CYP17A1 - Gene browser | 3billion

CYP17A1

CYP17A1

cytochrome P450 family 17 subfamily A member 1

HCNC Approved Symbol: CYP17A1 (HGNC:2593)
Genomic Coordinates: 10:102,830,531 - 102,837,413 (10q24.32)
Synonyms: P450C17, CPT7, S17AH, CYP17
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the CYP17A1 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

Amenorrhea: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Hypertension: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Mucopolysacchariduria: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Obesity: 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

CYP17A1 - Gene browser | 3billion