OrDB
Olfactory Receptors Database
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Gene Name
Data
Name
FMR1 FMRP
Description
Mutations of this gene causes cognitive (fragile X syndrome, intellectual disability, autism, Parkinson's) and female reproductive function deficits.
Genebank name
FMR1
Gene type
protein coding
Phenotype
fragile x, mental retardation, premature ovarian failure
Other categories referring to
FMR1 FMRP
Revisions:
1
Last Time:
6/10/2020 1:51:30 PM
Reviewer:
Tom Morse - MoldelDB admin
Owner:
Tom Morse - MoldelDB admin