Maniola jurtina chromosome 17, ilManJurt1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Papilionoidea; Nymphalidae; Satyrinae; Satyrini; Maniolina; Maniola.
REFSEQ INFORMATION: The reference sequence is identical to\nHG995224.1.\nAssembly name: ilManJurt1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2021/03/19. The original whole-genome shotgun project has the\naccession CAJOSP000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Maniola jurtina Annotation Release\n 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 81% 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
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: 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
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: 3 Proteins, and 96% 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: 6 Proteins, and 48% 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sarcoplasmic calcium-binding proteins I, III, and IV-like
protein transport protein Sec31A, transcript variant X4
protein transport protein Sec31A, transcript variant X5
protein transport protein Sec31A, transcript variant X3
protein transport protein Sec31A, transcript variant X2
protein transport protein Sec31A, transcript variant X1
protein transport protein Sec31A isoform X4
protein transport protein Sec31A isoform X5
protein transport protein Sec31A isoform X3
protein transport protein Sec31A isoform X2
protein transport protein Sec31A isoform X1
vicilin-like seed storage protein At2g18540
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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
pericentrin-like, transcript variant X10
golgin subfamily A member 4-like isoform X2
golgin subfamily A member 4-like isoform 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 5 samples with support for all annotated introns
golgin subfamily A member 4-like isoform 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 3 samples with support for all annotated introns
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
SET domain-containing protein SmydA-8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
SET domain-containing protein SmydA-8, 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
SET domain-containing protein SmydA-8, 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 14 samples with support for all annotated introns
SET domain-containing protein SmydA-8 isoform X1
SET domain-containing protein SmydA-8 isoform X2
SET domain-containing protein SmydA-8, transcript variant X4
SET domain-containing protein SmydA-8, transcript variant X6
SET domain-containing protein SmydA-8, transcript variant X5
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
SET domain-containing protein SmydA-8, transcript variant X7
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
SET domain-containing protein SmydA-8 isoform X3
SET domain-containing protein SmydA-8 isoform X4
SET domain-containing protein SmydA-8, 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
SET domain-containing protein SmydA-8, transcript variant X9
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 20 samples with support for all annotated introns
SET domain-containing protein SmydA-8 isoform X5
SET domain-containing protein SmydA-8 isoform X6
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 8 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 2 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 3 samples with support for all annotated introns
toll-like receptor 13, 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 1 sample with support for all annotated introns
toll-like receptor 13, transcript variant X1
protein spaetzle 4, 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
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 5 samples with support for all annotated introns
nucleosomal histone kinase 1-like, transcript variant X2
nucleosomal histone kinase 1-like, transcript variant X1
nucleosomal histone kinase 1-like isoform X1
nucleosomal histone kinase 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
insulin receptor substrate 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 3 samples with support for all annotated introns
insulin receptor substrate 1, 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 1 sample with support for all annotated introns
insulin receptor substrate 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
insulin receptor substrate 1, transcript variant X4
insulin receptor substrate 1, transcript variant X1
insulin receptor substrate 1, transcript variant X8
insulin receptor substrate 1, 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 4 samples with support for all annotated introns
insulin receptor substrate 1, transcript variant X7
insulin receptor substrate 1, transcript variant X11
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
insulin receptor substrate 1, transcript variant X10
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 4 samples with support for all annotated introns
insulin receptor substrate 1, transcript variant X9
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
insulin receptor substrate 1, transcript variant X14
insulin receptor substrate 1, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
insulin receptor substrate 1, transcript variant X12
insulin receptor substrate 1 isoform X13
insulin receptor substrate 1 isoform X12
insulin receptor substrate 1 isoform X11
insulin receptor substrate 1-B isoform X7
uncharacterized protein LOC123874130 isoform X5
insulin receptor substrate 1 isoform X10
insulin receptor substrate 1-B isoform X6
insulin receptor substrate 1-B isoform X4
insulin receptor substrate 1-B isoform X2
insulin receptor substrate 1-B isoform X3
insulin receptor substrate 1-B isoform X1
disks large homolog 5, transcript variant X4
disks large homolog 5, transcript variant X2
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 3 samples with support for all annotated introns
disks large homolog 5, transcript variant X6
disks large homolog 5, transcript variant X5
disks large homolog 5, transcript variant X3
uncharacterized LOC123874129, 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
uncharacterized LOC123874129, transcript variant X2
uncharacterized protein LOC123874129 isoform X1
uncharacterized protein LOC123874129 isoform X2
potassium voltage-gated channel protein Shaw-like, transcript variant X1
potassium voltage-gated channel protein Shaw-like isoform X1
potassium voltage-gated channel protein Shaw-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
potassium voltage-gated channel protein Shaw-like, transcript variant X4
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: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
potassium voltage-gated channel protein Shaw-like isoform X2
potassium voltage-gated channel protein Shaw-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123873831, transcript variant X2
uncharacterized LOC123873831, transcript variant X1
uncharacterized LOC123873831, transcript variant X3
uncharacterized protein LOC123873831 isoform X2
uncharacterized protein LOC123873831 isoform X1
uncharacterized protein LOC123873831 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123873907, transcript variant X2
uncharacterized LOC123873907, 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 2 samples with support for all annotated introns
uncharacterized LOC123873907, 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 10 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 5 samples with support for all annotated introns
uncharacterized LOC123873918, transcript variant X1
uncharacterized LOC123873918, transcript variant X2
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.
N6-adenosine-methyltransferase non-catalytic subunit
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN, transcript variant X1
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 isoform X2
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN isoform X1
nucleolar MIF4G domain-containing protein 1 homolog, transcript variant X2
nucleolar MIF4G domain-containing protein 1 homolog, transcript variant X3
nucleolar MIF4G domain-containing protein 1 homolog, transcript variant X1
nucleolar MIF4G domain-containing protein 1 homolog, transcript variant X4
nucleolar MIF4G domain-containing protein 1 isoform X3
nucleolar MIF4G domain-containing protein 1 isoform X2
nucleolar MIF4G domain-containing protein 1 isoform X1
nucleolar MIF4G domain-containing protein 1 homolog isoform X4
uncharacterized LOC123873916, 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 7 samples with support for all annotated introns
uncharacterized LOC123873916, transcript variant X2
uncharacterized LOC123873916, transcript variant X3
uncharacterized protein LOC123873916 isoform X1
uncharacterized protein LOC123873916 isoform X2
uncharacterized protein LOC123873916 isoform X3
uncharacterized LOC123873914, transcript variant X1
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
outer mitochondrial transmembrane helix translocase, transcript variant X1
outer mitochondrial transmembrane helix translocase, transcript variant X2
outer mitochondrial transmembrane helix translocase isoform X1
outer mitochondrial transmembrane helix translocase isoform X2
uncharacterized LOC123873914, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123873914, 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transfer RNA leucine (anticodon UAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger CCHC domain-containing protein 24-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 11 samples with support for all annotated introns
myeloid leukemia factor, transcript variant X3
myeloid leukemia factor, transcript variant X1
myeloid leukemia factor, transcript variant X2
mitochondrial 2-oxoglutarate/malate carrier protein-like
slowpoke-binding protein, 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 4 samples with support for all annotated introns
slowpoke-binding protein, transcript variant X2
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 1 sample with support for all annotated introns
slowpoke-binding protein, transcript variant X3
slowpoke-binding protein, 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 5 samples with support for all annotated introns
mitochondrial 2-oxoglutarate/malate carrier protein-like, transcript variant X2
mitochondrial 2-oxoglutarate/malate carrier protein-like, transcript variant X1
mitochondrial 2-oxoglutarate/malate carrier protein-like isoform X2
mitochondrial 2-oxoglutarate/malate carrier protein-like isoform X1
SET and MYND domain-containing protein 4-like, transcript variant X5
SET and MYND domain-containing protein 4-like, transcript variant X3
SET and MYND domain-containing protein 4-like, transcript variant X4
SET and MYND domain-containing protein 4-like, transcript variant X2
SET and MYND domain-containing protein 4-like, transcript variant X1
SET and MYND domain-containing protein 4-like isoform X1
SET and MYND domain-containing protein 4-like isoform X2
non-structural maintenance of chromosomes element 3 homolog, transcript variant X2
non-structural maintenance of chromosomes element 3 homolog, transcript variant X1
non-structural maintenance of chromosomes element 3 homolog isoform X1
non-structural maintenance of chromosomes element 3 homolog isoform X2
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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 160 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
zinc finger CCHC domain-containing protein 24-like, transcript variant X1
cyclin-dependent kinase-like 4, 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 1 sample with support for all annotated introns
cyclin-dependent kinase-like 4, transcript variant X3
cyclin-dependent kinase-like 4, transcript variant X2
SH2 domain-containing protein 4B-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 1 sample with support for all annotated introns
SH2 domain-containing protein 4B-like, transcript variant X1
protein ALP1-like, transcript variant X2
protein ALP1-like, transcript variant X1
uncharacterized protein LOC123873927 isoform X2
glyoxylate reductase/hydroxypyruvate reductase-like
thioredoxin domain-containing protein 15, transcript variant X1
thioredoxin domain-containing protein 15, transcript variant X2
thioredoxin domain-containing protein 15 isoform X1
thioredoxin domain-containing protein 15 isoform X2
NPC intracellular cholesterol transporter 1, transcript variant X3
NPC intracellular cholesterol transporter 1, transcript variant X2
NPC intracellular cholesterol transporter 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
NPC intracellular cholesterol transporter 1 isoform X2
NPC intracellular cholesterol transporter 1 isoform X4
NPC intracellular cholesterol transporter 1, transcript variant X4
NPC intracellular cholesterol transporter 1 isoform X3
NPC intracellular cholesterol transporter 1, transcript variant X1
NPC intracellular cholesterol transporter 1 isoform X1
G patch domain and ankyrin repeat-containing protein 1 homolog, transcript variant X2
myb/SANT-like DNA-binding domain-containing protein 3
G patch domain and ankyrin repeat-containing protein 1 homolog, transcript variant 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, transcript variant X2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A-like protein 1, transcript variant X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A-like protein 1 isoform X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A-like protein 1 isoform X2
serine protease inhibitor dipetalogastin-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
mitochondrial coenzyme A diphosphatase NUDT8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
chloride intracellular channel exc-4, 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 15 samples with support for all annotated introns
chloride intracellular channel exc-4, 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 15 samples with support for all annotated introns
chloride intracellular channel exc-4 isoform X2
chloride intracellular channel exc-4 isoform X1
uncharacterized LOC123873560, transcript variant X5
uncharacterized LOC123873560, 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 13 samples with support for all annotated introns
uncharacterized protein LOC123873560 isoform X5
uncharacterized protein LOC123873560 isoform X4
uncharacterized LOC123873560, transcript variant X3
uncharacterized LOC123873560, transcript variant X2
uncharacterized LOC123873560, transcript variant X1
uncharacterized protein LOC123873560 isoform X3
uncharacterized protein LOC123873560 isoform X2
uncharacterized protein LOC123873560 isoform X1
ragulator complex protein LAMTOR3 homolog
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 15 samples with support for all annotated introns
protein atonal homolog 8, 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 16 samples with support for all annotated introns
protein atonal homolog 8, transcript variant X2
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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
uncharacterized LOC123873559, transcript variant X6
uncharacterized LOC123873559, transcript variant X4
uncharacterized LOC123873559, transcript variant X1
uncharacterized LOC123873559, transcript variant X3
uncharacterized LOC123873559, transcript variant X7
uncharacterized LOC123873559, transcript variant X5
uncharacterized LOC123873559, transcript variant X2
uncharacterized protein LOC123873559 isoform X1
uncharacterized protein LOC123873559 isoform X2
uncharacterized protein LOC123873559 isoform X3
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
uncharacterized LOC123873689, transcript variant X1
uncharacterized LOC123873689, transcript variant X2
transfer RNA threonine (anticodon CGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ATPase family AAA domain-containing protein 2-like
monocyte to macrophage differentiation factor 2
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
DNA-directed RNA polymerase, mitochondrial, transcript variant X2
DNA-directed RNA polymerase, mitochondrial, 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 6 samples with support for all annotated introns
DNA-directed RNA polymerase, mitochondrial isoform X2
DNA-directed RNA polymerase, mitochondrial isoform X1
zinc finger protein 37 homolog, transcript variant X1
uncharacterized protein LOC123873842 isoform X1
zinc finger protein 37 homolog, transcript variant X2
zinc finger protein 37 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
transmembrane inner ear expressed protein
actin-related protein 2/3 complex subunit 2
serine/threonine-protein kinase Tor-like, 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 1 sample with support for all annotated introns
cytidine deaminase-like, 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 1 sample with support for all annotated introns
cytidine deaminase-like, transcript variant X1
serine/threonine-protein kinase Tor-like, transcript variant X1
serine/threonine-protein kinase Tor-like
ubiA prenyltransferase domain-containing protein 1 homolog
hybrid signal transduction histidine kinase M-like, transcript variant X2
hybrid signal transduction histidine kinase M-like, transcript variant X1
hybrid signal transduction histidine kinase M-like, transcript variant X3
hybrid signal transduction histidine kinase M-like, transcript variant X4
hybrid signal transduction histidine kinase M-like
ubiquitin carboxyl-terminal hydrolase isozyme L5
voltage-dependent anion-selective channel-like, transcript variant X1
voltage-dependent anion-selective channel-like isoform X1
voltage-dependent anion-selective channel-like, transcript variant X2
voltage-dependent anion-selective channel-like isoform X2
protein lin-54 homolog, transcript variant X3
protein lin-54 homolog, transcript variant X1
protein lin-54 homolog, transcript variant X2
SET and MYND domain-containing protein DDB_G0273589-like
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial, transcript variant X1
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial, transcript variant X3
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial, transcript variant X2
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial, transcript variant X4
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial
trichohyalin-like, transcript variant X2
trichohyalin-like, transcript variant X1
reversion-inducing cysteine-rich protein with Kazal motifs, transcript variant X1
reversion-inducing cysteine-rich protein with Kazal motifs, transcript variant X2
reversion-inducing cysteine-rich protein with Kazal motifs, transcript variant X3
reversion-inducing cysteine-rich protein with Kazal motifs
brefeldin A-inhibited guanine nucleotide-exchange protein 3, transcript variant X1
brefeldin A-inhibited guanine nucleotide-exchange protein 3, transcript variant X2
brefeldin A-inhibited guanine nucleotide-exchange protein 3, transcript variant X3
brefeldin A-inhibited guanine nucleotide-exchange protein 3 isoform X1
brefeldin A-inhibited guanine nucleotide-exchange protein 3 isoform X2
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 5, mitochondrial-like
pancreatic lipase-related protein 2, 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 9 samples with support for all annotated introns
pancreatic lipase-related protein 2, 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 9 samples with support for all annotated introns
pancreatic lipase-related protein 2 isoform X1
pancreatic lipase-related protein 2 isoform X2
malate dehydrogenase, mitochondrial-like, transcript variant X3
malate dehydrogenase, mitochondrial-like, transcript variant X4
malate dehydrogenase, mitochondrial-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 4 samples with support for all annotated introns
uncharacterized protein LOC123873846 isoform X3
uncharacterized protein LOC123873846 isoform X4
malate dehydrogenase, mitochondrial-like isoform X1
malate dehydrogenase, mitochondrial-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 5 samples with support for all annotated introns
malate dehydrogenase, mitochondrial-like isoform X2
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
class E basic helix-loop-helix protein 40-like, transcript variant X2
uncharacterized LOC123873854, transcript variant X1
uncharacterized LOC123873854, transcript variant X2
uncharacterized protein LOC123873854 isoform X1
uncharacterized protein LOC123873854 isoform X2
class E basic helix-loop-helix protein 40-like, 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 3 samples with support for all annotated introns
class E basic helix-loop-helix protein 40-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
probable ATP-dependent RNA helicase DDX46
U6 snRNA-associated Sm-like protein LSm3
U3 small nucleolar RNA-associated protein 14 homolog A
uncharacterized LOC123873947, transcript variant X3
uncharacterized LOC123873947, transcript variant X2
uncharacterized LOC123873947, transcript variant X1
uncharacterized protein LOC123873947 isoform X2
uncharacterized protein LOC123873947 isoform X1
uncharacterized protein LOC123873947 isoform X3
early boundary activity protein 1-like, transcript variant X1
early boundary activity protein 1-like, transcript variant X2
probable ribonuclease ZC3H12B, transcript variant X1
probable ribonuclease ZC3H12D isoform X1
probable ribonuclease ZC3H12B, transcript variant X2
probable ribonuclease ZC3H12B isoform X2
pre-mRNA-processing factor 6, transcript variant X2
uncharacterized LOC123873948, transcript variant X1
uncharacterized LOC123873948, transcript variant X2
uncharacterized protein LOC123873948 isoform X2
uncharacterized protein LOC123873948 isoform X1
pre-mRNA-processing factor 6, transcript variant X1
centrosomal protein of 162 kDa-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
centrosomal protein of 162 kDa-like isoform X1
centrosomal protein of 162 kDa-like, transcript variant X2
centrosomal protein of 162 kDa-like isoform X2
pre-mRNA-splicing regulator female-lethal(2)D
runt-related transcription factor 3-like, transcript variant X2
runt-related transcription factor 3-like, transcript variant X1
runt-related transcription factor 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
runt-related transcription factor 3, transcript variant X1
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 1 sample with support for all annotated introns
runt-related transcription factor 3, 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 1 sample with support for all annotated introns
runt-related transcription factor 3 isoform X1
runt-related transcription factor 3 isoform X2
carboxypeptidase B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
carboxypeptidase B-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 3 samples with support for all annotated introns
carboxypeptidase B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
runt-related transcription factor 1-like, transcript variant X2
runt-related transcription factor 1-like, transcript variant X1
runt-related transcription factor 1-like isoform X2
runt-related transcription factor 3-like isoform X1
peptidyl-prolyl cis-trans isomerase-like 4
mitogen-activated protein kinase kinase kinase 7-like
polypeptide N-acetylgalactosaminyltransferase 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 5, 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 10 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 5, 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 4 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 5 isoform X2
polypeptide N-acetylgalactosaminyltransferase 5 isoform X1
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial, transcript variant X1
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial, transcript variant X3
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial, transcript variant X2
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial isoform X1
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial isoform X3
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial isoform X2
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial, transcript variant X4
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial isoform X4
MORN repeat-containing protein 4-like, transcript variant X1
MORN repeat-containing protein 4-like, transcript variant X2
short-chain dehydrogenase/reductase family 16C member 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
chitin deacetylase 1, transcript variant X3
chitin deacetylase 1, transcript variant X2
chitin deacetylase 1, transcript variant X1
U6 snRNA-associated Sm-like protein LSm7, transcript variant X2
U6 snRNA-associated Sm-like protein LSm7, transcript variant X1
U6 snRNA-associated Sm-like protein LSm7
protein brunelleschi, transcript variant X2
protein brunelleschi, transcript variant X1
uncharacterized LOC123873774, transcript variant X2
uncharacterized protein LOC123873774 isoform X2
uncharacterized LOC123873774, transcript variant X1
uncharacterized protein LOC123873774 isoform X1
zinc finger protein 271-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
zinc finger protein 271-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 3 samples with support for all annotated introns
zinc finger protein 271-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 11 samples with support for all annotated introns
uncharacterized LOC123873762, transcript variant X1
uncharacterized LOC123873762, transcript variant X2
uncharacterized protein LOC123873762 isoform X1
uncharacterized protein LOC123873762 isoform X2
histone-lysine N-methyltransferase MECOM-like, transcript variant X1
histone-lysine N-methyltransferase MECOM-like, transcript variant X2
histone-lysine N-methyltransferase MECOM-like isoform X1
histone-lysine N-methyltransferase MECOM-like isoform X2
histone-lysine N-methyltransferase MECOM-like, transcript variant X3
histone-lysine N-methyltransferase MECOM-like isoform X3
uncharacterized LOC123873775, transcript variant X3
uncharacterized LOC123873775, transcript variant X1
uncharacterized LOC123873775, transcript variant X2
uncharacterized protein LOC123873775 isoform X3
uncharacterized protein LOC123873775 isoform X1
uncharacterized protein LOC123873775 isoform X2
transcription factor hamlet-like, transcript variant X1
transcription factor hamlet-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 25 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 3-like
ATP-dependent DNA/RNA helicase DHX36-like
enoyl-CoA hydratase domain-containing protein 3, mitochondrial
putative uncharacterized protein DDB_G0277255, transcript variant X4
putative uncharacterized protein DDB_G0287457 isoform X4
putative uncharacterized protein DDB_G0277255, transcript variant X6
putative uncharacterized protein DDB_G0277255, transcript variant X5
putative uncharacterized protein DDB_G0277255, transcript variant X1
putative uncharacterized protein DDB_G0277255, transcript variant X2
MATH and LRR domain-containing protein PFE0570w isoform X6
putative uncharacterized protein DDB_G0287457 isoform X1
putative uncharacterized protein DDB_G0277255 isoform X2
putative uncharacterized protein DDB_G0287457 isoform X5
putative uncharacterized protein DDB_G0277255, transcript variant X3
putative uncharacterized protein DDB_G0287457 isoform X3
transcription initiation factor TFIID subunit 11
succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial
uncharacterized LOC123873681, transcript variant X2
uncharacterized LOC123873681, transcript variant X1
iron-sulfur cluster assembly 2 homolog, mitochondrial
protein split ends, transcript variant X1
protein split ends, transcript variant X5
protein split ends, transcript variant X2
protein split ends, transcript variant X4
protein split ends, transcript variant X3
protein split ends, transcript variant X10
protein split ends, transcript variant X6
protein split ends, transcript variant X7
protein split ends, transcript variant X8
protein split ends, transcript variant X9
uncharacterized LOC123873760, transcript variant X3
uncharacterized LOC123873760, transcript variant X2
uncharacterized LOC123873760, transcript variant X1
uncharacterized LOC123873541, transcript variant X1
uncharacterized protein LOC123873541 isoform X1
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like
uncharacterized LOC123873541, transcript variant X2
uncharacterized protein LOC123873541 isoform X2
protein quick-to-court, transcript variant X1
protein quick-to-court, transcript variant X2
protein smoothened, transcript variant X4
protein smoothened, transcript variant X3
protein smoothened, transcript variant X1
protein smoothened, transcript variant X2
pre-mRNA 3' end processing protein WDR33
cytochrome P450 4V2-like, transcript variant X1
cytochrome P450 4V2-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 4 samples with support for all annotated introns
androgen-induced gene 1 protein-like, transcript variant X2
androgen-induced gene 1 protein-like, transcript variant X1
dynein regulatory complex protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dynein regulatory complex protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dynein regulatory complex protein 1 isoform X2
dynein regulatory complex protein 1 isoform X1
zinc finger protein OZF-like, transcript variant X1
zinc finger protein OZF-like, transcript variant X6
zinc finger protein OZF-like, transcript variant X5
zinc finger protein OZF-like, transcript variant X3
zinc finger protein OZF-like, transcript variant X15
zinc finger protein OZF-like, transcript variant X2
zinc finger protein OZF-like, transcript variant X9
zinc finger protein OZF-like, transcript variant X10
zinc finger protein OZF-like, transcript variant X4
zinc finger protein OZF-like, transcript variant X11
zinc finger protein OZF-like, transcript variant X7
zinc finger protein OZF-like, transcript variant X8
zinc finger protein OZF-like, transcript variant X12
zinc finger protein OZF-like, transcript variant X19
zinc finger protein OZF-like, transcript variant X13
zinc finger protein OZF-like, transcript variant X17
zinc finger protein OZF-like, transcript variant X14
zinc finger protein OZF-like, transcript variant X16
zinc finger protein OZF-like, transcript variant X20
zinc finger protein OZF-like, transcript variant X18
zinc finger protein OZF-like, transcript variant X21
zinc finger protein OZF-like, transcript variant X22
zinc finger protein 2 homolog isoform X1
zinc finger protein 2 homolog isoform X3
zinc finger protein 2 homolog isoform X15
zinc finger protein 2 homolog isoform X6
zinc finger protein 2 homolog isoform X16
zinc finger protein 2 homolog isoform X4
zinc finger protein 431-like isoform X14
zinc finger protein 182-like isoform X18
zinc finger protein OZF-like isoform X22
actin-related protein 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
26S proteasome non-ATPase regulatory subunit 14, transcript variant X3
actin-related protein 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 5 samples with support for all annotated introns
V-type proton ATPase subunit H, transcript variant X5
V-type proton ATPase subunit H, transcript variant X3
V-type proton ATPase subunit H, transcript variant X1
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 X5
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, transcript variant X1
26S proteasome non-ATPase regulatory subunit 14, transcript variant X2
26S proteasome non-ATPase regulatory subunit 14
uncharacterized LOC123873628, transcript variant X2
uncharacterized LOC123873628, transcript variant X1
uncharacterized protein LOC123873628 isoform X2
uncharacterized protein LOC123873628 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase pakE-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 8 samples with support for all annotated introns
serine/threonine-protein kinase pakE-like, transcript variant X2
serine/threonine-protein kinase pakE-like isoform X1
uncharacterized protein LOC123873644 isoform X2
cytochrome b5 reductase 4, 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 8 samples with support for all annotated introns
cytochrome b5 reductase 4, 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 9 samples with support for all annotated introns
uncharacterized LOC123873547, transcript variant X3
uncharacterized LOC123873547, transcript variant X2
uncharacterized LOC123873547, transcript variant X1
uncharacterized protein LOC123873547 isoform X3
uncharacterized protein LOC123873547 isoform X2
uncharacterized protein LOC123873547 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123874124, transcript variant X2
uncharacterized LOC123874124, transcript variant X7
uncharacterized LOC123874124, transcript variant X5
uncharacterized LOC123874124, transcript variant X4
uncharacterized LOC123874124, transcript variant X3
uncharacterized LOC123874124, transcript variant X6
uncharacterized LOC123874124, transcript variant X1
uncharacterized protein LOC123874124 isoform X2
uncharacterized protein LOC123874124 isoform X7
uncharacterized protein LOC123874124 isoform X5
uncharacterized protein LOC123874124 isoform X3
uncharacterized protein LOC123874124 isoform X6
uncharacterized protein LOC123874124 isoform X1
uncharacterized protein LOC123874124 isoform 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 8 samples with support for all annotated introns
uncharacterized transporter slc-17.2-like
arginyl-tRNA--protein transferase 1, transcript variant X2
arginyl-tRNA--protein transferase 1, transcript variant X1
arginyl-tRNA--protein transferase 1 isoform X2
arginyl-tRNA--protein transferase 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
2-hydroxyacyl-CoA lyase 1, transcript variant X2
2-hydroxyacyl-CoA lyase 1, transcript variant X1
EF-hand domain-containing protein D2 homolog
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 7 samples with support for all annotated introns
zinc finger CCCH domain-containing protein 13-like, transcript variant X5
zinc finger CCCH domain-containing protein 13-like, transcript variant X7
zinc finger CCCH domain-containing protein 13-like, transcript variant X6
zinc finger CCCH domain-containing protein 13-like, transcript variant X4
zinc finger CCCH domain-containing protein 13-like, transcript variant X3
zinc finger CCCH domain-containing protein 13-like, transcript variant X2
zinc finger CCCH domain-containing protein 13-like, transcript variant X1
zinc finger CCCH domain-containing protein 13-like isoform X5
zinc finger CCCH domain-containing protein 13-like isoform X7
zinc finger CCCH domain-containing protein 13-like isoform X6
zinc finger CCCH domain-containing protein 13-like isoform X4
zinc finger CCCH domain-containing protein 13-like isoform X3
zinc finger CCCH domain-containing protein 13-like isoform X2
zinc finger CCCH domain-containing protein 13-like isoform 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 27 samples with support for all annotated introns
uncharacterized LOC123873963, transcript variant X2
uncharacterized LOC123873963, transcript variant X1
protein gooseberry-neuro-like, transcript variant X2
protein gooseberry-neuro-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein gooseberry-neuro-like, transcript variant X3
protein gooseberry-neuro-like isoform X2
protein gooseberry-neuro-like isoform X1
protein gooseberry-neuro-like isoform X3
protein gooseberry, transcript variant X1
protein gooseberry, transcript variant X3
protein gooseberry, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
rap1 GTPase-activating protein 1, transcript variant X5
rap1 GTPase-activating protein 1, transcript variant X4
rap1 GTPase-activating protein 1, transcript variant X3
rap1 GTPase-activating protein 1, transcript variant X7
rap1 GTPase-activating protein 1, transcript variant X2
rap1 GTPase-activating protein 1, transcript variant X6
rap1 GTPase-activating protein 1, transcript variant X1
rap1 GTPase-activating protein 1, transcript variant X8
rap1 GTPase-activating protein 1 isoform X3
rap1 GTPase-activating protein 1 isoform X5
rap1 GTPase-activating protein 1 isoform X2
rap1 GTPase-activating protein 1 isoform X4
rap1 GTPase-activating protein 1 isoform X1
rap1 GTPase-activating protein 1 isoform X6
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 X5
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, transcript variant X2
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
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
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
long-chain-fatty-acid--CoA ligase 5, transcript variant X3
long-chain-fatty-acid--CoA ligase 5, transcript variant X4
long-chain-fatty-acid--CoA ligase 5, transcript variant X2
long-chain-fatty-acid--CoA ligase 5, transcript variant X1
long-chain-fatty-acid--CoA ligase 5, transcript variant X5
long-chain-fatty-acid--CoA ligase 5 isoform X2
long-chain-fatty-acid--CoA ligase 5 isoform X1
long-chain-fatty-acid--CoA ligase 5 isoform X3
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X4
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X3
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X1
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X13
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X12
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X11
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X5
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X14
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X9
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X7
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X10
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X6
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X2
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11, transcript variant X8
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11 isoform X2
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11 isoform X1
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11 isoform X4
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11 isoform X3
dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11 isoform X5
probable G-protein coupled receptor CG31760, 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 2 samples with support for all annotated introns
probable G-protein coupled receptor CG31760, transcript variant X2
probable G-protein coupled receptor CG31760
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
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
flocculation protein FLO11-like, transcript variant X2
flocculation protein FLO11-like, transcript variant X1
uncharacterized protein PB18E9.04c-like isoform X2
flocculation protein FLO11-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
NFU1 iron-sulfur cluster scaffold homolog, mitochondrial-like
protein drumstick, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 69% coverage of the annotated genomic feature by RNAseq alignments
protein drumstick, transcript variant X4
protein drumstick, transcript variant X1
protein drumstick, transcript variant X5
protein drumstick, transcript variant X2
uncharacterized protein LOC123873593 isoform X2
protein sister of odd and bowel-like, transcript variant X2
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 1 sample with support for all annotated introns
protein sister of odd and bowel-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
zinc finger BED domain-containing protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44% coverage of the annotated genomic feature by RNAseq alignments, including 15 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 11 samples with support for all annotated introns
uncharacterized LOC123873499, transcript variant X4
uncharacterized LOC123873499, transcript variant X7
uncharacterized LOC123873499, transcript variant X6
uncharacterized LOC123873499, transcript variant X3
uncharacterized LOC123873499, transcript variant X5
uncharacterized LOC123873499, transcript variant X2
uncharacterized LOC123873499, transcript variant X1
uncharacterized LOC123873499, transcript variant X8
uncharacterized protein LOC123873499 isoform X4
uncharacterized protein LOC123873499 isoform X7
uncharacterized protein LOC123873499 isoform X6
uncharacterized protein LOC123873499 isoform X3
uncharacterized protein LOC123873499 isoform X5
uncharacterized protein LOC123873499 isoform X2
uncharacterized protein LOC123873499 isoform X1
uncharacterized protein LOC123873499 isoform X8
facilitated trehalose transporter Tret1-2 homolog, transcript variant X1
facilitated trehalose transporter Tret1-2 homolog, transcript variant X11
facilitated trehalose transporter Tret1-2 homolog, transcript variant X2
facilitated trehalose transporter Tret1-2 homolog, transcript variant X6
facilitated trehalose transporter Tret1-2 homolog, transcript variant X5
facilitated trehalose transporter Tret1-2 homolog, transcript variant X4
facilitated trehalose transporter Tret1-2 homolog isoform X1
facilitated trehalose transporter Tret1-like isoform X2
facilitated trehalose transporter Tret1-like isoform X11
facilitated trehalose transporter Tret1-2 homolog isoform X6
facilitated trehalose transporter Tret1-2 homolog isoform X5
facilitated trehalose transporter Tret1-2 homolog isoform X4
facilitated trehalose transporter Tret1-2 homolog, transcript variant X3
facilitated trehalose transporter Tret1-like isoform X3
facilitated trehalose transporter Tret1-2 homolog, transcript variant X7
facilitated trehalose transporter Tret1-2 homolog, transcript variant X9
facilitated trehalose transporter Tret1-2 homolog, transcript variant X10
facilitated trehalose transporter Tret1-like isoform X7
facilitated trehalose transporter Tret1-like isoform X9
sugar transporter ERD6-like 9 isoform X10
facilitated trehalose transporter Tret1-2 homolog, transcript variant X12
facilitated trehalose transporter Tret1-2 homolog, transcript variant X13
facilitated trehalose transporter Tret1-2 homolog, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
facilitated trehalose transporter Tret1-2 homolog isoform X8
facilitated trehalose transporter Tret1-2 homolog isoform X12
facilitated trehalose transporter Tret1-2 homolog isoform X13
facilitated trehalose transporter Tret1-2 homolog, transcript variant X14
uncharacterized protein LOC123873500 isoform X14
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
MOXD1 homolog 1-like, transcript variant X1
MOXD1 homolog 1-like, transcript variant X2
uncharacterized LOC123873550, transcript variant X2
uncharacterized LOC123873550, transcript variant X1
uncharacterized protein LOC123873550 isoform X2
uncharacterized protein LOC123873550 isoform X1
neuropeptide CCHamide-2 receptor-like, transcript variant X2
neuropeptide CCHamide-2 receptor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neuropeptide CCHamide-2 receptor-like isoform X2
neuropeptide CCHamide-2 receptor-like isoform X1
uncharacterized LOC123873890, transcript variant X2
uncharacterized LOC123873890, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123873893, transcript variant X2
uncharacterized LOC123873893, transcript variant X1
uncharacterized protein LOC123873893 isoform X2
uncharacterized protein LOC123873893 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
SET and MYND domain-containing protein 4-like
nuclear pore membrane glycoprotein 210, transcript variant X3
nuclear pore membrane glycoprotein 210, transcript variant X2
nuclear pore membrane glycoprotein 210, transcript variant X1
nuclear pore membrane glycoprotein 210 isoform X2
nuclear pore membrane glycoprotein 210 isoform X1
uncharacterized LOC123873883, transcript variant X2
uncharacterized LOC123873883, 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
uncharacterized LOC123873883, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC123873892, transcript variant X2
uncharacterized LOC123873892, transcript variant X1
uncharacterized protein LOC123873892 isoform X1
uncharacterized protein LOC123873892 isoform 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 4 samples with support for all annotated introns
ralBP1-associated Eps domain-containing protein 1
glyceraldehyde-3-phosphate dehydrogenase 2-like
PI-PLC X domain-containing protein 3, transcript variant X1
PI-PLC X domain-containing protein 3, transcript variant X4
PI-PLC X domain-containing protein 3, transcript variant X2
PI-PLC X domain-containing protein 3, transcript variant X6
PI-PLC X domain-containing protein 3, transcript variant X3
PI-PLC X domain-containing protein 3, transcript variant X5
PI-PLC X domain-containing protein 3 isoform X1
PI-PLC X domain-containing protein 3 isoform X2
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase-like, transcript variant X1
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase-like, transcript variant X2
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase-like isoform X1
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase-like, transcript variant X3
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase-like, transcript variant X4
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase-like isoform X3
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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 2 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 17 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 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
39S ribosomal protein L41, mitochondrial
guided entry of tail-anchored proteins factor 1-like
glutathione S-transferase C-terminal domain-containing protein homolog
mitochondrial carrier protein Rim2, transcript variant X2
mitochondrial carrier protein Rim2, transcript variant X3
mitochondrial carrier protein Rim2, transcript variant X1
mitochondrial carrier protein Rim2 isoform X2
mitochondrial carrier protein Rim2 isoform X1
superoxide dismutase [Mn], mitochondrial
kinesin-like protein unc-104, transcript variant X7
kinesin-like protein unc-104, transcript variant X5
kinesin-like protein unc-104, transcript variant X20
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 4 samples with support for all annotated introns
kinesin-like protein unc-104, transcript variant X1
kinesin-like protein unc-104, transcript variant X6
kinesin-like protein unc-104, transcript variant X9
kinesin-like protein unc-104, transcript variant X3
kinesin-like protein unc-104, transcript variant X12
kinesin-like protein unc-104, transcript variant X10
kinesin-like protein unc-104, transcript variant X14
kinesin-like protein unc-104, transcript variant X8
kinesin-like protein unc-104, transcript variant X16
kinesin-like protein unc-104, transcript variant X11
kinesin-like protein unc-104, transcript variant X13
kinesin-like protein unc-104, transcript variant X15
kinesin-like protein unc-104, transcript variant X17
kinesin-like protein unc-104, transcript variant X18
kinesin-like protein unc-104, transcript variant X19
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
kinesin-like protein unc-104, transcript variant X2
kinesin-like protein unc-104, transcript variant X4
kinesin-like protein unc-104 isoform X10
kinesin-like protein unc-104 isoform X14
kinesin-like protein unc-104 isoform X11
kinesin-like protein unc-104 isoform X13
kinesin-like protein unc-104 isoform X15
kinesin-like protein unc-104 isoform X12
kinesin-like protein unc-104 isoform X16
kinesin-like protein unc-104 isoform X17
uncharacterized LOC123873806, transcript variant X6
uncharacterized LOC123873806, transcript variant X3
uncharacterized LOC123873806, transcript variant X4
uncharacterized LOC123873806, transcript variant X2
uncharacterized LOC123873806, transcript variant X7
uncharacterized LOC123873806, transcript variant X5
uncharacterized LOC123873806, transcript variant X8
uncharacterized LOC123873806, transcript variant X11
uncharacterized LOC123873806, transcript variant X12
uncharacterized LOC123873806, transcript variant X10
uncharacterized LOC123873806, transcript variant X9
uncharacterized LOC123873806, transcript variant X1
vacuolar protein sorting-associated protein 11 homolog
beta-1,4-N-acetylgalactosaminyltransferase bre-4, transcript variant X2
beta-1,4-N-acetylgalactosaminyltransferase bre-4, transcript variant X1
beta-1,4-N-acetylgalactosaminyltransferase bre-4
uncharacterized LOC123873804, transcript variant X2
uncharacterized LOC123873804, transcript variant X1
uncharacterized protein LOC123873804 isoform X1
uncharacterized protein LOC123873804 isoform 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 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
PAT complex subunit CCDC47, transcript variant X2
PAT complex subunit CCDC47, transcript variant X3
PAT complex subunit CCDC47, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
low density lipoprotein receptor adapter protein 1-like
serine/arginine repetitive matrix protein 1
guanine nucleotide-binding protein subunit beta-like protein
serine/threonine-protein phosphatase 2A catalytic subunit beta isoform, transcript variant X1
serine/threonine-protein phosphatase 2A catalytic subunit beta isoform isoform X1
serine/threonine-protein phosphatase 2A catalytic subunit beta isoform, transcript variant X2
serine/threonine-protein phosphatase 2A catalytic subunit beta isoform isoform X2
graves disease carrier protein-like, transcript variant X1
graves disease carrier protein-like, transcript variant X2
graves disease carrier protein-like isoform X2
graves disease carrier protein-like isoform 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
5-methylcytosine rRNA methyltransferase NSUN4
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 23 samples with support for all annotated introns
tudor and KH domain-containing protein homolog, transcript variant X3
tudor and KH domain-containing protein homolog, transcript variant X1
tudor and KH domain-containing protein homolog, transcript variant X2
tudor and KH domain-containing protein homolog isoform X2
tudor and KH domain-containing protein homolog isoform X1
uncharacterized LOC123873529, transcript variant X3
uncharacterized LOC123873529, transcript variant X1
uncharacterized LOC123873529, transcript variant X2
X-ray repair cross-complementing protein 5-like
eukaryotic translation initiation factor 4E-binding protein, 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 2 samples with support for all annotated introns
eukaryotic translation initiation factor 4E-binding protein, transcript variant X1
eukaryotic translation initiation factor 4E-binding protein
chromosome transmission fidelity protein 18 homolog, transcript variant X1
chromosome transmission fidelity protein 18 homolog, transcript variant X2
chromosome transmission fidelity protein 18 homolog, transcript variant X3
chromosome transmission fidelity protein 18 homolog isoform X1
chromosome transmission fidelity protein 18 homolog isoform X2
chromosome transmission fidelity protein 18 homolog isoform X3
dorsal root ganglia homeobox protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 5A, transcript variant X3
eukaryotic translation initiation factor 5A, transcript variant X1
eukaryotic translation initiation factor 5A, transcript variant X2
eukaryotic translation initiation factor 5A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
atypical protein kinase C, transcript variant X6
atypical protein kinase C, transcript variant X5
atypical protein kinase C, transcript variant X1
atypical protein kinase C, transcript variant X2
atypical protein kinase C, transcript variant X3
atypical protein kinase C, transcript variant X4
atypical protein kinase C, transcript variant X8
atypical protein kinase C, transcript variant X7
inositol-3-phosphate synthase, transcript variant X3
inositol-3-phosphate synthase, transcript variant X2
inositol-3-phosphate synthase, transcript variant X1
protein phosphatase 1 regulatory subunit 7, transcript variant X1
protein phosphatase 1 regulatory subunit 7, transcript variant X2
protein phosphatase 1 regulatory subunit 7 isoform X1
protein phosphatase 1 regulatory subunit 7 isoform X2
H/ACA ribonucleoprotein complex non-core subunit NAF1
zinc finger and BTB domain-containing protein 7A-like, transcript variant X1
zinc finger and BTB domain-containing protein 7A-like, transcript variant X3
zinc finger and BTB domain-containing protein 7A-like, transcript variant X2
zinc finger and BTB domain-containing protein 7A-like, transcript variant X4
zinc finger and BTB domain-containing protein 7A-like, transcript variant X5
zinc finger and BTB domain-containing protein 7A-like, transcript variant X6
zinc finger and BTB domain-containing protein 7A-like isoform X6
zinc finger and BTB domain-containing protein 7A-like isoform X5
zinc finger and BTB domain-containing protein 7A-like isoform X4
zinc finger and BTB domain-containing protein 7A-like isoform X3
zinc finger and BTB domain-containing protein 7A-like isoform X2
zinc finger and BTB domain-containing protein 7A-like isoform X1
uncharacterized LOC123873814, transcript variant X2
uncharacterized LOC123873814, transcript variant X1
uncharacterized LOC123873814, transcript variant X3
uncharacterized protein LOC123873814 isoform X2
uncharacterized protein LOC123873814 isoform X1
uncharacterized protein LOC123873814 isoform X3
GMP synthase [glutamine-hydrolyzing], transcript variant X4
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 7 samples with support for all annotated introns
GMP synthase [glutamine-hydrolyzing], transcript variant X5
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 6 samples with support for all annotated introns
GMP synthase [glutamine-hydrolyzing], 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 1 sample with support for all annotated introns
GMP synthase [glutamine-hydrolyzing] isoform X3
GMP synthase [glutamine-hydrolyzing], transcript variant X6
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
GMP synthase [glutamine-hydrolyzing], transcript variant X2
GMP synthase [glutamine-hydrolyzing] isoform X2
GMP synthase [glutamine-hydrolyzing], transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
GMP synthase [glutamine-hydrolyzing] isoform X1
GMP synthase [glutamine-hydrolyzing] isoform X4
protein MCM10 homolog, transcript variant X1
protein MCM10 homolog, transcript variant X2
cell wall protein DAN4-like, transcript variant X2
cell wall protein DAN4-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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% 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
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
mitochondrial import receptor subunit TOM40 homolog
rho-related GTP-binding protein RhoN-like isoform X1
rho-related GTP-binding protein RhoN-like isoform 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 10 samples with support for all annotated introns
zinc finger-containing ubiquitin peptidase 1-like
protein bicaudal C homolog 1, transcript variant X1
protein bicaudal C homolog 1, transcript variant X3
protein bicaudal C homolog 1, transcript variant X2
sodium-coupled neutral amino acid transporter 9 homolog
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 27 samples with support for all annotated introns
fatty-acid amide hydrolase 2-A-like, transcript variant X1
fatty-acid amide hydrolase 2-A-like, transcript variant X2
fatty-acid amide hydrolase 2-A-like, transcript variant X3
fatty-acid amide hydrolase 2-A-like isoform X1
fatty-acid amide hydrolase 2-A-like isoform X2
fatty-acid amide hydrolase 2-A-like, transcript variant X4
fatty-acid amide hydrolase 2-A-like isoform X3
fatty-acid amide hydrolase 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 3 samples with support for all annotated introns
fatty-acid amide hydrolase 2-like, transcript variant X2
fatty-acid amide hydrolase 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 1 sample with support for all annotated introns
fatty-acid amide hydrolase 2-like, transcript variant X1
S-adenosylmethionine decarboxylase proenzyme, transcript variant X1
S-adenosylmethionine decarboxylase proenzyme, transcript variant X2
S-adenosylmethionine decarboxylase proenzyme isoform X2
S-adenosylmethionine decarboxylase proenzyme isoform X1
uncharacterized LOC123873743, transcript variant X2
uncharacterized LOC123873743, transcript variant X1
activating signal cointegrator 1 complex subunit 2
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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
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: 85 Proteins, and 93% 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:RF00548
ubiquitin carboxyl-terminal hydrolase 16, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 16, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 16, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 16, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 16 isoform X1
ubiquitin carboxyl-terminal hydrolase 16 isoform X3
ubiquitin carboxyl-terminal hydrolase 16 isoform X2
ubiquitin carboxyl-terminal hydrolase 16 isoform X4
recQ-mediated genome instability protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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 X1
Ig-like and fibronectin type-III domain-containing protein 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
histone acetyltransferase KAT6B, transcript variant X1
histone acetyltransferase KAT6B, transcript variant X2
histone acetyltransferase KAT6B, transcript variant X3
histone acetyltransferase KAT6B isoform X3
histone acetyltransferase KAT6B isoform X2
histone acetyltransferase KAT6B isoform X1
tyrosine-protein phosphatase non-receptor type 13-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 26 samples with support for all annotated introns
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 LOC123873723, transcript variant X3
uncharacterized LOC123873723, transcript variant X2
uncharacterized LOC123873723, transcript variant X1
general vesicular transport factor p115, transcript variant X2
general vesicular transport factor p115, 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 10 samples with support for all annotated introns
general vesicular transport factor p115 isoform X1
general vesicular transport factor p115 isoform X2
40-kDa huntingtin-associated protein, transcript variant X3
40-kDa huntingtin-associated protein, 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 5 samples with support for all annotated introns
40-kDa huntingtin-associated protein, transcript variant X1
bone morphogenetic protein receptor type-1B, transcript variant X2
bone morphogenetic protein receptor type-1B 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 10 samples with support for all annotated introns
bone morphogenetic protein receptor type-1B, transcript variant X1
bone morphogenetic protein receptor type-1B isoform X1
bone morphogenetic protein receptor type-1B, transcript variant X3
bone morphogenetic protein receptor type-1B isoform X3
RNA-binding protein lark, transcript variant X2
RNA-binding protein lark, transcript variant X3
RNA-binding protein lark, transcript variant X1
stress-activated protein kinase JNK, transcript variant X1
stress-activated protein kinase JNK, transcript variant X2
stress-activated protein kinase JNK isoform X1
stress-activated protein kinase JNK, transcript variant X3
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
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 27 samples with support for all annotated introns
inositol polyphosphate multikinase, transcript variant X2
inositol polyphosphate multikinase, transcript variant X3
PEST proteolytic signal-containing nuclear protein-like, transcript variant X2
PEST proteolytic signal-containing nuclear protein-like, transcript variant X1
PEST proteolytic signal-containing nuclear protein-like isoform X2
PEST proteolytic signal-containing nuclear protein-like isoform X1
uncharacterized LOC123873703, transcript variant X1
uncharacterized LOC123873703, transcript variant X2
uncharacterized protein LOC123873703 isoform X1
uncharacterized protein LOC123873703 isoform X2
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
nucleolar pre-ribosomal-associated protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
stimulator of interferon genes protein, transcript variant X3
stimulator of interferon genes protein, transcript variant X1
stimulator of interferon genes protein, transcript variant X2
stimulator of interferon genes protein isoform X3
stimulator of interferon genes protein isoform X2
stimulator of interferon genes protein isoform X1
zinc finger CCCH domain-containing protein 16-like, transcript variant X1
zinc finger CCCH domain-containing protein 16-like, transcript variant X2
zinc finger CCCH domain-containing protein 16-like
U5 small nuclear ribonucleoprotein 40 kDa protein
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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123873978, transcript variant X1
uncharacterized LOC123873978, transcript variant X3
uncharacterized LOC123873978, transcript variant X2
uncharacterized LOC123873978, transcript variant X4
uncharacterized LOC123873978, 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 13 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 14 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 13 samples with support for all annotated introns
uncharacterized LOC123873970, transcript variant X1
uncharacterized LOC123873970, transcript variant X2
uncharacterized protein LOC123873970 isoform X1
uncharacterized protein LOC123873970 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC123873977, transcript variant X4
uncharacterized LOC123873977, transcript variant X3
uncharacterized LOC123873977, transcript variant X1
uncharacterized LOC123873977, transcript variant X5
uncharacterized LOC123873977, transcript variant X2
uncharacterized LOC123873829, transcript variant X1
uncharacterized LOC123873829, transcript variant X2
uncharacterized protein LOC123873829 isoform X1
uncharacterized protein LOC123873829 isoform X2
microsomal triacylglycerol transfer protein