Portunus trituberculatus isolate SZX2019 chromosome 34, ASM1759143v1, whole genome shotgun sequence.
Portunus trituberculatus (swimming crab)
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Crustacea; Multicrustacea; Malacostraca; Eumalacostraca; Eucarida; Decapoda; Pleocyemata; Brachyura; Eubrachyura; Portunoidea; Portunidae; Portunus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM030104.1.\nAssembly name: ASM1759143v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Center for Ecological and\nEnvironmental Sciences on 2021/03/30. The original whole-genome\nshotgun project has the accession JAGGDN000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Center for Ecological and Environmental\n Sciences\nAssembly Method :: Wtdbg v. 2.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 54.74x\nSequencing Technology :: Oxford Nanopore; Illumina\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Portunus trituberculatus Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123512772, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized LOC123512772, transcript variant X2
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.
alpha-(1,3)-fucosyltransferase 7-like, transcript variant X1
alpha-(1,3)-fucosyltransferase 7-like, transcript variant X2
alpha-(1,3)-fucosyltransferase 7-like isoform X1
alpha-(1,3)-fucosyltransferase 7-like isoform X2
WD repeat-containing protein 55-like, transcript variant X2
WD repeat-containing protein 55-like, transcript variant X1
WD repeat-containing protein 55-like isoform X2
WD repeat-containing protein 55-like isoform X1
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial-like
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC123512532, transcript variant X1
uncharacterized LOC123512532, transcript variant X2
uncharacterized LOC123512532, transcript variant X4
uncharacterized LOC123512532, transcript variant X5
uncharacterized LOC123512532, transcript variant X6
uncharacterized LOC123512532, transcript variant X3
uncharacterized protein LOC123512532 isoform X1
uncharacterized protein LOC123512532 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
TNF receptor-associated factor family protein DDB_G0272098-like
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA proline (anticodon UGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized protein LOC123512823 isoform X3
uncharacterized protein LOC123512823 isoform X1
uncharacterized protein LOC123512823 isoform X2
MTOR-associated protein MEAK7-like, transcript variant X2
MTOR-associated protein MEAK7-like, transcript variant X6
MTOR-associated protein MEAK7-like, transcript variant X4
MTOR-associated protein MEAK7-like, transcript variant X1
MTOR-associated protein MEAK7-like, transcript variant X3
MTOR-associated protein MEAK7-like, transcript variant X5
putative nuclease HARBI1, transcript variant X1
putative nuclease HARBI1, transcript variant X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins
probable E3 SUMO-protein ligase RNF212, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
probable E3 SUMO-protein ligase RNF212, 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
probable E3 SUMO-protein ligase RNF212, transcript variant X1
probable E3 SUMO-protein ligase RNF212 isoform X1
probable E3 SUMO-protein ligase RNF212 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC123512834, transcript variant X4
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
uncharacterized LOC123512834, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC123512834, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC123512834, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC123512834, transcript variant X5
uncharacterized protein LOC123512834 isoform X2
uncharacterized protein LOC123512834 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
zinc finger protein OZF-like, transcript variant X1
zinc finger protein OZF-like, transcript variant X2
zinc finger protein 493-like, transcript variant X1
zinc finger protein 493-like, transcript variant X2
zinc finger protein 493-like, transcript variant X3
zinc finger protein 493-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
G-patch domain and KOW motifs-containing protein-like, transcript variant X1
G-patch domain and KOW motifs-containing protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
G-patch domain and KOW motifs-containing protein-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
G-patch domain and KOW motifs-containing protein-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
G-patch domain and KOW motifs-containing protein-like, transcript variant X2
G-patch domain and KOW motifs-containing protein-like isoform X2
G-patch domain and KOW motifs-containing protein-like isoform X1
G-patch domain and KOW motifs-containing protein-like isoform X3
uncharacterized LOC123512883, transcript variant X1
uncharacterized LOC123512883, transcript variant X2
uncharacterized protein LOC123512883 isoform X1
uncharacterized protein LOC123512883 isoform X2
uncharacterized LOC123512789, transcript variant X1
uncharacterized LOC123512789, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
tumor susceptibility gene 101 protein-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: tumor susceptibility gene 101 protein-like
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, including 4 samples with support for all annotated introns
TBC1 domain family member 31-like, transcript variant X2
TBC1 domain family member 31-like, transcript variant X1
TBC1 domain family member 31-like, transcript variant X5
TBC1 domain family member 31-like, transcript variant X4
TBC1 domain family member 31-like, transcript variant X3
TBC1 domain family member 31-like isoform X2
TBC1 domain family member 31-like isoform X1
TBC1 domain family member 31-like 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
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.
innexin inx2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
innexin inx2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
innexin inx2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
innexin inx2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
innexin inx2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 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 1 sample with support for all annotated introns
small nuclear ribonucleoprotein-associated protein B-like
forkhead box protein P1-like, transcript variant X15
forkhead box protein P1-like, transcript variant X18
forkhead box protein P1-like isoform X15
forkhead box protein P1-like isoform X12
forkhead box protein P1-like, transcript variant X6
forkhead box protein P1-like, transcript variant X13
forkhead box protein P1-like, transcript variant X16
forkhead box protein P1-like isoform X10
forkhead box protein P1-like isoform X13
forkhead box protein P1-like, transcript variant X7
forkhead box protein P1-like, transcript variant X8
forkhead box protein P1-like, transcript variant X9
forkhead box protein P1-like, transcript variant X10
forkhead box protein P1-like, transcript variant X17
forkhead box protein P1-like isoform X14
forkhead box protein P1-like, transcript variant X11
forkhead box protein P1-like, transcript variant X14
forkhead box protein P1-like, transcript variant X1
forkhead box protein P1-like, transcript variant X3
forkhead box protein P1-like, transcript variant X4
forkhead box protein P1-like, transcript variant X19
forkhead box protein P1-like, transcript variant X5
forkhead box protein P1-like, transcript variant X12
forkhead box protein P1-like, transcript variant X22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
forkhead box protein P1-like, transcript variant X2
forkhead box protein P1-like isoform X11
forkhead box protein P1-like isoform X16
forkhead box protein P1-like isoform X19
forkhead box protein P1-like, transcript variant X20
forkhead box protein P1-like, transcript variant X21
forkhead box protein P1-like isoform X17
forkhead box protein P2-like isoform X18
uncharacterized LOC123512844, transcript variant X1
uncharacterized LOC123512844, transcript variant X2
solute carrier family 25 member 40-like, transcript variant X1
solute carrier family 25 member 40-like, transcript variant X2
solute carrier family 25 member 40-like isoform X2
solute carrier family 25 member 40-like isoform X1
glycerophosphocholine cholinephosphodiesterase ENPP6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
RNA-binding protein lark-like, transcript variant X1
RNA-binding protein lark-like, transcript variant X3
RNA-binding protein lark-like, transcript variant X2
polyadenylate-binding protein 5-like isoform X1
RNA-binding protein lark-like 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transcription factor GAGA-like
uncharacterized LOC123512780, transcript variant X3
uncharacterized LOC123512780, transcript variant X2
uncharacterized LOC123512780, transcript variant X1
uncharacterized protein LOC123512780 isoform X1
uncharacterized protein LOC123512780 isoform X2
sperm-associated antigen 1-like, transcript variant X2
sperm-associated antigen 1-like, transcript variant X3
sperm-associated antigen 1-like, transcript variant X1
sperm-associated antigen 1-like isoform X1
fork head domain-containing protein FD5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
fork head domain-containing protein FD4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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
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: palmitoyltransferase ZDHHC16B-like
uncharacterized LOC123512819, 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 8 samples with support for all annotated introns
uncharacterized LOC123512819, 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
DNA damage-inducible transcript 4-like protein
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
histone-lysine N-methyltransferase 2D-like
uncharacterized protein At4g17910-like, transcript variant X1
uncharacterized protein At4g17910-like, transcript variant X2
transient receptor potential cation channel subfamily A member 1 homolog
LOW QUALITY PROTEIN: transient receptor potential cation channel subfamily A member 1 homolog
uncharacterized LOC123512695, transcript variant X2
uncharacterized LOC123512695, transcript variant X3
uncharacterized LOC123512695, transcript variant X1
uncharacterized protein LOC123512695 isoform X1
uncharacterized protein LOC123512695 isoform X2
uncharacterized LOC123512695, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized protein LOC123512695 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
centromere-associated protein E-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
centromere-associated protein E-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
centromere-associated protein E-like isoform X2
centromere-associated protein E-like isoform X1
SH3 domain-binding glutamic acid-rich protein homolog, transcript variant X1
SH3 domain-binding glutamic acid-rich protein homolog, transcript variant X2
SH3 domain-binding glutamic acid-rich protein homolog isoform X1
SH3 domain-binding glutamic acid-rich protein homolog isoform X2
probable U3 small nucleolar RNA-associated protein 11
uncharacterized LOC123512529, transcript variant X1
uncharacterized LOC123512529, transcript variant X3
uncharacterized LOC123512529, transcript variant X2
uncharacterized protein LOC123512529 isoform X1
uncharacterized protein LOC123512529 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: homeobox protein unc-4 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
LOW QUALITY PROTEIN: kinesin-like protein KIF7
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
cationic amino acid transporter 2, vacuolar-like
LOW QUALITY PROTEIN: cationic amino acid transporter 2, vacuolar-like
deoxynucleoside kinase-like, transcript variant X5
deoxynucleoside kinase-like, transcript variant X1
deoxynucleoside kinase-like, transcript variant X2
deoxynucleoside kinase-like, transcript variant X4
deoxynucleoside kinase-like, transcript variant X3
neural Wiskott-Aldrich syndrome protein-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
LOW QUALITY PROTEIN: neural Wiskott-Aldrich syndrome protein-like
formin-like protein 14, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
formin-like protein 14, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
formin-like protein 14, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
formin-like protein 14, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
formin-like protein 14, transcript variant X5
zinc finger matrin-type protein 5-like, transcript variant X1
zinc finger matrin-type protein 5-like, transcript variant X2
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial-like, transcript variant X2
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial-like, transcript variant X1
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial-like isoform X1
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial-like isoform X2
uncharacterized LOC123512806, transcript variant X1
uncharacterized LOC123512806, 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
spermatogenesis-associated protein 20-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: spermatogenesis-associated protein 20-like
eukaryotic translation elongation factor 1 epsilon-1-like
solute carrier family 45 member 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
solute carrier family 45 member 3-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 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
protein N-terminal asparagine amidohydrolase-like
vacuolar protein sorting-associated protein 13B-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: vacuolar protein sorting-associated protein 13B-like
one cut domain family member 2-like, transcript variant X16
one cut domain family member 2-like, transcript variant X13
one cut domain family member 2-like, transcript variant X15
one cut domain family member 2-like, transcript variant X14
one cut domain family member 2-like, transcript variant X11
one cut domain family member 2-like, transcript variant X9
one cut domain family member 2-like, transcript variant X20
one cut domain family member 2-like, transcript variant X21
one cut domain family member 2-like, transcript variant X18
one cut domain family member 2-like, transcript variant X19
one cut domain family member 2-like, transcript variant X17
homeobox protein onecut-like isoform X20
homeobox protein onecut-like isoform X21
homeobox protein onecut-like isoform X18
homeobox protein onecut-like isoform X19
homeobox protein onecut-like isoform X17
homeobox protein onecut-like isoform X16
homeobox protein onecut-like isoform X13
homeobox protein onecut-like isoform X15
homeobox protein onecut-like isoform X14
homeobox protein onecut-like isoform X11
one cut domain family member 2-like isoform X9
one cut domain family member 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
one cut domain family member 2-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
one cut domain family member 2-like, transcript variant X6
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
one cut domain family member 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
one cut domain family member 2-like, transcript variant X2
one cut domain family member 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
one cut domain family member 2-like, transcript variant X1
one cut domain family member 2-like, transcript variant X12
one cut domain family member 2-like, transcript variant X10
one cut domain family member 2-like, transcript variant X8
trithorax group protein osa-like isoform X12
trithorax group protein osa-like isoform X10
trithorax group protein osa-like isoform X7
trithorax group protein osa-like isoform X3
trithorax group protein osa-like isoform X6
trithorax group protein osa-like isoform X5
trithorax group protein osa-like isoform X4
trithorax group protein osa-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein IMPACT-B-like, transcript variant X2
protein IMPACT-B-like, transcript variant X4
protein IMPACT-B-like, transcript variant X1
protein IMPACT-B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
peroxiredoxin 1-like, transcript variant X1
peroxiredoxin 1-like, transcript variant X2
hydroxyacylglutathione hydrolase, mitochondrial-like, transcript variant X1
hydroxyacylglutathione hydrolase, mitochondrial-like, transcript variant X2
hydroxyacylglutathione hydrolase, mitochondrial-like, transcript variant X3
hydroxyacylglutathione hydrolase, mitochondrial-like isoform X1
hydroxyacylglutathione hydrolase, mitochondrial-like isoform X2
oxysterol-binding protein-related protein 9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
protein aurora borealis-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
protein aurora borealis-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 long SRA reads, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
protein aurora borealis-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 long SRA reads, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized protein LOC123512708 isoform X2
uncharacterized protein LOC123512708 isoform X3
uncharacterized protein LOC123512708 isoform X1
protein aurora borealis-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 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: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: actin-related protein 3-like
glycoprotein 3-alpha-L-fucosyltransferase A-like, transcript variant X3
glycoprotein 3-alpha-L-fucosyltransferase A-like, transcript variant X2
glycoprotein 3-alpha-L-fucosyltransferase A-like, transcript variant X1
glycoprotein 3-alpha-L-fucosyltransferase A-like, transcript variant X4
glycoprotein 3-alpha-L-fucosyltransferase A-like, transcript variant X5
glycoprotein 3-alpha-L-fucosyltransferase A-like, transcript variant X6
glycoprotein 3-alpha-L-fucosyltransferase A-like isoform X2
glycoprotein 3-alpha-L-fucosyltransferase A-like isoform X1
glycoprotein 3-alpha-L-fucosyltransferase A-like isoform X3
facilitated trehalose transporter Tret1-like
platelet-activating factor acetylhydrolase IB subunit alpha2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 24 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
metal-response element-binding transcription factor 2-like, transcript variant X1
metal-response element-binding transcription factor 2-like, transcript variant X5
metal-response element-binding transcription factor 2-like, transcript variant X3
metal-response element-binding transcription factor 2-like, transcript variant X6
metal-response element-binding transcription factor 2-like, transcript variant X2
metal-response element-binding transcription factor 2-like, transcript variant X4
metal-response element-binding transcription factor 2-like isoform X1
metal-response element-binding transcription factor 2-like isoform X3
metal-response element-binding transcription factor 2-like isoform X2
metal-response element-binding transcription factor 2-like isoform X4
probable histone-arginine methyltransferase CARMER
LOW QUALITY PROTEIN: probable histone-arginine methyltransferase CARMER
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit-like, transcript variant X1
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit-like, transcript variant X2
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit-like isoform X1
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit-like isoform X2
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit-like, transcript variant X3
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit-like isoform X3
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit-like, transcript variant X4
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit-like isoform X4
uncharacterized LOC123512724, transcript variant X2
uncharacterized LOC123512724, transcript variant X1
uncharacterized protein LOC123512724 isoform X2
uncharacterized protein LOC123512724 isoform X1
glucose-6-phosphate 1-dehydrogenase-like
succinate--CoA ligase [GDP-forming] subunit beta, mitochondrial-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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 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 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC123512727
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
cytoplasmic dynein 2 intermediate chain 2-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 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: cytoplasmic dynein 2 intermediate chain 2-like
cold shock domain-containing protein CG9705-like
monocarboxylate transporter 10-like, transcript variant X1
monocarboxylate transporter 10-like, transcript variant X3
monocarboxylate transporter 10-like isoform X1
monocarboxylate transporter 10-like isoform X3
monocarboxylate transporter 10-like, transcript variant X4
monocarboxylate transporter 10-like, transcript variant X2
monocarboxylate transporter 10-like isoform X2
monocarboxylate transporter 10-like isoform X4
C-Maf-inducing protein-like, transcript variant X2
C-Maf-inducing protein-like, transcript variant X1
C-Maf-inducing protein-like, transcript variant X5
C-Maf-inducing protein-like, transcript variant X3
C-Maf-inducing protein-like, transcript variant X4
C-Maf-inducing protein-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
protein wntless-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein wntless-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein wntless-like, transcript variant X1
vascular endothelial growth factor receptor kdr-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 long SRA reads, 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
vascular endothelial growth factor receptor kdr-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 long SRA reads, 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
vascular endothelial growth factor receptor kdr-like isoform X2
vascular endothelial growth factor receptor kdr-like isoform X1
probable low-specificity L-threonine aldolase 2
LOW QUALITY PROTEIN: protein bicaudal D-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 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: 21 long SRA reads, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein LOC123512554
dual specificity testis-specific protein kinase 1-like
LOW QUALITY PROTEIN: dual specificity testis-specific protein kinase 1-like
RING finger and SPRY domain-containing protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
RING finger and SPRY domain-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
RING finger and SPRY domain-containing protein 1-like, transcript variant X3
RING finger and SPRY domain-containing protein 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
RING finger and SPRY domain-containing protein 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
RING finger and SPRY domain-containing protein 1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
RING finger and SPRY domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
5-formyltetrahydrofolate cyclo-ligase-like
microtubule-associated protein futsch-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: microtubule-associated protein futsch-like
haloacid dehalogenase-like hydrolase domain-containing 5
pollen-specific leucine-rich repeat extensin-like protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
pollen-specific leucine-rich repeat extensin-like protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
pollen-specific leucine-rich repeat extensin-like protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
pollen-specific leucine-rich repeat extensin-like protein 2, 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 14 samples with support for all annotated introns
pollen-specific leucine-rich repeat extensin-like protein 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 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 2, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
pollen-specific leucine-rich repeat extensin-like protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pollen-specific leucine-rich repeat extensin-like protein 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
pollen-specific leucine-rich repeat extensin-like protein 2, transcript variant X11
pollen-specific leucine-rich repeat extensin-like protein 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
pollen-specific leucine-rich repeat extensin-like protein 2, transcript variant X9
pollen-specific leucine-rich repeat extensin-like protein 2, transcript variant X12
pollen-specific leucine-rich repeat extensin-like protein 2, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
uncharacterized protein LOC123512644 isoform X2
uncharacterized protein LOC123512644 isoform X3
pollen-specific leucine-rich repeat extensin-like protein 2 isoform X1
formin-like protein 5, transcript variant X1
formin-like protein 5, transcript variant X2
LOW QUALITY PROTEIN: glutathione S-transferase 1-1-like
trifunctional purine biosynthetic protein adenosine-3-like, transcript variant X1
trifunctional purine biosynthetic protein adenosine-3-like isoform X1
trifunctional purine biosynthetic protein adenosine-3-like, transcript variant X7
trifunctional purine biosynthetic protein adenosine-3-like, transcript variant X3
trifunctional purine biosynthetic protein adenosine-3-like, transcript variant X4
trifunctional purine biosynthetic protein adenosine-3-like, transcript variant X6
trifunctional purine biosynthetic protein adenosine-3-like, transcript variant X5
trifunctional purine biosynthetic protein adenosine-3-like, transcript variant X9
trifunctional purine biosynthetic protein adenosine-3-like, transcript variant X2
trifunctional purine biosynthetic protein adenosine-3-like isoform X2
trifunctional purine biosynthetic protein adenosine-3-like isoform X3
trifunctional purine biosynthetic protein adenosine-3-like, transcript variant X8
trifunctional purine biosynthetic protein adenosine-3-like isoform X4
trifunctional purine biosynthetic protein adenosine-3-like isoform X5
uncharacterized LOC123512649, transcript variant X1
uncharacterized LOC123512649, transcript variant X2
translation initiation factor IF-2-like, transcript variant X2
translation initiation factor IF-2-like, transcript variant X3
translation initiation factor IF-2-like, transcript variant X1
deoxyuridine 5'-triphosphate nucleotidohydrolase-like
serine/threonine-protein phosphatase 4 regulatory subunit 2-A-like
uncharacterized LOC123512631, transcript variant X2
uncharacterized LOC123512631, transcript variant X1
bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase, mitochondrial-like
dnaJ-like protein 60, transcript variant X2
dnaJ-like protein 60, transcript variant X1
dnaJ-like protein 60, transcript variant X3
serine-threonine kinase receptor-associated protein-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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
double C2-like domain-containing protein beta
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 85% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: double C2-like domain-containing protein beta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC123512584, transcript variant X1
uncharacterized LOC123512584, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 18 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 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 2 bases in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: beta-1-syntrophin-like
uncharacterized LOC123512591, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC123512591, transcript variant 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: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: protein O-mannosyl-transferase 2-like
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
RNA-binding protein lark-like isoform X1
RNA-binding protein lark-like isoform X3
uncharacterized LOC123512593, transcript variant X3
uncharacterized LOC123512593, transcript variant X1
uncharacterized LOC123512593, transcript variant X2
uncharacterized protein LOC123512593 isoform X1
uncharacterized protein LOC123512593 isoform X3
uncharacterized protein LOC123512593 isoform 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: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
LOW QUALITY PROTEIN: popeye domain-containing protein 3-like
LOW QUALITY PROTEIN: blood vessel epicardial substance-like
uncharacterized LOC123512782, transcript variant X1
uncharacterized LOC123512782, transcript variant X2
uncharacterized LOC123512782, transcript variant X4
uncharacterized LOC123512782, transcript variant X3
uncharacterized protein LOC123512782 isoform X1
uncharacterized protein LOC123512782 isoform X2
ATP-binding cassette sub-family C member 12-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ATP-binding cassette sub-family C member 12-like
uncharacterized LOC123512741, transcript variant X1
uncharacterized LOC123512741, 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 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
putative uncharacterized protein DDB_G0290521
LOW QUALITY PROTEIN: putative uncharacterized protein DDB_G0290521
sec1 family domain-containing protein 2-like
LOW QUALITY PROTEIN: sec1 family domain-containing protein 2-like
protein diaphanous-like, transcript variant X2
protein diaphanous-like, transcript variant X5
protein diaphanous-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
protein diaphanous-like, transcript variant X1
protein diaphanous-like, transcript variant X6
protein diaphanous-like, transcript variant X7
protein diaphanous-like, transcript variant X4
protein diaphanous-like, transcript variant X3
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
LOW QUALITY PROTEIN: glutathione S-transferase theta-1-like
serine/threonine-protein kinase OSR1-like, transcript variant X2
serine/threonine-protein kinase OSR1-like, transcript variant X1
serine/threonine-protein kinase OSR1-like, transcript variant X4
serine/threonine-protein kinase OSR1-like isoform X1
serine/threonine-protein kinase OSR1-like isoform X2
serine/threonine-protein kinase OSR1-like isoform X4
serine/threonine-protein kinase OSR1-like, transcript variant X3
serine/threonine-protein kinase OSR1-like isoform X3
serine/threonine-protein kinase OSR1-like, transcript variant X5
serine/threonine-protein kinase OSR1-like isoform X5
serine/threonine-protein kinase OSR1-like, transcript variant X6
serine/threonine-protein kinase OSR1-like, transcript variant X7
serine/threonine-protein kinase OSR1-like isoform X6
protein ABHD11-like, transcript variant X2
protein ABHD11-like, transcript variant X1
protein ABHD11-like, transcript variant X3
peptidyl-tRNA hydrolase ICT1, mitochondrial-like
uncharacterized LOC123512694, transcript variant X1
uncharacterized LOC123512694, transcript variant X2
uncharacterized LOC123512694, transcript variant X3
uncharacterized protein LOC123512694 isoform X2
uncharacterized protein LOC123512694 isoform X1
transcription factor Spi-B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
transcription factor Spi-B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transcription factor Spi-B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
transcription factor Spi-B-like isoform X1
transcription factor Spi-B-like isoform X2
transcription factor Spi-B-like isoform X3
uncharacterized LOC123512684, transcript variant X2
uncharacterized LOC123512684, transcript variant X1
uncharacterized LOC123512791, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123512791, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123512791, 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 3 samples with support for all annotated introns
DNA helicase MCM9-like, transcript variant X5
DNA helicase MCM9-like, transcript variant X2
DNA helicase MCM9-like, transcript variant X4
DNA helicase MCM9-like, transcript variant X1
DNA helicase MCM9-like, transcript variant X3
DNA helicase MCM9-like, transcript variant X6
RNA polymerase II-associated protein 1-like, transcript variant X1
RNA polymerase II-associated protein 1-like isoform X1
RNA polymerase II-associated protein 1-like, transcript variant X2
RNA polymerase II-associated protein 1-like isoform X2
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 8-like
vesicle transport protein SEC20-like, transcript variant X1
vesicle transport protein SEC20-like, transcript variant X2
vesicle transport protein SEC20-like isoform X1
vesicle transport protein SEC20-like isoform X2
flocculation protein FLO11-like, transcript variant X2
flocculation protein FLO11-like, transcript variant X3
flocculation protein FLO11-like, transcript variant X1
flocculation protein FLO11-like isoform X1
flocculation protein FLO11-like isoform X2
probable methylthioribulose-1-phosphate dehydratase, transcript variant X2
probable methylthioribulose-1-phosphate dehydratase, transcript variant X1
probable methylthioribulose-1-phosphate dehydratase, transcript variant X3
probable methylthioribulose-1-phosphate dehydratase
nuclear factor related to kappa-B-binding protein-like
tubulin-specific chaperone cofactor E-like protein, transcript variant X2
tubulin-specific chaperone cofactor E-like protein, transcript variant X3
tubulin-specific chaperone cofactor E-like protein, transcript variant X1
tubulin-specific chaperone cofactor E-like protein isoform X1
tubulin-specific chaperone cofactor E-like protein isoform X2
persulfide dioxygenase ETHE1, mitochondrial-like
LOW QUALITY PROTEIN: persulfide dioxygenase ETHE1, mitochondrial-like
DNA-directed RNA polymerase II subunit RPB1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fibrinogen C domain-containing protein 1-A-like
LOW QUALITY PROTEIN: fibrinogen C domain-containing protein 1-A-like
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
calcium-activated chloride channel regulator 1-like, transcript variant X2
calcium-activated chloride channel regulator 1-like, transcript variant X1
calcium-activated chloride channel regulator 1-like
dopamine beta-hydroxylase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
dopamine beta-hydroxylase-like, transcript variant X2
dopamine beta-hydroxylase-like, transcript variant X1
dopamine beta-hydroxylase-like, transcript variant X5
dopamine beta-hydroxylase-like, transcript variant X4
dopamine beta-hydroxylase-like isoform X3
dopamine beta-hydroxylase-like isoform X2
dopamine beta-hydroxylase-like isoform X1
microfibril-associated glycoprotein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
uncharacterized LOC123512863, transcript variant X2
uncharacterized LOC123512863, transcript variant X1
centrosome and spindle pole-associated protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
centrosome and spindle pole-associated protein 1-like, transcript variant X2
centrosome and spindle pole-associated protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
centrosome and spindle pole-associated protein 1-like isoform X2
centrosome and spindle pole-associated protein 1-like isoform X1
uncharacterized protein LOC123512874 isoform X3
uncharacterized LOC123512877, 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 2 samples with support for all annotated introns
uncharacterized LOC123512877, transcript variant X1
uncharacterized LOC123512877, transcript variant X3
uncharacterized protein LOC123512877 isoform X3
uncharacterized protein LOC123512877 isoform X1
uncharacterized protein LOC123512877 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 2-like, transcript variant X4
glutamate receptor ionotropic, kainate 2-like isoform X3
glutamate receptor ionotropic, kainate 2-like, transcript variant X1
glutamate receptor ionotropic, kainate 2-like, transcript variant X2
glutamate receptor ionotropic, kainate 2-like, transcript variant X3
glutamate receptor ionotropic, kainate 2-like isoform X1
glutamate receptor ionotropic, kainate 2-like isoform X2
uncharacterized LOC123512785, transcript variant X1
uncharacterized LOC123512785, transcript variant X2
uncharacterized LOC123512751, transcript variant X2
uncharacterized LOC123512751, transcript variant X1
uncharacterized protein LOC123512751 isoform X1
uncharacterized protein LOC123512751 isoform X2
transient receptor potential-gamma protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transient receptor potential-gamma protein-like, transcript variant X2
transient receptor potential-gamma protein-like, transcript variant X9
transient receptor potential-gamma protein-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transient receptor potential-gamma protein-like, transcript variant X3
transient receptor potential-gamma protein-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 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-gamma protein-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transient receptor potential-gamma protein-like, transcript variant X12
transient receptor potential-gamma protein-like, transcript variant X4
transient receptor potential-gamma protein-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transient receptor potential-gamma protein-like, transcript variant X8
transient receptor potential-gamma protein-like, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
transient receptor potential-gamma protein-like, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
transient receptor potential-gamma protein-like, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transient receptor potential-gamma protein-like, transcript variant X17
transient receptor potential-gamma protein-like isoform X1
transient receptor potential-gamma protein-like isoform X2
transient receptor potential-gamma protein-like isoform X9
transient receptor potential-gamma protein-like isoform X5
transient receptor potential-gamma protein-like isoform X3
transient receptor potential-gamma protein-like isoform X10
transient receptor potential-gamma protein-like isoform X7
transient receptor potential-gamma protein-like isoform X12
transient receptor potential-gamma protein-like isoform X4
transient receptor potential-gamma protein-like isoform X6
transient receptor potential-gamma protein-like isoform X8
transient receptor potential-gamma protein-like isoform X11
transient receptor potential-gamma protein-like isoform X14
transient receptor potential-gamma protein-like isoform X16
transient receptor potential-gamma protein-like isoform X17
transient receptor potential-gamma protein-like, transcript variant X13
transient receptor potential-gamma protein-like, transcript variant X15
transient receptor potential-gamma protein-like, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 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-gamma protein-like isoform X13
transient receptor potential-gamma protein-like isoform X15
transient receptor potential-gamma protein-like isoform X18
uncharacterized LOC123512681, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC123512681, transcript variant X2
uncharacterized LOC123512681, transcript variant X1
uncharacterized protein LOC123512681 isoform X1
uncharacterized protein LOC123512681 isoform X2
uncharacterized LOC123512682, transcript variant X2
uncharacterized LOC123512681, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC123512682, transcript variant X3
uncharacterized LOC123512682, transcript variant X1
uncharacterized protein LOC123512682 isoform X2
uncharacterized protein LOC123512682 isoform X1
spermine synthase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
spermine synthase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 52 samples with support for all annotated introns
GTP-binding protein 2-like, transcript variant X3
GTP-binding protein 2-like, transcript variant X2
GTP-binding protein 2-like, transcript variant X5
GTP-binding protein 2-like, transcript variant X1
GTP-binding protein 2-like, transcript variant X4
cleavage and polyadenylation specificity factor subunit 4-like
protein zyg-11 homolog B-like, transcript variant X2
protein zyg-11 homolog B-like, transcript variant X1
protein zyg-11 homolog B-like isoform X2
protein zyg-11 homolog B-like isoform X1
histidine ammonia-lyase-like, transcript variant X2
histidine ammonia-lyase-like, transcript variant X3
histidine ammonia-lyase-like, transcript variant X1
uncharacterized LOC123512613, transcript variant X2
uncharacterized LOC123512613, transcript variant X3
uncharacterized LOC123512613, transcript variant X1
uncharacterized LOC123512613, transcript variant X4
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
G protein-activated inward rectifier potassium channel 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 13 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
G protein-activated inward rectifier potassium channel 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 13 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
G protein-activated inward rectifier potassium channel 3-like
methyltransferase-like protein 25, transcript variant X2
methyltransferase-like protein 25, transcript variant X4
methyltransferase-like protein 25, transcript variant X3
methyltransferase-like protein 25, transcript variant X1
polyribonucleotide nucleotidyltransferase 1, mitochondrial-like
pyrroline-5-carboxylate reductase 3-like, transcript variant X2
pyrroline-5-carboxylate reductase 3-like, transcript variant X1
pyrroline-5-carboxylate reductase 3-like
E3 ubiquitin-protein ligase TRIM23-like, transcript variant X2
E3 ubiquitin-protein ligase TRIM23-like, transcript variant X1
E3 ubiquitin-protein ligase TRIM23-like isoform X2
E3 ubiquitin-protein ligase TRIM23-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
soluble calcium-activated nucleotidase 1-like, transcript variant X2
soluble calcium-activated nucleotidase 1-like, transcript variant X4
soluble calcium-activated nucleotidase 1-like, transcript variant X1
soluble calcium-activated nucleotidase 1-like, transcript variant X3
soluble calcium-activated nucleotidase 1-like
putative inorganic phosphate cotransporter
LOW QUALITY PROTEIN: protein spaetzle 4-like
transmembrane protein 114-like, transcript variant X2
transmembrane protein 114-like, transcript variant X1
uncharacterized protein LOC123512602 isoform X2
transmembrane protein 114-like isoform X1
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: 37 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
LOW QUALITY PROTEIN: protein KIAA0100-like
uncharacterized LOC123512535, transcript variant X2
uncharacterized LOC123512535, transcript variant X1
28S ribosomal protein S5, mitochondrial-like
probable G-protein coupled receptor B0563.6, transcript variant X2
probable G-protein coupled receptor B0563.6, transcript variant X1
probable G-protein coupled receptor B0563.6
ubiquitin carboxyl-terminal hydrolase 1-like, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 1-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 1-like, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 1-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 1-like isoform X1
ubiquitin carboxyl-terminal hydrolase 1-like isoform X2
ubiquitin carboxyl-terminal hydrolase 1-like, transcript variant X5
ubiquitin carboxyl-terminal hydrolase 1-like isoform X3
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: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
meiotic recombination protein SPO11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123512738, transcript variant X1
uncharacterized LOC123512738, transcript variant X2
uncharacterized protein LOC123512738 isoform X1
uncharacterized protein LOC123512738 isoform X2
gastrula zinc finger protein XlCGF49.1-like
probable DNA helicase MCM9, transcript variant X1
probable DNA helicase MCM9, transcript variant X2
uncharacterized LOC123512808, transcript variant X2
uncharacterized LOC123512808, transcript variant X1
uncharacterized LOC123512807, transcript variant X1
uncharacterized LOC123512807, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123512656, 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
uncharacterized LOC123512656, transcript variant X2
uncharacterized LOC123512655, transcript variant X2
uncharacterized LOC123512655, transcript variant X3
ras-related C3 botulinum toxin substrate 1-like, transcript variant X3
ras-related C3 botulinum toxin substrate 1-like, transcript variant X1
ras-related C3 botulinum toxin substrate 1-like, transcript variant X2
ras-related C3 botulinum toxin substrate 1-like isoform X3
ras-related C3 botulinum toxin substrate 2-like isoform X1
ras-related C3 botulinum toxin substrate 1-like isoform X2
uncharacterized LOC123512655, transcript variant X1
uncharacterized LOC123512655, transcript variant X5
uncharacterized LOC123512655, transcript variant X6
uncharacterized LOC123512655, transcript variant X4
uncharacterized protein LOC123512655 isoform X1
uncharacterized protein LOC123512655 isoform X2
uncharacterized protein LOC123512655 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 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: 64% coverage of the annotated genomic feature by RNAseq alignments
kinesin-like protein KIF28P, transcript variant X2
kinesin-like protein KIF28P, transcript variant X1