C1QTNF5 - Gene browser | 3billion

C1QTNF5

C1QTNF5

C1q and TNF related 5

HCNC Approved Symbol: C1QTNF5 (HGNC:14344)
Genomic Coordinates: 11:119,338,942 - 119,346,705 (11q23.3)
Synonyms: CTRP5, DKFZp586B0621, LORD
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the C1QTNF5 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

Retinitis pigmentosa: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Congenital stationary night blindness: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Retinal disease: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)

Last updated: 2024-06-30

C1QTNF5 - Gene browser | 3billion