Version: 8.0.0Date: Tue Jan 28 2025
Category
Mrm1
(Rattus norvegicus)Gene
Name: mitochondrial rRNA methyltransferase 1
Synonyms: LOC363661, mitochondrial rRNA methyltransferase 1 homolog, mitochondrial rRNA methyltransferase 1 homolog (S. cerevisiae), rRNA methyltransferase 1, mitochondrial, RGD1566232, similar to hypothetical protein FLJ22578
Source: RGD:1566232
Biotype: protein coding gene
Symbol: Mrm1 (Rno)
Symbol: Mrm1
Gene Synopsis: Orthologous to human MRM1 (mitochondrial rRNA methyltransferase 1); INTERACTS WITH 2,2',4,4'-Tetrabromodiphenyl
Automated Gene Synopsis: Orthologous to human MRM1 (mitochondrial rRNA methyltransferase 1).
Strict Orthology Symbols: mrm1
MRM1
(Saccharomyces cerevisiae)Gene
Name: Mitochondrial rRNA Methyltransferase
Synonyms: PET56, YOR201C
Source: SGD:S000005727
Biotype: protein coding gene
Symbol: MRM1 (Sce)
Symbol: MRM1
Automated Gene Synopsis: Orthologous to human MRM1 (mitochondrial rRNA methyltransferase 1).
Strict Orthology Symbols: mrm1
Alleles: mrm1-Δ (Sce)
mrm1
(Danio rerio)Gene
Name: mitochondrial rRNA methyltransferase 1 homolog (S. cerevisiae)
Synonyms: si:dkey-189h5.1
Source: ZFIN:ZDB-GENE-060526-229
Biotype: protein coding gene
Symbol: mrm1 (Dre)
Symbol: mrm1
Automated Gene Synopsis: Orthologous to human MRM1 (mitochondrial rRNA methyltransferase 1).
Strict Orthology Symbols: MRM1...Mrm1
MRM1
(Homo sapiens)Gene
Name: mitochondrial rRNA methyltransferase 1
Synonyms: 16S rRNA (guanosine(1145)-2'-O)-methyltransferase, CTB-75G16.3, 16S rRNA [Gm1145] 2'-O-methyltransferase, mitochondrial large ribosomal RNA ribose methylase, FLJ22578, mitochondrial rRNA methyltransferase 1 homolog, rRNA methyltransferase 1, mitochondrial
Source: HGNC:26202
Biotype: protein coding gene
Symbol: MRM1 (Hsa)
Symbol: MRM1
Strict Orthology Symbols: mrm1
Mrm1
(Mus musculus)Gene
Name: mitochondrial rRNA methyltransferase 1
Synonyms: RIKEN cDNA A530065E19 gene, RGD1566232, A530065E19Rik
Source: MGI:2443470
Biotype: protein coding gene
Symbol: Mrm1 (Mmu)
Symbol: Mrm1
Automated Gene Synopsis: Orthologous to human MRM1 (mitochondrial rRNA methyltransferase 1).
Strict Orthology Symbols: mrm1
Alleles: Mrm1
Mrm1tm2a(EUCOMM)Wtsi
(Mus musculus)Allele/Variant
Source: MGI:5472694
Genes: Mrm1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Mrm1
Genes: Mrm1 (Mmu)
Symbol: Mrm1tm2a(EUCOMM)Wtsi
mrm1-Δ
(Saccharomyces cerevisiae)Allele/Variant
Source: SGD:S000281840
Genes: MRM1 (Sce)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: mrm1-Δ (Sce)
Genes: MRM1 (Sce)
Symbol: mrm1-Δ
Mrm1tm2a(EUCOMM)Wtsi/Mrm1tm2a(EUCOMM)Wtsi [background:] C57BL/6N-Mrm1tm2a(EUCOMM)Wtsi/Wtsi
(Mus musculus)Model
Id: MGI:5639398
Synonyms: Not Available
Symbol: Mrm1/Mrm1 [background:] C57BL/6N-Mrm1/Wtsi (Mmu
Genes: Mrm1 (Mmu)
Alleles: Mrm1
Name: Mrm1/Mrm1 [background:] C57BL/6N-Mrm1/Wtsi
Y45F3A.9
(Caenorhabditis elegans)Gene
Name: rRNA methyltransferase 1, mitochondrial
Synonyms: CELE_Y45F3A.9
Source: WB:WBGene00012864
Biotype: protein coding gene
Gene Synopsis: Is an ortholog of human MRM1 (mitochondrial rRNA methyltransferase 1).
Automated Gene Synopsis: Orthologous to human MRM1 (mitochondrial rRNA methyltransferase 1).
Strict Orthology Symbols: mrm1
Gene Ontology
Source: GO:0000154
Synonyms:
- rRNA editing
Branch: biological process
Genes: MRM1 (Sce)...Mrm1 (Rno)...Mrm1 (Mmu)...MRM1 (Hsa)
Gene Ontology
Source: GO:0016435
Synonyms: Not Available
Branch: molecular function
Genes: MRM1 (Sce)...Mrm1 (Rno)...Mrm1 (Mmu)...MRM1 (Hsa)
Gene Ontology
Source: GO:0070039
Synonyms: Not Available
Branch: molecular function
Genes: Mrm1 (Mmu)...Mrm1 (Rno)...MRM1 (Hsa)
Gene Ontology
Source: GO:0000451
Synonyms: Not Available
Branch: biological process
Genes: Mrm1 (Mmu)...Mrm1 (Rno)...MRM1 (Hsa)
Gene Ontology
Source: GO:0008989
Synonyms:
- S-adenosyl-L-methionine:rRNA (guanine-1-N-)-methyltransferase activity
- S-adenosyl-L-methionine:rRNA (guanine-N1-)-methyltransferase activity
Branch: molecular function
Genes: MRM1 (Sce)
Gene Ontology
Source: GO:0008173
Synonyms: Not Available
Branch: molecular function
Genes: MRM1 (Hsa)...mrm1 (Dre)...MRM1 (Sce)
Gene Ontology
Source: GO:0031167
Synonyms: Not Available
Branch: biological process
Genes: MRM1 (Hsa)...mrm1 (Dre)...MRM1 (Sce)
Gene Ontology
Source: GO:0016070
Synonyms:
- RNA metabolism
Branch: biological process
Genes: MRM1 (Sce)
Gene Ontology
Source: GO:0008168
Synonyms:
- methylase
Branch: molecular function
Genes: mrm1 (Dre)...MRM1 (Sce)...MRM1 (Hsa)
Gene Ontology
Source: GO:0006364
Synonyms:
- 35S primary transcript processing
Branch: biological process
Genes: MRM1 (Sce)...Mrm1 (Rno)...MRM1 (Hsa)
Gene Ontology
Source: GO:0032259
Synonyms: Not Available
Branch: biological process
Genes: mrm1 (Dre)...MRM1 (Sce)...MRM1 (Hsa)
Gene Ontology
Source: GO:0005759
Synonyms:
- mitochondrial lumen
- mitochondrial stroma
Branch: cellular component
Genes: Mrm1 (Mmu)...Mrm1 (Rno)...MRM1 (Hsa)
Gene Ontology
Source: GO:0003723
Synonyms:
- base pairing with RNA
- poly(A) RNA binding
Branch: molecular function
Genes: MRM1 (Sce)...Mrm1 (Rno)...MRM1 (Hsa)...mrm1 (Dre)...Mrm1 (Mmu)
Gene Ontology
Source: GO:0006396
Synonyms: Not Available
Branch: biological process
Genes: mrm1 (Dre)
Gene Ontology
Source: GO:0010467
Synonyms: Not Available
Branch: biological process
Genes: MRM1 (Sce)
Gene Ontology
Source: GO:0005739
Synonyms:
- mitochondria
Branch: cellular component
Genes: Mrm1 (Rno)...Mrm1 (Mmu)...MRM1 (Sce)...MRM1 (Hsa)
sa38510
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-161003-15986
Genes: mrm1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: mrm1 (Dre)
Gene Ontology
Source: GO:0016740
Synonyms: Not Available
Branch: molecular function
Genes: mrm1 (Dre)
Gene Ontology
Source: GO:0005737
Synonyms: Not Available
Branch: cellular component
Genes: MRM1 (Hsa)...MRM1 (Sce)
(GRCh38)17:36602145G>A
(Homo sapiens)Allele/Variant
Source: rs780596708
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36602145G>A
(GRCh38)17:36608267G>A
(Homo sapiens)Allele/Variant
Source: rs138168313
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36608267G>A
(GRCh38)17:36608367C>G
(Homo sapiens)Allele/Variant
Source: rs2074950407
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36608367C>G
(GRCh38)17:36601821T>C
(Homo sapiens)Allele/Variant
Source: rs779554507
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36601821T>C
(GRCh38)17:36601832C>T
(Homo sapiens)Allele/Variant
Source: rs772345695
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36601832C>T
(GRCh38)17:36602049G>A
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.36602049G>A
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36602049G>A
(GRCh38)17:36607742G>A
(Homo sapiens)Allele/Variant
Source: rs201130891
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36607742G>A
(GRCh38)17:36608405A>G
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.36608405A>G
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36608405A>G
(GRCh38)17:36602169G>C
(Homo sapiens)Allele/Variant
Source: rs78943308
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36602169G>C
(GRCh38)17:36608293G>T
(Homo sapiens)Allele/Variant
Source: rs111861323
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36608293G>T
(GRCh38)17:36601827C>T
(Homo sapiens)Allele/Variant
Source: rs200927938
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36601827C>T
(GRCh38)17:36602210G>T
(Homo sapiens)Allele/Variant
Source: rs1410869599
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36602210G>T
(GRCh38)17:36602567C>T
(Homo sapiens)Allele/Variant
Source: rs367649431
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36602567C>T
(GRCh38)17:36608282T>C
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.36608282T>C
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36608282T>C
(GRCh38)17:36602006C>A
(Homo sapiens)Allele/Variant
Source: rs150793618
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36602006C>A
(GRCh38)17:36602037C>G
(Homo sapiens)Allele/Variant
Source: rs138056291
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36602037C>G
(GRCh38)17:36607690G>T
(Homo sapiens)Allele/Variant
Source: rs1314562699
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36607690G>T
(GRCh38)17:36602324G>C
(Homo sapiens)Allele/Variant
Source: rs545927735
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36602324G>C
(GRCh38)17:36602635G>A
(Homo sapiens)Allele/Variant
Source: rs749460262
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36602635G>A
(GRCh38)17:36607719G>A
(Homo sapiens)Allele/Variant
Source: rs776572568
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36607719G>A
(GRCh38)17:36601875A>T
(Homo sapiens)Allele/Variant
Source: rs753441297
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36601875A>T
(GRCh38)17:36602048G>A
(Homo sapiens)Allele/Variant
Source: rs1448904534
Genes: MRM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)17:36602048G>A