CWC27 - Gene browser

CWC27

CWC27 spliceosome associated cyclophilin

HCNC Approved Symbol: CWC27 (HGNC:10664)
Genomic Coordinates: 5:64,768,918 - 65,018,763 (5q12.3)
Synonyms: NY-CO-10, SDCCAG-10, SDCCAG10
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

1Patient

In total, 1 patient was diagnosed with a variant in the CWC27 gene.

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

01
Patient count

Mental retardation: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Retinitis pigmentosa: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Unilateral renal agenesis: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Ventricular septal defect: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)