CEP63 Chromosome 3

Centrosomal protein 63
36 variants 36 Health Risk

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What This Gene Does
This gene encodes a protein with six coiled-coil domains. The protein is localized to the centrosome, a non-membraneous organelle that functions as the major microtubule-organizing center in animal cells. Several alternatively spliced transcript variants have been found, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]
Associated Conditions (4)
Seckel syndrome 6
Familial cancer of breast
Inborn genetic diseases
Papillary renal cell carcinoma type 1
Key Variants
All Variants (36)
RSID Category Clinical Significance Conditions
RS142766824 Health Risk Conflicting classifications of pathogenicity —
RS372685774 Health Risk Conflicting classifications of pathogenicity Seckel syndrome 6, Seckel syndrome 6
RS529386244 Health Risk Conflicting classifications of pathogenicity —
RS752207334 Health Risk Conflicting classifications of pathogenicity Seckel syndrome 6, Familial cancer of breast, Seckel syndrome 6
RS763001827 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS765783970 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS797045459 Health Risk Conflicting classifications of pathogenicity —
RS1185168725 Health Risk Likely pathogenic —
RS1396633264 Health Risk Likely pathogenic —
RS150764448 Health Risk Likely pathogenic Papillary renal cell carcinoma type 1, Papillary renal cell carcinoma type 1
RS1956657659 Health Risk Likely pathogenic —
RS2109591981 Health Risk Likely pathogenic Seckel syndrome 6, Seckel syndrome 6
RS2547181177 Health Risk Likely pathogenic Seckel syndrome 6, Seckel syndrome 6
RS746387482 Health Risk Likely pathogenic Seckel syndrome 6, Seckel syndrome 6
RS753579827 Health Risk Likely pathogenic Seckel syndrome 6, Seckel syndrome 6
RS769414976 Health Risk Likely pathogenic —
RS773725359 Health Risk Likely pathogenic Seckel syndrome 6, Seckel syndrome 6
RS867015582 Health Risk Likely pathogenic —
RS1164567042 Health Risk Pathogenic Seckel syndrome 6, Seckel syndrome 6
RS1187435534 Health Risk Pathogenic —
RS1266747910 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1358372238 Health Risk Pathogenic —
RS1378870937 Health Risk Pathogenic —
RS141121335 Health Risk Pathogenic —
RS1953288507 Health Risk Pathogenic —
RS2546774426 Health Risk Pathogenic —
RS2546848928 Health Risk Pathogenic Seckel syndrome 6, Seckel syndrome 6
RS2546985015 Health Risk Pathogenic —
RS2547015012 Health Risk Pathogenic —
RS368122278 Health Risk Pathogenic —
RS753461493 Health Risk Pathogenic —
RS756469612 Health Risk Pathogenic —
RS771949417 Health Risk Pathogenic —
RS774485513 Health Risk Pathogenic —
RS775712041 Health Risk Pathogenic —
RS933176029 Health Risk Pathogenic —
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