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Phenotypes Associated with This Genotype
Genotype
MGI:5446444
Allelic
Composition
Gpr89tm1.1Ymae/Gpr89tm1.1Ymae
Tg(KRT5-cre)1Tak/0
Genetic
Background
involves: C3H * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gpr89tm1.1Ymae mutation (0 available); any Gpr89 mutation (36 available)
Tg(KRT5-cre)1Tak mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• half of mice die within 1 month

reproductive system
• impaired development of external genitalia

integument
• 4-fold increase in transepidermal water loss at P5
• at 1 month, inflammatory cells containing melanin with enlarged sebaceous glands are observed in the dermis
• associated with scaly skin
• ballooning basal cells
• intracellular vacuoles and intracytoplasmic droplets in the basal layer
• abnormal formation of lamellar structures between corneum layers
• abnormal and decreased formation of contents of lamellar granules
• in newborn mice but not at P5
• aberrant lamellar granules
• apparent 1 week after birth

growth/size/body
• impaired development

hearing/vestibular/ear
• impaired development

homeostasis/metabolism
• 4-fold increase in transepidermal water loss at P5

pigmentation
• apparent 4 days after birth

craniofacial
• impaired development

endocrine/exocrine glands

immune system
• at 1 month, inflammatory cells containing melanin with enlarged sebaceous glands are observed in the dermis


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