FSHR Back

follicle stimulating hormone receptor

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NCBI Description of FSHR

The protein encoded by this gene belongs to family 1 of G-protein coupled receptors. It is the receptor for follicle stimulating hormone and functions in gonad development. Mutations in this gene cause ovarian dysgenesis type 1, and also ovarian hyperstimulation syndrome. Alternative splicing results in multiple transcript variants.

Community Annotation of FSHR Add / Edit FSHR: Annotations

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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

FSHR is highly significantly mutated in
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FSHR is significantly mutated in
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FSHR is near significance in
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Click on a tumor type to see its full list of significant genes.

Data details


Mutation list for FSHR