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Symbol
Name
ID
Ophn1
oligophrenin 1
MGI:2151070
Phenotype annotations related to reproductive system
Darker colors indicate more annotations
Human Phenotypes
Cryptorchidism
Micropenis
Microphallus
Scrotal hypoplasia
Disease(s) Associated with OPHN1
X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance

Mouse Phenotypes
asthenozoospermia
decreased litter size
Availability Mouse Genotype
Ophn1Wtgr/Ophn1+
Ophn1Wtgr/Y

Contributing Projects:
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
03/03/2020
MGI 6.15
The Jackson Laboratory