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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rbp4tm1.1Mma
targeted mutation 1.1, Manuel Mark
MGI:3625605
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rbp4tm1.1Mma/Rbp4tm1.1Mma involves: 129 * C57BL/6J MGI:3629679
ht2
Rbp4tm1.1Mma/Rbp4+ involves: 129 * C57BL/6J MGI:3629703


Genotype
MGI:3629679
hm1
Allelic
Composition
Rbp4tm1.1Mma/Rbp4tm1.1Mma
Genetic
Background
involves: 129 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rbp4tm1.1Mma mutation (0 available); any Rbp4 mutation (21 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• serum retinol levels were decreased by 98% in 15 week old mutant mice compared to wild-type littermates

reproductive system
• prolonged vitamin A deficiency results in progressive testis degeneration
• immature spermatids are released during spermatogenesis
• testes show chronic loss of immature germ cells
• immature germ cells, as well as spermatozoa, are shed into the epidydimides
• mild vitamin A deficiency results in desquamation of round spermatids
• mild vitamin A deficiency results in partial spermiation failure
• IX and X spermatids are retained in seminiferous tubules longer than normal
• some immature round spermatids detach from seminiferous epithelium and are released into tubule lumen
• at 6 weeks of age, testicular levels of serum retinol and retinyl palmitate are 50% lower in mutant mice than in wild-type littermates

endocrine/exocrine glands
• prolonged vitamin A deficiency results in progressive testis degeneration
• immature spermatids are released during spermatogenesis
• testes show chronic loss of immature germ cells

cellular
• mild vitamin A deficiency results in desquamation of round spermatids




Genotype
MGI:3629703
ht2
Allelic
Composition
Rbp4tm1.1Mma/Rbp4+
Genetic
Background
involves: 129 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rbp4tm1.1Mma mutation (0 available); any Rbp4 mutation (21 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• serum retinol levels are decreased by 40% in heterozygous compared to levels in wild-type mice





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last database update
12/17/2024
MGI 6.24
The Jackson Laboratory