FAH Back

fumarylacetoacetate hydrolase (fumarylacetoacetase)

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NCBI Description of FAH
This gene encodes the last enzyme in the tyrosine catabolism pathway. FAH deficiency is associated with Type 1 hereditary tyrosinemia (HT).

Community Annotation of FAH Add / Edit FAH: Annotations

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Sort mutations by: Tumor type  Mutation type  Position  
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Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

FAH is highly significantly mutated in
(none)
FAH is significantly mutated in
(none)
FAH is near significance in
(none)

Click on a tumor type to see its full list of significant genes.

Data details


• Mutation list for FAH