CFC1

cripto, FRL-1, cryptic family 1
OMIM: 605194, ClinGen, DECIPHER

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green CFC1 in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.430	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Expert list Phenotypes Heterotaxy, visceral, 2, MIM# 605376
Red CFC1 in Ciliopathies Level 2: Dysmorphic and congenital abnormality syndromes Version 1.62	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Heterotaxy, visceral, 2, autosomal 605376
Green CFC1 in Heterotaxy Level 2: Dysmorphic and congenital abnormality syndromes Version 1.36	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Heterotaxy, visceral, 2, autosomal 605376
Green CFC1 in Mendeliome Version 1.2302	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Heterotaxy, visceral, 2, autosomal 605376
Green CFC1 in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category A gene Expert Review Green Phenotypes Congenital heart defects
Green CFC1 in Fetal anomalies Version 1.313	1 review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Genomics England PanelApp Expert list Phenotypes Heterotaxy, visceral, 2, autosomal 605376
Red CFC1 in BabyScreen+ newborn screening Level 2: Screening Version 1.116	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red BabySeq Category A gene Phenotypes Heterotaxy, visceral, 2, autosomal MIM#605376