Vespula pensylvanica isolate Volc-1 chromosome 13, ASM1446617v1, whole genome shotgun sequence.
Vespula pensylvanica (western yellowjacket)
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Hymenoptera; Apocrita; Aculeata; Vespoidea; Vespidae; Vespinae; Vespula.
High-Quality Assemblies for Three Invasive Social Wasps from the Vespula Genus
Publication Status: Available-Online prior to print
REFSEQ INFORMATION: The reference sequence is identical to\nCM025348.1.\nAssembly name: ASM1446617v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the University of Otago on\n2020/09/09. The original whole-genome shotgun project has the\naccession JACSDY000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: University of Otago\nAssembly Date :: 03-JUL-2020\nAssembly Method :: meraculous v. 2.2.6\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 644x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Vespula pensylvanica 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.
COORDINATES: polyA evidence [ECO:0006239]
serine/arginine repetitive matrix protein 2, transcript variant X2
serine/arginine repetitive matrix protein 2, transcript variant X3
serine/arginine repetitive matrix protein 2, transcript variant X1
serine/arginine repetitive matrix protein 2 isoform X2
serine/arginine repetitive matrix protein 2 isoform X3
serine/arginine repetitive matrix protein 2 isoform X1
myosin light chain alkali, transcript variant X1
myosin light chain alkali, transcript variant X2
uncharacterized LOC122633686, 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 LOC122633686, 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 11 samples with support for all annotated introns
uncharacterized protein LOC122633686 isoform X2
uncharacterized protein LOC122633686 isoform X1
protein unc-80 homolog, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
protein unc-80 homolog, transcript variant X11
protein unc-80 homolog, transcript variant X13
protein unc-80 homolog, transcript variant X10
protein unc-80 homolog, transcript variant X1
protein unc-80 homolog, transcript variant X2
protein unc-80 homolog, transcript variant X8
protein unc-80 homolog, transcript variant X3
protein unc-80 homolog, transcript variant X15
protein unc-80 homolog, transcript variant X5
protein unc-80 homolog, transcript variant X4
protein unc-80 homolog, transcript variant X6
protein unc-80 homolog, transcript variant X14
protein unc-80 homolog, transcript variant X7
protein unc-80 homolog, transcript variant X9
carboxypeptidase Q-like, transcript variant X2
carboxypeptidase Q-like, transcript variant X1
CUGBP Elav-like family member 4, transcript variant X7
CUGBP Elav-like family member 4, transcript variant X11
CUGBP Elav-like family member 4, transcript variant X10
CUGBP Elav-like family member 4, transcript variant X5
CUGBP Elav-like family member 4, transcript variant X4
CUGBP Elav-like family member 4, transcript variant X2
CUGBP Elav-like family member 4, transcript variant X3
CUGBP Elav-like family member 4, transcript variant X6
CUGBP Elav-like family member 4, transcript variant X1
CUGBP Elav-like family member 4, transcript variant X8
CUGBP Elav-like family member 4, transcript variant X13
CUGBP Elav-like family member 4, transcript variant X18
CUGBP Elav-like family member 4, transcript variant X12
CUGBP Elav-like family member 4, transcript variant X15
CUGBP Elav-like family member 4, transcript variant X14
CUGBP Elav-like family member 4, transcript variant X17
CUGBP Elav-like family member 4, transcript variant X9
CUGBP Elav-like family member 4, transcript variant X16
CUGBP Elav-like family member 4, transcript variant X19
CUGBP Elav-like family member 4 isoform X7
CUGBP Elav-like family member 4 isoform X6
CUGBP Elav-like family member 3 isoform X5
CUGBP Elav-like family member 3 isoform X3
CUGBP Elav-like family member 3 isoform X4
CUGBP Elav-like family member 3 isoform X2
CUGBP Elav-like family member 3 isoform X1
CUGBP Elav-like family member 4 isoform X8
CUGBP Elav-like family member 4 isoform X12
CUGBP Elav-like family member 4 isoform X9
CUGBP Elav-like family member 4 isoform X13
CUGBP Elav-like family member 4 isoform X10
CUGBP Elav-like family member 4 isoform X11
membrane-associated protein Hem, transcript variant X1
membrane-associated protein Hem isoform X1
membrane-associated protein Hem, transcript variant X2
membrane-associated protein Hem isoform X2
disintegrin and metalloproteinase domain-containing protein 10
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
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: 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
carbonic anhydrase-related protein-like, transcript variant X2
carbonic anhydrase-related protein-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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein C15orf61 homolog, transcript variant X1
uncharacterized protein C15orf61 homolog, transcript variant X3
uncharacterized protein C15orf61 homolog, transcript variant X2
uncharacterized protein C15orf61 homolog, transcript variant X5
uncharacterized protein C15orf61 homolog isoform X1
uncharacterized protein C15orf61 homolog, transcript variant X4
uncharacterized protein C15orf61 homolog isoform X2
50S ribosomal protein L1, transcript variant X2
50S ribosomal protein L1, transcript variant X1
GTP-binding protein SAR1b, transcript variant X1
GTP-binding protein SAR1b, transcript variant X2
dimethylaniline monooxygenase [N-oxide-forming] 2-like, transcript variant X2
dimethylaniline monooxygenase [N-oxide-forming] 2-like, transcript variant X1
dimethylaniline monooxygenase [N-oxide-forming] 2-like, transcript variant X3
dimethylaniline monooxygenase [N-oxide-forming] 2-like isoform X1
dimethylaniline monooxygenase [N-oxide-forming] 2-like isoform X2
RNA exonuclease 4, transcript variant X1
RNA exonuclease 4, transcript variant X2
protein-tyrosine sulfotransferase, transcript variant X3
protein-tyrosine sulfotransferase, transcript variant X1
protein-tyrosine sulfotransferase, transcript variant X2
ABC transporter G family member 14, 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 6 samples with support for all annotated introns
ABC transporter G family member 14, 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 30 samples with support for all annotated introns
ABC transporter G family member 14 isoform X2
ABC transporter G family member 14 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 5 samples with support for all annotated introns
TBC1 domain family member 1, transcript variant X2
TBC1 domain family member 1, transcript variant X3
TBC1 domain family member 1, transcript variant X1
TBC1 domain family member 1, transcript variant X4
ras-related protein Rap-1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
ras-related protein Rap-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 15 samples with support for all annotated introns
ras-related protein Rap-1, 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 10 samples with support for all annotated introns
leucine-rich PPR motif-containing protein, mitochondrial-like
facilitated trehalose transporter Tret1-like
lateral signaling target protein 2 homolog, transcript variant X1
lateral signaling target protein 2 homolog, transcript variant X2
lateral signaling target protein 2 homolog isoform X1
lateral signaling target protein 2 homolog isoform X2
urea transporter 2-like, transcript variant X3
urea transporter 2-like, transcript variant X1
urea transporter 2-like, transcript variant X2
collagen alpha chain CG42342, transcript variant X7
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 9 samples with support for all annotated introns
collagen alpha chain CG42342, transcript variant X5
collagen alpha chain CG42342, transcript variant X4
collagen alpha chain CG42342, transcript variant X2
collagen alpha chain CG42342, transcript variant X3
collagen alpha chain CG42342, transcript variant X1
collagen alpha chain CG42342, transcript variant X8
collagen alpha chain CG42342, transcript variant X10
collagen alpha chain CG42342, transcript variant X6
collagen alpha chain CG42342, transcript variant X11
collagen alpha chain CG42342, transcript variant X9
collagen alpha chain CG42342, transcript variant X12
collagen alpha chain CG42342 isoform X12
collagen alpha chain CG42342 isoform X10
collagen alpha chain CG42342 isoform X11
collagen alpha chain CG42342, transcript variant X15
collagen alpha chain CG42342, transcript variant X13
collagen alpha chain CG42342 isoform X13
collagen alpha chain CG42342 isoform X15
collagen alpha chain CG42342, transcript variant X16
collagen alpha chain CG42342, transcript variant X14
collagen alpha chain CG42342 isoform X14
collagen alpha chain CG42342 isoform X16
putative peptidyl-tRNA hydrolase PTRHD1, transcript variant X2
putative peptidyl-tRNA hydrolase PTRHD1, transcript variant X1
putative uncharacterized protein DDB_G0282133
glutathione S-transferase-like, transcript variant X2
glutathione S-transferase-like, transcript variant X1
mitochondrial enolase superfamily member 1-like, transcript variant X1
mitochondrial enolase superfamily member 1-like, transcript variant X2
mitochondrial enolase superfamily member 1-like isoform X1
mitochondrial enolase superfamily member 1-like isoform X2
histidine triad nucleotide-binding protein 3
uncharacterized LOC122633698, transcript variant X2
uncharacterized LOC122633698, transcript variant X1
uncharacterized LOC122633698, transcript variant X3
uncharacterized protein LOC122633698 isoform X1
uncharacterized protein LOC122633698 isoform X2
uncharacterized protein LOC122633698 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 47% coverage of the annotated genomic feature by RNAseq alignments
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X4
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 7 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, 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
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X6
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 27 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X7
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
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X9
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X23
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X36
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 25 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X38
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X21
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 32 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X30
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X26
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 17 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X27
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X25
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 28 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X22
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 23 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X24
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 27 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X10
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 21 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X33
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X17
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
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X42
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 18 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X32
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X28
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 37 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X44
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
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X39
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X15
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
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X37
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X11
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X34
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X40
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 12 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X12
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X16
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X31
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 1 sample with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X18
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X13
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X43
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X8
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X41
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 3 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X29
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X19
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 36 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X20
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X14
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 26 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X35
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X2
longitudinals lacking protein, isoforms A/B/D/L, transcript variant X3
longitudinals lacking protein, isoforms A/B/D/L isoform X19
longitudinals lacking protein, isoforms F/I/K/T isoform X1
longitudinals lacking protein isoform X32
longitudinals lacking protein, isoforms N/O/W/X/Y isoform X26
longitudinals lacking protein isoform X22
longitudinals lacking protein, isoforms A/B/D/L isoform X23
longitudinals lacking protein, isoforms A/B/D/L isoform X21
longitudinals lacking protein, isoforms F/I/K/T isoform X3
longitudinals lacking protein isoform X18
longitudinals lacking protein, isoforms A/B/D/L isoform X6
longitudinals lacking protein isoform X13
longitudinals lacking protein, isoforms A/B/D/L isoform X38
longitudinals lacking protein, isoforms A/B/D/L isoform X2
longitudinals lacking protein, isoforms A/B/D/L isoform X28
longitudinals lacking protein, isoforms A/B/D/L isoform X11
longitudinals lacking protein, isoforms A/B/D/L isoform X33
longitudinals lacking protein, isoforms A/B/D/L isoform X7
longitudinals lacking protein, isoforms A/B/D/L isoform X30
longitudinals lacking protein, isoforms A/B/D/L isoform X36
longitudinals lacking protein, isoforms A/B/D/L isoform X8
longitudinals lacking protein, isoforms N/O/W/X/Y isoform X12
longitudinals lacking protein, isoforms A/B/D/L isoform X27
longitudinals lacking protein, isoforms A/B/D/L isoform X14
longitudinals lacking protein, isoforms N/O/W/X/Y isoform X9
longitudinals lacking protein, isoforms A/B/D/L isoform X39
longitudinals lacking protein, isoforms A/B/D/L isoform X37
longitudinals lacking protein, isoforms A/B/D/L isoform X25
zinc finger and BTB domain-containing protein 17 isoform X4
longitudinals lacking protein, isoforms A/B/D/L isoform X31
uncharacterized LOC122633715, transcript variant X2
uncharacterized LOC122633715, transcript variant X1
longitudinals lacking protein, isoforms A/B/D/L-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 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 9 samples with support for all annotated introns
cytochrome c oxidase assembly protein COX11, mitochondrial
cytosolic Fe-S cluster assembly factor NUBP1 homolog
lysosomal alpha-glucosidase-like, transcript variant X1
lysosomal alpha-glucosidase-like, transcript variant X3
lysosomal alpha-glucosidase-like, transcript variant X2
protein N-terminal asparagine amidohydrolase, 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 32 samples with support for all annotated introns
protein N-terminal asparagine amidohydrolase, 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 41 samples with support for all annotated introns
protein N-terminal asparagine amidohydrolase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
protein N-terminal asparagine amidohydrolase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
protein N-terminal asparagine amidohydrolase
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 5 samples with support for all annotated introns
cullin-associated NEDD8-dissociated protein 1, transcript variant X1
cullin-associated NEDD8-dissociated protein 1, transcript variant X2
cullin-associated NEDD8-dissociated protein 1
DDB1- and CUL4-associated factor 7, transcript variant X2
DDB1- and CUL4-associated factor 7, transcript variant X1
DDB1- and CUL4-associated factor 7, transcript variant X3
LIM domain kinase 1, transcript variant X1
LIM domain kinase 1, transcript variant X2
uncharacterized LOC122633658, 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
uncharacterized LOC122633658, 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 2 samples with support for all annotated introns
optomotor-blind protein-like, transcript variant X5
optomotor-blind protein-like, transcript variant X4
optomotor-blind protein-like, transcript variant X2
optomotor-blind protein-like, transcript variant X1
optomotor-blind protein-like, transcript variant X3
Fanconi anemia group J protein homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Fanconi anemia group J protein homolog, transcript variant X3
Fanconi anemia group J protein homolog, transcript variant X2
Fanconi anemia group J protein homolog, 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 6 samples with support for all annotated introns
Fanconi anemia group J protein homolog isoform X1
Fanconi anemia group J protein homolog isoform X3
Fanconi anemia group J protein homolog isoform X2
Fanconi anemia group J protein homolog isoform X4
coiled-coil domain-containing protein 86
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 39 samples with support for all annotated introns
phospholipase A2 isozymes PA3A/PA3B/PA5-like, transcript variant X2
phospholipase A2 isozymes PA3A/PA3B/PA5-like, transcript variant X1
phospholipase A2 isozymes PA3A/PA3B/PA5-like
arginine/serine-rich coiled-coil protein 2-like, transcript variant X1
arginine/serine-rich coiled-coil protein 2-like, transcript variant X3
arginine/serine-rich coiled-coil protein 2-like, transcript variant X2
arginine/serine-rich coiled-coil protein 2-like isoform X1
arginine/serine-rich coiled-coil protein 2-like isoform X2
arginine/serine-rich coiled-coil protein 2-like isoform X3
ragulator complex protein LAMTOR1, transcript variant X2
ragulator complex protein LAMTOR1 isoform X2
ragulator complex protein LAMTOR1, transcript variant X1
ragulator complex protein LAMTOR1 isoform X1
nuclear transcription factor Y subunit alpha, transcript variant X1
nuclear transcription factor Y subunit alpha, transcript variant X2
nuclear transcription factor Y subunit alpha isoform X1
nuclear transcription factor Y subunit alpha isoform X2
nuclear transcription factor Y subunit alpha, transcript variant X4
nuclear transcription factor Y subunit alpha, transcript variant X6
nuclear transcription factor Y subunit alpha, transcript variant X3
nuclear transcription factor Y subunit alpha, transcript variant X7
nuclear transcription factor Y subunit alpha, transcript variant X5
nuclear transcription factor Y subunit alpha isoform 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 1 sample with support for all annotated introns
U8-agatoxin-Ao1a-like, transcript variant X2
U8-agatoxin-Ao1a-like, transcript variant X1
uncharacterized LOC122633964, 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
uncharacterized LOC122633964, 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 4 samples with support for all annotated introns
uncharacterized LOC122633964, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
uncharacterized protein LOC122633964 isoform X2
uncharacterized protein LOC122633964 isoform X1
uncharacterized LOC122633968, transcript variant X1
uncharacterized LOC122633968, transcript variant X2
probable serine/threonine-protein kinase DDB_G0278845, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
probable serine/threonine-protein kinase DDB_G0278845, transcript variant X2
probable serine/threonine-protein kinase DDB_G0278845 isoform X1
probable serine/threonine-protein kinase DDB_G0278845 isoform X2
uncharacterized LOC122633973, 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 36 samples with support for all annotated introns
uncharacterized LOC122633973, transcript variant X2
uncharacterized LOC122633965, transcript variant X3
uncharacterized protein LOC122633965 isoform X3
uncharacterized LOC122633965, transcript variant X1
uncharacterized LOC122633965, transcript variant X2
uncharacterized protein LOC122633965 isoform X1
uncharacterized protein LOC122633965 isoform X2
ADP-ribosylation factor-like protein 6-interacting protein 1
DNA-directed RNA polymerase III subunit RPC6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
DNA-directed RNA polymerase III subunit RPC6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
probable DNA-directed RNA polymerase III subunit RPC6 isoform X1
DNA-directed RNA polymerase III subunit RPC6 isoform X2
dihydrolipoyllysine-residue succinyltransferase component of 2-oxoglutarate dehydrogenase complex, mitochondrial
trafficking protein particle complex subunit 8
tudor domain-containing protein 7-like, transcript variant X1
tudor domain-containing protein 7-like, transcript variant X2
adenylyl cyclase 78C, transcript variant X1
adenylyl cyclase 78C, transcript variant X2
adenylyl cyclase 78C, transcript variant X3
adenylyl cyclase 78C, transcript variant X4
adenylyl cyclase 78C, transcript variant X5
histone demethylase UTY, transcript variant X2
histone demethylase UTY, transcript variant X1
histone demethylase UTY, transcript variant X3
FUN14 domain-containing protein 1A, transcript variant X2
FUN14 domain-containing protein 1A, transcript variant X1
FUN14 domain-containing protein 1A, transcript variant X4
FUN14 domain-containing protein 1 isoform X1
FUN14 domain-containing protein 1A isoform X3
FUN14 domain-containing protein 1A, transcript variant X3
FUN14 domain-containing protein 1 isoform X2
integrator complex subunit 9, transcript variant X1
integrator complex subunit 9, transcript variant X2
metallo-beta-lactamase domain-containing protein 1, transcript variant X1
metallo-beta-lactamase domain-containing protein 1, transcript variant X2
metallo-beta-lactamase domain-containing protein 1 isoform X1
metallo-beta-lactamase domain-containing protein 1 isoform X2
sodium/hydrogen exchanger 7, transcript variant X4
sodium/hydrogen exchanger 7, transcript variant X7
sodium/hydrogen exchanger 7, transcript variant X3
sodium/hydrogen exchanger 7, transcript variant X2
sodium/hydrogen exchanger 7, transcript variant X1
sodium/hydrogen exchanger 7, transcript variant X8
sodium/hydrogen exchanger 7, transcript variant X6
sodium/hydrogen exchanger 7, transcript variant X5
conserved oligomeric Golgi complex subunit 3
conserved oligomeric Golgi complex subunit 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
conserved oligomeric Golgi complex subunit 1, transcript variant X1
conserved oligomeric Golgi complex subunit 1 isoform X1
conserved oligomeric Golgi complex subunit 1 isoform X2
ras-related protein Rab-32, transcript variant X4
ras-related protein Rab-32, transcript variant X3
ras-related protein Rab-32, transcript variant X1
ras-related protein Rab-32, transcript variant X2
ras and EF-hand domain-containing protein homolog isoform X1
ras and EF-hand domain-containing protein homolog isoform X2
ras-related protein Rab-32, transcript variant X5
protein brown-like, transcript variant X1
protein brown-like, transcript variant X3
protein brown-like, transcript variant X2
protein scarlet-like, transcript variant X3
protein scarlet-like, 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 3 samples with support for all annotated introns
protein scarlet-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
probable peroxisomal acyl-coenzyme A oxidase 1, transcript variant X1
probable peroxisomal acyl-coenzyme A oxidase 1, transcript variant X2
probable peroxisomal acyl-coenzyme A oxidase 1, transcript variant X3
probable peroxisomal acyl-coenzyme A oxidase 1 isoform X1
probable peroxisomal acyl-coenzyme A oxidase 1 isoform X2
probable peroxisomal acyl-coenzyme A oxidase 1 isoform X3
translation initiation factor eIF-2B subunit delta, transcript variant X1
translation initiation factor eIF-2B subunit delta, transcript variant X2
translation initiation factor eIF-2B subunit delta, transcript variant X3
translation initiation factor eIF-2B subunit delta, transcript variant X4
translation initiation factor eIF-2B subunit delta, transcript variant X5
translation initiation factor eIF-2B subunit delta isoform X1
translation initiation factor eIF-2B subunit delta, transcript variant X6
translation initiation factor eIF-2B subunit delta isoform X2
transcription termination factor 5, mitochondrial
uncharacterized LOC122633766, transcript variant X1
uncharacterized LOC122633766, transcript variant X2
phospholipid scramblase 1, transcript variant X6
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 47 samples with support for all annotated introns
phospholipid scramblase 1, 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 24 samples with support for all annotated introns
phospholipid scramblase 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
phospholipid scramblase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
phospholipid scramblase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
phospholipid scramblase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
phospholipid scramblase 1, 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 40 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
1,2-dihydroxy-3-keto-5-methylthiopentene dioxygenase
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 48 samples with support for all annotated introns
ribonucleoside-diphosphate reductase subunit M2 B, transcript variant X1
ribonucleoside-diphosphate reductase subunit M2 B, transcript variant X2
ribonucleoside-diphosphate reductase subunit M2 B isoform X1
ribonucleoside-diphosphate reductase subunit M2 B isoform X2
uncharacterized LOC122633770, transcript variant X1
uncharacterized LOC122633770, transcript variant X2
uncharacterized protein LOC122633770 isoform X1
uncharacterized LOC122633770, transcript variant X3
uncharacterized LOC122633770, transcript variant X4
uncharacterized LOC122633770, transcript variant X5
uncharacterized protein LOC122633770 isoform X2
uncharacterized protein LOC122633770 isoform X3
uncharacterized LOC122633901, transcript variant X3
uncharacterized LOC122633901, transcript variant X2
uncharacterized LOC122633901, transcript variant X1
uncharacterized protein LOC122633901 isoform X1
uncharacterized LOC122633901, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
uncharacterized protein LOC122633901 isoform X2
uncharacterized LOC122633905, transcript variant X1
uncharacterized LOC122633905, transcript variant X2
uncharacterized LOC122633905, transcript variant X3
uncharacterized LOC122633902, transcript variant X3
uncharacterized LOC122633902, transcript variant X2
uncharacterized LOC122633902, transcript variant X1
uncharacterized LOC122633902, transcript variant X4
uncharacterized LOC122633906, transcript variant X3
uncharacterized LOC122633906, transcript variant X4
uncharacterized LOC122633906, 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 8 samples with support for all annotated introns
uncharacterized LOC122633906, 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 4 samples with support for all annotated introns
vacuolar protein-sorting-associated protein 36, 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 10 samples with support for all annotated introns
vacuolar protein-sorting-associated protein 36, transcript variant X1
vacuolar protein-sorting-associated protein 36
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
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 11 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 5 samples with support for all annotated introns
uncharacterized LOC122633898, transcript variant X2
uncharacterized LOC122633898, transcript variant X3
uncharacterized LOC122633898, 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 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 16 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
caseinolytic peptidase B protein homolog
97 kDa heat shock protein, transcript variant X1
97 kDa heat shock protein, transcript variant X2
vacuolar ATPase assembly integral membrane protein VMA21 homolog
uncharacterized LOC122633977, transcript variant X1
uncharacterized LOC122633977, transcript variant X4
uncharacterized LOC122633977, transcript variant X2
uncharacterized LOC122633977, transcript variant X3
uncharacterized protein LOC122633977 isoform X1
uncharacterized protein LOC122633977 isoform X2
uncharacterized LOC122633790, 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 15 samples with support for all annotated introns
uncharacterized LOC122633790, 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 28 samples with support for all annotated introns
uncharacterized protein LOC122633790 isoform X2
uncharacterized protein LOC122633790 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 19 samples with support for all annotated introns
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 23 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
calcium-dependent secretion activator, transcript variant X8
calcium-dependent secretion activator, transcript variant X6
calcium-dependent secretion activator, transcript variant X7
calcium-dependent secretion activator, transcript variant X5
calcium-dependent secretion activator, transcript variant X2
calcium-dependent secretion activator, transcript variant X4
calcium-dependent secretion activator, transcript variant X1
calcium-dependent secretion activator, transcript variant X3
calcium-dependent secretion activator isoform X5
calcium-dependent secretion activator isoform X3
calcium-dependent secretion activator isoform X4
calcium-dependent secretion activator isoform X2
calcium-dependent secretion activator isoform X1
beta-1,3-galactosyltransferase 5-like, transcript variant X4
beta-1,3-galactosyltransferase 5-like, transcript variant X5
beta-1,3-galactosyltransferase 5-like, transcript variant X6
beta-1,3-galactosyltransferase 5-like, transcript variant X2
beta-1,3-galactosyltransferase 5-like, transcript variant X3
beta-1,3-galactosyltransferase 5-like, transcript variant X1
beta-1,3-galactosyltransferase 5-like, transcript variant X7
beta-1,3-galactosyltransferase 5-like isoform X1
beta-1,3-galactosyltransferase 5-like isoform X2
WW domain-binding protein 2, transcript variant X2
WW domain-binding protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
ubiquitin domain-containing protein UBFD1-like, transcript variant X2
ubiquitin domain-containing protein UBFD1-like, transcript variant X1
ubiquitin domain-containing protein UBFD1-like, transcript variant X3
ubiquitin domain-containing protein UBFD1-like, transcript variant X4
ubiquitin domain-containing protein UBFD1-like isoform X1
ubiquitin domain-containing protein UBFD1-like isoform X2
ubiquitin domain-containing protein UBFD1-like isoform X3
polycomb protein suz12-B, transcript variant X3
polycomb protein suz12-B, transcript variant X1
polycomb protein suz12-B, transcript variant X2
protein disulfide-isomerase, transcript variant X4
protein disulfide-isomerase, transcript variant X3
protein disulfide-isomerase, transcript variant X1
protein disulfide-isomerase, transcript variant X2
dynein axonemal intermediate chain 2-like, transcript variant X4
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 22 samples with support for all annotated introns
dynein axonemal intermediate chain 2-like, transcript variant X3
dynein axonemal intermediate chain 2-like isoform X3
dynein axonemal intermediate chain 2-like isoform X2
dynein axonemal intermediate chain 2-like, 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 5 samples with support for all annotated introns
dynein axonemal intermediate chain 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein disulfide-isomerase TMX3, transcript variant X5
protein disulfide-isomerase TMX3, transcript variant X1
protein disulfide-isomerase TMX3, transcript variant X3
protein disulfide-isomerase TMX3, transcript variant X4
protein disulfide-isomerase TMX3, transcript variant X2
protein disulfide-isomerase TMX3 isoform X1
protein disulfide-isomerase TMX3 isoform X2
uncharacterized LOC122633912, 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 35 samples with support for all annotated introns
uncharacterized LOC122633912, transcript variant X2
uncharacterized protein LOC122633912 isoform X1
uncharacterized protein LOC122633912 isoform X2
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC122633918, transcript variant X2
uncharacterized protein LOC122633918 isoform X2
uncharacterized LOC122633918, transcript variant X3
uncharacterized LOC122633918, transcript variant X1
uncharacterized LOC122633918, transcript variant X4
uncharacterized protein LOC122633918 isoform X1
uncharacterized protein LOC122633918 isoform X3
3-hydroxyisobutyryl-CoA hydrolase, mitochondrial-like
peptide deformylase, mitochondrial-like, transcript variant X2
peptide deformylase, mitochondrial-like, transcript variant X1
peptide deformylase, mitochondrial-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
peptide deformylase, mitochondrial-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
tachykinin-like peptides receptor 99D, transcript variant X2
tachykinin-like peptides receptor 99D isoform X2
tachykinin-like peptides receptor 99D, transcript variant X1
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 22 samples with support for all annotated introns
tachykinin-like peptides receptor 99D 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 23 samples with support for all annotated introns
sphingosine-1-phosphate lyase, transcript variant X2
sphingosine-1-phosphate lyase, transcript variant X1
sphingosine-1-phosphate lyase isoform X2
sphingosine-1-phosphate lyase isoform X1
tubby-related protein 4, transcript variant X2
tubby-related protein 4, transcript variant X3
tubby-related protein 4, transcript variant X1
NADP-dependent malic enzyme, transcript variant X2
NADP-dependent malic enzyme, transcript variant X3
NADP-dependent malic enzyme, transcript variant X4
NADP-dependent malic enzyme, 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 18 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 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC122633820, transcript variant X2
uncharacterized LOC122633820, transcript variant X1
uncharacterized LOC122633820, transcript variant X6
uncharacterized LOC122633820, transcript variant X3
uncharacterized LOC122633820, transcript variant X5
uncharacterized LOC122633820, transcript variant X4
uncharacterized protein LOC122633820 isoform X1
uncharacterized protein LOC122633820 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
WD repeat-containing protein 44, transcript variant X5
WD repeat-containing protein 44, transcript variant X3
WD repeat-containing protein 44, transcript variant X4
WD repeat-containing protein 44, transcript variant X2
WD repeat-containing protein 44, transcript variant X1
WD repeat-containing protein 44 isoform X5
WD repeat-containing protein 44 isoform X3
WD repeat-containing protein 44 isoform X4
WD repeat-containing protein 44 isoform X2
WD repeat-containing protein 44 isoform X1
fragile X mental retardation syndrome-related protein 1, transcript variant X1
fragile X mental retardation syndrome-related protein 1, transcript variant X4
fragile X mental retardation syndrome-related protein 1, transcript variant X2
fragile X mental retardation syndrome-related protein 1, transcript variant X3
fragile X mental retardation syndrome-related protein 1, transcript variant X5
fragile X mental retardation syndrome-related protein 1, 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 17 samples with support for all annotated introns
fragile X mental retardation syndrome-related protein 1, transcript variant X7
fragile X mental retardation syndrome-related protein 1, transcript variant X8
synaptic functional regulator FMR1 isoform X1
synaptic functional regulator FMR1 isoform X4
synaptic functional regulator FMR1 isoform X2
fragile X mental retardation syndrome-related protein 1 isoform X3
fragile X mental retardation syndrome-related protein 1 isoform X5
synaptic functional regulator FMR1 isoform X6
synaptic functional regulator FMR1 isoform X7
synaptic functional regulator FMR1 isoform X8
E3 ubiquitin-protein ligase RNF19A-like, transcript variant X4
E3 ubiquitin-protein ligase RNF19A-like, transcript variant X1
E3 ubiquitin-protein ligase RNF19A-like, transcript variant X2
E3 ubiquitin-protein ligase RNF19A-like, transcript variant X3
E3 ubiquitin-protein ligase RNF19A-like isoform X1
E3 ubiquitin-protein ligase RNF19A-like isoform X2
E3 ubiquitin-protein ligase RNF19A-like isoform X3
E3 ubiquitin-protein ligase RNF19A-like isoform X4
E3 ubiquitin-protein ligase RNF19A-like, transcript variant X5
E3 ubiquitin-protein ligase RNF19A-like, transcript variant X6
E3 ubiquitin-protein ligase RNF19A-like isoform X5
trafficking protein particle complex subunit 1
sodium-dependent proline transporter-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 10 samples with support for all annotated introns
sodium-dependent proline transporter-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
sodium-dependent proline transporter-like isoform X1
sodium- and chloride-dependent glycine transporter 1-like isoform X2
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X1
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X4
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X3
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X2
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X5
acid sphingomyelinase-like phosphodiesterase 3b isoform X1
acid sphingomyelinase-like phosphodiesterase 3b isoform X2
uncharacterized LOC122633845, transcript variant X2
uncharacterized LOC122633845, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 171 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: 94 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: 91 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
neuropeptide SIFamide receptor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
neuropeptide SIFamide receptor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 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: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
inner membrane metabolite transport protein YgcS-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
uncharacterized LOC122633729, transcript variant X2
uncharacterized LOC122633729, transcript variant X1
uncharacterized protein LOC122633729 isoform X2
uncharacterized protein LOC122633729 isoform X1
replication protein A 70 kDa DNA-binding subunit
protein Skeletor, isoforms B/C, transcript variant X15
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
protein Skeletor, isoforms B/C, transcript variant X17
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
protein Skeletor, isoforms B/C, transcript variant X16
protein Skeletor, isoforms B/C, transcript variant X7
protein Skeletor, isoforms B/C, transcript variant X6
protein Skeletor, isoforms B/C, transcript variant X11
protein Skeletor, isoforms B/C, transcript variant X10
protein Skeletor, isoforms B/C, transcript variant X8
protein Skeletor, isoforms B/C, transcript variant X1
protein Skeletor, isoforms B/C, transcript variant X13
protein Skeletor, isoforms B/C, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
protein Skeletor, isoforms B/C, transcript variant X3
protein Skeletor, isoforms B/C, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
protein Skeletor, isoforms B/C, transcript variant X4
protein Skeletor, isoforms B/C, transcript variant X12
protein Skeletor, isoforms B/C, transcript variant X14
protein Skeletor, isoforms B/C, transcript variant X9
protein Skeletor, isoforms B/C, transcript variant X5
protein Skeletor, isoforms B/C isoform X2
protein Skeletor, isoforms B/C isoform X1
uncharacterized LOC122633930, transcript variant X2
uncharacterized LOC122633930, transcript variant X1
F-box/LRR-repeat protein 7, 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 4 samples with support for all annotated introns
F-box/LRR-repeat protein 7, 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 33 samples with support for all annotated introns
F-box/LRR-repeat protein 7, 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 26 samples with support for all annotated introns
F-box/LRR-repeat protein 7, 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 3 samples with support for all annotated introns
F-box/LRR-repeat protein 7, 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 33 samples with support for all annotated introns
complement component 1 Q subcomponent-binding protein, mitochondrial
receptor-type guanylate cyclase daf-11, 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 13 samples with support for all annotated introns
receptor-type guanylate cyclase daf-11, transcript variant X5
receptor-type guanylate cyclase daf-11, transcript variant X1
receptor-type guanylate cyclase daf-11, transcript variant X6
receptor-type guanylate cyclase daf-11, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
receptor-type guanylate cyclase daf-11, transcript variant X2
receptor-type guanylate cyclase daf-11, transcript variant X17
receptor-type guanylate cyclase daf-11, transcript variant X14
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
receptor-type guanylate cyclase daf-11, transcript variant X12
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
receptor-type guanylate cyclase daf-11, transcript variant X11
receptor-type guanylate cyclase daf-11, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
receptor-type guanylate cyclase daf-11, transcript variant X15
receptor-type guanylate cyclase daf-11, transcript variant X13
receptor-type guanylate cyclase daf-11, transcript variant X8
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 19 samples with support for all annotated introns
receptor-type guanylate cyclase daf-11, transcript variant X10
receptor-type guanylate cyclase daf-11, transcript variant X9
receptor-type guanylate cyclase daf-11, transcript variant X7
receptor-type guanylate cyclase daf-11 isoform X1
receptor-type guanylate cyclase daf-11 isoform X2
geranylgeranyl transferase type-2 subunit alpha
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
purine nucleoside phosphorylase, transcript variant X1
purine nucleoside phosphorylase, transcript variant X3
purine nucleoside phosphorylase isoform X1
purine nucleoside phosphorylase isoform X3
purine nucleoside phosphorylase, transcript variant X4
purine nucleoside phosphorylase, transcript variant X2
purine nucleoside phosphorylase, transcript variant X5
purine nucleoside phosphorylase, transcript variant X6
purine nucleoside phosphorylase isoform X2
purine nucleoside phosphorylase isoform X4
purine nucleoside phosphorylase isoform X5
purine nucleoside phosphorylase isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
beta-1-syntrophin, transcript variant X1
beta-1-syntrophin, transcript variant X2
unconventional myosin-Va, 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
unconventional myosin-Va, transcript variant X2
estradiol 17-beta-dehydrogenase 11-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
estradiol 17-beta-dehydrogenase 11-like, transcript variant X1
estradiol 17-beta-dehydrogenase 11-like isoform X1
estradiol 17-beta-dehydrogenase 11-like isoform X3
estradiol 17-beta-dehydrogenase 11-like, transcript variant X2
short-chain dehydrogenase/reductase family 16C member 6-like isoform X2
17-beta-hydroxysteroid dehydrogenase 13-like, transcript variant X2
17-beta-hydroxysteroid dehydrogenase 13-like, transcript variant X1
17-beta-hydroxysteroid dehydrogenase 13-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122633786, transcript variant X3
uncharacterized LOC122633786, transcript variant X2
uncharacterized LOC122633786, transcript variant X7
uncharacterized LOC122633786, transcript variant X6
uncharacterized LOC122633786, transcript variant X1
uncharacterized LOC122633786, transcript variant X5
uncharacterized LOC122633786, transcript variant X9
uncharacterized protein LOC122633786 isoform X4
uncharacterized protein LOC122633786 isoform X1
uncharacterized LOC122633786, transcript variant X4
uncharacterized protein LOC122633786 isoform X2
uncharacterized LOC122633786, transcript variant X8
uncharacterized protein LOC122633786 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 25% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122633824, transcript variant X4
uncharacterized LOC122633824, transcript variant X2
uncharacterized LOC122633824, transcript variant X1
uncharacterized LOC122633824, transcript variant X3
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
active regulator of SIRT1-like, transcript variant X2
active regulator of SIRT1-like, transcript variant X1
active regulator of SIRT1-like isoform X2
active regulator of SIRT1-like 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
fatty acid synthase, transcript variant X1
fatty acid synthase, transcript variant X2
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
serine/threonine-protein kinase dyf-5, 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 12 samples with support for all annotated introns
serine/threonine-protein kinase dyf-5, 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 17 samples with support for all annotated introns
serine/threonine-protein kinase dyf-5, 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 16 samples with support for all annotated introns
serine/threonine-protein kinase ICK isoform X1
serine/threonine-protein kinase ICK isoform X2
serine/threonine-protein kinase dyf-5 isoform X3
equilibrative nucleoside transporter 4, 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 16 samples with support for all annotated introns
equilibrative nucleoside transporter 4, 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 20 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 41 samples with support for all annotated introns
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
putative uncharacterized protein DDB_G0274405
LIM/homeobox protein Awh-like, transcript variant X2
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 2 samples with support for all annotated introns
LIM/homeobox protein Awh-like, 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 17 samples with support for all annotated introns
LIM/homeobox protein Awh-like, transcript variant X1
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 17 samples with support for all annotated introns
LIM/homeobox protein Awh-like isoform X1
LIM/homeobox protein Awh-like isoform X2
TBC1 domain family member 13, transcript variant X2
TBC1 domain family member 13, transcript variant X1
TBC1 domain family member 13, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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
short-chain dehydrogenase/reductase family 16C member 6-like
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
retinol dehydrogenase 10-B-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 21 samples with support for all annotated introns
retinol dehydrogenase 10-B-like, transcript variant X2
retinol dehydrogenase 10-B-like isoform X1
retinol dehydrogenase 10-B-like isoform X2
OVARIAN TUMOR DOMAIN-containing deubiquitinating enzyme 9-like, transcript variant X5
OVARIAN TUMOR DOMAIN-containing deubiquitinating enzyme 9-like, transcript variant X4
OVARIAN TUMOR DOMAIN-containing deubiquitinating enzyme 9-like, transcript variant X2
OVARIAN TUMOR DOMAIN-containing deubiquitinating enzyme 9-like, transcript variant X1
OVARIAN TUMOR DOMAIN-containing deubiquitinating enzyme 9-like, transcript variant X6
OVARIAN TUMOR DOMAIN-containing deubiquitinating enzyme 9-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein LOC122633674 isoform X2
uncharacterized protein LOC122633674 isoform X1
OVARIAN TUMOR DOMAIN-containing deubiquitinating enzyme 9-like isoform X3
sodium/potassium-transporting ATPase subunit beta-1-interacting protein, 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 44 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit beta-1-interacting protein, 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 38 samples with support for all annotated introns
uncharacterized protein LOC122633673 isoform X1
sodium/potassium-transporting ATPase subunit beta-1-interacting protein isoform X2
glutaminase kidney isoform, mitochondrial, transcript variant X1
glutaminase kidney isoform, mitochondrial, transcript variant X4
glutaminase kidney isoform, mitochondrial, transcript variant X2
glutaminase kidney isoform, mitochondrial, transcript variant X5
glutaminase kidney isoform, mitochondrial, transcript variant X3
glutaminase liver isoform, mitochondrial isoform X1
glutaminase kidney isoform, mitochondrial isoform X3
glutaminase kidney isoform, mitochondrial isoform X4
glutaminase liver isoform, mitochondrial isoform X2
glutaminase kidney isoform, mitochondrial isoform X5
glutaminase kidney isoform, mitochondrial, transcript variant X6
glutaminase kidney isoform, mitochondrial, transcript variant X8
glutaminase kidney isoform, mitochondrial isoform X6
glutaminase kidney isoform, mitochondrial isoform X8
glutaminase kidney isoform, mitochondrial, transcript variant X7
glutaminase kidney isoform, mitochondrial isoform X7
uncharacterized PE-PGRS family protein PE_PGRS46-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
uncharacterized PE-PGRS family protein PE_PGRS46-like, transcript variant X1
uncharacterized PE-PGRS family protein PE_PGRS46-like, transcript variant X3
uncharacterized transmembrane protein DDB_G0289901-like isoform X1
uncharacterized PE-PGRS family protein PE_PGRS46-like isoform X3
uncharacterized PE-PGRS family protein PE_PGRS46-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
uncharacterized LOC122633813, transcript variant X1
uncharacterized protein LOC122633813 isoform X1
uncharacterized LOC122633813, transcript variant X2
uncharacterized protein LOC122633813 isoform X2
EF-hand calcium-binding domain-containing protein 1-like
splicing factor 3B subunit 5, 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 24 samples with support for all annotated introns
splicing factor 3B subunit 5, transcript variant X1
ATP synthase subunit C lysine N-methyltransferase
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 35 samples with support for all annotated introns
sodium-coupled neutral amino acid transporter 9 homolog, transcript variant X1
sodium-coupled neutral amino acid transporter 9 homolog, transcript variant X2
sodium-coupled neutral amino acid transporter 9-like isoform X1
sodium-coupled neutral amino acid transporter 9 homolog isoform X2
phosphoglucomutase, transcript variant X1
phosphoglucomutase, transcript variant X2
U3 small nucleolar ribonucleoprotein protein IMP3
uncharacterized LOC122633876, 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 38 samples with support for all annotated introns
uncharacterized LOC122633876, 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 12 samples with support for all annotated introns
uncharacterized LOC122633876, transcript variant X3
uncharacterized LOC122633876, 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 20 samples with support for all annotated introns
uncharacterized LOC122633876, transcript variant X1
uncharacterized protein LOC122633876 isoform X4
uncharacterized protein LOC122633876 isoform X2
uncharacterized protein LOC122633876 isoform X1
uncharacterized protein LOC122633876 isoform X3
transmembrane protein 267, transcript variant X2
transmembrane protein 267, 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 44 samples with support for all annotated introns
single-minded homolog 2, transcript variant X6
single-minded homolog 2, transcript variant X5
single-minded homolog 2, transcript variant X4
single-minded homolog 2, transcript variant X7
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
single-minded homolog 2, 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 1 sample with support for all annotated introns
single-minded homolog 2, 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
single-minded homolog 2, transcript variant X1
GTP-binding protein Di-Ras2, transcript variant X1
GTP-binding protein Di-Ras2, transcript variant X2
GTP-binding protein Di-Ras2, transcript variant X3
regulator of MON1-CCZ1 complex, transcript variant X2
regulator of MON1-CCZ1 complex, transcript variant X1
regulator of MON1-CCZ1 complex isoform X2
regulator of MON1-CCZ1 complex isoform X1
1-phosphatidylinositol 3-phosphate 5-kinase, transcript variant X1
1-phosphatidylinositol 3-phosphate 5-kinase, transcript variant X2
1-phosphatidylinositol 3-phosphate 5-kinase isoform X1
1-phosphatidylinositol 3-phosphate 5-kinase isoform X2
protein dissatisfaction-like, transcript variant X4
protein dissatisfaction-like, transcript variant X1
protein dissatisfaction-like, transcript variant X2
protein dissatisfaction-like, transcript variant X3
uncharacterized LOC122633853, transcript variant X4
uncharacterized LOC122633853, transcript variant X1
uncharacterized LOC122633853, transcript variant X5
uncharacterized LOC122633853, 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 15 samples with support for all annotated introns
uncharacterized LOC122633853, transcript variant X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
uncharacterized LOC122633854, transcript variant X2
uncharacterized LOC122633854, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
inhibitor of nuclear factor kappa-B kinase subunit alpha-like, transcript variant X2
inhibitor of nuclear factor kappa-B kinase subunit alpha-like, transcript variant X1
inhibitor of nuclear factor kappa-B kinase subunit alpha-like isoform X2
inhibitor of nuclear factor kappa-B kinase subunit alpha-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
transfer RNA aspartic acid (anticodon GUC); 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 6 samples with support for all annotated introns