- decreased mean corpuscular hemoglobin / IMPC
B6Brd;B6N-Tyrc-Brd Srctm2a(EUCOMM)Wtsi/WtsiCnbc
Status | Available to order |
EMMA ID | EM:05380 |
International strain name | B6Brd;B6N-Tyrc-Brd Srctm2a(EUCOMM)Wtsi/WtsiCnbc |
Alternative name | EPD0058_2_D10 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Srctm2a(EUCOMM)Wtsi |
Gene/Transgene symbol | Src |
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 EPD0058_2_D10. 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 |
Animals used for archiving | heterozygous C57BL/6N, wild-type C57BL/6J |
Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Hereditary thrombocytopenia with early-onset myelofibrosis / Orphanet_480851
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- decreased mean corpuscular hemoglobin / IMPC
MGI phenotypes (gene matching)
- abnormal bone marrow cavity morphology / MGI
- osteopetrosis / MGI
- abnormal tooth eruption / MGI
- failure of tooth eruption / MGI
- absent incisors / MGI
- decreased compact bone thickness / MGI
- diluted coat color / MGI
- shortened head / MGI
- abnormal femur morphology / MGI
- decreased body weight / MGI
- decreased body size / MGI
- delayed eyelid opening / MGI
- abnormal social investigation / MGI
- hyperactivity / MGI
- impaired coordination / MGI
- increased startle reflex / MGI
- abnormal vocalization / MGI
- increased inflammatory response / MGI
- female infertility / MGI
- abnormal learning/memory/conditioning / MGI
- abnormal motor capabilities/coordination/movement / MGI
- premature death / MGI
- abnormal tooth morphology / MGI
- abnormal limb morphology / MGI
- abnormal craniofacial bone morphology / MGI
- abnormal bone marrow morphology / MGI
- increased thigmotaxis / MGI
- abnormal motor learning / MGI
- delayed endochondral bone ossification / MGI
- abnormal response to novel object / MGI
- nervous system phenotype / MGI
- abnormal long bone morphology / MGI
- abnormal bone structure / MGI
- abnormal decidualization / MGI
- abnormal long bone diaphysis morphology / MGI
- decreased length of long bones / MGI
- abnormal behavior / MGI
- decreased bone resorption / MGI
- abnormal anterior eye segment morphology / MGI
- hematopoietic system phenotype / MGI
- increased long bone epiphyseal plate size / MGI
- decreased molar number / MGI
- abnormal spatial reference memory / MGI
- impaired cued conditioning behavior / MGI
- decreased grip strength / MGI
- mortality/aging / MGI
- abnormal bone trabecula morphology / MGI
- increased trabecular bone mass / MGI
- postnatal lethality, incomplete penetrance / MGI
- abnormal head shape / MGI
- abnormal response to social novelty / MGI
- abnormal social recognition / MGI
- broad face / MGI
- periodontium inflammation / MGI
- short basicranium / 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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