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Symbol
Name
ID
Apc
APC, WNT signaling pathway regulator
MGI:88039
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Progressive macrocephaly
Delayed cranial suture closure
Supernumerary tooth
Eruption failure
Carious teeth
Odontoma
Disease(s) Associated with APC
familial adenomatous polyposis 1
medulloblastoma

Mouse Phenotypes
abnormal craniofacial morphology
abnormal cranium morphology
absent upper incisors
abnormal tooth development
absent teeth
abnormal mandible morphology
absent mandible
acrania
increased forehead pigmentation
abnormal ear shape
increased ear pigmentation
Availability Mouse Genotype
ApcMin/Apctm1Tno
Apctm1.1Tno/Apctm1Tno
Apctm1Rsmi/Apctm1Rsmi
Tg(Col2a1-cre)1Rsjo/0  (conditional)
Apctm2Rak/Apctm2Rak
Tg(KRT14-cre)8Brn/0  (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