FERMT1
Sign in to saveAlso known as C20orf42, DTGCU2, KIND1, UNC112A, URP1, fermitin family member 1, FERM domain containing kindlin 1
Fermitin family homolog 1 is a protein that in humans is encoded by the FERMT1 gene.
Gene data
FERMT1- Name
- FERM domain containing kindlin 1
- Type
- protein-coding
- Position
- 6,070,288–6,123,644 (−)
- Aliases
- C20orf42, DTGCU2, KIND1, UNC112A, URP1
- Ensembl
- ENSG00000101311
- RefSeq RNA
- NM_017671.5, XM_024451935.2, XM_047440259.1, XM_047440260.1, XM_054323631.1
- RefSeq protein
- NP_060141.3, XP_024307703.1, XP_047296215.1, XP_047296216.1, XP_054179606.1
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 Ontology
Biological process
Molecular function
via MyGene.info
Gene · Ensembl
FERM domain containing kindlin 1
- Symbol
- FERMT1
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 20:6,070,288-6,123,644
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Image
- Mouse Fermitin family homolog 1 4BBK.png
Show 5 more facts
- HomoloGene ID
- 9773
- exact match
- identifiers.org/ncbigene/55612
- genomic start
- 6055492
- genomic end
- 6123030
- cytogenetic location
- 20p12.3
Sources (4)
via Wikidata · CC0
~1 min read
Article
3 sectionsContents
- References
- External links
- Further reading
Fermitin family homolog 1 is a protein that in humans is encoded by the FERMT1 gene.
==References==