- 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 |
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:
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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 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 |
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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