FERMT2
Sign in to saveAlso known as KIND2, MIG2, PLEKHC1, UNC112, UNC112B, mig-2, fermitin family member 2, URP2SF
Fermitin family homolog 2 (FERMT2) also known as pleckstrin homology domain-containing family C member 1 (PLEKHC1) or kindlin-2 is a protein that in humans is encoded by the FERMT2 gene.
In the Vinony graph
Vinony's link graph records 7 inbound references to FERMT2, and connects out to PubMed, human chromosome 14 and Ensembl genome database project.
It is catalogued under the topic Genes on human chromosome 14.
Vinony links it to 5 Wikipedia language editions.
Gene data
FERMT2- Name
- FERM domain containing kindlin 2
- Type
- protein-coding
- Position
- 52,856,943–52,952,435 (−)
- Aliases
- KIND2, MIG2, PLEKHC1, UNC112, UNC112B, mig-2
- Ensembl
- ENSG00000073712
- RefSeq RNA
- NM_001134999.2, NM_001135000.2, NM_006832.3, XM_005267285.4, XM_006720008.4
- RefSeq protein
- NP_001128471.1, NP_001128472.1, NP_006823.1, XP_005267342.1, XP_006720071.1
Enables several functions, including actin binding activity; phosphatidylinositol-3,4,5-trisphosphate binding activity; and type I transforming growth factor beta receptor binding activity. Involved in several processes, including cell surface receptor signaling pathway; positive regulation of cell differentiation; and positive regulation of cellular component biogenesis. Acts upstream of or within cell adhesion and protein localization to cell junction. Located in cytosol; focal adhesion; and nucleoplasm. Is extrinsic component of cytoplasmic side of plasma membrane. Part of adherens junction and plasma membrane. Biomarker of acute myeloid leukemia. [provided by Alliance of Genome Resources, Apr 2022]
Gene Ontology
Biological process
Molecular function
Cellular component
Pathways
via MyGene.info
Gene · Ensembl
FERM domain containing kindlin 2
- Symbol
- FERMT2
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 14:52,856,943-52,952,435
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 8 more facts
- HomoloGene ID
- 4976
- cytogenetic location
- 14q22.1
- genetic association
- Alzheimer's disease
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/10979
- genomic end
- 53419153
- genomic start
- 53323986
- chromosome
- human chromosome 14
via Wikidata · CC0
~2 min read
Encyclopedic overview
6 sectionsContents
- Function
- Interactions
- Role in health and diseases
- References
- Further reading
- External links
Fermitin family homolog 2 (FERMT2) also known as pleckstrin homology domain-containing family C member 1 (PLEKHC1) or kindlin-2 is a protein that in humans is encoded by the FERMT2 gene.
Kindlin-2 is the first of the kindlin protein to be discovered in 1994. It was detected in a screen for epidermal growth factor (EGF)-induced mRNAs and initially named mitogen-inducible gene 2 (Mig-2) protein.
Excerpted from Wikipedia’s “FERMT2” article, available under the CC BY-SA 4.0 licence.