MP:0000333 | decreased bone marrow cell number | "decreased number of cells that make up the core cavities of bones when compared to the norm" [tc:Teresa Chu , Mouse Genome Informatics Curator, J:60896] |
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Allelic Composition: Tnnt2tm2Mmto/Tnnt2+ Genetic Background: involves: 129S/SvEv * C57BL/6
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MP:0001601 | abnormal myelopoiesis | "atypical process of bone marrow cell formation and/or bone marrow-derived blood cells" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:tc] |
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Allelic Composition: Tnnt2tm2Mmto/Tnnt2+ Genetic Background: involves: 129S/SvEv * 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: Tnnt2tm2Mmto/Tnnt2+ Genetic Background: involves: 129S/SvEv * C57BL/6
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MP:0002123 | abnormal hematopoiesis | "abnormal development of the enucleated fetal and adult erythrocytes that develop in the aorta, genital ridge and mesonephros region and later in the fetal and adult liver" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Tnnt2tm2Mmto/Tnnt2+ Genetic Background: involves: 129S/SvEv * C57BL/6
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MP:0002144 | abnormal B lymphocyte development | "atypical production of or inability to produce mature B cells, and/or accumulation of B cell precursors" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Tnnt2tm2Mmto/Tnnt2+ Genetic Background: involves: 129S/SvEv * C57BL/6
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MP:0002447 | abnormal erythrocyte morphology | "structural anomaly of the cells in the blood that carry oxygen, red blood cells" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Tnnt2tm2Mmto/Tnnt2+ Genetic Background: involves: 129S/SvEv * C57BL/6
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MP:0003406 | failure of zygotic cell division | "inability of a fertilized oocyte to initiate or complete early cell divisions" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Cacna1ctm2Hfm/Cacna1ctm2Hfm Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0004957 | abnormal blastocyst morphology | "any structural anomaly of the preimplantation embryo of mammals consisting of a hollow sphere of cells with an outer cell layer (trophoblast) that forms the placenta, a fluid-filled cavity (blastocoele), and a cluster of cells on the interior (the inner cell mass) that forms the embryo" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Cacna1ctm2Hfm/Cacna1ctm2Hfm Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0004964 | absent inner cell mass | "absence of the cells of the blastocyst that develop into the body of the embryo" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Cacna1ctm2Hfm/Cacna1ctm2Hfm Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0008190 | decreased transitional stage B cell number | "reduced number of immature B cells of an intermediate stage between the pre-B cell stage and the mature naive stage; transitional B cells express surface immunoglobulin, and are subject to the process of B cell selection" [CL:0000818, ISBN:0781735149, MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Tnnt2tm2Mmto/Tnnt2+ Genetic Background: involves: 129S/SvEv * C57BL/6
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MP:0008208 | decreased pro-B cell number | "reduced number of the progenitor cells of the B cell lineage, with some lineage specific activity such as early stages of recombination of B cell receptor genes, but are not yet fully committed to the B cell lineage until the expression of PAX5 occurs" [CL:0000826, ISBN:0781735149, MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Tnnt2tm2Mmto/Tnnt2+ Genetic Background: involves: 129S/SvEv * C57BL/6
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MP:0011094 | complete embryonic lethality before implantation | "death of all organisms of a given genotype in a population between fertilization and implantation (Mus: E0 to less than E4.5)" [MGI:csmith] |
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Allelic Composition: Cacna1ctm2Hfm/Cacna1ctm2Hfm Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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