PCNT: Difference between revisions
CSV import Tags: mobile edit mobile web edit |
CSV import |
||
| Line 30: | Line 30: | ||
{{stub}} | {{stub}} | ||
{{No image}} | |||
Revision as of 19:15, 10 February 2025
PCNT (Pericentrin) is a protein that in humans is encoded by the PCNT gene. It is a component of the centrosome, an organelle responsible for microtubule organization and cell cycle progression. Mutations in the PCNT gene are associated with Microcephalic osteodysplastic primordial dwarfism type II (MOPD II), a rare genetic disorder characterized by severe growth retardation and microcephaly.
Function
Pericentrin is a large coiled-coil protein of the centrosome, a cell organelle involved in cell division. It plays a crucial role in microtubule organization and the progression of the cell cycle. Pericentrin also anchors the gamma-tubulin ring complex, a multiprotein complex involved in microtubule nucleation.
Clinical significance
Mutations in the PCNT gene are associated with Microcephalic osteodysplastic primordial dwarfism type II (MOPD II), a rare genetic disorder characterized by severe growth retardation and microcephaly. Patients with MOPD II also exhibit skeletal abnormalities, including hip dislocation and short stature.
See also
References
<references />


