| Gene Symbol | PCNT |
| Entrez Gene ID | 5116 |
| Full Name | pericentrin |
| Synonyms | KEN,MOPD2,PCN,PCNT2,PCNTB,PCTN2,SCKL4 |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | The protein encoded by this gene binds to calmodulin and is expressed in the centrosome. It is an integral component of the pericentriolar material (PCM). The protein contains a series of coiled-coil domains and a highly conserved PCM targeting motif called the PACT domain near its C-terminus. The protein interacts with the microtubule nucleation component gamma-tubulin and is likely important to normal functioning of the centrosomes, cytoskeleton, and cell-cycle progression. Mutations in this gene cause Seckel syndrome-4 and microcephalic osteodysplastic primordial dwarfism type II. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]. |
| Disorder MIM: | |
| Disorder Html: | Microcephalic osteodysplastic primordial dwarfism, type II, 210720 (3) |







































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