MT-ND1 - Gene browser

MT-ND1

mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1

HCNC Approved Symbol: MT-ND1 (HGNC:7455)
Genomic Coordinates: -:- - - (mitochondria)
Synonyms: ND1, NAD1, MTND1
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-ND1 gene.

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

06
Patient count

Cognitive delay: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)
Hypotonia: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)
Seizures: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)
Speech delay: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)
Developmental delay: 1 (16.7%)
Patient Count: 1 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
1 (16.7%)