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5 Possible Causes for Mutation in the CENPE Gene

  • Autosomal Recessive Primary Microcephaly 13

    […] in the PHC1 gene ({602978}) on 12p13; MCPH12 ({616080}), caused by mutation in the CDK6 gene ({603368}) on 7q21; MCPH13 ({616051}), caused by mutation in the CENPE gene ([diseaseinfosearch.org] {117143}) on 4q24; MCPH14 ({616402}), caused by mutation in the SASS6 gene ({609321}) on 1p21; MCPH15 ({616486}), caused by mutation in the MFSD2A gene ({614397}) on 1p34;[diseaseinfosearch.org] }), caused by mutation in the CEP152 gene ({613529}) on 15q21; MCPH10 ({615095}), caused by mutation in the ZNF335 gene ({610827}) on 20q13; MCPH11 ({615414}), caused by mutation[diseaseinfosearch.org]

  • Autosomal Recessive Primary Microcephaly 12

    […] in the PHC1 gene ({602978}) on 12p13; MCPH12 ({616080}), caused by mutation in the CDK6 gene ({603368}) on 7q21; MCPH13 ({616051}), caused by mutation in the CENPE gene ([diseaseinfosearch.org] {117143}) on 4q24; MCPH14 ({616402}), caused by mutation in the SASS6 gene ({609321}) on 1p21; MCPH15 ({616486}), caused by mutation in the MFSD2A gene ({614397}) on 1p34;[diseaseinfosearch.org] }), caused by mutation in the CEP152 gene ({613529}) on 15q21; MCPH10 ({615095}), caused by mutation in the ZNF335 gene ({610827}) on 20q13; MCPH11 ({615414}), caused by mutation[diseaseinfosearch.org]

  • Autosomal Recessive Primary Microcephaly 11

    […] in the PHC1 gene ({602978}) on 12p13; MCPH12 ({616080}), caused by mutation in the CDK6 gene ({603368}) on 7q21; MCPH13 ({616051}), caused by mutation in the CENPE gene ([diseaseinfosearch.org] {117143}) on 4q24; MCPH14 ({616402}), caused by mutation in the SASS6 gene ({609321}) on 1p21; MCPH15 ({616486}), caused by mutation in the MFSD2A gene ({614397}) on 1p34;[diseaseinfosearch.org] }), caused by mutation in the CEP152 gene ({613529}) on 15q21; MCPH10 ({615095}), caused by mutation in the ZNF335 gene ({610827}) on 20q13; MCPH11 ({615414}), caused by mutation[diseaseinfosearch.org]

  • Autosomal Dominant Microcephaly

    […] in the PHC1 gene ({602978}) on 12p13; MCPH12 ({616080}), caused by mutation in the CDK6 gene ({603368}) on 7q21; MCPH13 ({616051}), caused by mutation in the CENPE gene ([diseaseinfosearch.org] {117143}) on 4q24; MCPH14 ({616402}), caused by mutation in the SASS6 gene ({609321}) on 1p21; MCPH15 ({616486}), caused by mutation in the MFSD2A gene ({614397}) on 1p34;[diseaseinfosearch.org] }), caused by mutation in the CEP152 gene ({613529}) on 15q21; MCPH10 ({615095}), caused by mutation in the ZNF335 gene ({610827}) on 20q13; MCPH11 ({615414}), caused by mutation[diseaseinfosearch.org]

  • X-Linked Intellectual Disability Type Cantagrel

    […] in the CENPE gene (117143) on chromosome 4q24.[findzebra.com] […] in the centromeric protein E gene (CENPE, 117143.0001) Giant congenital nevus A giant congenital nevus is a dark-colored, often hairy patch of skin that is present at birth[findzebra.com] […] corpus callosum (in 1 of 2 sibs); Cerebellar hypoplasia (in 1 of 2 sibs) MISCELLANEOUS: Two sibs have been reported (last curated October 2014) MOLECULAR BASIS: Caused by mutation[findzebra.com]

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