Annotation Detail
Information
- Associated Genes
- CFH
- Associated Variants
-
ENSG00000289697 p.Ser1191Leu (p.S1191L), CFH p.Ser1191Leu (p.S1191L)
(
ENST00000696029.1,
ENST00000695976.1,
ENST00000696028.1,
ENST00000696027.1,
ENST00000695984.1,
ENST00000695981.1,
ENST00000695971.1,
ENST00000695974.1,
ENST00000695970.1,
ENST00000367429.9 )
ENSG00000289697 p.Ser1191Leu (p.S1191L), CFH p.Ser1191Leu (p.S1191L) ( ENST00000367429.9, ENST00000695970.1, ENST00000695971.1, ENST00000695974.1, ENST00000695976.1, ENST00000695981.1, ENST00000695984.1, ENST00000696027.1, ENST00000696028.1, ENST00000696029.1 ) - Associated Disease
- Atypical Hemolytic Uremic Syndrome
- Source Database
- DisGeNET
- Description
- Renal transplantation in patients with the S1191L mutation of the CFH gene carries a high risk of failure due to recurrence of aHUS in the renal graft.
- Pubmed
- 19856002
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.231606809293154
- Year of publication
- 2010
Drugs