Symbol Name ID |
Tcf7l2
transcription factor 7 like 2, T cell specific, HMG box MGI:1202879 |
Darker colors indicate more annotations |
Human Phenotypes | Hereditary nonpolyposis colorectal carcinoma |
Colon cancer |
Intestinal pseudo-obstruction |
Neoplasm of the stomach |
Intermittent diarrhea |
Nausea and vomiting |
Functional intestinal obstruction |
Neoplasm of the liver |
Disease(s) Associated with TCF7L2 | ||||||||
colorectal cancer | ||||||||
pancreatic cancer |
Mouse Phenotypes | abnormal intestinal goblet cell morphology |
abnormal colon goblet cell morphology |
abnormal small intestine goblet cell morphology |
increased enterocyte apoptosis |
abnormal enterocyte proliferation |
abnormal cecum position |
abnormal intestine development |
abnormal intestinal enteroendocrine cell morphology |
abnormal intestine morphology |
abnormal intestinal epithelium morphology |
abnormal enterocyte morphology |
decreased enterocyte cell number |
abnormal crypts of Lieberkuhn morphology |
decreased Paneth cell number |
absent Paneth cells |
ectopic Paneth cells |
abnormal colon morphology |
abnormal small intestine morphology |
increased susceptibility to induced colitis |
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Availability | Mouse Genotype | |||||||||||||||||||
Tcf7l2m1Btlr/Tcf7l2m1Btlr | ||||||||||||||||||||
Tcf7l2tm1.1(EGFP/cre)Mrc/Tcf7l2tm1.1(EGFP/cre)Mrc | ||||||||||||||||||||
Tcf7l2tm1a(EUCOMM)Wtsi/Tcf7l2tm1a(EUCOMM)Wtsi | ||||||||||||||||||||
Tcf7l2tm1Cle/Tcf7l2tm1Cle | ||||||||||||||||||||
Tcf7l2tm2.2Mrc/Tcf7l2tm2.2Mrc | ||||||||||||||||||||
Tcf7l2tm2.1Cle/Tcf7l2tm2.1Cle Tg(Vil1-cre/ERT2)23Syr/0 (conditional) |
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Tcf7l2tm1(EGFP/cre)Mrc/Tcf7l2tm2.1Mrc (conditional) | ||||||||||||||||||||
Tcf7l2tm1.1(EGFP/cre)Mrc/Tcf7l2tm2.1Mrc (conditional) | ||||||||||||||||||||
Tcf7l2tm1.1(EGFP/cre)Mrc/Tcf7l2tm2.2Mrc (conditional) |
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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