MOCS2 - Gene browser

MOCS2

molybdenum cofactor synthesis 2

HCNC Approved Symbol: MOCS2 (HGNC:7193)
Genomic Coordinates: 5:53,095,679 - 53,109,757 (5q11.2)
Synonyms: MOCO1, MOCS2A, MOCS2B
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

3Patients

In total, 3 patients were diagnosed with a variant in the MOCS2 gene.

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

03
Patient count

Abnormal basal ganglia mri signal intensity: 1 (33.3%)
Patient Count: 1 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (33.3%)
Decreased muscle strength: 1 (33.3%)
Patient Count: 1 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (33.3%)
Diffuse cerebral atrophy: 1 (33.3%)
Patient Count: 1 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (33.3%)
Elevated serum cpk: 1 (33.3%)
Patient Count: 1 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (33.3%)
Emg: myopathic changes: 1 (33.3%)
Patient Count: 1 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (33.3%)