FERMT1( Human )

Entrez Gene 55612 Entrez Gene 55612
fermitin family member 1

Alias

C20orf42|DTGCU2|KIND1|UNC112A|URP1

This gene encodes a member of the fermitin family, and contains a FERM domain and a pleckstrin homology domain. The encoded protein is involved in integrin signaling and linkage of the actin cytoskeleton to the extracellular matrix. Mutations in this gene have been linked to Kindler syndrome. [provided by RefSeq, Dec 2009].

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