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Symbol
Name
ID
Wnt5a
wingless-type MMTV integration site family, member 5A
MGI:98958
Phenotype annotations related to renal/urinary system
Darker colors indicate more annotations
Human Phenotypes
Hydronephrosis
Renal duplication
Disease(s) Associated with WNT5A
autosomal dominant Robinow syndrome 1

Mouse Phenotypes
abnormal kidney morphology
abnormal urinary bladder morphology
Availability Mouse Genotype
Wnt5ab2b3077.1Clo/Wnt5ab2b3077.1Clo
Wnt5atm1Amc/Wnt5atm1Amc

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