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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nintm1c(EUCOMM)Hmgu
targeted mutation 1c, Helmholtz Zentrum Muenchen GmbH
MGI:6358683
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Nintm1c(EUCOMM)Hmgu/Nintm1c(EUCOMM)Hmgu
Tg(KRT14-cre)1Ipc/0
involves: C57BL/6 * C57BL/6N * SJL MGI:6358685


Genotype
MGI:6358685
cn1
Allelic
Composition
Nintm1c(EUCOMM)Hmgu/Nintm1c(EUCOMM)Hmgu
Tg(KRT14-cre)1Ipc/0
Genetic
Background
involves: C57BL/6 * C57BL/6N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nintm1c(EUCOMM)Hmgu mutation (0 available); any Nin mutation (82 available)
Tg(KRT14-cre)1Ipc mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• transepidermal water loss is increased in newborns, indicating that inside-out barrier is slightly compromised

integument
• transepidermal water loss is increased in newborns, indicating that inside-out barrier is slightly compromised
• skin shows reduced desmosome numbers and size
• desmosomes have an irregular morphology, with a faint, kinked desmoglea and with plaques appearing less dense with less keratin filaments attached
• relative thickness of the basal and spinous layers is 74% of wild-type
• the granular layer appears thinner, with cells that have less and smaller keratohyalin granules
• relative thickness of the granular layer is 49% of wild-type
• relative thickness of the basal and spinous layers is 74% of wild-type
• newborns exhibit a thinner epidermis, with relative thickness of the epidermis being 67% of wild-type epidermis
• E17.5 mutants show dye penetration almost all over their surface indicating defective epidermal barrier formation, however by E18.5, epidermal barrier is normal and no dye penetration is seen





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory