MP:0000136 | abnormal microglial cell morphology | "anomalous structure, number, or composition of the small neuroglial cells, possibly of mesodermal origin, which may become phagocytic, in areas of neural damage or inflammation" [ava:Anna V. Anagnostopoulos , Mouse Genome Informatics Curator, J:71688] |
Show
Allelic Composition: Cx3cl1tm1Lira/Cx3cl1tm1Lira Genetic Background: involves: C57BL/6
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J
|
MP:0000223 | decreased monocyte count | "fewer than normal monocyte numbers" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
Show
Allelic Composition: Rasgrf1enu1H/Rasgrf1+ Genetic Background: involves: BALB/c * C3H/HeN * C57BL/6JOlaHsd
|
MP:0000753 | paralysis | "loss of power of voluntary movement in a muscle through injury or disease of its nerve supply" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129P2-Cx3cr1tm1Litt
Allelic Composition: Cd1d1tm1Luc/Cd1d1tm1Luc,Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129-Cd1d1tm1Luc Cx3cr1tm1Litt
|
MP:0000754 | partial paralysis | "partial loss of power of voluntary movement in a muscle through injury or disease of it or its nerve supply" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129P2-Cx3cr1tm1Litt
|
MP:0000921 | demyelination | "loss of the myelin sheath without loss of axons or fiber tracts" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129P2-Cx3cr1tm1Litt
|
MP:0001325 | abnormal retina morphology | "structural or developmental anomaly of the thin layer of neural tissue lining the back of the eyeball which contains visual receptors " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
Show
Allelic Composition: Rasgrf1enu1H/Rasgrf1+ Genetic Background: involves: BALB/c * C3H/HeN * C57BL/6JOlaHsd
Allelic Composition: Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: C.129-Cx3cr1tm1Zm
Allelic Composition: Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: involves: 129 * C57BL/6
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: involves: 129 * 129S4/SvJae
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J
|
MP:0001326 | retinal degeneration | "pathological change in the thin layer of neural tissue lining the back of the eyeball, which contains visual receptors and can result in the impairment or cessation of retinal neural function" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, NMF:Stephanie Pretel, Neuroscience Mutagenesis Facility Curator] |
Show
Allelic Composition: Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: C.129-Cx3cr1tm1Zm
Allelic Composition: Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: involves: 129 * C57BL/6
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J
|
MP:0001847 | brain inflammation | "local accumulation of fluid, plasma proteins, and leukocytes in the brain" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129P2-Cx3cr1tm1Litt
|
MP:0001935 | reduced litter size | "fewer live born pups in a litter compared to average" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: involves: 129 * 129S4/SvJae
|
MP:0002083 | premature death | "death after 3 weeks of age, but before normal life span" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1+ Genetic Background: B6.129P2-Cx3cr1tm1Litt
|
MP:0002376 | abnormal dendritic cell physiology | "failure or atypical function of the immunocompetent cells of the lymphoid and hemopoietic systems and skin, which function to process antigens and present them to T cells, thus stimulating cellular immunity" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, J:85808] |
Show
Allelic Composition: Pomctm1Low/Pomctm1Low,Tg(Pomc)#Low/Tg(Pomc)#Low Genetic Background: involves: 129 * C57BL/6 * CBA * DBA/2 * Swiss Webster
|
MP:0002411 | decreased susceptibility to bacterial infection | "reduced likelihood that an organism will develop ill effects from a bacterial infection or from components of or toxins produced by bacteria " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
Show
Allelic Composition: Runx2tm1.1Yyon/Runx2tm1.1Yyon,Tg(Col2a1-cre)1Star/0 Genetic Background: involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj
|
MP:0002442 | abnormal leukocyte physiology | "abnormal function of any of the white blood cells (basophils, eosinophils, neutrophils, lymphocytes, or monocytes) " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
Show
Allelic Composition: Rasgrf1enu1H/Rasgrf1+ Genetic Background: involves: BALB/c * C3H/HeN * C57BL/6JOlaHsd
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129P2-Cx3cr1tm1Litt
Allelic Composition: Ccr2tm2.1Ifc/Ccr2tm2.1Ifc,Cx3cr1tm1Litt/Cx3cr1+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * FVB/N
Allelic Composition: Ccr2tm2.1Ifc/Ccr2tm2.1Ifc,Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * FVB/N
|
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] |
Show
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J
|
MP:0003203 | increased neuron apoptosis | "increase in the number of neurons undergoing programmed cell death" [RGD:Rat Genome Database submission] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129P2-Cx3cr1tm1Litt
|
MP:0003224 | neuron degeneration | "a retrogressive impairment of function or destruction of the functional cells of the nervous system that receive, conduct, and transmit impulses " [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1+,Psen1tm1Mpm/Psen1tm1Mpm,Tg(APPSwe,tauP301L)1Lfa/0,Tg(Thy1-YFP)HJrs/0 Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
|
MP:0003691 | abnormal microglial cell function | "anomalous activity of the small neuroglial cells, possibly of mesodermal origin, which may become phagocytic, in areas of neural damage or inflammation" [hdene:Howard Dene , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129P2-Cx3cr1tm1Litt
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1+,Psen1tm1Mpm/Psen1tm1Mpm,Tg(APPSwe,tauP301L)1Lfa/0,Tg(Thy1-YFP)HJrs/0 Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
|
MP:0003728 | abnormal photoreceptor layer | "malformation/anomalous structure of the photoreceptor layer" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator] |
Show
Allelic Composition: Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: C.129-Cx3cr1tm1Zm
Allelic Composition: Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: involves: 129 * C57BL/6
|
MP:0003730 | abnormal photoreceptor inner segments | "malformation/anomalous structure of the photoreceptor layer which contains the machinery of the cell (mitochondria, golgi, endoplasmic reticulum, etc)" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator] |
Show
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J
|
MP:0003799 | impaired macrophage migration | "defect in the ability of macrophages to move up a chemotactic gradient" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
Show
Allelic Composition: Trp53tm1Tyj/Trp53tm1Tyj,Tsg101tm1Mak/Tsg101tm1Mak Genetic Background: involves: 129P3/J * 129S2/SvPas * C57BL/6 * CD-1
Allelic Composition: Apoetm1Bres/Apoetm1Bres,Cx3cr1tm1Ifc/Cx3cr1tm1Ifc Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: involves: 129P2/OlaHsd * C57BL/6
|
MP:0004042 | decreased susceptibility to kidney reperfusion injury | "a diminished likelihood or extent of damage to the kidney when the blood supply is restored after a period of ischemia" [brs:Beverly Richards-Smith, Mouse Genome Informatics Curator] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: involves: 129P2/OlaHsd * C57BL/6
|
MP:0004799 | increased susceptibility to experimental autoimmune encephalomyelitis | "greater 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"] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129P2-Cx3cr1tm1Litt
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1+ Genetic Background: B6.129P2-Cx3cr1tm1Litt
Allelic Composition: Cd1d1tm1Luc/Cd1d1tm1Luc,Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129-Cd1d1tm1Luc Cx3cr1tm1Litt
|
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"] |
Show
Allelic Composition: Ccr2tm2.1Ifc/Ccr2tm2.1Ifc,Cx3cr1tm1Litt/Cx3cr1+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * FVB/N
Allelic Composition: Ccr2tm2.1Ifc/Ccr2tm2.1Ifc,Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * FVB/N
|
MP:0004883 | abnormal blood vessel healing | "anomaly in the repair process of blood vessels after injury" [MGI:monikat "Monika Tomczuk, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129P2-Cx3cr1tm1Litt
|
MP:0005025 | response to infection | "the body s reaction to invasion and multiplication of microorganisms in its tissues, or the body s reaction to components of or toxins produced by pathogenic mircroorganisms " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
Show
Allelic Composition: Pomctm1Low/Pomctm1Low,Tg(Pomc)#Low/Tg(Pomc)#Low Genetic Background: involves: 129 * C57BL/6 * CBA * DBA/2 * Swiss Webster
|
MP:0005103 | abnormal retinal pigmentation | "anomalous coloring of the thin layer of neural tissue lining the back of the eyeball which contains visual receptors " [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: involves: 129 * 129S4/SvJae
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J
|
MP:0005201 | abnormal retinal pigment epithelium morphology | "anomaly in the epithelial layer of the retina composed of cells containing pigment granules " [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
Show
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: involves: 129 * 129S4/SvJae
|
MP:0005239 | abnormal Bruch membrane morphology | "anomalous structure of the transparent, nearly structureless inner layer of the choroid in contact with the pigmented layer of the retina" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: involves: 129 * 129S4/SvJae
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J
|
MP:0005240 | abnormal amacrine cell morphology | "anomalous structure of the interneurons of the retina" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
Show
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J
|
MP:0005341 | decreased susceptibility to atherosclerosis | "less likely than the norm to develop thickening and loss of elasticity of arterial walls, involving lipid deposition and thickening of intimal layers within arteries" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
Show
Allelic Composition: Apoetm1Bres/Apoetm1Bres,Cx3cr1tm1Ifc/Cx3cr1tm1Ifc Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6
Allelic Composition: Apoetm1Unc/Apoetm1Unc,Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: B6.129-Apoetm1Unc Cx3cr1tm1Zm
Allelic Composition: Apoetm1Unc/Apoetm1Unc,Cx3cr1tm1Zm/Cx3cr1+ Genetic Background: B6.129-Apoetm1Unc Cx3cr1tm1Zm
|
MP:0005546 | choroidal neovascularization | "new, abnormal, vessel development of the thin, highly vascularized membrane covering most of the posterior of the eye between the retina and the sclera" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: Rasgrf1enu1H/Rasgrf1+ Genetic Background: involves: BALB/c * C3H/HeN * C57BL/6JOlaHsd
Allelic Composition: Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: involves: 129 * C57BL/6
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: involves: 129 * 129S4/SvJae
|
MP:0005547 | abnormal Muller cell morphology | "anomalous structure of the elongated neuroglial cells that traverse all the layers of the retina and that act as supporting elements" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J
|
MP:0005548 | retinal pigment epithelium atrophy | "wasting or decreased size of the epithelial layer of the retina composed of cells containing pigment granules " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
Show
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: involves: 129 * 129S4/SvJae
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J
|
MP:0005549 | retinal pigment epithelium hyperplasia | "increased numbers of cells in the epithelial layer of the retina composed of cells containing pigment granules " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
Show
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: involves: 129 * 129S4/SvJae
|
MP:0005595 | abnormal vascular smooth muscle physiology | "anomalous function of the nonstriated, involuntary muscle tissue of the blood vessels" [RGD:Rat Genome Database submission, MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129P2-Cx3cr1tm1Litt
|
MP:0005671 | response to transplant | "the body s reaction to the grafting of organs, tissues, or cells taken from the same individual for another area of the body or from another individual" [MeSH:National Library of Medicine - Medical Subject Headings, 2003, cwg:Carroll-Ann W. Goldsmith, Mouse Genome Informatics curator, J:52834] |
Show
Allelic Composition: Trp53tm1Tyj/Trp53tm1Tyj,Tsg101tm1Mak/Tsg101tm1Mak Genetic Background: involves: 129P3/J * 129S2/SvPas * C57BL/6 * CD-1
|
MP:0006051 | brainstem hemorrhage | "bleeding into the brain stem" [smb:Susan M Bello, Mouse Genome Informatics Curator, RGD:Rat Genome Database submission] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129P2-Cx3cr1tm1Litt
|
MP:0006187 | retinal deposits | "abnormal accumulation of material on the retina" [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator] |
Show
Allelic Composition: Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: involves: 129 * C57BL/6
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: involves: 129 * 129S4/SvJae
|
MP:0008045 | decreased NK cell number | "reduction in the number of 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"] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129P2-Cx3cr1tm1Litt
Allelic Composition: Cd1d1tm1Luc/Cd1d1tm1Luc,Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129-Cd1d1tm1Luc Cx3cr1tm1Litt
|
MP:0008108 | abnormal small intestinal villus morphology | "any structural anomaly of the tiny hair-like projections that protrude from the inside of the small intestine that contain blood vessels that capture digested nutrients that are absorbed through the intestinal wall; the villi increase the absorptive surface area of the small intestine by approximately 30-fold" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", MGI:rbabiuk "Randall Babiuk, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Pomctm1Low/Pomctm1Low,Tg(Pomc)#Low/Tg(Pomc)#Low Genetic Background: involves: 129 * C57BL/6 * CBA * DBA/2 * Swiss Webster
|
MP:0008126 | increased dendritic cell number | "greater 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"] |
Show
Allelic Composition: Pomctm1Low/Pomctm1Low,Tg(Pomc)#Low/Tg(Pomc)#Low Genetic Background: involves: 129 * C57BL/6 * CBA * DBA/2 * Swiss Webster
|
MP:0008450 | retinal photoreceptor degeneration | "a retrogressive impairment of function or destruction of a cell specialized to detect and transduce light, including rods and cones of the retina" [MESH:A08.663.650.650, MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: involves: 129 * 129S4/SvJae
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J
|
MP:0008515 | thin retinal outer nuclear layer | "reduced thickness of the retinal layer that contains the nuclei and cell bodies of rods and cones" [MGI:monikat "Monika Tomczuk, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: involves: 129 * C57BL/6
|
MP:0008586 | disorganized photoreceptor outer segment | "derangement of the pattern of the photoreceptor region that is rich in the visual pigment rhodopsin" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: involves: 129 * 129S4/SvJae
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J
|
MP:0008918 | microgliosis | "a proliferation or spread of microglia in the area of a degenerative lesion or damaged tissue" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129P2-Cx3cr1tm1Litt
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1+ Genetic Background: B6.129P2-Cx3cr1tm1Litt
|
MP:0008948 | decreased neuron number | "fewer than normal numbers of the cells of the nervous system that receive, conduct, and transmit impulses" [MESH:A08.663] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1+ Genetic Background: B6.129P2-Cx3cr1tm1Litt
|
MP:0009333 | abnormal splenocyte physiology | "any functional anomaly of a cell of the spleen" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Dcxtm1Caw/Dcx+ Genetic Background: involves: 129S6/SvEvTac * 129X1/SvJ * Black Swiss
|
MP:0009763 | increased sensitivity to induced morbidity/mortality | "decrease in the amount of an external agent required to cause death or diseased state" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129P2-Cx3cr1tm1Litt
|
MP:0009788 | increased susceptibility to bacterial infection induced morbidity/mortality | "increased likelihood that an organism will display the expected moribund state caused by a bacterial invasion or from components of or toxins produced by bacteria" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Pomctm1Low/Pomctm1Low,Tg(Pomc)#Low/Tg(Pomc)#Low Genetic Background: involves: 129 * C57BL/6 * CBA * DBA/2 * Swiss Webster
|
MP:0010016 | variable depigmentation | "absence or loss of normal pigment in the skin in various and irregular patterns" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Zm/Cx3cr1tm1Zm Genetic Background: involves: 129 * 129S4/SvJae
|
MP:0010053 | decreased grip strength | "reduced ability to grasp and hold objects, often measured as time spent hanging from an object or wire" [ISBN:0471316393 "Crawley, JN, What s Wrong with my Mouse: Behavioral Phenotyping of Transgenic and Knockout Mice"] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1+ Genetic Background: B6.129P2-Cx3cr1tm1Litt
|
MP:0010180 | increased susceptibility to weight loss | "greater decrease in body weight over time when compared to the average decrease in weight in response to dietary modification, fasting or caloric restriction" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1+ Genetic Background: B6.129P2-Cx3cr1tm1Litt
|
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] |
Show
Allelic Composition: Trp53tm1Tyj/Trp53tm1Tyj,Tsg101tm1Mak/Tsg101tm1Mak Genetic Background: involves: 129P3/J * 129S2/SvPas * C57BL/6 * CD-1
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129P2-Cx3cr1tm1Litt
|
MP:0011451 | increased susceptibility to dopaminergic neuron neurotoxicity | "greater than normal amount of dopaminergic neuronal cell death following exposure to a neurotoxic compound, such as MPTP-induced cell death occurring through interference in mitochondrial metabolism" [MGI:csmith] |
Show
Allelic Composition: Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: B6.129P2-Cx3cr1tm1Litt
|
MP:0020448 | increased microglial cell activation | "increase in the change in morphology and behavior of a microglial cell resulting from exposure to a cytokine, chemokine, cellular ligand, or soluble factor, during the maturation to the fully active phagocytic form" [GO:0001774] |
Show
Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Cx3cr1tm1Litt/Cx3cr1tm1Litt Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J
|