- 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 |
Citation information | RRID:IMSR_EM:10642 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
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/6NTac males |
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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