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FMR1

fragile X messenger ribonucleoprotein 1

HCNC Approved Symbol
FMR1 (HGNC:3775)
Genomic Coordinates
23:147,911,919 - 147,951,125 (Xq27.3)
Synonyms
FMRP, FRAXA, MGC87458, POF1, POF
Disease Associations
This gene is associated with the following 3 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Fragile X syndrome
300624X-linked dominant
Fragile X tremor/ataxia syndrome
300623X-linked dominant
Premature ovarian failure 1
311360XL

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the FMR1 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results