all annotated introns
facilitated trehalose transporter Tret1-2 homolog
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
glycosylphosphatidylinositol anchor attachment 1 protein
similar to RNA sequence (same species):INSD:GFMO01007777.1
annotated by transcript or proteomic data
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 108 bases not found in genome assembly; 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 38 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 37 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.