ZIC1

Zic family member 1
OMIM: 600470, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green ZIC1 in Craniosynostosis Level 2: Dysmorphic and congenital abnormality syndromes Version 1.68	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Structural brain anomalies with impaired intellectual development and craniosynostosis, MIM# 618736 Craniosynostosis 6, MIM# 616602
Red ZIC1 in Joubert syndrome and other neurological ciliopathies Level 2: Neurology and neurodevelopmental disorders Version 1.28	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Structural brain anomalies with impaired intellectual development and craniosynostosis (MIM#618736)
Green ZIC1 in Mendeliome Version 1.2374	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Structural brain anomalies with impaired intellectual development and craniosynostosis, OMIM#618736
Green ZIC1 in Callosome Level 2: Neurology and neurodevelopmental disorders Version 0.540	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Red ZIC1 in Regression Level 2: Neurology and neurodevelopmental disorders Version 0.573	review	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services
Green ZIC1 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.83	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Structural brain anomalies with impaired intellectual development and craniosynostosis OMIM #618736 
Green ZIC1 in Fetal anomalies Version 1.314	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp Expert list Victorian Clinical Genetics Services Phenotypes Structural brain anomalies with impaired intellectual development and craniosynostosis OMIM#618736