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Phenotypes Associated with This Genotype
Genotype
MGI:3589670
Allelic
Composition
Sox9tm2Crm/Sox9tm2Crm
Tg(WT1-cre)1Asc/0
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sox9tm2Crm mutation (1 available); any Sox9 mutation (33 available)
Tg(WT1-cre)1Asc mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
integument
• increase of apoptosis in the precortex of the hair bulb
• different types of hair are impossible to distinguish
• appear hairless in the caudal part of the body, however further observation shows the presence of small, atrophic hair
• hair shaft is fragile as hair broke off easily
• between P6 and P14, show a marked change in follicular epithelium
• by P8, show an increased cellularity in the dermis
• reduction in cell proliferation in the matrix region
• by P8, show a decreased number of bulb matrix cells
• increase of apoptosis in the lower part of the outer root sheath
• bulge (the hair stem cell compartment) of the outer root sheath is absent
• hair follicles remain after the first hair cycle, however their number is reduced with a marked decrease at P60
• degeneration of the hair follicle after the first hair cycle

cellular
• increase of apoptosis in the precortex of the hair bulb


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
01/28/2026
MGI 6.24
The Jackson Laboratory