- increased circulating glucose level / IMPC
- decreased bone mineral content / IMPC
- increased circulating alkaline phosphatase level / IMPC
- decreased lean body mass / IMPC
- impaired glucose tolerance / IMPC
- abnormal bone structure / IMPC
- abnormal gait / IMPC
- increased circulating fructosamine level / IMPC
- increased total body fat amount / IMPC
- decreased grip strength / IMPC
- decreased bone mineral density / IMPC
- increased circulating aspartate transaminase level / IMPC
- thrombocytopenia / IMPC
- short tibia / IMPC
- decreased respiratory quotient / IMPC
- decreased circulating triglyceride level / IMPC
- increased monocyte cell number / IMPC
- increased leukocyte cell number / IMPC
- decreased heart weight / IMPC
- increased hematocrit / IMPC
- increased circulating alanine transaminase level / IMPC
- increased fasting circulating glucose level / IMPC
- increased hemoglobin content / IMPC
- abnormal retina morphology / IMPC
- increased lymphocyte cell number / IMPC
- increased mean corpuscular volume / IMPC
- tremors / IMPC
C57BL/6NTac-Bbs5tm1a(EUCOMM)Wtsi/H
Status | Available to order |
EMMA ID | EM:06028 |
International strain name | C57BL/6NTac-Bbs5tm1a(EUCOMM)Wtsi/H |
Alternative name | EPD0227_3_C06 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Bbs5tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Bbs5 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0227_3_C06. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Bardet-Biedl syndrome / Orphanet_110
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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