- decreased bone mineral density / IMPC
- increased circulating calcium level / IMPC
- abnormal coat/ hair morphology / IMPC
- abnormal tibia morphology / IMPC
- decreased body length / IMPC
- decreased body weight / IMPC
- abnormal lens morphology / IMPC
- cataract / IMPC
- abnormal coat/hair pigmentation / IMPC
- abnormal eye morphology / IMPC
- abnormal tooth morphology / IMPC
- increased circulating alanine transaminase level / IMPC
- increased lactate dehydrogenase level / IMPC
- abnormal humerus morphology / IMPC
- increased circulating creatine kinase level / IMPC
- abnormal incisor color / IMPC
- decreased bone mineral content / IMPC
B6Dnk;B6Brd;B6N-Tyrc-Brd Sparctm1a(EUCOMM)Wtsi/WtsiCnbc
Status | Available to order |
EMMA ID | EM:05296 |
International strain name | B6Dnk;B6Brd;B6N-Tyrc-Brd Sparctm1a(EUCOMM)Wtsi/WtsiCnbc |
Alternative name | EPD0060_1_A07 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Sparctm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Sparc |
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 EPD0060_1_A07. 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 | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Osteogenesis imperfecta type 4 / Orphanet_216820
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- abnormal coat/hair pigmentation / IMPC
- increased lactate dehydrogenase level / IMPC
- abnormal incisor color / IMPC
- abnormal humerus morphology / IMPC
- decreased body weight / IMPC
- increased circulating creatine kinase level / IMPC
- abnormal lens morphology / IMPC
- decreased bone mineral density / IMPC
- decreased body length / IMPC
- cataract / IMPC
- abnormal tibia morphology / IMPC
- abnormal eye morphology / IMPC
- abnormal tooth morphology / IMPC
- decreased bone mineral content / IMPC
- increased circulating alanine transaminase level / IMPC
- increased circulating calcium level / IMPC
- abnormal coat/ hair morphology / IMPC
MGI phenotypes (allele matching)
- abnormal tibia morphology / MGI
- decreased body weight / MGI
- abnormal lens morphology / MGI
- cataract / MGI
- abnormal coat/hair pigmentation / MGI
- abnormal eye morphology / MGI
- abnormal tooth morphology / MGI
- abnormal humerus morphology / MGI
- decreased mean corpuscular hemoglobin concentration / MGI
- abnormal incisor color / MGI
MGI phenotypes (gene matching)
- decreased bone mineral density / MGI
- abnormal trabecular bone morphology / MGI
- abnormal tibia morphology / MGI
- decreased body weight / MGI
- abnormal lens morphology / MGI
- cataract / MGI
- retinal degeneration / MGI
- hypoactivity / MGI
- abnormal skeleton physiology / MGI
- abnormal bone strength / MGI
- eye inflammation / MGI
- abnormal coat/hair pigmentation / MGI
- abnormal eye morphology / MGI
- abnormal tooth morphology / MGI
- enhanced wound healing / MGI
- abnormal lens fiber morphology / MGI
- delayed wound healing / MGI
- abnormal bone remodeling / MGI
- retinal detachment / MGI
- abnormal lens capsule morphology / MGI
- abnormal lens epithelium morphology / MGI
- increased tumor growth/size / MGI
- abnormal retinal layer morphology / MGI
- abnormal osteoclast morphology / MGI
- decreased osteoclast cell number / MGI
- abnormal osteoblast morphology / MGI
- decreased osteoblast cell number / MGI
- abnormal humerus morphology / MGI
- hematopoietic system phenotype / MGI
- abnormal skeleton morphology / MGI
- decreased mean corpuscular hemoglobin concentration / MGI
- vitreous body inflammation / MGI
- ruptured lens capsule / MGI
- abnormal incisor color / MGI
- subcapsular cataracts / MGI
- posterior subcapsular cataracts / MGI
- cortical cataracts / 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
- Identification of genes important for cutaneous function revealed by a large scale reverse genetic screen in the mouse.;DiTommaso Tia, Jones Lynelle K, Cottle Denny L, null null, Gerdin Anna-Karin, Vancollie Valerie E, Watt Fiona M, Ramirez-Solis Ramiro, Bradley Allan, Steel Karen P, Sundberg John P, White Jacqueline K, Smyth Ian M, ;2014;PLoS genetics;10;e1004705; 25340873
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