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NDUFA13

NADH:ubiquinone oxidoreductase subunit A13

HCNC Approved Symbol
NDUFA13 (HGNC:17194)
Genomic Coordinates
19:19,516,225 - 19,528,198 (19p13.11)
Synonyms
CGI-39, CDA016, GRIM-19, GRIM19, B16.6
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Mitochondrial complex I deficiency, nuclear type 28
618249AR
{Thyroid carcinoma, Hurthle cell}
607464-

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the NDUFA13 gene.

Frequently observed phenotypes

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

No Results