FTSJ1

Putative ribosomal RNA methyltransferase 1 is an enzyme that in humans is encoded by the FTSJ1 gene.[5][6][7]

FTSJ1
Identifiers
AliasesFTSJ1, CDLIV, MRX44, MRX9, SPB1, TRMT7, JM23, FtsJ RNA methyltransferase homolog 1 (E. coli), FtsJ RNA methyltransferase homolog 1, FtsJ RNA 2'-O-methyltransferase 1, XLID9
External IDsOMIM: 300499 MGI: 1859648 HomoloGene: 5372 GeneCards: FTSJ1
Orthologs
SpeciesHumanMouse
Entrez

24140

54632

Ensembl

ENSG00000068438

ENSMUSG00000031171

UniProt

Q9UET6

n/a

RefSeq (mRNA)

NM_001282157
NM_012280
NM_177439

NM_001290430
NM_133991

RefSeq (protein)

NP_001269086
NP_036412
NP_803188

n/a

Location (UCSC)Chr X: 48.48 – 48.49 MbChr X: 8.1 – 8.12 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

The protein encoded by this gene is a member of the S-adenosylmethionine-binding protein family. It is a nucleolar protein and may be involved in the processing and modification of rRNA. Three alternatively spliced transcript variants encoding different isoforms have been described for this gene.[7]

References

  1. GRCh38: Ensembl release 89: ENSG00000068438 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000031171 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Ramser J, Winnepenninckx B, Lenski C, Errijgers V, Platzer M, Schwartz CE, Meindl A, Kooy RF (Sep 2004). "A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9)". J Med Genet. 41 (9): 679–83. doi:10.1136/jmg.2004.019000. PMC 1735884. PMID 15342698.
  6. Freude K, Hoffmann K, Jensen LR, Delatycki MB, des Portes V, Moser B, Hamel B, van Bokhoven H, Moraine C, Fryns JP, Chelly J, Gecz J, Lenzner S, Kalscheuer VM, Ropers HH (Aug 2004). "Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardation". Am J Hum Genet. 75 (2): 305–9. doi:10.1086/422507. PMC 1216064. PMID 15162322.
  7. "Entrez Gene: FTSJ1 FtsJ homolog 1 (E. coli)".

Further reading


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