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Symbol Name ID |
Icam1
intercellular adhesion molecule 1 MGI:96392 |
| Darker colors indicate more annotations |
| Human Phenotypes | Raynaud phenomenon |
Congestive heart failure |
Lymphadenopathy |
Splenomegaly |
Erythema |
| Disease(s) Associated with ICAM1 | |||||
| Behcet's disease | |||||
| biliary atresia | |||||
| Graves' disease | |||||
| multiple myeloma |
| Mouse Phenotypes | decreased susceptibility to induced choroidal neovascularization |
abnormal retina vasculature morphology |
decreased angiogenesis |
abnormal cardiac muscle contractility |
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| Availability | Mouse Genotype | ||||
| Icam1tm1Bay/Icam1tm1Bay | |||||
| Icam1tm1Jcgr/Icam1tm1Jcgr | |||||
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 03/25/2025 MGI 6.24 |
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