IFT52 - Gene browser

IFT52

intraflagellar transport 52

HCNC Approved Symbol: IFT52 (HGNC:15901)
Genomic Coordinates: 20:43,590,937 - 43,647,299 (20q13.12)
Synonyms: CGI-53, NGD5, dJ1028D15.1, NGD2, C20orf9
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

0Patient

There are no patients diagnosed with a variant in the IFT52 gene.

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

No Results