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Phenotypes Associated with This Genotype
Genotype
MGI:3051020
Allelic
Composition
Cux1tm1Mbu/Cux1tm1Mbu
Genetic
Background
involves: OF1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cux1tm1Mbu mutation (0 available); any Cux1 mutation (111 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• the majority of homozygotes survive on the outbred OF1 background

growth/size/body
• homozygotes are severely growth-retarded
• growth retardation is not caused by dysfunction of the thyroid or pituitary glands

reproductive system
N
• surprisingly, matings of OF1 mutant males with wild-type females resulted in litters of normal size, indicating normal male fertility

integument
• the mutant pelage contains twisted, bifurcated, circle, and corkscrew hair as well as hair with nodules or longitudinal grooving
• rare survivors (1%) have only a sparse pelage of abnormal hair
• at P7, mutants start to lose most of their pelage hair
• morphogenesis of hair follicles is disrupted in 3-wk-old mutants: they appear misoriented, cystic or even sclerotic, and contain more than one degenerated hair shaft
• scales are absent, suggesting aberrant development of the cuticle cell layers in the hair follicle
• the inner root sheath is reduced in mutant hair follicles
• pups are born with curly whiskers
• pups are born with only a few stunted whiskers


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
04/30/2024
MGI 6.23
The Jackson Laboratory