Annotation Detail
Information
- Associated Genes
- POLG
- Associated Variants
-
POLG p.Pro1073Leu (p.P1073L)
(
ENST00000636937.2,
ENST00000442287.6,
ENST00000268124.11 )
POLG p.Pro1073Leu (p.P1073L) ( ENST00000268124.11, ENST00000442287.6, ENST00000636937.2 ) - Associated Disease
- hepatic encephalopathy
- Source Database
- DisGeNET
- Description
- To describe a novel POLG missense mutation (c.3218C>T; p.P1073L) that, in association with 2 previously described mutations, caused an Alpers-like hepatocerebral syndrome in 4 children.
- Pubmed
- 20142534
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000271441872080303
- Year of publication
- 2010
Drugs