FERMT1, fermitin family member 1

FERMT1, fermitin family member 1

• 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]

• Gene Synonyms (C20orf42, DTGCU2, KIND1, UNC112A, URP1, fermitin family homolog 1, UNC112 related protein 1, kindlerin, kindlin 1, kindlin syndrome protein, unc-112-related protein 1,)
• NCBI Gene ID: 55612
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q54A15
  UNIPROT ID#>>Q9BQL6
  UNIPROT ID#>>Q49AC8
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

fermitin family member 1 interacts with:

• fermitin family member 3
  MAD2 mitotic arrest deficient-like 1
  membrane associated guanylate kinase, WW and PDZ domain containing 3
  parvin alpha
  ribonuclease H2 subunit B
  threonyl-tRNA synthetase 3

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.