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Symbol
Name
ID
Wnt5a
wingless-type MMTV integration site family, member 5A
MGI:98958
Phenotype annotations related to reproductive system
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Clitoral hypoplasia
Hypoplastic labia majora
Micropenis
Cryptorchidism
Disease(s) Associated with WNT5A
autosomal dominant Robinow syndrome 1

Mouse Phenotypes
reproductive system phenotype
decreased primordial germ cell number
increased primordial germ cell apoptosis
abnormal primordial germ cell migration
abnormal maternal decidual layer morphology
abnormal reproductive system morphology
absent external female genitalia
abnormal uterus morphology
absent external male genitalia
genital tubercle hypoplasia
abnormal embryo attachment
abnormal uterine-embryonic axis
impaired embryo implantation
impaired spacing of implantation sites
twin decidual capsule
reduced female fertility
decreased litter size
Availability Mouse Genotype
Wnt5atm1Amc/Wnt5atm1Amc
Pgrtm2(cre)Lyd/Pgr+
Wnt5atm1.1Tpy/Wnt5atm1.1Tpy  (conditional)
*
Gt(ROSA)26Sortm1(CAG-Wnt5a,-AcGFP)Skde/Gt(ROSA)26Sor+
Pgrtm2(cre)Lyd/Pgr+  (conditional)
*

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
04/30/2024
MGI 6.23
The Jackson Laboratory