MP:0000065 | abnormal bone marrow cavities | "absence or abnormal size or shape of the medullary cavities of the bones" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61295] |
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Allelic Composition: Tyrobptm1Lll/Tyrobptm1Lll Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0000067 | osteopetrosis | "excessive formation of dense trabecular bone and excessive calcified cartilage formation; may lead to anemia and extramedullary hematopoiesis " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MeSH:National Library of Medicine - Medical Subject Headings, 2003] |
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Allelic Composition: Tyrobptm1Lll/Tyrobptm1Lll Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0000130 | abnormal cancellous bone morphology | "structural anomaly of bone that has a latticelike or spongy structure" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Tyrobptm1Lll/Tyrobptm1Lll Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0000715 | decreased thymocyte number | "fewer than expected number of precursors to T cells; these cells are lymphoid cells found in the thymus " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7] |
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Allelic Composition: Cd247tm1Lov/Cd247tm1Lov,Fcer1gtm1Rav/Fcer1gtm1Rav Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6
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MP:0001265 | reduced body size | "smaller than average body weight, height and/or length of an organism compared to controls" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:23170] |
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Allelic Composition: Tyrobptm1Lll/Tyrobptm1Lll Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0001405 | impaired coordination | "reduced ability to execute integrated movements of muscle" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Hexbtm1Rlp/Hexbtm1Rlp Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6
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MP:0001541 | abnormal osteoclast function | "reduced ability or inability of osteoclasts to absorb and remove osseous tissue" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:58795] |
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Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Tyrobptm1Lll/Tyrobptm1Lll Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Hcst/Tyrobptm1Ttk/Hcst/Tyrobptm1Ttk Genetic Background: involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6
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MP:0001547 | abnormal lipid level | "anomalous concentrations of fat-soluble substances (molecules composed of carbon and hydrogen and are characteristically insoluble in water) in the body" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Hexbtm1Rlp/Hexbtm1Rlp Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6
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MP:0001588 | hemoglobin abnormalities | "defects in the levels or the function of the oxygen-carrying protein of erythrocytes" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Celsr1Crsh/Celsr1+,Ptk7chz/Ptk7+ Genetic Background: involves: 101/H * BALB/c * BALB/cAnN * C3H/HeH
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MP:0001798 | impaired macrophage phagocytosis | "reduced ability of these phagocytic cells to internalize particulate matter" [Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Spta1sph-2Bc/Spta1sph-2Bc Genetic Background: involves: SELH
Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6
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MP:0001805 | decreased IgG | "less than normal immunoglobulin class G level" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6
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MP:0001819 | abnormal immune cell physiology | "abnormal function of the cells of the immune system" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Spta1sph-2Bc/Spta1sph-2Bc Genetic Background: involves: SELH
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MP:0001828 | abnormal T cell activation | "anomaly in the process of producing effector T cells from naive T cells" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7] |
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Allelic Composition: Spta1sph-2Bc/Spta1sph-2Bc Genetic Background: involves: SELH
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MP:0001835 | abnormal antigen presentation | "aberration in the process by which peptide is presented to lymphocytes in a form they can recognize " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Th/Th Genetic Background: Not Specified
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MP:0001864 | vasculitis | "inflammation of a blood or lymph vessel" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Faslpr/Faslpr,Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: MRL.Cg-Fcer1gtm1Tks Faslpr
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MP:0001876 | decreased inflammatory response | "less than expected response to injury, infection, or insult" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Th/Th Genetic Background: Not Specified
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MP:0001921 | reduced fertility | "diminished ability to produce live offspring" [J:65030] |
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Allelic Composition: Il4tm1.1Wep/Il4tm1.1Wep Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Tyrobptm1.1Viv/Tyrobptm1.1Viv Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0002083 | premature death | "death after 3 weeks of age, but before normal life span" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Hexbtm1Rlp/Hexbtm1Rlp Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6
Allelic Composition: Faslpr/Faslpr,Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: MRL.Cg-Fcer1gtm1Tks Faslpr
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MP:0002423 | abnormal mast cell physiology | "anomalous response of the granulated cells found in most tissues and which contain large amounts of histamine and heparin in granules" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Spta1sph-2Bc/Spta1sph-2Bc Genetic Background: involves: SELH
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MP:0002435 | abnormal effector T cell morphology/development | "anomalous structure, formation, or numbers of the set of T lymphocytes that are able to respond immediately upon contact with cells bearing the appropriate peptide:MHC complex for the cell" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Cd247tm1Lov/Cd247tm1Lov,Fcer1gtm1Rav/Fcer1gtm1Rav Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6
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MP:0002451 | abnormal macrophage physiology | "abnormal function or response of the phagocytic leukocytes involved in innate immunity, early non-adaptive phases of host-defense, antigen presentation, and which act as effector cells in humoral and cell-mediated immunity" [Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6
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MP:0002455 | abnormal dendritic cell antigen presentation | "impairment of these specialized cells to process and present antigen to T lymphoytes" [Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7] |
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Allelic Composition: Spta1sph-2Bc/Spta1sph-2Bc Genetic Background: involves: SELH
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MP:0002461 | increased circulating immunoglobulin concentration | "greater than normal immunoglobulin level" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Hexbtm1Rlp/Hexbtm1Rlp Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6
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MP:0002490 | abnormal circulating immunoglobulin concentration | "deviation from the normal levels of glycoproteins present in the blood and other tissue, often functioning as antibodies" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Spta1sph-2Bc/Spta1sph-2Bc Genetic Background: involves: SELH
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MP:0002493 | increased IgG | "greater than normal immunoglobulin class G level" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Faslpr/Faslpr,Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: MRL.Cg-Fcer1gtm1Tks Faslpr
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MP:0002497 | increased IgE | "greater than normal immunoglobulin class E level" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Spta1sph-2Bc/Spta1sph-2Bc Genetic Background: involves: SELH
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MP:0002743 | glomerulonephritis | "glomerular disease characterized by diffuse inflammatory reaction that is not the acute response to infection of the kidneys" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator] |
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Allelic Composition: Faslpr/Faslpr,Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: MRL.Cg-Fcer1gtm1Tks Faslpr
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MP:0002962 | increased protein excretion | "greater than the normal amount of serum proteins voided by the kidneys" [RGD:Rat Genome Database submission] |
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Allelic Composition: Faslpr/Faslpr,Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: MRL.Cg-Fcer1gtm1Tks Faslpr
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MP:0003038 | decreased infarction size | "decreased size of necrotic area from normal of the myocardium resulting from a sudden insufficiency of arterial or venous blood supply due to emboli, thrombi or mechanical factors" [MeSH:National Library of Medicine - Medical Subject Headings, 2003, Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8, RGD:Rat Genome Database submission] |
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Allelic Composition: Spta1sph-2Bc/Spta1sph-2Bc Genetic Background: involves: SELH
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MP:0003109 | short femur | "reduced length of the long bone of the thigh" [ava:Anna V. Anagnostopoulos, Mouse Genome Informatics Curator, Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Tyrobptm1Lll/Tyrobptm1Lll Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0003606 | kidney failure | "cessation of renal function" [ncbi:Matthew Mailman, NCBI request] |
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Allelic Composition: Faslpr/Faslpr,Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: MRL.Cg-Fcer1gtm1Tks Faslpr
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MP:0003795 | abnormal bone structure | |
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Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Tyrobptm1Lll/Tyrobptm1Lll Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0004256 | abnormal maternal decidual layer morphology | "anomaly in the structure of the maternal uterine-derived portion of the placenta" [PMID:11433360] |
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Allelic Composition: Il4tm1.1Wep/Il4tm1.1Wep Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Tyrobptm1.1Viv/Tyrobptm1.1Viv Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0004259 | small placenta | "reduced size of the size or shape of the organ of metabolic interchange between fetus and mother" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Tyrobptm1.1Viv/Tyrobptm1.1Viv Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0004260 | enlarged placenta | "increased size of the size or shape of the organ of metabolic interchange between fetus and mother" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Il4tm1.1Wep/Il4tm1.1Wep Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0004762 | increased anti-double stranded DNA antibody level | "increase in the level of antibodies that recognize double stranded DNA" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Faslpr/Faslpr,Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: MRL.Cg-Fcer1gtm1Tks Faslpr
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MP:0004800 | decreased susceptibility to experimental autoimmune encephalomyelitis | "reduced likelihood that an organism will develop disease symptoms similar to human multiple sclerosis upon induction with antigens to Myelin Basic Protein (MBP), Proteolipid Protein (PLP), and/or Myelin Oligodendrocyte glycoprotein (MOG)" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Spta1sph-2Bc/Spta1sph-2Bc Genetic Background: involves: SELH
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MP:0004804 | decreased susceptibility to autoimmune diabetes | "reduced likelihood that an organism will develop inflammatory pancreatic disease resulting from the body attacking and destroying the insulin-producing beta islet cells of the pancreas" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: 1700016L21RikTg(Itgax-DTR/EGFP)57Lan/0 Genetic Background: B6.FVB-1700016L21RikTg(Itgax-DTR/EGFP)57Lan/J
Allelic Composition: C3tm1Crr/C3tm1Crr,Fcer1gtm1Rav/Fcer1gtm1Rav,Tg(Ins2-TFRC/OVA)296Wehi/0 Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6
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MP:0004828 | decreased susceptibility to autoimmune hemolytic anemia | "reduced likelihood that an organism will develop an abnormality of the immune system that destroys red blood cells (hemolysis) prematurely" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Atp1b1tm1.1Akra/Atp1b1tm1.1Akra,Myl2tm1(cre)Krc/Myl2+ Genetic Background: involves: 129S/SvEv * 129S4/SvJae
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MP:0004867 | decreased platelet calcium level | "decreased concentration in the platelet of this bivalent element" [RGD:Rat Genome Database submission] |
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Allelic Composition: Spta1sph-2Bc/Spta1sph-2Bc Genetic Background: involves: SELH
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MP:0004952 | increased spleen weight | "greater than average weight of the organ that functions to filter blood and to store red corpuscles and platelets" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Faslpr/Faslpr,Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: MRL.Cg-Fcer1gtm1Tks Faslpr
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MP:0004993 | decreased bone resorption | "reduced amount of degradation of the organic and inorganic phases of bone by absorption, usually by the abnormal function or number of osteoclasts" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Tyrobptm1Lll/Tyrobptm1Lll Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0005027 | increased susceptibility to parasitic infection | "greater likelihood that an organism will develop ill effects from a parasitic infection or from components of or toxins produced by parasites " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Celsr1Crsh/Celsr1+,Ptk7chz/Ptk7+ Genetic Background: involves: 101/H * BALB/c * BALB/cAnN * C3H/HeH
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MP:0005070 | defective NK cell cytolysis | "impaired ability of these cells to destroy or dissolve targeted cells" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:6213] |
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Allelic Composition: Cd247tm1Lov/Cd247tm1Lov,Fcer1gtm1Rav/Fcer1gtm1Rav Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6
Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6
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MP:0005090 | increased double-negative T cells count | "greater than expected numbers of the subset of T cells found in the thymus that express neither CD4 nor CD8" [Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7] |
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Allelic Composition: Faslpr/Faslpr,Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: MRL.Cg-Fcer1gtm1Tks Faslpr
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MP:0005095 | decreased T cell proliferation | "reduced clonal expansion of naive T cells in response to stimuli" [Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7] |
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Allelic Composition: 1700016L21RikTg(Itgax-DTR/EGFP)57Lan/0 Genetic Background: B6.FVB-1700016L21RikTg(Itgax-DTR/EGFP)57Lan/J
Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6
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MP:0005463 | abnormal CD4+ T cell physiology | "anomalous response of the subset of T lymphocytes that carry the CD4 marker, recognize intravesicular peptides bound to MHC class-II molecules, and turn on antibody production" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6
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MP:0005465 | abnormal T helper 1 physiology | "anomalous response of the subset of helper T cells that enhance cell-mediated immune responses; these cells secrete IL-1 and gamma-IFN and are generally involved in inflammatory responses" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7] |
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Allelic Composition: Cd247tm1Lov/Cd247tm1Lov,Fcer1gtm1Rav/Fcer1gtm1Rav Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6
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MP:0005597 | decreased susceptibility to type I hypersensitivity reaction | "less likelihood or resistance to developing a response manifested by localized or generalized reaction that occurs immediately (minutes) after exposure to an antigen to which the person/animal was previously sensitized; it is IgE-mediated, and mast cell activation and degranulation are hallmarks" [Pathology:ISBN 0-397-51047-0, J:68588, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Spta1sph-2Bc/Spta1sph-2Bc Genetic Background: involves: SELH
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MP:0005605 | increased bone mass | "an increase in the total amount of bone tissue contained in the skeleton" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Tyrobptm1Lll/Tyrobptm1Lll Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0005614 | decreased susceptibility to type III hypersensitivity reaction | "less likelihood of or resistance to developing tissue injury mediated by immune complexes; generally involves immune complexes formed in the blood via Abs encountering circulating Ag; Ag-Ab complexes then deposit in tissues (especially blood vessels and glomeruli), induce complement activation, and result in tissue injury " [Pathology:ISBN 0-397-51047-0, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Faslpr/Faslpr,Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: MRL.Cg-Fcer1gtm1Tks Faslpr
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MP:0005616 | decreased susceptibility to type IV hypersensitivity reaction | "less likelihood of or resistance to developing an antigen-elicited cellular immune reaction that results in tissue damage, but does not require Ab participation; the response is seen at the area of contact" [Pathology:ISBN 0-397-51047-0, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6
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MP:0006043 | decreased apoptosis | "less than normal cell death" [RGD:Rat Genome Database submission, smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Hexbtm1Rlp/Hexbtm1Rlp Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6
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MP:0006298 | abnormal platelet activation | "anomaly in the series of progressive, overlapping events triggered by exposure of platelets to signals from subendothelial tissue, including shape change, adhesiveness, aggregation, and release reactions; when carried through to completion, these events lead to the formation of a stable hemostatic plug" [GO:0030168, MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Spta1sph-2Bc/Spta1sph-2Bc Genetic Background: involves: SELH
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MP:0008042 | abnormal NK T cell physiology | "any functional anomaly of the distinct lineage of T cells expressing natural killer cell markers and having T cell receptors characterized by the usage of a restricted repertoire of variable region gene segments" [GO:0001865] |
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6
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MP:0008127 | decreased dendritic cell number | "reduction in the number of a cells of hematopoietic origin, typically resident in particular tissues, specialized in the uptake, processing, and transport of antigens to lymph nodes for the purpose of stimulating an immune response via T cell activation" [ISBN:0781735149, MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Clec4etm1Tks/Clec4etm1Tks Genetic Background: involves: 129S1/Sv * 129X1/SvJ
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MP:0008158 | increased diameter of femur | "increased width of the cross-sectional distance that extends from one lateral edge of the femur, through its center and to the opposite lateral edge" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Tyrobptm1Lll/Tyrobptm1Lll Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0008352 | absent gamma-delta intraepithelial T cell | "absence of a gamma-delta T cell present in columnar epithelia such as in the gastrointestinal tract; intraepithelial T cells often have distinct developmental pathways and activation requirements" [CL:0000801, ISBN:0781735149] |
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Allelic Composition: Cd247tm1Lov/Cd247tm1Lov,Fcer1gtm1Rav/Fcer1gtm1Rav Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6
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MP:0008396 | abnormal osteoclast differentiation | "atypical production of or inability to produce bone resorpting cells that remove bone tissue by degrading the mineralized matrix" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Tyrobptm1Lll/Tyrobptm1Lll Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0008495 | decreased IgG1 level | "less than normal immunoglobulin class G1 level" [MGI:tmeehan "Terry Meehan, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6
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MP:0008496 | decreased IgG2a level | "less than normal immunoglobulin class G2a level" [MGI:tmeehan "Terry Meehan, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6
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MP:0008497 | decreased IgG2b level | "less than normal immunoglobulin class G2b level" [MGI:tmeehan "Terry Meehan, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6
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MP:0008498 | decreased IgG3 level | "less than normal immunoglobulin class G3 level" [MGI:tmeehan "Terry Meehan, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6
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MP:0008559 | abnormal interferon-gamma secretion | "anomaly in the production or release of the major interferon produced by mitogenically or antigenically stimulated lymphocytes that is involved in immunoregulation" [MESH:D12.644.276.374.440.893] |
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Allelic Composition: Clec4etm1Tks/Clec4etm1Tks Genetic Background: involves: 129S1/Sv * 129X1/SvJ
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MP:0008561 | decreased tumor necrosis factor secretion | "reduction in the production or release of a serum glycoprotein produced by activated macrophages and NK cells and involved in initiating local inflammatory responses, particularly by its action on the endothelium of local blood vessels; its actions result in increased vascular permeability and induction of expression of adhesion molecules on the endothelium" [ISBN:0-8153-1691-7 "Immunobiology, The Immune System in Health and Disease", MESH:D12.644.276.374.500.800] |
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Allelic Composition: ArTfm/Ar+,EdaTa-25H/Eda+ Genetic Background: involves: 101/H * C3H/HeH
Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6J
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MP:0008567 | decreased interferon-gamma secretion | "reduction in the production or release of the major interferon produced by mitogenically or antigenically stimulated lymphocytes that is involved in immunoregulation" [MESH:D12.644.276.374.440.893] |
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Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Tyrobptm1.1Viv/Tyrobptm1.1Viv Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6
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MP:0008658 | decreased interleukin-1 beta secretion | "reduction in the production or release of an interleukin-1 subtype that is synthesized as an inactive membrane-bound pro-protein on monocytes, macrophages and other cells; proteolytic processing of the precursor form by caspase 1 results in release of the active form of interleukin-1beta from the membrane" [MESH:D12.644.276.374.465.501.600] |
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Allelic Composition: ArTfm/Ar+,EdaTa-25H/Eda+ Genetic Background: involves: 101/H * C3H/HeH
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MP:0008661 | decreased interleukin-10 secretion | "reduction in the production or release of a cytokine produced by a variety of cell types, including T-cells, monocytes, dendritic cells and epithelial cells that exerts a variety of effects on immunoregulation and inflammation" [MESH:D12.644.276.374.465.510] |
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Allelic Composition: ArTfm/Ar+,EdaTa-25H/Eda+ Genetic Background: involves: 101/H * C3H/HeH
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MP:0008670 | decreased interleukin-12b secretion | "reduction in the production or release of the p40 cytokine subunit that is a component of both interleukin-12 and interleukin-23" [MESH:D12.644.276.374.465.512.500] |
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Allelic Composition: ArTfm/Ar+,EdaTa-25H/Eda+ Genetic Background: involves: 101/H * C3H/HeH
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MP:0008680 | abnormal interleukin-17 secretion | "anomaly in the production or release of a proinflammatory cytokine produced primarily by T-cells or their precursors" [MESH:D12.644.276.374.465.517] |
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6J
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MP:0008688 | decreased interleukin-2 secretion | "reduction in the production or release of a soluble substance elaborated by antigen- or mitogen-stimulated T-cells which induces DNA synthesis in naive lymphocytes" [MESH:D12.644.276.374.465.502] |
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6
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MP:0008691 | decreased interleukin-23 secretion | "reduction in the production or release of a heterodimeric cytokine that plays a role in innate and adaptive immune responses; it is produced by dendritic cells, macrophages and a variety of other immune cells" [MESH:D12.644.276.374.465.759] |
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Allelic Composition: ArTfm/Ar+,EdaTa-25H/Eda+ Genetic Background: involves: 101/H * C3H/HeH
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MP:0008706 | decreased interleukin-6 secretion | "reduction in the production or release of a cytokine that stimulates the growth and differentiation of B-cells and is also a growth factor for hybridomas and plasmacytomas, and is produced by many different cells including T-cells, monocytes and fibroblasts" [MESH:D12.644.276.374.465.506] |
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Allelic Composition: ArTfm/Ar+,EdaTa-25H/Eda+ Genetic Background: involves: 101/H * C3H/HeH
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MP:0008722 | abnormal chemokine secretion | "anomaly in the production or cellular release of any of the class of pro-inflammatory cytokines that attract and activate leukocytes" [MESH:D12.644.276.374.200] |
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6
Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6J
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MP:0008817 | hematoma | "an abnormal localized accumulation of clotted or partially clotted blood in an organ or a soft tissue space as a result of localized hemorrhage" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
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Allelic Composition: Celsr1Crsh/Celsr1+,Ptk7chz/Ptk7+ Genetic Background: involves: 101/H * BALB/c * BALB/cAnN * C3H/HeH
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MP:0008874 | decreased sensitivity to xenobiotics | "increase in the dose or concentration of a foreign compound required to induce a specific level of response" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6J
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MP:0008876 | decreased uterine NK cell number | "reduced number of the uterine subset of the non-T, non-B lymphocytes, having a granular morphology and which are important in innate immunity to viruses and other intracellular pathogens; in addition, these cells can kill certain tumor cells" [ISBN:0-8153-1691-7 "Immunobiology, The Immune System in Health and Disease"] |
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Allelic Composition: Il4tm1.1Wep/Il4tm1.1Wep Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Tyrobptm1.1Viv/Tyrobptm1.1Viv Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0009549 | impaired platelet aggregation | "decrease in the ability of one platelet to one or more other platelets via adhesion molecules" [GO:0070527] |
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Allelic Composition: Spta1sph-2Bc/Spta1sph-2Bc Genetic Background: involves: SELH
Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav Genetic Background: involves: 129P2/OlaHsd
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MP:0009764 | decreased sensitivity to induced morbidity/mortality | "increase in the amount of an external agent required to cause death or diseased state" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6
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MP:0009767 | decreased sensitivity to xenobiotic induced morbidity/mortality | "increase in the amount of a foreign compound required to cause death or diseased state" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6J
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MP:0010138 | arteritis | "inflammation of the walls of arteries, usually as a result of infection or auto-immune response" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Faslpr/Faslpr,Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: MRL.Cg-Fcer1gtm1Tks Faslpr
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MP:0010766 | abnormal NK cell physiology | "any functional anomaly of a lymphocyte that can spontaneously kill a variety of target cells without prior antigenic activation via germline encoded activation receptors, and also regulate immune responses via cytokine release and direct contact with other cells" [GOC:add, ISBN:0781735149, MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", PMID:15771571] |
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Allelic Composition: Spta1sph-2Bc/Spta1sph-2Bc Genetic Background: involves: SELH
Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: involves: C57BL/6
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MP:0011110 | partial preweaning lethality | "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms between fertilization and weaning age (Mus: approximately 3-4 weeks of age)" [MGI:csmith] |
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Allelic Composition: Clrn1tm1.1(KOMP)Vlcg/Clrn1tm1.1(KOMP)Vlcg Genetic Background: C57BL/6N-Clrn1tm1.1(KOMP)Vlcg/Ucd
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MP:0011427 | mesangial cell hyperplasia | "increased number of the phagocytic cells in the capillary tuft of the renal glomerulus, interposed between endothelial cells and the basement membrane in the central or stalk region of the tuft" [MGI:anna] |
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Allelic Composition: Faslpr/Faslpr,Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: MRL.Cg-Fcer1gtm1Tks Faslpr
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MP:0011440 | increased kidney cell proliferation | "increase in the expansion rate of any kidney cell population by cell division" [MGI:anna] |
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Allelic Composition: Faslpr/Faslpr,Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: MRL.Cg-Fcer1gtm1Tks Faslpr
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MP:0011453 | abnormal glomerular capillary endothelium morphology | "any structural anomaly of the thin, extremely flattened layer of cells that line the interior surface of glomerular capillaries and is densely perforated by large transcellular pores (aka fenestrae or fenestrations) that, unlike those of other fenestrated capillaries, are generally thought to lack diaphragms" [MGI:anna] |
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Allelic Composition: Faslpr/Faslpr,Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: MRL.Cg-Fcer1gtm1Tks Faslpr
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MP:0011506 | glomerular crescent | "formation of a crescent-shaped (semi-lunar) glomerular lesion corresponding to extracapillary proliferation of Bowman s capsular epithelium and acquiring a fibroblast-like spindled morphology, possibly stimulated by release of fibrinogen from a ruptured glomerular basement membrane; epithelial crescents occur in aggressive forms of glomerulonephritis, may be accompanied by collagen and fibrin deposition and/or monocyte and macrophage proliferation, may protrude into Bowman s space, and ultimately compress and destroy the glomerular tuft" [MGI:anna] |
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Allelic Composition: Faslpr/Faslpr,Fcer1gtm1Tks/Fcer1gtm1Tks Genetic Background: MRL.Cg-Fcer1gtm1Tks Faslpr
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MP:0012529 | abnormal decidua basalis morphology | "any structural anomaly of the area of uterine endometrium found between the implanted chorionic vesicle and the myometrium; with continued growth of the embryo, the decidua basalis becomes incorporated into the maternal component of the definitive placenta" [MGI:anna] |
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Allelic Composition: Il4tm1.1Wep/Il4tm1.1Wep Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Tyrobptm1.1Viv/Tyrobptm1.1Viv Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0012726 | abnormal uterine spiral artery morphology | "any structural anomaly of the corkscrew-like arteries in premenstrual or progestational endometrium; uterine spiral arteries play a vital role in supplying nutrients to the placenta and fetus, and are thus remodeled into highly dilated inelastic vessels by the action of invading trophoblast (physiological change)" [MGI:anna] |
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Allelic Composition: Il4tm1.1Wep/Il4tm1.1Wep Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Tyrobptm1.1Viv/Tyrobptm1.1Viv Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0012727 | abnormal uterine spiral artery remodeling | "any anomaly of the physiological conversion of the uterine spiral arteries into highly dilated vessels by the action of invading trophoblast; in pregnancy, trophoblast invasion and uterine spiral artery remodeling are important for lowering maternal vascular resistance and increasing uteroplacental blood flow; this process involves loss of smooth muscle and elastic lamina from the vessel wall, and significant dilation at the mouth of the vessel; impaired spiral artery remodeling has been implicated in preeclampsia, fetal growth restriction, and preterm labor" [MGI:anna] |
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Allelic Composition: Il4tm1.1Wep/Il4tm1.1Wep Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Tyrobptm1.1Viv/Tyrobptm1.1Viv Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0030072 | round face | "facial appearance is more circular than usual as viewed from the front" [HP:0000311] |
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Allelic Composition: Fcer1gtm1Rav/Fcer1gtm1Rav,Tyrobptm1Lll/Tyrobptm1Lll Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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