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FERMT1

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For Research Use Only. Not For Clinical Use.


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.
FERMT1
Protein class

Disease related genes, Human disease related genes

Predicted location

Intracellular

Single cell type specificity

Cell type enhanced (Pancreatic endocrine cells, Oligodendrocyte precursor cells, Basal squamous epithelial cells, Undifferentiated cells)

Immune cell specificity

Not detected in immune cells

Cell line specificity

Cell line enhanced (CAPAN-2, HaCaT, HBEC3-KT, OE19, RT4)

Interaction

Interacts with the cytoplasmic domain of integrins ITGB1 and ITGB3.

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