XB-FEAT-5960334: Difference between revisions
Jump to navigation
Jump to search
imported>Xenbase gene generator No edit summary |
imported>Xenbase |
||
| Line 1: | Line 1: | ||
=fermt1= | =fermt1= | ||
This is the community wiki page for the gene ''fermt1'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | This is the community wiki page for the gene ''fermt1'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | ||
=nomenclature changes = | |||
02.17.2021 | |||
Human name has changed for Entrez Gene: 55612. From fermitin family member 1 to FERM domain containing kindlin 1 | |||
=Summary for human FERMT1 from NCBI= | |||
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] | |||
Latest revision as of 14:48, 19 February 2021
fermt1
This is the community wiki page for the gene fermt1 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
nomenclature changes
02.17.2021
Human name has changed for Entrez Gene: 55612. From fermitin family member 1 to FERM domain containing kindlin 1
Summary for human FERMT1 from NCBI
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]