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Intellectual_disability

Gene: CEP152

Red List (low evidence)

CEP152 (centrosomal protein 152)
EnsemblGeneIds (GRCh38): ENSG00000103995
EnsemblGeneIds (GRCh37): ENSG00000103995
OMIM: 613529, Gene2Phenotype
CEP152 is in 5 panels

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Details

Sources
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Microcephaly 9, primary, autosomal recessive, 614852Seckel syndrome 5, 613823
OMIM
613529
Clinvar variants
Variants in CEP152
Penetrance
Complete
Panels with this gene

History Filter Activity

8 Oct 2015, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

CEP152 was added to Intellectual_disabilitypanel. Sources: Radboud University Medical Center, Nijmegen