ZNF408 - Gene browser | 3billion

ZNF408

ZNF408

zinc finger protein 408

HCNC Approved Symbol: ZNF408 (HGNC:20041)
Genomic Coordinates: 11:46,701,031 - 46,705,912 (11p11.2)
Synonyms: FLJ12827
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

5Patients

In total, 5 patients were diagnosed with a variant in the ZNF408 gene.

Frequently observed phenotypes(Top 5 only)

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

05
Patient count

Retinitis pigmentosa: 5 (100.0%)
Patient Count: 5 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
5 (100.0%)
Hearing loss: 2 (40.0%)
Patient Count: 2 (40.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (40.0%)
Rod-cone dystrophy: 1 (20.0%)
Patient Count: 1 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (20.0%)
Hearing impairment: 1 (20.0%)
Patient Count: 1 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (20.0%)

Last updated: 2024-06-30

ZNF408 - Gene browser | 3billion