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Phenotypes Associated with This Genotype
Genotype
MGI:3688736
Allelic
Composition
Apctm2Rak/Apctm2Rak
Tg(KRT14-cre)8Brn/0
Genetic
Background
involves: 129/Sv * C57BL/6J * FVB/N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apctm2Rak mutation (0 available); any Apc mutation (152 available)
Tg(KRT14-cre)8Brn mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Stunted growth, short whiskers, sparse hair coat and abnormal tooth development in the Apctm2Rak/Apctm2Rak Tg(KRT14-cre)8Brn/0 mouse

mortality/aging
• some pups have died by P8-10 and none survive to weaning; time of death is variable with some dying within 1-2 days of birth, while some survive almost to weaning

growth/size/body
• maxillary incisors are often absent or underdeveloped
• initiation of ectopic tooth buds is evident by E15.5
• at time of death, animals are toothless
• at E17.5-18.5 mutants display a patch of dark pigmentation on the forehead
• external ears or pinnae are shriveled in appearance
• external ears or pinnae are pigmented compared to littermates
• by P8-10, mutant pups are considerably smaller than wild-type
• mutants start to lose weight from P10 onwards

cellular
• mutants show aberrant proliferation and differentiation of keratinocytes leading to massive squamous metaplasia, rather than forming medullary or cortical thymic epithelial cells
• in skin, proliferating cells are observed in cells in bulbs at base of hair cells and in bulb-like structures budding from outer root sheaths of existing hair follicles

behavior/neurological
• by P16-17, mice are lethargic

craniofacial
• maxillary incisors are often absent or underdeveloped
• initiation of ectopic tooth buds is evident by E15.5
• at time of death, animals are toothless
• at E17.5-18.5 mutants display a patch of dark pigmentation on the forehead
• external ears or pinnae are shriveled in appearance
• external ears or pinnae are pigmented compared to littermates

endocrine/exocrine glands
• hyperplasia in salivary gland squamous epithelium is observed
• at P12-17, thymi frequently contain black deposits within the tissue
• in more severely affected mutants, by P3, distinct thymic epithelial compartments are lost as well as most lymphocytes
• at P10-13, thymus consists of numerous enlarged Hassall's corpuscle-like structures surrounding large keratin deposits, and show large numbers of infiltrating neutrophils and macrophages in response to keratins
• numerous enlarged Hassall's corpuscle-like structures surrounding large keratin deposits
• thymi are inconspicuous and small for pups' age; this is evident by P3
• no thymocytes are detectable at P10-13
• hyperplasia in squamous epithelium is observed

digestive/alimentary system
• hyperplasia in salivary gland squamous epithelium is observed
• stomach is small at time of death, and contains no solid food

pigmentation
• at E17.5-18.5 mutants display patch of dark pigmentation on forehead and a dark median line running caudally from head to tail
• at E17.5-18.5 mutants display a patch of dark pigmentation on the forehead
• external ears or pinnae are pigmented compared to littermates

hematopoietic system
• at P12-17, thymi frequently contain black deposits within the tissue
• in more severely affected mutants, by P3, distinct thymic epithelial compartments are lost as well as most lymphocytes
• at P10-13, thymus consists of numerous enlarged Hassall's corpuscle-like structures surrounding large keratin deposits, and show large numbers of infiltrating neutrophils and macrophages in response to keratins
• numerous enlarged Hassall's corpuscle-like structures surrounding large keratin deposits
• thymi are inconspicuous and small for pups' age; this is evident by P3
• no thymocytes are detectable at P10-13

immune system
• at P12-17, thymi frequently contain black deposits within the tissue
• in more severely affected mutants, by P3, distinct thymic epithelial compartments are lost as well as most lymphocytes
• at P10-13, thymus consists of numerous enlarged Hassall's corpuscle-like structures surrounding large keratin deposits, and show large numbers of infiltrating neutrophils and macrophages in response to keratins
• numerous enlarged Hassall's corpuscle-like structures surrounding large keratin deposits
• thymi are inconspicuous and small for pups' age; this is evident by P3
• no thymocytes are detectable at P10-13

skeleton
• maxillary incisors are often absent or underdeveloped
• initiation of ectopic tooth buds is evident by E15.5
• at time of death, animals are toothless

vision/eye
• hyperplasia in squamous epithelium of cornea occurs
• by P17, animals hardly keep eyes open

hearing/vestibular/ear
• external ears or pinnae are shriveled in appearance
• external ears or pinnae are pigmented compared to littermates

integument
• mutants show aberrant proliferation and differentiation of keratinocytes leading to massive squamous metaplasia, rather than forming medullary or cortical thymic epithelial cells
• at ~P8, mutants are hairless while normal littermates have a smooth thin coat
• around P10-12, mice display short, shaggy coats
• at P3, follicles are often irregularly spaced and seen as disoriented and clamped invaginations that become more noticeable at P12
• clusters of dysplastic follicular structures are frequently observed throughout the epidermis, while other regions display gaps with no follicles
• bulbs are often bent and irregularly angled to one another, with variable size and location
• ectopic hair follicle morphogenesis is observed in epithelium of cornea, oral, salivary, and Harderian glands
• at P12, some hair follicles are not properly formed or shorter than normal
• around P10-12, mutants display short and misshapen vibrissae
• ridged skin regions look scaly
• at P17, development of thick ridges in the skin around the ears, eyelids, forehead, nose and paws becomes noticeable
• mutants have wrinkled skin at P8
• at E17.5-18.5 mutants display patch of dark pigmentation on forehead and a dark median line running caudally from head to tail
• at E17.5-18.5 mutants display a patch of dark pigmentation on the forehead
• external ears or pinnae are pigmented compared to littermates


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
03/31/2026
MGI 6.24
The Jackson Laboratory