MT-ND6 - Gene browser

MT-ND6

mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6

HCNC Approved Symbol: MT-ND6 (HGNC:7462)
Genomic Coordinates: -:- - - (mitochondria)
Synonyms: NAD6, ND6, MTND6
Disease Associations: Currently, this gene is not associated with any human disease in OMIM.

6Patients

In total, 6 patients were diagnosed with a variant in the MT-ND6 gene.

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

06
Patient count

Seizures: 2 (33.3%)
Patient Count: 2 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
2 (33.3%)
Afebrile seizures: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)
Branchial anomaly: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)
Hypoglycemia: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)
Neurogenic bladder: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)