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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Bbs7tm1Vcs
targeted mutation 1, Val C Sheffield
MGI:5315475
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Bbs7tm1Vcs/Bbs7tm1Vcs involves: 129S1/Sv * 129X1/SvJ * C57BL/6J MGI:5705386
hm2
Bbs7tm1Vcs/Bbs7tm1Vcs Not Specified MGI:5315587
cx3
Bbs7tm1Vcs/Bbs7tm1Vcs
Ift88Tg737Rpw/Ift88Tg737Rpw
involves: FVB/N MGI:5315588


Genotype
MGI:5705386
hm1
Allelic
Composition
Bbs7tm1Vcs/Bbs7tm1Vcs
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bbs7tm1Vcs mutation (0 available); any Bbs7 mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mating of heterozygotes results in a sub-Mendelian ratio of homozygous offspring (19% versus expected 25%)

growth/size/body
• homozygotes are runts at birth
• at 3 weeks of age, homozygotes weigh less than wild-type controls
• after weaning, homozygotes begin to gain more weight than wild-type mice due to increased food intake
• at 12 weeks of age, both male and female homozygotes weigh significantly more than wild-type controls, and differences become greater as mice age
• by 7 months, homozygotes weigh 41.1 +/- 3.25 g whereas wild-type controls weigh 28.7 +/- 2.8 g

behavior/neurological
• after weaning, homozygotes begin to gain more weight than wild-type mice due to increased food intake

reproductive system
• at 4-8 months of age, mutant seminiferous tubules exhibit a paucity of sperm flagella
• some mutant sperm have abnormal flagella
• in the principal piece, outer dense fibers surrounding the microtubular structure are highly disorganized
• only 8.8% of mutant sperm flagella have normal 9+2 axonemal structures
• abnormal sperm flagella show disorganized microtubule structures
• a ring-type of microtubule structure is frequently observed
• TEM analysis revealed that the microtubular structures and the outer dense fibers surrounding the microtubular structure in the principal piece are highly disorganized
• most mutant sperm lack a flagellar tail
• male infertility is associated with abnormal sperm flagellar axonemes

nervous system
N
• at 4-8 months of age, homozygotes show no apparent defects in overall cerebellum morphology or foliation
• cerebellar Purkinje cells appear normal
• at 3 weeks of age, TEM analysis revealed short and bulged cilia with vesicles, and motile cilia with defective axonemal structures
• at 3 months of age, remaining cilia are shorter than normal
• at 3 months of age, homozygotes show a significantly reduced number of motile cilia in the brain ependymal layer
• at 4-8 months of age, homozygotes show enlarged lateral ventricles
• at 4-8 months of age, homozygotes show an enlarged dorsal third ventricle
• at 4-8 months of age, homozygotes show a reduction in the size of the corpus striatum
• at 4-8 months of age, homozygotes show a reduction in the size of the hippocampus
• at 4-8 months of age, homozygotes show thinning of the cerebral cortex
• at 4-8 months of age, mutant eyes show a significant degeneration of the inner segment of photoreceptor cells
• at 4-8 months of age, mutant eyes show a significant degeneration of the outer segment of photoreceptor cells

vision/eye
• at 4-8 months of age, mutant eyes show a significant degeneration of the inner segment of photoreceptor cells
• at 4-8 months of age, mutant eyes show a significant degeneration of the outer segment of photoreceptor cells
• at 4-8 months of age, mutant eyes show a significant degeneration of the retinal outer nuclear layer
• at 4-8 months of age, homozygotes display photoreceptor cell loss

cellular
N
• homozygotes show normal primary cilia numbers and cilia length in the kidney and pancreas
• primary cilia form and appear grossly normal in cultured kidney epithelial cells and mouse embryonic fibroblasts
• motile cilia in the trachea have normal 9+2 axonemal structures
• homozygotes show abnormal accumulation of the dopamine D1 receptor to the ciliary membrane in multiple brain regions including the striatum and amygdala, unlike wild-type controls
• at 3 weeks of age, TEM analysis revealed short and bulged cilia with vesicles, and motile cilia with defective axonemal structures
• at 3 months of age, remaining cilia are shorter than normal
• at 3 months of age, homozygotes show a significantly reduced number of motile cilia in the brain ependymal layer
• at 4-8 months of age, mutant seminiferous tubules exhibit a paucity of sperm flagella
• some mutant sperm have abnormal flagella
• in the principal piece, outer dense fibers surrounding the microtubular structure are highly disorganized
• only 8.8% of mutant sperm flagella have normal 9+2 axonemal structures
• abnormal sperm flagella show disorganized microtubule structures
• a ring-type of microtubule structure is frequently observed
• TEM analysis revealed that the microtubular structures and the outer dense fibers surrounding the microtubular structure in the principal piece are highly disorganized
• most mutant sperm lack a flagellar tail

taste/olfaction
N
• bitter taste receptors in cultured mutant kidney cells are functional, as shown by normal Ca2+ mobilization following stimulation with the bitter compound denatonium

renal/urinary system
N
• homozygotes lack kidney cysts
• in culture, mutant primary kidney cells show normal ciliary membrane localization of polycystin-1, and polycystin-2, and bitter taste receptors
• bitter taste receptors in mutant kidney cells are functional, as shown by normal Ca2+ mobilization following stimulation with the bitter compound denatonium

limbs/digits/tail
N
• homozygotes do not exhibit polydactyly of the forelimbs or hindlimbs




Genotype
MGI:5315587
hm2
Allelic
Composition
Bbs7tm1Vcs/Bbs7tm1Vcs
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bbs7tm1Vcs mutation (0 available); any Bbs7 mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
N
• mice exhibit normal limb development

nervous system
N
• mice exhibit normal neurocranial development

vision/eye
N
• mice exhibit eye development at E11.5 to E13.5




Genotype
MGI:5315588
cx3
Allelic
Composition
Bbs7tm1Vcs/Bbs7tm1Vcs
Ift88Tg737Rpw/Ift88Tg737Rpw
Genetic
Background
involves: FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bbs7tm1Vcs mutation (0 available); any Bbs7 mutation (43 available)
Ift88Tg737Rpw mutation (0 available); any Ift88 mutation (48 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

limbs/digits/tail
• lack of calcification at E12.5
• broad at E12.5 relative to E11.5 wild-type limb buds, suggesting polydactyly
• delayed at E11.5 and E12.5

embryo
• broad at E12.5 relative to E11.5 wild-type limb buds, suggesting polydactyly

vision/eye
• absent eyes at E11.5 to E13.5

cardiovascular system
• at E11.5 to E13.5

craniofacial
• at E11.5 to E13.5

nervous system
• at E11.5 to E13.5

homeostasis/metabolism
• at E11.5 to E13.5

digestive/alimentary system
• at E11.5 to E13.5

growth/size/body
• at E11.5 to E13.5





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory