DNM2 - Gene browser

DNM2

dynamin 2

HCNC Approved Symbol: DNM2 (HGNC:2974)
Genomic Coordinates: 19:10,718,079 - 10,831,903 (19p13.2)
Synonyms: DYNII, DYN2, CMTDIB, CMTDI1, DI-CMTB, CMT2M
Disease Associations: This gene is associated with the following 4 diseases in OMIM.

10Patients

In total, 10 patients were diagnosed with a variant in the DNM2 gene.

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

010
Patient count

Muscular dystrophy: 2 (20.0%)
Patient Count: 2 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (20.0%)
Myopathy: 2 (20.0%)
Patient Count: 2 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (20.0%)
Gait disturbance: 1 (10.0%)
Patient Count: 1 (10.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (10.0%)
Lower limb hyperreflexia: 1 (10.0%)
Patient Count: 1 (10.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (10.0%)
Motor delay: 1 (10.0%)
Patient Count: 1 (10.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (10.0%)