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Symbol
Name
ID
Smad4
SMAD family member 4
MGI:894293
Phenotype annotations related to mortality/aging
Darker colors indicate more annotations
Human Phenotypes
Death in early adulthood
Death in infancy
Miscarriage
Disease(s) Associated with SMAD4
hereditary hemorrhagic telangiectasia
Lynch syndrome

Mouse Phenotypes
decreased tumor-free survival time
premature death
perinatal lethality, incomplete penetrance
postnatal lethality, complete penetrance
postnatal lethality, incomplete penetrance
embryonic lethality during organogenesis, complete penetrance
embryonic lethality during organogenesis, incomplete penetrance
embryonic lethality between implantation and somite formation, complete penetrance
embryonic lethality between implantation and somite formation, incomplete penetrance
embryonic lethality between somite formation and embryo turning, incomplete penetrance
embryonic lethality, complete penetrance
prenatal lethality, complete penetrance
Availability Mouse Genotype
Smad4E6sad/Smad4E6sad
Smad4m4Mag/Smad4m4Mag
Smad4tm1Cxd/Smad4tm1Cxd
Smad4tm1Mak/Smad4tm1Mak
Smad4tm1Mmt/Smad4tm1Mmt
Smad4tm2.2Cxd/Smad4tm2.2Cxd
Smad4tm2Cxd/Smad4tm2Cxd
Smad4E6sad/Smad4+
Smad4m4Mag/Smad4tm1Cxd
Smad4tm2.1Cxd/Smad4tm2.1Cxd
Tg(KRT5-cre)1Xya/0  (conditional)
Smad4tm2.1Cxd/Smad4tm2.1Cxd
Tg(Nes-cre)1Atp/0  (conditional)
Smad4tm2.1Cxd/Smad4tm2.1Cxd
Kdrtm1(cre)Sato/Kdr+  (conditional)
Smad4tm2.1Cxd/Smad4tm2.1Cxd
Tg(ACTA1-cre)AMcle/0  (conditional)
Smad4tm2.1Cxd/Smad4tm2.1Cxd
Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0  (conditional)
Bmp7tm6(cre)Rob/Bmp7+
Smad4tm1Rob/Smad4tm1.1Rob  (conditional)
Smad4tm1Rob/Smad4tm1.1Rob
Edil3Tg(Sox2-cre)1Amc/Edil3+  (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
04/09/2024
MGI 6.23
The Jackson Laboratory