Fraxa

Human FMR1 wild-type allele is located in the vicinity of Xq27.3 and is approximately 39 kb in length. This allele, which encodes fragile X mental retardation protein 1, may play a role in the mediation of mRNA transport. Amplification of a trinucleotide repeat (CGG) within the gene is associated with fragile X syndrome.

Disease Alternative Name

fmrp
premature ovarian failure 1 gene
fragile x mental retardation 1 wt allele
fmr1 wt allele
mgc87458
pof
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