- increased circulating calcium level / IMPC
- decreased bone mineral density / IMPC
- abnormal auditory brainstem response / IMPC
- abnormal radius morphology / IMPC
- increased circulating cholesterol level / IMPC
- decreased bone mineral content / IMPC
- decreased KLRG1-positive NK cell number / IMPC
- decreased grip strength / IMPC
- decreased effector memory T-helper cell number / IMPC
- abnormal tibia morphology / IMPC
- increased mean corpuscular hemoglobin concentration / IMPC
- decreased leukocyte cell number / IMPC
- increased circulating creatinine level / IMPC
- abnormal clavicle morphology / IMPC
- abnormal hair growth / IMPC
- abnormal joint morphology / IMPC
- increased circulating fructosamine level / IMPC
- increased CD4-positive, alpha-beta T cell number / IMPC
- abnormal thoracic cage shape / IMPC
- decreased Ly6C low monocyte number / IMPC
- increased effector memory CD8-positive, alpha-beta T cell number / IMPC
- increased lean body mass / IMPC
- decreased lean body mass / IMPC
- abnormal vertebral arch morphology / IMPC
- decreased mature B cell number / IMPC
- decreased red blood cell distribution width / IMPC
- increased T cell number / IMPC
- decreased immature B cell number / IMPC
- decreased memory-marker gamma-delta T cell number / IMPC
- increased mean corpuscular hemoglobin / IMPC
- decreased hematocrit / IMPC
- abnormal femur morphology / IMPC
- increased circulating iron level / IMPC
- increased alpha-beta T cell number / IMPC
- decreased circulating glucose level / IMPC
- decreased erythrocyte cell number / IMPC
- abnormal vertebrae morphology / IMPC
- increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number / IMPC
- increased circulating sodium level / IMPC
- increased circulating LDL cholesterol level / IMPC
- abnormal humerus morphology / IMPC
- increased total body fat amount / IMPC
- decreased B cell number / IMPC
- increased circulating total protein level / IMPC
- decreased B-2 B cell number / IMPC
- decreased CD8-positive, alpha-beta T cell number / IMPC
- increased neutrophil cell number / IMPC
- absent pinna reflex / IMPC
- increased circulating serum albumin level / IMPC
- increased blood urea nitrogen level / IMPC
- decreased transitional stage T1 B cell number / IMPC
- decreased heart weight / IMPC
- abnormal zygomatic bone morphology / IMPC
- abnormal ulna morphology / IMPC
- increased CD8-positive, naive alpha-beta T cell number / IMPC
- decreased circulating thyroxine level / IMPC
- increased plasmacytoid dendritic cell number / IMPC
- increased circulating HDL cholesterol level / IMPC
- abnormal snout morphology / IMPC
- abnormal cranium morphology / IMPC
- decreased body length / IMPC
- decreased hemoglobin content / IMPC
- increased CD8-positive, alpha-beta T cell number / IMPC
- abnormal bone structure / IMPC
- decreased follicular B cell number / IMPC
- decreased circulating amylase level / IMPC
- increased T-helper cell number / IMPC
- abnormal head morphology / IMPC
- decreased total body fat amount / IMPC
- improved glucose tolerance / IMPC
- abnormal eyelid morphology / IMPC
- increased fasting circulating glucose level / IMPC
- abnormal iris morphology / IMPC
- decreased NK cell number / IMPC
- decreased CD11b-high dendritic cell number / IMPC
- decreased memory CD4-positive, CD25-positive, alpha-beta regulatory T cell number / IMPC
- decreased mean platelet volume / IMPC
C57BL/6N-Atm1Brd Duoxa2tm1a(KOMP)Wtsi/WtsiOrl
Status | Available to order |
EMMA ID | EM:09460 |
Citation information | RRID:IMSR_EM:09460 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-Atm1Brd Duoxa2tm1a(KOMP)Wtsi/WtsiOrl |
Alternative name | EPD0899_5_A06 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Duoxa2tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Duoxa2 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from KOMP ES clone EPD0899_5_A06. 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 | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6NTac males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Familial thyroid dyshormonogenesis / Orphanet_95716
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- no abnormal phenotype detected / MGI
Information on how we integrate external resources can be found here
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