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Symbol
Name
ID
Ctnnb1
catenin beta 1
MGI:88276
Phenotype annotations related to digestive/alimentary system
Darker colors indicate more annotations
Human Phenotypes
Hereditary nonpolyposis colorectal carcinoma
Adenomatous colonic polyposis
Neoplasm of the stomach
Nausea and vomiting
Dysphagia
Hepatocellular carcinoma
Disease(s) Associated with CTNNB1
autosomal dominant intellectual developmental disorder 19
colorectal cancer
hepatocellular carcinoma
medulloblastoma

Mouse Phenotypes
abnormal small intestinal crypt cell proliferation
abnormal maxillary shelf morphology
cleft secondary palate
cleft palate
abnormal tongue morphology
abnormal filiform papillae morphology
tracheoesophageal fistula
abnormal exocrine pancreas morphology
pancreatic acinar hypoplasia
abnormal intestinal epithelium morphology
abnormal crypts of Lieberkuhn morphology
decreased Paneth cell number
ectopic Paneth cells
abnormal small intestine morphology
intestine polyps
increased intestinal adenoma incidence
Availability Mouse Genotype
Ctnnb1tm1Mmt/Ctnnb1+
Ctnnb1tm1Mmt/Ctnnb1tm1Mmt
Osr2tm5(cre)Jian/Osr2+  (conditional)
Ctnnb1tm1Mmt/Ctnnb1tm1Mmt
Shhtm1(EGFP/cre)Cjt/Shh+  (conditional)
Ctnnb1tm2Kem/Ctnnb1tm2Kem
Tg(Cyp1a1-cre)1Dwi/0  (conditional)
Ctnnb1tm2Kem/Ctnnb1tm2Kem
Tg(Tcfap2a-cre)1Will/0  (conditional)
Ctnnb1tm2Kem/Ctnnb1tm2Kem
Tg(KRT14-cre)#Smr/0  (conditional)
Ctnnb1tm4Wbm/Ctnnb1tm4Wbm
Tg(Pdx1-cre)6Tuv/0  (conditional)
Bmi1tm1(cre/ERT)Mrc/Bmi1+
Ctnnb1tm1Mmt/Ctnnb1+  (conditional)
Ctnnb1tm1Mmt/Ctnnb1+
Krt19tm1(cre)Mmt/Krt19+  (conditional)
Ctnnb1tm1Mmt/Ctnnb1+
Tg(Fabp1-cre)1Mmt/?  (conditional)
Ctnnb1tm1Mmt/Ctnnb1+
Lgr5tm1(cre/ERT2)Cle/Lgr5+  (conditional)
Ctnnb1tm2Kem/Ctnnb1+
Osr2tm2(cre)Jian/Osr2+  (conditional)

Contributing Projects:
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
The Jackson Laboratory