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Basic information of VDR :

Official Symbol of Gene VDR
Species Homo sapiens
Entrez Gene ID 7421
Official Full Name vitamin D receptor
Also known as NR1I1; PPP1R163
Gene Type protein coding
dbXrefs Ensembl:ENSG00000111424 MIM:601769; AllianceGenome:HGNC:12679
Map Location 12q13.11
Variation Type intragenic restriction fragment length polymorphisms
refSNP ID N/A

Sample information of multiple sclerosis:

Detected Sample peripheral blood
Sample Detail PBMC
Detected Method PCR
Disease MS
Disease subtype RRMS,PPMS,SPMS
Population Australian
Sample Size 208

Literature information of multiple sclerosis :

Pubmed ID 16076630
Year 2005
Title VARIATION IN THE VITAMIN D RECEPTOR GENE IS ASSOCIATED WITH MULTIPLE SCLEROSIS IN AN AUSTRALIAN POPULATION

Results of multiple sclerosis :

Risk Type Disease risk
Main Result Positive
Result Our results support a role for the VDR gene increasing the risk of developing multiple sclerosis, particularly the progressive clinical subtypes of MS.
Mechanism/Pathway The Taq and Apa variants are in very strong and significant linkage disequilibrium (D0 0.96, P < 0.0001). The genotypic associations are strongest for the progressive forms of MS (SP–MS and PP–MS)