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Phenotypes Associated with This Genotype
Genotype
MGI:4442842
Allelic
Composition
Fntbtm1.1Mbrg/Fntbtm1.1Mbrg
Tg(KRT14-cre)1Amc/?
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fntbtm1.1Mbrg mutation (0 available); any Fntb mutation (207 available)
Tg(KRT14-cre)1Amc mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• most of the hair shafts are dysmorphic
• all of the layers of the shaft develop but the shafts are smaller and not as straight as in controls

integument
• apoptotic cells are detected in the hair follicle at P1 and are even more numerous at P4, P6 and P8
• scattered apoptotic cells are detected in the interfollicular epidermis at P4, P6 and P8
• marked proliferation defect in culture cells
• by P6 alopecia is virtually complete and persists throughout life
• hair follicles are stunted in appearance
• hair follicles appear normal at E17.5 but stunting of hair follicles is easily apparent at all post-natal time points
• most of the hair shafts are improperly angled and few penetrated the surface of the skin
• hair follicles have largely disappeared by P120
• keratinocytes in culture have a flattened morphology

cellular
• apoptotic cells are detected in the hair follicle at P1 and are even more numerous at P4, P6 and P8
• scattered apoptotic cells are detected in the interfollicular epidermis at P4, P6 and P8
• marked proliferation defect in culture cells


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
03/18/2025
MGI 6.24
The Jackson Laboratory