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
RS1029955995 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, Inborn genetic diseases, PCNT-related disorder
RS1064793985 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS112231246 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS112633352 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS113208348 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS113342730 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, PCNT-related disorder, Inborn genetic diseases
RS113591604 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Intellectual disability
RS113731555 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS115369710 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS1170990391 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS1229663143 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS1234384421 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS1292668105 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS137912192 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS138506849 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS138543824 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS138617654 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS138868039 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS138962786 Health Risk Conflicting classifications of pathogenicity Global developmental delay, Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder
RS139383288 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS139581644 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS140290722 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS140398533 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS140416280 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS140836847 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS140912550 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS141211481 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS141276542 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS141635334 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS141771795 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS142080697 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Inborn genetic diseases, PCNT-related disorder
RS142413458 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS142800774 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS143064269 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS143511166 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS143560718 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS143671774 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS143776463 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS144342729 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS144445891 Health Risk Conflicting classifications of pathogenicity
RS144633170 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder
RS144651746 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS144683591 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS144775948 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS144869229 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS145119952 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephaly, PCNT-related disorder
RS146657011 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Hepatocellular carcinoma
RS146717642 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS146792192 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Inborn genetic diseases, PCNT-related disorder
RS147358856 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II, Inborn genetic diseases
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