Pieris rapae chromosome 18, ilPieRapa1.1, 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\nLR990600.1.\nAssembly name: ilPieRapa1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Wellcome Sanger Institute on\n2021/01/28. The original whole-genome shotgun project has the\naccession CAJHWY000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Pieris rapae Annotation Release 101\nAnnotation Version :: 101\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.
uncharacterized LOC110999595, 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 14 samples with support for all annotated introns
uncharacterized protein LOC110999595 isoform X1
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized LOC110999595, 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
uncharacterized protein LOC110999595 isoform X2
uncharacterized LOC110999599, 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
uncharacterized LOC110999599, 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 14 samples with support for all annotated introns
uncharacterized protein LOC110999599 isoform X2
uncharacterized protein LOC110999599 isoform X1
solute carrier family 41 member 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
solute carrier family 41 member 1, transcript variant X1
solute carrier family 41 member 1, transcript variant X2
solute carrier family 41 member 1 isoform X1
solute carrier family 41 member 1, transcript variant X4
solute carrier family 41 member 1 isoform X2
plasma membrane calcium-transporting ATPase 3, transcript variant X3
plasma membrane calcium-transporting ATPase 3, transcript variant X6
plasma membrane calcium-transporting ATPase 3, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3, transcript variant X7
plasma membrane calcium-transporting ATPase 3, transcript variant X1
plasma membrane calcium-transporting ATPase 3, transcript variant X4
plasma membrane calcium-transporting ATPase 3, transcript variant X5
plasma membrane calcium-transporting ATPase 3, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3, transcript variant X2
plasma membrane calcium-transporting ATPase 2 isoform X1
plasma membrane calcium-transporting ATPase 2 isoform X4
plasma membrane calcium-transporting ATPase 2 isoform X2
plasma membrane calcium-transporting ATPase 2 isoform X3
plasma membrane calcium-transporting ATPase 3 isoform X6
plasma membrane calcium-transporting ATPase 3 isoform X7
plasma membrane calcium-transporting ATPase 3 isoform X5
plasma membrane calcium-transporting ATPase 3 isoform X8
WEB family protein At3g02930, chloroplastic, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
WEB family protein At3g02930, chloroplastic, 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 15 samples with support for all annotated introns
WEB family protein At3g02930, chloroplastic, 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 7 samples with support for all annotated introns
WEB family protein At3g02930, chloroplastic isoform X3
WEB family protein At3g02930, chloroplastic isoform X1
WEB family protein At3g02930, chloroplastic isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
tyrosine-protein phosphatase 69D, transcript variant X2
tyrosine-protein phosphatase 69D, transcript variant X1
tyrosine-protein phosphatase 69D isoform X2
tyrosine-protein phosphatase 69D isoform X1
uncharacterized LOC110994580, transcript variant X1
uncharacterized LOC110994580, transcript variant X2
uncharacterized protein LOC110994580 isoform X1
uncharacterized protein LOC110994580 isoform X2
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC110994585, transcript variant X2
uncharacterized LOC110994585, transcript variant X1
uncharacterized protein LOC110994585 isoform X2
uncharacterized protein LOC110994585 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
dual specificity protein phosphatase MPK-4-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
transcriptional activator cubitus interruptus, transcript variant X3
transcriptional activator cubitus interruptus, transcript variant X1
transcriptional activator cubitus interruptus, transcript variant X2
transcriptional activator cubitus interruptus isoform X2
transcriptional activator cubitus interruptus isoform X1
facilitated trehalose transporter Tret1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 53 samples with support for all annotated introns
facilitated trehalose transporter Tret1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
facilitated trehalose transporter Tret1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Na(+)/H(+) exchange regulatory cofactor NHE-RF2
epidermal growth factor receptor kinase substrate 8, transcript variant X1
epidermal growth factor receptor kinase substrate 8, transcript variant X2
epidermal growth factor receptor kinase substrate 8, transcript variant X3
epidermal growth factor receptor kinase substrate 8 isoform X1
epidermal growth factor receptor kinase substrate 8 isoform X3
epidermal growth factor receptor kinase substrate 8 isoform X2
epidermal growth factor receptor kinase substrate 8, transcript variant X4
epidermal growth factor receptor kinase substrate 8-like protein 1 isoform X4
uncharacterized LOC110991611, transcript variant X3
uncharacterized LOC110991611, transcript variant X1
uncharacterized LOC110991611, transcript variant X2
uncharacterized LOC110991611, transcript variant X4
uncharacterized protein LOC110991611 isoform X1
uncharacterized protein LOC110991611 isoform X2
uncharacterized protein LOC110991611 isoform X4
uncharacterized protein LOC110991611 isoform X3
transcriptional activator protein Pur-alpha, transcript variant X1
transcriptional activator protein Pur-alpha, transcript variant X2
transcriptional activator protein Pur-alpha isoform X1
transcriptional activator protein Pur-alpha isoform X2
transcriptional activator protein Pur-alpha, transcript variant X3
transcriptional activator protein Pur-beta isoform X3
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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 103 samples with support for all annotated introns
uncharacterized LOC110991614, transcript variant X1
uncharacterized LOC110991614, transcript variant X2
uncharacterized protein LOC110991614 isoform X1
uncharacterized protein LOC110991614 isoform 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 20 samples with support for all annotated introns
chloride channel protein 2, transcript variant X2
chloride channel protein 2, transcript variant X1
chloride channel protein 2, transcript variant X3
transfer RNA serine (anticodon GCU); 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 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 94% 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: 87 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 102 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100 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: 87 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: 87 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
vitellogenin-like, transcript variant X2
vitellogenin-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 4 samples with support for all annotated introns
forkhead box protein P1, transcript variant X4
forkhead box protein P1, transcript variant X1
forkhead box protein P1, transcript variant X3
forkhead box protein P1, transcript variant X2
forkhead box protein P1, transcript variant X5
forkhead box protein P1, transcript variant X6
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
calcium-dependent secretion activator, transcript variant X14
calcium-dependent secretion activator, transcript variant X13
calcium-dependent secretion activator, transcript variant X12
calcium-dependent secretion activator, transcript variant X4
calcium-dependent secretion activator, transcript variant X5
calcium-dependent secretion activator, transcript variant X2
calcium-dependent secretion activator, transcript variant X11
calcium-dependent secretion activator, transcript variant X10
calcium-dependent secretion activator, transcript variant X6
calcium-dependent secretion activator, transcript variant X8
calcium-dependent secretion activator, transcript variant X3
calcium-dependent secretion activator, transcript variant X7
calcium-dependent secretion activator, transcript variant X1
calcium-dependent secretion activator, transcript variant X9
calcium-dependent secretion activator isoform X4
calcium-dependent secretion activator isoform X14
calcium-dependent secretion activator isoform X5
calcium-dependent secretion activator isoform X13
calcium-dependent secretion activator isoform X2
calcium-dependent secretion activator isoform X11
calcium-dependent secretion activator isoform X10
calcium-dependent secretion activator isoform X12
calcium-dependent secretion activator isoform X6
calcium-dependent secretion activator isoform X8
calcium-dependent secretion activator isoform X3
calcium-dependent secretion activator isoform X7
calcium-dependent secretion activator isoform X1
calcium-dependent secretion activator isoform X9
MAM and LDL-receptor class A domain-containing protein 1, transcript variant X2
MAM and LDL-receptor class A domain-containing protein 1, transcript variant X1
MAM and LDL-receptor class A domain-containing protein 1 isoform X2
MAM and LDL-receptor class A domain-containing protein 1 isoform X1
zinc finger protein OZF, 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 12 samples with support for all annotated introns
zinc finger protein OZF, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sodium- and chloride-dependent GABA transporter 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
sodium- and chloride-dependent GABA transporter 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
sodium- and chloride-dependent GABA transporter 1
NACHT and WD repeat domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC111001524, 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 16 samples with support for all annotated introns
uncharacterized LOC111001524, transcript variant X1
solute carrier family 12 member 9, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
solute carrier family 12 member 9, 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 12 samples with support for all annotated introns
solute carrier family 12 member 9, 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 8 samples with support for all annotated introns
solute carrier family 12 member 9, transcript variant X1
solute carrier family 12 member 9 isoform X2
solute carrier family 12 member 9 isoform X1
solute carrier family 12 member 9 isoform X3
probable small nuclear ribonucleoprotein G
transcription factor EB, transcript variant X1
transcription factor EB, transcript variant X2
transcription factor EB, transcript variant X5
transcription factor EB, transcript variant X3
transcription factor EB, 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 2 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized LOC111004292, transcript variant X5
uncharacterized LOC111004292, transcript variant X7
uncharacterized LOC111004292, transcript variant X6
uncharacterized LOC111004292, transcript variant X3
uncharacterized LOC111004292, transcript variant X1
uncharacterized LOC111004292, transcript variant X12
uncharacterized LOC111004292, transcript variant X10
uncharacterized LOC111004292, transcript variant X11
uncharacterized LOC111004292, transcript variant X2
uncharacterized LOC111004292, transcript variant X8
uncharacterized LOC111004292, transcript variant X4
uncharacterized LOC111004292, transcript variant X9
uncharacterized protein LOC111004292 isoform X4
uncharacterized protein LOC111004292 isoform X2
uncharacterized protein LOC111004292 isoform X3
uncharacterized protein LOC111004292 isoform X1
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1
ATP-binding cassette sub-family D member, 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 21 samples with support for all annotated introns
ATP-binding cassette sub-family D member, transcript variant X1
ATP-binding cassette sub-family D member
IQ motif and SEC7 domain-containing protein 2, transcript variant X1
IQ motif and SEC7 domain-containing protein 2, transcript variant X8
IQ motif and SEC7 domain-containing protein 2, transcript variant X2
IQ motif and SEC7 domain-containing protein 2, transcript variant X7
IQ motif and SEC7 domain-containing protein 3 isoform X1
IQ motif and SEC7 domain-containing protein 2 isoform X3
IQ motif and SEC7 domain-containing protein 2, transcript variant X4
IQ motif and SEC7 domain-containing protein 2, transcript variant X3
IQ motif and SEC7 domain-containing protein 2, transcript variant X6
IQ motif and SEC7 domain-containing protein 2, transcript variant X5
IQ motif and SEC7 domain-containing protein 3 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 2 samples with support for all annotated introns
fat-like cadherin-related tumor suppressor homolog, transcript variant X2
fat-like cadherin-related tumor suppressor homolog, transcript variant X1
fat-like cadherin-related tumor suppressor homolog isoform X2
fat-like cadherin-related tumor suppressor homolog isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 1 Protein, 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
protein O-mannosyl-transferase TMTC1-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
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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine protease inhibitor dipetalogastin-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
serine protease inhibitor Kazal-type 5-like, transcript variant X1
serine protease inhibitor Kazal-type 5-like, transcript variant X3
serine protease inhibitor Kazal-type 5-like, transcript variant X2
serine protease inhibitor Kazal-type 5-like, transcript variant X5
serine protease inhibitor Kazal-type 5-like, transcript variant X4
serine protease inhibitor Kazal-type 5-like isoform X5
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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
beta-1,4-glucuronyltransferase 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
troponin T, skeletal muscle, transcript variant X2
troponin T, skeletal muscle, transcript variant X1
troponin T, skeletal muscle, transcript variant X3
troponin T, skeletal muscle, transcript variant X5
troponin T, skeletal muscle, transcript variant X9
troponin T, skeletal muscle, transcript variant X4
troponin T, skeletal muscle, transcript variant X6
troponin T, skeletal muscle, transcript variant X7
troponin T, skeletal muscle, transcript variant X8
troponin T, skeletal muscle, transcript variant X10
coatomer subunit beta, transcript variant X1
coatomer subunit beta, transcript variant X2
probable U3 small nucleolar RNA-associated protein 11
zinc finger matrin-type protein CG9776, transcript variant X1
zinc finger matrin-type protein CG9776, transcript variant X3
zinc finger matrin-type protein CG9776, transcript variant X2
zinc finger matrin-type protein CG9776 isoform X1
zinc finger matrin-type protein CG9776 isoform X3
zinc finger matrin-type protein CG9776 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
glycine N-methyltransferase, transcript variant X1
glycine N-methyltransferase, transcript variant X2
protein transport protein Sec61 subunit gamma, transcript variant X1
protein transport protein Sec61 subunit gamma, transcript variant X2
protein transport protein Sec61 subunit gamma
uncharacterized LOC110995132, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
uncharacterized LOC110995132, 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 17 samples with support for all annotated introns
uncharacterized LOC110995132, 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 15 samples with support for all annotated introns
uncharacterized LOC110995132, transcript variant X4
uncharacterized LOC110995132, transcript variant X1
uncharacterized protein LOC110995132 isoform X2
uncharacterized protein LOC110995132 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 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 5 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 79% coverage of the annotated genomic feature by RNAseq alignments
protein O-mannosyl-transferase TMTC1-like, transcript variant X2
protein O-mannosyl-transferase TMTC1-like, transcript variant X1
protein O-mannosyl-transferase TMTC1-like isoform X2
protein O-mannosyl-transferase TMTC1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
V-type proton ATPase 16 kDa proteolipid subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins, 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: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
proton-coupled amino acid transporter-like protein CG1139, transcript variant X2
proton-coupled amino acid transporter-like protein CG1139, transcript variant X4
proton-coupled amino acid transporter-like protein CG1139, transcript variant X3
proton-coupled amino acid transporter-like protein CG1139, transcript variant X1
proton-coupled amino acid transporter-like protein CG1139 isoform X1
proton-coupled amino acid transporter-like protein CG1139 isoform X2
proton-coupled amino acid transporter-like protein pathetic, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
proton-coupled amino acid transporter-like protein pathetic, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
proton-coupled amino acid transporter-like protein pathetic isoform X1
proton-coupled amino acid transporter-like protein pathetic isoform X2
glycine receptor subunit alpha-1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
glycine receptor subunit alpha-1, 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 3 samples with support for all annotated introns
glycine receptor subunit alpha-1 isoform X2
glycine receptor subunit alpha-1 isoform X1
MORN repeat-containing protein 4 homolog
elongation of very long chain fatty acids protein 4
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 13 samples with support for all annotated introns
proton-coupled amino acid transporter-like protein CG1139
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
DNA-binding protein D-ETS-4, transcript variant X2
DNA-binding protein D-ETS-4, transcript variant X1
DNA-binding protein D-ETS-4, transcript variant X4
DNA-binding protein D-ETS-4, 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 3 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 1 Protein, and 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: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
zinc finger protein jing, transcript variant X1
zinc finger protein jing, transcript variant X2
SH3 and multiple ankyrin repeat domains protein 3, transcript variant X2
SH3 and multiple ankyrin repeat domains protein 3, transcript variant X1
SH3 and multiple ankyrin repeat domains protein 3, transcript variant X3
SH3 and multiple ankyrin repeat domains protein 3, transcript variant X5
SH3 and multiple ankyrin repeat domains protein 3, transcript variant X6
SH3 and multiple ankyrin repeat domains protein 3, transcript variant X4
SH3 and multiple ankyrin repeat domains protein 3, transcript variant X9
SH3 and multiple ankyrin repeat domains protein 3, transcript variant X7
SH3 and multiple ankyrin repeat domains protein 3, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
SH3 and multiple ankyrin repeat domains protein 3 isoform X1
SH3 and multiple ankyrin repeat domains protein 3 isoform X2
SH3 and multiple ankyrin repeat domains protein 3 isoform X5
SH3 and multiple ankyrin repeat domains protein 3 isoform X3
SH3 and multiple ankyrin repeat domains protein 3 isoform X8
SH3 and multiple ankyrin repeat domains protein 3 isoform X6
SH3 and multiple ankyrin repeat domains protein 3 isoform X7
probable arginine--tRNA ligase, mitochondrial
CREB-binding protein, transcript variant X1
CREB-binding protein, transcript variant X2
CREB-binding protein, transcript variant X5
CREB-binding protein, transcript variant X7
CREB-binding protein, transcript variant X4
CREB-binding protein, transcript variant X6
CREB-binding protein, transcript variant X3
CREB-binding protein, transcript variant X8
membrane-associated progesterone receptor component 1, transcript variant X2
membrane-associated progesterone receptor component 1, transcript variant X1
membrane-associated progesterone receptor component 1
uncharacterized LOC123689963, transcript variant X1
uncharacterized LOC123689963, transcript variant X2
GDP-fucose transporter 1, transcript variant X2
GDP-fucose transporter 1, transcript variant X1
iduronate 2-sulfatase, 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 2 samples with support for all annotated introns
iduronate 2-sulfatase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
TNF receptor-associated factor 6-A, transcript variant X1
TNF receptor-associated factor 6-A, transcript variant X2
TNF receptor-associated factor 6-A isoform X1
TNF receptor-associated factor 6 isoform X2
uncharacterized LOC111001411, 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 3 samples with support for all annotated introns
uncharacterized LOC111001411, transcript variant X2
uncharacterized protein LOC111001411 isoform X1
uncharacterized LOC111001411, transcript variant X3
uncharacterized protein LOC111001411 isoform X2
nose resistant to fluoxetine protein 6, transcript variant X2
nose resistant to fluoxetine protein 6, transcript variant X1
nose resistant to fluoxetine protein 6 isoform X2
nose resistant to fluoxetine protein 6 isoform X1
uncharacterized LOC110997359, transcript variant X2
uncharacterized LOC110997359, transcript variant X1
uncharacterized protein LOC110997359 isoform X2
uncharacterized protein LOC110997359 isoform X1
dehydrodolichyl diphosphate synthase complex subunit DHDDS
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
RNA transcription, translation and transport factor protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 100 samples with support for all annotated introns
mitochondrial import inner membrane translocase subunit Tim8
N(4)-(Beta-N-acetylglucosaminyl)-L-asparaginase, transcript variant X3
adenosine deaminase-like protein, 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 18 samples with support for all annotated introns
adenosine deaminase-like protein, transcript variant X1
adenosine deaminase-like protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
adenosine deaminase-like protein, 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 3 samples with support for all annotated introns
adenosine deaminase-like protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
adenosine deaminase-like protein isoform X1
adenosine deaminase-like protein isoform X2
N(4)-(Beta-N-acetylglucosaminyl)-L-asparaginase, transcript variant X1
N(4)-(Beta-N-acetylglucosaminyl)-L-asparaginase, transcript variant X2
probable DNA-directed RNA polymerases I and III subunit RPAC2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 95 samples with support for all annotated introns
cytochrome P450 CYP12A2, transcript variant X1
cytochrome P450 CYP12A2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 101 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
trimethyllysine dioxygenase, mitochondrial, transcript variant X3
trimethyllysine dioxygenase, mitochondrial, transcript variant X1
trimethyllysine dioxygenase, mitochondrial, transcript variant X2
trimethyllysine dioxygenase, mitochondrial isoform X3
trimethyllysine dioxygenase, mitochondrial isoform X1
trimethyllysine dioxygenase, mitochondrial isoform X2
trimethyllysine dioxygenase, mitochondrial
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
venom dipeptidyl peptidase 4, transcript variant X2
venom dipeptidyl peptidase 4, transcript variant X1
venom dipeptidyl peptidase 4, transcript variant X3
zinc finger C3H1 domain-containing protein, transcript variant X1
zinc finger C3H1 domain-containing protein, transcript variant X2
zinc finger C3H1 domain-containing protein isoform X2
uncharacterized protein LOC110994519 isoform X1
TBC domain-containing protein kinase-like protein, transcript variant X2
TBC domain-containing protein kinase-like protein, transcript variant X1
TBC domain-containing protein kinase-like protein
cyclic AMP response element-binding protein A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 109 samples with support for all annotated introns
heparan-alpha-glucosaminide N-acetyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha, transcript variant X1
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha, transcript variant X2
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha isoform X2
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha isoform X1
GRB10-interacting GYF protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
GRB10-interacting GYF protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
GRB10-interacting GYF protein 2-like isoform X1
GRB10-interacting GYF protein 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC110994494, transcript variant X1
uncharacterized protein LOC110994494 isoform X1
uncharacterized LOC110994494, transcript variant X2
uncharacterized protein LOC110994494 isoform X2
retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit delta
uncharacterized LOC110994517, transcript variant X2
uncharacterized LOC110994517, 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 4 samples with support for all annotated introns
eukaryotic translation initiation factor 5B, transcript variant X2
eukaryotic translation initiation factor 5B, transcript variant X1
eukaryotic translation initiation factor 5B isoform X2
eukaryotic translation initiation factor 5B isoform X1
ATP-dependent RNA helicase SUV3 homolog, mitochondrial
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 75 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
cytochrome P450 4d2, transcript variant X1
cytochrome P450 4d2, transcript variant X2
lipopolysaccharide-induced tumor necrosis factor-alpha factor homolog
roundabout homolog 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
roundabout homolog 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
uncharacterized LOC111001249, transcript variant X2
uncharacterized LOC111001249, transcript variant X1
uncharacterized protein LOC111001249 isoform X2
uncharacterized protein LOC111001249 isoform X1
proton channel OtopLc, 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
proton channel OtopLc, 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 7 samples with support for all annotated introns
proton channel OtopLc, 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 2 samples with support for all annotated introns
proton channel OtopLc, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
proton channel OtopLc, transcript variant X6
proton channel OtopLc, transcript variant X7
proton channel OtopLc, transcript variant X8
proton channel OtopLc, transcript variant X5
proton channel OtopLc, transcript variant X10
proton channel OtopLc, transcript variant X11
proton channel OtopLc, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
protein BCL9 homolog, transcript variant X3
protein BCL9 homolog, transcript variant X4
protein BCL9 homolog, transcript variant X5
protein BCL9 homolog, transcript variant X6
protein BCL9 homolog, transcript variant X1
protein BCL9 homolog, transcript variant X2
kelch domain-containing protein 3, transcript variant X2
kelch domain-containing protein 3, 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 46 samples with support for all annotated introns
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
latrophilin Cirl-like, transcript variant X1
latrophilin Cirl-like, transcript variant X4
latrophilin Cirl-like, transcript variant X3
latrophilin Cirl-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
latrophilin Cirl-like, transcript variant X2
glycine receptor subunit alpha-4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glycine receptor subunit alpha-4-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 20 samples with support for all annotated introns
endothelin-converting enzyme homolog, transcript variant X2
endothelin-converting enzyme homolog, transcript variant X1
endothelin-converting enzyme homolog isoform X2
endothelin-converting enzyme homolog isoform X1
dihydropyrimidinase, transcript variant X3
dihydropyrimidinase, transcript variant X4
dihydropyrimidinase, transcript variant X1
dihydropyrimidinase, transcript variant X2
dihydropyrimidinase, transcript variant X5
regulation of nuclear pre-mRNA domain-containing protein 2, transcript variant X2
regulation of nuclear pre-mRNA domain-containing protein 2, transcript variant X1
regulation of nuclear pre-mRNA domain-containing protein 2 isoform X2
uncharacterized protein LOC110995547 isoform X1
uncharacterized LOC123689983, transcript variant X2
uncharacterized LOC123689983, 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
uncharacterized LOC110995552, transcript variant X1
uncharacterized LOC110995552, transcript variant X2
uncharacterized protein LOC110995552 isoform X1
uncharacterized protein LOC110995552 isoform X2
CDK-activating kinase assembly factor MAT1, transcript variant X2
CDK-activating kinase assembly factor MAT1, transcript variant X1
CDK-activating kinase assembly factor MAT1
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 6 samples with support for all annotated introns
uncharacterized LOC123689960, transcript variant X2
uncharacterized LOC123689960, transcript variant X1
uncharacterized protein LOC123689960 isoform X2
uncharacterized protein LOC123689960 isoform 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone]-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glucose dehydrogenase [FAD, quinone]-like, transcript variant X1
glucose dehydrogenase [FAD, quinone]-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC111000614, transcript variant X2
uncharacterized LOC111000614, transcript variant X1
uncharacterized protein LOC111000614 isoform X2
uncharacterized protein LOC111000614 isoform X1
E3 ubiquitin-protein ligase MARCHF2, transcript variant X1
E3 ubiquitin-protein ligase MARCHF2, transcript variant X2
uncharacterized protein LOC111000615 isoform X1
E3 ubiquitin-protein ligase MARCHF2 isoform X2
nuclear pore glycoprotein p62, 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 6 samples with support for all annotated introns
nuclear pore glycoprotein p62, 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 50 samples with support for all annotated introns
nuclear pore glycoprotein p62 isoform X1
nuclear pore glycoprotein p62 isoform X2
putative ATP-dependent RNA helicase TDRD12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
putative ATP-dependent RNA helicase TDRD12, transcript variant X3
putative ATP-dependent RNA helicase TDRD12, 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 15 samples with support for all annotated introns
putative ATP-dependent RNA helicase TDRD12 isoform X3
putative ATP-dependent RNA helicase TDRD12 isoform X1
putative ATP-dependent RNA helicase TDRD12 isoform X2
checkpoint protein HUS1, transcript variant X2
checkpoint protein HUS1, 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 11 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 18 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 19 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 9 samples with support for all annotated introns
Down syndrome cell adhesion molecule-like protein Dscam2, 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 2 samples with support for all annotated introns
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X2
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X1
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X2
glycine-rich cell wall structural protein 1.8-like, transcript variant X1
glycine-rich cell wall structural protein 1.8-like, transcript variant X2
glycine-rich cell wall structural protein 1.8-like isoform X1
glycine-rich cell wall structural protein-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, 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: 11 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 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: 15 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: 1 Protein, and 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 3
immunoglobulin superfamily member 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
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 59 samples with support for all annotated introns
photoreceptor-specific nuclear receptor-like
ATP-dependent RNA helicase DHX30, 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 16 samples with support for all annotated introns
ATP-dependent RNA helicase DHX30, transcript variant X1
ATP-dependent RNA helicase DHX30 isoform X1
ATP-dependent RNA helicase DHX30 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Down syndrome cell adhesion molecule-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Down syndrome cell adhesion molecule-like protein Dscam2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC111000007 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 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 12 samples with support for all annotated introns
phenoloxidase-activating enzyme, transcript variant X1
phenoloxidase-activating enzyme isoform X1
phenoloxidase-activating enzyme, transcript variant X2
phenoloxidase-activating enzyme 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 4 samples with support for all annotated introns
structural maintenance of chromosomes protein 5, transcript variant X2
structural maintenance of chromosomes protein 5, transcript variant X1
structural maintenance of chromosomes protein 5
armadillo repeat-containing protein 6 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
PRKCA-binding protein, transcript variant X2
PRKCA-binding protein, transcript variant X1
PRKCA-binding protein, transcript variant X4
PRKCA-binding protein, transcript variant X3
uncharacterized LOC111000015, transcript variant X2
uncharacterized LOC111000015, transcript variant X1
chymotrypsin-like elastase family member 2A
regulator of hypoxia-inducible factor 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 4% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 52 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 33 samples with support for all annotated introns
cleavage and polyadenylation specificity factor subunit 1
MIP18 family protein galla-1, transcript variant X1
autophagy-related protein 13 homolog isoform X1
MIP18 family protein galla-1, transcript variant X2
40S ribosomal protein S11, transcript variant X2
40S ribosomal protein S11, transcript variant X1
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC111001379, transcript variant X1
uncharacterized LOC111001379, transcript variant X2
uncharacterized LOC111001379, transcript variant X3
uncharacterized protein LOC111001379 isoform X1
uncharacterized protein LOC111001379 isoform X2
uncharacterized protein LOC111001379 isoform X3
insulin gene enhancer protein ISL-1, 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 14 samples with support for all annotated introns
insulin gene enhancer protein ISL-1, transcript variant X2
insulin gene enhancer protein ISL-1 isoform X1
insulin gene enhancer protein ISL-1 isoform X2
endoplasmic reticulum metallopeptidase 1, transcript variant X2
endoplasmic reticulum metallopeptidase 1, transcript variant X1
endoplasmic reticulum metallopeptidase 1, transcript variant X4
endoplasmic reticulum metallopeptidase 1 isoform X1
endoplasmic reticulum metallopeptidase 1 isoform X2
endoplasmic reticulum metallopeptidase 1 isoform X4
endoplasmic reticulum metallopeptidase 1, transcript variant X3
endoplasmic reticulum metallopeptidase 1, transcript variant X5
endoplasmic reticulum metallopeptidase 1 isoform X3
endoplasmic reticulum metallopeptidase 1 isoform X5
serine/arginine repetitive matrix protein 1, transcript variant X2
serine/arginine repetitive matrix protein 1, transcript variant X1
microtubule-associated protein futsch isoform X2
serine/arginine repetitive matrix protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
hyaluronidase-like, transcript variant X1
hyaluronidase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
G protein-activated inward rectifier potassium channel 3
ATP-sensitive inward rectifier potassium channel 11-like
uncharacterized LOC111001376, transcript variant X1
uncharacterized LOC111001376, transcript variant X2
uncharacterized protein LOC111001376 isoform X1
uncharacterized protein LOC111001376 isoform 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
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 2 samples with support for all annotated introns
hydroxylysine kinase, transcript variant X1
hydroxylysine kinase, transcript variant X2
doublesex- and mab-3-related transcription factor A2
probable 5-hydroxyisourate hydrolase R09H10.3
RNA-binding protein 5-A, 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 73 samples with support for all annotated introns
RNA-binding protein 5-A, 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 95 samples with support for all annotated introns
uncharacterized LOC111001354, 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 8 samples with support for all annotated introns
uncharacterized LOC111001354, 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 21 samples with support for all annotated introns
uncharacterized LOC111001354, transcript variant X3
uncharacterized protein LOC111001354 isoform X1
uncharacterized protein LOC111001354 isoform X2
uncharacterized protein LOC111001354 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 1 sample with support for all annotated introns
39S ribosomal protein L54, mitochondrial
outer dense fiber protein 3-like protein 2
pyridine nucleotide-disulfide oxidoreductase domain-containing protein 1
probable galactose-1-phosphate uridylyltransferase
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 galactose-1-phosphate uridylyltransferase