ZIC1

Zic family member 1
OMIM: 600470, Gene2Phenotype

7 panels

Panel Reviews Mode of inheritance Details
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