Pieris napi chromosome 22, ilPieNapi1.2, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Papilionoidea; Pieridae; Pierinae; Pieris.
REFSEQ INFORMATION: The reference sequence is identical to\nFR997716.1.\nAssembly name: ilPieNapi1.2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2022/01/30. The original whole-genome shotgun project has the\naccession CAJQFT000000000.2.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Pieris napi Annotation Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
membrane-bound alkaline phosphatase-like
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 29 samples with support for all annotated introns
sarcoplasmic calcium-binding proteins I, III, and IV-like
protein transport protein Sec31A, transcript variant X1
protein transport protein Sec31A, transcript variant X2
protein transport protein Sec31A, transcript variant X3
protein transport protein Sec31A, transcript variant X4
protein transport protein Sec31A isoform X3
protein transport protein Sec31A isoform X2
protein transport protein Sec31A isoform X4
protein transport protein Sec31A isoform X1
centrosome-associated protein CEP250 isoform X5
centrosome-associated protein CEP250 isoform X1
uncharacterized LOC125061054, transcript variant X1
uncharacterized LOC125061054, transcript variant X2
uncharacterized protein LOC125061054 isoform X1
uncharacterized protein LOC125061054 isoform X2
protein phosphatase inhibitor 2-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 72 samples with support for all annotated introns
protein phosphatase inhibitor 2-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 168 samples with support for all annotated introns
protein phosphatase inhibitor 2-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 76 samples with support for all annotated introns
protein phosphatase inhibitor 2-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 50 samples with support for all annotated introns
SET domain-containing protein SmydA-8, transcript variant X2
SET domain-containing protein SmydA-8 isoform X2
SET domain-containing protein SmydA-8, transcript variant X1
SET domain-containing protein SmydA-8 isoform X1
protein spaetzle 4, 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 81 samples with support for all annotated introns
protein spaetzle 4, 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
serine/threonine-protein kinase VRK1-like
facilitated trehalose transporter Tret1-like, transcript variant X1
facilitated trehalose transporter Tret1-like isoform X1
facilitated trehalose transporter Tret1-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 9 samples with support for all annotated introns
facilitated trehalose transporter Tret1-like isoform X2
facilitated trehalose transporter Tret1-like, transcript variant X3
facilitated trehalose transporter Tret1-like isoform X3
insulin receptor substrate 1-like, transcript variant X6
insulin receptor substrate 1-like, transcript variant X4
insulin receptor substrate 1-like, transcript variant X3
insulin receptor substrate 1-like, transcript variant X5
insulin receptor substrate 1-like, transcript variant X2
insulin receptor substrate 1-like, transcript variant X1
insulin receptor substrate 1-like isoform X6
insulin receptor substrate 1-like isoform X4
insulin receptor substrate 1-like isoform X3
insulin receptor substrate 1-like isoform X5
insulin receptor substrate 1-like isoform X2
insulin receptor substrate 1-like isoform X1
facilitated trehalose transporter Tret1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
disks large homolog 5, 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
disks large homolog 5, 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 28 samples with support for all annotated introns
disks large homolog 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
disks large homolog 5, 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 20 samples with support for all annotated introns
uncharacterized LOC125060971, transcript variant X1
uncharacterized LOC125060971, transcript variant X2
uncharacterized protein LOC125060971 isoform X1
uncharacterized protein LOC125060971 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
potassium voltage-gated channel protein Shaw-like, transcript variant X2
potassium voltage-gated channel protein Shaw-like, transcript variant X1
potassium voltage-gated channel protein Shaw-like
potassium voltage-gated channel protein Shaw-like, transcript variant X3
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 22 samples with support for all annotated introns
potassium voltage-gated channel protein Shaw-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
potassium voltage-gated channel protein Shaw-like, transcript variant X5
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 8 samples with support for all annotated introns
potassium voltage-gated channel protein Shaw-like, transcript variant X4
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 36 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 10 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 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
N6-adenosine-methyltransferase non-catalytic subunit
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN, transcript variant X2
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN, transcript variant X3
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN isoform X3
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN isoform X2
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN, 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 124 samples with support for all annotated introns
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN isoform X1
nucleolar MIF4G domain-containing protein 1 homolog
outer mitochondrial transmembrane helix translocase-like, transcript variant X1
outer mitochondrial transmembrane helix translocase-like, transcript variant X2
outer mitochondrial transmembrane helix translocase-like isoform X1
outer mitochondrial transmembrane helix translocase-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 8 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 25 samples with support for all annotated introns
uncharacterized LOC125060982, transcript variant X2
uncharacterized LOC125060982, transcript variant X1
uncharacterized LOC125060992, transcript variant X1
uncharacterized LOC125060992, transcript variant X2
transfer RNA leucine (anticodon UAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
myeloid leukemia factor, transcript variant X1
myeloid leukemia factor, transcript variant X2
myeloid leukemia factor, transcript variant X3
probable serine/threonine-protein kinase DDB_G0280133
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 168 samples with support for all annotated introns
mitochondrial 2-oxoglutarate/malate carrier protein-like
myb/SANT-like DNA-binding domain-containing protein 3
mitochondrial 2-oxoglutarate/malate carrier protein
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 169 samples with support for all annotated introns
SET and MYND domain-containing protein 4-like
non-structural maintenance of chromosomes element 3 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
zinc finger CCHC domain-containing protein 24-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 37 samples with support for all annotated introns
zinc finger CCHC domain-containing protein 24-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 62 samples with support for all annotated introns
zinc finger CCHC domain-containing protein 24-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 126 samples with support for all annotated introns
zinc finger CCHC domain-containing protein 24-like isoform X2
zinc finger CCHC domain-containing protein 24-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glyoxylate reductase/hydroxypyruvate reductase
thioredoxin domain-containing protein 15
sarcoplasmic calcium-binding protein 1, transcript variant X1
sarcoplasmic calcium-binding protein 1, transcript variant X2
sarcoplasmic calcium-binding protein 1 isoform X1
sarcoplasmic calcium-binding protein 1 isoform X2
NPC intracellular cholesterol transporter 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 164 samples with support for all annotated introns
NPC intracellular cholesterol transporter 1 isoform X2
NPC intracellular cholesterol transporter 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 63 samples with support for all annotated introns
NPC intracellular cholesterol transporter 1 isoform X4
NPC intracellular cholesterol transporter 1, transcript variant X3
NPC intracellular cholesterol transporter 1 isoform X3
NPC intracellular cholesterol transporter 1, transcript variant X1
NPC intracellular cholesterol transporter 1, transcript variant X5
NPC intracellular cholesterol transporter 1 isoform X5
NPC intracellular cholesterol transporter 1 isoform X1
G patch domain and ankyrin repeat-containing protein 1 homolog
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A-like protein 1
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 161 samples with support for all annotated introns
serine protease inhibitor dipetalogastin-like
mitochondrial coenzyme A diphosphatase NUDT8-like
chloride intracellular channel exc-4, transcript variant X1
chloride intracellular channel exc-4, transcript variant X2
chloride intracellular channel exc-4 isoform X2
chloride intracellular channel exc-4 isoform X1
uncharacterized LOC125060613, 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 18 samples with support for all annotated introns
uncharacterized protein LOC125060613 isoform X4
uncharacterized LOC125060613, 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 120 samples with support for all annotated introns
uncharacterized protein LOC125060613 isoform X3
uncharacterized LOC125060613, transcript variant X1
uncharacterized LOC125060613, transcript variant X2
uncharacterized LOC125060613, transcript variant X3
uncharacterized protein LOC125060613 isoform X2
uncharacterized protein LOC125060613 isoform X1
ragulator complex protein LAMTOR3 homolog
glyoxylate reductase/hydroxypyruvate reductase-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 5 samples with support for all annotated introns
zinc finger HIT domain-containing protein 1
general transcription factor IIH subunit 5
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 168 samples with support for all annotated introns
meiotic nuclear division protein 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
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 108 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 8 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 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
protein jim lovell, transcript variant X1
protein jim lovell, transcript variant X2
ATPase family AAA domain-containing protein 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ATPase family AAA domain-containing protein 2-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 6 samples with support for all annotated introns
ATPase family AAA domain-containing protein 2-like, transcript variant X4
ATPase family AAA domain-containing protein 2-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 31 samples with support for all annotated introns
ATPase family AAA domain-containing protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
ATPase family AAA domain-containing protein 2-like isoform X3
ATPase family AAA domain-containing protein 2-like isoform X2
ATPase family AAA domain-containing protein 2-like isoform X1
ATPase family AAA domain-containing protein 2-like isoform X4
monocyte to macrophage differentiation factor 2, 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 50 samples with support for all annotated introns
monocyte to macrophage differentiation factor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 145 samples with support for all annotated introns
monocyte to macrophage differentiation factor 2 isoform X1
monocyte to macrophage differentiation factor 2 isoform 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
DNA-directed RNA polymerase, mitochondrial, transcript variant X1
DNA-directed RNA polymerase, mitochondrial, transcript variant X2
DNA-directed RNA polymerase, mitochondrial
zinc finger and BTB domain-containing protein 41-like, transcript variant X1
uncharacterized protein LOC125060996 isoform X1
zinc finger and BTB domain-containing protein 41-like, transcript variant X2
zinc finger and BTB domain-containing protein 41-like isoform X2
putative leucine-rich repeat-containing protein DDB_G0290503
UPF0047 protein YjbQ, transcript variant X2
UPF0047 protein YjbQ, transcript variant X1
actin-related protein 2/3 complex subunit 2, transcript variant X1
actin-related protein 2/3 complex subunit 2, transcript variant X2
actin-related protein 2/3 complex subunit 2 isoform X1
actin-related protein 2/3 complex subunit 2 isoform X2
serine/threonine-protein kinase mTOR, 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 11 samples with support for all annotated introns
serine/threonine-protein kinase mTOR, 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 101 samples with support for all annotated introns
serine/threonine-protein kinase mTOR isoform X2
serine/threonine-protein kinase mTOR isoform X1
serine/threonine-protein kinase mTOR-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 82 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 166 samples with support for all annotated introns
ubiA prenyltransferase domain-containing protein 1 homolog
dyslexia-associated protein KIAA0319-like protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dyslexia-associated protein KIAA0319-like protein, 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 8 samples with support for all annotated introns
dyslexia-associated protein KIAA0319-like protein, transcript variant X2
dyslexia-associated protein KIAA0319-like protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 116 samples with support for all annotated introns
dyslexia-associated protein KIAA0319-like protein isoform X3
dyslexia-associated protein KIAA0319-like protein isoform X1
dyslexia-associated protein KIAA0319-like protein isoform X2
dyslexia-associated protein KIAA0319-like protein, transcript variant X5
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 7 samples with support for all annotated introns
dyslexia-associated protein KIAA0319-like protein isoform 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 1 sample with support for all annotated introns
pre-mRNA 3' end processing protein WDR33, 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 168 samples with support for all annotated introns
protein smoothened, transcript variant X1
pre-mRNA 3' end processing protein WDR33, 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 24 samples with support for all annotated introns
pre-mRNA 3' end processing protein WDR33
protein smoothened, transcript variant X2
protein quick-to-court, transcript variant X2
protein quick-to-court, transcript variant X1
protein quick-to-court, transcript variant X3
uncharacterized LOC125060888, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125060888, 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
protein split ends-like, transcript variant X6
protein split ends-like, transcript variant X7
protein split ends-like, transcript variant X3
protein split ends-like, transcript variant X5
protein split ends-like, transcript variant X2
protein split ends-like, transcript variant X4
protein split ends-like, transcript variant X1
iron-sulfur assembly protein IscA-like 2, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 169 samples with support for all annotated introns
succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial
transcription initiation factor TFIID subunit 11
putative uncharacterized protein DDB_G0277255, transcript variant X3
putative uncharacterized protein DDB_G0277255, transcript variant X4
putative uncharacterized protein DDB_G0277255, transcript variant X1
putative uncharacterized protein DDB_G0277255, transcript variant X2
putative uncharacterized protein DDB_G0277255 isoform X3
putative uncharacterized protein DDB_G0277255 isoform X4
putative uncharacterized protein DDB_G0277255 isoform X1
putative uncharacterized protein DDB_G0277255 isoform X2
putative uncharacterized protein DDB_G0277255, 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 12 samples with support for all annotated introns
uncharacterized protein MAL13P1.304 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
enoyl-CoA hydratase domain-containing protein 3, mitochondrial
ATP-dependent DNA/RNA helicase DHX36-like, transcript variant X2
ATP-dependent DNA/RNA helicase DHX36-like, transcript variant X1
ATP-dependent DNA/RNA helicase DHX36-like isoform X2
ATP-dependent DNA/RNA helicase DHX36-like isoform X1
polypeptide N-acetylgalactosaminyltransferase 3-like, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase 3-like, transcript variant X2
polypeptide N-acetylgalactosaminyltransferase 3-like isoform X1
polypeptide N-acetylgalactosaminyltransferase 3-like isoform 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 101 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments
probable small nuclear ribonucleoprotein Sm D2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
histone-lysine N-methyltransferase PRDM16-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
histone-lysine N-methyltransferase PRDM16-like, 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 1 sample with support for all annotated introns
histone-lysine N-methyltransferase PRDM16-like, transcript variant X3
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 9 samples with support for all annotated introns
histone-lysine N-methyltransferase PRDM16-like isoform X2
histone-lysine N-methyltransferase PRDM16-like isoform X1
histone-lysine N-methyltransferase PRDM16-like isoform X3
uncharacterized LOC125060880, 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 82 samples with support for all annotated introns
uncharacterized LOC125060880, 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 143 samples with support for all annotated introns
uncharacterized LOC125060880, 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 146 samples with support for all annotated introns
uncharacterized LOC125060897, transcript variant X2
uncharacterized LOC125060897, transcript variant X1
uncharacterized protein LOC125060897 isoform X2
uncharacterized protein LOC125060897 isoform X1
U6 snRNA-associated Sm-like protein LSm7
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 49 samples with support for all annotated introns
short-chain dehydrogenase/reductase family 16C member 6
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 59 samples with support for all annotated introns
V-type proton ATPase subunit H, transcript variant X1
V-type proton ATPase subunit H, transcript variant X3
V-type proton ATPase subunit H, transcript variant X2
V-type proton ATPase subunit H, transcript variant X4
V-type proton ATPase subunit H isoform X3
V-type proton ATPase subunit H isoform X1
V-type proton ATPase subunit H isoform X4
V-type proton ATPase subunit H isoform X2
COX assembly mitochondrial protein homolog
26S proteasome non-ATPase regulatory subunit 14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
uncharacterized LOC125060967, transcript variant X1
uncharacterized LOC125060967, transcript variant X2
cytochrome b5 reductase 4, transcript variant X1
cytochrome b5 reductase 4, transcript variant X2
fatty-acid amide hydrolase 2-A-like, transcript variant X1
fatty-acid amide hydrolase 2-A-like isoform X1
fatty-acid amide hydrolase 2-A-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 3 samples with support for all annotated introns
fatty-acid amide hydrolase 2-A-like isoform X2
cytochrome b5 reductase 4, transcript variant X3
cytochrome b5 reductase 4, transcript variant X4
troponin C, slow skeletal and cardiac muscles-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 7 samples with support for all annotated introns
homologous recombination OB-fold protein-like
uncharacterized LOC125060662, 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 69 samples with support for all annotated introns
uncharacterized LOC125060662, 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 141 samples with support for all annotated introns
uncharacterized protein LOC125060662 isoform X1
uncharacterized protein LOC125060662 isoform X2
enoyl-[acyl-carrier-protein] reductase, mitochondrial, transcript variant X2
enoyl-[acyl-carrier-protein] reductase, mitochondrial, transcript variant X1
enoyl-[acyl-carrier-protein] reductase, mitochondrial isoform X2
enoyl-[acyl-carrier-protein] reductase, mitochondrial isoform X1
uncharacterized LOC125060664, transcript variant X2
uncharacterized LOC125060664, transcript variant X1
uncharacterized protein LOC125060664 isoform X2
uncharacterized protein LOC125060664 isoform X1
putative inorganic phosphate cotransporter, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
putative inorganic phosphate cotransporter, transcript variant X2
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 90 samples with support for all annotated introns
putative inorganic phosphate cotransporter isoform X1
putative inorganic phosphate cotransporter isoform X2
uncharacterized LOC125060817, transcript variant X16
uncharacterized LOC125060817, transcript variant X2
uncharacterized LOC125060817, transcript variant X1
uncharacterized LOC125060817, transcript variant X3
uncharacterized LOC125060817, transcript variant X4
uncharacterized LOC125060817, transcript variant X5
uncharacterized LOC125060817, transcript variant X8
uncharacterized LOC125060817, transcript variant X9
uncharacterized LOC125060817, transcript variant X6
uncharacterized LOC125060817, transcript variant X7
uncharacterized LOC125060817, transcript variant X10
uncharacterized LOC125060817, transcript variant X11
uncharacterized LOC125060817, transcript variant X12
uncharacterized LOC125060817, transcript variant X14
uncharacterized LOC125060817, transcript variant X13
uncharacterized LOC125060817, transcript variant X15
uncharacterized protein LOC125060817 isoform X1
uncharacterized LOC125060817, transcript variant X17
uncharacterized protein LOC125060817 isoform X2
uncharacterized protein LOC125060817 isoform X3
uncharacterized protein LOC125060817 isoform X4
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 152 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
2-hydroxyacyl-CoA lyase 1, 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 24 samples with support for all annotated introns
2-hydroxyacyl-CoA lyase 1, transcript variant X2
2-hydroxyacyl-CoA lyase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 169 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 73 samples with support for all annotated introns
DNA-binding protein RFXANK, transcript variant X1
DNA-binding protein RFXANK, transcript variant X2
pickpocket protein 28-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
pickpocket protein 28-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pickpocket protein 28-like, transcript variant X4
EF-hand domain-containing protein D2 homolog
pickpocket protein 28-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 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 71% 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 89% 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% 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 74 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00147
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC125060912, 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 9 samples with support for all annotated introns
uncharacterized LOC125060912, 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 19 samples with support for all annotated introns
protein gooseberry-neuro, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein gooseberry-neuro, 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 9 samples with support for all annotated introns
protein gooseberry-neuro, 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 17 samples with support for all annotated introns
protein gooseberry, transcript variant X1
protein gooseberry, transcript variant X3
protein gooseberry, transcript variant X2
acidic juvenile hormone-suppressible protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 84 samples with support for all annotated introns
basic juvenile hormone-suppressible protein 2-like
synaptotagmin-15-like, transcript variant X2
synaptotagmin-15-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 6 samples with support for all annotated introns
synaptotagmin-15-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 12 samples with support for all annotated introns
synaptotagmin-15-like, transcript variant X4
rap1 GTPase-activating protein 1, 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 35 samples with support for all annotated introns
rap1 GTPase-activating protein 1, 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 18 samples with support for all annotated introns
rap1 GTPase-activating protein 1, transcript variant X1
rap1 GTPase-activating 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 57 samples with support for all annotated introns
rap1 GTPase-activating protein 1, 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
rap1 GTPase-activating protein 1, 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 29 samples with support for all annotated introns
rap1 GTPase-activating protein 1 isoform X3
rap1 GTPase-activating protein 1 isoform X5
rap1 GTPase-activating protein 1 isoform X4
rap1 GTPase-activating protein 1 isoform X1
rap1 GTPase-activating protein 1 isoform X2
rap1 GTPase-activating protein 1 isoform X6
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
cGMP-dependent protein kinase, isozyme 2 forms cD4/T1/T3A/T3B, transcript variant X2
cGMP-dependent protein kinase, isozyme 2 forms cD4/T1/T3A/T3B, transcript variant X3
cGMP-dependent protein kinase, isozyme 2 forms cD4/T1/T3A/T3B, transcript variant X4
cGMP-dependent protein kinase, isozyme 2 forms cD4/T1/T3A/T3B, transcript variant X1
cGMP-dependent protein kinase, isozyme 2 forms cD4/T1/T3A/T3B isoform X2
cGMP-dependent protein kinase, isozyme 2 forms cD4/T1/T3A/T3B isoform X3
cGMP-dependent protein kinase, isozyme 2 forms cD5/T2 isoform X1
long-chain-fatty-acid--CoA ligase 5, 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 68 samples with support for all annotated introns
long-chain-fatty-acid--CoA ligase 5, 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 93 samples with support for all annotated introns
long-chain-fatty-acid--CoA ligase 5 isoform X1
long-chain-fatty-acid--CoA ligase 5 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 43 samples with support for all annotated introns
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X5
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X4
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X2
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X1
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X3
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11 isoform X1
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11 isoform X2
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11 isoform X3
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11 isoform X4
probable G-protein coupled receptor CG31760
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 169 samples with support for all annotated introns
flocculation protein FLO11-like, transcript variant X2
flocculation protein FLO11-like, transcript variant X1
flocculation protein FLO11-like isoform X2
flocculation protein FLO11-like isoform 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 116 samples with support for all annotated introns
NFU1 iron-sulfur cluster scaffold homolog, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
protein drumstick, 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 141 samples with support for all annotated introns
protein drumstick, 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 118 samples with support for all annotated introns
protein drumstick, 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 154 samples with support for all annotated introns
protein drumstick, 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 142 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 148 samples with support for all annotated introns
uncharacterized LOC125060711, transcript variant X2
uncharacterized LOC125060711, transcript variant X1
uncharacterized protein LOC125060711 isoform X2
uncharacterized protein LOC125060711 isoform X1
MOXD1 homolog 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 108 samples with support for all annotated introns
MOXD1 homolog 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 108 samples with support for all annotated introns
neuropeptide CCHamide-2 receptor-like, transcript variant X1
neuropeptide CCHamide-2 receptor-like isoform X1
neuropeptide CCHamide-2 receptor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neuropeptide CCHamide-2 receptor-like isoform X2
uncharacterized LOC125060846, transcript variant X1
uncharacterized LOC125060846, transcript variant X2
uncharacterized LOC125060829, transcript variant X1
uncharacterized LOC125060829, transcript variant X2
protein 5NUC-like, transcript variant X1
protein 5NUC-like, transcript variant X3
protein 5NUC-like, transcript variant X2
protein 5NUC-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 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 42 samples with support for all annotated introns
putative uncharacterized protein DDB_G0277255
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 88 samples with support for all annotated introns
transcription factor A, mitochondrial, transcript variant X2
transcription factor A, mitochondrial, transcript variant X3
transcription factor A, mitochondrial, transcript variant X1
eukaryotic translation initiation factor 5A, transcript variant X2
eukaryotic translation initiation factor 5A, transcript variant X1
eukaryotic translation initiation factor 5A
WAS/WASL-interacting protein family member 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 36 samples with support for all annotated introns
chromosome transmission fidelity protein 18 homolog
eukaryotic translation initiation factor 4E-binding protein
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 106 samples with support for all annotated introns
X-ray repair cross-complementing protein 5-like
uncharacterized LOC125060741, transcript variant X1
uncharacterized LOC125060741, transcript variant X2
tudor and KH domain-containing protein homolog, 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 130 samples with support for all annotated introns
tudor and KH domain-containing protein homolog, 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 132 samples with support for all annotated introns
tudor and KH domain-containing protein homolog isoform X1
tudor and KH domain-containing protein homolog isoform 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 64 samples with support for all annotated introns
5-methylcytosine rRNA methyltransferase NSUN4
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 125 samples with support for all annotated introns
graves disease carrier protein-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 130 samples with support for all annotated introns
graves disease carrier protein-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 166 samples with support for all annotated introns
graves disease carrier protein-like isoform X1
graves disease carrier protein-like isoform X2
serine/threonine-protein phosphatase 2A catalytic subunit beta isoform
guanine nucleotide-binding protein subunit beta-like protein
wiskott-Aldrich syndrome protein family member 3
low density lipoprotein receptor adapter protein 1-A-like
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 23 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
beta-1,4-N-acetylgalactosaminyltransferase bre-4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
vacuolar protein sorting-associated protein 11 homolog
kinesin-like protein unc-104, transcript variant X4
kinesin-like protein unc-104, transcript variant X2
kinesin-like protein unc-104, transcript variant X15
kinesin-like protein unc-104, transcript variant X10
kinesin-like protein unc-104, transcript variant X18
kinesin-like protein unc-104, transcript variant X16
kinesin-like protein unc-104, transcript variant X5
kinesin-like protein unc-104, transcript variant X9
kinesin-like protein unc-104, transcript variant X14
kinesin-like protein unc-104, transcript variant X8
kinesin-like protein unc-104, transcript variant X17
kinesin-like protein unc-104, transcript variant X13
kinesin-like protein unc-104, transcript variant X6
kinesin-like protein unc-104, transcript variant X12
kinesin-like protein unc-104, transcript variant X7
kinesin-like protein unc-104, transcript variant X11
kinesin-like protein unc-104, transcript variant X1
kinesin-like protein unc-104, transcript variant X3
kinesin-like protein unc-104 isoform X13
kinesin-like protein unc-104 isoform X11
kinesin-like protein unc-104 isoform X10
kinesin-like protein unc-104 isoform X12
kinesin-like protein unc-104 isoform X15
kinesin-like protein unc-104 isoform X14
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like
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
superoxide dismutase [Mn], mitochondrial
guided entry of tail-anchored proteins factor 1-like
glutathione S-transferase C-terminal domain-containing protein homolog
39S ribosomal protein L41, mitochondrial
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase-like
PI-PLC X domain-containing protein 3, transcript variant X3
PI-PLC X domain-containing protein 3, transcript variant X1
PI-PLC X domain-containing protein 3 isoform X1
PI-PLC X domain-containing protein 3, transcript variant X2
PI-PLC X domain-containing protein 3, transcript variant X4
PI-PLC X domain-containing protein 3 isoform X2
uncharacterized LOC125060779, transcript variant X1
uncharacterized LOC125060779, transcript variant X2
uncharacterized protein LOC125060779 isoform X1
uncharacterized protein LOC125060779 isoform X2
glyceraldehyde-3-phosphate dehydrogenase 1-like
ralBP1-associated Eps domain-containing protein 1
F-actin-capping protein subunit beta, transcript variant X1
F-actin-capping protein subunit beta, transcript variant X2
F-actin-capping protein subunit beta, transcript variant X3
F-actin-capping protein subunit beta isoform X3
F-actin-capping protein subunit beta isoform X1
F-actin-capping protein subunit beta isoform X2
atypical protein kinase C, transcript variant X4
atypical protein kinase C, transcript variant X3
atypical protein kinase C, transcript variant X2
atypical protein kinase C, transcript variant X1
atypical protein kinase C, transcript variant X6
atypical protein kinase C, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 159 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 44-like, transcript variant X1
zinc finger and BTB domain-containing protein 44-like, transcript variant X3
zinc finger and BTB domain-containing protein 44-like, transcript variant X2
zinc finger and BTB domain-containing protein 44-like isoform X1
zinc finger and BTB domain-containing protein 44-like isoform X3
zinc finger and BTB domain-containing protein 44-like isoform X2
H/ACA ribonucleoprotein complex non-core subunit NAF1
protein phosphatase 1 regulatory subunit 7-like
uncharacterized LOC125060825, transcript variant X2
uncharacterized LOC125060825, transcript variant X1
uncharacterized protein LOC125060825 isoform X2
uncharacterized protein LOC125060825 isoform X1
GMP synthase [glutamine-hydrolyzing], transcript variant X2
GMP synthase [glutamine-hydrolyzing], transcript variant X1
GMP synthase [glutamine-hydrolyzing] isoform X1
GMP synthase [glutamine-hydrolyzing] isoform 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 1 sample 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 129 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 121 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 168 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
rho-related GTP-binding protein RhoN-like, transcript variant X2
rho-related GTP-binding protein RhoN-like, transcript variant X1
rho-related GTP-binding protein RhoN-like, transcript variant X3
uncharacterized LOC125060804, transcript variant X1
uncharacterized LOC125060804, transcript variant X2
rho-related GTP-binding protein RhoN-like isoform X1
GTP-binding protein rho1-like isoform X2
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon CCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger-containing ubiquitin peptidase 1-like
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 157 samples with support for all annotated introns
protein bicaudal C homolog 1, transcript variant X1
protein bicaudal C homolog 1, transcript variant X3
protein bicaudal C homolog 1, transcript variant X2
protein bicaudal C homolog 1, transcript variant X4
sodium-coupled neutral amino acid transporter 9 homolog, transcript variant X1
sodium-coupled neutral amino acid transporter 9 homolog, transcript variant X2
sodium-coupled neutral amino acid transporter 9 homolog isoform X1
sodium-coupled neutral amino acid transporter 9 homolog isoform X2
fatty-acid amide hydrolase 2-like, transcript variant X2
fatty-acid amide hydrolase 2-like, transcript variant X3
fatty-acid amide hydrolase 2-like, transcript variant X1
fatty-acid amide hydrolase 2-like, transcript variant X4
fatty-acid amide hydrolase 2-like isoform X1
fatty-acid amide hydrolase 2-like isoform X3
fatty-acid amide hydrolase 2-like isoform X2
S-adenosylmethionine decarboxylase proenzyme
activating signal cointegrator 1 complex subunit 2, 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 65 samples with support for all annotated introns
activating signal cointegrator 1 complex subunit 2, 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 28 samples with support for all annotated introns
activating signal cointegrator 1 complex subunit 2, transcript variant X1
activating signal cointegrator 1 complex subunit 2 isoform X1
activating signal cointegrator 1 complex subunit 2 isoform X2
activating signal cointegrator 1 complex subunit 2 isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
Golgi-specific brefeldin A-resistance guanine nucleotide exchange factor 1, transcript variant X2
Golgi-specific brefeldin A-resistance guanine nucleotide exchange factor 1, transcript variant X1
Golgi-specific brefeldin A-resistance guanine nucleotide exchange factor 1 isoform X2
Golgi-specific brefeldin A-resistance guanine nucleotide exchange factor 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00548
ubiquitin carboxyl-terminal hydrolase 16
recQ-mediated genome instability protein 1-like, transcript variant X1
recQ-mediated genome instability protein 1-like, transcript variant X2
recQ-mediated genome instability protein 1-like isoform X2
recQ-mediated genome instability protein 1-like isoform 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 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
Ig-like and fibronectin type-III domain-containing protein 2, transcript variant X1
Ig-like and fibronectin type-III domain-containing protein 2, transcript variant X2
Ig-like and fibronectin type-III domain-containing protein 2 isoform X2
Ig-like and fibronectin type-III domain-containing protein 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
cytochrome P450 4g15-like, transcript variant X2
cytochrome P450 4g15-like, transcript variant X1
histone acetyltransferase KAT6B, transcript variant X2
histone acetyltransferase KAT6B, transcript variant X1
histone acetyltransferase KAT6B isoform X2
histone acetyltransferase KAT6A isoform X1
tyrosine-protein phosphatase non-receptor type 13-like, transcript variant X1
tyrosine-protein phosphatase non-receptor type 13-like, transcript variant X2
tyrosine-protein phosphatase non-receptor type 13-like
vesicle transport through interaction with t-SNAREs homolog 1A
uncharacterized LOC125060872, 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 7 samples with support for all annotated introns
uncharacterized LOC125060872, 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 9 samples with support for all annotated introns
uncharacterized protein LOC125060872 isoform X1
uncharacterized protein LOC125060872 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 60% coverage of the annotated genomic feature by RNAseq alignments
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 17 samples with support for all annotated introns
bone morphogenetic protein receptor type-1B, transcript variant X4
bone morphogenetic protein receptor type-1B isoform X4
uncharacterized LOC125060735, transcript variant X2
uncharacterized LOC125060735, transcript variant X1
uncharacterized protein LOC125060735 isoform X1
uncharacterized protein LOC125060735 isoform X2
uncharacterized LOC125060735, transcript variant X3
uncharacterized protein LOC125060735 isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
bone morphogenetic protein receptor type-1B, transcript variant X2
bone morphogenetic protein receptor type-1B isoform X2
bone morphogenetic protein receptor type-1B, transcript variant X3
bone morphogenetic protein receptor type-1B isoform X3
bone morphogenetic protein receptor type-1B, transcript variant X1
bone morphogenetic protein receptor type-1B isoform X1
RNA-binding protein lark, transcript variant X2
RNA-binding protein lark, transcript variant X1
RNA-binding protein lark, 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 169 samples with support for all annotated introns
stress-activated protein kinase JNK, transcript variant X1
stress-activated protein kinase JNK, transcript variant X5
stress-activated protein kinase JNK, transcript variant X3
stress-activated protein kinase JNK, transcript variant X2
stress-activated protein kinase JNK, transcript variant X6
stress-activated protein kinase JNK, transcript variant X4
stress-activated protein kinase JNK isoform X1
stress-activated protein kinase JNK, transcript variant X7
stress-activated protein kinase JNK isoform X2
transcription initiation factor TFIID subunit 9
hydroxyacyl-coenzyme A dehydrogenase, mitochondrial-like
inositol polyphosphate multikinase, transcript variant X1
probable 3-hydroxyacyl-CoA dehydrogenase B0272.3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
probable 3-hydroxyacyl-CoA dehydrogenase B0272.3, transcript variant X1
probable 3-hydroxyacyl-CoA dehydrogenase B0272.3 isoform X2
probable 3-hydroxyacyl-CoA dehydrogenase B0272.3 isoform X1
inositol polyphosphate multikinase, transcript variant X2
AN1-type zinc finger protein 4-like, transcript variant X2
AN1-type zinc finger protein 4-like, transcript variant X1
AN1-type zinc finger protein 4-like isoform X2
uncharacterized protein LOC125060647 isoform X1
PEST proteolytic signal-containing nuclear protein-like
mitochondrial tRNA methylthiotransferase CDK5RAP1
stimulator of interferon genes protein-like
U5 small nuclear ribonucleoprotein 40 kDa protein
enkurin domain-containing protein 1-like, transcript variant X2
enkurin domain-containing protein 1-like, transcript variant X1
enkurin domain-containing protein 1-like isoform X2
enkurin domain-containing protein 1-like isoform X1
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125060885, transcript variant X2
uncharacterized LOC125060885, transcript variant X1
uncharacterized protein LOC125060885 isoform X2
uncharacterized protein LOC125060885 isoform 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 157 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 90 samples with support for all annotated introns
microsomal triacylglycerol transfer protein