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Phenotypes Associated with This Genotype
Genotype
MGI:5792863
Allelic
Composition
Bbs10tm1.2Vmar/Bbs10tm1.2Vmar
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bbs10tm1.2Vmar mutation (0 available); any Bbs10 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• homozygotes show decreased body weight at 4 to 7 weeks of age but recover equivalent body weight with wild-type controls by 8 weeks of age
• homozygotes gain more weight from 8 weeks onwards and are significantly heavier than wild-type controls at 11-12 weeks of age
• homozygotes develop obesity by 3 months of age

behavior/neurological
• homozygotes develop hyperphagia from 8 weeks of age

vision/eye
• retinas show ongoing apoptosis of photoreceptors, as revealed by increased number of TUNEL+ nuclei
• homozygotes display gradual loss of the inner segment of retinal photoreceptors
• a marked reduction of rhodopsin content is observed in the outer segment at 3 months of age
• homozygotes display gradual loss of the outer segment of retinal photoreceptors
• homozygotes display gradual loss of retinal photoreceptors
• however, the connecting cilium is still be detectable next to the centriole
• homozygotes display gradual loss of the outer nuclear layer
• homozygotes exhibit retinal thinning by 3 months of age
• homozygotes develop severe retinal degeneration by 3 months of age
• at 2- and 3 months of age, scotopic electroretinogram (ERG) recordings show a significant reduction of the a-wave and b-wave magnitudes

renal/urinary system
• at 3 months of age, homozygotes show a significant increase in urine microalbumin levels
• however, creatinine clearance is normal
• at 3 months of age, primary and secondary podocyte structures are absent
• at 3 months of age, GBM thickness is substantially reduced
• renal tubular epithelial cells contain large intracytoplasmic vacuoles, unlike wild-type cells
• however, no cystic lesions are observed and tubular epithelial cells are normally ciliated and correctly polarized
• following 24-h fluid deprivation, homozygotes show a significant increase in urinary volume (diuresis) relative to similarly treated wild-type controls
• homozygotes display polyuria associated with high circulating antidiuretic hormone levels

homeostasis/metabolism
• homozygotes show a drastic increase in circulating AVP levels irrespective of fluid intake, unlike wild-type controls which exhibit a normal physiological response upon fluid restriction
• homozygotes show severe hyperleptinemia at 3 months with a circulating leptin level of 125 ng/mL
• at 3 months of age, homozygotes are not hyperglycemic but show a significant delay in the rate of decrease of glucose levels following a glucose tolerance test (GTT)
• however, insulin sensitivity is normal, indicating that the delay in glucose handling in GTT is not related to insulin resistance
• at 3 months of age, homozygotes show a significant increase in urine microalbumin levels
• however, creatinine clearance is normal

cellular
• retinas show ongoing apoptosis of photoreceptors, as revealed by increased number of TUNEL+ nuclei

nervous system
• homozygotes display gradual loss of the inner segment of retinal photoreceptors
• a marked reduction of rhodopsin content is observed in the outer segment at 3 months of age
• homozygotes display gradual loss of the outer segment of retinal photoreceptors
• homozygotes display gradual loss of retinal photoreceptors
• however, the connecting cilium is still be detectable next to the centriole

adipose tissue
N
• despite the obese phenotype, visceral adipocytes show no significant differences in cellular diameter relative to wild-type adipocytes

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Bardet-Biedl syndrome 10 DOID:0110132 OMIM:615987
J:227230


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
11/12/2024
MGI 6.24
The Jackson Laboratory