IFT57 - Gene browser

IFT57

intraflagellar transport 57

HCNC Approved Symbol: IFT57 (HGNC:17367)
Genomic Coordinates: 3:108,160,812 - 108,222,424 (3q13.12-q13.13)
Synonyms: FLJ10147, HIPPI, MHS4R2, ESRRBL1
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

0Patient

There are no patients diagnosed with a variant in the IFT57 gene.

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

No Results