Trmt10c - tRNA methyltransferase 10C, mitochondrial RNase P subunit Gene

Mus musculus

Also known as Rnmtd1; Rg9mtd1; D16Ertd454e; 1300018J16Rik

Gene ID: 52575 | Gene type: protein coding

About Trmt10c

Summary

Predicted to enable RNA methyltransferase activity; identical protein binding activity; and tRNA binding activity. Predicted to be involved in RNA metabolic process and positive regulation of mitochondrial translation. Predicted to act upstream of or within methylation. Located in mitochondrion. Is expressed in several structures, including central nervous system; metanephros; phalanx; skin; and tooth. Human ortholog(s) of this gene implicated in combined Oxidative Phosphorylation deficiency 30. Orthologous to human TRMT10C (tRNA methyltransferase 10C, mitochondrial RNase P subunit). [provided by Alliance of Genome Resources, Apr 2022]

Trmt10c Products(1)

mRNA	Protein	Name
NM_029092.4	NP_083368.1	tRNA methyltransferase 10 homolog C precursor

Gene Ontology

Cellular Component

Cellular Component GO Annotation	Evidence	Reference	Source
located in mitochondrion	IDA IDA: Inferred from direct assay	24703694	MGI

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

Protein Preferred Names

Protein Names

tRNA methyltransferase 10 homolog C

RNA (guanine-9-) methyltransferase domain containing 1	RNA (guanine-9-)-methyltransferase domain-containing protein 1
mRNA methyladenosine-N(1)-methyltransferase	mitochondrial RNase P protein 1
mitochondrial ribonuclease P protein 1	tRNA (adenine(9)-

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS15088	TRMT10C Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Homo sapiens	Trmt10c	NCBI	NCBI:54931

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