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Symbol
Name
ID
Smad4
SMAD family member 4
MGI:894293
Phenotype annotations related to renal/urinary system
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Hematuria
Nephrolithiasis
Renal neoplasm
Disease(s) Associated with SMAD4
hereditary hemorrhagic telangiectasia
Lynch syndrome

Mouse Phenotypes
renal/urinary system phenotype
kidney cyst
decreased kidney collecting duct number
abnormal renal glomerulus morphology
abnormal kidney development
small kidney
hydroureter
Availability Mouse Genotype
Bmp7tm6(cre)Rob/Bmp7+
Smad4tm1Rob/Smad4tm1.1Rob  (conditional)
Smad4tm1Rob/Smad4tm1.1Rob
Tg(Hoxb7-cre)1Rob/0  (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
04/23/2024
MGI 6.23
The Jackson Laboratory