Leguminivora glycinivorella isolate SPB_JAAS2020 chromosome 3, LegGlyc_1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Tortricoidea; Tortricidae; Olethreutinae; Grapholitini; Leguminivora.
REFSEQ INFORMATION: The reference sequence is identical to\nCM041123.1.\nAssembly name: LegGlyc_1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the USDA-ARS on 2022/04/22. The\noriginal whole-genome shotgun project has the accession\nJAKXMO000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: USDA-ARS\nAssembly Date :: 08-OCT-2021\nAssembly Method :: NextDeNovo v. 2.5.0\nAssembly Name :: LegGlyc_1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 85.48x\nSequencing Technology :: Oxford Nanopore GridION\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Leguminivora glycinivorella\n Annotation Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
acetylcholine receptor subunit alpha-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 256 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
acetylcholine receptor subunit alpha-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
acetylcholine receptor subunit alpha-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 252 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
acetylcholine receptor subunit alpha-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
acetylcholine receptor subunit alpha-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
acetylcholine receptor subunit alpha-like isoform X4
acetylcholine receptor subunit alpha-like isoform X2
acetylcholine receptor subunit alpha-like isoform X3
acetylcholine receptor subunit alpha-like 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 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
uncharacterized LOC125242721, 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 12 samples with support for all annotated introns
uncharacterized LOC125242721, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized LOC125242719, transcript variant X1
uncharacterized LOC125242719, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
uncharacterized LOC125242720, transcript variant X1
uncharacterized LOC125242720, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 13 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 6 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
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
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
NKAP family protein CG6066, 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 3 samples with support for all annotated introns
NKAP family protein CG6066, 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 13 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 64% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 1, 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 7 samples with support for all annotated introns
zinc finger protein 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 5 samples with support for all annotated introns
zinc finger protein 1, transcript variant X1
zinc finger protein 1, 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 8 samples with support for all annotated introns
zinc finger 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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein K02A2.6-like, transcript variant X3
uncharacterized protein LOC125224796 isoform X3
uncharacterized protein K02A2.6-like, transcript variant X1
uncharacterized protein K02A2.6-like, transcript variant X2
uncharacterized protein K02A2.6-like isoform X2
uncharacterized protein K02A2.6-like isoform X1
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.
transfer RNA arginine (anticodon CCU); 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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125224769, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC125224769, transcript variant X2
uncharacterized protein LOC125224769 isoform X1
uncharacterized protein LOC125224769 isoform X2
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
flexible cuticle protein 12-like, transcript variant X2
flexible cuticle protein 12-like, transcript variant X1
flexible cuticle protein 12-like isoform X2
flexible cuticle protein 12-like isoform X1
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: flexible cuticle protein 12-like
uncharacterized LOC125242520, 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
uncharacterized LOC125242520, 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 1 sample with support for all annotated introns
uncharacterized protein LOC125242520 isoform X1
uncharacterized protein LOC125242520 isoform X2
L-aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase
3-hydroxyisobutyryl-CoA hydrolase, mitochondrial, 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 12 samples with support for all annotated introns
3-hydroxyisobutyryl-CoA hydrolase, mitochondrial, 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 10 samples with support for all annotated introns
3-hydroxyisobutyryl-CoA hydrolase, mitochondrial
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 87% 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: 12 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 161B, 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
transmembrane protein 161B, 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 10 samples with support for all annotated introns
V-type proton ATPase 116 kDa subunit a 1, transcript variant X1
V-type proton ATPase 116 kDa subunit a 1, transcript variant X4
V-type proton ATPase 116 kDa subunit a 1, transcript variant X5
V-type proton ATPase 116 kDa subunit a 1, transcript variant X2
V-type proton ATPase 116 kDa subunit a 1, transcript variant X3
V-type proton ATPase 116 kDa subunit a 1, transcript variant X7
V-type proton ATPase 116 kDa subunit a 1, transcript variant X8
V-type proton ATPase 116 kDa subunit a 1, transcript variant X9
V-type proton ATPase 116 kDa subunit a 1, transcript variant X10
V-type proton ATPase 116 kDa subunit a 1 isoform X4
V-type proton ATPase 116 kDa subunit a 1 isoform X1
V-type proton ATPase 116 kDa subunit a 1 isoform X2
V-type proton ATPase 116 kDa subunit a 1 isoform X3
V-type proton ATPase 116 kDa subunit a 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: protoporphyrinogen oxidase
phospholipase B1, membrane-associated-like
palmitoyltransferase ZDHHC6, 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 1 sample with support for all annotated introns
palmitoyltransferase ZDHHC6, 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 10 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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 3 samples with support for all annotated introns
glutenin, high molecular weight subunit PW212-like, transcript variant X2
glutenin, high molecular weight subunit PW212-like, transcript variant X1
glutenin, high molecular weight subunit PW212-like
cell wall protein DAN4-like, transcript variant X3
cell wall protein DAN4-like, transcript variant X2
cell wall protein DAN4-like, transcript variant X1
uncharacterized protein LOC125224846 isoform X3
cell wall integrity and stress response component 4-like isoform X2
transfer RNA isoleucine (anticodon AAU); 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 3 samples with support for all annotated introns
pollen-specific leucine-rich repeat extensin-like protein 1
angiotensin-converting enzyme-like, transcript variant X3
angiotensin-converting enzyme-like, transcript variant X4
angiotensin-converting enzyme-like, transcript variant X1
angiotensin-converting enzyme-like, transcript variant X2
angiotensin-converting enzyme-like isoform X1
angiotensin-converting enzyme-like isoform X2
angiotensin-converting enzyme-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
LOW QUALITY PROTEIN: centaurin-gamma-1A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC125242637, transcript variant X1
uncharacterized LOC125242637, transcript variant X4
uncharacterized LOC125242637, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC125242637, 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 2 samples with support for all annotated introns
uncharacterized LOC125242637, transcript variant X2
uncharacterized LOC125242637, transcript variant X3
uncharacterized protein LOC125242637 isoform X1
uncharacterized protein LOC125242637 isoform X2
uncharacterized protein LOC125242637 isoform X3
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
acid sphingomyelinase-like phosphodiesterase 3a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acid sphingomyelinase-like phosphodiesterase 3a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acid sphingomyelinase-like phosphodiesterase 3a isoform X1
acid sphingomyelinase-like phosphodiesterase 3a isoform X2
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
calcium-binding mitochondrial carrier protein Aralar1
bone morphogenetic protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
bone morphogenetic protein 1, transcript variant X2
methionine aminopeptidase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
methionine aminopeptidase 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 13 samples with support for all annotated introns
immunoglobulin A1 protease autotransporter-like, transcript variant X2
immunoglobulin A1 protease autotransporter-like, transcript variant X1
immunoglobulin A1 protease autotransporter-like isoform X2
immunoglobulin A1 protease autotransporter-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 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 1 sample 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% 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
LOW QUALITY PROTEIN: uncharacterized protein LOC125242743
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
uncharacterized LOC125242659, transcript variant X2
uncharacterized LOC125242659, transcript variant X1
uncharacterized protein LOC125242659 isoform X2
uncharacterized protein LOC125242659 isoform X1
uncharacterized LOC125224679, transcript variant X2
uncharacterized protein LOC125224679 isoform X2
uncharacterized LOC125224679, transcript variant X1
uncharacterized protein LOC125224679 isoform X1
uncharacterized LOC125242546, 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 6 samples with support for all annotated introns
uncharacterized protein LOC125242546 isoform X1
uncharacterized LOC125242546, transcript variant X5
uncharacterized protein LOC125242546 isoform X3
uncharacterized LOC125242546, 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 12 samples with support for all annotated introns
uncharacterized LOC125242546, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC125242546, 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 4 samples with support for all annotated introns
uncharacterized protein LOC125242546 isoform X2
mannosyl-oligosaccharide alpha-1,2-mannosidase IA
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA valine (anticodon GAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA proline (anticodon CGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
STAM-binding protein-like A, transcript variant X1
STAM-binding protein-like A, transcript variant X2
uncharacterized LOC125242556, transcript variant X3
uncharacterized LOC125242556, transcript variant X2
uncharacterized LOC125242556, transcript variant X1
CDGSH iron-sulfur domain-containing protein 2 homolog
PH and SEC7 domain-containing protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PH and SEC7 domain-containing protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
PH and SEC7 domain-containing protein isoform X2
PH and SEC7 domain-containing protein isoform X1
LOW QUALITY PROTEIN: BRISC and BRCA1-A complex member 1-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, transcript variant X3
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
cytoplasmic dynein 1 intermediate chain, transcript variant X18
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 7 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, transcript variant X13
cytoplasmic dynein 1 intermediate chain, transcript variant X19
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
cytoplasmic dynein 1 intermediate chain, transcript variant X16
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 7 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, transcript variant X15
cytoplasmic dynein 1 intermediate chain, transcript variant X10
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 6 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, transcript variant X12
cytoplasmic dynein 1 intermediate chain, transcript variant X7
cytoplasmic dynein 1 intermediate chain, transcript variant X17
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 5 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, transcript variant X11
cytoplasmic dynein 1 intermediate chain, transcript variant X9
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 7 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, transcript variant X4
cytoplasmic dynein 1 intermediate chain, transcript variant X8
cytoplasmic dynein 1 intermediate chain, transcript variant X14
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 3 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, transcript variant X6
cytoplasmic dynein 1 intermediate chain, transcript variant X5
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 5 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, 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 5 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, transcript variant X1
cytoplasmic dynein 1 intermediate chain isoform X18
cytoplasmic dynein 1 intermediate chain isoform X13
cytoplasmic dynein 1 intermediate chain isoform X19
cytoplasmic dynein 1 intermediate chain isoform X16
cytoplasmic dynein 1 intermediate chain isoform X15
cytoplasmic dynein 1 intermediate chain isoform X10
cytoplasmic dynein 1 intermediate chain isoform X12
cytoplasmic dynein 1 intermediate chain isoform X7
cytoplasmic dynein 1 intermediate chain isoform X17
cytoplasmic dynein 1 intermediate chain isoform X11
cytoplasmic dynein 1 intermediate chain isoform X9
cytoplasmic dynein 1 intermediate chain isoform X4
cytoplasmic dynein 1 intermediate chain isoform X8
cytoplasmic dynein 1 intermediate chain isoform X14
cytoplasmic dynein 1 intermediate chain isoform X6
cytoplasmic dynein 1 intermediate chain isoform X5
cytoplasmic dynein 1 intermediate chain isoform X2
cytoplasmic dynein 1 intermediate chain isoform X1
cytoplasmic dynein 1 intermediate chain isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
MICOS complex subunit MIC13 homolog QIL1
DNA polymerase zeta catalytic subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
DNA polymerase zeta catalytic subunit, transcript variant X1
DNA polymerase zeta catalytic subunit, 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 9 samples with support for all annotated introns
DNA polymerase zeta catalytic subunit, 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 2 samples with support for all annotated introns
DNA polymerase zeta catalytic subunit isoform X4
DNA polymerase zeta catalytic subunit isoform X2
DNA polymerase zeta catalytic subunit isoform X1
DNA polymerase zeta catalytic subunit isoform X3
uncharacterized LOC125242665, transcript variant X2
uncharacterized LOC125242665, transcript variant X1
uncharacterized protein LOC125242665 isoform X2
uncharacterized protein LOC125242665 isoform 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
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: putative malate dehydrogenase 1B
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
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
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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC125242625, transcript variant X1
uncharacterized LOC125242625, transcript variant X2
uncharacterized LOC125242625, transcript variant X3
angiomotin-like protein 2, transcript variant X2
angiomotin-like protein 2, transcript variant X1
putative thiosulfate sulfurtransferase, mitochondrial, transcript variant X2
putative thiosulfate sulfurtransferase, mitochondrial isoform X2
putative thiosulfate sulfurtransferase, mitochondrial, transcript variant X1
putative thiosulfate sulfurtransferase, mitochondrial isoform X1
rhodanese domain-containing protein CG4456-like, transcript variant X2
rhodanese domain-containing protein CG4456-like, transcript variant X1
rhodanese domain-containing protein CG4456-like isoform X1
rhodanese domain-containing protein CG4456-like isoform X2
LOW QUALITY PROTEIN: peroxiredoxin-4-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC125242698
cytosolic carboxypeptidase-like protein 5
uncharacterized LOC125242688, transcript variant X1
uncharacterized LOC125242688, transcript variant X3
uncharacterized LOC125242688, transcript variant X2
uncharacterized protein LOC125242688 isoform X1
uncharacterized protein LOC125242688 isoform X3
uncharacterized protein LOC125242688 isoform X2
uncharacterized LOC125224723, transcript variant X1
uncharacterized LOC125224723, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
tachykinin-like peptides receptor 99D, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tachykinin-like peptides receptor 99D, transcript variant X2
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
activity-regulated cytoskeleton associated protein 1-like
thioredoxin-1-like, transcript variant X1
thioredoxin-1-like, transcript variant X2
TPR repeat-containing thioredoxin TDX-like isoform X1
tachykinin-like peptides receptor 99D isoform X1
tachykinin-like peptides receptor 99D isoform X2
serine/arginine repetitive matrix protein 1-like, transcript variant X7
serine/arginine repetitive matrix protein 1-like, transcript variant X11
serine/arginine repetitive matrix protein 1-like, transcript variant X16
serine/arginine repetitive matrix protein 1-like, transcript variant X15
serine/arginine repetitive matrix protein 1-like, transcript variant X12
serine/arginine repetitive matrix protein 1-like, transcript variant X9
serine/arginine repetitive matrix protein 1-like, transcript variant X1
serine/arginine repetitive matrix protein 1-like, transcript variant X10
serine/arginine repetitive matrix protein 1-like, transcript variant X2
serine/arginine repetitive matrix protein 1-like, transcript variant X14
serine/arginine repetitive matrix protein 1-like, transcript variant X6
serine/arginine repetitive matrix protein 1-like, transcript variant X3
serine/arginine repetitive matrix protein 1-like, transcript variant X8
serine/arginine repetitive matrix protein 1-like, transcript variant X4
serine/arginine repetitive matrix protein 1-like, transcript variant X5
serine/arginine repetitive matrix protein 1-like, transcript variant X13
serine/arginine repetitive matrix protein 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; 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
LOW QUALITY PROTEIN: ubiquitin carboxyl-terminal hydrolase 1
pyruvate kinase-like, transcript variant X4
pyruvate kinase-like, transcript variant X5
uncharacterized LOC125242682, transcript variant X2
uncharacterized LOC125242682, transcript variant X1
uncharacterized protein LOC125242682 isoform X2
uncharacterized protein LOC125242682 isoform X1
pyruvate kinase-like, transcript variant X9
pyruvate kinase-like, transcript variant X7
pyruvate kinase-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
pyruvate kinase-like, transcript variant X2
pyruvate kinase-like, transcript variant X3
pyruvate kinase-like, transcript variant X1
pyruvate kinase-like, transcript variant X6
geranylgeranyl pyrophosphate synthase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
geranylgeranyl pyrophosphate synthase, 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 8 samples with support for all annotated introns
geranylgeranyl pyrophosphate synthase isoform X1
geranylgeranyl pyrophosphate synthase isoform X2
calcium-activated potassium channel slowpoke, transcript variant X7
calcium-activated potassium channel slowpoke, transcript variant X4
calcium-activated potassium channel slowpoke, transcript variant X11
calcium-activated potassium channel slowpoke, transcript variant X2
calcium-activated potassium channel slowpoke, transcript variant X10
calcium-activated potassium channel slowpoke, transcript variant X9
calcium-activated potassium channel slowpoke, transcript variant X6
calcium-activated potassium channel slowpoke, transcript variant X1
calcium-activated potassium channel slowpoke, transcript variant X5
calcium-activated potassium channel slowpoke, transcript variant X8
calcium-activated potassium channel slowpoke, transcript variant X3
calcium-activated potassium channel slowpoke isoform X11
calcium-activated potassium channel slowpoke isoform X2
calcium-activated potassium channel slowpoke isoform X7
calcium-activated potassium channel slowpoke isoform X4
calcium-activated potassium channel slowpoke isoform X10
calcium-activated potassium channel slowpoke isoform X9
calcium-activated potassium channel slowpoke isoform X6
calcium-activated potassium channel slowpoke isoform X1
calcium-activated potassium channel slowpoke isoform X5
calcium-activated potassium channel slowpoke isoform X8
calcium-activated potassium channel slowpoke isoform X3
uncharacterized LOC125224872, 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 13 samples with support for all annotated introns
uncharacterized protein LOC125224872 isoform X2
uncharacterized LOC125224872, transcript variant X1
uncharacterized protein LOC125224872 isoform X1
uncharacterized LOC125224872, 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 4 samples with support for all annotated introns
uncharacterized protein LOC125224872 isoform X3
uncharacterized LOC125224749, transcript variant X2
uncharacterized protein LOC125224749 isoform X2
uncharacterized LOC125224749, transcript variant X1
uncharacterized LOC125224749, transcript variant X3
uncharacterized protein LOC125224749 isoform X1
uncharacterized protein LOC125224749 isoform X3
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
xanthan lyase-like, transcript variant X2
xanthan lyase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 98% 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: cell division cycle 5-like protein
NEDD8-activating enzyme E1 catalytic subunit
signal peptidase complex catalytic subunit SEC11A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein K02A2.6-like
uncharacterized LOC125242646, transcript variant X3
uncharacterized LOC125242646, transcript variant X2
uncharacterized protein LOC125242646 isoform X2
uncharacterized LOC125242646, transcript variant X1
uncharacterized protein LOC125242646 isoform X1
corticotropin-releasing factor-binding protein
acetylcholinesterase-like, transcript variant X1
acetylcholinesterase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 68% coverage of the annotated genomic feature by RNAseq alignments
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
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 12 samples with support for all annotated introns
putative serine protease K12H4.7, transcript variant X2
putative serine protease K12H4.7 isoform X2
putative serine protease K12H4.7, transcript variant X1
putative serine protease K12H4.7 isoform X1
S-adenosylmethionine synthase, transcript variant X2
S-adenosylmethionine synthase, transcript variant X1
S-adenosylmethionine synthase isoform X1
S-adenosylmethionine synthase isoform X2
pituitary adenylate cyclase-activating polypeptide type I receptor-like, transcript variant X1
pituitary adenylate cyclase-activating polypeptide type I receptor-like, transcript variant X2
pituitary adenylate cyclase-activating polypeptide type I receptor-like, transcript variant X3
uncharacterized protein LOC125242618 isoform X1
pituitary adenylate cyclase-activating polypeptide type I receptor-like isoform X2
uncharacterized protein LOC125242618 isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 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; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: tubulin-specific chaperone D
arylsulfatase B-like, transcript variant X1
arylsulfatase B-like, transcript variant X3
arylsulfatase B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 96% 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: 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized protein LOC125224746 isoform X2
LOW QUALITY PROTEIN: PHD finger protein 14
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 4 samples with support for all annotated introns
RNA-binding motif protein, X-linked 2-like
transcription initiation factor TFIID subunit 13, transcript variant X2
transcription initiation factor TFIID subunit 13, transcript variant X3
transcription initiation factor TFIID subunit 13, transcript variant X1
transcription initiation factor TFIID subunit 13
uncharacterized LOC125224711, transcript variant X2
uncharacterized LOC125224711, transcript variant X1
uncharacterized LOC125224711, transcript variant X3
uncharacterized protein LOC125224711 isoform X2
uncharacterized protein LOC125224711 isoform X1
uncharacterized protein LOC125224711 isoform X3
uncharacterized LOC125224714, transcript variant X7
uncharacterized LOC125224714, transcript variant X2
uncharacterized LOC125224714, transcript variant X1
uncharacterized LOC125224714, transcript variant X3
uncharacterized LOC125224714, transcript variant X5
uncharacterized protein LOC125224714 isoform X1
uncharacterized protein LOC125224714 isoform X2
uncharacterized LOC125224714, transcript variant X4
uncharacterized LOC125224714, transcript variant X6
uncharacterized protein LOC125224714 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
poly(rC)-binding protein 3, transcript variant X11
poly(rC)-binding protein 3, transcript variant X15
poly(rC)-binding protein 3, transcript variant X14
poly(rC)-binding protein 3, transcript variant X13
poly(rC)-binding protein 3, transcript variant X2
poly(rC)-binding protein 3, transcript variant X6
poly(rC)-binding protein 3, transcript variant X5
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
poly(rC)-binding protein 3, transcript variant X1
poly(rC)-binding protein 3, transcript variant X10
poly(rC)-binding protein 3, transcript variant X9
poly(rC)-binding protein 3, transcript variant X7
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
poly(rC)-binding protein 3, transcript variant X4
poly(rC)-binding protein 3, transcript variant X8
poly(rC)-binding protein 3, transcript variant X3
poly(rC)-binding protein 3, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA serine (anticodon CGA); 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: 13 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
migration and invasion enhancer 1, transcript variant X1
migration and invasion enhancer 1, transcript variant X3
migration and invasion enhancer 1, transcript variant X4
migration and invasion enhancer 1, 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 8 samples with support for all annotated introns
PDZ and LIM domain protein 2-like, transcript variant X1
PDZ and LIM domain protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
PDZ and LIM domain protein 5-like isoform X1
PDZ and LIM domain protein 2-like isoform X2
PDZ and LIM domain protein 2-like, transcript variant X3
microtubule-associated serine/threonine-protein kinase 3-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
putative sodium-dependent multivitamin transporter
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 13 samples with support for all annotated introns
putative sodium-dependent multivitamin transporter, 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 3 samples with support for all annotated introns
putative sodium-dependent multivitamin transporter, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
putative sodium-dependent multivitamin transporter isoform X1
putative sodium-dependent multivitamin transporter isoform X2
odorant receptor 45a, 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 2 samples with support for all annotated introns
odorant receptor 45a, transcript variant X2
odorant receptor 45a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC125224822 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 10 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 12 samples with support for all annotated introns
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: homeobox protein ceh-19-like
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
alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
acidic leucine-rich nuclear phosphoprotein 32 family member A, transcript variant X1
acidic leucine-rich nuclear phosphoprotein 32 family member A, transcript variant X2
acidic leucine-rich nuclear phosphoprotein 32 family member A isoform X1
acidic leucine-rich nuclear phosphoprotein 32 family member A isoform X2
LOW QUALITY PROTEIN: origin recognition complex subunit 2
THAP domain-containing protein 1-like, transcript variant X1
THAP domain-containing protein 1-like, transcript variant X2
THAP domain-containing protein 1-like isoform X1
THAP domain-containing protein 1-like isoform X2
protein amalgam-like, transcript variant X1
protein amalgam-like, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein LOC125224640
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X1
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X2
guanine nucleotide-binding protein G(q) subunit alpha
fatty-acid amide hydrolase 2-B, transcript variant X2
fatty-acid amide hydrolase 2-B, transcript variant X1
fatty-acid amide hydrolase 2-B isoform X1
fatty-acid amide hydrolase 2-B isoform X2
uncharacterized LOC125224786, transcript variant X2
uncharacterized LOC125224786, transcript variant X1
uncharacterized protein LOC125224786 isoform X1
uncharacterized LOC125224786, transcript variant X3
uncharacterized protein LOC125224786 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
LOW QUALITY PROTEIN: trypsin alpha-3-like
zinc finger MIZ domain-containing protein 1
dentin sialophosphoprotein-like, transcript variant X1
dentin sialophosphoprotein-like, transcript variant X3
dentin sialophosphoprotein-like, transcript variant X2
dentin sialophosphoprotein-like isoform X1
dentin sialophosphoprotein-like, transcript variant X4
dentin sialophosphoprotein-like isoform X2
LOW QUALITY PROTEIN: probable phosphoserine aminotransferase
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cytochrome b5-related protein-like, 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 11 samples with support for all annotated introns
cytochrome b5-related protein-like, 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 5 samples with support for all annotated introns
uncharacterized LOC125242672, transcript variant X2
uncharacterized LOC125242672, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125224918, transcript variant X3
uncharacterized LOC125224918, transcript variant X1
uncharacterized LOC125224918, transcript variant X2
uncharacterized protein LOC125224918 isoform X2
uncharacterized protein LOC125224918 isoform X1
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 4 samples with support for all annotated introns
ras-related and estrogen-regulated growth inhibitor-like protein
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
major facilitator superfamily domain-containing protein 9-like
major facilitator superfamily domain-containing protein 9-like, 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 6 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 9-like, transcript variant X2
major facilitator superfamily domain-containing protein 9-like isoform X1
major facilitator superfamily domain-containing protein 9-like isoform X2
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 2, mitochondrial-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 4 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 4 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: CD2-associated protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
leucine-rich melanocyte differentiation-associated protein-like
aldehyde dehydrogenase 1A1-like, transcript variant X1
aldehyde dehydrogenase 1A1-like, transcript variant X3
aldehyde dehydrogenase 1A1-like, transcript variant X4
aldehyde dehydrogenase 1A1-like, transcript variant X2
aldehyde dehydrogenase 1A1-like isoform X1
aldehyde dehydrogenase 1A1-like isoform X3
aldehyde dehydrogenase 1A1-like isoform X4
aldehyde dehydrogenase, cytosolic 2-like isoform X2
LOW QUALITY PROTEIN: aldehyde dehydrogenase 1A1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
aldehyde dehydrogenase 1A1-like isoform X2
transfer RNA alanine (anticodon GGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA aspartic acid (anticodon AUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC125242622, transcript variant X3
uncharacterized LOC125242622, transcript variant X1
uncharacterized LOC125242622, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
cell wall protein PRY3-like, transcript variant X3
cell wall protein PRY3-like, transcript variant X2
cell wall protein PRY3-like, transcript variant X1
bifunctional purine biosynthesis protein ATIC, transcript variant X3
bifunctional purine biosynthesis protein ATIC, transcript variant X2
bifunctional purine biosynthesis protein ATIC, transcript variant X1
bifunctional purine biosynthesis protein ATIC isoform X1
bifunctional purine biosynthesis protein ATIC isoform X2
nuclear factor NF-kappa-B p105 subunit, transcript variant X1
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 11 samples with support for all annotated introns
nuclear factor NF-kappa-B p105 subunit, 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 11 samples with support for all annotated introns
nuclear factor NF-kappa-B p110 subunit isoform X1
nuclear factor NF-kappa-B p110 subunit isoform X2
nuclear factor NF-kappa-B p105 subunit, 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
nuclear factor NF-kappa-B p105 subunit isoform X3
uncharacterized protein C15orf61 homolog, transcript variant X1
uncharacterized protein C15orf61 isoform X1
uncharacterized protein C15orf61 homolog, transcript variant X2
uncharacterized protein C15orf61 homolog isoform 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
odorant receptor 4-like, transcript variant X3
odorant receptor 4-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 4 samples with support for all annotated introns
odorant receptor 4-like, transcript variant X1
uncharacterized protein LOC125242593 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125224785, transcript variant X1
uncharacterized LOC125224785, transcript variant X2
uncharacterized LOC125224908, transcript variant X2
uncharacterized LOC125224908, transcript variant X5
uncharacterized LOC125224908, transcript variant X4
uncharacterized LOC125224908, transcript variant X3
uncharacterized LOC125224908, transcript variant X6
uncharacterized LOC125224908, transcript variant X1
uncharacterized LOC125224908, transcript variant X7
uncharacterized protein LOC125224908 isoform X4
uncharacterized protein LOC125224908 isoform X2
uncharacterized protein LOC125224908 isoform X3
uncharacterized protein LOC125224908 isoform X5
uncharacterized protein LOC125224908 isoform X1
uncharacterized protein LOC125224908 isoform X6
uncharacterized LOC125224908, transcript variant X11
uncharacterized LOC125224908, transcript variant X10
uncharacterized LOC125224908, transcript variant X9
uncharacterized LOC125224908, transcript variant X12
uncharacterized protein LOC125224908 isoform X10
uncharacterized protein LOC125224908 isoform X9
uncharacterized protein LOC125224908 isoform X8
uncharacterized protein LOC125224908 isoform X11
uncharacterized LOC125224908, transcript variant X8
uncharacterized protein LOC125224908 isoform X7
tetratricopeptide repeat protein 21B-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
LOW QUALITY PROTEIN: tetratricopeptide repeat protein 21B-like
V-type proton ATPase 116 kDa subunit a 1-like
LOW QUALITY PROTEIN: V-type proton ATPase 116 kDa subunit a 1-like
thiamin pyrophosphokinase 1, transcript variant X1
thiamin pyrophosphokinase 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 7 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 13 samples with support for all annotated introns
synaptic vesicle glycoprotein 2C-like, transcript variant X2
synaptic vesicle glycoprotein 2C-like, transcript variant X1
synaptic vesicle glycoprotein 2C-like isoform X2
synaptic vesicle glycoprotein 2C-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein LOC125242767
A disintegrin and metalloproteinase with thrombospondin motifs 3-like, transcript variant X1
A disintegrin and metalloproteinase with thrombospondin motifs 3-like, transcript variant X2
A disintegrin and metalloproteinase with thrombospondin motifs 3-like isoform X1
A disintegrin and metalloproteinase with thrombospondin motifs 3-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein LOC125224657
peptidyl-prolyl cis-trans isomerase-like
disintegrin and metalloproteinase domain-containing protein 10
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 4 samples with support for all annotated introns
zinc finger protein 800, transcript variant X1
zinc finger protein 800, transcript variant X2
ATP synthase subunit beta, mitochondrial-like
ubiquinol-cytochrome-c reductase complex assembly factor 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: sphingomyelin phosphodiesterase 1-like
uncharacterized LOC125242579, transcript variant X2
uncharacterized LOC125242579, transcript variant X3
uncharacterized LOC125242579, transcript variant X1
ATP synthase subunit beta, mitochondrial
importin subunit alpha-7, transcript variant X3
importin subunit alpha-7, transcript variant X2
importin subunit alpha-7, transcript variant X1
importin subunit alpha-7, transcript variant X4
esterase FE4-like, transcript variant X2
esterase FE4-like, transcript variant X1
uncharacterized LOC125242566, transcript variant X4
uncharacterized LOC125242566, transcript variant X1
uncharacterized LOC125242566, transcript variant X3
uncharacterized LOC125242566, transcript variant X2
uncharacterized protein LOC125242566 isoform X2
uncharacterized protein LOC125242566 isoform X1
uncharacterized protein LOC125242566 isoform X3
uncharacterized LOC125242566, transcript variant X5
uncharacterized protein LOC125242566 isoform X4
leucine-rich repeat and death domain-containing protein 1-like
uncharacterized LOC125224720, transcript variant X2
uncharacterized LOC125224720, transcript variant X1
uncharacterized LOC125224721, transcript variant X1
uncharacterized LOC125224721, transcript variant X2
uncharacterized LOC125224603, transcript variant X3
uncharacterized LOC125224603, transcript variant X4
uncharacterized LOC125224603, transcript variant X2
uncharacterized LOC125224603, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32% 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, including 2 samples with support for all annotated introns
protein timeless homolog, transcript variant X1
protein timeless homolog, transcript variant 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
U3 small nucleolar RNA-associated protein 18 homolog
LOW QUALITY PROTEIN: dnaJ homolog subfamily A member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
meiosis-specific nuclear structural protein 1-like, transcript variant X1
meiosis-specific nuclear structural protein 1-like isoform X1
meiosis-specific nuclear structural protein 1-like, transcript variant X2
meiosis-specific nuclear structural protein 1-like isoform X2
cytochrome P450 4V2-like, transcript variant X2
cytochrome P450 4V2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
myosin heavy chain 95F, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
myosin heavy chain 95F, transcript variant X1
2-acylglycerol O-acyltransferase 2-A-like, transcript variant X3
2-acylglycerol O-acyltransferase 2-A-like, transcript variant X4
2-acylglycerol O-acyltransferase 2-A-like, transcript variant X1
2-acylglycerol O-acyltransferase 2-A-like, transcript variant X2
2-acylglycerol O-acyltransferase 2-A-like isoform X3
2-acylglycerol O-acyltransferase 2-A-like isoform X1
2-acylglycerol O-acyltransferase 2-A-like isoform X2
2-acylglycerol O-acyltransferase 2-A-like isoform X4
set1/Ash2 histone methyltransferase complex subunit ASH2, transcript variant X1
set1/Ash2 histone methyltransferase complex subunit ASH2 isoform X1
set1/Ash2 histone methyltransferase complex subunit ASH2, transcript variant X2
set1/Ash2 histone methyltransferase complex subunit ASH2 isoform X2
phosphatidylinositol 4-kinase beta, transcript variant X1
phosphatidylinositol 4-kinase beta, transcript variant X3
phosphatidylinositol 4-kinase beta isoform X1
phosphatidylinositol 4-kinase beta isoform X3
phosphatidylinositol 4-kinase beta, transcript variant X2
phosphatidylinositol 4-kinase beta isoform X2
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ATP-dependent RNA helicase dbp10
uncharacterized LOC125242624, transcript variant X1
uncharacterized protein LOC125242624 isoform X1
uncharacterized LOC125242624, transcript variant X2
uncharacterized protein LOC125242624 isoform X2
beta-1,3-glucan-binding protein-like, transcript variant X1
beta-1,3-glucan-binding protein-like, transcript variant X2
uncharacterized protein LOC125224994 isoform X1
beta-1,3-glucan-binding protein-like, transcript variant X3
beta-1,3-glucan-binding protein-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
E3 ubiquitin-protein ligase MARCHF7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 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: 79% coverage of the annotated genomic feature by RNAseq alignments
tyrosine kinase receptor Cad96Ca, 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 13 samples with support for all annotated introns
tyrosine kinase receptor Cad96Ca, 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 12 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 84% coverage of the annotated genomic feature by RNAseq alignments
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
uncharacterized LOC125224802, transcript variant X1
uncharacterized LOC125224802, transcript variant X2
sodium- and chloride-dependent glycine transporter 1-like
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, including 1 sample with support for all annotated introns
acid sphingomyelinase-like phosphodiesterase 3a
uncharacterized LOC125242669, transcript variant X2
uncharacterized LOC125242669, transcript variant X1
protein AAR2 homolog, transcript variant X2
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, including 2 samples with support for all annotated introns
protein AAR2 homolog, transcript variant 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, including 13 samples with support for all annotated introns
MKI67 FHA domain-interacting nucleolar phosphoprotein-like, transcript variant X2
MKI67 FHA domain-interacting nucleolar phosphoprotein-like, transcript variant X1
MKI67 FHA domain-interacting nucleolar phosphoprotein-like isoform X2
MKI67 FHA domain-interacting nucleolar phosphoprotein-like isoform X1
NAD-dependent protein deacylase sirtuin-5, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
dynactin subunit 6-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 5 samples with support for all annotated introns
dynactin subunit 6-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 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
juvenile hormone acid O-methyltransferase-like
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
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transient receptor potential channel pyrexia-like, transcript variant X4
transient receptor potential channel pyrexia-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transient receptor potential channel pyrexia-like, transcript variant X1
transient receptor potential channel pyrexia-like isoform X1
uncharacterized protein LOC125224868 isoform X4
transient receptor potential channel pyrexia-like isoform X2
transient receptor potential channel pyrexia-like, transcript variant X3
transient receptor potential channel pyrexia-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125224894, transcript variant X3
uncharacterized LOC125224894, transcript variant X2
uncharacterized LOC125224894, transcript variant X5
uncharacterized LOC125224894, transcript variant X7
uncharacterized LOC125224894, transcript variant X6
uncharacterized LOC125224894, transcript variant X4
uncharacterized LOC125224894, transcript variant X1
uncharacterized protein LOC125224894 isoform X3
uncharacterized protein LOC125224894 isoform X2
uncharacterized protein LOC125224894 isoform X5
uncharacterized protein LOC125224894 isoform X7
uncharacterized protein LOC125224894 isoform X6
uncharacterized protein LOC125224894 isoform X4
uncharacterized protein LOC125224894 isoform X1
putative uncharacterized protein DDB_G0271974
uncharacterized LOC125242691, transcript variant X1
uncharacterized LOC125242691, transcript variant X2
uncharacterized LOC125242691, transcript variant X3
uncharacterized protein LOC125242691 isoform X1
uncharacterized protein LOC125242691 isoform X2
uncharacterized protein LOC125242691 isoform X3
uncharacterized LOC125242690, transcript variant X1
uncharacterized protein LOC125242690 isoform X1
uncharacterized LOC125242690, transcript variant X3
uncharacterized protein LOC125242690 isoform X3
uncharacterized LOC125242690, transcript variant X2
uncharacterized protein LOC125242690 isoform X2
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like
forkhead box protein O, transcript variant X2
forkhead box protein O, transcript variant X1
uncharacterized LOC125224806, transcript variant X1
uncharacterized protein LOC125224806 isoform X1
uncharacterized LOC125224805, transcript variant X1
uncharacterized LOC125224805, transcript variant X2
uncharacterized LOC125224806, transcript variant X2
uncharacterized protein LOC125224806 isoform X2
wiskott-Aldrich syndrome protein family member 1-like
vacuolar protein sorting-associated protein 13-like
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: vacuolar protein sorting-associated protein 13-like
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
COORDINATES: nucleotide motif:Rfam:12.0:RF00618
early nodulin-75-like, transcript variant X7
early nodulin-75-like, transcript variant X2
early nodulin-75-like, transcript variant X3
early nodulin-75-like, transcript variant X4
early nodulin-75-like, transcript variant X1
early nodulin-75-like, transcript variant X6
early nodulin-75-like, transcript variant X8
early nodulin-75-like, transcript variant X5
altered inheritance of mitochondria protein 3-like isoform X1
class E vacuolar protein-sorting machinery protein HSE1-like isoform X6
activating signal cointegrator 1 complex subunit 2 homolog isoform X4
AT-rich interactive domain-containing protein 1A-like isoform X7
probable E3 ubiquitin-protein ligase HERC4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: probable E3 ubiquitin-protein ligase HERC4
zinc finger SWIM domain-containing protein 8 homolog
alanine--glyoxylate aminotransferase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
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
immunoglobulin superfamily member 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 67% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125242596, transcript variant X1
uncharacterized LOC125242596, transcript variant X2
uncharacterized LOC125242543, transcript variant X2
uncharacterized LOC125242543, transcript variant X1
uncharacterized protein LOC125242543 isoform X1
uncharacterized protein LOC125242543 isoform X2
transfer RNA threonine (anticodon GGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
signal recognition particle 19 kDa protein
tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit wuho
mitotic checkpoint serine/threonine-protein kinase BUB1 beta-like
ATP-dependent (S)-NAD(P)H-hydrate dehydratase, transcript variant X2
ATP-dependent (S)-NAD(P)H-hydrate dehydratase, transcript variant X1
ATP-dependent (S)-NAD(P)H-hydrate dehydratase
26S proteasome non-ATPase regulatory subunit 5
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
LOW QUALITY PROTEIN: dnaJ homolog subfamily C member 9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC125242561, transcript variant X1
uncharacterized LOC125242561, transcript variant X3
uncharacterized LOC125242561, transcript variant X2
uncharacterized protein LOC125242561 isoform X1
uncharacterized protein LOC125242561 isoform X2
uncharacterized protein LOC125242561 isoform X3
coiled-coil domain-containing protein 12
all trans-polyprenyl-diphosphate synthase PDSS1
39S ribosomal protein L32, mitochondrial
protein draper-like, transcript variant X1
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 1 sample with support for all annotated introns
protein draper-like, transcript variant X3
protein draper-like, transcript variant X2
protein draper-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein draper-like, transcript variant X4
uncharacterized LOC125224761, transcript variant X2
uncharacterized LOC125224761, transcript variant X1
uncharacterized LOC125224761, transcript variant X4
uncharacterized LOC125224761, transcript variant X5
uncharacterized LOC125224761, transcript variant X3
uncharacterized protein LOC125224761 isoform X2
uncharacterized protein LOC125224761 isoform X1
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 3 samples with support for all annotated introns
methionyl-tRNA formyltransferase, mitochondrial, transcript variant X1
methionyl-tRNA formyltransferase, mitochondrial isoform X1
methionyl-tRNA formyltransferase, mitochondrial, transcript variant X2
methionyl-tRNA formyltransferase, mitochondrial isoform X2
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic, 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 9 samples with support for all annotated introns
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic isoform X3
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic, transcript variant X4
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 5 samples with support for all annotated introns
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic isoform X4
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic isoform X1
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic, transcript variant X2
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 1 sample with support for all annotated introns
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic isoform 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 9 samples with support for all annotated introns
inner nuclear membrane protein Man1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: inner nuclear membrane protein Man1-like
2-oxoisovalerate dehydrogenase subunit beta, mitochondrial, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
2-oxoisovalerate dehydrogenase subunit beta, mitochondrial, transcript variant X1
2-oxoisovalerate dehydrogenase subunit beta, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
histone-lysine N-methyltransferase SETMAR-like
protein GDAP2 homolog, transcript variant X2
protein GDAP2 homolog, transcript variant X1
phosphatidylinositol-glycan biosynthesis class F protein
5-aminolevulinate synthase, erythroid-specific, mitochondrial
LOW QUALITY PROTEIN: 5-aminolevulinate synthase, erythroid-specific, mitochondrial
LOW QUALITY PROTEIN: pre-mRNA-processing factor 17
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 13 samples with support for all annotated introns
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, including 3 samples with support for all annotated introns
vacuolar protein sorting-associated protein 51 homolog
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: vacuolar protein sorting-associated protein 51 homolog
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
aminopeptidase N-like, transcript variant X2
aminopeptidase N-like, transcript variant X1
aminopeptidase N-like, transcript variant X3
WAP four-disulfide core domain protein 2-like
hyphally regulated cell wall protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125224830, transcript variant X1
uncharacterized LOC125224830, transcript variant X3
uncharacterized LOC125224830, transcript variant X2
uncharacterized protein LOC125224830 isoform X2
uncharacterized protein LOC125224830 isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: muscarinic acetylcholine receptor M5
facilitated trehalose transporter Tret1-like, transcript variant X1
facilitated trehalose transporter Tret1-like, transcript variant X2
facilitated trehalose transporter Tret1-like isoform X1
facilitated trehalose transporter Tret1-like isoform X2
putative uncharacterized protein DDB_G0271974, transcript variant X2
putative uncharacterized protein DDB_G0271974, 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 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 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: 90 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: membrane alanyl aminopeptidase-like
membrane alanyl aminopeptidase-like, transcript variant X3
membrane alanyl aminopeptidase-like, transcript variant X2
membrane alanyl aminopeptidase-like, transcript variant X1
membrane alanyl aminopeptidase-like isoform X1
membrane alanyl aminopeptidase-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
V-type proton ATPase 116 kDa subunit a 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
V-type proton ATPase 116 kDa subunit a 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
katanin p60 ATPase-containing subunit A1-like, transcript variant X2
katanin p60 ATPase-containing subunit A1-like, transcript variant X3
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
katanin p60 ATPase-containing subunit A1-like, 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 3 samples with support for all annotated introns
katanin p60 ATPase-containing subunit A1-like isoform X2
katanin p60 ATPase-containing subunit A1-like isoform X3
katanin p60 ATPase-containing subunit A1-like isoform X1
nuclear envelope integral membrane protein 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: sphingosine-1-phosphate lyase
dynein regulatory complex protein 11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA glutamic acid (anticodon CUC); 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: 76% 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: 99% coverage of the annotated genomic feature by RNAseq alignments
pickpocket protein 28-like, transcript variant X1
pickpocket protein 28-like, transcript variant X2
uncharacterized protein LOC125224905 isoform X2
SH2 domain-containing protein 5-like, transcript variant X2
SH2 domain-containing protein 5-like, transcript variant X1
SH2 domain-containing protein 5-like, transcript variant X3
SH2 domain-containing protein 5-like isoform X2
SH2 domain-containing protein 5-like isoform X1