| Protein Name | formin homology 2 domain containing 1 |
|---|---|
| Organism | Homo sapiens |
| Gene ID | 29109 |
| Gene Symbol | FHOD1 |
| UniProt | Q9Y613 (FHOD1_HUMAN), A0A068F7M9 (A0A068F7M9_HUMAN) |
| Relationships |
Total Number of functionally related compound(s) :
17
Total Number of Articles : 12 |
Description |
formin homology 2 domain containing 1 |
| Gene Summary |
This gene encodes a protein which is a member of the formin/diaphanous family of proteins. The gene is ubiquitously expressed but is found in abundance in the spleen. The encoded protein has sequence homology to diaphanous and formin proteins within the Formin Homology (FH)1 and FH2 domains. It also contains a coiled-coil domain, a collagen-like domain, two nuclear localization signals, and several potential PKC and PKA phosphorylation sites. It is a predominantly cytoplasmic protein and is expressed in a variety of human cell lines. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015] |
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