PPP1R21 - Gene browser

PPP1R21

protein phosphatase 1 regulatory subunit 21

HCNC Approved Symbol: PPP1R21 (HGNC:30595)
Genomic Coordinates: 2:48,440,766 - 48,515,386 (2p16.3)
Synonyms: FLJ16566, Fy-2, FERRY2, CCDC128, KLRAQ1
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 PPP1R21 gene.

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

02
Patient count

Abnormality of the cerebral white matter: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Areflexia: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Atrial septal defect: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Decreased fetal movement: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Failure to thrive: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)