Annotation Detail
Information
- Associated Genes
- MUTYH
- Associated Variants
-
MUTYH p.Gly393Asp (p.G393D), ENSG00000288208 p.Gly564Asp (p.G564D)
(
ENST00000531105.5,
ENST00000672818.3,
ENST00000448481.5,
ENST00000372098.7,
ENST00000529892.6,
ENST00000710952.2,
ENST00000713750.1,
ENST00000372110.7,
ENST00000529984.5,
ENST00000372115.7,
ENST00000672314.2,
ENST00000483127.2,
ENST00000456914.7,
ENST00000354383.10,
ENST00000372104.5,
ENST00000528013.6,
ENST00000412971.6,
ENST00000355498.6,
ENST00000713751.1,
ENST00000488731.6 )
MUTYH p.Tyr176Cys (p.Y176C), ENSG00000288208 p.Tyr347Cys (p.Y347C) ( ENST00000372098.7, ENST00000448481.5, ENST00000529892.6, ENST00000531105.5, ENST00000672818.3, ENST00000713750.1, ENST00000372110.7, ENST00000710952.2, ENST00000528013.6, ENST00000412971.6, ENST00000372104.5, ENST00000355498.6, ENST00000372115.7, ENST00000529984.5, ENST00000456914.7, ENST00000354383.10, ENST00000672314.2, ENST00000483127.2, ENST00000488731.6, ENST00000713751.1 )
MUTYH p.Gly393Asp (p.G393D), ENSG00000288208 p.Gly564Asp (p.G564D) ( ENST00000354383.10, ENST00000355498.6, ENST00000372098.7, ENST00000372104.5, ENST00000372110.7, ENST00000372115.7, ENST00000412971.6, ENST00000448481.5, ENST00000456914.7, ENST00000483127.2, ENST00000488731.6, ENST00000528013.6, ENST00000529892.6, ENST00000529984.5, ENST00000531105.5, ENST00000672314.2, ENST00000672818.3, ENST00000710952.2, ENST00000713750.1, ENST00000713751.1 )
MUTYH p.Tyr176Cys (p.Y176C), ENSG00000288208 p.Tyr347Cys (p.Y347C) ( ENST00000354383.10, ENST00000355498.6, ENST00000372098.7, ENST00000372104.5, ENST00000372110.7, ENST00000372115.7, ENST00000412971.6, ENST00000448481.5, ENST00000456914.7, ENST00000483127.2, ENST00000488731.6, ENST00000528013.6, ENST00000529892.6, ENST00000529984.5, ENST00000531105.5, ENST00000672314.2, ENST00000672818.3, ENST00000710952.2, ENST00000713750.1, ENST00000713751.1 ) - Associated Disease
- Colorectal Adenomatous Polyposis, Autosomal Recessive
- Source Database
- DisGeNET
- Description
- Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors.
- Pubmed
- 11818965
- Original source reporting the Gene Disease association
- UNIPROT
- DisGENET score for the Gene Disease association
- 0.48027144187208
- Year of publication
- 2002
Drugs