PSAP - Gene browser | 3billion

PSAP

PSAP

prosaposin

HCNC Approved Symbol: PSAP (HGNC:9498)
Genomic Coordinates: 10:71,816,298 - 71,851,251 (10q22.1)
Synonyms: SAP1, GLBA, SAP2
Disease Associations: This gene is associated with the following 5 diseases in OMIM.

Diagnosed Cases

1Patient

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

Frequently observed phenotypes(Top 5 only)

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

01
Patient count

Cerebral palsy: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Poor speech: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)

Last updated: 2024-06-30

PSAP - Gene browser | 3billion