FMR1 gene

FMR1 gene
[fragile X mental retardation 1] a gene expressed in human brain and testes cells and associated with fragile X syndrome (q.v.).

Medical dictionary. 2011.

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  • FMR1 — [ thumb|280px|Location of FMR1 on the X chromosome. ] FMR1 (fragile X mental retardation 1) is a human gene that codes for a protein called fragile X mental retardation protein , or FMRP. This protein is normally made in many tissues, especially… …   Wikipedia

  • FMR1 — The gene responsible for the production of a protein called FMRP. Lack of FMRP results in the fragile X syndrome. (FMRP is an acronym composed of the first letters of Familial Mental Retardation Protein). * * * SYN: fragile X syndrome …   Medical dictionary

  • Fragile X syndrome — Classification and external resources Location of FMR1 gene ICD 10 Q99.2 …   Wikipedia

  • Síndrome X frágil — Localización del gen FMR 1. Clasificación y recursos externos CIE 10 Q …   Wikipedia Español

  • Fragile X syndrome — One of the most common causes of inherited mental retardation and neuropsychiatric disease in human beings, affects as many as one in 2000 males and one in 4000 females. The syndrome is also known as FRAXA (the fragile X chromosome itself) and as …   Medical dictionary

  • CGGBP1 — CGG triplet repeat binding protein 1, also known as CGGBP1, is a human gene.cite web | title = Entrez Gene: CGGBP1 CGG triplet repeat binding protein 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=8545|… …   Wikipedia

  • Wim Crusio — Wim E. Crusio Wim Crusio, August 2006 Born 20 December 1954 (1954 12 …   Wikipedia

  • Chromosomal fragile site — Silencing of the FMR1 gene in Fragile X syndrome. FMR1 co localizes with a rare fragile site, visible here as a gap on the long arms of the X chromosome. A chromosomal fragile site is a specific heritable point on a chromosome that tends to form… …   Wikipedia

  • Cherubism — Classification and external resources Facial appearance of 37 year old woman diagnosed with cherubism. ICD 10 K …   Wikipedia

  • ZFP161 — Zinc finger protein 161 homolog (mouse), also known as ZFP161, is a human gene.cite web | title = Entrez Gene: ZFP161 zinc finger protein 161 homolog (mouse)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… …   Wikipedia

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