Symbol Name ID |
Fmr1
fragile X messenger ribonucleoprotein 1 MGI:95564 |
Darker colors indicate more annotations |
Human Phenotypes | Macroorchidism |
Congenital macroorchidism |
Macroorchidism, postpubertal |
Premature ovarian insufficiency |
Irregular menstruation |
Impotence |
Disease(s) Associated with FMR1 | ||||||
fragile X syndrome | ||||||
fragile X-associated tremor/ataxia syndrome | ||||||
primary ovarian insufficiency 1 |
Mouse Phenotypes | abnormal female germ cell morphology |
abnormal female meiosis |
abnormal ovary morphology |
decreased corpora lutea number |
abnormal granulosa cell morphology |
abnormal cumulus oophorus morphology |
abnormal ovarian follicle number |
increased atretic ovarian follicle number |
abnormal tertiary ovarian follicle morphology |
small ovary |
ovary atrophy |
ovary cyst |
increased testis weight |
enlarged testis |
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Availability | Mouse Genotype | ||||||||||||||
Fmr1tm1Usdn/Fmr1tm1Usdn | |||||||||||||||
Fmr1tm1.2Cidz/Y | |||||||||||||||
Fmr1tm1Cgr/Y | |||||||||||||||
Fmr1tm1Rbd/Y | |||||||||||||||
Fmr1tm1Usdn/Y |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 09/03/2024 MGI 6.24 |
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