Symbol Name ID |
Apc
APC, WNT signaling pathway regulator MGI:88039 |
Darker colors indicate more annotations |
Human Phenotypes | Breast carcinoma |
Fibroadenoma of the breast |
Jaundice |
Hyperpigmentation of the skin |
Keloids |
Epidermoid cyst |
Disease(s) Associated with APC | ||||||
familial adenomatous polyposis 1 | ||||||
hereditary desmoid disease | ||||||
pancreatic cancer |
Mouse Phenotypes | abnormal keratinocyte differentiation |
increased forehead pigmentation |
increased ear pigmentation |
abnormal mammary gland development |
absent nipple |
increased mammary gland tumor incidence |
increased mammary adenocarcinoma incidence |
mammary gland hyperplasia |
absent male preputial gland |
skin cyst |
epidermal cyst |
delayed hair appearance |
short hair |
abnormal hair follicle morphology |
abnormal hair follicle bulb morphology |
abnormal hair follicle development |
underdeveloped hair follicles |
abnormal hair follicle orientation |
short vibrissae |
blistering |
scaly skin |
skin ridges |
wrinkled skin |
abnormal skin pigmentation |
increased skin tumor incidence |
increased pilomatricoma incidence |
increased trichoepithelioma incidence |
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Availability | Mouse Genotype | |||||||||||||||||||||||||||
Apctm1Rfo/Apctm1Rfo | ||||||||||||||||||||||||||||
ApcM1Tno/Apc+ | ||||||||||||||||||||||||||||
ApcMin/Apc+ | ||||||||||||||||||||||||||||
Apctm1.1Rsmi/Apc+ | ||||||||||||||||||||||||||||
Apctm1Cip/Apc+ | ||||||||||||||||||||||||||||
Apctm1Rak/Apc+ | ||||||||||||||||||||||||||||
Apctm2Rfo/Apc+ | ||||||||||||||||||||||||||||
Apctm1Rsmi/Apctm1Rsmi Tg(Col2a1-cre)1Rsjo/0 (conditional) |
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Apctm2Rak/Apctm2Rak Tg(KRT14-cre)8Brn/0 (conditional) |
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Apctm1Tno/Apc+ Tg(CDX2-cre)101Erf/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 04/16/2024 MGI 6.23 |
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