CEP135

centrosomal protein 135
OMIM: 611423, ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green CEP135 in Mendeliome Version 1.2302	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Microcephalic primordial dwarfism Microcephaly 8, primary, autosomal recessive, 614673
Green CEP135 in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.295	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Microcephalic primordial dwarfism Microcephaly 8, primary, autosomal recessive, 614673
Red CEP135 in Callosome Level 2: Neurology and neurodevelopmental disorders Version 0.540	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Microcephalic primordial dwarfism Microcephaly 8, primary, autosomal recessive, 614673
Green CEP135 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.63	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genetic Health Queensland Phenotypes Microcephalic primordial dwarfism Microcephaly 8, primary, autosomal recessive, 614673
Green CEP135 in Fetal anomalies Version 1.313	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Genetic Health Queensland Phenotypes Microcephaly 8, primary, autosomal recessive, OMIM:614673 Microcephaly 8, primary, autosomal recessive, MONDO:0013849 Microcephalic primordial dwarfism