AFF2

AF4/FMR2 family, member 2
Identifiers
Symbols	AFF2 ; FMR2; FRAXE; MRX2; OX19
External IDs	Template:OMIM5 Template:MGI HomoloGene: 1532
Gene ontology Biological process Template:GNF GO Template:GNF GO
RNA expression pattern
More reference expression data
Orthologs
Template:GNF Ortholog box
Species	Human	Mouse
Entrez	n/a	n/a
Ensembl	n/a	n/a
UniProt	n/a	n/a
RefSeq (mRNA)	n/a	n/a
RefSeq (protein)	n/a	n/a
Location (UCSC)	n/a	n/a
PubMed search	n/a	n/a

AF4/FMR2 family, member 2, also known as AFF2, is a human gene.

Further reading

• Mulley JC, Yu S, Loesch DZ; et al. (1995). "FRAXE and mental retardation". J. Med. Genet. 32 (3): 162–9. PMID 7783162.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Gecz J, Gedeon AK, Sutherland GR, Mulley JC (1996). "Identification of the gene FMR2, associated with FRAXE mental retardation". Nat. Genet. 13 (1): 105–8. doi:10.1038/ng0596-105. PMID 8673085.CS1 maint: Multiple names: authors list (link)
• Gu Y, Shen Y, Gibbs RA, Nelson DL (1996). "Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island". Nat. Genet. 13 (1): 109–13. doi:10.1038/ng0596-109. PMID 8673086.CS1 maint: Multiple names: authors list (link)
• Chakrabarti L, Knight SJ, Flannery AV, Davies KE (1996). "A candidate gene for mild mental handicap at the FRAXE fragile site". Hum. Mol. Genet. 5 (2): 275–82. PMID 8824884.CS1 maint: Multiple names: authors list (link)
• Gécz J, Oostra BA, Hockey A; et al. (1997). "FMR2 expression in families with FRAXE mental retardation". Hum. Mol. Genet. 6 (3): 435–41. PMID 9147647.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Gecz J, Bielby S, Sutherland GR, Mulley JC (1997). "Gene structure and subcellular localization of FMR2, a member of a new family of putative transcription activators". Genomics. 44 (2): 201–13. doi:10.1006/geno.1997.4867. PMID 9299237.CS1 maint: Multiple names: authors list (link)
• Chakrabarti L, Bristulf J, Foss GS, Davies KE (1998). "Expression of the murine homologue of FMR2 in mouse brain and during development". Hum. Mol. Genet. 7 (3): 441–8. PMID 9467002.CS1 maint: Multiple names: authors list (link)
• Gecz J, Mulley JC (1999). "Characterisation and expression of a large, 13.7 kb FMR2 isoform". Eur. J. Hum. Genet. 7 (2): 157–62. doi:10.1038/sj.ejhg.5200279. PMID 10196698.
• Murray A, Webb J, Dennis N; et al. (1999). "Microdeletions in FMR2 may be a significant cause of premature ovarian failure". J. Med. Genet. 36 (10): 767–70. PMID 10528856.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Dias Neto E, Correa RG, Verjovski-Almeida S; et al. (2000). "Shotgun sequencing of the human transcriptome with ORF expressed sequence tags". Proc. Natl. Acad. Sci. U.S.A. 97 (7): 3491–6. PMID 10737800.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Lo Nigro C, Faravelli F, Cavani S; et al. (2000). "FRAXE mutation in a mentally retarded subject and in his phenotypically normal twin brother". Eur. J. Hum. Genet. 8 (3): 157–62. doi:10.1038/sj.ejhg.5200425. PMID 10780779.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Tzeng CC, Tzeng PY, Sun HS; et al. (2000). "Implication of screening for FMR1 and FMR2 gene mutation in individuals with nonspecific mental retardation in Taiwan". Diagn. Mol. Pathol. 9 (2): 75–80. PMID 10850542.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Musumeci SA, Scuderi C, Ferri R; et al. (2000). "Does a peculiar EEG pattern exist also for FRAXE mental retardation?". Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 111 (9): 1632–6. PMID 10964075.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Hillman MA, Gecz J (2001). "Fragile XE-associated familial mental retardation protein 2 (FMR2) acts as a potent transcription activator". J. Hum. Genet. 46 (5): 251–9. PMID 11355014.
• Strausberg RL, Feingold EA, Grouse LH; et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Kitano T, Schwarz C, Nickel B, Pääbo S (2004). "Gene diversity patterns at 10 X-chromosomal loci in humans and chimpanzees". Mol. Biol. Evol. 20 (8): 1281–9. doi:10.1093/molbev/msg134. PMID 12777533.CS1 maint: Multiple names: authors list (link)
• Ross MT, Grafham DV, Coffey AJ; et al. (2005). "The DNA sequence of the human X chromosome". Nature. 434 (7031): 325–37. doi:10.1038/nature03440. PMID 15772651.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Brylawski BP, Chastain PD, Cohen SM; et al. (2007). "Mapping of an origin of DNA replication in the promoter of fragile X gene FMR1". Exp. Mol. Pathol. 82 (2): 190–6. doi:10.1016/j.yexmp.2006.10.004. PMID 17196195.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)