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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.
View More Disease Info
Disease NameOMIM IDInheritance
Short-rib thoracic dysplasia 16 with or without polydactyly
617102AR

Diagnosed Cases

0Patient

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

Frequently observed phenotypes

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

No Results