MP:0000061 | fragile skeleton | "easily damaged or broken bones" [J:14208] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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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: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0000066 | osteoporosis | "reduction in bone mass or atrophy of skeletal tissue; may lead to skeletal fragility" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:57315] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
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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: Snai2tm2Grid/Snai2tm2Grid Genetic Background: involves: 129S1/Sv
Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0000109 | abnormal parietal bone morphology | "malformed curved bone forming part of the vault of the cranium" [J:17489] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0000121 | failure of tooth eruption | "inability of the teeth to grow into the oral cavity" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61295] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0000124 | absent teeth | "missing bony structures of the upper and lower jaws used in mastication" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61295] |
Show
Allelic Composition: Csf1op/Csf1op,Csf2tm1Ard/Csf2tm1Ard Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0000125 | absent incisors | "missing long pointed teeth; most anterior and prominent in the jaw" [J:17489] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
Allelic Composition: Csf1op/Csf1op,Galctwi/Galctwi Genetic Background: involves: C3HeB/Fe * C57BL/6J * CE/J
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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: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0000135 | reduced cortical bone thickness | "thinner than normal superficial layer of compact bone " [J:61509] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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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] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
Allelic Composition: Csf1op/Csf1op Genetic Background: B6;C3Fe a/a-Csf1op/J
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MP:0000165 | abnormal hypertrophic chondrocyte zone | "anomaly of the cartilage cell matrix layer " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:58795] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0000198 | hypophosphatemia | "abnormally low concentrations of phosphates in the circulating blood" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
Show
Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0000219 | increased neutrophil count | "greater than normal neutrophil numbers" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Csf1op/Csf1op,Csf2tm1Ard/Csf2tm1Ard Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0000221 | decreased WBC count | "fewer than normal numbers of WBCs" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
Show
Allelic Composition: Csf1op/Csf1op,Csf2tm1Ard/Csf2tm1Ard Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0000223 | decreased monocyte count | "fewer than normal monocyte numbers" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0000240 | extramedullary hematopoiesis | "formation and development of blood cells outside the bone marrow, e.g., in the spleen, liver, or lymph nodes" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
Show
Allelic Composition: Csf1op/Csf1op,Csf2tm1Ard/Csf2tm1Ard Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0000322 | increased granulocyte number | "greater than expected number of leukocytes that have abundant granules in the cytoplasm: basophils, neutrophils, or eosinophils" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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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: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0000440 | domed skull | |
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Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
Allelic Composition: Csf1op/Csf1op,Galctwi/Galctwi Genetic Background: involves: C3HeB/Fe * C57BL/6J * CE/J
Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0000547 | short limbs | "reduced average length of the extremities" [MGI:CLS, J:61509] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
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MP:0000558 | abnormal tibia morphology | "atructural anomaly of the medial and larger of the two bones of the lower leg" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0000559 | abnormal femur morphology | "structural anomaly of the long bone of the thigh" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0000572 | abnormal autopod morphology | "malformation of the hand or foot" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
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MP:0000592 | short tail | "reduced length of tail compared to control " [J:55583] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
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MP:0000628 | abnormal mammary gland development | "aberration in the differentiation of the mammary gland during early embryogenesis or during sexual maturity" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0000662 | abnormal branching of the mammary ductal tree | "anomaly in the development of the channels that secrete milk and direct milk to the nipple" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0000692 | small spleen | "decreased spleen size" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0000711 | thymic cortex hypoplasia | "reduced cell number in the outer portion of the thymus" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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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: Csf1op/Csf1op,Galctwi/Galctwi Genetic Background: involves: C3HeB/Fe * C57BL/6J * CE/J
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MP:0000755 | hindlimb paralysis | "loss of power of voluntary movement in the muscles of the hindlimb through injury or disease of it or its nerve supply" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Csf1op/Csf1op,Galctwi/Galctwi Genetic Background: involves: C3HeB/Fe * C57BL/6J * CE/J
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MP:0000783 | abnormal forebrain morphology | "malformed or absent anterior primitive cerebral vesicle; most rostral of three primary vesicles of the embryonic neural tube" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:38857] |
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Allelic Composition: Csf1op/Csf1op,Galctwi/Galctwi Genetic Background: involves: C3HeB/Fe * C57BL/6J * CE/J
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MP:0000920 | abnormal myelination | "atypical or altered myelination in axon sheaths" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Mpztm1Msch/Mpz+ Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
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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] |
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Allelic Composition: Csf1op/Csf1op,Galctwi/Galctwi Genetic Background: involves: C3HeB/Fe * C57BL/6J * CE/J
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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: Csf1op/Csf1op,Galctwi/Galctwi Genetic Background: involves: C3HeB/Fe * C57BL/6J * CE/J
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MP:0000954 | reduced oligodendrocyte progenitor number | "fewer cells that differentiate into a type of glial cell in the central nervous system" [J:15108] |
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Allelic Composition: Csf1op/Csf1op,Galctwi/Galctwi Genetic Background: involves: C3HeB/Fe * C57BL/6J * CE/J
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MP:0001126 | abnormal ovary morphology | "malformed female reproductive gland containing the germ cells" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:35782] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0001130 | abnormal ovarian folliculogenesis | "atypical formation or failure to form the spherical ovum in the ovary" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:35782] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6;C3Fe a/a-Csf1op/J
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MP:0001262 | decreased body weight | "lower than normal average weight " [J:61295] |
Show
Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0001263 | weight loss | "progressive reduction of body weight below normal average for age" [J:45400] |
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Allelic Composition: Csf1op/Csf1op,Galctwi/Galctwi Genetic Background: involves: C3HeB/Fe * C57BL/6J * CE/J
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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: Csf1op/Csf1op,Galctwi/Galctwi Genetic Background: involves: C3HeB/Fe * C57BL/6J * CE/J
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MP:0001377 | abnormal copulation | "reduced or absent attempt of sexual contact between a male and a receptive female " [MeSH:National Library of Medicine - Medical Subject Headings, 2003] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0001380 | male reduced copulation without impotence | "males do not initiate sexual behavior as scored by the presence of copulation plugs (not due to infertility)" [J:57125] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0001431 | abnormal eating behavior | "inability to consume or atypical consumption pattern" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:19212] |
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Allelic Composition: Hoxd8tm1Jdes/Hoxd8+ Genetic Background: involves: 129S2/SvPas * FVB
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MP:0001562 | abnormal circulating calcium level | "anomalous concentration in the blood of this bivalent element" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0001729 | impaired implantation | "impaired ability of the blastocyst to attach to the endometrium of the uterus" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0001731 | abnormal postnatal growth | "anomaly in reaching a developmental stage or stages after birth" [il:Ira Lu, Mouse Genome Informatics Curator] |
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Allelic Composition: Ccl2tm1Rol/Ccl2tm1Rol,Ccr2tm1Mae/Ccr2tm1Mae Genetic Background: B6.129-Ccr2tm1Mae Ccl2tm1Rol
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MP:0001732 | postnatal growth retardation | "slow or limited development after birth " [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0001790 | abnormal immune system physiology | "deviation from the normal function of the immune system " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Csf1tm1.1(CSF1)Flv/Csf1tm1.1(CSF1)Flv,Il2rgtm1.1Flv/Il2rgtm1.1Flv,Rag2tm1.1Flv/Rag2tm1.1Flv Genetic Background: involves: 129P2/OlaHsd * 129S/SvEv * 129S4/SvJae * BALB/cAnNTac
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MP:0001860 | liver inflammation | "local accumulation of fluid, plasma proteins, and leukocytes in the liver" [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: Csf1op/Csf1op,Sh3bp2tm1Bjro/Sh3bp2tm1Bjro Genetic Background: involves: 129S4/SvJae * BALB/cJ * C57BL/6J
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MP:0001861 | lung inflammation | "local accumulation of fluid, plasma proteins, and leukocytes in the lung" [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: Csf1op/Csf1op,Csf2tm1Ard/Csf2tm1Ard Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0001862 | interstitial pneumonia | "disorder of the lower respiratory tract, primarily affecting the alveolar wall, but may also involve the small airways and blood vessels of the lung parencyma; this is usually inflammatory in nature" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Csf1op/Csf1op,Csf2tm1Ard/Csf2tm1Ard Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0001882 | abnormal lactation | "atypical production of milk from the mammary gland" [J:51296] |
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Allelic Composition: ApcMin/Apc+,Hptm1Skl/Hptm1Skl Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0001921 | reduced fertility | "diminished ability to produce live offspring" [J:65030] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
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MP:0001922 | reduced male fertility | "reduced ability of male to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61340] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0001923 | reduced female fertility | "reduced ability of female to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0001928 | abnormal ovulation | "aberration in the release of an ovum from a rupturing Graafin follicle, normally regulated by a surge in lutenizing hormone" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
Show
Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
Allelic Composition: Csf1op/Csf1op Genetic Background: B6;C3Fe a/a-Csf1op/J
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MP:0001935 | reduced litter size | "fewer live born pups in a litter compared to average" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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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: Snai2tm2Grid/Snai2tm2Grid Genetic Background: involves: 129S1/Sv
Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
Allelic Composition: Csf1op/Csf1op,Galctwi/Galctwi Genetic Background: involves: C3HeB/Fe * C57BL/6J * CE/J
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MP:0002270 | abnormal alveoli morphology | "any structural anomaly of the outpouching of the respiratory system where gas exchange occurs" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Snai2tm2Grid/Snai2tm2Grid Genetic Background: involves: 129S1/Sv
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MP:0002356 | abnormal spleen red pulp morphology | "anomalous structure of the area of the spleen that screens and eliminates defective or foreign cells" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Pathology:ISBN 0-397-51047-0] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0002397 | abnormal bone marrow morphology | "structural anomalies in the soft tissue that fills the cavities of bones" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Snai2tm2Grid/Snai2tm2Grid Genetic Background: involves: 129S1/Sv
Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0002398 | abnormal bone marrow cell morphology/development | "anomalous structure or formation of the cells found in the bone marrow" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0002673 | abnormal sperm count | "increased or decreased numbers of spermatozoa " [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0002680 | decreased number of corpora lutea | "fewer than normal numbers of yellow endocrine body formed in the ovary after follicle rupture in a given oestrus cycle" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0002682 | reduced number of mature ovarian follicles | "fewer than normal numbers of spehroidal cell aggregations in the ovary containing the ovum" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6;C3Fe a/a-Csf1op/J
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MP:0002687 | oligozoospermia | "reduced concentration of spermatozoa " [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:57312] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0002780 | decreased circulating testosterone level | "less than the normal blood concentration of this most potent androgen" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0002872 | polycythemia | "an excess of circulating red blood cells" [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: Csf1op/Csf1op,Csf2tm1Ard/Csf2tm1Ard Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0002998 | abnormal bone remodeling | "aberrant process of the turnover of bone matrix that involves a balance of resorbtion and formation by osteoclasts and osteoblasts, respectively" [ava:Anna V. Anagnostopoulos , Mouse Genome Informatics Curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0003329 | amyloid beta deposits | |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0003355 | reduced ovulation | "reduction in the frequency in which an ovum is released from a rupturing ovarian follicle" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0003357 | impaired granulosa cell differentiation | "atypical differentiation of the layer of small cells that forms the wall of an ovarian follicle" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator, J:43075] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6;C3Fe a/a-Csf1op/J
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MP:0003408 | increased width of hypertrophic chondrocyte zone | "increased width of cartilage cell matrix layer " [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0003572 | abnormal uterus development | "abnormal morphogenesis of the female muscular organ of gestation" [ncbi:Matthew Mailman, NCBI request] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0003795 | abnormal bone structure | |
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Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0003797 | abnormal compact bone morphology | "structural anomaly of the outer layers of solid, hard bone that covers spongy bone; consists of parallel osteons containing mineral deposits and interstitial lamellae" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, hdene:Howard Dene , Mouse Genome Informatics Curator] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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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] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6;C3Fe a/a-Csf1op/J
Allelic Composition: Csf1op/Csf1op,Galctwi/Galctwi Genetic Background: involves: C3HeB/Fe * C57BL/6J * CE/J
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MP:0003884 | decreased macrophage count | "fewer than the normal numbers of macrophages" [acv:Alicia Valenzuela, Genetic Resources Curator] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
Allelic Composition: Csf1op/Csf1op Genetic Background: B6;C3Fe a/a-Csf1op/J
Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0004235 | abnormal masseter muscle morphology | "any structural anomaly of the masticatory muscle of posterior cheek with origin from the inferior border and medial surface of the zygomatic arch, with insertion into the lateral surface of the ramus of the mandible, with nerve supply from the masseteric nerve, and whose action closes the jaw during chewing" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0004686 | decreased length of long bones | "reduced end-to-end length of the several elongated bones of the extremities" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0004698 | abnormal thyroid parafollicular C-cells | "any structural anomaly of the calcitonin-producing C-cells which are derived from the ultimobranchial body (a sac-like structure emanating from the neural crest) and constitute the minor component of the thyroid gland" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0004738 | abnormal brainstem auditory evoked potential | "anomaly in the electrical activity generated in response to short tone bursts; may be used to evaluate sensorineural hearing function" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator", MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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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: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0004808 | abnormal hematopoietic stem cell morphology | "any structural anomaly of the multipotent, self-renewing stem cells found in the bone marrow and the fetal liver; these give rise to all the types of both the myeloid and lymphoid cell lineages" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0004851 | increased testis weight | "greater average weight of the male reproductive glands" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0004884 | abnormal testicular physiology | "anomaly or loss either the production of male germ cells or the endocrine cells for the production testosterone" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0004953 | decreased spleen weight | "reduction in the 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: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0004982 | abnormal osteoclast morphology | "any structural anomaly of the 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: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0004983 | abnormal osteoclast cell number | "deviation from the average number of the 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: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0004985 | decreased osteoclast cell number | "reduced number of the 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: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0004986 | abnormal osteoblast morphology | "any structural anomaly of a bone-forming cell, which normally forms an osseous matrix (osteoid) in which it becomes enclosed as an osteocyte" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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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: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0005006 | abnormal osteoblast function | "anomalous function of this bone-forming cell, which normally forms an osseous matrix in which it becomes enclosed as an osteocyte " [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
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MP:0005015 | increased T cell number | "greater than normal T cell numbers" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0005016 | decreased lymphocyte number | "fewer than normal white blood cell numbers " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0005017 | decreased B cell number | "fewer than normal B cell numbers" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0005178 | increased total circulating cholesterol level | "greater than the normal concentration in the blood of these most abundant steroids in animal tissues, and precursors to steroid hormones and bile salts; also components of plasma membranes" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Apoetm1Unc/Apoe+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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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] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
Allelic Composition: Apoetm1Unc/Apoetm1Unc,Csf1op/Csf1op Genetic Background: involves: 129P2/OlaHsd * C3HeB/Fe * C57BL/6
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MP:0005362 | abnormal Langerhans cell physiology | "atypical or failure of normal function of the phagocytic dendritic cells principally found in the epidemis" [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: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0005422 | osteosclerosis | "abnormal hardening or eburnation (change in exposed subchondral bone in degenerative joint disease in which bone is converted into a dense substance with a smooth surface) of bone " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, cml:Cathy M Lutz , Mouse Genome Informatics Curator] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0005508 | abnormal skeleton morphology | "malformation of the bony framework of the body in vertebrates" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
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MP:0005564 | increased hemoglobin content | "increase in the total hemoglobin content in the circulating blood" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, RGD:Rat Genome Database submission] |
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Allelic Composition: Csf1op/Csf1op,Csf2tm1Ard/Csf2tm1Ard Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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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: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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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] |
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Allelic Composition: Csf1tm1.1(CSF1)Flv/Csf1tm1.1(CSF1)Flv,Il2rgtm1.1Flv/Il2rgtm1.1Flv,Csf2/Il3tm1.1(CSF2,IL3)Flv/Csf2/Il3tm1.1(CSF2,IL3)Flv,Rag2tm1.1Flv/Rag2tm1.1Flv,Thpotm1.1(TPO)Flv/Thpotm1.1(TPO)Flv Genetic Background: involves: 129S4/SvJae * BALB/cAnNTac
Allelic Composition: Csf1tm1.1(CSF1)Flv/Csf1tm1.1(CSF1)Flv,Csf2/Il3tm1.1(CSF2,IL3)Flv/Csf2/Il3tm1.1(CSF2,IL3)Flv,Il2rgtm1.1Flv/Il2rgtm1.1Flv,Rag2tm1.1Flv/Rag2tm1.1Flv,Thpotm1.1(TPO)Flv/Thpotm1.1(TPO)Flv Genetic Background: involves: 129S4/SvJae * BALB/cAnNTac
Allelic Composition: Csf1tm1.1(CSF1)Flv/Csf1tm1.1(CSF1)Flv,Il2rgtm1.1Flv/Il2rgtm1.1Flv,Csf2/Il3tm1.1(CSF2,IL3)Flv/Csf2/Il3tm1.1(CSF2,IL3)Flv,Rag2tm1.1Flv/Rag2tm1.1Flv,Tg(SIRPA)1Flv/0,Thpotm1.1(TPO)Flv/Thpotm1.1(TPO)Flv Genetic Background: involves: 129S4/SvJae * BALB/cAnNTac
Allelic Composition: Csf1tm1.1(CSF1)Flv/Csf1tm1.1(CSF1)Flv,Csf2/Il3tm1.1(CSF2,IL3)Flv/Csf2/Il3tm1.1(CSF2,IL3)Flv,Il2rgtm1.1Flv/Il2rgtm1.1Flv,Rag2tm1.1Flv/Rag2tm1.1Flv,Tg(SIRPA)1Flv/0,Thpotm1.1(TPO)Flv/Thpotm1.1(TPO)Flv Genetic Background: involves: 129S4/SvJae * BALB/cAnNTac
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MP:0006269 | abnormal mammary gland growth during pregnancy | "anomaly in the extensive and rapid branching of the mammary ducts, expansion of mammary epithelium in the stroma between the ducts with or without abnormalities in nipple maturation " [llw2:Linda Washburn , Mouse Genome Informatics Curator] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0006270 | abnormal mammary gland growth during lactation | "anomaly in the final stage of mammary growth that occurs during the start of lactation" [llw2:Linda Washburn , Mouse Genome Informatics Curator] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0006398 | increased long bone epiphyseal plate size | "greater than the normal size of the cartilaginous center of ossification on the long bones permitting growth of the bone in both directions during development" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0008114 | abnormal Kupffer cell morphology | "any structural anomaly of the phagocytic macrophages residing on the luminal surface of the hepatic sinusoids" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0008117 | abnormal Langerhans cell morphology | "any structural anomaly of a stellate dendritic cell of myeloid origin, that appears clear on light microscopy and has a dark-staining, indented nucleus and characteristic inclusions (Birbeck granules) in the cytoplasm; Langerhans cells are found principally in the stratum spinosum of the epidermis, but they also occur in other stratified epithelia and have been identified in the lung, lymph nodes, spleen, and thymus" [CL:0000453, ISBN:0781735149, MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0008118 | absent Langerhans cell | "absence of stellate dendritic cells of myeloid origin, that appear clear on light microscopy and has a dark-staining, indented nucleus and characteristic inclusions (Birbeck granules) in the cytoplasm; Langerhans cells are found principally in the stratum spinosum of the epidermis, but they also occur in other stratified epithelia and have been identified in the lung, lymph nodes, spleen, and thymus" [ISBN:0781735149, MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0008242 | abnormal perivascular macrophage morphology | "any structural anomaly of macrophages that line the small blood vessels" [PMID:16322748] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0008250 | abnormal myeloid leukocyte morphology | "any structural anomaly of a cell of the monocyte, granulocyte, or mast cell lineage" [CL:0000766] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * 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: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0008415 | abnormal neurite morphology | "any structural anomaly of a neuronal process, either a dendrite or an axon in vivo, or a filamentous projection from a neuron such as is seen in tissue culture" [PMID:12951572] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6;C3Fe a/a-Csf1op/J
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MP:0008489 | postnatal slow weight gain | "the weight gain over a span of postnatal developmental time is slower than controls, with or without ever attaining a similar weight to controls as adults" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
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MP:0008553 | increased circulating tumor necrosis factor level | "greater amount in the blood 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: Csf1op/Csf1op,Sh3bp2tm1Bjro/Sh3bp2tm1Bjro Genetic Background: involves: 129S4/SvJae * BALB/cJ * C57BL/6J
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MP:0008753 | abnormal osteocyte morphology | "any structural anomaly of a mature osteoblast that has become embedded in the bone matrix (osteoid) in small cavities called lacuna and is connected to adjacent osteocytes via protoplasmic projections called canaliculi" [MESH:A.11.329.629.500] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0008826 | abnormal splenic cell ratio | "deviation from the standard ratios of splenocyte subpopulations compared to control samples" [MGI:mberry "Melissa Berry, Genetics Resources Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0008828 | abnormal lymph node cell ratio | "deviation from the standard ratios of lymph node cell subpopulations compared to control samples" [MGI:mberry "Melissa Berry, Genetics Resources Curator"] |
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Allelic Composition: Csf1op/Csf1op,Sh3bp2tm1Bjro/Sh3bp2tm1Bjro Genetic Background: involves: 129S4/SvJae * BALB/cJ * C57BL/6J
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MP:0008871 | abnormal ovarian follicle number | "abnormal numbers of spheroid cell aggregations in the ovary" [MGI:mnk "Michelle Knowlton, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6;C3Fe a/a-Csf1op/J
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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: Csf1op/Csf1op Genetic Background: B6;C3Fe a/a-Csf1op/J
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MP:0008917 | abnormal oligodendrocyte physiology | "any functional anomaly of the neuroglia of the central nervous system that form the insulating myelin sheath of axons in the CNS" [MESH:A08.637.600] |
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Allelic Composition: Csf1op/Csf1op,Galctwi/Galctwi Genetic Background: involves: C3HeB/Fe * C57BL/6J * CE/J
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MP:0009006 | prolonged estrous cycle | "increase in the length of the sexual cycle of female animals" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0009013 | abnormal proestrus | "any anomaly or aberrant timing of the first phase of the estrous cycle which begins when a new batch of eggs reach maturity within ovarian follicles that are ripe and large; external examination of the female usually shows a bloated vulva with an open vagina" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0009090 | myometrium hypoplasia | "underdevelopment or reduced size, usually due to a reduced number of cells, of the smooth muscle coat of the uterus, which forms the main mass of the organ and surrounds and supports the endometrium" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0009091 | endometrium hypoplasia | "underdevelopment or reduced size, usually due to a reduced number of cells, of the glandular mucous membrane lining of the uterine cavity that is hormonally responsive during the estrous/menstrual cycle and during pregnancy" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0009325 | necrospermia | "condition in which spermatozoa in seminal fluid are dead or motionless" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0009333 | abnormal splenocyte physiology | "any functional anomaly of a cell of the spleen" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0009346 | decreased cancellous bone thickness | "thinner than normal bone with a lattice-like or spongy structure" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0009505 | abnormal mammary gland lobule morphology | "any structural anomaly of a group of alveoli and the intralobular portion of the terminal duct of the mammary gland" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0009506 | abnormal mammary gland alveolus morphology | "any structural anomaly of the sac-like structure of the mammary gland that secretes milk after pregnancy" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0009647 | decreased fertilization frequency | "he number of secondary oocytes each penetrated by a spermatozoon followed by fusion of the male and female pronuclei are fewer than expected" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: involves: C3HeB/FeJ * C57BL/6J
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MP:0009808 | reduced oligodendrocyte number | "significantly fewer than the expected number of cells of the central nervous system that form the insulating myelin sheath of axons in the CNS are present" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op,Galctwi/Galctwi Genetic Background: involves: C3HeB/Fe * C57BL/6J * CE/J
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MP:0009971 | decreased hippocampus pyramidal cell number | "decreased number of the projection neurons in the pyramidal layer of the hippocampus" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0010748 | abnormal visual evoked potential | "anomaly in the electroencephalographic pattern recorded from the occipital area generated in response to retinal stimulation such as flashing lights or inverting a contrasting image; may be used to evaluate optic nerve damage or visual perception" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
Allelic Composition: Csf1op/Csf1op Genetic Background: B6;C3Fe a/a-Csf1op/J
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MP:0010868 | increased bone trabecula number | "increased number of intersecting plates and spicules in cancellous bone which form a meshwork of intercommunicating spaces filled with blood vessels and marrow; in mature bone, the trabeculae are aligned in parallel with the lines of major compressive or tensile force" [http://www.dorlands.com/ "Dorland s Illustrated Medical Dictionary, 31st edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0010872 | increased trabecular bone mass | "greater total amount of trabecular bone tissue contained in the skeleton" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0010878 | increased trabecular bone volume | "increase in the amount of space occupied by trabecular bone tissue in the skeleton" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0010998 | pulmonary alveolar proteinosis | "abnormal intra-alveolar accumulation of an amorphous, largely cell-free, surfactant-like lipoproteinaceous material that is not easily cleared from the lungs" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Csf1op/Csf1op,Csf2tm1Ard/Csf2tm1Ard Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0011086 | partial postnatal 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 anytime between the neonatal period and weaning age (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0011129 | decreased secondary ovarian follicle number | "fewer than normal numbers of the ovarian follicle in which the primary oocyte attains its full size and is surrounded by an extracellular glycoprotein layer (zona pellucida) that separates it from a peripheral layer of follicular cells permeated by one or more fluid-filled antra; the primary oocyte occupies the cumulus oophorus while the theca of the follicle develops into internal and external layers" [MGI:csmith] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6;C3Fe a/a-Csf1op/J
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MP:0011165 | abnormal tooth root development | "aberrant or incomplete formation of the part of a tooth that is implanted in the gum; the root is normally located below the neck of the tooth, covered by cementum rather than enamel, and attached by the periodontal ligament to the alveolar bone" [MGI:anna] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0011711 | decreased osteoblast differentiation | |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0011966 | abnormal auditory brainstem response waveform shape | "any anomaly in the characteristic pattern of electrical activity recording of a series of vertex positive waves generated by neurons in the ascending auditory system, that can be recorded from scalp electrograms by using computer-averaged responses to short tone bursts" [MGI:csmith] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6;C3Fe a/a-Csf1op/J
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MP:0013586 | thymus medulla atrophy | "acquired diminution of the inner area of thymus lobules associated with wasting as from death and reabsorbtion of cells, diminished cellular proliferation, decreased cellular volume, pressure, ischemia, malnutrition, reduced function or malfunction, or hormonal changes" [MGI:Anna] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: B6C3Fe a/a-Csf1op/J
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MP:0020137 | decreased bone mineralization | "decrease in the rate at which minerals are deposited into bone" [] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0030188 | round snout | "appearance of the anterior facial part of the face or muzzle containing the oral and nasal regions is more circular than usual" [MGI:anna] |
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Allelic Composition: Csf1op/Csf1op Genetic Background: C57BL/6J-Csf1op
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MP:0030451 | abnormal dentin mineralization | "anomaly in the process by which calcium salts are deposited into dentin" [GO:0097188] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0030479 | increased osteocyte apoptosis | "increase in the number of osteocytes undergoing programmed cell death" [MGI:anna] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0030484 | abnormal osteocyte lacuna morphology | "any structural anomaly of the small cavity within the bone matrix that is occupied by an osteocyte cell body, and from which slender canaliculi radiate and penetrate the adjacent lamellae to anastomose with the canaliculi of neighboring lacunae, thus forming a system of cavities interconnected by minute canals" [https://medical-dictionary.thefreedictionary.com/osteocyte+lacuna] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0030487 | abnormal osteocyte dendritic process morphology | "any structural anomaly of the long, slender cytoplasmic processes by which mature osteocytes communicate with one another, receive mechanosensory signals and participate in the regulation of bone turnover; these processes radiate from the osteocyte cell body, run along narrow canaliculi, and are linked to other neighboring osteocytes processes by gap junctions, as well as to cytoplasmic processes of osteoblasts and bone lining cells on the bone surface" [https://www.hindawi.com/journals/bmri/2015/421746/, PMID:24419319] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0030506 | abnormal dental follicle morphology | "any structural anomaly of the loose ectomesenchyme-derived connective tissue sac that surrounds the enamel organ and the dental papilla of the developing tooth germ before eruption; it is believed that this tissue contains stem cells and lineage-committed progenitor cells or precursor cells for cementoblasts, periodontal ligament (PDL) cells and osteoblasts; dental follicle cells form the PDL by differentiating into PDL fibroblasts that secrete collagen and interact with fibers on the surface of adjacent bone and cementum" [PMID:21035344] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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MP:0030543 | abnormal predentin morphology | "any structural anomaly of the initial type I collagen-rich unmineralized extracellular matrix synthesized and secreted by odontoblasts and located at the dentin-pulp interface; predentin is converted to dentin when hydroxyapatite crystals are deposited on the predentin" [https://books.google.com/books?isbn=0470958332] |
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Allelic Composition: Csf1tm1.2Sabw/Csf1tm1.2Sabw Genetic Background: involves: 129S4/SvJaeSor * C57BL/6
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