CXorf66 chromosome X open reading frame 66

Information
Symbol
CXorf66
Type
protein-coding
Description
chromosome X open reading frame 66
Entrez Gene ID
347487
Genome
hg19
Position
chrX:139,037,887-139,047,680
Genome
hg38
Position
chrX:139,955,728-139,965,521
HGNC
HGNC:33743 HGNC
Ensembl
ENSG00000203933 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 6 0
Uncertain significance 0 4
Ranking
ClinVar
0
0
0
6
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 SGPX
HGNC HGNC:33743 HGNC
Ensembl ENSG00000203933 Ensembl
AllianceGenome HGNC:33743
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000370540.2 hg38 chrX 139,955,728 139,965,521 9,794
ENST00000370540.2 hg19 chrX 139,037,887 139,047,680 9,794
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