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CFC1

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]
Protein class

Disease related genes, Human disease related genes

Predicted location

Secreted

Single cell type specificity

Group enriched (Enteroendocrine cells, Bipolar cells)

Immune cell specificity

Not detected in immune cells

Cell line specificity

Group enriched (RPMI-8226, SCLC-21H, SuSa)

Molecular function

Developmental protein

More Types Infomation

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For Research Use Only. Not For Clinical Use.

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