Vespula pensylvanica isolate Volc-1 chromosome 24, 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\nCM025359.1.\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.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
protein kinase C, brain isozyme, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
protein kinase C, brain isozyme, transcript variant X2
protein kinase C, brain isozyme, transcript variant X5
protein kinase C, brain isozyme, transcript variant X3
protein kinase C, brain isozyme, transcript variant X4
protein kinase C, brain isozyme isoform X2
protein kinase C, brain isozyme isoform X1
protein kinase C, brain isozyme isoform X3
protein kinase C, brain isozyme isoform X4
cationic amino acid transporter 3, transcript variant X1
cationic amino acid transporter 3 isoform X1
cationic amino acid transporter 3, transcript variant X3
cationic amino acid transporter 3, transcript variant X2
cationic amino acid transporter 3 isoform X2
cationic amino acid transporter 3 isoform X3
uncharacterized LOC122637110, transcript variant X3
uncharacterized LOC122637110, transcript variant X2
uncharacterized LOC122637110, transcript variant X1
uncharacterized protein LOC122637110 isoform X2
uncharacterized protein LOC122637110 isoform X1
uncharacterized LOC122637110, transcript variant X4
uncharacterized protein LOC122637110 isoform X3
phospholipase DDHD1-like, transcript variant X3
phospholipase DDHD1-like, transcript variant X2
phospholipase DDHD1-like, transcript variant X1
phospholipase DDHD1-like, transcript variant X4
max-binding protein MNT-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 32 samples with support for all annotated introns
max-binding protein MNT-like, 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 27 samples with support for all annotated introns
max-binding protein MNT-like, 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 17 samples with support for all annotated introns
max-binding protein MNT-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 28 samples with support for all annotated introns
max-binding protein MNT-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 29 samples with support for all annotated introns
max-binding protein MNT-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 23 samples with support for all annotated introns
max-binding protein MNT-like, transcript variant X10
max-binding protein MNT-like, transcript variant X11
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 24 samples with support for all annotated introns
max-binding protein MNT-like, transcript variant X7
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
max-binding protein MNT-like, transcript variant X9
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 19 samples with support for all annotated introns
max-binding protein MNT-like, transcript variant X8
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 33 samples with support for all annotated introns
max-binding protein MNT-like, transcript variant X12
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 37 samples with support for all annotated introns
phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform, transcript variant X2
phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform, transcript variant X1
phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform isoform X2
phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform isoform X1
coiled-coil domain-containing protein 93
proton-coupled amino acid transporter-like protein pathetic, transcript variant X2
proton-coupled amino acid transporter-like protein pathetic, transcript variant X3
proton-coupled amino acid transporter-like protein pathetic, transcript variant X1
proton-coupled amino acid transporter-like protein pathetic, transcript variant X4
proton-coupled amino acid transporter-like protein pathetic isoform X2
proton-coupled amino acid transporter-like protein pathetic isoform X1
proton-coupled amino acid transporter-like protein pathetic isoform X3
autophagy-related protein 13, transcript variant X2
autophagy-related protein 13, transcript variant X1
autophagy-related protein 13, transcript variant X3
autophagy-related protein 13 homolog isoform X2
phospholipid-transporting ATPase ID, transcript variant X8
phospholipid-transporting ATPase ID, transcript variant X7
phospholipid-transporting ATPase ID, transcript variant X9
phospholipid-transporting ATPase ID, transcript variant X10
phospholipid-transporting ATPase ID isoform X6
phospholipid-transporting ATPase ID, transcript variant X11
phospholipid-transporting ATPase ID, transcript variant X1
phospholipid-transporting ATPase ID, transcript variant X2
phospholipid-transporting ATPase ID, transcript variant X3
phospholipid-transporting ATPase ID, transcript variant X4
phospholipid-transporting ATPase ID, transcript variant X5
phospholipid-transporting ATPase ID, transcript variant X6
phospholipid-transporting ATPase ID isoform X1
phospholipid-transporting ATPase ID isoform X2
phospholipid-transporting ATPase ID isoform X3
phospholipid-transporting ATPase ID isoform X4
phospholipid-transporting ATPase ID isoform X5
protein distal antenna-like, transcript variant X2
protein distal antenna-like, transcript variant X1
dynein regulatory complex subunit 7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
autophagy-related protein 2 homolog B, transcript variant X2
autophagy-related protein 2 homolog B, transcript variant X3
autophagy-related protein 2 homolog B, transcript variant X1
autophagy-related protein 2 homolog B isoform X2
autophagy-related protein 2 homolog A isoform X1
autophagy-related protein 2 homolog B isoform X3
autophagy-related protein 2 homolog B, 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 21 samples with support for all annotated introns
autophagy-related protein 2 homolog B isoform X4
dimethyladenosine transferase 2, mitochondrial
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
set1/Ash2 histone methyltransferase complex subunit ASH2
probable JmjC domain-containing histone demethylation protein 2C, transcript variant X2
probable JmjC domain-containing histone demethylation protein 2C, transcript variant X3
probable JmjC domain-containing histone demethylation protein 2C, transcript variant X1
probable JmjC domain-containing histone demethylation protein 2C, transcript variant X4
probable JmjC domain-containing histone demethylation protein 2C, transcript variant X6
probable JmjC domain-containing histone demethylation protein 2C, transcript variant X5
probable JmjC domain-containing histone demethylation protein 2C isoform X2
probable JmjC domain-containing histone demethylation protein 2C isoform X4
probable JmjC domain-containing histone demethylation protein 2C isoform X3
probable JmjC domain-containing histone demethylation protein 2C isoform X1
uncharacterized protein LOC122637149 isoform X6
uncharacterized protein LOC122637149 isoform X5
putative cyclin-dependent serine/threonine-protein kinase DDB_G0272797/DDB_G0274007, transcript variant X2
putative cyclin-dependent serine/threonine-protein kinase DDB_G0272797/DDB_G0274007, transcript variant X1
putative cyclin-dependent serine/threonine-protein kinase DDB_G0272797/DDB_G0274007
uncharacterized protein T19C3.4-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized protein T19C3.4-like isoform X5
uncharacterized protein T19C3.4-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 17 samples with support for all annotated introns
uncharacterized protein T19C3.4-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 18 samples with support for all annotated introns
uncharacterized protein T19C3.4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized protein T19C3.4-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 39 samples with support for all annotated introns
uncharacterized protein T19C3.4-like, transcript variant X4
receptor expression-enhancing protein 4-like isoform X1
receptor expression-enhancing protein 4-like isoform X2
uncharacterized protein T19C3.4-like isoform X4
receptor expression-enhancing protein 2-like isoform X3
condensin-2 complex subunit G2-like, transcript variant X1
condensin-2 complex subunit G2-like, transcript variant X3
condensin-2 complex subunit G2-like, transcript variant X2
condensin-2 complex subunit G2-like isoform X2
condensin-2 complex subunit G2-like isoform X1
condensin-2 complex subunit G2-like isoform X3
condensin-2 complex subunit G2-like, transcript variant X4
condensin-2 complex subunit G2-like isoform X4
condensin-2 complex subunit G2-like, transcript variant X5
condensin-2 complex subunit G2-like isoform X5
conserved oligomeric Golgi complex subunit 7
uncharacterized LOC122637175, transcript variant X5
uncharacterized LOC122637175, transcript variant X30
uncharacterized LOC122637175, transcript variant X25
uncharacterized LOC122637175, transcript variant X28
uncharacterized LOC122637175, transcript variant X40
uncharacterized LOC122637175, transcript variant X11
uncharacterized LOC122637175, transcript variant X24
uncharacterized LOC122637175, transcript variant X32
uncharacterized LOC122637175, transcript variant X38
uncharacterized LOC122637175, transcript variant X12
uncharacterized LOC122637175, transcript variant X39
uncharacterized LOC122637175, transcript variant X16
uncharacterized LOC122637175, transcript variant X41
uncharacterized LOC122637175, transcript variant X26
uncharacterized LOC122637175, transcript variant X33
uncharacterized LOC122637175, transcript variant X31
uncharacterized LOC122637175, transcript variant X21
uncharacterized LOC122637175, transcript variant X27
uncharacterized LOC122637175, transcript variant X35
uncharacterized LOC122637175, transcript variant X9
uncharacterized LOC122637175, transcript variant X18
uncharacterized LOC122637175, transcript variant X10
uncharacterized LOC122637175, transcript variant X6
uncharacterized LOC122637175, transcript variant X13
uncharacterized LOC122637175, transcript variant X2
uncharacterized LOC122637175, transcript variant X29
uncharacterized LOC122637175, transcript variant X8
uncharacterized LOC122637175, transcript variant X20
uncharacterized LOC122637175, transcript variant X17
uncharacterized LOC122637175, transcript variant X37
uncharacterized LOC122637175, transcript variant X14
uncharacterized LOC122637175, transcript variant X34
uncharacterized LOC122637175, transcript variant X4
uncharacterized LOC122637175, transcript variant X1
uncharacterized LOC122637175, transcript variant X19
uncharacterized LOC122637175, transcript variant X22
uncharacterized LOC122637175, transcript variant X23
uncharacterized LOC122637175, transcript variant X15
uncharacterized LOC122637175, transcript variant X3
uncharacterized LOC122637175, transcript variant X7
uncharacterized LOC122637175, transcript variant X36
uncharacterized LOC122637175, transcript variant X42
uncharacterized LOC122637157, transcript variant X1
uncharacterized LOC122637157, transcript variant X2
uncharacterized protein LOC122637157 isoform X1
uncharacterized protein LOC122637157 isoform 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 38 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 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
TAR DNA-binding protein 43-like, transcript variant X3
TAR DNA-binding protein 43-like, transcript variant X1
TAR DNA-binding protein 43-like, transcript variant X4
TAR DNA-binding protein 43-like isoform X3
TAR DNA-binding protein 43-like isoform X1
TAR DNA-binding protein 43-like isoform X4
TAR DNA-binding protein 43-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 43 samples with support for all annotated introns
uncharacterized protein LOC122637160 isoform X2
DNA replication ATP-dependent helicase/nuclease DNA2
uncharacterized LOC122637162, transcript variant X3
uncharacterized LOC122637162, transcript variant X2
uncharacterized protein LOC122637162 isoform X2
uncharacterized LOC122637162, transcript variant X1
uncharacterized protein LOC122637162 isoform X1
uncharacterized protein LOC122637162 isoform X3
vitamin K epoxide reductase complex subunit 1-like protein 1
autism susceptibility gene 2 protein-like, transcript variant X2
autism susceptibility gene 2 protein-like, transcript variant X1
autism susceptibility gene 2 protein-like, transcript variant X5
autism susceptibility gene 2 protein-like, transcript variant X3
autism susceptibility gene 2 protein-like, transcript variant X4
autism susceptibility gene 2 protein-like isoform X1
autism susceptibility gene 2 protein-like isoform X3
autism susceptibility gene 2 protein-like isoform X4
autism susceptibility gene 2 protein-like isoform X2
autism susceptibility gene 2 protein-like, transcript variant X6
autism susceptibility gene 2 protein-like isoform X5
RNA-binding protein with serine-rich domain 1-B-like, transcript variant X2
RNA-binding protein with serine-rich domain 1-B-like, transcript variant X1
RNA-binding protein with serine-rich domain 1-B-like isoform X2
RNA-binding protein with serine-rich domain 1-like isoform X1
mediator of RNA polymerase II transcription subunit 19
RNA-binding protein cabeza-like, transcript variant X1
RNA-binding protein cabeza-like isoform X1
RNA-binding protein cabeza-like, transcript variant X2
RNA-binding protein cabeza-like isoform X2
transducin beta-like protein 2, transcript variant X8
transducin beta-like protein 2, transcript variant X9
transducin beta-like protein 2 isoform X7
transducin beta-like protein 2 isoform X6
transducin beta-like protein 2, 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 5 samples with support for all annotated introns
transducin beta-like protein 2, transcript variant X4
transducin beta-like protein 2, 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 8 samples with support for all annotated introns
transducin beta-like protein 2, 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 38 samples with support for all annotated introns
transducin beta-like protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
transducin beta-like protein 2, 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 42 samples with support for all annotated introns
transducin beta-like protein 2, 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 39 samples with support for all annotated introns
uncharacterized protein LOC122636958 isoform X5
uncharacterized protein LOC122636958 isoform X4
uncharacterized protein LOC122636958 isoform X3
uncharacterized protein LOC122636958 isoform X2
uncharacterized protein LOC122636958 isoform X1
coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial-like, 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 6 samples with support for all annotated introns
coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial-like, transcript variant X2
coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial-like, transcript variant X3
coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial-like, transcript variant X5
coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial-like, transcript variant X1
coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial-like isoform X1
coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial-like isoform X3
coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial-like isoform X2
coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial
mitochondrial Rho GTPase, transcript variant X1
mitochondrial Rho GTPase, transcript variant X3
mitochondrial Rho GTPase, transcript variant X2
DNA polymerase theta, 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 23 samples with support for all annotated introns
DNA polymerase theta, 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 10 samples with support for all annotated introns
ER membrane protein complex subunit 2-like
tRNA (guanine(10)-N2)-methyltransferase homolog
cytochrome c oxidase assembly protein COX19
phosphopantothenoylcysteine decarboxylase
matrix metalloproteinase-2-like, transcript variant X2
matrix metalloproteinase-2-like, transcript variant X1
matrix metalloproteinase-2-like, transcript variant X4
matrix metalloproteinase-2-like, transcript variant X5
matrix metalloproteinase-2-like, transcript variant X3
matrix metalloproteinase-2-like isoform X2
matrix metalloproteinase-2-like isoform X1
matrix metalloproteinase-2-like isoform X3
cytadherence high molecular weight protein 1-like isoform X6
cytadherence high molecular weight protein 1-like isoform X10
uncharacterized protein LOC122636972 isoform X8
uncharacterized protein LOC122636972 isoform X13
uncharacterized protein LOC122636972 isoform X12
uncharacterized protein LOC122636972 isoform X16
uncharacterized protein LOC122636972 isoform X18
ubiquitin carboxyl-terminal hydrolase 30 homolog, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 30 homolog, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 30 homolog isoform X2
ubiquitin carboxyl-terminal hydrolase 30 homolog isoform X1
zinc finger and BTB domain-containing protein 16-A-like
BUB3-interacting and GLEBS motif-containing protein ZNF207-like, transcript variant X2
BUB3-interacting and GLEBS motif-containing protein ZNF207-like, transcript variant X1
BUB3-interacting and GLEBS motif-containing protein ZNF207-like, transcript variant X4
BUB3-interacting and GLEBS motif-containing protein ZNF207-like, transcript variant X5
BUB3-interacting and GLEBS motif-containing protein ZNF207-like, transcript variant X3
BUB3-interacting and GLEBS motif-containing protein ZNF207-like isoform X1
BUB3-interacting and GLEBS motif-containing protein ZNF207-like isoform X2
BUB3-interacting and GLEBS motif-containing protein ZNF207-like isoform X4
BUB3-interacting and GLEBS motif-containing protein ZNF207-like isoform X3
putative phospholipase B-like lamina ancestor, transcript variant X2
putative phospholipase B-like lamina ancestor, transcript variant X1
putative phospholipase B-like lamina ancestor, transcript variant X4
putative phospholipase B-like lamina ancestor, transcript variant X3
putative phospholipase B-like lamina ancestor
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 30 samples with support for all annotated introns
active breakpoint cluster region-related protein, transcript variant X1
active breakpoint cluster region-related protein, transcript variant X2
active breakpoint cluster region-related protein isoform X2
active breakpoint cluster region-related protein isoform 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 30 samples with support for all annotated introns
cytochrome P450 315a1, mitochondrial, transcript variant X5
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 11 samples with support for all annotated introns
cytochrome P450 315a1, mitochondrial, transcript variant X4
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 6 samples with support for all annotated introns
cytochrome P450 315a1, mitochondrial, transcript variant X3
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 5 samples with support for all annotated introns
cytochrome P450 315a1, mitochondrial, 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 8 samples with support for all annotated introns
cytochrome P450 315a1, mitochondrial, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
probable cytochrome P450 301a1, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
uncharacterized LOC122637192, transcript variant X2
uncharacterized LOC122637192, transcript variant X1
uncharacterized protein LOC122637192 isoform X1
uncharacterized protein LOC122637192 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 100% coverage of the annotated genomic feature by RNAseq alignments
U11/U12 small nuclear ribonucleoprotein 25 kDa protein
distal membrane-arm assembly complex protein 2
uncharacterized LOC122637185, 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 22 samples with support for all annotated introns
uncharacterized LOC122637185, 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 15 samples with support for all annotated introns
uncharacterized LOC122637185, 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
uncharacterized protein LOC122637185 isoform X3
uncharacterized protein LOC122637185 isoform X1
uncharacterized protein LOC122637185 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 3 samples with support for all annotated introns
uncharacterized LOC122637194, transcript variant X2
uncharacterized LOC122637194, transcript variant X1
calcium uptake protein 3, mitochondrial, transcript variant X2
calcium uptake protein 3, mitochondrial, transcript variant X1
calcium uptake protein 3, mitochondrial, transcript variant X5
calcium uptake protein 3, mitochondrial, transcript variant X3
calcium uptake protein 3, mitochondrial, transcript variant X4
calcium uptake protein 3, mitochondrial isoform X5
calcium uptake protein 3, mitochondrial isoform X2
calcium uptake protein 3, mitochondrial isoform X4
calcium uptake protein 3, mitochondrial isoform X3
calcium uptake protein 3, mitochondrial isoform X1
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
general transcriptional corepressor trfA
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
squamous cell carcinoma antigen recognized by T-cells 3-like
meiotic nuclear division protein 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Hermansky-Pudlak syndrome 5 protein homolog, 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 6 samples with support for all annotated introns
Hermansky-Pudlak syndrome 5 protein homolog, transcript variant X1
Hermansky-Pudlak syndrome 5 protein homolog isoform X1
Hermansky-Pudlak syndrome 5 protein homolog isoform X2
cleavage and polyadenylation specificity factor subunit 6, transcript variant X3
cleavage and polyadenylation specificity factor subunit 6, transcript variant X7
cleavage and polyadenylation specificity factor subunit 6, transcript variant X5
cleavage and polyadenylation specificity factor subunit 6, transcript variant X9
cleavage and polyadenylation specificity factor subunit 6, transcript variant X8
cleavage and polyadenylation specificity factor subunit 6, transcript variant X4
cleavage and polyadenylation specificity factor subunit 6, transcript variant X1
cleavage and polyadenylation specificity factor subunit 6, transcript variant X2
cleavage and polyadenylation specificity factor subunit 6, transcript variant X6
cleavage and polyadenylation specificity factor subunit 6 isoform X5
cleavage and polyadenylation specificity factor subunit 6 isoform X3
cleavage and polyadenylation specificity factor subunit 6 isoform X7
cleavage and polyadenylation specificity factor subunit 6 isoform X6
cleavage and polyadenylation specificity factor subunit 6 isoform X2
cleavage and polyadenylation specificity factor subunit 6 isoform X1
cleavage and polyadenylation specificity factor subunit 6 isoform X4
cleavage and polyadenylation specificity factor subunit 6, transcript variant X10
cleavage and polyadenylation specificity factor subunit 6 isoform X8
vacuolar protein sorting-associated protein 33A
serine/threonine-protein kinase Tao, transcript variant X1
serine/threonine-protein kinase Tao, transcript variant X2
microprocessor complex subunit DGCR8, transcript variant X2
microprocessor complex subunit DGCR8, transcript variant X4
microprocessor complex subunit DGCR8, transcript variant X3
microprocessor complex subunit DGCR8, transcript variant X5
microprocessor complex subunit DGCR8, transcript variant X1
microprocessor complex subunit DGCR8 isoform X1
microprocessor complex subunit DGCR8, transcript variant X6
microprocessor complex subunit DGCR8 isoform X2
RILP-like protein homolog, transcript variant X3
RILP-like protein homolog, 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 24 samples with support for all annotated introns
RILP-like protein homolog, transcript variant X1
RILP-like protein homolog, 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 21 samples with support for all annotated introns
clathrin heavy chain, transcript variant X1
clathrin heavy chain, transcript variant X2
39S ribosomal protein L44, mitochondrial
uncharacterized LOC122636985, transcript variant X1
uncharacterized LOC122636985, transcript variant X3
uncharacterized LOC122636985, transcript variant X4
uncharacterized LOC122636985, transcript variant X2
uncharacterized LOC122636985, transcript variant X5
uncharacterized LOC122636981, transcript variant X1
uncharacterized LOC122636981, transcript variant X4
uncharacterized LOC122636981, transcript variant X2
uncharacterized LOC122636981, transcript variant X3
uncharacterized protein LOC122636981 isoform X1
uncharacterized protein LOC122636981 isoform X4
uncharacterized protein LOC122636981 isoform X2
uncharacterized protein LOC122636981 isoform X3
uncharacterized LOC122636981, transcript variant X5
uncharacterized protein LOC122636981 isoform X5
rhomboid-related protein 2-like, transcript variant X4
rhomboid-related protein 2-like, transcript variant X5
rhomboid-related protein 2-like, transcript variant X1
rhomboid-related protein 2-like, transcript variant X3
rhomboid-related protein 2-like, transcript variant X2
rhomboid-related protein 2-like isoform X1
rhomboid-related protein 2-like isoform X2
Meckel syndrome type 1 protein homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Meckel syndrome type 1 protein homolog, 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 9 samples with support for all annotated introns
Meckel syndrome type 1 protein homolog isoform X1
Meckel syndrome type 1 protein-like isoform X2
serine protease gd-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
serine protease gd-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
serine protease gd-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 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 45 samples with support for all annotated introns
kinetochore-associated protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
kinetochore-associated protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
kinetochore-associated protein 1, transcript variant X3
BTB/POZ domain-containing protein 17-like
glutathione S-transferase 1-like, transcript variant X2
glutathione S-transferase 1-like, transcript variant X1
glutathione S-transferase 1-like, transcript variant X4
glutathione S-transferase 1-like, transcript variant X3
putative thiamine transporter SLC35F3, transcript variant X9
putative thiamine transporter SLC35F3, transcript variant X8
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
putative thiamine transporter SLC35F3 isoform X6
putative thiamine transporter SLC35F3 isoform X5
putative thiamine transporter SLC35F3, transcript variant X6
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
putative thiamine transporter SLC35F3, 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 11 samples with support for all annotated introns
putative thiamine transporter SLC35F3, 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 9 samples with support for all annotated introns
putative thiamine transporter SLC35F3, 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 10 samples with support for all annotated introns
putative thiamine transporter SLC35F3, 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 12 samples with support for all annotated introns
putative thiamine transporter SLC35F3, transcript variant X2
putative thiamine transporter SLC35F3, 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 13 samples with support for all annotated introns
putative thiamine transporter SLC35F3 isoform X4
putative thiamine transporter SLC35F3 isoform X3
putative thiamine transporter SLC35F3 isoform X1
putative thiamine transporter SLC35F3 isoform X2
putative thiamine transporter SLC35F3, transcript variant X10
putative thiamine transporter SLC35F3 isoform X7
serine/arginine repetitive matrix 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 38 samples with support for all annotated introns
serine/arginine repetitive matrix protein 1-like isoform X2
serine/arginine repetitive matrix protein 1-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 38 samples with support for all annotated introns
serine/arginine repetitive matrix protein 1-like isoform X1
major facilitator superfamily domain-containing protein 10, transcript variant X2
major facilitator superfamily domain-containing protein 10, 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 24 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 10 isoform X2
major facilitator superfamily domain-containing protein 10 isoform X1
uncharacterized LOC122636969, 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
uncharacterized LOC122636969, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein PTCD3 homolog, mitochondrial, transcript variant X3
protein PTCD3 homolog, mitochondrial, transcript variant X1
protein PTCD3 homolog, mitochondrial, transcript variant X2
protein PTCD3 homolog, mitochondrial isoform X1
protein PTCD3 homolog, mitochondrial isoform X2
protein PTCD3 homolog, mitochondrial isoform X3
SWI/SNF complex subunit SMARCC2, transcript variant X1
SWI/SNF complex subunit SMARCC2, transcript variant X2
SWI/SNF complex subunit SMARCC2, transcript variant X3
SWI/SNF complex subunit SMARCC2, transcript variant X4
SWI/SNF complex subunit SMARCC2 isoform X2
SWI/SNF complex subunit SMARCC2 isoform X3
SWI/SNF complex subunit SMARCC2 isoform X1
SWI/SNF complex subunit SMARCC2 isoform X4
uncharacterized LOC122637098, transcript variant X2
uncharacterized LOC122637098, 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 34 samples with support for all annotated introns
methyltransferase-like protein 25, transcript variant X1
methyltransferase-like protein 25, transcript variant X2
methyltransferase-like protein 25 isoform X1
methyltransferase-like protein 25 isoform X2
cell division cycle-associated protein 7-like, transcript variant X2
cell division cycle-associated protein 7-like, transcript variant X1
cell division cycle-associated protein 7-like
ornithine aminotransferase, mitochondrial-like, transcript variant X2
ornithine aminotransferase, mitochondrial-like, transcript variant X1
ornithine aminotransferase, mitochondrial-like
putative uncharacterized protein DDB_G0277255
protein king tubby, 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 13 samples with support for all annotated introns
protein king tubby, 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 29 samples with support for all annotated introns
THO complex subunit 3, transcript variant X1
THO complex subunit 3, transcript variant X2
uncharacterized LOC122636874, transcript variant X2
uncharacterized LOC122636874, 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 45 samples with support for all annotated introns
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B, transcript variant X3
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B, transcript variant X2
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B, transcript variant X1
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B isoform X1
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B isoform X3
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B isoform X2
zinc finger protein 271-like, transcript variant X2
zinc finger protein 271-like, transcript variant X3
zinc finger protein 271-like, transcript variant X1
zinc finger protein 271-like, transcript variant X4
B-box type zinc finger protein ncl-1-like, transcript variant X2
B-box type zinc finger protein ncl-1-like, transcript variant X1
B-box type zinc finger protein ncl-1-like
probable ATP-dependent RNA helicase DDX43
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
probable ATP-dependent RNA helicase DDX17, transcript variant X1
probable ATP-dependent RNA helicase DDX17, 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 16 samples with support for all annotated introns
probable ATP-dependent RNA helicase DDX17, 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 40 samples with support for all annotated introns
probable ATP-dependent RNA helicase DDX17 isoform X1
probable ATP-dependent RNA helicase DDX17 isoform X2
probable ATP-dependent RNA helicase DDX17 isoform X3
uncharacterized protein ZC84.1, transcript variant X1
uncharacterized protein ZC84.1, transcript variant X3
uncharacterized protein ZC84.1, transcript variant X4
uncharacterized protein ZC84.1, transcript variant X2
protein kinase C-like, 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 17 samples with support for all annotated introns
protein kinase C-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
unconventional myosin-X, transcript variant X2
unconventional myosin-X, transcript variant X1
kinesin-like protein Klp98A, transcript variant X1
kinesin-like protein Klp98A, transcript variant X2
kinesin-like protein Klp98A, transcript variant X3
fibril-forming collagen alpha chain-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
structural maintenance of chromosomes protein 1A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
fork head domain transcription factor slp1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122637068, transcript variant X1
uncharacterized LOC122637068, transcript variant X2
NADH-cytochrome b5 reductase 3, transcript variant X3
NADH-cytochrome b5 reductase 3, transcript variant X2
NADH-cytochrome b5 reductase 3, transcript variant X5
NADH-cytochrome b5 reductase 3, transcript variant X1
NADH-cytochrome b5 reductase 3, transcript variant X4
NADH-cytochrome b5 reductase 3 isoform X3
NADH-cytochrome b5 reductase 3 isoform X2
NADH-cytochrome b5 reductase 3 isoform X1
NADH-cytochrome b5 reductase 3 isoform X5
NADH-cytochrome b5 reductase 3 isoform X4
uncharacterized LOC122637071, transcript variant X3
uncharacterized LOC122637071, transcript variant X2
uncharacterized LOC122637071, transcript variant X1
uncharacterized protein LOC122637071 isoform X1
uncharacterized LOC122637071, transcript variant X4
uncharacterized protein LOC122637071 isoform X2
myosin light chain kinase, smooth muscle-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 24 samples with support for all annotated introns
myosin light chain kinase, smooth muscle-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 39 samples with support for all annotated introns
myosin light chain kinase, smooth muscle-like, transcript variant X4
myosin light chain kinase, smooth muscle-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 21 samples with support for all annotated introns
myosin light chain kinase, smooth muscle-like
U11/U12 small nuclear ribonucleoprotein 35 kDa protein-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 17 samples with support for all annotated introns
U11/U12 small nuclear ribonucleoprotein 35 kDa protein-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 2 samples with support for all annotated introns
U11/U12 small nuclear ribonucleoprotein 35 kDa protein-like
troponin T, skeletal muscle, transcript variant X17
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
troponin T, skeletal muscle, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
troponin T, skeletal muscle, transcript variant X18
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 35 samples with support for all annotated introns
troponin T, skeletal muscle, transcript variant X19
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 21 samples with support for all annotated introns
troponin T, skeletal muscle, transcript variant X20
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 38 samples with support for all annotated introns
troponin T, skeletal muscle, transcript variant X22
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 48 samples with support for all annotated introns
troponin T, skeletal muscle, transcript variant X23
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 45 samples with support for all annotated introns
troponin T, skeletal muscle, transcript variant X21
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 49 samples with support for all annotated introns
troponin T, skeletal muscle, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
troponin T, skeletal muscle, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
troponin T, skeletal muscle, 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 24 samples with support for all annotated introns
troponin T, skeletal muscle, transcript variant X5
troponin T, skeletal muscle, transcript variant X8
troponin T, skeletal muscle, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
troponin T, skeletal muscle, transcript variant X6
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 31 samples with support for all annotated introns
troponin T, skeletal muscle, transcript variant X7
troponin T, skeletal muscle, transcript variant X9
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
troponin T, skeletal muscle, transcript variant X10
troponin T, skeletal muscle, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
troponin T, skeletal muscle, transcript variant X13
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 10 samples with support for all annotated introns
troponin T, skeletal muscle, transcript variant X14
troponin T, skeletal muscle, transcript variant X15
troponin T, skeletal muscle, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
transmembrane reductase CYB561D2-like, 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 6 samples with support for all annotated introns
transmembrane reductase CYB561D2-like, 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 18 samples with support for all annotated introns
transmembrane reductase CYB561D2-like, 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 27 samples with support for all annotated introns
transmembrane reductase CYB561D2-like, 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 19 samples with support for all annotated introns
transmembrane reductase CYB561D2-like, 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 31 samples with support for all annotated introns
transmembrane reductase CYB561D2-like, 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 42 samples with support for all annotated introns
sodium- and chloride-dependent glycine transporter 1-like, transcript variant X1
sodium- and chloride-dependent glycine transporter 1-like, transcript variant X2
sodium- and chloride-dependent glycine transporter 1-like
ubiquitin-protein ligase E3A, transcript variant X2
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 29 samples with support for all annotated introns
ubiquitin-protein ligase E3A, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
ubiquitin-protein ligase E3A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
ubiquitin-protein ligase E3A, transcript variant X3
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 32 samples with support for all annotated introns
ubiquitin-protein ligase E3A, 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 39 samples with support for all annotated introns
ubiquitin-protein ligase E3A, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
uncharacterized LOC122637183, transcript variant X2
uncharacterized LOC122637183, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
chromatin-remodeling complex ATPase chain Iswi-like
uncharacterized protein LOC122636869 isoform X2
facilitated trehalose transporter Tret1-2 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
tight junction protein ZO-2, 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 7 samples with support for all annotated introns
tight junction protein ZO-2, transcript variant X5
tight junction protein ZO-2, transcript variant X2
tight junction protein ZO-2, transcript variant X1
tight junction protein ZO-2, transcript variant X3
tight junction protein ZO-2, 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
nuclear fragile X mental retardation-interacting protein 1, transcript variant X1
nuclear fragile X mental retardation-interacting protein 1, transcript variant X2
nuclear fragile X mental retardation-interacting protein 1
RNA cytidine acetyltransferase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
RNA cytidine acetyltransferase, transcript variant X4
RNA cytidine acetyltransferase isoform X3
RNA cytidine acetyltransferase isoform X4
RNA cytidine acetyltransferase, transcript variant X1
RNA cytidine acetyltransferase, transcript variant X2
RNA cytidine acetyltransferase isoform X1
RNA cytidine acetyltransferase isoform X2
acidic mammalian chitinase-like, transcript variant X3
acidic mammalian chitinase-like, transcript variant X1
acidic mammalian chitinase-like, transcript variant X2
acidic mammalian chitinase-like isoform X1
acidic mammalian chitinase-like isoform X2
39S ribosomal protein L54, mitochondrial
leucine-rich repeat-containing protein 49
doublesex- and mab-3-related transcription factor A2-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 4 samples with support for all annotated introns
anaphase-promoting complex subunit 5-like, transcript variant X1
anaphase-promoting complex subunit 5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
putative uncharacterized protein DDB_G0282133 isoform X1
anaphase-promoting complex subunit 5-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 4 samples with support for all annotated introns
anaphase-promoting complex subunit 5-like isoform X2
anaphase-promoting complex subunit 5-like, transcript variant X4
anaphase-promoting complex subunit 5-like isoform X3
general transcription factor 3C polypeptide 3, transcript variant X1
general transcription factor 3C polypeptide 3, transcript variant X2
general transcription factor 3C polypeptide 3
membrane-bound transcription factor site-1 protease, transcript variant X2
membrane-bound transcription factor site-1 protease, transcript variant X3
membrane-bound transcription factor site-1 protease, transcript variant X1
membrane-bound transcription factor site-1 protease isoform X1
membrane-bound transcription factor site-1 protease isoform X2
membrane-bound transcription factor site-1 protease, transcript variant X4
membrane-bound transcription factor site-1 protease isoform X3
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9, mitochondrial
E3 ubiquitin-protein ligase TRIP12, transcript variant X1
E3 ubiquitin-protein ligase TRIP12, transcript variant X2
E3 ubiquitin-protein ligase TRIP12 isoform X1
E3 ubiquitin-protein ligase TRIP12 isoform X2
probable tubulin polyglutamylase ttll-15, transcript variant X1
probable tubulin polyglutamylase ttll-15, transcript variant X2
probable tubulin polyglutamylase ttll-15 isoform X1
probable tubulin polyglutamylase ttll-15 isoform X2
single-strand selective monofunctional uracil DNA glycosylase
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
RNA helicase aquarius, transcript variant X1
RNA helicase aquarius, transcript variant X2
probable G-protein coupled receptor Mth-like 5
probable G-protein coupled receptor Mth-like 3, transcript variant X3
probable G-protein coupled receptor Mth-like 3, transcript variant X1
probable G-protein coupled receptor Mth-like 3, transcript variant X2
probable G-protein coupled receptor Mth-like 3, transcript variant X4
probable G-protein coupled receptor Mth-like 3
uncharacterized LOC122637105, transcript variant X2
uncharacterized LOC122637105, transcript variant X1
uncharacterized protein LOC122637105 isoform X2
uncharacterized protein LOC122637105 isoform X1
uncharacterized protein LOC122637106 isoform X1
adipocyte plasma membrane-associated protein
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 42 samples with support for all annotated introns
uncharacterized LOC122637107, transcript variant X1
uncharacterized LOC122637107, transcript variant X2
uncharacterized protein LOC122637107 isoform X1
uncharacterized protein LOC122637107 isoform X2
uncharacterized LOC122637107, transcript variant X3
uncharacterized protein LOC122637107 isoform X3
MATH and LRR domain-containing protein PFE0570w-like, transcript variant X3
MATH and LRR domain-containing protein PFE0570w-like, transcript variant X2
MATH and LRR domain-containing protein PFE0570w-like, transcript variant X1
MATH and LRR domain-containing protein PFE0570w-like
proteasome activator complex subunit 4B-like, transcript variant X1
proteasome activator complex subunit 4B-like isoform X1
proteasome activator complex subunit 4B-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 25 samples with support for all annotated introns
proteasome activator complex subunit 4-like isoform X2
N-alpha-acetyltransferase 40, transcript variant X1
N-alpha-acetyltransferase 40, transcript variant X3
N-alpha-acetyltransferase 40, transcript variant X2
3'-5' ssDNA/RNA exonuclease TatD, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
3'-5' ssDNA/RNA exonuclease TatD, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC122636955, transcript variant X1
uncharacterized LOC122636955, transcript variant X2
uncharacterized protein LOC122636955 isoform X1
uncharacterized protein LOC122636955 isoform X2
multiple RNA-binding domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
cilia- and flagella-associated protein 97-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
translation initiation factor IF-2, mitochondrial
proline hydroxylase buaE-like, transcript variant X3
proline hydroxylase buaE-like, transcript variant X4
proline hydroxylase buaE-like, transcript variant X1
proline hydroxylase buaE-like, transcript variant X2
jasmonate-induced oxygenase 2-like isoform X2
proline hydroxylase buaE-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
transcription factor SPT20 homolog, transcript variant X1
transcription factor SPT20 homolog, transcript variant X2
transcription factor SPT20 homolog, transcript variant X3
transcription factor SPT20 homolog isoform X1
transcription factor SPT20 homolog 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 7 samples with support for all annotated introns
homeobox protein SIX2-like, transcript variant X1
homeobox protein SIX2-like, transcript variant X3
homeobox protein SIX2-like, transcript variant X2
probable Rho GTPase-activating protein CG5521, transcript variant X1
probable Rho GTPase-activating protein CG5521, transcript variant X4
probable Rho GTPase-activating protein CG5521, transcript variant X3
probable Rho GTPase-activating protein CG5521, transcript variant X6
probable Rho GTPase-activating protein CG5521, transcript variant X2
probable Rho GTPase-activating protein CG5521, 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 20 samples with support for all annotated introns
ral GTPase-activating protein subunit alpha-1 isoform X1
ral GTPase-activating protein subunit alpha-1 isoform X4
ral GTPase-activating protein subunit alpha-1 isoform X3
probable Rho GTPase-activating protein CG5521 isoform X6
ral GTPase-activating protein subunit alpha-1 isoform X2
ral GTPase-activating protein subunit alpha-1 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
lysosomal alpha-mannosidase, transcript variant X1
lysosomal alpha-mannosidase, transcript variant X2
uncharacterized LOC122636945, transcript variant X4
uncharacterized LOC122636945, transcript variant X3
uncharacterized LOC122636945, transcript variant X2
uncharacterized LOC122636945, transcript variant X1
uncharacterized protein LOC122636945 isoform X2
uncharacterized protein LOC122636945 isoform X1
uncharacterized protein LOC122636945 isoform X3
uncharacterized protein LOC122636945 isoform X4
alkylglycerol monooxygenase-like, transcript variant X4
alkylglycerol monooxygenase-like, transcript variant X5
alkylglycerol monooxygenase-like, transcript variant X1
alkylglycerol monooxygenase-like, transcript variant X2
alkylglycerol monooxygenase-like, transcript variant X3
alkylglycerol monooxygenase-like isoform X1
alkylglycerol monooxygenase-like isoform X3
alkylglycerol monooxygenase-like isoform 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 34 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 22 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 14 samples with support for all annotated introns
UDP-N-acetylglucosamine transferase subunit ALG14 homolog, transcript variant X1
UDP-N-acetylglucosamine transferase subunit ALG14 homolog, transcript variant X2
UDP-N-acetylglucosamine transferase subunit ALG14 homolog
signal transducer and activator of transcription 5B, transcript variant X2
signal transducer and activator of transcription 5B, transcript variant X3
signal transducer and activator of transcription 5B, transcript variant X4
signal transducer and activator of transcription 5B, transcript variant X1
signal transducer and activator of transcription 5B, transcript variant X7
signal transducer and activator of transcription 5B isoform X1
signal transducer and activator of transcription 5B isoform X3
signal transducer and activator of transcription 5B, transcript variant X5
signal transducer and activator of transcription 5B, transcript variant X6
signal transducer and activator of transcription 5B isoform X2
stabilizer of axonemal microtubules 2-like
phosphatidylinositol 4-kinase type 2-alpha
armadillo-like helical domain-containing protein 3, transcript variant X1
armadillo-like helical domain-containing protein 3 isoform X1
armadillo-like helical domain-containing protein 3, 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 5 samples with support for all annotated introns
armadillo-like helical domain-containing protein 3 isoform X2
hydroxymethylglutaryl-CoA lyase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mediator of RNA polymerase II transcription subunit 8, transcript variant X1
mediator of RNA polymerase II transcription subunit 8, transcript variant X2
mediator of RNA polymerase II transcription subunit 8 isoform X1
mediator of RNA polymerase II transcription subunit 8 isoform X2
ATP-dependent zinc metalloprotease YME1L
mediator of RNA polymerase II transcription subunit 16, transcript variant X1
mediator of RNA polymerase II transcription subunit 16, transcript variant X3
mediator of RNA polymerase II transcription subunit 16, transcript variant X2
mediator of RNA polymerase II transcription subunit 16 isoform X1
mediator of RNA polymerase II transcription subunit 16 isoform X2
thioredoxin-like protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
thioredoxin-like protein 1, transcript variant X1
uncharacterized LOC122637012, transcript variant X8
uncharacterized LOC122637012, transcript variant X3
uncharacterized LOC122637012, transcript variant X9
uncharacterized LOC122637012, transcript variant X11
uncharacterized LOC122637012, transcript variant X13
uncharacterized LOC122637012, transcript variant X1
uncharacterized LOC122637012, transcript variant X10
uncharacterized LOC122637012, transcript variant X14
uncharacterized LOC122637012, transcript variant X12
uncharacterized protein LOC122637012 isoform X3
uncharacterized protein LOC122637012 isoform X1
uncharacterized protein LOC122637012 isoform X9
uncharacterized protein LOC122637012 isoform X8
uncharacterized LOC122637012, transcript variant X6
uncharacterized protein LOC122637012 isoform X6
uncharacterized LOC122637012, transcript variant X4
uncharacterized protein LOC122637012 isoform X4
uncharacterized protein LOC122637012 isoform X10
uncharacterized LOC122637012, transcript variant X2
uncharacterized LOC122637012, transcript variant X5
uncharacterized LOC122637012, transcript variant X7
uncharacterized protein LOC122637012 isoform X2
uncharacterized protein LOC122637012 isoform X5
uncharacterized protein LOC122637012 isoform X7
uncharacterized protein LOC122637012 isoform X11
inner nuclear membrane protein Man1, 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 31 samples with support for all annotated introns
inner nuclear membrane protein Man1, transcript variant X2
inner nuclear membrane protein Man1, transcript variant X1
inner nuclear membrane protein Man1 isoform X1
inner nuclear membrane protein Man1 isoform X2
inner nuclear membrane protein Man1 isoform X3
ATP-binding cassette sub-family G member 1-like
acyl-CoA synthetase short-chain family member 3, mitochondrial, transcript variant X1
acyl-CoA synthetase short-chain family member 3, mitochondrial, transcript variant X2
acyl-CoA synthetase short-chain family member 3, mitochondrial
uncharacterized LOC122637009, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC122637009, transcript variant X4
uncharacterized LOC122637009, 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 11 samples with support for all annotated introns
uncharacterized LOC122637009, transcript variant X2
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
hydroxysteroid dehydrogenase-like protein 2
tRNA:m(4)X modification enzyme TRM13 homolog, transcript variant X2
tRNA:m(4)X modification enzyme TRM13 homolog, transcript variant X1
tRNA:m(4)X modification enzyme TRM13 homolog isoform X1
tRNA:m(4)X modification enzyme TRM13 homolog isoform X2
divergent protein kinase domain 1C, transcript variant X2
divergent protein kinase domain 1C, transcript variant X1
divergent protein kinase domain 1C, transcript variant X3
divergent protein kinase domain 1C isoform X1
divergent protein kinase domain 1C isoform X2
uncharacterized LOC122637000, transcript variant X1
uncharacterized protein LOC122637000 isoform X1
uncharacterized LOC122637000, transcript variant X2
uncharacterized protein LOC122637000 isoform X2
heparan sulfate 2-O-sulfotransferase pipe, transcript variant X2
heparan sulfate 2-O-sulfotransferase pipe, transcript variant X1
heparan sulfate 2-O-sulfotransferase pipe
ATP-binding cassette sub-family G member 4-like
ATP-binding cassette sub-family G member 1, transcript variant X4
ATP-binding cassette sub-family G member 1, transcript variant X2
ATP-binding cassette sub-family G member 1, transcript variant X1
ATP-binding cassette sub-family G member 1, transcript variant X3
ATP-binding cassette sub-family G member 1, transcript variant X5
ATP-binding cassette sub-family G member 1 isoform X2
ATP-binding cassette sub-family G member 1 isoform X1
ATP-binding cassette sub-family G member 4 isoform X3
lysine-specific demethylase 4A-like, transcript variant X4
lysine-specific demethylase 4A-like, transcript variant X3
lysine-specific demethylase 4A-like, transcript variant X2
lysine-specific demethylase 4A-like, transcript variant X1
lysine-specific demethylase 4A-like isoform X3
lysine-specific demethylase 4A-like isoform X1
lysine-specific demethylase 4A-like isoform X2
ATP-binding cassette sub-family G member 4-like, transcript variant X1
ATP-binding cassette sub-family G member 4-like, transcript variant X3
ATP-binding cassette sub-family G member 1-like isoform X1
ATP-binding cassette sub-family G member 1-like isoform X3
ATP-binding cassette sub-family G member 4-like, transcript variant X2
ATP-binding cassette sub-family G member 4-like, transcript variant X4
ATP-binding cassette sub-family G member 4-like, transcript variant X7
ATP-binding cassette sub-family G member 1-like isoform X2
ATP-binding cassette sub-family G member 4-like, transcript variant X6
ATP-binding cassette sub-family G member 4-like isoform X4
ATP-binding cassette sub-family G member 4-like, transcript variant X5
ATP-binding cassette sub-family G member 4-like isoform X5
ETS-related transcription factor Elf-5-like, transcript variant X2
ETS-related transcription factor Elf-5-like, transcript variant X1
uncharacterized protein LOC122636885 isoform X2
ETS-related transcription factor Elf-5-like isoform X1
U6 snRNA-associated Sm-like protein LSm3
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
putative inorganic phosphate cotransporter
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns