About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory