Symbol Name ID |
Smad4
SMAD family member 4 MGI:894293 |
Darker colors indicate more annotations |
Human Phenotypes | Epistaxis |
Spontaneous, recurrent epistaxis |
Gastrointestinal hemorrhage |
Hematemesis |
Hematochezia |
Melena |
Cerebral hemorrhage |
Subarachnoid hemorrhage |
Pulmonary hemorrhage |
Spontaneous hematomas |
Anemia |
Polycythemia |
Venous thrombosis |
Hematological neoplasm |
Hepatosplenomegaly |
Disease(s) Associated with SMAD4 | |||||||||||||||
hereditary hemorrhagic telangiectasia | |||||||||||||||
juvenile polyposis syndrome | |||||||||||||||
juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome | |||||||||||||||
Lynch syndrome | |||||||||||||||
pancreatic cancer |
Mouse Phenotypes | abnormal embryonic hematopoiesis |
small thymus |
abnormal thymus physiology |
decreased osteoclast cell number |
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Availability | Mouse Genotype | ||||
Smad4tm2.1Cxd/Smad4tm2.1Cxd Kdrtm1(cre)Sato/Kdr+ (conditional) |
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Smad4tm2.1Cxd/Smad4tm2.1Cxd Tg(Foxn1-cre)8Ghr/0 (conditional) |
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Smad4tm2.1Cxd/Smad4tm2.1Cxd Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0 (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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