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Symbol Name ID |
Neurog3
neurogenin 3 MGI:893591 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Diarrhea |
Vomiting |
| Disease(s) Associated with NEUROG3 | ||
| congenital malabsorptive diarrhea 4 |
| Mouse Phenotypes | abnormal intestinal goblet cell morphology |
abnormal small intestinal crypt cell proliferation |
digestive/alimentary phenotype |
abnormal intestine development |
abnormal intestinal enteroendocrine cell morphology |
decreased enteroendocrine cell number |
abnormal pancreatic acinar cell morphology |
pancreatic acinar cell zymogen granule accumulation |
abnormal small intestine crypts of Lieberkuhn morphology |
abnormal large intestine morphology |
abnormal small intestinal villus morphology |
abnormal small intestinal microvillus morphology |
decreased small intestinal microvillus size |
disorganized stomach mucosa |
increased stomach mucosa thickness |
regional gastric metaplasia |
small stomach |
increased defecation amount |
diarrhea |
abnormal intestinal lipid absorption |
steatorrhea |
abnormal intestinal transit time |
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| Availability | Mouse Genotype | ||||||||||||||||||||||
| Neurog3tm1(EGFP)Khk/Neurog3tm1(EGFP)Khk | |||||||||||||||||||||||
| Neurog3tm1Fgu/Neurog3tm1Fgu | |||||||||||||||||||||||
| Neurog3tm3.1Ggr/Neurog3tm3.1Ggr Tg(Vil1-cre)20Syr/0 (conditional) |
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| Neurog3tm3.1Ggr/Neurog3tm3.1Ggr Tg(CDX2-cre)101Erf/0 (conditional) |
* | ||||||||||||||||||||||
| Neurog3tm1Fgu/Neurog3tm3.1Ggr Tg(Vil1-cre)20Syr/0 (conditional) |
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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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