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MRPL39

mitochondrial ribosomal protein L39

HCNC Approved Symbol
MRPL39 (HGNC:14027)
Genomic Coordinates
21:25,585,656 - 25,607,859 (21q21.3)
Synonyms
RPML5, MRP-L5, MGC104174, PRED66, PRED22, C21orf92, L39mt, MSTP003, MGC3400, FLJ20451, mL39
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Combined oxidative phosphorylation deficiency 59
620646AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the MRPL39 gene.

Frequently observed phenotypes

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

No Results