Pieris napi chromosome 6, ilPieNapi1.2, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Papilionoidea; Pieridae; Pierinae; Pieris.
REFSEQ INFORMATION: The reference sequence is identical to\nFR997700.1.\nAssembly name: ilPieNapi1.2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2022/01/30. The original whole-genome shotgun project has the\naccession CAJQFT000000000.2.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Pieris napi Annotation Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
COORDINATES: polyA evidence [ECO:0006239]
poly(U)-binding-splicing factor half pint, transcript variant X1
poly(U)-binding-splicing factor half pint, transcript variant X2
poly(U)-binding-splicing factor half pint isoform X1
poly(U)-binding-splicing factor half pint isoform X2
protein amalgam-like, transcript variant X2
protein amalgam-like, transcript variant X1
bile salt-activated lipase-like, transcript variant X1
bile salt-activated lipase-like, transcript variant X2
bile salt-activated lipase-like isoform X1
bile salt-activated lipase-like isoform X2
T-lymphocyte activation antigen CD86-like, transcript variant X1
T-lymphocyte activation antigen CD86-like, transcript variant X4
T-lymphocyte activation antigen CD86-like, transcript variant X3
T-lymphocyte activation antigen CD86-like, transcript variant X2
T-lymphocyte activation antigen CD86-like isoform X2
phosphate carrier protein, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
snRNA-activating protein complex subunit 3, transcript variant X2
snRNA-activating protein complex subunit 3, transcript variant X1
snRNA-activating protein complex subunit 3, transcript variant X3
snRNA-activating protein complex subunit 3 isoform X1
snRNA-activating protein complex subunit 3 isoform X2
immediate early response 3-interacting protein 1
zinc finger RNA-binding protein, transcript variant X1
zinc finger RNA-binding protein, transcript variant X4
zinc finger RNA-binding protein, transcript variant X7
zinc finger RNA-binding protein, transcript variant X5
zinc finger RNA-binding protein, transcript variant X3
zinc finger RNA-binding protein, transcript variant X6
zinc finger RNA-binding protein, transcript variant X2
zinc finger RNA-binding protein isoform X1
zinc finger RNA-binding protein isoform X4
zinc finger RNA-binding protein isoform X7
zinc finger RNA-binding protein isoform X5
zinc finger RNA-binding protein isoform X3
zinc finger RNA-binding protein isoform X6
zinc finger RNA-binding protein isoform X2
ecdysone oxidase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
ecdysone oxidase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
poly(A) RNA polymerase gld-2 homolog A-like
neither inactivation nor afterpotential protein G
probable ribosome biogenesis protein RLP24
uncharacterized LOC125050317, transcript variant X2
uncharacterized LOC125050317, transcript variant X3
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized protein LOC125050317 isoform X2
uncharacterized LOC125050317, transcript variant X1
uncharacterized protein LOC125050317 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 3 samples with support for all annotated introns
bumetanide-sensitive sodium-(potassium)-chloride cotransporter, transcript variant X1
bumetanide-sensitive sodium-(potassium)-chloride cotransporter, transcript variant X2
bumetanide-sensitive sodium-(potassium)-chloride cotransporter isoform X1
bumetanide-sensitive sodium-(potassium)-chloride cotransporter isoform X2
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
arrestin domain-containing protein 17-like
arrestin domain-containing protein 1-like
uncharacterized LOC125050180, transcript variant X1
uncharacterized LOC125050180, transcript variant X2
uncharacterized protein LOC125050180 isoform X1
uncharacterized protein LOC125050180 isoform X2
mitochondrial import inner membrane translocase subunit TIM50-C-like
uncharacterized LOC125050122, transcript variant X1
uncharacterized protein LOC125050122 isoform X1
uncharacterized LOC125050122, 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 78 samples with support for all annotated introns
uncharacterized protein LOC125050122 isoform X2
uncharacterized LOC125050590, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125050590, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized protein LOC125050590 isoform X1
uncharacterized protein LOC125050590 isoform X2
uncharacterized LOC125050590, transcript variant X2
ral GTPase-activating protein subunit beta, transcript variant X3
ral GTPase-activating protein subunit beta, transcript variant X5
ral GTPase-activating protein subunit beta, transcript variant X4
ral GTPase-activating protein subunit beta, transcript variant X1
ral GTPase-activating protein subunit beta, transcript variant X6
ral GTPase-activating protein subunit beta, transcript variant X2
ral GTPase-activating protein subunit beta isoform X6
ral GTPase-activating protein subunit beta isoform X3
ral GTPase-activating protein subunit beta isoform X5
ral GTPase-activating protein subunit beta isoform X4
ral GTPase-activating protein subunit beta isoform X2
ral GTPase-activating protein subunit beta isoform X1
B-cell receptor-associated protein 31-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 143 samples with support for all annotated introns
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
collagen and calcium-binding EGF domain-containing protein 1-like, transcript variant X2
collagen and calcium-binding EGF domain-containing protein 1-like, transcript variant X1
collagen and calcium-binding EGF domain-containing protein 1-like isoform X2
collagen and calcium-binding EGF domain-containing protein 1-like isoform X1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
neuroendocrine convertase 1-like, transcript variant X1
neuroendocrine convertase 1-like, transcript variant X2
neuroendocrine convertase 1-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 1 sample with support for all annotated introns
neuroendocrine convertase 1-like isoform X1
neuroendocrine convertase 1-like isoform X2
neuroendocrine convertase 1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
alpha-tocopherol transfer protein-like, transcript variant X1
alpha-tocopherol transfer protein-like isoform X1
alpha-tocopherol transfer protein-like, transcript variant X2
alpha-tocopherol transfer protein-like, transcript variant X3
alpha-tocopherol transfer protein-like isoform X2
ankyrin repeat domain-containing protein 29-like, transcript variant X1
ankyrin repeat domain-containing protein 29-like, transcript variant X2
ankyrin repeat domain-containing protein 29-like isoform X1
ankyrin repeat domain-containing protein 29-like isoform X2
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
heterogeneous nuclear ribonucleoprotein 27C, transcript variant X4
heterogeneous nuclear ribonucleoprotein 27C, transcript variant X3
heterogeneous nuclear ribonucleoprotein 27C, transcript variant X2
heterogeneous nuclear ribonucleoprotein 27C, transcript variant X1
heterogeneous nuclear ribonucleoprotein 27C, transcript variant X7
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 28 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein 27C isoform X3
heterogeneous nuclear ribonucleoprotein 27C isoform X4
heterogeneous nuclear ribonucleoprotein 27C isoform X2
heterogeneous nuclear ribonucleoprotein 27C isoform X1
heterogeneous nuclear ribonucleoprotein 27C isoform X7
heterogeneous nuclear ribonucleoprotein 27C, transcript variant X6
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 10 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein 27C isoform X6
heterogeneous nuclear ribonucleoprotein 27C, transcript variant X8
heterogeneous nuclear ribonucleoprotein 27C, transcript variant X5
heterogeneous nuclear ribonucleoprotein 27C isoform X8
heterogeneous nuclear ribonucleoprotein 27C isoform X5
uncharacterized LOC125050168, transcript variant X3
uncharacterized LOC125050168, 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 4 samples with support for all annotated introns
uncharacterized LOC125050168, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125050168, 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 11 samples with support for all annotated introns
uncharacterized protein LOC125050168 isoform X1
uncharacterized protein LOC125050168 isoform X4
uncharacterized protein LOC125050168 isoform X2
uncharacterized protein LOC125050168 isoform X3
serine protease snake-like, transcript variant X3
serine protease snake-like, transcript variant X1
serine protease snake-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 158 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
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
acetylcholine receptor subunit alpha-like 2
acetylcholine receptor subunit alpha-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 255 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
acetylcholine receptor subunit beta-like 2, transcript variant X4
acetylcholine receptor subunit beta-like 2, transcript variant X2
acetylcholine receptor subunit beta-like 2, transcript variant X5
acetylcholine receptor subunit beta-like 2, transcript variant X3
acetylcholine receptor subunit beta-like 2, transcript variant X1
acetylcholine receptor subunit beta-like 2 isoform X4
acetylcholine receptor subunit beta-like 2 isoform X2
acetylcholine receptor subunit beta-like 2 isoform X5
acetylcholine receptor subunit beta-like 2 isoform X3
acetylcholine receptor subunit beta-like 2 isoform X1
acetylcholine receptor subunit beta-like 2, transcript variant X6
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 46 samples with support for all annotated introns
acetylcholine receptor subunit beta-like 2 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC125050373, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125050373, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 75 samples with support for all annotated introns
uncharacterized LOC125050243, 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 152 samples with support for all annotated introns
uncharacterized LOC125050243, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
uncharacterized LOC125050243, 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 50 samples with support for all annotated introns
SKI family transcriptional corepressor 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 6-like
uncharacterized LOC125050175, transcript variant X1
uncharacterized LOC125050175, transcript variant X2
protein fem-1 homolog CG6966, transcript variant X3
protein fem-1 homolog CG6966, transcript variant X1
protein fem-1 homolog CG6966, transcript variant X2
protein groucho-like, transcript variant X1
protein groucho-like, transcript variant X3
protein groucho-like, transcript variant X4
protein groucho-like, transcript variant X2
protein groucho-like, transcript variant X5
protein groucho-like, transcript variant X8
protein groucho-like, transcript variant X6
protein groucho-like, transcript variant X7
protein groucho-like, transcript variant X9
protein groucho-like, transcript variant X10
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
conserved oligomeric Golgi complex subunit 1, transcript variant X1
conserved oligomeric Golgi complex subunit 1 isoform X1
conserved oligomeric Golgi complex subunit 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
conserved oligomeric Golgi complex subunit 1 isoform X2
ribose-phosphate pyrophosphokinase 1-like
maltase-glucoamylase-like, transcript variant X1
maltase-glucoamylase-like, transcript variant X2
maltase-glucoamylase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
lysosomal alpha-glucosidase-like isoform X3
adipokinetic hormone/corazonin-related peptide receptor variant I-like
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
actin-binding Rho-activating protein-like
protein unc-13 homolog A, transcript variant X7
protein unc-13 homolog A, transcript variant X6
protein unc-13 homolog A, transcript variant X3
protein unc-13 homolog A, transcript variant X4
protein unc-13 homolog A, transcript variant X5
protein unc-13 homolog A, transcript variant X2
protein unc-13 homolog A, transcript variant X1
protein unc-13 homolog A, transcript variant X9
protein unc-13 homolog A, transcript variant X12
protein unc-13 homolog A, transcript variant X10
protein unc-13 homolog A, transcript variant X11
protein unc-13 homolog A, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
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 34 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
protein prenyltransferase alpha subunit repeat-containing protein 1
ras GTPase-activating protein 1, transcript variant X1
ras GTPase-activating protein 1, transcript variant X2
ras GTPase-activating protein 1 isoform X2
ras GTPase-activating protein 1 isoform X1
dmX-like protein 2, transcript variant X5
dmX-like protein 2, transcript variant X1
dmX-like protein 2, transcript variant X8
dmX-like protein 2, transcript variant X7
dmX-like protein 2, transcript variant X3
dmX-like protein 2, transcript variant X10
dmX-like protein 2, transcript variant X2
dmX-like protein 2, transcript variant X9
dmX-like protein 2, transcript variant X6
dmX-like protein 2, transcript variant X4
E3 ubiquitin-protein ligase arih1l, 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 159 samples with support for all annotated introns
E3 ubiquitin-protein ligase arih1l, 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 169 samples with support for all annotated introns
E3 ubiquitin-protein ligase ariadne-1 isoform X1
E3 ubiquitin-protein ligase arih1l isoform X2
sodium channel protein para, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sodium channel protein para, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium channel protein para, transcript variant X37
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sodium channel protein para, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sodium channel protein para, transcript variant X2
sodium channel protein para, transcript variant X19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sodium channel protein para, transcript variant X25
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sodium channel protein para, transcript variant X13
sodium channel protein para, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sodium channel protein para, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sodium channel protein para, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sodium channel protein para, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sodium channel protein para, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sodium channel protein para, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
sodium channel protein para, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
sodium channel protein para, transcript variant X35
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sodium channel protein para, transcript variant X28
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sodium channel protein para, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sodium channel protein para, transcript variant X21
sodium channel protein para, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sodium channel protein para, transcript variant X34
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium channel protein para, transcript variant X36
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sodium channel protein para, transcript variant X24
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
sodium channel protein para, transcript variant X33
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sodium channel protein para, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
sodium channel protein para, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sodium channel protein para, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
sodium channel protein para, transcript variant X23
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
sodium channel protein para, transcript variant X27
sodium channel protein para, transcript variant X20
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sodium channel protein para, transcript variant X26
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
sodium channel protein para, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
sodium channel protein para, transcript variant X29
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
sodium channel protein para, transcript variant X22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
sodium channel protein para, transcript variant X30
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
sodium channel protein para, transcript variant X31
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium channel protein para, transcript variant X32
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
unconventional myosin-IXAa-like, transcript variant X1
unconventional myosin-IXAa-like, transcript variant X2
unconventional myosin-IXAa-like, transcript variant X5
unconventional myosin-IXAa-like, transcript variant X3
unconventional myosin-IXAa-like, transcript variant X4
unconventional myosin-IXAa-like, transcript variant X6
unconventional myosin-IXAa-like isoform X1
unconventional myosin-IXAa-like isoform X2
unconventional myosin-IXa-like isoform X5
unconventional myosin-IXAa-like isoform X3
unconventional myosin-IXAa-like isoform X4
unconventional myosin-IXa-like isoform X6
unconventional myosin-IXAa-like, transcript variant X7
unconventional myosin-IXAa-like isoform X7
probable phospholipid-transporting ATPase IM
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: probable phospholipid-transporting ATPase IM
methyl-CpG-binding domain protein 2, transcript variant X1
methyl-CpG-binding domain protein 2, transcript variant X2
methyl-CpG-binding domain protein 2 isoform X1
methyl-CpG-binding domain protein 2 isoform X2
GPI mannosyltransferase 2, transcript variant X3
GPI mannosyltransferase 2, transcript variant X1
GPI mannosyltransferase 2, transcript variant X2
tubulin polyglutamylase TTLL13-like, transcript variant X1
tubulin polyglutamylase TTLL13-like, transcript variant X2
tubulin polyglutamylase TTLL13-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
tyrosine-protein kinase CSK, transcript variant X1
tyrosine-protein kinase CSK, transcript variant X3
tyrosine-protein kinase CSK, transcript variant X2
cytochrome c oxidase assembly protein COX16 homolog, mitochondrial
ADAM 17-like protease, transcript variant X2
ADAM 17-like protease, transcript variant X1
dynein heavy chain, cytoplasmic, transcript variant X5
dynein heavy chain, cytoplasmic, transcript variant X3
dynein heavy chain, cytoplasmic, transcript variant X4
dynein heavy chain, cytoplasmic, transcript variant X1
dynein heavy chain, cytoplasmic, transcript variant X2
dynein heavy chain, cytoplasmic isoform X5
dynein heavy chain, cytoplasmic isoform X3
dynein heavy chain, cytoplasmic isoform X4
dynein heavy chain, cytoplasmic isoform X1
dynein heavy chain, cytoplasmic isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins
hemicentin-2-like, transcript variant X1
hemicentin-2-like, transcript variant X2
hemicentin-2-like, transcript variant X3
hemicentin-2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 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: 13 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: 100% coverage of the annotated genomic feature by RNAseq alignments
heterogeneous nuclear ribonucleoprotein M-like, transcript variant X7
heterogeneous nuclear ribonucleoprotein M-like, transcript variant X6
heterogeneous nuclear ribonucleoprotein M-like, transcript variant X4
heterogeneous nuclear ribonucleoprotein M-like, transcript variant X5
heterogeneous nuclear ribonucleoprotein M-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein M-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein M-like, transcript variant X3
heterogeneous nuclear ribonucleoprotein M-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 169 samples with support for all annotated introns
regulator of nonsense transcripts 1-like
A disintegrin and metalloproteinase with thrombospondin motifs 7
G kinase-anchoring protein 1-like, transcript variant X2
G kinase-anchoring protein 1-like isoform X2
G kinase-anchoring protein 1-like, transcript variant X1
G kinase-anchoring protein 1-like, transcript variant X3
G kinase-anchoring protein 1-like, transcript variant X4
G kinase-anchoring protein 1-like isoform X1
G kinase-anchoring protein 1-like isoform X3
uncharacterized LOC125050142, transcript variant X2
uncharacterized LOC125050142, transcript variant X1
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 3-like
dynein regulatory complex subunit 6-like
mitochondrial import inner membrane translocase subunit Tim29
probable 39S ribosomal protein L23, mitochondrial
tyrosine-protein phosphatase non-receptor type 9, transcript variant X2
tyrosine-protein phosphatase non-receptor type 9 isoform X2
tyrosine-protein phosphatase non-receptor type 9, transcript variant X1
tyrosine-protein phosphatase non-receptor type 9 isoform X1
tyrosine-protein phosphatase non-receptor type 9, transcript variant X3
tyrosine-protein phosphatase non-receptor type 9 isoform X3
bumetanide-sensitive sodium-(potassium)-chloride cotransporter-like
bumetanide-sensitive sodium-(potassium)-chloride cotransporter
tRNA-uridine aminocarboxypropyltransferase 2, transcript variant X2
tRNA-uridine aminocarboxypropyltransferase 2, transcript variant X3
tRNA-uridine aminocarboxypropyltransferase 2, transcript variant X1
tRNA-uridine aminocarboxypropyltransferase 2 isoform X2
tRNA-uridine aminocarboxypropyltransferase 2 isoform X1
tRNA-uridine aminocarboxypropyltransferase 2 isoform X3
histone-lysine N-methyltransferase ash1, transcript variant X1
histone-lysine N-methyltransferase ash1 isoform X1
histone-lysine N-methyltransferase ash1, transcript variant X2
histone-lysine N-methyltransferase ash1 isoform X2
synaptic vesicle glycoprotein 2B-like, transcript variant X4
synaptic vesicle glycoprotein 2B-like, transcript variant X2
synaptic vesicle glycoprotein 2B-like, transcript variant X1
synaptic vesicle glycoprotein 2B-like isoform X1
synaptic vesicle glycoprotein 2B-like, transcript variant X3
synaptic vesicle glycoprotein 2B-like isoform X2
ejaculatory bulb-specific protein 3, transcript variant X2
ejaculatory bulb-specific protein 3, transcript variant X1
uncharacterized protein LOC125050291 isoform X2
ejaculatory bulb-specific protein 3 isoform X1
protein pygopus-like, transcript variant X4
protein pygopus-like, transcript variant X3
protein pygopus-like, transcript variant X2
protein pygopus-like, transcript variant X1
ubiquitin-like modifier-activating enzyme ATG7
uncharacterized LOC125050215, transcript variant X1
uncharacterized LOC125050215, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125050215, transcript variant X2
uncharacterized protein LOC125050215 isoform X1
uncharacterized protein LOC125050215 isoform X2
geranylgeranyl transferase type-1 subunit beta, transcript variant X1
geranylgeranyl transferase type-1 subunit beta isoform X1
geranylgeranyl transferase type-1 subunit beta, transcript variant X2
geranylgeranyl transferase type-1 subunit beta isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 55% 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 44% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial inner membrane protein OXA1L
U3 small nucleolar RNA-associated protein 15 homolog
DENN domain-containing protein Crag, 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 108 samples with support for all annotated introns
DENN domain-containing protein Crag, 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 15 samples with support for all annotated introns
DENN domain-containing protein Crag, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 110 samples with support for all annotated introns
DENN domain-containing protein Crag, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 124 samples with support for all annotated introns
DENN domain-containing protein Crag, 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 125 samples with support for all annotated introns
DENN domain-containing protein Crag, 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 12 samples with support for all annotated introns
DENN domain-containing protein Crag isoform X1
DENN domain-containing protein Crag isoform X3
DENN domain-containing protein Crag isoform X2
DENN domain-containing protein Crag isoform X4
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125050080, transcript variant X2
uncharacterized LOC125050080, transcript variant X1
uncharacterized LOC125050080, transcript variant X3
uncharacterized protein LOC125050080 isoform X2
uncharacterized protein LOC125050080 isoform 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 169 samples with support for all annotated introns
uncharacterized LOC125050144, transcript variant X1
uncharacterized LOC125050144, transcript variant X2
uncharacterized protein LOC125050144 isoform X1
uncharacterized protein LOC125050144 isoform X2
furin-like protease 1, isoforms 1/1-X/2, transcript variant X1
furin-like protease 1, isoforms 1/1-X/2, transcript variant X7
furin-like protease 1, isoforms 1/1-X/2, transcript variant X6
furin-like protease 1, isoforms 1/1-X/2, transcript variant X2
furin-like protease 1, isoforms 1/1-X/2, transcript variant X3
furin-like protease 1, isoforms 1/1-X/2, transcript variant X4
furin-like protease 1, isoforms 1/1-X/2, transcript variant X5
furin-like protease 1, isoforms 1/1-X/2 isoform X3
dual specificity mitogen-activated protein kinase kinase dSOR1, transcript variant X2
dual specificity mitogen-activated protein kinase kinase dSOR1, transcript variant X1
dual specificity mitogen-activated protein kinase kinase dSOR1
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 127 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 134 samples with support for all annotated introns
protein giant-lens, transcript variant X1
protein giant-lens, transcript variant X2
limbic system-associated membrane protein-like, transcript variant X2
limbic system-associated membrane protein-like, transcript variant X1
limbic system-associated membrane protein-like, transcript variant X3
limbic system-associated membrane protein-like
G-patch domain and KOW motifs-containing protein
uncharacterized membrane protein C20F10.07-like, transcript variant X1
uncharacterized membrane protein C20F10.07-like, transcript variant X3
uncharacterized membrane protein C20F10.07-like, transcript variant X2
membrane-anchored lipid-binding protein LAM4-like isoform X1
uncharacterized membrane protein C20F10.07-like isoform X3
uncharacterized membrane protein C20F10.07-like isoform X2
uncharacterized LOC125050100, transcript variant X1
uncharacterized protein LOC125050100 isoform X1
uncharacterized LOC125050100, transcript variant X2
uncharacterized protein LOC125050100 isoform X2
death-inducer obliterator 1-like, transcript variant X2
death-inducer obliterator 1-like, transcript variant X1
RNA polymerase II elongation factor ELL, transcript variant X1
RNA polymerase II elongation factor ELL, transcript variant X2
RNA polymerase II elongation factor ELL isoform X2
RNA polymerase II elongation factor ELL isoform X1
putative uncharacterized protein DDB_G0282499
uncharacterized protein DDB_G0283357-like, transcript variant X2
uncharacterized protein DDB_G0283357-like, transcript variant X1
uncharacterized protein DDB_G0283357-like isoform X2
uncharacterized protein DDB_G0283357-like isoform X1
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
small conductance calcium-activated potassium channel protein, transcript variant X1
small conductance calcium-activated potassium channel protein, transcript variant X3
small conductance calcium-activated potassium channel protein, transcript variant X4
small conductance calcium-activated potassium channel protein, transcript variant X5
small conductance calcium-activated potassium channel protein, transcript variant X2
small conductance calcium-activated potassium channel protein, transcript variant X6
small conductance calcium-activated potassium channel protein, transcript variant X7
small conductance calcium-activated potassium channel protein, transcript variant X8
small conductance calcium-activated potassium channel protein isoform X1
small conductance calcium-activated potassium channel protein isoform X3
small conductance calcium-activated potassium channel protein isoform X4
small conductance calcium-activated potassium channel protein isoform X5
small conductance calcium-activated potassium channel protein isoform X2
small conductance calcium-activated potassium channel protein isoform X6
small conductance calcium-activated potassium channel protein isoform X7
small conductance calcium-activated potassium channel protein isoform X8
gonadotropin-releasing hormone receptor, transcript variant X2
gonadotropin-releasing hormone receptor, transcript variant X1
gonadotropin-releasing hormone receptor isoform X1
gonadotropin-releasing hormone receptor isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
cell adhesion molecule 1, transcript variant X1
cell adhesion molecule 1, transcript variant X3
cell adhesion molecule 1, transcript variant X2
beta-ureidopropionase-like, transcript variant X5
beta-ureidopropionase-like, transcript variant X3
beta-ureidopropionase-like, transcript variant X1
beta-ureidopropionase-like, transcript variant X4
beta-ureidopropionase-like, transcript variant X2
eukaryotic translation initiation factor 2 subunit 2
28S ribosomal protein S30, mitochondrial, transcript variant X2
28S ribosomal protein S30, mitochondrial, transcript variant X1
28S ribosomal protein S30, mitochondrial
leucine-rich repeat protein 1, transcript variant X1
leucine-rich repeat protein 1 isoform X1
leucine-rich repeat protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 136 samples with support for all annotated introns
leucine-rich repeat protein 1 isoform X2
nonsense-mediated mRNA decay factor SMG5, transcript variant X1
nonsense-mediated mRNA decay factor SMG5, transcript variant X2
nonsense-mediated mRNA decay factor SMG5
39S ribosomal protein L34, mitochondrial
mitochondrial outer membrane protein SLC25A46-like, transcript variant X2
mitochondrial outer membrane protein SLC25A46-like, transcript variant X1
mitochondrial outer membrane protein SLC25A46-like isoform X2
mitochondrial outer membrane protein SLC25A46-like isoform X1
uncharacterized LOC125050296, transcript variant X1
uncharacterized LOC125050296, transcript variant X2
uncharacterized protein LOC125050296 isoform X1
uncharacterized protein LOC125050296 isoform X2
voltage-dependent calcium channel subunit alpha-2/delta-4-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 12 samples with support for all annotated introns
uncharacterized PE-PGRS family protein PE_PGRS54-like
protein AF-9-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 142 samples with support for all annotated introns
protein AF-9-like, transcript variant X1
protein AF-9-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 77 samples with support for all annotated introns
uncharacterized protein LOC125050460 isoform X1
uncharacterized protein LOC125050460 isoform X2
protein AF-9-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 3-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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
WD repeat-containing protein 61-like, transcript variant X2
WD repeat-containing protein 61-like, transcript variant X1
WD repeat-containing protein 61-like isoform X2
WD repeat-containing protein 61-like isoform X1
secretory carrier-associated membrane protein 5B, transcript variant X1
secretory carrier-associated membrane protein 5B, transcript variant X2
secretory carrier-associated membrane protein 5B isoform X2
secretory carrier-associated membrane protein 5B 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 65 samples with support for all annotated introns
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase 2, mitochondrial, transcript variant X2
bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase 2, mitochondrial, transcript variant X1
bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase 2, mitochondrial, transcript variant X3
bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase 2, mitochondrial isoform X2
bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase 2, mitochondrial isoform X3
bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase 2, mitochondrial 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
probable ATP-dependent RNA helicase DHX34
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 150 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
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 94 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 130 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 129 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
uncharacterized LOC125050377, transcript variant X1
uncharacterized LOC125050377, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 67% coverage of the annotated genomic feature by RNAseq alignments, including 146 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 45% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125050297, transcript variant X1
uncharacterized protein LOC125050297 isoform X1
uncharacterized LOC125050297, transcript variant X2
uncharacterized protein LOC125050297 isoform X2
aldehyde dehydrogenase, mitochondrial-like
NAD-dependent protein deacetylase Sirt6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 53 samples with support for all annotated introns
NAD-dependent protein deacetylase Sirt6, 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 168 samples with support for all annotated introns
NAD-dependent protein deacetylase Sirt6 isoform X1
NAD-dependent protein deacetylase Sirt6 isoform X2
tropomyosin-1, isoforms 9A/A/B isoform X21
tropomyosin-1, isoforms 9A/A/B isoform X22
tropomyosin-1, isoforms 9A/A/B isoform X20
tropomyosin-1, isoforms 9A/A/B isoform X11
tropomyosin-1, isoforms 9A/A/B isoform X24
tropomyosin-1, isoforms 9A/A/B isoform X23
tumor necrosis factor alpha-induced protein 8-like protein
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 120 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 134 samples with support for all annotated introns
dual specificity protein kinase splA-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 95 samples with support for all annotated introns
dual specificity protein kinase splA-like, transcript variant X1
dual specificity protein kinase splA-like, transcript variant X2
dual specificity protein kinase splA-like isoform X2
uncharacterized protein LOC125050305 isoform X4
dual specificity protein kinase splA-like, transcript variant X3
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 13
very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase
phosphatidylinositol 5-phosphate 4-kinase type-2 alpha, transcript variant X1
phosphatidylinositol 5-phosphate 4-kinase type-2 alpha, transcript variant X2
phosphatidylinositol 5-phosphate 4-kinase type-2 alpha isoform X1
phosphatidylinositol 5-phosphate 4-kinase type-2 alpha isoform X2
uncharacterized LOC125050496, transcript variant X2
uncharacterized LOC125050496, 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
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COUP transcription factor 2, transcript variant X2
COUP transcription factor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 124 samples with support for all annotated introns
piggyBac transposable element-derived protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 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 54 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 34 samples with support for all annotated introns
triosephosphate isomerase, transcript variant X1
triosephosphate isomerase, transcript variant X2
histone H4 transcription factor, transcript variant X3
histone H4 transcription factor, transcript variant X1
histone H4 transcription factor, transcript variant X2
spermine oxidase-like, transcript variant X3
spermine oxidase-like, transcript variant X1
spermine oxidase-like, transcript variant X2
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
esterase FE4-like, transcript variant X4
esterase FE4-like, transcript variant X1
esterase FE4-like, transcript variant X5
esterase FE4-like, transcript variant X2
esterase FE4-like, transcript variant X3
uncharacterized LOC125050582, transcript variant X2
uncharacterized LOC125050582, transcript variant X1
uncharacterized protein LOC125050582 isoform X2
uncharacterized protein LOC125050582 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125050464, transcript variant X2
uncharacterized LOC125050464, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
A-kinase anchor protein 17A, transcript variant X2
A-kinase anchor protein 17A, transcript variant X1
A-kinase anchor protein 17A, transcript variant X3
A-kinase anchor protein 17A, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
A-kinase anchor protein 17A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 82 samples with support for all annotated introns
uncharacterized LOC125050221, transcript variant X2
uncharacterized LOC125050221, transcript variant X1
uncharacterized protein LOC125050221 isoform X2
uncharacterized protein LOC125050221 isoform X1
zinc finger protein ZFP2-like, transcript variant X1
zinc finger protein ZFP2-like isoform X1
zinc finger protein ZFP2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 60 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 29 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 132 samples with support for all annotated introns
zinc finger protein ZFP2-like isoform X2
zinc finger protein ZFP2-like, transcript variant X3
zinc finger protein ZFP2-like isoform X3
zinc finger protein 660-like, transcript variant X1
zinc finger protein 660-like, transcript variant X2
zinc finger protein 431-like, transcript variant X1
zinc finger protein 431-like, transcript variant X2
omega-amidase NIT2, transcript variant X2
omega-amidase NIT2, transcript variant X1
general transcription and DNA repair factor IIH helicase subunit XPD
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 118 samples with support for all annotated introns
RNA-binding protein NOB1, transcript variant X1
RNA-binding protein NOB1, transcript variant X2
FAM172 family protein homolog CG10038, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 169 samples with support for all annotated introns
FAM172 family protein homolog CG10038, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 138 samples with support for all annotated introns
FAM172 family protein homolog CG10038, 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 96 samples with support for all annotated introns
FAM172 family protein homolog CG10038 isoform X1
FAM172 family protein homolog CG10038 isoform X3
FAM172 family protein homolog CG10038 isoform X2
glycosylated lysosomal membrane protein A-like
probable tRNA (guanine(26)-N(2))-dimethyltransferase, transcript variant X3
probable tRNA (guanine(26)-N(2))-dimethyltransferase, transcript variant X1
probable tRNA (guanine(26)-N(2))-dimethyltransferase, transcript variant X2
probable tRNA (guanine(26)-N(2))-dimethyltransferase, transcript variant X4
probable tRNA (guanine(26)-N(2))-dimethyltransferase isoform X2
probable tRNA (guanine(26)-N(2))-dimethyltransferase isoform X1
probable tRNA (guanine(26)-N(2))-dimethyltransferase isoform X3
lon protease homolog, mitochondrial, transcript variant X1
lon protease homolog, mitochondrial, transcript variant X2
lon protease homolog, mitochondrial isoform X1
lon protease homolog, mitochondrial isoform X2
conserved oligomeric Golgi complex subunit 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
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 66 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
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 161 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 156 samples with support for all annotated introns
ras-specific guanine nucleotide-releasing factor 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ras-specific guanine nucleotide-releasing factor 1-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 2 samples with support for all annotated introns
ras-specific guanine nucleotide-releasing factor 1-like, transcript variant X3
ras-specific guanine nucleotide-releasing factor 1-like, transcript variant X5
ras-specific guanine nucleotide-releasing factor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ras-specific guanine nucleotide-releasing factor 1-like isoform X4
ras-specific guanine nucleotide-releasing factor 1-like isoform X2
ras-specific guanine nucleotide-releasing factor 1-like isoform X3
ras-specific guanine nucleotide-releasing factor 1-like isoform X5
ras-specific guanine nucleotide-releasing factor 1-like isoform X1
BTB/POZ domain-containing protein 2-like
katanin p60 ATPase-containing subunit A-like 2
phosphatidylinositol 3-kinase catalytic subunit type 3, 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 156 samples with support for all annotated introns
phosphatidylinositol 3-kinase catalytic subunit type 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 129 samples with support for all annotated introns
phosphatidylinositol 3-kinase catalytic subunit type 3 isoform X1
phosphatidylinositol 3-kinase catalytic subunit type 3 isoform X2
phosphatidylinositol 3-kinase catalytic subunit type 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
phosphatidylinositol 3-kinase catalytic subunit type 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 56 samples with support for all annotated introns
phosphatidylinositol 3-kinase catalytic subunit type 3 isoform X3
vacuolar protein sorting-associated protein 33B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 161 samples with support for all annotated introns
probable isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial, transcript variant X3
probable isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial, transcript variant X4
probable isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial isoform X4
probable isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial isoform X3
probable isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial, transcript variant X1
probable isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial, transcript variant X2
probable isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial isoform X2
probable isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial isoform X1
U11/U12 small nuclear ribonucleoprotein 59 kDa protein-like
DDB1- and CUL4-associated factor 12 homolog
geranylgeranyl pyrophosphate synthase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
myogenesis-regulating glycosidase, transcript variant X1
myogenesis-regulating glycosidase, transcript variant X2
myogenesis-regulating glycosidase, transcript variant X3
myogenesis-regulating glycosidase, transcript variant X4
myogenesis-regulating glycosidase, transcript variant X5
myogenesis-regulating glycosidase isoform X1
myogenesis-regulating glycosidase isoform X2
myogenesis-regulating glycosidase isoform X3
myogenesis-regulating glycosidase isoform X4
ATP-dependent Clp protease ATP-binding subunit clpX-like, mitochondrial, transcript variant X4
ATP-dependent Clp protease ATP-binding subunit clpX-like, mitochondrial, transcript variant X3
ATP-dependent Clp protease ATP-binding subunit clpX-like, mitochondrial, transcript variant X1
ATP-dependent Clp protease ATP-binding subunit clpX-like, mitochondrial, transcript variant X2
ATP-dependent Clp protease ATP-binding subunit clpX-like, mitochondrial isoform X2
ATP-dependent Clp protease ATP-binding subunit clpX-like, mitochondrial isoform X3
ATP-dependent Clp protease ATP-binding subunit clpX-like, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
probable mitochondrial-processing peptidase subunit alpha-2, chloroplastic/mitochondrial
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
G patch domain-containing protein 1 homolog
transmembrane protein 68, transcript variant X2
transmembrane protein 68, transcript variant X1
mediator of RNA polymerase II transcription subunit 25, transcript variant X2
mediator of RNA polymerase II transcription subunit 25, transcript variant X3
mediator of RNA polymerase II transcription subunit 25, transcript variant X1
mediator of RNA polymerase II transcription subunit 25, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 102 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 25 isoform X2
mediator of RNA polymerase II transcription subunit 25 isoform X3
mediator of RNA polymerase II transcription subunit 25 isoform X1
mediator of RNA polymerase II transcription subunit 25 isoform X4
peptidyl-prolyl cis-trans isomerase FKBP1A-like
nuclear inhibitor of protein phosphatase 1
myrosinase 1-like, transcript variant X2
myrosinase 1-like, 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 40 samples with support for all annotated introns
uncharacterized LOC125050300, transcript variant X2
uncharacterized LOC125050300, transcript variant X1
uncharacterized LOC125050303, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
uncharacterized LOC125050303, transcript variant X2
snake venom 5'-nucleotidase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 samples with support for all annotated introns
snake venom 5'-nucleotidase, 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 60 samples with support for all annotated introns
phospholipase A1-like, transcript variant X2
phospholipase A1-like, transcript variant X1
phospholipase A1-like, transcript variant X3
piggyBac transposable element-derived protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
transfer RNA arginine (anticodon UCU); 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: 1 Protein, and 76% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
gastrulation defective protein 1 homolog
39S ribosomal protein L39, mitochondrial
EKC/KEOPS complex subunit TP53RK, transcript variant X1
EKC/KEOPS complex subunit TP53RK, transcript variant X2
coactosin-like 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 169 samples with support for all annotated introns
coactosin-like protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: probable aminopeptidase NPEPL1
oxysterol-binding protein-related protein 6-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
oxysterol-binding protein-related protein 6-like, transcript variant X6
oxysterol-binding protein-related protein 6-like, transcript variant X1
oxysterol-binding protein-related protein 6-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
oxysterol-binding protein-related protein 6-like, transcript variant X2
oxysterol-binding protein-related protein 6-like, transcript variant X4
oxysterol-binding protein-related protein 6-like, transcript variant X5
oxysterol-binding protein-related protein 6-like isoform X7
oxysterol-binding protein-related protein 3-like isoform X6
oxysterol-binding protein-related protein 3-like isoform X5
oxysterol-binding protein-related protein 3-like isoform X4
oxysterol-binding protein-related protein 3-like isoform X2
oxysterol-binding protein-related protein 3-like isoform X1
oxysterol-binding protein-related protein 3-like isoform X3
uncharacterized LOC125050184, transcript variant X1
uncharacterized LOC125050184, transcript variant X2
lipase member H-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
lipase member H-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
tigger transposable element-derived protein 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 169 samples with support for all annotated introns
oxidative stress-induced growth inhibitor 1-like, transcript variant X2
oxidative stress-induced growth inhibitor 1-like, transcript variant X1
oxidative stress-induced growth inhibitor 1-like
trafficking protein particle complex subunit 2-like protein
uridine 5'-monophosphate synthase-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 154 samples with support for all annotated introns
uridine 5'-monophosphate synthase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 151 samples with support for all annotated introns
uridine 5'-monophosphate synthase-like isoform X1
uridine 5'-monophosphate synthase-like isoform X2
activin receptor type-1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 158 samples with support for all annotated introns
activin receptor type-1, 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 48 samples with support for all annotated introns
activin receptor type-1, 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 119 samples with support for all annotated introns
activin receptor type-1, 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 47 samples with support for all annotated introns
uncharacterized LOC125050456, transcript variant X2
uncharacterized LOC125050456, transcript variant X1
uncharacterized protein LOC125050456 isoform X1
uncharacterized protein LOC125050456 isoform X2
cilia- and flagella-associated protein 45-like
S-adenosylmethionine mitochondrial carrier protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 168 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 134 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 66 samples with support for all annotated introns
uncharacterized LOC125050524, transcript variant X6
uncharacterized LOC125050524, transcript variant X3
uncharacterized LOC125050524, transcript variant X5
uncharacterized LOC125050524, transcript variant X4
uncharacterized LOC125050524, transcript variant X2
uncharacterized LOC125050524, transcript variant X1
uncharacterized protein LOC125050524 isoform X6
uncharacterized protein LOC125050524 isoform X3
uncharacterized protein LOC125050524 isoform X5
uncharacterized protein LOC125050524 isoform X4
uncharacterized protein LOC125050524 isoform X2
uncharacterized protein LOC125050524 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
pancreatic triacylglycerol lipase-like, transcript variant X2
pancreatic triacylglycerol lipase-like, transcript variant X3
pancreatic triacylglycerol lipase-like, transcript variant X1
pancreatic triacylglycerol lipase-like isoform X1
pancreatic triacylglycerol lipase-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
protein 4.1 homolog, transcript variant X4
protein 4.1 homolog, transcript variant X3
protein 4.1 homolog, transcript variant X1
protein 4.1 homolog, transcript variant X2
protein 4.1 homolog, transcript variant X5
protein 4.1 homolog, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
vacuolar protein sorting-associated protein 28 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
replication stress response regulator SDE2
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 23 samples with support for all annotated introns
uncharacterized LOC125050718, transcript variant X2
uncharacterized LOC125050718, transcript variant X5
uncharacterized LOC125050718, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125050718, transcript variant X3
uncharacterized LOC125050718, transcript variant X4
uncharacterized protein LOC125050718 isoform X2
uncharacterized protein LOC125050718 isoform X1
uncharacterized protein LOC125050718 isoform X3
uncharacterized protein LOC125050718 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
uncharacterized LOC125050094, 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
uncharacterized LOC125050094, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125050094, 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 12 samples with support for all annotated introns
uncharacterized protein LOC125050094 isoform X2
uncharacterized protein LOC125050094 isoform 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
non-canonical poly(A) RNA polymerase protein Trf4-1-like
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 33 samples with support for all annotated introns
prolow-density lipoprotein receptor-related protein 1
counting factor associated protein D-like
zinc finger protein ubi-d4, transcript variant X2
transfer RNA leucine (anticodon UAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein ubi-d4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 87 samples with support for all annotated introns
zinc finger protein ubi-d4, 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 135 samples with support for all annotated introns
nuclear transcription factor Y subunit gamma, 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 103 samples with support for all annotated introns
nuclear transcription factor Y subunit gamma, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 162 samples with support for all annotated introns
nuclear transcription factor Y subunit gamma isoform X1
nuclear transcription factor Y subunit gamma isoform X2
RNA-binding protein fusilli, transcript variant X2
RNA-binding protein fusilli, transcript variant X3
RNA-binding protein fusilli, 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 146 samples with support for all annotated introns
guanine nucleotide-binding protein G(s) subunit alpha, transcript variant X3
guanine nucleotide-binding protein G(s) subunit alpha, transcript variant X2
guanine nucleotide-binding protein G(s) subunit alpha, transcript variant X1
guanine nucleotide-binding protein G(s) subunit alpha
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 160 samples with support for all annotated introns
protein tyrosine phosphatase domain-containing protein 1-like
WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing 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 35 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 57 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 68 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 69 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 114 samples with support for all annotated introns
phosphoenolpyruvate carboxykinase [GTP]-like, transcript variant X2
phosphoenolpyruvate carboxykinase [GTP]-like isoform X2
phosphoenolpyruvate carboxykinase [GTP]-like, transcript variant X1
phosphoenolpyruvate carboxykinase [GTP]-like isoform X1
sister chromatid cohesion protein DCC1, transcript variant X1
sister chromatid cohesion protein DCC1, transcript variant X2
sister chromatid cohesion protein DCC1 isoform X1
sister chromatid cohesion protein DCC1 isoform X2
mitochondrial import inner membrane translocase subunit Tim23
stromal membrane-associated protein 1, transcript variant X3
stromal membrane-associated protein 1, transcript variant X2
stromal membrane-associated protein 1, transcript variant X1
stromal membrane-associated protein 1 isoform X3
stromal membrane-associated protein 2 isoform X2
stromal membrane-associated protein 1 isoform X1
phosphoinositide 3-kinase regulatory subunit 4, transcript variant X2
phosphoinositide 3-kinase regulatory subunit 4, transcript variant X1
phosphoinositide 3-kinase regulatory subunit 4 isoform X1
phosphoinositide 3-kinase regulatory subunit 4 isoform X2
uncharacterized LOC125050289, transcript variant X1
uncharacterized LOC125050289, transcript variant X2
uncharacterized LOC125050289, transcript variant X3
uncharacterized LOC125050289, transcript variant X4
uncharacterized LOC125050289, transcript variant X6
uncharacterized LOC125050289, transcript variant X7
uncharacterized LOC125050289, transcript variant X8
uncharacterized LOC125050289, transcript variant X5
uncharacterized protein LOC125050289 isoform X1
uncharacterized protein LOC125050289 isoform X5
uncharacterized protein LOC125050289 isoform X2
uncharacterized protein LOC125050289 isoform X3
uncharacterized protein LOC125050289 isoform X4
uncharacterized protein LOC125050289 isoform X6
uncharacterized protein LOC125050289 isoform X7
uncharacterized protein LOC125050289 isoform X8
laminin subunit alpha-like, transcript variant X3
laminin subunit alpha-like, transcript variant X1
laminin subunit alpha-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: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 132 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 148 samples with support for all annotated introns
heparan-alpha-glucosaminide N-acetyltransferase-like
dolichol-phosphate mannosyltransferase subunit 1
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 82 samples with support for all annotated introns
NF-kappa-B inhibitor-interacting Ras-like protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 158 samples with support for all annotated introns
NF-kappa-B inhibitor-interacting Ras-like protein, 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 166 samples with support for all annotated introns
NF-kappa-B inhibitor-interacting Ras-like protein isoform X1
NF-kappa-B inhibitor-interacting Ras-like protein isoform X2
sodium-dependent neutral amino acid transporter B(0)AT3, 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 16 samples with support for all annotated introns
sodium-dependent neutral amino acid transporter B(0)AT3, 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 19 samples with support for all annotated introns
sodium-dependent neutral amino acid transporter B(0)AT3 isoform X2
sodium-dependent neutral amino acid transporter B(0)AT3 isoform X1
sodium-dependent neutral amino acid transporter B(0)AT3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 58 samples with support for all annotated introns
sodium-dependent neutral amino acid transporter B(0)AT3 isoform X3
uncharacterized LOC125050242, transcript variant X1
uncharacterized LOC125050242, transcript variant X2
cytochrome c oxidase subunit 5B, mitochondrial-like
uncharacterized LOC125050276, transcript variant X2
uncharacterized LOC125050276, transcript variant X1
uncharacterized protein LOC125050276 isoform X1
uncharacterized protein LOC125050276 isoform X2
coiled-coil domain-containing protein 102A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 168 samples with support for all annotated introns
protein piccolo-like, transcript variant X3
protein piccolo-like, transcript variant X1
protein piccolo-like, transcript variant X2
NACHT domain- and WD repeat-containing protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
NACHT domain- and WD repeat-containing protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
NACHT domain- and WD repeat-containing protein 1 isoform X2
NACHT domain- and WD repeat-containing protein 1 isoform X1
MTOR-associated protein MEAK7, transcript variant X3
MTOR-associated protein MEAK7, transcript variant X4
MTOR-associated protein MEAK7, transcript variant X1
MTOR-associated protein MEAK7, transcript variant X2
MTOR-associated protein MEAK7 isoform X2
MTOR-associated protein MEAK7 isoform X1
uncharacterized LOC125050610, 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 101 samples with support for all annotated introns
uncharacterized LOC125050610, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 117 samples with support for all annotated introns
uncharacterized protein LOC125050610 isoform X1
uncharacterized protein LOC125050610 isoform X2
dipeptidyl aminopeptidase-like protein 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
dipeptidyl aminopeptidase-like protein 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
dipeptidyl aminopeptidase-like protein 6 isoform X2
dipeptidyl aminopeptidase-like protein 6 isoform X1
zinc finger protein 836-like, transcript variant X2
zinc finger protein 836-like, transcript variant X1
nucleolar protein 4, transcript variant X1
nucleolar protein 4, transcript variant X2
nucleolar protein 4, transcript variant X3
nucleolar protein 4, transcript variant X4
uncharacterized protein LOC125050054 isoform X4
intraflagellar transport protein 52 homolog
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
eyes absent homolog 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
eyes absent homolog 2, 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 73 samples with support for all annotated introns
eyes absent homolog 2, 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 77 samples with support for all annotated introns
stress-associated endoplasmic reticulum protein 2
sodium-dependent noradrenaline transporter-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 2 samples with support for all annotated introns
uncharacterized LOC125050445, transcript variant X1
uncharacterized LOC125050445, transcript variant X2
uncharacterized protein LOC125050445 isoform X1
uncharacterized protein LOC125050445 isoform X2
far upstream element-binding protein 1, transcript variant X1
far upstream element-binding protein 1, transcript variant X3
far upstream element-binding protein 1, transcript variant X2
far upstream element-binding protein 1, transcript variant X4
far upstream element-binding protein 1, transcript variant X5
far upstream element-binding protein 1 isoform X1
far upstream element-binding protein 1 isoform X3
far upstream element-binding protein 1 isoform X2
far upstream element-binding protein 1 isoform X4
far upstream element-binding protein 2 isoform X5
uncharacterized LOC125050346, transcript variant X1
uncharacterized LOC125050346, transcript variant X2
uncharacterized LOC125050425, transcript variant X3
uncharacterized LOC125050425, transcript variant X4
uncharacterized LOC125050425, transcript variant X2
uncharacterized LOC125050425, transcript variant X1
uncharacterized protein LOC125050425 isoform X2
uncharacterized protein LOC125050425 isoform X1
probable phenylalanine--tRNA ligase, mitochondrial
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 69 samples with support for all annotated introns
eukaryotic translation initiation factor 2 subunit 1
collagen alpha-1(IX) chain-like, transcript variant X1
collagen alpha-1(IX) chain-like, transcript variant X2
collagen alpha-1(XIX) chain-like isoform X1
collagen alpha-1(IX) chain-like isoform X2
uncharacterized LOC125050626, 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 9 samples with support for all annotated introns
uncharacterized LOC125050626, transcript variant X1
uncharacterized protein LOC125050626 isoform X2
uncharacterized protein LOC125050626 isoform X1
histone-arginine methyltransferase CARMER
vacuolar protein sorting-associated protein 35, transcript variant X2
vacuolar protein sorting-associated protein 35, transcript variant X1
vacuolar protein sorting-associated protein 35
trafficking protein particle complex subunit 12
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 137 samples with support for all annotated introns
KH domain-containing, RNA-binding, signal transduction-associated protein 2-like, transcript variant X3
KH domain-containing, RNA-binding, signal transduction-associated protein 2-like, transcript variant X2
KH domain-containing, RNA-binding, signal transduction-associated protein 2-like, transcript variant X1
KH domain-containing, RNA-binding, signal transduction-associated protein 2-like, transcript variant X4
KH domain-containing, RNA-binding, signal transduction-associated protein 2-like isoform X3
KH domain-containing, RNA-binding, signal transduction-associated protein 2-like isoform X2
KH domain-containing, RNA-binding, signal transduction-associated protein 2-like isoform X1
transfer RNA methionine (anticodon CAU); 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: 2 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential channel pyrexia-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
dynein light chain roadblock-type 2-like
dynein light chain roadblock-type 1-like
glycine-rich protein GRP33-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 89 samples with support for all annotated introns
glycine-rich protein GRP33-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 89 samples with support for all annotated introns
glycine-rich protein GRP33-like isoform X3
glycine-rich protein GRP33-like, transcript variant X2
glycine-rich protein GRP33-like, transcript variant X3
SH3 domain-binding protein 5-like, transcript variant X1
SH3 domain-binding protein 5-like, transcript variant X2
zinc transporter 2-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 54 samples with support for all annotated introns
zinc transporter 2-like, transcript variant X2
probable ATP-dependent RNA helicase DDX27
uncharacterized LOC125050652, transcript variant X6
uncharacterized LOC125050652, transcript variant X3
uncharacterized LOC125050652, transcript variant X2
uncharacterized LOC125050652, transcript variant X4
uncharacterized LOC125050652, transcript variant X5
uncharacterized LOC125050652, transcript variant X1
uncharacterized protein LOC125050652 isoform X1
uncharacterized protein LOC125050652 isoform X3
uncharacterized protein LOC125050652 isoform X2
uncharacterized protein LOC125050652 isoform X4
uncharacterized protein LOC125050652 isoform X5
uncharacterized protein LOC125050652 isoform X6
trifunctional enzyme subunit beta, mitochondrial
putative vitellogenin receptor, transcript variant X1
putative vitellogenin receptor, transcript variant X4
putative vitellogenin receptor, transcript variant X5
putative vitellogenin receptor, transcript variant X6
putative vitellogenin receptor, transcript variant X2
putative vitellogenin receptor, transcript variant X3
putative vitellogenin receptor isoform X1
putative vitellogenin receptor isoform X2
putative vitellogenin receptor isoform X3
putative vitellogenin receptor isoform X4
putative vitellogenin receptor isoform X5
putative vitellogenin receptor isoform X6
malonate--CoA ligase ACSF3, mitochondrial
probable sodium-coupled neutral amino acid transporter 6
ornithine decarboxylase 1-like, transcript variant X1
ornithine decarboxylase 1-like, transcript variant X2
glutathione synthetase-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 96 samples with support for all annotated introns
glutathione synthetase-like, transcript variant X1
glutathione synthetase-like, transcript variant X5
glutathione synthetase-like, transcript variant X2
glutathione synthetase-like, transcript variant X3
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 10, mitochondrial
EARP and GARP complex-interacting protein 1-like
uncharacterized LOC125050246, transcript variant X2
uncharacterized LOC125050246, transcript variant X3
uncharacterized LOC125050246, transcript variant X1
uncharacterized protein LOC125050246 isoform X2
uncharacterized protein LOC125050246 isoform X1
uncharacterized LOC125050501, transcript variant X2
uncharacterized LOC125050501, transcript variant X1
uncharacterized protein LOC125050501 isoform X1
uncharacterized protein LOC125050501 isoform X2
uncharacterized LOC125050621, transcript variant X2
uncharacterized LOC125050621, transcript variant X1
uncharacterized LOC125050042, transcript variant X1
uncharacterized LOC125050042, transcript variant X3
uncharacterized LOC125050042, transcript variant X4
uncharacterized LOC125050042, transcript variant X2
uncharacterized LOC125050042, transcript variant X5
peptidyl-prolyl cis-trans isomerase FKBP1B-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 35 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 22 samples with support for all annotated introns