Gene: TRMT10C

Alternate names for this Gene: COXPD30|HNYA|MRPP1|RG9MTD1

Gene Summary: This gene encodes the precursor of a subunit of the mitochondrial ribonuclease P, which is involved in 5' processing of mitochondrial tRNAs. The encoded protein may confer RNA-binding capacity to mitochondrial ribonuclease P and may be essential for transcript processing, RNA modification, translation and mitochondrial respiration.

Gene is located in Chromosome: 3

Location in Chromosome : 3q12.3

Description of this Gene: tRNA methyltransferase 10C, mitochondrial RNase P subunit

Type of Gene: protein-coding

rs199730889 in TRMT10C gene and COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30 PMID 27132592 2016 Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies.

rs199730889 in TRMT10C gene and Mitochondrial Diseases PMID 27132592 2016 Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies.