MP:0000163 | abnormal cartilage morphology | "anomalous structure or development of the nonvascular, resilient, flexible connective tissue found primarily in joints, walls of the throax, and tubular structures, but which also comprises most of the skeleton in early fetal life " [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0000352 | decreased cell proliferation | "less than the normal growth and reproduction of similar cells" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
Allelic Composition: Igf2bp1Gt(OST33739)Lex/Igf2bp1Gt(OST33739)Lex Genetic Background: involves: 129S5/SvEvBrd
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MP:0000445 | short snout | "reduced length of the anterior facial part of the muzzle" [J:53370] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0000477 | abnormal intestine morphology | "malformation of the digestive tube passing from the stomach to the anus" [J:48968] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0000478 | delayed intestine development | "slowed progression to a structurally mature intestine" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0000496 | abnormal small intestine morphology | "structural or developmental anomalies of the intestinum tenue " [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0000511 | abnormal intestinal mucosa morphology | "structural or developmental anomalies of the mucous lining of the intestine; this consists of epithelium, lamina, propria, and a layer of smooth muscle cells" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0000528 | delayed kidney development | "late onset of the induction and/or differentiation of the kidney" [J:18048] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0000585 | kinked tail | "a sharp bend or zig-zag in the tail" [J:61295] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0000694 | spleen hypoplasia | "small size due to reduced cell number in the spleen" [J:43971] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0000774 | reduced brain size | "smaller appearance of the brain" [J:35802] |
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Allelic Composition: Igf2bp1Gt(OST33739)Lex/Igf2bp1Gt(OST33739)Lex Genetic Background: involves: 129S5/SvEvBrd
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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: Igf2bp1Gt(OST33739)Lex/Igf2bp1Gt(OST33739)Lex Genetic Background: involves: 129S5/SvEvBrd
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MP:0000823 | abnormal lateral ventricle morphology | "malformation or absence of cavity in each of the cerebral hemispheres derived from the cavity of the embryonic neural tube; they are separated from each other by the septum pellucidum, and each communicates with the third ventricle by the foramen of Monro, through which also the choroid plexuses of the lateral ventricles become continuous with that of the third ventricle" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Igf2bp1Gt(OST33739)Lex/Igf2bp1Gt(OST33739)Lex Genetic Background: involves: 129S5/SvEvBrd
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MP:0000952 | abnormal CNS glia | "anomalous structure, number or composition of non-neuronal cells of the central nervous system that form the myelin insulation of nervous pathways, guide neuronal migration during development, and exchange metabolites with neurons" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Igf2bp1Gt(OST33739)Lex/Igf2bp1Gt(OST33739)Lex Genetic Background: involves: 129S5/SvEvBrd
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MP:0001258 | decreased body length | "decreased crown to tail distance compared to controls" [cwg:Carroll W. Goldsmith, Mouse Genome Informatics Curator] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0001262 | decreased body weight | "lower than normal average weight " [J:61295] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0001363 | increased anxiety-related response | "when compared to controls, subjects exhibit more responses thought to be indicative of anxiety in behavioral tests" [cwg:Carroll-Ann W. Goldsmith, Mouse Genome Informatics curator, J:49752, J:53060] |
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Allelic Composition: Itktm1Lex/Itktm1Lex Genetic Background: involves: 129S5/SvEvBrd * C57BL/6J
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MP:0001394 | circling | "repeated, compulsive movement in a circle; often associated with inner ear defects" [MGI:CLS, J:61295] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0001399 | hyperactivity | "general restlessness or excessive movement; more frequent movement from one place to another" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409, J:57125] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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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: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0001417 | decreased exploration in new environment | "less amount of time spent investigating a new location" [J:79870] |
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Allelic Composition: Itktm1Lex/Itktm1Lex Genetic Background: involves: 129S5/SvEvBrd * C57BL/6J
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MP:0001429 | dehydration | "excessive water loss from the body or from an organ or bodily part" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:50053] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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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: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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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: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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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: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0002019 | abnormal tumor incidence | "deviation from the expected number of abnormal growths of a specific tissue in a specific population" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Tpotee-2J/Tpotee-2J Genetic Background: C3.B6(NOD)-Tpotee-2J/Kjn
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MP:0002427 | dwarfism | "abnormally undersized with disproportionate body parts" [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: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0002628 | fatty liver | "an accumulation of fat deposits in the liver " [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0003077 | abnormal cell cycle | "failure to progress or abnormal progression through the stages of of the cell cycle" [smb:Susan M. Bello, Mouse Genome Informatics Curator, J:91266] |
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Allelic Composition: Igf2bp1Gt(OST33739)Lex/Igf2bp1Gt(OST33739)Lex Genetic Background: involves: 129S5/SvEvBrd
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MP:0003424 | premature neuronal precursor differentiation | "earlier than normal transformation of neuronal precursor cells into neurons" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:94391] |
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Allelic Composition: Igf2bp1Gt(OST33739)Lex/Igf2bp1Gt(OST33739)Lex Genetic Background: involves: 129S5/SvEvBrd
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MP:0003446 | renal hypoplasia | "decreased cell number in the kidney leading to reduced size" [llw2:Linda Washburn , Mouse Genome Informatics Curator] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0004201 | fetal growth retardation | "slow or limited development during the fetal period (sensu Mus: from E14 through birth)" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0004754 | abnormal kidney collecting duct | "any structural anomaly of the duct that drains fluid from the nephron and either allows bodily reabsorbtion of water or allows the fluid to drain to the bladder via the ureter; the collecting duct system also maintains acid-base homeostasis" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0004842 | abnormal large intestine crypts of Lieberkuhn morphology | "any structural anomaly in the tubular intestinal glands found in the mucosal membranes of the large intestine" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0004921 | decreased placenta weight | "reduction in the weight of the organ of metabolic interchange between fetus and mother" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0005325 | abnormal glomerulus | "anomalous structure of the capillary loops of the kidney that normally function as a filtration unit" [J:57971, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0005621 | abnormal cell physiology | "aberration in the vital processes of the cell " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, hdene:Howard Dene , Mouse Genome Informatics Curator] |
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Allelic Composition: Relatm1Rsch/Relatm1Rsch,Tg(Cd4-cre)1Cwi/0 Genetic Background: involves: C57BL/6 * DBA/2
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MP:0005655 | increased aggression | "when compared to controls, subjects exhibit greater than the normal level of domineering, assaultive posture and/or hostile physical action" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, cwg:Carroll-Ann W. Goldsmith, Mouse Genome Informatics curator] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0008109 | abnormal small intestinal microvillus morphology | "any structural anomaly of the additional extensions of the villi of the small intestine which protrude from the apical surface of the epithelial cells lining the villi; the microvilli increase the absorptive surface area of the small intestine by approximately 600-fold" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", MGI:rbabiuk "Randall Babiuk, Mouse Genome Informatics Curator"] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0008142 | decreased small intestinal villus size | "reduced size of the tiny hair-like projections that protrude from the inside of the small intestine that contain blood vessels that capture digested nutrients that are absorbed through the intestinal wall; the villi increase the absorptive surface area of the small intestine by approximately 30-fold" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", MGI:rbabiuk "Randall Babiuk, Mouse Genome Informatics Curator"] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0008770 | decreased survivor rate | "a smaller percentage of organisms than expected survive to adulthood and have a lifespan similar to controls" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0008802 | abnormal intestinal smooth muscle morphology | "any structural anomaly of the nonstriated, involuntary muscle tissue lining the intestine" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0008987 | abnormal liver lobule morphology | "any structural anomaly of the polygonal structure of the liver that consists of hepatocytes radiating outward from a hepatic vein" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0009431 | decreased fetal weight | "reduced weight of a fetus compared to controls (sensu Mus: from E14 through birth)" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0009674 | decreased birth weight | "reduction in average weight at birth compared to controls" [RGD:cur "Rat Genome Database submission"] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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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: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0011090 | partial perinatal 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 within the perinatal period (Mus: E18.5 through postnatal day 1)" [MGI:csmith] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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MP:0011110 | partial preweaning lethality | "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms between fertilization and weaning age (Mus: approximately 3-4 weeks of age)" [MGI:csmith] |
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Allelic Composition: Itktm1Lex/Itktm1Lex Genetic Background: involves: 129S5/SvEvBrd * C57BL/6J
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MP:0012203 | abnormal neuronal stem cell morphology | "any structural anomaly of an undifferentiated cell that originates from the neuroectoderm and has the capacity both to perpetually self-renew without differentiating and to generate multiple types of lineage-restricted progenitors" [CL:0000047] |
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Allelic Composition: Igf2bp1Gt(OST33739)Lex/Igf2bp1Gt(OST33739)Lex Genetic Background: involves: 129S5/SvEvBrd
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MP:0012207 | decreased neuronal stem cell self-renewal | "an decreased rate in the process by which stem cells divide and proliferate to make more stem cells, perpetuating an decrease in the stem cell pool; self-renewal is division with maintenance of the undifferentiated state" [PMID:19575646] |
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Allelic Composition: Igf2bp1Gt(OST33739)Lex/Igf2bp1Gt(OST33739)Lex Genetic Background: involves: 129S5/SvEvBrd
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MP:0013795 | abnormal colon goblet cell morphology | "any structural anomaly of the glandular simple columnar epithelial cell found in the mucosal lining of the colon, whose primary function is to secrete gel-forming mucins, the major components of mucus" [MGI:Anna, PMID:25872481] |
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Allelic Composition: X/Srydl1Rlb,Tg(Sry)2Ei/0 Genetic Background: involves: 129S6/SvEv * C3H * C57BL/6JEi * MF1
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