CEP63, centrosomal protein 63, 80254

N. diseases: 44; N. variants: 15
Disease: SECKEL SYNDROME 6 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3553582
Disease: SECKEL SYNDROME 6
SECKEL SYNDROME 6 		0.400 Biomarker disease GENOMICS_ENGLAND Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family. 26400686 2015
CUI: C3553582
Disease: SECKEL SYNDROME 6
SECKEL SYNDROME 6 		0.400 Biomarker disease GENOMICS_ENGLAND CEP63 deficiency promotes p53-dependent microcephaly and reveals a role for the centrosome in meiotic recombination. 26158450 2015
CUI: C3553582
Disease: SECKEL SYNDROME 6
SECKEL SYNDROME 6 		0.400 GeneticVariation disease CLINVAR A primary microcephaly protein complex forms a ring around parental centrioles. 21983783 2011
CUI: C3553582
Disease: SECKEL SYNDROME 6
SECKEL SYNDROME 6 		0.400 Biomarker disease GENOMICS_ENGLAND A primary microcephaly protein complex forms a ring around parental centrioles. 21983783 2011
CUI: C3553582
Disease: SECKEL SYNDROME 6
SECKEL SYNDROME 6 		0.400 Biomarker disease GENOMICS_ENGLAND A primary microcephaly protein complex forms a ring around parental centrioles. 21983783 2011
CUI: C3553582
Disease: SECKEL SYNDROME 6
SECKEL SYNDROME 6 		0.400 CausalMutation disease CLINVAR