DNM1 - Gene browser

DNM1

dynamin 1

HCNC Approved Symbol: DNM1 (HGNC:2972)
Genomic Coordinates: 9:128,203,379 - 128,255,244 (9q34.11)
Synonyms: DNM
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

14Patients

In total, 14 patients were diagnosed with a variant in the DNM1 gene.

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

014
Patient count

Epilepsy: 5 (35.7%)
Patient Count: 5 (35.7%)
% of total patients presenting each phenotype is shown in parentheses.
5 (35.7%)
Developmental delay: 4 (28.6%)
Patient Count: 4 (28.6%)
% of total patients presenting each phenotype is shown in parentheses.
4 (28.6%)
Global developmental delay: 3 (21.4%)
Patient Count: 3 (21.4%)
% of total patients presenting each phenotype is shown in parentheses.
3 (21.4%)
Seizures: 3 (21.4%)
Patient Count: 3 (21.4%)
% of total patients presenting each phenotype is shown in parentheses.
3 (21.4%)
Developmental regression: 2 (14.3%)
Patient Count: 2 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
2 (14.3%)