SPANXA2-OT1 SPANXA2 overlapping transcript 1

Information
Symbol
SPANXA2-OT1
Type
ncRNA
Description
SPANXA2 overlapping transcript 1
Entrez Gene ID
619455
Genome
hg19
Position
chrX:140,271,469-140,307,747
Genome
hg38
Position
chrX:141,177,284-141,213,568
HGNC
HGNC:31683 HGNC
Ensembl
ENSG00000277215 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 0
Ranking
ClinVar
0
0
0
0
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM CXorf18
HGNC HGNC:31683 HGNC
Ensembl ENSG00000277215 Ensembl
AllianceGenome HGNC:31683
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000666501.1 hg38 chrX 141,177,314 141,213,572 36,259
ENST00000662492.1 hg38 chrX 141,177,323 141,649,175 471,853
ENST00000665569.1 hg38 chrX 141,177,284 141,213,568 36,285
ENST00000665569.1 hg19 chrX 140,271,469 140,307,747 36,279
ENST00000666501.1 hg19 chrX 140,271,499 140,307,751 36,253
ENST00000662492.1 hg19 chrX 140,271,508 140,737,305 465,798
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