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TRMT10C

tRNA methyltransferase 10C, mitochondrial RNase P subunit

HCNC Approved Symbol
TRMT10C (HGNC:26022)
Genomic Coordinates
3:101,561,868 - 101,566,446 (3q12.3)
Synonyms
FLJ20432, MRPP1, RG9MTD1
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Combined oxidative phosphorylation deficiency 30
616974AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the TRMT10C gene.

Frequently observed phenotypes

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

No Results