Symbol Name ID |
Wnt4
wingless-type MMTV integration site family, member 4 MGI:98957 |
Darker colors indicate more annotations |
Human Phenotypes | Renal agenesis |
Unilateral renal agenesis |
Disease(s) Associated with WNT4 | ||
Mullerian aplasia and hyperandrogenism |
Mouse Phenotypes | decreased renal glomerulus number |
abnormal kidney development |
abnormal kidney mesenchyme morphology |
abnormal metanephric mesenchyme morphology |
abnormal nephrogenic mesenchyme morphogenesis |
small metanephros |
delayed kidney development |
small kidney |
absent kidney |
kidney failure |
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Availability | Mouse Genotype | ||||||||||
Wnt4tm1.2Boer/Wnt4tm1.2Boer | |||||||||||
Wnt4tm1Amc/Wnt4tm1Amc | |||||||||||
Wnt4tm1.1Svo/Wnt4tm1.1Svo Tg(CAG-cre)13Miya/0 (conditional) |
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Amhr2tm3(cre)Bhr/Amhr2+ Wnt4tm1.1Boer/Wnt4tm1.2Boer (conditional) |
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Wnt4tm2(EGFP/cre)Svo/Wnt4tm1Svo (conditional) |
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 04/23/2024 MGI 6.23 |
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