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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rbp1tm1Ipc
targeted mutation 1, Pierre Chambon
MGI:2181412
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rbp1tm1Ipc/Rbp1tm1Ipc involves: 129S2/SvPas MGI:3039735
hm2
Rbp1tm1Ipc/Rbp1tm1Ipc involves: 129S2/SvPas * C57BL/6 MGI:3700284


Genotype
MGI:3039735
hm1
Allelic
Composition
Rbp1tm1Ipc/Rbp1tm1Ipc
Genetic
Background
involves: 129S2/SvPas
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rbp1tm1Ipc mutation (2 available); any Rbp1 mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
• contact between retinal pigment epithelium and outer segments of photoreceptors disrupted on a vitamin A deficient diet

endocrine/exocrine glands
• sloughing of immature germ cells after 14 weeks on a vitamin A deficient diet
• irregular vacuoles in the epithelium
• tubules reduced in size by 23 weeks
• contain only Sertoli cells

growth/size/body
• on a vitamin A deficient diet growth was slower from 5 weeks to 12 weeks of age and then stopped

hematopoietic system
• marked expansion of entire granulocyte population when vitamin A is deficient
• increased neutrophil numbers in spleen and blood

homeostasis/metabolism
• serum levels of retinol stay stable on a vitamin A deficient diet until liver levels drop very low
• uptake by liver about half normal rate
• turnover time about 6X less than normal

immune system
• marked expansion of entire granulocyte population when vitamin A is deficient
• increased neutrophil numbers in spleen and blood

liver/biliary system
• fewer and smaller fat droplets in hepatic stellate cells
• retinyl palmitate stores in the liver are rapidly depleted on a vitamin A deficient diet

reproductive system
• sloughing of immature germ cells after 14 weeks on a vitamin A deficient diet
• irregular vacuoles in the epithelium
• tubules reduced in size by 23 weeks
• contain only Sertoli cells

vision/eye
• outer segments distorted due to swelling of lamellar disks when vitamin A deficient
• contact between retinal pigment epithelium and outer segments of photoreceptors disrupted on a vitamin A deficient diet
• electroretinogram response dramatically reduced when vitamin A deficient
• "a and b wave" amplitudes are decreased and latency is increased
• under vitamin A deficient conditions, dark adaptation is delayed 2X

nervous system
• outer segments distorted due to swelling of lamellar disks when vitamin A deficient




Genotype
MGI:3700284
hm2
Allelic
Composition
Rbp1tm1Ipc/Rbp1tm1Ipc
Genetic
Background
involves: 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rbp1tm1Ipc mutation (2 available); any Rbp1 mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
N
• contrary to expectation, E18.5 homozygotes show normal cochlear morphology with no structural changes at the level of the organ of Corti relative to wild-type mice
• in addition, homozygotes show no significant differences in ABR thresholds and latencies or DPOAEs relative to wild-type mice, indicating normal auditory function





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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
11/12/2024
MGI 6.24
The Jackson Laboratory