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Symbol Name ID |
Fermt1
fermitin family member 1 MGI:2443583 |
| Darker colors indicate more annotations |
| Human Phenotypes | Esophageal stenosis |
Dysphagia |
| Disease(s) Associated with FERMT1 | ||
| Kindler syndrome |
| Mouse Phenotypes | abnormal intestine morphology |
abnormal colon morphology |
abnormal ileum morphology |
distended ileum |
distended stomach |
large intestinal inflammation |
ileum inflammation |
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| Availability | Mouse Genotype | |||||||
| Fermt1tm1Ref/Fermt1tm1Ref | ||||||||
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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