- increased monocyte cell number / IMPC
- tremors / IMPC
- abnormal gait / IMPC
- increased circulating aspartate transaminase level / IMPC
- decreased exploration in new environment / IMPC
- thrombocytosis / IMPC
- increased circulating iron level / IMPC
- abnormal locomotor behavior / IMPC
- increased circulating alkaline phosphatase level / IMPC
- decreased circulating fructosamine level / IMPC
C57BL/6N-Hexbtm1a(EUCOMM)Hmgu/H
Status | Available to order |
EMMA ID | EM:10642 |
International strain name | C57BL/6N-Hexbtm1a(EUCOMM)Hmgu/H |
Alternative name | HEPD0741_7_G09 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Hexbtm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Hexb |
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 HEPD0741_7_G09. 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 |
Animals used for archiving | heterozygous C57BL/6N Tac |
Breeding at archiving centre | The mutation is on an isogenic C57BL/6NTac background |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Sandhoff disease, juvenile form / Orphanet_309162
- Sandhoff disease, adult form / Orphanet_309169
- Sandhoff disease, infantile form / Orphanet_309155
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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