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CFP

complement factor properdin

HCNC Approved Symbol
CFP (HGNC:8864)
Genomic Coordinates
23:47,623,282 - 47,630,305 (Xp11.23)
Synonyms
PFC
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the CFP gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results
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