Rmrp Gene Summary [Mouse]

Acts upstream of or within in utero embryonic development. Is expressed in early conceptus and secondary oocyte. Human ortholog(s) of this gene implicated in anauxetic dysplasia 1 and cartilage-hair hypoplasia. Orthologous to human RMRP (RNA component of mitochondrial RNA processing endoribonuclease). [provided by Alliance of Genome Resources, Jul 2025]

Details

Type
Ribozyme
Official Symbol
Rmrp
Official Name
RNA component of mitochondrial RNAase P [Source:MGI Symbol;Acc:MGI:97937]
Ensembl ID
ENSMUSG00000088088
Bio databases IDs NCBI: 19782 Ensembl: ENSMUSG00000088088
Aliases RNA component of mitochondrial RNAase P
Synonyms 1110032O22Rik, AL732506.1, CHH, NME1, RMRPR, RNA component of mitochondrial RNAase P, RNA component of mitochondrial RNA processing endoribonuclease, RRP2
Species
Mouse, Mus musculus
OrthologiesHuman

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • neoplasia
  • colorectal cancer
  • cartilage-hair hypoplasia
  • anauxetic dysplasia
  • anauxetic dysplasia type 1
  • lung adenocarcinoma
  • lung adenocarcinoma formation
  • autosomal dominant polycystic kidney disease
  • metaphyseal dysplasia without hypotrichosis
  • multiple sclerosis
regulated by
regulates
role in cell
  • binding in
  • expression in
  • migration
  • accumulation in
  • phosphorylation in
  • proliferation
  • apoptosis
  • growth
  • colony formation
  • invasion by

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Cytoplasm

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.