FTSJ1

FtsJ homolog 1 (E. coli), also known as FTSJ1, is a human gene.cite web | title = Entrez Gene: FTSJ1 FtsJ homolog 1 (E. coli)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=24140| accessdate = ]

PBB_Summary
section_title =
summary_text = 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.cite web | title = Entrez Gene: FTSJ1 FtsJ homolog 1 (E. coli)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=24140| accessdate = ]

References

Further reading

PBB_Further_reading
citations =
*cite journal | author=Mulley JC, Kerr B, Stevenson R, Lubs H |title=Nomenclature guidelines for X-linked mental retardation. |journal=Am. J. Med. Genet. |volume=43 |issue= 1-2 |pages= 383–91 |year= 1992 |pmid= 1605216 |doi=
*cite journal | author=Willems P, Vits L, Buntinx I, "et al." |title=Localization of a gene responsible for nonspecific mental retardation (MRX9) to the pericentromeric region of the X chromosome. |journal=Genomics |volume=18 |issue= 2 |pages= 290–4 |year= 1994 |pmid= 8288232 |doi= 10.1006/geno.1993.1468
*cite journal | author=Hamel BC, Smits AP, van den Helm B, "et al." |title=Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: clinical and psychometric data and results of linkage analysis. |journal=Am. J. Med. Genet. |volume=85 |issue= 3 |pages= 290–304 |year= 2000 |pmid= 10398246 |doi=
*cite journal | author=Pintard L, Kressler D, Lapeyre B |title=Spb1p is a yeast nucleolar protein associated with Nop1p and Nop58p that is able to bind S-adenosyl-L-methionine in vitro. |journal=Mol. Cell. Biol. |volume=20 |issue= 4 |pages= 1370–81 |year= 2000 |pmid= 10648622 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Ropers HH, Hoeltzenbein M, Kalscheuer V, "et al." |title=Nonsyndromic X-linked mental retardation: where are the missing mutations? |journal=Trends Genet. |volume=19 |issue= 6 |pages= 316–20 |year= 2003 |pmid= 12801724 |doi=
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Freude K, Hoffmann K, Jensen LR, "et al." |title=Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardation. |journal=Am. J. Hum. Genet. |volume=75 |issue= 2 |pages= 305–9 |year= 2004 |pmid= 15162322 |doi= 10.1086/422507
*cite journal | author=Ramser J, Winnepenninckx B, Lenski C, "et al." |title=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). |journal=J. Med. Genet. |volume=41 |issue= 9 |pages= 679–83 |year= 2005 |pmid= 15342698 |doi= 10.1136/jmg.2004.019000
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Ross MT, Grafham DV, Coffey AJ, "et al." |title=The DNA sequence of the human X chromosome. |journal=Nature |volume=434 |issue= 7031 |pages= 325–37 |year= 2005 |pmid= 15772651 |doi= 10.1038/nature03440
*cite journal | author=Froyen G, Bauters M, Boyle J, "et al." |title=Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region. |journal=Hum. Genet. |volume=121 |issue= 5 |pages= 539–47 |year= 2007 |pmid= 17333282 |doi= 10.1007/s00439-007-0343-1

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