MP:0000160 | kyphosis | "forward curvature of the spine, characterized by extensive flexion. " [J:62023, J:66943, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, cml:Cathleen M. Lutz , Mouse Genome Informatics Curator] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
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MP:0000208 | decreased hematocrit | "less than the average percentage of a volume of a blood sample occupied by red blood cells" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Ireb2tm1Mwh/Ireb2tm1Mwh Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Allelic Composition: Ireb2tm1.2Mwh/Ireb2tm1.2Mwh Genetic Background: involves: 129P2/OlaHsd * BALB/c * C57BL/6 * SJL
Allelic Composition: Fbxl5tm1Kei/Fbxl5tm1Kei,Ireb2tm1Roua/Ireb2tm1Roua Genetic Background: B6.Cg-Fbxl5tm1Kei Ireb2tm1Roua
Allelic Composition: Ireb2tm1Roua/Ireb2tm1Roua Genetic Background: B6.Cg-Ireb2tm1Roua
Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0000745 | tremors | "repetitive, cyclical movements of the body or a body part; usually involuntary, but can also manifest in response to an attempt at movement" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
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MP:0000780 | abnormal corpus callosum morphology | "malformation or absence of a thick bundle of nerve fibers comprising a commissural plate connecting the two cerebral hemispheres; it consists of contralateral axon projections that provides communications between the right and left cerebral hemispheres" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Col8a2tm1.1Asj/Col8a2tm1.1Asj Genetic Background: involves: 129S6/SvEvTac
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MP:0000788 | abnormal cerebral cortex morphology | "malformed gray cellular mantle covering the surface of the brain" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:38857] |
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Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0000832 | abnormal thalamus morphology | "malformation or absence of the large ovoid mass of paired bodies containing mostly gray matter and forming part of the lateral wall of the third ventricle of the brain" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0000849 | abnormal cerebellum morphology | "any malformation or absence of the part of the metencephalon that lies in the posterior cranial fossa dorsal to the pons and medulla that is concerned with the coordination of movement and learning of motor skills" [J:50311, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
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MP:0000876 | Purkinje cell degeneration | "a retrogressive impairment of function or destruction of the large neurons located at the interface of the molecular and internal granule layers of the cerebellar cortex" [J:46854] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
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MP:0000877 | abnormal Purkinje cell | "any structural anomaly of the neurons located at the interface of the molecular and internal granule layers of the cerebellar cortex; these inhibitory neurons provide the output of the cerebellar cortex through axons that project into the white matter, and extensive dendritic trees from the Purkinje cells extend upward in a single plane into the molecular layer where they synapse with parallel fibers of granule cells" [J:46140, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3] |
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Allelic Composition: Col8a2tm1.1Asj/Col8a2tm1.1Asj Genetic Background: involves: 129S6/SvEvTac
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MP:0000880 | decreased Purkinje cell number | "fewer than normal neuronal cells that are located in the interface of the molecular and granular layers of the cerebellar cortex" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:45302] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
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MP:0000899 | abnormal colliculi | "malformed inferior and superior colliculus" [J:50311] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
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MP:0000904 | abnormal superior colliculus | "dysmorphology or disorganization of the paired superior eminence of the mesencephalic tectum that is involved in auditory processing" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0000953 | abnormal oligodendrocyte morphology | "anomalous structure, number or composition of the neuroglia of the central nervous system that form the insulating myelin sheath of axons in the CNS" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Col8a2tm1.1Asj/Col8a2tm1.1Asj Genetic Background: involves: 129S6/SvEvTac
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MP:0001392 | abnormal locomotor activity | "altered ability or inability to move from place to place" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
Allelic Composition: Ireb2tm1Mwh/Ireb2tm1Mwh Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Allelic Composition: Ireb2tm1.2Mwh/Ireb2tm1.2Mwh Genetic Background: involves: 129P2/OlaHsd * BALB/c * C57BL/6 * SJL
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MP:0001393 | ataxia | "inability to coordinate voluntary muscular movements" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:67231] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
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MP:0001402 | hypoactivity | "reduced movement from one place to another" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, J:64289] |
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Allelic Composition: Col8a2tm1.1Asj/Col8a2tm1.1Asj Genetic Background: involves: 129S6/SvEvTac
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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: Col8a2tm1.1Asj/Col8a2tm1.1Asj Genetic Background: involves: 129S6/SvEvTac
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MP:0001406 | abnormal gait | "unusual or distinctive way of walking" [J:65038] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
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MP:0001504 | abnormal posture | "atypical position of the limbs or carriage of the body" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:18984] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
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MP:0001525 | impaired balance | "reduced ability of an animal to maintain equilibrium" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:64962, J:17123] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
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MP:0001577 | anemia | "less than normal levels of red blood cells, hemoglobin or volume of packed red blood cells " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:53370] |
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Allelic Composition: Fbxl5Gt(OST386421)Lex/Fbxl5+ Genetic Background: involves: 129S5/SvEvBrd * C57BL/6
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MP:0001770 | abnormal iron level | "anomalous concentrations of this metallic element that normally occurs in the heme of hemoglobin, myoglobin, transferrin, ferritin, and iron-containing porphyrins; it is an essential component of enzymes such as catalase, peroxidase, and various cytochromes" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Col8a2tm1.1Asj/Col8a2tm1.1Asj Genetic Background: involves: 129S6/SvEvTac
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MP:0001973 | increased thermal nociceptive threshold | "a greater than average point at which thermal pain sensation is first detectable" [What s Wrong With My Mouse?:ISBN 0-471-31639-3, J:17194] |
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Allelic Composition: Col8a2tm1.1Asj/Col8a2tm1.1Asj Genetic Background: involves: 129S6/SvEvTac
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MP:0002169 | no phenotype detected | "normal, viable and fertile appearance and behavior; indistinguishable from controls" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Ireb2tm1Mwh/Ireb2tm1Mwh Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
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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: Ireb2tm1Mwh/Ireb2tm1Mwh Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Allelic Composition: Ireb2tm1.2Mwh/Ireb2tm1.2Mwh Genetic Background: involves: 129P2/OlaHsd * BALB/c * C57BL/6 * SJL
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MP:0002591 | decreased mean corpuscular volume | "less than the average amount of space occupied by each red blood cell, calculated from the hematocrit and red cell count, in erythrocyte indices" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Ireb2tm1Mwh/Ireb2tm1Mwh Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Allelic Composition: Fbxl5tm1Kei/Fbxl5tm1Kei,Ireb2tm1Roua/Ireb2tm1Roua Genetic Background: B6.Cg-Fbxl5tm1Kei Ireb2tm1Roua
Allelic Composition: Ireb2tm1Roua/Ireb2tm1Roua Genetic Background: B6.Cg-Ireb2tm1Roua
Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0002757 | reduced vertical activity | "lesser than average time spent jumping or rearing" [J:82829, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator] |
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Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0002810 | microcytic anemia | "anemia in which the circulating erythrocyte corpuscular volume is smaller than normal" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0002813 | microcytosis | "the presence of unusually small erythrocytes in the circulating blood" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Ireb2tm1Mwh/Ireb2tm1Mwh Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Allelic Composition: Ireb2tm1.2Mwh/Ireb2tm1.2Mwh Genetic Background: involves: 129P2/OlaHsd * BALB/c * C57BL/6 * SJL
Allelic Composition: Fbxl5tm1Kei/Fbxl5tm1Kei,Ireb2tm1Roua/Ireb2tm1Roua Genetic Background: B6.Cg-Fbxl5tm1Kei Ireb2tm1Roua
Allelic Composition: Ireb2tm1Roua/Ireb2tm1Roua Genetic Background: B6.Cg-Ireb2tm1Roua
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MP:0002874 | decreased hemoglobin content | "decrease in the total hemoglobin content in the circulating blood" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Ireb2tm1Mwh/Ireb2tm1Mwh Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Allelic Composition: Ireb2tm1.2Mwh/Ireb2tm1.2Mwh Genetic Background: involves: 129P2/OlaHsd * BALB/c * C57BL/6 * SJL
Allelic Composition: Fbxl5tm1Kei/Fbxl5tm1Kei,Ireb2tm1Roua/Ireb2tm1Roua Genetic Background: B6.Cg-Fbxl5tm1Kei Ireb2tm1Roua
Allelic Composition: Ireb2tm1Roua/Ireb2tm1Roua Genetic Background: B6.Cg-Ireb2tm1Roua
Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0002875 | decreased erythrocyte count | "reduced number of the cells in the blood that carry oxygen, red blood cells, per unit" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Ireb2tm1.2Mwh/Ireb2tm1.2Mwh Genetic Background: involves: 129P2/OlaHsd * BALB/c * C57BL/6 * SJL
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MP:0003179 | decreased platelet count | "fewer than the normal numbers of the non-nucleated cells found in the blood and involved in blood coagulation " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, hdene:Howard Dene , Mouse Genome Informatics Curator, J:93052] |
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Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0003271 | abnormal duodenum morphology | "malformation in the first division of the small intestine that extends from the pyloris to the junction with the jejunum " [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Ireb2tm1.2Mwh/Ireb2tm1.2Mwh Genetic Background: involves: 129P2/OlaHsd * BALB/c * C57BL/6 * SJL
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MP:0004102 | abnormal dorsal striatum morphology | "any structural abnormality of the regions of the caudate nucleus and the putamen that lie dorsal to the anterior commissure" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0004147 | increased porphyrin level | "elevated concentration of porphyrins or protoporphyrins" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0004742 | abnormal vestibular system physiology | "any functional anomaly of the sensory system responsible for the sense of head position and movement of the body through space; such anomalies may include impaired balance, dizziness, poor regulation of postural muscle tone and inability to detect quick movements of the head " [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
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MP:0005156 | bradykinesia | "decreased spontaneity and movement" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:83301] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
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MP:0005404 | abnormal axon morphology | "anomaly in the structure of the single process of a nerve cell that normally conducts impulses away from the cell body" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0005562 | decreased mean corpuscular hemoglobin | "less than the average levels of hemoglobin contained in an erythrocyte" [RGD:Rat Genome Database submission, Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Fbxl5tm1Kei/Fbxl5tm1Kei,Ireb2tm1Roua/Ireb2tm1Roua Genetic Background: B6.Cg-Fbxl5tm1Kei Ireb2tm1Roua
Allelic Composition: Ireb2tm1Roua/Ireb2tm1Roua Genetic Background: B6.Cg-Ireb2tm1Roua
Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0005637 | abnormal iron homeostasis | "anomaly in the state of equilibrium in the body with respect to this metallic element that normally occurs in the heme of hemoglobin, myoglobin, transferrin, ferritin, and iron-containing porphyrins; it is an essential component of enzymes such as catalase, peroxidase, and various cytochromes" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:64456] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
Allelic Composition: Ireb2tm1Mwh/Ireb2tm1Mwh Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Allelic Composition: Ireb2tm1.2Mwh/Ireb2tm1.2Mwh Genetic Background: involves: 129P2/OlaHsd * BALB/c * C57BL/6 * SJL
Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0005642 | decreased mean corpuscular hemoglobin concentration | "less than the normal Hgb/Hct; the average hemoglobin concentration in a given volume of packed red cells, calculated from the hemoglobin therein and the hematocrit, in erythrocyte indices" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:8936] |
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Allelic Composition: Fbxl5tm1Kei/Fbxl5tm1Kei,Ireb2tm1Roua/Ireb2tm1Roua Genetic Background: B6.Cg-Fbxl5tm1Kei Ireb2tm1Roua
Allelic Composition: Ireb2tm1Roua/Ireb2tm1Roua Genetic Background: B6.Cg-Ireb2tm1Roua
Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0005654 | porphyria | "aquired or inherited group of disorders characterized by excessive production of porphyrins or their precursors; if aquired, it results from inhibition of enzymes in the heme metabolic pathway by drugs, toxins or abnormal metabolites" [MeSH:National Library of Medicine - Medical Subject Headings, 2003, anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator] |
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Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0008743 | decreased liver iron level | "reduction in the amount of iron present in the liver tissue" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fbxl5tm1Kei/Fbxl5tm1Kei,Ireb2tm1Roua/Ireb2tm1Roua Genetic Background: B6.Cg-Fbxl5tm1Kei Ireb2tm1Roua
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MP:0008807 | increased liver iron level | "increase in the amount of iron present in the liver tissue" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
Allelic Composition: Ireb2tm1Mwh/Ireb2tm1Mwh Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Allelic Composition: Ireb2tm1.2Mwh/Ireb2tm1.2Mwh Genetic Background: involves: 129P2/OlaHsd * BALB/c * C57BL/6 * SJL
Allelic Composition: Ireb2tm1Roua/Ireb2tm1Roua Genetic Background: B6.Cg-Ireb2tm1Roua
Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0008808 | decreased spleen iron level | "reduction in the amount of iron present in the spleen tissue" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Ireb2tm1Mwh/Ireb2tm1Mwh Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Allelic Composition: Ireb2tm1.2Mwh/Ireb2tm1.2Mwh Genetic Background: involves: 129P2/OlaHsd * BALB/c * C57BL/6 * SJL
Allelic Composition: Ireb2tm1Roua/Ireb2tm1Roua Genetic Background: B6.Cg-Ireb2tm1Roua
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MP:0008810 | increased circulating iron level | "elevation in the concentration of iron in the blood" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fbxl5tm1Kei/Fbxl5tm1Kei,Ireb2tm1Roua/Ireb2tm1Roua Genetic Background: B6.Cg-Fbxl5tm1Kei Ireb2tm1Roua
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MP:0008935 | decreased mean platelet volume | "reduced average content of platelet cells over normal" [MGI:mberry "Melissa Berry, Genetics Resources Curator"] |
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Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0009940 | abnormal hippocampus pyramidal cell morphology | "any structural anomaly of the projection neuron in the pyramidal layer of the hippocampus" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0009978 | abnormal cerebellum white matter morphology | |
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Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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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"] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
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MP:0010067 | increased red blood cell distribution width | "higher than normal coefficient of variance (reference range) of the red blood cell volume for an organism" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", NCI:C64800 "NCI Thesaurus (Code C64800)"] |
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Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0010375 | increased kidney iron level | "increase in the amount of iron present in the renal tissue" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
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Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0011890 | increased circulating ferritin level | "elevated concentration in the blood of ferritin, a ubiquitous intracellular protein that stores iron and releases it in a controlled fashion; some ferritin is also found in the blood and is measured in tests for overall iron levels, anemia and chronic diseases" [MGI:csmith] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0011897 | decreased circulating unsaturated transferrin level | "reduction in the concentration of transferrin that is not saturated (bound) with iron; this represents the reserve capacity of transferrin and is often measured by the Unsaturated Iron Binding Capacity (UIBC) test" [MGI:csmith] |
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Allelic Composition: Fbxl5tm1Kei/Fbxl5tm1Kei,Ireb2tm1Roua/Ireb2tm1Roua Genetic Background: B6.Cg-Fbxl5tm1Kei Ireb2tm1Roua
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MP:0020338 | abnormal hippocampal pyramidal neuron dendrite morphology | "structural anomaly of the highly branched tree-like process of the hippocampal neurons that have a pyramid-shaped soma with the apex and an apical dendrite pointed toward the pial surface and other dendrites and an axon emerging from the base" [CL_1001571, ORCID: orcid.org/0000-0003-4606-0597] |
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Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0020365 | increased brain iron level | "increase in the amount of iron present in the brain tissue" [MGI:Anna] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0020366 | decreased brain iron level | "reduction in the amount of iron present in the brain tissue" [MGI:Anna] |
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Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0020368 | decreased heart iron level | "reduction in the amount of iron present in the heart tissue" [MGI:Anna] |
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Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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MP:0020369 | increased intestinal iron level | "increase in the amount of iron present in the large or small intestinal tissue" [MGI:Anna] |
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Allelic Composition: Ihhtm1Amc/Ihhtm2Amc,Pth1rtm1Hmk/Pth1rtm2Hmk,Tg(Bglap2-cre)1Kry/0 Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB
Allelic Composition: Ireb2tm1Mwh/Ireb2tm1Mwh Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Allelic Composition: Ireb2tm1.2Mwh/Ireb2tm1.2Mwh Genetic Background: involves: 129P2/OlaHsd * BALB/c * C57BL/6 * SJL
Allelic Composition: Ireb2tm1.1Eal/Ireb2tm1.1Eal Genetic Background: B6J.129-Ireb2tm1.1Eal
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