Fibroblast growth factor receptor

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== Disease ==
== Disease ==
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Mutation in FGFR3 causes achondroplasia and is involved in myeloma. Mutations in FGFR2 cause Crouzon syndrome.
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Mutation in FGFR3 causes achondroplasia<ref>PMID:9718331</ref> and is involved in myeloma<ref>PMID:11529856</ref>. Mutations in FGFR2 cause Crouzon syndrome<ref>PMID:7493034</ref>.
== Structural insights ==
== Structural insights ==

Revision as of 08:18, 16 May 2017

Human fibroblast growth factor receptor 1 ligand-binding domain modules D2 and D3 (pink and yellow) complex with fibroblast growth factor 1 (cyan and green) and sulfate (PDB code 1evt)

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3D structures of fibroblast growth factor receptor

Updated on 16-May-2017

Proteopedia Page Contributors and Editors (what is this?)

Michal Harel, Alexander Berchansky

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