|
Symbol Name ID |
Itgam
integrin alpha M MGI:96607 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormality of the nervous system |
Choroid plexus cyst |
Ventriculomegaly |
Chiari malformation |
Syringomyelia |
Sleep abnormality |
Headache |
Global developmental delay |
Seizure |
| Disease(s) Associated with ITGAM | |||||||||
| persistent fetal circulation syndrome | |||||||||
| pre-eclampsia |
| Mouse Phenotypes | decreased cerebral infarct size |
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| Availability | Mouse Genotype | |
| Itgamtm1Myd/Itgamtm1Myd | ||
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 04/30/2024 MGI 6.23 |
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