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Phenotypes Associated with This Genotype
Genotype
MGI:3641079
Allelic
Composition
Dicer1tm1Smr/Dicer1tm1Smr
Tg(KRT14-cre)52Smr/0
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6J * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dicer1tm1Smr mutation (1 available); any Dicer1 mutation (95 available)
Tg(KRT14-cre)52Smr mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• less affected mice survive up to 2.5 months
• severely affected mutants die within a few days of birth

growth/size/body
• newborn mice appear normal but by P7 are stunted with respect to growth compared to wild-type lettermates

integument
• at P7 mice lack external hair growth
• hair shaft structures are underdeveloped, and hair shafts do not extend beyond the level of the epidermis
• the hair bulbs are smaller than those in controls
• in newborn skin, follicle growth is stunted
• secondary hair follicles fail to extend into the dermis
• when viewed from the dermal aspect, hair follicles are misangled and fail to display the normal anterior-posterior polarity seen in control skin
• by P7, mutant hair follicles are misangled and wavy
• by P49 hair follicles have degenerated in large stretches of mutant skin and have been replaced by cyst structures or clumps of disorganized epithelial cells
• hair follicle proliferation is reduced in newborns
• the skin of mutants displays evaginating dermal cells which are engulfed by epidermal cells
• at P7 epidermal proliferation is increased compared with controls
• the epidermis is expanded compared to controls at P7 and is that way at P49
• at P49 and P63, mutant epidermis is thickened with increased numbers of basal and suprabasal layers


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