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CFAP47

cilia and flagella associated protein 47

HCNC Approved Symbol
CFAP47 (HGNC:26708)
Genomic Coordinates
23:35,919,734 - 36,385,317 (Xp21.1)
Synonyms
FLJ36601, RP13-11B7.1, MGC34831, CXorf59, CXorf22, CXorf30, CHDC2
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Spermatogenic failure, X-linked 3
301059X-linked recessive

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the CFAP47 gene.

Frequently observed phenotypes

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

No Results