Plutella xylostella chromosome 27, ilPluXylo3.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Yponomeutoidea; Plutellidae; Plutella.
REFSEQ INFORMATION: The reference sequence is identical to\nOW026578.1.\nAssembly name: ilPluXylo3.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2022/03/10. The original whole-genome shotgun project has the\naccession CAKNZZ000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Plutella xylostella Annotation\n Release 103\nAnnotation Version :: 103\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 79 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: 1 Protein, and 97% 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: 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 103 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 59 samples with support for all annotated introns
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 26 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 103 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89 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 97% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
forkhead box protein P1, transcript variant X2
forkhead box protein P1, transcript variant X1
forkhead box protein P1, transcript variant X3
forkhead box protein P1, transcript variant X4
forkhead box protein P1, transcript variant X5
forkhead box protein P1, transcript variant X6
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
calcium-dependent secretion activator, 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 16 samples with support for all annotated introns
calcium-dependent secretion activator, transcript variant X11
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
calcium-dependent secretion activator, 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
calcium-dependent secretion activator, 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 13 samples with support for all annotated introns
calcium-dependent secretion activator, transcript variant X8
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
calcium-dependent secretion activator, 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 16 samples with support for all annotated introns
calcium-dependent secretion activator, 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 16 samples with support for all annotated introns
calcium-dependent secretion activator, transcript variant X7
calcium-dependent secretion activator, transcript variant X1
calcium-dependent secretion activator, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
calcium-dependent secretion activator, transcript variant X3
calcium-dependent secretion activator isoform X4
calcium-dependent secretion activator isoform X11
calcium-dependent secretion activator isoform X2
calcium-dependent secretion activator isoform X9
calcium-dependent secretion activator isoform X8
calcium-dependent secretion activator isoform X10
calcium-dependent secretion activator isoform X5
calcium-dependent secretion activator isoform X7
calcium-dependent secretion activator isoform X3
calcium-dependent secretion activator isoform X1
calcium-dependent secretion activator isoform X6
MAM and LDL-receptor class A domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
sodium- and chloride-dependent GABA transporter 1
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
NACHT and WD repeat domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% 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 84% coverage of the annotated genomic feature by RNAseq alignments
probable small nuclear ribonucleoprotein G
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 66 samples with support for all annotated introns
transcription factor EB, transcript variant X3
transcription factor EB, 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 65 samples with support for all annotated introns
transcription factor EB, 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 47 samples with support for all annotated introns
transcription factor EB, transcript variant X1
transcription factor EB, transcript variant X9
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 44 samples with support for all annotated introns
transcription factor EB, 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 43 samples with support for all annotated introns
transcription factor EB, 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 61 samples with support for all annotated introns
transcription factor EB, transcript variant X7
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 63 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 34 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 33 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 ESTs, 170 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
heat shock protein 83; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309114.1
annotated by transcript or proteomic data
The RefSeq transcript has 45 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001296043.1
The RefSeq protein has 4 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
facilitated trehalose transporter Tret1, transcript variant X4
facilitated trehalose transporter Tret1, transcript variant X3
facilitated trehalose transporter Tret1, transcript variant X2
facilitated trehalose transporter Tret1, transcript variant X1
facilitated trehalose transporter Tret1, transcript variant X5
facilitated trehalose transporter Tret1 isoform X2
facilitated trehalose transporter Tret1 isoform X1
facilitated trehalose transporter Tret1 isoform X3
uncharacterized LOC105388662, transcript variant X6
uncharacterized LOC105388662, transcript variant X8
uncharacterized LOC105388662, transcript variant X1
uncharacterized LOC105388662, transcript variant X7
uncharacterized LOC105388662, transcript variant X3
uncharacterized LOC105388662, transcript variant X4
uncharacterized LOC105388662, transcript variant X2
uncharacterized LOC105388662, transcript variant X5
uncharacterized protein LOC105388662 isoform X3
uncharacterized protein LOC105388662 isoform X1
uncharacterized protein LOC105388662 isoform X2
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, transcript variant X1
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1 isoform X1
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 60 samples with support for all annotated introns
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1 isoform X2
ATP-binding cassette sub-family D member, transcript variant X1
ATP-binding cassette sub-family D member, transcript variant X3
ATP-binding cassette sub-family D member, transcript variant X2
ATP-binding cassette sub-family D member isoform X2
ATP-binding cassette sub-family D member isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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: 29 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105395204, transcript variant X1
uncharacterized LOC105395204, transcript variant X2
uncharacterized protein LOC105395204 isoform X2
uncharacterized protein LOC105395204 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 62 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 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 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 12 samples with support for all annotated introns
androgen-dependent TFPI-regulating protein
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 85 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 97% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 2, facilitated glucose transporter member 8
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 62 samples with support for all annotated introns
facilitated trehalose transporter Tret1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 78 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 21 samples with support for all annotated introns
transcriptional activator protein Pur-alpha, transcript variant X2
transcriptional activator protein Pur-alpha, transcript variant X1
transcriptional activator protein Pur-alpha isoform X2
transcriptional activator protein Pur-alpha isoform X1
trithorax group protein osa, transcript variant X8
trithorax group protein osa, transcript variant X3
trithorax group protein osa, transcript variant X11
trithorax group protein osa, transcript variant X5
trithorax group protein osa, transcript variant X7
trithorax group protein osa, transcript variant X6
trithorax group protein osa, transcript variant X4
trithorax group protein osa, transcript variant X10
trithorax group protein osa, transcript variant X9
trithorax group protein osa, transcript variant X2
trithorax group protein osa, transcript variant X1
histone-lysine N-methyltransferase PRDM9
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
epidermal growth factor receptor kinase substrate 8-like protein 1
Na(+)/H(+) exchange regulatory cofactor NHE-RF1
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 78 samples with support for all annotated introns
uncharacterized LOC105382892, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
uncharacterized LOC105382892, transcript variant X2
uncharacterized protein LOC105382892 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 58 samples with support for all annotated introns
uncharacterized LOC105392544, transcript variant X4
uncharacterized LOC105392544, transcript variant X3
uncharacterized LOC105392544, transcript variant X1
uncharacterized LOC105392544, transcript variant X2
uncharacterized protein LOC105392544 isoform X1
uncharacterized protein LOC105392544 isoform X2
uncharacterized LOC105382892, transcript variant X3
uncharacterized protein LOC105382892 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
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 X3
solute carrier family 41 member 1 isoform X2
solute carrier family 41 member 1, transcript variant X4
solute carrier family 41 member 1 isoform X3
plasma membrane calcium-transporting ATPase 3, transcript variant X4
plasma membrane calcium-transporting ATPase 3, transcript variant X3
plasma membrane calcium-transporting ATPase 3, transcript variant X5
plasma membrane calcium-transporting ATPase 3, transcript variant X8
plasma membrane calcium-transporting ATPase 3, transcript variant X7
plasma membrane calcium-transporting ATPase 3, transcript variant X12
plasma membrane calcium-transporting ATPase 3, transcript variant X10
plasma membrane calcium-transporting ATPase 3, transcript variant X9
plasma membrane calcium-transporting ATPase 3, transcript variant X13
plasma membrane calcium-transporting ATPase 3, transcript variant X11
plasma membrane calcium-transporting ATPase 3, transcript variant X1
plasma membrane calcium-transporting ATPase 3, transcript variant X2
plasma membrane calcium-transporting ATPase 3, transcript variant X6
plasma membrane calcium-transporting ATPase 2 isoform X1
plasma membrane calcium-transporting ATPase 2 isoform X5
plasma membrane calcium-transporting ATPase 2 isoform X2
plasma membrane calcium-transporting ATPase 2 isoform X4
plasma membrane calcium-transporting ATPase 2 isoform X3
plasma membrane calcium-transporting ATPase 2 isoform X9
plasma membrane calcium-transporting ATPase 2 isoform X7
plasma membrane calcium-transporting ATPase 3 isoform X6
plasma membrane calcium-transporting ATPase 3 isoform X10
plasma membrane calcium-transporting ATPase 3 isoform X8
calponin homology domain-containing protein DDB_G0272472
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
facilitated trehalose transporter Tret1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 495 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: 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
protein lethal(2)essential for life-like; Derived by automated computational analysis using gene prediction method: BestRefSeq.
protein lethal(2)essential for life-like
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309117.1
The RefSeq transcript has 12 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 161 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: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105398197, 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 51 samples with support for all annotated introns
uncharacterized LOC105398197, 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 55 samples with support for all annotated introns
uncharacterized LOC105398197, 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 72 samples with support for all annotated introns
uncharacterized protein LOC105398197 isoform X2
uncharacterized protein LOC105398197 isoform X1
uncharacterized LOC105398197, transcript variant X3
uncharacterized LOC105383550, transcript variant X1
uncharacterized LOC105383550, transcript variant X2
uncharacterized LOC105381260, transcript variant X2
uncharacterized LOC105381260, transcript variant X3
uncharacterized LOC105381260, transcript variant X4
uncharacterized LOC105381260, transcript variant X5
uncharacterized LOC105381260, transcript variant X1
uncharacterized protein LOC105381260 isoform X2
uncharacterized protein LOC105381260 isoform X3
uncharacterized protein LOC105381260 isoform X4
uncharacterized protein LOC105381260 isoform X5
uncharacterized protein LOC105381260 isoform X1
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
dual specificity protein phosphatase 1B, 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 27 samples with support for all annotated introns
dual specificity protein phosphatase 1B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
dual specificity protein phosphatase 3 isoform X1
dual specificity protein phosphatase 1B isoform X2
IQ motif and SEC7 domain-containing protein 1, transcript variant X1
IQ motif and SEC7 domain-containing protein 1, transcript variant X10
IQ motif and SEC7 domain-containing protein 1, transcript variant X3
IQ motif and SEC7 domain-containing protein 1, transcript variant X12
IQ motif and SEC7 domain-containing protein 1, transcript variant X2
IQ motif and SEC7 domain-containing protein 3 isoform X1
IQ motif and SEC7 domain-containing protein 3 isoform X4
IQ motif and SEC7 domain-containing protein 3 isoform X2
IQ motif and SEC7 domain-containing protein 3 isoform X6
IQ motif and SEC7 domain-containing protein 1, transcript variant X13
IQ motif and SEC7 domain-containing protein 1, transcript variant X4
IQ motif and SEC7 domain-containing protein 1, transcript variant X6
IQ motif and SEC7 domain-containing protein 1, transcript variant X7
IQ motif and SEC7 domain-containing protein 1, transcript variant X5
IQ motif and SEC7 domain-containing protein 1, transcript variant X8
IQ motif and SEC7 domain-containing protein 1, transcript variant X9
IQ motif and SEC7 domain-containing protein 3 isoform X3
IQ motif and SEC7 domain-containing protein 1, transcript variant X11
IQ motif and SEC7 domain-containing protein 3 isoform X5
IQ motif and SEC7 domain-containing protein 1 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105383545, transcript variant X4
uncharacterized LOC105383545, transcript variant X3
uncharacterized LOC105383545, transcript variant X1
uncharacterized LOC105383545, transcript variant X2
uncharacterized protein LOC105383545 isoform X1
uncharacterized protein LOC105383545 isoform X3
uncharacterized protein LOC105383545 isoform X2
uncharacterized protein LOC105383545 isoform X4
plasminogen activator inhibitor 2, macrophage
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
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309098.1
The RefSeq transcript has 7 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001296027.1
The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
alpha-crystallin A chain-like; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001309064.1
The RefSeq transcript has 8 substitutions, 2 non-frameshifting indels compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001295993.1
The RefSeq protein has 2 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001306116.1
The RefSeq transcript has 8 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001293045.1
transmembrane and coiled-coil domains protein 2, transcript variant X5
transmembrane and coiled-coil domains protein 2, transcript variant X3
transmembrane and coiled-coil domains protein 2, transcript variant X6
transmembrane and coiled-coil domains protein 2, transcript variant X4
transmembrane and coiled-coil domains protein 2, transcript variant X1
transmembrane and coiled-coil domains protein 2, transcript variant X7
transmembrane and coiled-coil domains protein 2, transcript variant X2
transmembrane and coiled-coil domains protein 2 isoform X4
transmembrane and coiled-coil domains protein 2 isoform X2
transmembrane and coiled-coil domains protein 2 isoform X6
transmembrane and coiled-coil domains protein 2 isoform X5
transmembrane and coiled-coil domains protein 2 isoform X3
transmembrane and coiled-coil domains protein 2 isoform X1
dual specificity tyrosine-phosphorylation-regulated kinase 2
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
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
DNA-directed RNA polymerases I, II, and III subunit RPABC5
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 24 samples with support for all annotated introns
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
pyrroline-5-carboxylate reductase, transcript variant X1
pyrroline-5-carboxylate reductase isoform X1
pyrroline-5-carboxylate reductase, transcript variant X2
pyrroline-5-carboxylate reductase isoform X2
dual specificity protein phosphatase CDC14A
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
delta(24)-sterol reductase, 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 56 samples with support for all annotated introns
delta(24)-sterol reductase, 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 60 samples with support for all annotated introns
delta(24)-sterol reductase, 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 62 samples with support for all annotated introns
delta(24)-sterol reductase, 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 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 52 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 82 samples with support for all annotated introns
uncharacterized LOC105383676, transcript variant X2
uncharacterized LOC105383676, transcript variant X1
uncharacterized LOC105383676, transcript variant X3
uncharacterized LOC105383676, transcript variant X5
uncharacterized LOC105383676, transcript variant X4
uncharacterized LOC105383676, transcript variant X6
uncharacterized LOC105383676, transcript variant X7
uncharacterized LOC105383676, transcript variant X8
uncharacterized protein LOC105383676 isoform X2
uncharacterized protein LOC105383676 isoform X1
uncharacterized protein LOC105383676 isoform X5
uncharacterized protein LOC105383676 isoform X3
uncharacterized protein LOC105383676 isoform X4
uncharacterized LOC105381158, transcript variant X6
uncharacterized LOC105381158, transcript variant X2
uncharacterized LOC105381158, transcript variant X1
uncharacterized LOC105381158, transcript variant X9
uncharacterized LOC105381158, transcript variant X8
uncharacterized LOC105381158, transcript variant X7
uncharacterized LOC105381158, transcript variant X13
uncharacterized LOC105381158, transcript variant X4
uncharacterized LOC105381158, transcript variant X12
uncharacterized LOC105381158, transcript variant X3
uncharacterized LOC105381158, transcript variant X16
uncharacterized LOC105381158, transcript variant X15
uncharacterized LOC105381158, transcript variant X11
uncharacterized LOC105381158, transcript variant X10
uncharacterized protein LOC105381158 isoform X5
uncharacterized protein LOC105381158 isoform X2
uncharacterized protein LOC105381158 isoform X1
uncharacterized protein LOC105381158 isoform X8
uncharacterized protein LOC105381158 isoform X7
uncharacterized protein LOC105381158 isoform X6
uncharacterized protein LOC105381158 isoform X12
uncharacterized protein LOC105381158 isoform X11
uncharacterized protein LOC105381158 isoform X3
uncharacterized protein LOC105381158 isoform X9
uncharacterized LOC105381158, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein LOC105381158 isoform X10
uncharacterized LOC105381158, transcript variant X5
uncharacterized protein LOC105381158 isoform X4
uncharacterized LOC105381160, transcript variant X2
uncharacterized LOC105381160, transcript variant X3
uncharacterized LOC105381160, transcript variant X1
uncharacterized LOC105381160, transcript variant X4
uncharacterized protein LOC105381160 isoform X1
uncharacterized protein LOC105381160 isoform X2
uncharacterized LOC105381188, transcript variant X3
uncharacterized LOC105381188, transcript variant X5
uncharacterized LOC105381188, transcript variant X4
uncharacterized protein LOC105381188 isoform X3
uncharacterized protein LOC105381188 isoform X4
uncharacterized protein LOC105381188 isoform X2
uncharacterized LOC105381188, transcript variant X6
uncharacterized protein LOC105381188 isoform X5
uncharacterized LOC105381188, transcript variant X7
uncharacterized protein LOC105381188 isoform X6
uncharacterized LOC105381188, transcript variant X1
uncharacterized LOC105381188, transcript variant X10
uncharacterized LOC105381188, 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 5 samples with support for all annotated introns
uncharacterized LOC105381188, transcript variant X2
uncharacterized protein LOC105381188 isoform X1
uncharacterized protein LOC105381188 isoform X9
uncharacterized protein LOC105381188 isoform X7
uncharacterized LOC105381188, transcript variant X9
uncharacterized protein LOC105381188 isoform X8
uncharacterized LOC105381163, transcript variant X2
uncharacterized LOC105381163, transcript variant X1
uncharacterized LOC105381190, transcript variant X2
uncharacterized LOC105381190, transcript variant X1
uncharacterized protein LOC105381190 isoform X2
uncharacterized protein LOC105381190 isoform X1
collagen alpha-1(I) chain, transcript variant X2
collagen alpha-1(I) chain, transcript variant X1
collagen alpha-1(I) chain, transcript variant X4
collagen alpha-1(I) chain, transcript variant X5
collagen alpha-1(I) chain, transcript variant X6
collagen alpha-1(I) chain, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
growth/differentiation factor 8, transcript variant X2
growth/differentiation factor 8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutamate-gated chloride channel alpha-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 79 samples with support for all annotated introns
uncharacterized LOC105381170, 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 53 samples with support for all annotated introns
uncharacterized LOC105381170, 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 52 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, transcript variant X3
endothelin-converting enzyme homolog isoform X2
endothelin-converting enzyme homolog isoform X1
endothelin-converting enzyme homolog isoform X3
dihydropyrimidinase, transcript variant X2
dihydropyrimidinase, transcript variant X6
dihydropyrimidinase, transcript variant X1
dihydropyrimidinase, transcript variant X3
dihydropyrimidinase, transcript variant X4
dihydropyrimidinase, transcript variant X5
protein pangolin, isoforms A/H/I/S, transcript variant X7
protein pangolin, isoforms A/H/I/S, transcript variant X11
protein pangolin, isoforms A/H/I/S, transcript variant X8
protein pangolin, isoforms A/H/I/S, transcript variant X6
protein pangolin, isoforms A/H/I/S, transcript variant X3
protein pangolin, isoforms A/H/I/S, transcript variant X5
protein pangolin, isoforms A/H/I/S, transcript variant X2
protein pangolin, isoforms A/H/I/S, transcript variant X4
protein pangolin, isoforms A/H/I/S, transcript variant X1
protein pangolin, isoforms A/H/I/S isoform X7
protein pangolin, isoforms A/H/I/S isoform X11
protein pangolin, isoforms A/H/I/S isoform X8
protein pangolin, isoforms A/H/I/S isoform X6
protein pangolin, isoforms A/H/I/S isoform X3
protein pangolin, isoforms A/H/I/S isoform X5
protein pangolin, isoforms A/H/I/S isoform X2
protein pangolin, isoforms A/H/I/S isoform X4
protein pangolin, isoforms A/H/I/S isoform X1
protein pangolin, isoforms A/H/I/S, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
protein pangolin, isoforms A/H/I/S, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
protein pangolin, isoforms A/H/I/S isoform X10
protein pangolin, isoforms A/H/I/S isoform X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
uncharacterized LOC105381196, transcript variant X1
uncharacterized LOC105381196, transcript variant X2
uncharacterized protein LOC105381196 isoform X1
uncharacterized protein LOC105381196 isoform X2
uncharacterized LOC105395957, 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 44 samples with support for all annotated introns
uncharacterized protein LOC105395957 isoform X1
uncharacterized LOC105395957, 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 13 samples with support for all annotated introns
uncharacterized protein LOC105395957 isoform X2
uncharacterized LOC105395957, 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 53 samples with support for all annotated introns
uncharacterized protein LOC105395957 isoform X3
uncharacterized LOC105382669, transcript variant X1
uncharacterized LOC105382669, transcript variant X2
uncharacterized protein LOC105382669 isoform X1
uncharacterized protein LOC105382669 isoform X2
uncharacterized LOC105382669, transcript variant X3
uncharacterized protein LOC105382669 isoform 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 70 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 7 samples with support for all annotated introns
two pore potassium channel protein sup-9
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 4 samples with support for all annotated introns
dynein regulatory complex protein 8, transcript variant X1
dynein regulatory complex protein 8, transcript variant X2
dynein regulatory complex protein 8, transcript variant X3
dynein regulatory complex protein 8 isoform X2
dynein regulatory complex protein 8 isoform X1
lysophospholipase-like protein 1, 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 46 samples with support for all annotated introns
lysophospholipase-like protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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
orphan steroid hormone receptor 2, transcript variant X3
orphan steroid hormone receptor 2, transcript variant X2
orphan steroid hormone receptor 2, transcript variant X1
orphan steroid hormone receptor 2 isoform X3
orphan steroid hormone receptor 2 isoform X2
orphan steroid hormone receptor 2 isoform X1
U3 small nucleolar ribonucleoprotein protein MPP10
nuclear factor 1 B-type, 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 25 samples with support for all annotated introns
nuclear factor 1 B-type, 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 21 samples with support for all annotated introns
nuclear factor 1 B-type, transcript variant X4
nuclear factor 1 B-type, 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 20 samples with support for all annotated introns
nuclear factor 1 B-type, 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 25 samples with support for all annotated introns
nuclear factor 1 B-type, transcript variant X10
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
nuclear factor 1 B-type, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
nuclear factor 1 B-type, transcript variant X8
nuclear factor 1 B-type, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
nuclear factor 1 B-type, transcript variant X9
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
homeobox protein onecut, transcript variant X1
homeobox protein onecut, transcript variant X2
potassium voltage-gated channel protein Shal, transcript variant X1
potassium voltage-gated channel protein Shal, transcript variant X2
potassium voltage-gated channel protein Shal isoform X1
potassium voltage-gated channel protein Shal isoform X2
paired box protein Pax-2-B, 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 12 samples with support for all annotated introns
paired box protein Pax-2-B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
paired box protein Pax-2-B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC105387766, transcript variant X2
uncharacterized LOC105387766, 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 13 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 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: 1 Protein
uncharacterized LOC105387779, transcript variant X6
uncharacterized LOC105387779, transcript variant X4
uncharacterized LOC105387779, transcript variant X1
uncharacterized LOC105387779, transcript variant X3
uncharacterized LOC105387779, transcript variant X5
uncharacterized protein LOC105387779 isoform X1
uncharacterized protein LOC105387779 isoform X3
uncharacterized protein LOC105387779 isoform X5
uncharacterized protein LOC105387779 isoform X4
uncharacterized protein LOC105387779 isoform X6
uncharacterized LOC105387779, transcript variant X2
uncharacterized protein LOC105387779 isoform X2
microtubule-associated serine/threonine-protein kinase 3, transcript variant X2
microtubule-associated serine/threonine-protein kinase 3, transcript variant X6
microtubule-associated serine/threonine-protein kinase 3, transcript variant X3
microtubule-associated serine/threonine-protein kinase 3, transcript variant X7
microtubule-associated serine/threonine-protein kinase 3, transcript variant X5
microtubule-associated serine/threonine-protein kinase 3, transcript variant X4
microtubule-associated serine/threonine-protein kinase 3, transcript variant X1
microtubule-associated serine/threonine-protein kinase 3, transcript variant X8
microtubule-associated serine/threonine-protein kinase 3, transcript variant X9
microtubule-associated serine/threonine-protein kinase 3 isoform X3
microtubule-associated serine/threonine-protein kinase 3 isoform X2
microtubule-associated serine/threonine-protein kinase 3 isoform X7
microtubule-associated serine/threonine-protein kinase 3 isoform X5
microtubule-associated serine/threonine-protein kinase 3 isoform X4
microtubule-associated serine/threonine-protein kinase 3 isoform X6
microtubule-associated serine/threonine-protein kinase 3 isoform X1
microtubule-associated serine/threonine-protein kinase 3 isoform X8
pollen-specific leucine-rich repeat extensin-like protein 1
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: pollen-specific leucine-rich repeat extensin-like protein 1
protein transport protein sec31, transcript variant X1
protein transport protein sec31, transcript variant X2
protein transport protein sec31, transcript variant X3
protein transport protein sec31 isoform X1
protein transport protein sec31 isoform X2
protein MON2 homolog, 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 30 samples with support for all annotated introns
protein MON2 homolog, transcript variant X4
protein MON2 homolog, 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 33 samples with support for all annotated introns
protein MON2 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
serine/threonine-protein kinase WNK1, transcript variant X3
serine/threonine-protein kinase WNK1, transcript variant X5
serine/threonine-protein kinase WNK1, transcript variant X4
serine/threonine-protein kinase WNK1, transcript variant X1
serine/threonine-protein kinase WNK1, transcript variant X6
serine/threonine-protein kinase WNK1, transcript variant X8
serine/threonine-protein kinase WNK1, transcript variant X7
serine/threonine-protein kinase WNK1, transcript variant X2
serine/threonine-protein kinase WNK1 isoform X1
serine/threonine-protein kinase WNK1 isoform X3
serine/threonine-protein kinase WNK1 isoform X5
serine/threonine-protein kinase WNK1 isoform X4
serine/threonine-protein kinase WNK1 isoform X2
serine/threonine-protein kinase WNK1, transcript variant X9
serine/threonine-protein kinase WNK1 isoform X6
serine/threonine-protein kinase WNK1, transcript variant X10
serine/threonine-protein kinase WNK1 isoform X7
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: 1 Protein, 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: 6 Proteins, and 99% 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: 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: 98% 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125490759, transcript variant X2
uncharacterized LOC125490759, 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 73 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 6 samples with support for all annotated introns
trypsin CFT-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
trypsin CFT-1-like, transcript variant X1
uncharacterized LOC125490760, transcript variant X2
uncharacterized LOC125490760, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
transposon TX1 uncharacterized 149 kDa protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC105385439, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized LOC105385439, transcript variant X1
uncharacterized protein LOC105385439 isoform X1
uncharacterized LOC105385439, transcript variant X3
uncharacterized protein LOC105385439 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 65 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
trypsin CFT-1-like, transcript variant X4
trypsin CFT-1-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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 53 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC125490742, transcript variant X9
uncharacterized LOC125490742, transcript variant X7
uncharacterized LOC125490742, transcript variant X5
uncharacterized LOC125490742, transcript variant X2
uncharacterized LOC125490742, transcript variant X1
uncharacterized LOC125490742, transcript variant X8
uncharacterized LOC125490742, transcript variant X6
uncharacterized LOC125490742, transcript variant X4
uncharacterized LOC125490742, 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 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 70 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 9 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 9 samples with support for all annotated introns
trypsin, alkaline B-like, transcript variant X2
trypsin, alkaline B-like, transcript variant X3
trypsin, alkaline B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
trypsin, alkaline B, transcript variant X2
trypsin, alkaline B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% 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: 4 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: 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: 10 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 80 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 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 3 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 62 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
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 71 samples with support for all annotated introns
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105382816, transcript variant X1
uncharacterized LOC105382816, transcript variant X2
zinc finger protein rotund, 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
zinc finger protein rotund, transcript variant X1
zinc finger protein rotund, transcript variant X3
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein 628, transcript variant X3
zinc finger protein 628, transcript variant X2
zinc finger protein 628, transcript variant X1
zinc finger protein 628, transcript variant X4
zinc finger protein 628, transcript variant X9
zinc finger protein 628, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein 628, transcript variant X5
zinc finger protein 628, transcript variant X7
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
zinc finger protein 628, transcript variant X6
zinc finger and BTB domain-containing protein 24 isoform X4
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
leucine-rich repeat-containing protein 71
mitochondrial import receptor subunit TOM40 homolog 1
gamma-aminobutyric acid type B receptor subunit 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
gamma-aminobutyric acid type B receptor subunit 2, transcript variant X2
gamma-aminobutyric acid type B receptor subunit 2 isoform X1
gamma-aminobutyric acid type B receptor subunit 2 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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
dual serine/threonine and tyrosine protein kinase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 72% 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 22 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 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 72% 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 75 samples with support for all annotated introns