PCNT Chromosome 21

Pericentrin
485 variants 485 Health Risk

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What This Gene Does
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]
Associated Conditions (13)
PCNT-related disorder
Inborn genetic diseases
Microcephalic osteodysplastic primordial dwarfism type II
Intellectual disability
Global developmental delay
Microcephaly
Hepatocellular carcinoma
Familial cancer of breast
Thymoma
Cervical cancer
See cases
Sarcoma
Melanoma
Key Variants
RS1029955995
Conflicting classifications of pathogenicity
PCNT-related disorder, Inborn genetic diseases, PCNT-related disorder
Health Risk
RS1064793985
Conflicting classifications of pathogenicity
Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
Health Risk
RS112231246
Conflicting classifications of pathogenicity
Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
Health Risk
RS112633352
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS113208348
Conflicting classifications of pathogenicity
PCNT-related disorder, PCNT-related disorder
Health Risk
RS113342730
Conflicting classifications of pathogenicity
Inborn genetic diseases, PCNT-related disorder, Inborn genetic diseases
Health Risk
RS113591604
Conflicting classifications of pathogenicity
Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Intellectual disability
Health Risk
RS113731555
Conflicting classifications of pathogenicity
Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
Health Risk
RS115369710
Conflicting classifications of pathogenicity
Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
Health Risk
RS1170990391
Conflicting classifications of pathogenicity
Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
Health Risk
RS1229663143
Conflicting classifications of pathogenicity
Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
Health Risk
RS1234384421
Conflicting classifications of pathogenicity
Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
Health Risk
All Variants (485)
RSID Category Clinical Significance Conditions
RS202221024 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS2070426 Health Risk Conflicting classifications of pathogenicity
RS2085811037 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS2839217 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS35513449 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Inborn genetic diseases, PCNT-related disorder
RS367928364 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS368199588 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS368565898 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS368569999 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS368579694 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS369038814 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS369178196 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS369586175 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, Inborn genetic diseases, PCNT-related disorder
RS369876466 Health Risk Conflicting classifications of pathogenicity
RS370099497 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS370266308 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, See cases, Microcephalic osteodysplastic primordial dwarfism type II
RS370423096 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS371666981 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS371917839 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS372175239 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS372356069 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, See cases, PCNT-related disorder
RS372531708 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS373238616 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS374300652 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS374344594 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, PCNT-related disorder, Inborn genetic diseases
RS374903045 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, Inborn genetic diseases, PCNT-related disorder
RS375279759 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS375581809 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS376185703 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS376236418 Health Risk Conflicting classifications of pathogenicity
RS377164652 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS377552545 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS377749878 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS527590016 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS535358423 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder
RS541135644 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, Inborn genetic diseases, PCNT-related disorder
RS541260181 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS542099749 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, PCNT-related disorder, Inborn genetic diseases
RS544254673 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS546562229 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS548190846 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS559031201 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS562568796 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS569351854 Health Risk Conflicting classifications of pathogenicity
RS57046460 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Inborn genetic diseases, PCNT-related disorder
RS572321857 Health Risk Conflicting classifications of pathogenicity
RS572444748 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS575720246 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS576187743 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS58106867 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
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