- decreased bone mineral density / IMPC
- decreased hematocrit / IMPC
- abnormal cranium morphology / IMPC
- abnormal snout morphology / IMPC
- abnormal maxilla morphology / IMPC
- decreased body length / IMPC
- decreased body weight / IMPC
- abnormal tooth morphology / IMPC
- decreased hemoglobin content / IMPC
- decreased erythrocyte cell number / IMPC
- decreased lean body mass / IMPC
- decreased total body fat amount / IMPC
- decreased bone mineral content / IMPC
- hypoplasia / IMPC
- process of degenerative change / IMPC
- glomerulonephritis / IMPC
- lipid deposition / IMPC
- osteopenia / IMPC
- steatosis / IMPC
B6Brd;B6N-Tyrc-Brd Miga2tm1a(KOMP)Wtsi/Wtsi
Status | Available to order |
EMMA ID | EM:12034 |
International strain name | B6Brd;B6N-Tyrc-Brd Miga2tm1a(KOMP)Wtsi/Wtsi |
Alternative name | EPD0026_1_C12 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Miga2tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Miga2 |
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 EPD0026_1_C12. 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 |
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Information from EMMA
Archiving centre | Wellcome Trust Sanger Institute, Hinxton, United Kingdom |
Animals used for archiving | heterozygous C57BL/6Dnk;C57BL/6Brd-Tyr |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- decreased body weight / IMPC
- decreased lean body mass / IMPC
- process of degenerative change / IMPC
- hypoplasia / IMPC
- decreased erythrocyte cell number / IMPC
- decreased hematocrit / IMPC
- decreased bone mineral content / IMPC
- lipid deposition / IMPC
- decreased total body fat amount / IMPC
- osteopenia / IMPC
- abnormal cranium morphology / IMPC
- abnormal tooth morphology / IMPC
- steatosis / IMPC
- glomerulonephritis / IMPC
- abnormal snout morphology / IMPC
- abnormal maxilla morphology / IMPC
- decreased bone mineral density / IMPC
- decreased hemoglobin content / IMPC
- decreased body length / IMPC
MGI phenotypes (gene matching)
- decreased bone mineral density / MGI
- decreased circulating LDL cholesterol level / MGI
- decreased circulating HDL cholesterol level / MGI
- decreased hematocrit / MGI
- abnormal cranium morphology / MGI
- abnormal snout morphology / MGI
- abnormal maxilla morphology / MGI
- decreased body length / MGI
- decreased body weight / MGI
- hyperactivity / MGI
- abnormal tooth morphology / MGI
- decreased hemoglobin content / MGI
- decreased lean body mass / MGI
- abnormal behavior / MGI
- decreased circulating cholesterol level / MGI
- decreased circulating serum albumin level / MGI
- decreased circulating total protein level / MGI
- decreased lactate dehydrogenase level / MGI
- decreased circulating aspartate transaminase level / MGI
- decreased total body fat amount / MGI
- decreased bone mineral content / MGI
Literature references
- Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes.;White Jacqueline K, Gerdin Anna-Karin, Karp Natasha A, Ryder Ed, Buljan Marija, Bussell James N, Salisbury Jennifer, Clare Simon, Ingham Neil J, Podrini Christine, Houghton Richard, Estabel Jeanne, Bottomley Joanna R, Melvin David G, Sunter David, Adams Niels C, null null, Tannahill David, Logan Darren W, Macarthur Daniel G, Flint Jonathan, Mahajan Vinit B, Tsang Stephen H, Smyth Ian, Watt Fiona M, Skarnes William C, Dougan Gordon, Adams David J, Ramirez-Solis Ramiro, Bradley Allan, Steel Karen P, ;2013;Cell;154;452-64; 23870131
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