Gene
MRM2
mitochondrial rRNA methyltransferase 2
- HGNC 16352↗(opens in a new tab)
- Ensembl gene ENSG00000122687↗(opens in a new tab)
- NCBI Gene 29960↗(opens in a new tab)
Summary
- Cytogenetic location
- 7p22.3
- Coordinates
- Chromosome 7: 2,234,195–2,242,205 (GRCh38)
- Exons
- 3 exons across 8 kb
- Protein
- 246 amino acids
- Also known as
- FJH1, RRMJ2
- Previous symbols
- FTSJ2
- MANE Select transcript
- ENST00000242257.14NM_013393.3
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Primary Mitochondrial Disease
- Mitochondrial DNA Depletion Syndrome
Caused by variants in nuclear genes such as POLG, TWNK, TK2, DGUOK, MPV17, RRM2B and SUCLA2, which reduce the amount of mitochondrial DNA and can cause muscle, liver or brain disease.
- 1 GenCC submitter rates it definitive or strong
What knowing changes
Knowing is directly actionable: valproate must be avoided in POLG disease because of the risk of fatal liver failure, and TK2 deficiency has a nucleoside therapy.
How MRM2 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 1.7 kb of the gene's 8 kb; 741 of those bases code for the protein.
Genes linked to the same conditions
- AFG3L2AFG3 like matrix AAA peptidase subunit 2Shares 1 condition
- AGKacylglycerol kinaseShares 1 condition
- DGUOKdeoxyguanosine kinaseShares 1 condition
- DNA2DNA replication helicase/nuclease 2Shares 1 condition
- FBXL4F-box and leucine rich repeat protein 4Shares 1 condition
- GUK1guanylate kinase 1Shares 1 condition
- LIG3DNA ligase 3Shares 1 condition
- MGME1mitochondrial genome maintenance exonuclease 1Shares 1 condition
- MPV17mitochondrial inner membrane protein MPV17Shares 1 condition
- OPA1OPA1 mitochondrial dynamin like GTPaseShares 1 condition
- POLGDNA polymerase gamma, catalytic subunitShares 1 condition
- RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2BShares 1 condition
Traits linked to MRM2
The Human Phenotype Ontology lists these as features of the rare conditions MRM2 can cause. Each trait's page lists the other genes linked to it.
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). MRM2 gene: mitochondrial rRNA methyltransferase 2. Retrieved 16 October 2026, from https://dantelabs.com/genes/mrm2
Dante Labs. MRM2 gene: mitochondrial rRNA methyltransferase 2 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/mrm2
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