- 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/6N-Bbs5tm1c(EUCOMM)Wtsi/H
Status | Available to order |
EMMA ID | EM:09033 |
International strain name | C57BL/6N-Bbs5tm1c(EUCOMM)Wtsi/H |
Alternative name | EPD0227_3_C06 |
Strain type | Targeted Mutant Strains : Targeted Conditional |
Allele/Transgene symbol | Bbs5tm1c(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 line originates from EUCOMM ES clone EPD0227_3_C06, after breeding with a Flp recombinase deleter line to convert the original targeted allele tm1a (knock-out first allele) into a conditional allele tm1c. 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 |
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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)
Literature references
- A review of standardized high-throughput cardiovascular phenotyping with a link to metabolism in mice.;Lindovsky Jiri, Nichtova Zuzana, Dragano Nathalia R V, Pajuelo Reguera David, Prochazka Jan, Fuchs Helmut, Marschall Susan, Gailus-Durner Valerie, Sedlacek Radislav, Hrabě de Angelis Martin, Rozman Jan, Spielmann Nadine, ;2023;Mammalian genome : official journal of the International Mammalian Genome Society;34;107-122; 37326672
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