OrDB
Gene Name
  Data
FMR1 FMRP
Mutations of this gene causes cognitive (fragile X syndrome, intellectual disability, autism, Parkinson's) and female reproductive function deficits.
FMR1
protein coding
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