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Protein-coding gene in the species Homo sapiens
Fibroblast growth factor 16 is a protein which in humans is encoded by the FGF16 gene. The protein encoded by this gene is a member of the fibroblast growth
FGF16
Medical condition
caused by X-linked recessive mutations (alterations or duplications) in the FGF16 gene, in chromosome X. It is a feature of various rare disorders such as
Metacarpal_synostosis
Protein found in humans
FGFs that bind to and activate one or more of the FGFRs: FGF1 to FGF10 and FGF16 to FGF23. Fourteen of these, FGF1 to FGF6, FGF8, FGF10, FGF17, and FGF19
Fibroblast growth factor receptor 1
Fibroblast_growth_factor_receptor_1
HGNC:3668; P61328 5647 FGF13 HGNC:3670; Q92913 5648 FGF14 HGNC:3671; Q92915 5649 FGF16 HGNC:3672; O43320 5650 FGF17 HGNC:3673; O60258 5651 FGF18 HGNC:3674; O76093
List of human protein-coding genes 3
List_of_human_protein-coding_genes_3
FGF16
FGF16
FGF16
FGF16
FGF16
FGF16
FGF16
FGF16
FGF16