Symbol Name ID |
Lmna
lamin A MGI:96794 |
Darker colors indicate more annotations |
Human Phenotypes | Rectal prolapse |
Gastroesophageal reflux |
Gastrointestinal carcinoma |
Neoplasm of the small intestine |
Disease(s) Associated with LMNA | ||||
restrictive dermopathy 2 | ||||
Werner syndrome |
Mouse Phenotypes | abnormal hard palate morphology |
abnormal tongue morphology |
abnormal esophageal squamous epithelium morphology |
abnormal esophageal smooth muscle morphology |
dilated esophagus |
abnormal interstitial cell of Cajal morphology |
distended cecum |
abnormal colon morphology |
esophageal achalasia |
meteorism |
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Availability | Mouse Genotype | ||||||||||
LmnaDhe/LmnaDhe | |||||||||||
LmnaGt(S7-1F1)Sor/LmnaGt(S7-1F1)Sor | |||||||||||
Lmnatm2Stw/Lmnatm2Stw | |||||||||||
Lmnatm11Lgf/Lmna+ |
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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