IFT27 - Gene browser

IFT27

intraflagellar transport 27

HCNC Approved Symbol: IFT27 (HGNC:18626)
Genomic Coordinates: 22:36,758,211 - 36,776,119 (22q12.3)
Synonyms: RAYL, BBS19, FAP156, CFAP156, RABL4
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

0Patient

There are no patients diagnosed with a variant in the IFT27 gene.

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

No Results