CFC1 Chromosome 2

Cryptic, EGF-CFC family member 1
3 variants 3 Health Risk

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What This Gene Does
This gene encodes a member of the epidermal growth factor (EGF)- Cripto, Frl-1, and Cryptic (CFC) family, which are involved in signalling during embryonic development. Proteins in this family share a variant EGF-like motif, a conserved cysteine-rich domain, and a C-terminal hydrophobic region. The protein encoded by this gene is necessary for patterning the left-right embryonic axis. Mutations in this gene are associated with defects in organ development, including autosomal visceral heterotaxy and congenital heart disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]
Gene Info
Gene Group
EGF-CFC family
Locus Type
gene with protein product
Location
2q21.1
Ensembl
ENSG00000136698
Associated Conditions (4)
Heterotaxy
visceral
2
autosomal
Key Variants
All Variants (3)
RSID Category Clinical Significance Conditions
RS746231039 Health Risk Conflicting classifications of pathogenicity Heterotaxy, visceral, 2
RS104893611 Health Risk Pathogenic Heterotaxy, visceral, 2
RS863223280 Health Risk Pathogenic Heterotaxy, visceral, 2
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