VCX2 variable charge X-linked 2

Information
Symbol
VCX2
Type
protein-coding
Description
variable charge X-linked 2
Entrez Gene ID
51480
Genome
hg19
Position
chrX:8,137,985-8,139,308
Genome
hg38
Position
chrX:8,169,944-8,171,267
MIM
300532 OMIM
HGNC
HGNC:18158 HGNC
Ensembl
ENSG00000177504 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 20
not provided 8 0
Uncertain significance 0 74
Ranking
ClinVar
0
0
0
94
2
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 VCX-2r
SYNONYM VCX2R
SYNONYM VCXB
MIM 300532 OMIM
HGNC HGNC:18158 HGNC
Ensembl ENSG00000177504 Ensembl
AllianceGenome HGNC:18158
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000317103.5 hg38 chrX 8,169,944 8,171,267 1,324
ENST00000317103.5 hg19 chrX 8,137,985 8,139,308 1,324
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