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NDUFS2

NADH:ubiquinone oxidoreductase core subunit S2

HCNC Approved Symbol
NDUFS2 (HGNC:7708)
Genomic Coordinates
1:161,197,417 - 161,214,395 (1q23.3)
Synonyms
CI-49
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Leber-like hereditary optic neuropathy, autosomal recessive 2
620569AR
Mitochondrial complex I deficiency, nuclear type 6
618228AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the NDUFS2 gene.

Frequently observed phenotypes

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

No Results