- abnormal behavior / IMPC
- tremors / IMPC
- abnormal coat/ hair morphology / IMPC
- abnormal vocalization / IMPC
- increased circulating glucose level / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- decreased circulating LDL cholesterol level / IMPC
- increased blood uric acid level / IMPC
- decreased leukocyte cell number / IMPC
- decreased body weight / IMPC
129-Brd7tm2a(EUCOMM)Wtsi/WtsiH
Status | Available to order |
EMMA ID | EM:04469 |
Citation information | RRID:IMSR_EM:04469 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 | 129-Brd7tm2a(EUCOMM)Wtsi/WtsiH |
Alternative name | EPD0001_3_E04 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Brd7tm2a(EUCOMM)Wtsi |
Gene/Transgene symbol | Brd7 |
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 | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0001_3_E04. For further details on the construction of this clone see the page at the IKMC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
Breeding history | Current information may be viewed at the a href="http://www.sanger.ac.uk/mouseportal/search?query=Brd7"Sanger mouse portal/a: Viability at weaning, Fertility, General Observations |
References | None available |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (allele matching)
- decreased circulating LDL cholesterol level / MGI
- abnormal coat/ hair morphology / MGI
- decreased caudal vertebrae number / MGI
- abnormal behavior / MGI
- increased blood uric acid level / MGI
- abnormal blood vessel morphology / MGI
- decreased fetal size / MGI
- fetal growth retardation / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
- delayed limb development / MGI
MGI phenotypes (gene matching)
- decreased circulating LDL cholesterol level / MGI
- abnormal coat/ hair morphology / MGI
- decreased caudal vertebrae number / MGI
- abnormal blood vessel morphology / MGI
- abnormal social/conspecific interaction / MGI
- abnormal short term object recognition memory / MGI
- abnormal long term object recognition memory / MGI
- nervous system phenotype / MGI
- decreased fetal size / MGI
- fetal growth retardation / MGI
- abnormal behavior / MGI
- behavior/neurological phenotype / MGI
- abnormal dendrite morphology / MGI
- increased blood uric acid level / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
- impaired spatial learning / MGI
- delayed limb development / MGI
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