PGAP2 - Gene browser | 3billion

PGAP2

PGAP2

post-GPI attachment to proteins 2

HCNC Approved Symbol: PGAP2 (HGNC:17893)
Genomic Coordinates: 11:3,797,724 - 3,826,371 (11p15.4)
Synonyms: FRAG1, CWH43-N, MRT21, MRT17
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 PGAP2 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

Abnormal electroencephalogram: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Infantile spasms: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Muscular hypotonia: 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

PGAP2 - Gene browser | 3billion