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Symbol
Name
ID
Apc
APC, WNT signaling pathway regulator
MGI:88039
Phenotype annotations related to integument
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
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)
Apctm2Rak/Apctm2Rak
Tg(KRT14-cre)8Brn/0  (conditional)
Apctm1Tno/Apc+
Tg(CDX2-cre)101Erf/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