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IFT43

intraflagellar transport 43

HCNC Approved Symbol
IFT43 (HGNC:29669)
Genomic Coordinates
14:75,985,763 - 76,084,073 (14q24.3)
Synonyms
FLJ32173, MGC16028, C14orf179
Disease Associations
This gene is associated with the following 3 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Cranioectodermal dysplasia 3
614099AR
?Retinitis pigmentosa 81
617871AR
Short-rib thoracic dysplasia 18 with polydactyly
617866AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the IFT43 gene.

Frequently observed phenotypes

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

No Results