FAM161A - Gene browser | 3billion

FAM161A

FAM161A

FAM161 centrosomal protein A

HCNC Approved Symbol: FAM161A (HGNC:25808)
Genomic Coordinates: 2:61,800,240 - 61,854,060 (2p15)
Synonyms: FLJ13305, RP28
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

14Patients

In total, 14 patients were diagnosed with a variant in the FAM161A gene.

Frequently observed phenotypes(Top 5 only)

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

014
Patient count

Retinitis pigmentosa: 12 (85.7%)
Patient Count: 12 (85.7%)
% of total patients presenting each phenotype is shown in parentheses.
12 (85.7%)
Retinal dystrophy: 1 (7.1%)
Patient Count: 1 (7.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (7.1%)
Cone-rod dystrophy: 1 (7.1%)
Patient Count: 1 (7.1%)
% of total patients presenting each phenotype is shown in parentheses.
1 (7.1%)

Last updated: 2024-06-30

FAM161A - Gene browser | 3billion