Symbol Name ID |
Ctnnb1
catenin beta 1 MGI:88276 |
Darker colors indicate more annotations |
Human Phenotypes | Broad finger |
Disease(s) Associated with CTNNB1 | |
autosomal dominant intellectual developmental disorder 19 |
Mouse Phenotypes | abnormal apical ectodermal ridge morphology |
abnormal autopod morphology |
polydactyly |
abnormal forelimb morphology |
abnormal humerus morphology |
absent deltoid tuberosity |
decreased diameter of humerus |
absent radius |
abnormal ulna morphology |
short ulna |
abnormal hindlimb morphology |
absent hindlimb |
abnormal limb development |
ectopic limbs |
short limbs |
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Availability | Mouse Genotype | |||||||||||||||
Ctnnb1tm1Mmt/Ctnnb1tm1Mmt Tg(Msx2-cre)5Rem/0 (conditional) |
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Ctnnb1tm1Yy/Ctnnb1tm1Yy Tg(Col2a1-cre)1Bhr/0 (conditional) |
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Ctnnb1tm1Yy/Ctnnb1tm1Yy Tg(Prnp-GFP/cre)1Blw/0 (conditional) |
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Ctnnb1tm1Yy/Ctnnb1tm1Yy Tg(Prrx1-cre)1Cjt/0 (conditional) |
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Ctnnb1tm2Kem/Ctnnb1tm2Kem Tg(Col2a1-cre)1Bhr/0 (conditional) |
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Ctnnb1tm2Kem/Ctnnb1tm2Kem Tg(Msx2-cre)5Rem/0 (conditional) |
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Ctnnb1tm4Wbm/Ctnnb1tm4Wbm Tg(Prrx1-cre)98Mlgn/0 (conditional) |
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Ctnnb1tm1Max/Ctnnb1tm2Kem Tg(Msx2-cre)5Rem/0 (conditional) |
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Ctnnb1tm1Max/Ctnnb1tm2Kem Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0 (conditional) |
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Ctnnb1tm1Mmt/Ctnnb1+ Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0 (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 05/14/2024 MGI 6.23 |
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