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FMR1 gene

Known as: FRAXA, fragile X mental retardation 1, FRAGILE X MENTAL RETARDATION PROTEIN 
This gene may be involved in the regulation of mRNA trafficking.
National Institutes of Health

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Related topics

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FMR1 gene activation:NFr:Pt:Bld:Qn:MolgenFMR1 gene targeted mutation analysis:Prid:Pt:Amnio fld:Nar:MolgenFMR1 protein, humanFragile X Mental Retardation Protein

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FMR1 wt Allele

Papers overview

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2005
2005
DNA Methylation and Replication: Implications for the “Deletion Hotspot” Region of FMR1
Expansion and hyper-methylation of a CGG repeat tract are the main causes of fragile X syndrome (FRAXA). In some rare instances… 
2005
2005
A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotype [Letter To Jmg]
  • 2005
  • Corpus ID: 18550869
A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotype [Letter To Jmg… 
2005
2005
Haplotype Study of Intermediate-Length Alleles at the Fragile X (FMR1) Gene: ATL1, FMRB, and Microsatellite Haplotypes Differ from Those Found in Common-Size FMR1 Alleles
The CGG repeat within the X-chromosome-linked FMR1 gene, which in hyperexpansion (>200 copies) results in fragile X syndrome, is… 
2003
2003
FMR1 haplotype analyses among Indians: a weak founder effect and other findings
This study on allelic/haplotypic fragile X associations evaluated using STR (DXS548, FRAXAC1, FRAXAC2) and SNP (ATL1) markers… 
2002
2002
SNP genotyping using a simple and rapid single-tube modification of ARMS illustrated by analysis of 6 SNPs in a population of males with FRAXA repeat expansions.
Microsatellites have been used extensively in gene mapping, linkage and association studies but with the near completion of the… 
Review
2002
Review
2002
Cognitive and behavioral performance among FMR1 high-repeat allele carriers surveyed from special education classes.
The fragile X syndrome is caused by an unstable CGG repeat sequence in the 5' untranslated region of the X-linked, FMR1 gene… 
2001
2001
Analysis of FMR1 (CGG)n alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia
Fragile X syndrome, the most common form of inherited mental retardation, is caused by expansion of a (CGG)n repeat located in… 
1997
1997
Sequence analysis of long FMR1 arrays in the Japanese population: insights into the generation of long (CGG)n tracts
Abstract The human fragile-X syndrome is associated with expansions of a (CGG)n triplet repeat within the FMR1 gene. Whilst… 
1994
1994
Haplotype analysis at the FRAXA locus in the Japanese population.
Fragile X syndrome, one of the most common human genetic diseases, is characterized by a unique genetic mechanism which involves… 
1994
1994
Clonal determination by the fragile X (FMR1) and phosphoglycerate kinase (PGK) genes in hematological malignancies.
The polymerase chain reaction (PCR) clonality assay based on the principle of random X chromosome methylation in females provides… 
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