PCNT Chromosome 21

Pericentrin
485 variants 485 Health Risk

Upload your DNA to see your personal genotypes for variants in PCNT.

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
RS147670568 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS147868583 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS147878958 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, Familial cancer of breast, PCNT-related disorder
RS148444313 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS1486232846 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS149264703 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Inborn genetic diseases, PCNT-related disorder
RS149623054 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS150156962 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS150279909 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS150355356 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, Inborn genetic diseases, PCNT-related disorder
RS150436577 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS150554265 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS150882711 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS150892737 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS151138182 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS151325202 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS180775012 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS181165794 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS181294356 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS182378192 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Thymoma
RS182694054 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS193261408 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS199844366 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, PCNT-related disorder, Inborn genetic diseases
RS199847432 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS199857861 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS199864153 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS200137805 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS200174202 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS200294006 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS200559632 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, Inborn genetic diseases, PCNT-related disorder
RS200571944 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS200610141 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS200910675 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS201042435 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS201124068 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS201139850 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS201185279 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS201315836 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephaly, PCNT-related disorder
RS201503338 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS201507947 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, PCNT-related disorder, Inborn genetic diseases
RS201549624 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS201562329 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS201652457 Health Risk Conflicting classifications of pathogenicity
RS201798996 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS201809134 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS201944549 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, PCNT-related disorder, Microcephalic osteodysplastic primordial dwarfism type II
RS202005598 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
RS202096874 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Microcephalic osteodysplastic primordial dwarfism type II
RS202161810 Health Risk Conflicting classifications of pathogenicity Microcephalic osteodysplastic primordial dwarfism type II, Inborn genetic diseases, PCNT-related disorder
RS202170105 Health Risk Conflicting classifications of pathogenicity PCNT-related disorder, PCNT-related disorder
« Prev 1 2 3 4 5 ... 10 Next »
Sign Up to Analyze Your DNA Log In