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Symbol
Name
ID
Ctnnb1
catenin beta 1
MGI:88276
Phenotype annotations related to growth/size/body
Darker colors indicate more annotations
Human Phenotypes
Small for gestational age
Growth delay
Disease(s) Associated with CTNNB1
autosomal dominant intellectual developmental disorder 19

Mouse Phenotypes
absent lower incisors
abnormal tooth development
abnormal dental mesenchyme morphology
abnormal enamel knot morphology
growth retardation of incisors
growth retardation of molars
abnormal maxillary shelf morphology
abnormal facial morphology
abnormal face development
abnormal oral cavity morphology
cleft secondary palate
cleft palate
abnormal tongue morphology
abnormal filiform papillae morphology
flattened snout
broad head
absent outer ear
embryonic growth retardation
decreased embryo size
kidney cyst
abnormal head morphology
abnormal head size
decreased body size
Availability Mouse Genotype
Ctnnb1Bfc/Ctnnb1Bfc
Ctnnb1tm1Kba/Ctnnb1tm1Kba
Ctnnb1tm1Max/Ctnnb1tm1Max
Ctnnb1tm1Wbm/Ctnnb1tm1Wbm
Ctnnb1tm2Wbm/Ctnnb1tm2Wbm
Ctnnb1tm3Wbm/Ctnnb1tm3Wbm
Ctnnb1Bfc/Ctnnb1+
Ctnnb1tm1Mmt/Ctnnb1tm1Mmt
Osr2tm5(cre)Jian/Osr2+  (conditional)
Ctnnb1tm1Mmt/Ctnnb1tm1Mmt
Tcf21tm1(cre)Seq/Tcf21+  (conditional)
Ctnnb1tm2Kem/Ctnnb1tm2Kem
Emx1tm1(cre)Yql/Emx1+  (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)
Ctnnb1tm1Mmt/Ctnnb1+
Tg(Tcfap2a-cre)1Will/0  (conditional)
Ctnnb1tm1Mmt/Ctnnb1+
Tg(Col1a1-cre)1Kry/0  (conditional)
Ctnnb1tm1Mmt/Ctnnb1+
Tg(Cdh16-cre)91Igr/0  (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
04/16/2024
MGI 6.23
The Jackson Laboratory