Vespula pensylvanica isolate Volc-1 chromosome 23, 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\nCM025358.1.\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]
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
DNA ligase 1-like, transcript variant X1
DNA ligase 1-like, transcript variant X2
DNA ligase 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
coiled-coil domain-containing protein 34-like isoform X1
coiled-coil domain-containing protein 34-like isoform X2
uncharacterized LOC122636732, transcript variant X9
uncharacterized protein LOC122636732 isoform X5
uncharacterized LOC122636732, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC122636732, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC122636732, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC122636732, transcript variant X7
uncharacterized LOC122636732, transcript variant X8
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
uncharacterized LOC122636732, transcript variant X4
uncharacterized LOC122636732, 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
uncharacterized LOC122636732, 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 7 samples with support for all annotated introns
uncharacterized protein LOC122636732 isoform X3
uncharacterized protein LOC122636732 isoform X2
uncharacterized protein LOC122636732 isoform X1
uncharacterized protein LOC122636732 isoform X4
uncharacterized LOC122636736, transcript variant X2
uncharacterized protein LOC122636736 isoform X2
uncharacterized LOC122636736, transcript variant X1
uncharacterized protein LOC122636736 isoform X1
transport and Golgi organization protein 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transport and Golgi organization protein 1
uncharacterized LOC122636705, transcript variant X2
uncharacterized LOC122636705, transcript variant X1
uncharacterized protein LOC122636705 isoform X2
uncharacterized protein LOC122636705 isoform X1
EARP-interacting protein homolog, transcript variant X2
EARP-interacting protein homolog isoform X2
EARP-interacting protein homolog, transcript variant X1
EARP-interacting protein homolog isoform X1
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
ubiquitin carboxyl-terminal hydrolase isozyme L5
WD repeat-containing protein 55 homolog, transcript variant X1
WD repeat-containing protein 55 homolog, transcript variant X2
cytoplasmic FMR1-interacting protein, transcript variant X2
cytoplasmic FMR1-interacting protein, transcript variant X1
rho GTPase-activating protein 26, transcript variant X2
rho GTPase-activating protein 26, transcript variant X1
rho GTPase-activating protein 26, transcript variant X3
rho GTPase-activating protein 26 isoform X2
rho GTPase-activating protein 26 isoform X1
rho GTPase-activating protein 26 isoform X3
uridine-cytidine kinase, transcript variant X2
uridine-cytidine kinase, transcript variant X1
folylpolyglutamate synthase, mitochondrial-like, 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 6 samples with support for all annotated introns
folylpolyglutamate synthase, mitochondrial-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
folylpolyglutamate synthase, mitochondrial-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
folylpolyglutamate synthase, mitochondrial-like, 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 9 samples with support for all annotated introns
folylpolyglutamate synthase, mitochondrial-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
folylpolyglutamate synthase, mitochondrial-like, transcript variant X1
folylpolyglutamate synthase, mitochondrial-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
folylpolyglutamate synthase, mitochondrial-like
neuropathy target esterase sws, transcript variant X4
neuropathy target esterase sws, transcript variant X3
neuropathy target esterase sws, transcript variant X5
neuropathy target esterase sws, transcript variant X2
neuropathy target esterase sws, transcript variant X7
neuropathy target esterase sws, transcript variant X1
neuropathy target esterase sws, transcript variant X6
neuropathy target esterase sws isoform X4
neuropathy target esterase sws isoform X2
neuropathy target esterase sws isoform X7
neuropathy target esterase sws isoform X6
neuropathy target esterase sws isoform X1
neuropathy target esterase sws isoform X5
neuropathy target esterase sws isoform X3
neuropathy target esterase sws, 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 14 samples with support for all annotated introns
formin-binding protein 1-like, transcript variant X3
formin-binding protein 1-like, transcript variant X2
formin-binding protein 1-like, transcript variant X1
formin-binding protein 1-like, transcript variant X5
formin-binding protein 1-like, transcript variant X4
formin-binding protein 1-like, transcript variant X6
formin-binding protein 1-like, transcript variant X7
formin-binding protein 1-like isoform X1
formin-binding protein 1-like isoform X3
formin-binding protein 1-like isoform X2
formin-binding protein 1-like isoform X4
formin-binding protein 1-like isoform X5
formin-binding protein 1-like, transcript variant X9
formin-binding protein 1-like, transcript variant X8
formin-binding protein 1-like isoform X6
leucine-rich repeat-containing protein 20, transcript variant X1
leucine-rich repeat-containing protein 20, transcript variant X2
leucine-rich repeat-containing protein 20 isoform X1
leucine-rich repeat-containing protein 20 isoform X2
PDZ domain-containing protein 8, 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 25 samples with support for all annotated introns
PDZ domain-containing protein 8, 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 23 samples with support for all annotated introns
PDZ domain-containing protein 8, 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 39 samples with support for all annotated introns
PDZ domain-containing protein 8 isoform X3
PDZ domain-containing protein 8 isoform X1
PDZ domain-containing protein 8 isoform X2
PDZ domain-containing protein 8, 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 14 samples with support for all annotated introns
PDZ domain-containing protein 8 isoform X4
uncharacterized LOC122636709, transcript variant X1
uncharacterized LOC122636709, transcript variant X2
leucine-rich repeat-containing protein 4B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
leucine-rich repeat-containing protein 4B, transcript variant X5
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 8 samples with support for all annotated introns
leucine-rich repeat-containing protein 4B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
leucine-rich repeat-containing protein 4B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leucine-rich repeat-containing protein 4B, 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 5 samples with support for all annotated introns
leucine-rich repeat-containing protein 4B isoform X2
leucine-rich repeat-containing protein 4B isoform X1
ATP-dependent RNA helicase me31b, transcript variant X1
ATP-dependent RNA helicase me31b, transcript variant X2
protein odd-skipped-related 1-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 8 samples with support for all annotated introns
protein odd-skipped-related 1-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 12 samples with support for all annotated introns
protein odd-skipped-related 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
protein odd-skipped-related 1-like isoform X2
protein odd-skipped-related 1-like isoform X1
MOB kinase activator-like 2, transcript variant X1
MOB kinase activator-like 2, transcript variant X2
MOB kinase activator-like 2, transcript variant X3
palmitoyltransferase Hip14, transcript variant X3
palmitoyltransferase Hip14, transcript variant X1
palmitoyltransferase Hip14, transcript variant X2
putative mediator of RNA polymerase II transcription subunit 26, 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 22 samples with support for all annotated introns
putative mediator of RNA polymerase II transcription subunit 26, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
putative mediator of RNA polymerase II transcription subunit 26, transcript variant X3
putative mediator of RNA polymerase II transcription subunit 26, 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 31 samples with support for all annotated introns
putative mediator of RNA polymerase II transcription subunit 26, 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 32 samples with support for all annotated introns
putative mediator of RNA polymerase II transcription subunit 26 isoform X3
putative mediator of RNA polymerase II transcription subunit 26 isoform X4
putative mediator of RNA polymerase II transcription subunit 26 isoform X1
putative mediator of RNA polymerase II transcription subunit 26 isoform X2
putative mediator of RNA polymerase II transcription subunit 26, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
putative mediator of RNA polymerase II transcription subunit 26 isoform X5
leucine-rich repeat-containing protein 51-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 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
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
peroxisomal targeting signal 1 receptor, transcript variant X2
peroxisomal targeting signal 1 receptor, transcript variant X1
peroxisomal targeting signal 1 receptor isoform X1
peroxisomal targeting signal 1 receptor isoform X2
ribosome biogenesis protein BOP1 homolog
nucleoporin SEH1-A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
nucleoporin SEH1-A, transcript variant X2
guanine nucleotide-releasing factor 2, transcript variant X5
guanine nucleotide-releasing factor 2, transcript variant X4
guanine nucleotide-releasing factor 2, transcript variant X3
guanine nucleotide-releasing factor 2, transcript variant X1
guanine nucleotide-releasing factor 2, transcript variant X2
guanine nucleotide-releasing factor 2, transcript variant X6
guanine nucleotide-releasing factor 2 isoform X5
guanine nucleotide-releasing factor 2 isoform X4
guanine nucleotide-releasing factor 2 isoform X3
guanine nucleotide-releasing factor 2 isoform X2
guanine nucleotide-releasing factor 2 isoform X1
guanine nucleotide-releasing factor 2 isoform X6
leucine-rich repeat-containing protein 57-like
uncharacterized LOC122636740, transcript variant X1
uncharacterized LOC122636740, transcript variant X2
bromodomain-containing protein DDB_G0270170-like, transcript variant X1
bromodomain-containing protein DDB_G0270170-like, transcript variant X2
bromodomain-containing protein DDB_G0270170-like, transcript variant X3
bromodomain-containing protein DDB_G0270170-like isoform X1
uncharacterized protein LOC122636822 isoform X2
bromodomain-containing protein DDB_G0270170-like isoform X3
uncharacterized LOC122636826, 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 6 samples with support for all annotated introns
uncharacterized LOC122636826, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC122636826, transcript variant X1
succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
protein pinocchio, transcript variant X1
protein pinocchio, transcript variant X2
pre-mRNA-splicing factor 38, transcript variant X2
pre-mRNA-splicing factor 38, transcript variant X1
LHFPL tetraspan subfamily member 3 protein-like, transcript variant X1
LHFPL tetraspan subfamily member 3 protein-like, transcript variant X2
LHFPL tetraspan subfamily member 3 protein-like isoform X1
LHFPL tetraspan subfamily member 4 protein-like isoform X2
paired box protein Pax-9, transcript variant X2
paired box protein Pax-9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
DNA-directed RNA polymerases I, II, and III subunit RPABC4
serine-protein kinase ATM, transcript variant X1
serine-protein kinase ATM, transcript variant X2
serine-protein kinase ATM, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
probable histone-lysine N-methyltransferase CG1716, transcript variant X1
probable histone-lysine N-methyltransferase CG1716, transcript variant X3
probable histone-lysine N-methyltransferase CG1716, transcript variant X2
probable histone-lysine N-methyltransferase CG1716
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
putative inorganic phosphate cotransporter
uncharacterized LOC122636648, transcript variant X2
uncharacterized LOC122636648, transcript variant X1
myosin heavy chain, muscle, transcript variant X29
myosin heavy chain, muscle, transcript variant X10
myosin heavy chain, muscle, transcript variant X9
myosin heavy chain, muscle, transcript variant X24
myosin heavy chain, muscle, transcript variant X11
myosin heavy chain, muscle, transcript variant X25
myosin heavy chain, muscle, transcript variant X23
myosin heavy chain, muscle, transcript variant X15
myosin heavy chain, muscle, transcript variant X8
myosin heavy chain, muscle, transcript variant X2
myosin heavy chain, muscle, transcript variant X16
myosin heavy chain, muscle, transcript variant X33
myosin heavy chain, muscle, transcript variant X1
myosin heavy chain, muscle, transcript variant X22
myosin heavy chain, muscle, transcript variant X13
myosin heavy chain, muscle, transcript variant X3
myosin heavy chain, muscle, transcript variant X17
myosin heavy chain, muscle, transcript variant X14
myosin heavy chain, muscle, transcript variant X27
myosin heavy chain, muscle, transcript variant X6
myosin heavy chain, muscle, transcript variant X26
myosin heavy chain, muscle, transcript variant X5
myosin heavy chain, muscle, transcript variant X31
myosin heavy chain, muscle, transcript variant X20
myosin heavy chain, muscle, transcript variant X12
myosin heavy chain, muscle, transcript variant X7
myosin heavy chain, muscle, transcript variant X32
myosin heavy chain, muscle, transcript variant X21
myosin heavy chain, muscle, transcript variant X28
myosin heavy chain, muscle, transcript variant X18
myosin heavy chain, muscle, transcript variant X4
myosin heavy chain, muscle, transcript variant X30
myosin heavy chain, muscle, transcript variant X19
cytochrome b5-related protein, transcript variant X2
cytochrome b5-related protein, transcript variant X1
protein yellow-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
protein yellow-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 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 39 samples with support for all annotated introns
gonadotropin-releasing hormone II receptor, transcript variant X2
gonadotropin-releasing hormone II receptor, transcript variant X4
gonadotropin-releasing hormone II receptor, transcript variant X1
gonadotropin-releasing hormone II receptor, transcript variant X3
gonadotropin-releasing hormone receptor isoform X1
gonadotropin-releasing hormone II receptor isoform X2
gonadotropin-releasing hormone II receptor isoform X3
cartilage oligomeric matrix protein, transcript variant X1
cartilage oligomeric matrix protein, transcript variant X2
cartilage oligomeric matrix protein isoform X1
cartilage oligomeric matrix protein isoform X2
C-Maf-inducing protein-like, transcript variant X2
C-Maf-inducing protein-like, transcript variant X1
xaa-Pro dipeptidase, transcript variant X6
xaa-Pro dipeptidase, transcript variant X5
xaa-Pro dipeptidase, transcript variant X4
xaa-Pro dipeptidase, transcript variant X3
xaa-Pro dipeptidase, transcript variant X1
xaa-Pro dipeptidase, transcript variant X2
FAST kinase domain-containing protein 3, mitochondrial isoform X1
FAST kinase domain-containing protein 3, mitochondrial isoform X2
putative uncharacterized protein DDB_G0287113
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 37 samples with support for all annotated introns
bolA-like protein 3, transcript variant X2
bolA-like protein 3, 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 25 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC122636790, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC122636790, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC122636777, transcript variant X2
uncharacterized LOC122636777, transcript variant X1
uncharacterized LOC122636781, transcript variant X2
uncharacterized LOC122636781, transcript variant X1
uncharacterized LOC122636786, transcript variant X2
uncharacterized LOC122636786, 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 20 samples with support for all annotated introns
uncharacterized LOC122636789, transcript variant X1
uncharacterized LOC122636789, transcript variant X2
uncharacterized LOC122636784, transcript variant X2
uncharacterized LOC122636784, 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 13 samples with support for all annotated introns
putative sodium-coupled neutral amino acid transporter 7
SLIT-ROBO Rho GTPase-activating protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
SLIT-ROBO Rho GTPase-activating protein 1-like, 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 16 samples with support for all annotated introns
SLIT-ROBO Rho GTPase-activating protein 1-like, transcript variant X5
SLIT-ROBO Rho GTPase-activating protein 1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
SLIT-ROBO Rho GTPase-activating protein 1-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 30 samples with support for all annotated introns
SLIT-ROBO Rho GTPase-activating protein 1-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 24 samples with support for all annotated introns
SLIT-ROBO Rho GTPase-activating protein 1-like, transcript variant X10
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
SLIT-ROBO Rho GTPase-activating protein 1-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
SLIT-ROBO Rho GTPase-activating protein 1-like, transcript variant X9
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 15 samples with support for all annotated introns
SLIT-ROBO Rho GTPase-activating protein 1-like, transcript variant X8
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 32 samples with support for all annotated introns
SLIT-ROBO Rho GTPase-activating protein 1-like isoform X1
SLIT-ROBO Rho GTPase-activating protein 1-like isoform X2
SLIT-ROBO Rho GTPase-activating protein 1-like isoform X3
SLIT-ROBO Rho GTPase-activating protein 1-like isoform X4
female-specific protein transformer-like
RNA-binding protein 7, transcript variant X1
RNA-binding protein 7, transcript variant X2
glucose dehydrogenase [FAD, quinone]-like, transcript variant X2
glucose dehydrogenase [FAD, quinone]-like, transcript variant X1
glucose dehydrogenase [FAD, quinone]-like isoform X2
glucose dehydrogenase [FAD, quinone]-like isoform X1
regulator of microtubule dynamics protein 1-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 40 samples with support for all annotated introns
regulator of microtubule dynamics protein 1-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 16 samples with support for all annotated introns
regulator of microtubule dynamics protein 1-like isoform X1
regulator of microtubule dynamics protein 1-like isoform X2
protein Wnt-7b-like, transcript variant X5
protein Wnt-7b-like, transcript variant X6
protein Wnt-7b-like, transcript variant X3
protein Wnt-7b-like, transcript variant X4
protein Wnt-7b-like, transcript variant X1
protein Wnt-7b-like, transcript variant X2
uncharacterized LOC122636738, transcript variant X2
uncharacterized LOC122636738, transcript variant X1
patatin-like phospholipase domain-containing protein 2, transcript variant X1
patatin-like phospholipase domain-containing protein 2, transcript variant X2
patatin-like phospholipase domain-containing protein 2 isoform X1
patatin-like phospholipase domain-containing protein 2 isoform X2
transcription factor SPT20 homolog, transcript variant X2
transcription factor SPT20 homolog, transcript variant X3
transcription factor SPT20 homolog, transcript variant X1
transcription factor SPT20 homolog isoform X2
transcription factor SPT20 homolog isoform X1
histone acetyltransferase KAT7, transcript variant X4
histone acetyltransferase KAT7, transcript variant X5
histone acetyltransferase KAT7, transcript variant X2
histone acetyltransferase KAT7, transcript variant X3
histone acetyltransferase KAT7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
histone acetyltransferase KAT7, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
histone acetyltransferase KAT7, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
histone acetyltransferase KAT7, 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 1 sample with support for all annotated introns
histone acetyltransferase KAT7, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
histone acetyltransferase KAT7 isoform X1
histone acetyltransferase KAT7 isoform X2
histone acetyltransferase KAT7 isoform X4
histone acetyltransferase KAT7 isoform X3
histone acetyltransferase KAT7 isoform X5
nuclear transcription factor Y subunit gamma, transcript variant X1
nuclear transcription factor Y subunit gamma, transcript variant X2
nuclear transcription factor Y subunit gamma, transcript variant X4
nuclear transcription factor Y subunit gamma, transcript variant X7
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 18 samples with support for all annotated introns
nuclear transcription factor Y subunit gamma, transcript variant X5
nuclear transcription factor Y subunit gamma, transcript variant X6
nuclear transcription factor Y subunit gamma, transcript variant X3
nuclear transcription factor Y subunit gamma isoform X1
nuclear transcription factor Y subunit gamma isoform X2
nuclear transcription factor Y subunit gamma isoform X3
nuclear transcription factor Y subunit gamma isoform X4
protein split ends-like, transcript variant X2
protein split ends-like, transcript variant X3
protein split ends-like, transcript variant X1
protein split ends-like, transcript variant X5
protein split ends-like, transcript variant X4
dynein regulatory complex protein 1, transcript variant X3
dynein regulatory complex protein 1, 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 11 samples with support for all annotated introns
dynein regulatory complex protein 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 5 samples with support for all annotated introns
dynein regulatory complex protein 1, transcript variant X1
dynein regulatory complex protein 1, transcript variant X2
dynein regulatory complex protein 1 isoform X2
dynein regulatory complex protein 1 isoform X1
dynein regulatory complex protein 1 isoform X3
dynein regulatory complex protein 1 isoform X4
zinc finger protein 32-like, transcript variant X2
zinc finger protein 32-like, transcript variant X1
TWiK family of potassium channels protein 18-like, 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
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
TWiK family of potassium channels protein 18-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TWiK family of potassium channels protein 18-like, transcript variant X2
TWiK family of potassium channels protein 18-like, transcript variant X5
TWiK family of potassium channels protein 18-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
TWiK family of potassium channels protein 18-like
homeobox protein cut, transcript variant X2
homeobox protein cut, transcript variant X4
homeobox protein cut, transcript variant X3
homeobox protein cut, transcript variant X1
uncharacterized LOC122636763, transcript variant X1
uncharacterized LOC122636763, transcript variant X2
uncharacterized LOC122636763, transcript variant X3
uncharacterized LOC122636729, transcript variant X2
uncharacterized LOC122636729, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
putative uncharacterized protein DDB_G0274435, transcript variant X2
putative uncharacterized protein DDB_G0274435 isoform X2
putative uncharacterized protein DDB_G0274435, 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 6 samples with support for all annotated introns
zinc finger protein squeeze-like isoform X1
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC122636842, transcript variant X2
uncharacterized LOC122636842, transcript variant X1
uncharacterized LOC122636842, transcript variant X3
uncharacterized protein LOC122636842 isoform X1
uncharacterized protein LOC122636842 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 11 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 7 samples with support for all annotated introns
peptidyl-prolyl cis-trans isomerase H, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
peptidyl-prolyl cis-trans isomerase H, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
aromatic-L-amino-acid decarboxylase-like, transcript variant X1
aromatic-L-amino-acid decarboxylase-like, transcript variant X2
aromatic-L-amino-acid decarboxylase-like isoform X1
aromatic-L-amino-acid decarboxylase-like isoform X2
ribonuclease P protein subunit p25-like protein, transcript variant X1
ribonuclease P protein subunit p25-like protein, transcript variant X4
ribonuclease P protein subunit p25-like protein, transcript variant X2
ribonuclease P protein subunit p25-like protein, transcript variant X3
ribonuclease P protein subunit p25-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
26S proteasome non-ATPase regulatory subunit 2
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 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 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 28 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 33 samples with support for all annotated introns
uncharacterized protein LOC122636654 isoform X3
eukaryotic translation initiation factor 5B-like
CREB-regulated transcription coactivator 1-like, transcript variant X7
CREB-regulated transcription coactivator 1-like, transcript variant X5
CREB-regulated transcription coactivator 1-like, transcript variant X4
CREB-regulated transcription coactivator 1-like, transcript variant X8
CREB-regulated transcription coactivator 1-like, transcript variant X2
CREB-regulated transcription coactivator 1-like, transcript variant X14
CREB-regulated transcription coactivator 1-like, transcript variant X13
CREB-regulated transcription coactivator 1-like, transcript variant X12
CREB-regulated transcription coactivator 1-like, transcript variant X10
CREB-regulated transcription coactivator 1-like, transcript variant X9
CREB-regulated transcription coactivator 1-like, transcript variant X11
CREB-regulated transcription coactivator 1-like, transcript variant X3
CREB-regulated transcription coactivator 1-like, transcript variant X1
CREB-regulated transcription coactivator 1-like, transcript variant X6
CREB-regulated transcription coactivator 1-like, transcript variant X15
CREB-regulated transcription coactivator 1-like isoform X7
CREB-regulated transcription coactivator 1-like isoform X6
CREB-regulated transcription coactivator 1-like isoform X5
CREB-regulated transcription coactivator 1-like isoform X3
CREB-regulated transcription coactivator 1-like isoform X2
CREB-regulated transcription coactivator 1-like isoform X4
CREB-regulated transcription coactivator 1-like isoform X1
CREB-regulated transcription coactivator 1-like isoform X8
general odorant-binding protein 83a-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 40 samples with support for all annotated introns
probable 39S ribosomal protein L24, mitochondrial, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
probable 39S ribosomal protein L24, mitochondrial, transcript variant X4
probable 39S ribosomal protein L24, mitochondrial, transcript variant X3
probable 39S ribosomal protein L24, mitochondrial, transcript variant X1
probable 39S ribosomal protein L24, mitochondrial
uncharacterized LOC122636655, transcript variant X2
uncharacterized LOC122636655, transcript variant X1
insulin-like receptor, transcript variant X1
insulin-like receptor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
uncharacterized LOC122636692, transcript variant X1
uncharacterized LOC122636692, transcript variant X2
major facilitator superfamily domain-containing protein 12-like
uncharacterized LOC122636692, transcript variant X3
protein dead ringer-like, transcript variant X5
protein dead ringer-like, transcript variant X2
protein dead ringer-like, transcript variant X1
protein dead ringer-like, transcript variant X3
protein dead ringer-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 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
ejaculatory bulb-specific protein 3-like
protein RRNAD1-like, transcript variant X1
protein RRNAD1-like, transcript variant X2
protein RRNAD1-like, transcript variant X3
uncharacterized LOC122636695, transcript variant X2
uncharacterized LOC122636695, transcript variant X1
vesicular inhibitory amino acid transporter
ubiquitin carboxyl-terminal hydrolase 20
eukaryotic translation initiation factor 2 subunit 1
sister chromatid cohesion protein PDS5 homolog B, transcript variant X1
sister chromatid cohesion protein PDS5 homolog B, transcript variant X3
sister chromatid cohesion protein PDS5 homolog B, transcript variant X2
sister chromatid cohesion protein PDS5 homolog B isoform X1
sister chromatid cohesion protein PDS5 homolog B isoform X3
sister chromatid cohesion protein PDS5 homolog B isoform X2
probable ATP-dependent RNA helicase DDX27
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 30 samples with support for all annotated introns
reticulon-4-interacting protein 1 homolog, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
reticulon-4-interacting protein 1 homolog, mitochondrial-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
reticulon-4-interacting protein 1 homolog, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
reticulon-4-interacting protein 1 homolog, mitochondrial-like isoform X1
reticulon-4-interacting protein 1 homolog, mitochondrial-like isoform X2
WASH complex subunit 5, transcript variant X1
WASH complex subunit 5, transcript variant X2
uncharacterized LOC122636628, transcript variant X1
uncharacterized LOC122636628, transcript variant X2
uncharacterized LOC122636628, transcript variant X3
uncharacterized LOC122636628, transcript variant X4
uncharacterized LOC122636628, transcript variant X5
uncharacterized LOC122636628, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
uncharacterized protein LOC122636628 isoform X1
uncharacterized protein LOC122636628 isoform X2
uncharacterized protein LOC122636628 isoform X3
uncharacterized protein LOC122636628 isoform X4
uncharacterized protein LOC122636628 isoform X5
uncharacterized protein LOC122636628 isoform X6
uncharacterized LOC122636750, transcript variant X3
uncharacterized LOC122636750, transcript variant X1
uncharacterized LOC122636750, transcript variant X2
uncharacterized LOC122636750, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ammonium transporter Rh type A, transcript variant X6
ammonium transporter Rh type A, transcript variant X4
ammonium transporter Rh type A, transcript variant X3
ammonium transporter Rh type A, transcript variant X5
ammonium transporter Rh type A, transcript variant X2
ammonium transporter Rh type A, transcript variant X1
ammonium transporter Rh type A isoform X1
ammonium transporter Rh type A, transcript variant X7
ammonium transporter Rh type A, transcript variant X8
ammonium transporter Rh type A isoform X2
signal recognition particle receptor subunit alpha homolog
glycogen synthase kinase-3 beta, transcript variant X5
glycogen synthase kinase-3 beta, transcript variant X9
glycogen synthase kinase-3 beta, transcript variant X10
glycogen synthase kinase-3 beta isoform X5
glycogen synthase kinase-3 beta isoform X9
glycogen synthase kinase-3 beta isoform X10
glycogen synthase kinase-3 beta, transcript variant X11
glycogen synthase kinase-3 beta isoform X11
glycogen synthase kinase-3 beta, transcript variant X3
glycogen synthase kinase-3 beta, transcript variant X2
glycogen synthase kinase-3 beta, transcript variant X7
glycogen synthase kinase-3 beta, transcript variant X8
glycogen synthase kinase-3 beta, transcript variant X6
glycogen synthase kinase-3 beta, transcript variant X1
glycogen synthase kinase-3 beta, transcript variant X4
glycogen synthase kinase-3 beta isoform X3
glycogen synthase kinase-3 beta isoform X2
glycogen synthase kinase-3 beta isoform X7
glycogen synthase kinase-3 beta isoform X8
glycogen synthase kinase-3 beta isoform X6
glycogen synthase kinase-3 beta isoform X1
glycogen synthase kinase-3 beta isoform X4
glycogen synthase kinase-3 beta, transcript variant X13
glycogen synthase kinase-3 beta, transcript variant X12
glycogen synthase kinase-3 beta isoform X12
leucine-rich repeat-containing protein 58
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns