IFT74 - Gene browser | 3billion

IFT74

IFT74

intraflagellar transport 74

HCNC Approved Symbol: IFT74 (HGNC:21424)
Genomic Coordinates: 9:26,947,110 - 27,066,134 (9p21.2)
Synonyms: CMG1, CMG-1, FLJ22621, CCDC2
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the IFT74 gene.

Frequently observed phenotypes(Top 5 only)

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

02
Patient count

Myopia, severe: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Pigmentary retinopathy: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)

Last updated: 2024-06-30

IFT74 - Gene browser | 3billion