MP:0000150 | abnormal rib morphology | "malformed bones forming the bony wall of the chest" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:50311] |
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Allelic Composition: Arntltm1Bra/Arntltm1Weit,Syt10tm1.1(icre)Geno/Syt10tm1.1(icre)Geno Genetic Background: involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6
Allelic Composition: Fstl1tm1.2Mvdh/Fstl1+ Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
Allelic Composition: Fstl1tm2.1(cre/ERT2)Mvdh/Fstl1tm2.1(cre/ERT2)Mvdh Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Fstl1tm2.1(cre/ERT2)Mvdh/Fstl1+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0000519 | hydronephrosis | "dilation of the pelvis and calices of one or both kidneys" [J:56641] |
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Allelic Composition: Baxtm1Sjk/Baxtm1Sjk,Pcdhgtm1.1Tman/Pcdhgtm1.1Tman Genetic Background: involves: 129S4/SvJae * 129X1/SvJ * C57BL/6
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MP:0000534 | abnormal ureter morphology | "anomalous structure of the tube that conducts the urine from the renal pelvis to the bladder" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Baxtm1Sjk/Baxtm1Sjk,Pcdhgtm1.1Tman/Pcdhgtm1.1Tman Genetic Background: involves: 129S4/SvJae * 129X1/SvJ * C57BL/6
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MP:0000536 | hydroureter | "distention of the ureter with urine, due to blockage from any cause" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:Cml, J:13044] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: Fstl1tm1.1Nju/Fstl1tm1.1Nju Genetic Background: involves: 129 * C57BL/6 * FVB/N
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MP:0000961 | abnormal dorsal root ganglia morphology | "malformed group of nerve cell bodies of each segmental nerve projecting from the spinal cord " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:60159] |
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Allelic Composition: Fstl1tm1.1Nju/Fstl1tm1.1Nju Genetic Background: involves: 129 * C57BL/6 * FVB/N
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MP:0001175 | abnormal lung morphology | "malformed organ of respiration" [J:35802] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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MP:0001176 | abnormal lung development | "malformation or arrest of differentiation of the organs of respiration" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54931] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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MP:0001575 | cyanosis | "a dark bluish or purple skin discoloration resulting from deficient oxygenation of the blood" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60159] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
Allelic Composition: Fstl1tm2.1(cre/ERT2)Mvdh/Fstl1tm2.1(cre/ERT2)Mvdh Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0001625 | cardiac hypertrophy | "an increase in size of the cardiac tissue, not due to increased cell number " [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Cd68tm1Xfen/Cd68+ Genetic Background: C57BL/6J-Cd68tm1Xfen
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MP:0001951 | abnormal breathing | "irregular or atypical breathing pattern " [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:17489] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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MP:0001954 | respiratory distress | "physical difficulty or inability to breathe" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54931] |
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Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
Allelic Composition: Fstl1tm2.1(cre/ERT2)Mvdh/Fstl1tm2.1(cre/ERT2)Mvdh Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0002110 | abnormal digit morphology | "abnormal development of the digits resulting in structural abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Arntltm1Bra/Arntltm1Weit,Syt10tm1.1(icre)Geno/Syt10tm1.1(icre)Geno Genetic Background: involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6
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MP:0002151 | abnormal neural tube morphology/development | "anomalous structure of or development of the embryonic neural tube resulting in structural anomaly" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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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: Tbx1m1H/Tbx1m1H Genetic Background: involves: C3H/HeH * C57BL/6J
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MP:0002249 | abnormal larynx morphology | "any structural anomaly of the most superior portion of the respiratory tract" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Pathology , 2nd edition:ISBN 0-397-51047-0] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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MP:0002267 | abnormal bronchiole morphology | "any structural anomaly of the conducting airway of the lungs found terminal to the bronchi. These structures contain neither cartilage nor mucous-secreting glands; the epithelium of the bronchioles becomes thinner with each branching. " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Pathology , 2nd edition:ISBN 0-397-51047-0] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
Allelic Composition: Fstl1tm2.1(cre/ERT2)Mvdh/Fstl1tm2.1(cre/ERT2)Mvdh Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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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: Arntltm1Bra/Arntltm1Weit,Syt10tm1.1(icre)Geno/Syt10tm1.1(icre)Geno Genetic Background: involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6
Allelic Composition: Fstl1tm2.1(cre/ERT2)Mvdh/Fstl1tm2.1(cre/ERT2)Mvdh Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0002275 | abnormal type II pneumocyte morphology | "any structural anomaly of the epithelial cells lining the alveoli that produce surfactant " [Pathology , 2nd edition:ISBN 0-397-51047-0, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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MP:0002282 | abnormal trachea morphology | "structral anomaly of the tube descending from the larynx and branching into the right and left main bronchi" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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MP:0002285 | abnormal tracheal ciliated epithelium morphology | "structural anomaly of the epithelial lining of the trachea which contains numerous ciliated cells" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Pathology:ISBN 0-397-51047-0] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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MP:0002738 | hyperresponsive to tactile stimuli | "exaggerated reflex action normally induced by touch or pain" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Fstl1tm1.1Nju/Fstl1tm1.1Nju Genetic Background: involves: 129 * C57BL/6 * FVB/N
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MP:0002833 | increased heart weight | "greater than average weight of the heart compared to the average for a particular strain" [RGD:Rat Genome Database submission] |
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Allelic Composition: Cd68tm1Xfen/Cd68+ Genetic Background: C57BL/6J-Cd68tm1Xfen
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MP:0002910 | abnormal excitatory postsynaptic currents | "defect in the size or duration of currents detected in postsynaptic cells when an excitatory impulse arrives at the synapse causing depolarization" [Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3] |
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Allelic Composition: Fstl1tm1.1Nju/Fstl1tm1.1Nju Genetic Background: involves: 129 * C57BL/6 * FVB/N
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MP:0002989 | small kidney | "reduced physical bulk one or both of the organs responsible for urine secretion" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Fstl1tm1.1Nju/Fstl1tm1.1Nju Genetic Background: involves: 129 * C57BL/6 * FVB/N
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MP:0003073 | abnormal metacarpal bone morphology | "anomaly in the five bones of the forepaws that articulate proximally with the carpal bones and distally with the phlanges" [Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8, Anatomy of the Rat:Greene, EC, Hafner Publishing Co, 1935] |
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Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
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MP:0003120 | abnormal tracheal cartilage | "any structural anomaly of the cartilaginous structures that support the trachea" [smb:Susan M. Bello, Mouse Genome Informatics Curator, J:97123] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
Allelic Composition: Fstl1tm2.1(cre/ERT2)Mvdh/Fstl1tm2.1(cre/ERT2)Mvdh Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0003141 | cardiac fibrosis | "formation of fibrous tissue within the heart often resulting from inflammation or injury " [smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Cd68tm1Xfen/Cd68+ Genetic Background: C57BL/6J-Cd68tm1Xfen
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MP:0003586 | ureter dilation | "abnormal distention of the ureter due to accumulation of fluid" [ncbi:Matthew Mailman, NCBI request] |
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Allelic Composition: Fstl1tm1.1Nju/Fstl1tm1.1Nju Genetic Background: involves: 129 * C57BL/6 * FVB/N
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MP:0003588 | ureter stenosis | "abnormal narrowing or constriction of the ureter" [ncbi:Matthew Mailman, NCBI request] |
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Allelic Composition: Fstl1tm1.1Nju/Fstl1tm1.1Nju Genetic Background: involves: 129 * C57BL/6 * FVB/N
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MP:0003672 | abnormal ureter development | "anomalous differentiation of the tube that conducts the urine from the renal pelvis to the bladder" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:96485] |
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Allelic Composition: Fstl1tm1.1Nju/Fstl1tm1.1Nju Genetic Background: involves: 129 * C57BL/6 * FVB/N
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MP:0003723 | abnormal long bone morphology | "malformation of any of the several elongated bones of the extremities
" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator] |
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Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
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MP:0003856 | abnormal hindlimb stylopod morphology | |
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Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
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MP:0003857 | abnormal hindlimb zeugopod morphology | |
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Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
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MP:0003915 | increased left ventricle weight | "greater than average weight of the left ventricle compared to the average for a particular strain" [RGD:Rat Genome Database submission] |
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Allelic Composition: Cd68tm1Xfen/Cd68+ Genetic Background: C57BL/6J-Cd68tm1Xfen
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MP:0003998 | decreased thermal nociceptive threshold | "a lower than average point at which thermal pain sensation is first detectable" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Fstl1tm1.1Nju/Fstl1tm1.1Nju Genetic Background: involves: 129 * C57BL/6 * FVB/N
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MP:0004174 | abnormal spine curvature | "deviation from the typical S-shape of the spine" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
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MP:0004194 | abnormal kidney pelvis morphology | "any structural anomaly of the funnel shaped proximal portion of the ureter that is formed by convergence of the major calices" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fstl1tm1.1Nju/Fstl1tm1.1Nju Genetic Background: involves: 129 * C57BL/6 * FVB/N
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MP:0004202 | pulmonary hyperplasia | "overdevelopment or increased size, usually due an increased number of cells of the respiratory organ in all or part of the organ" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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MP:0004372 | bowed fibula | "increased curvature of the lateral and smaller bone of the lower limb" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
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MP:0004485 | increased response of heart to induced stress | "increase in severity of the physiological response of the heart to induced stress such as cardiac hypertrophy due to mechanical pressure overload from aortic banding" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Cd68tm1Xfen/Cd68+ Genetic Background: C57BL/6J-Cd68tm1Xfen
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MP:0004551 | decreased tracheal cartilage ring number | "less than the 16-20 incomplete rings of hyaline cartilage forming the skeleton of the trachea" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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MP:0004564 | enlarged myocardial fiber | "increased size of cardiac muscle fibers, the multinucleated muscle cells of the heart" [MGI:monikat "Monika Tomczuk, Mouse Genome Informatics Curator"] |
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Allelic Composition: Cd68tm1Xfen/Cd68+ Genetic Background: C57BL/6J-Cd68tm1Xfen
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MP:0004607 | abnormal cervical atlas morphology | "any structural anomaly of the first (topmost, C1) cervical vertebra which supports the globe of the head" [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: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
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MP:0004608 | abnormal cervical axis morphology | "any structural anomaly of the second cervical vertebra (C2) which forms the pivot upon which the first cervical (atlas, C1) vertebra rotates" [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: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
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MP:0004694 | absent patella | "absence of the large sesamoid bone that covers the anterior surface of the knee" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
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MP:0005140 | decreased cardiac muscle contractility | "inability or reduced ability of the heart muscle to shorten or to develop increased tension" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Cd68tm1Xfen/Cd68+ Genetic Background: C57BL/6J-Cd68tm1Xfen
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MP:0005293 | impaired glucose tolerance | "less than the normal response to oral consumption or intravenous injection of specified amounts of glucose and indicative of insulin resistance; measured by determining whole blood or plasma sugar level in a fasting state before and after taking glucose at specified intervals" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Fgf9tm1b(KOMP)Wtsi/Fgf9tm1b(KOMP)Wtsi Genetic Background: C57BL/6N-Fgf9tm1b(KOMP)Wtsi/H
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MP:0005402 | abnormal action potential | "change in the electric response of a nerve or other excitable tissue to its stimulation" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Fstl1tm1.1Nju/Fstl1tm1.1Nju Genetic Background: involves: 129 * C57BL/6 * FVB/N
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MP:0005440 | increased glycogen level | "greater than the normal concentration of this readily converted carbohydrate reserve, found in most tissues of the body, especially liver and muscle" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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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: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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MP:0005602 | decreased angiogenesis | "reduced process of blood vessel formation and the subsequent remodeling process; does not refer to the initial establishment of the vascular network" [RGD:Rat Genome Database submission] |
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Allelic Composition: Cd68tm1Xfen/Cd68+ Genetic Background: C57BL/6J-Cd68tm1Xfen
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MP:0006113 | abnormal heart septum morphology | "abnormality in the wall between the atria or ventricles of the heart, usually incomplete closure" [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Cd68tm1Xfen/Cd68+ Genetic Background: C57BL/6J-Cd68tm1Xfen
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MP:0006382 | abnormal lung epithelium morphology | "any structural anomaly of the epithelial layer of the lung" [MGI:rbabiuk "Randall Babiuk, Mouse Genome Informatics Curator", MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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MP:0006432 | abnormal costal cartilage morphology | "any structural anomaly of the nonvascular, resilient, flexible connective tissue that connects the end of a true rib to the sternum or the end of a false rib with the costal cartilage above" [ISBN:0-8036-0655-9 "Taber s Cyclopedic Medical Dictionary", MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
Allelic Composition: Fstl1tm2.1(cre/ERT2)Mvdh/Fstl1tm2.1(cre/ERT2)Mvdh Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0008146 | asymmetric rib-sternum attachment | "loss of bilateral symmetry in rib attachments to the sternum" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
Allelic Composition: Fstl1tm1.2Mvdh/Fstl1+ Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
Allelic Composition: Fstl1tm2.1(cre/ERT2)Mvdh/Fstl1tm2.1(cre/ERT2)Mvdh Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Fstl1tm2.1(cre/ERT2)Mvdh/Fstl1+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0008532 | decreased chemical nociceptive threshold | "a lower than average concentration at which chemically induced pain sensation is first detectable" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fstl1tm1.1Nju/Fstl1tm1.1Nju Genetic Background: involves: 129 * C57BL/6 * FVB/N
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MP:0008730 | fused phalanges | "anomaly of the long bones of the digits resulting in some or all the bones being joined together" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
Allelic Composition: Fstl1tm2.1(cre/ERT2)Mvdh/Fstl1tm2.1(cre/ERT2)Mvdh Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0009005 | abnormal sesamoid bone of gastrocnemius morphology | "any structural anomaly of the small sesamoid bones situated behind the condyles of the femur" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
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MP:0010018 | lung vascular congestion | "obstruction of the normal flux of blood within the blood vessel network of the lung" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Cd68tm1Xfen/Cd68+ Genetic Background: C57BL/6J-Cd68tm1Xfen
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MP:0010551 | abnormal coronary vessel morphology | "any structural anomaly of any of the arteries or veins that supply blood to the heart or return blood from the heart muscles to the circulation" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Cd68tm1Xfen/Cd68+ Genetic Background: C57BL/6J-Cd68tm1Xfen
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MP:0010579 | increased heart left ventricle size | "greater than average size of the left ventricle" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Cd68tm1Xfen/Cd68+ Genetic Background: C57BL/6J-Cd68tm1Xfen
|
MP:0010810 | increased type II pneumocyte number | "greater number of the granular and roughly cuboidal cells typically found at the alveolar-septal junction that modulate the fluid surrounding the alveolar epithelium by secreting and recycling surfactants, and also contribute to tissue repair and can differentiate after injury into a type I pneumocyte; type II cells cover a much smaller surface area than type I cells (less than 5 percent), but are much more numerous and contain lamellar bodies on the apical surface where surfactant is stored" [ISBN:0412046911, MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator", PMID:8540632] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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MP:0010816 | decreased type I pneumocyte number | "reduced number of the flattened, branched squamous cells that covers more than 98 percent of the alveolar surface, and have thin (50-100 nm) cytoplasmic extensions to form the air-blood barrier essential for normal gas exchange" [PMID:20054144] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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MP:0010819 | primary atelectasis | "nonexpansion of the lungs after birth, seen in stillborn organisms and in live born animals that do not establish respiration" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
Allelic Composition: Fstl1tm2.1(cre/ERT2)Mvdh/Fstl1tm2.1(cre/ERT2)Mvdh Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0010883 | trachea stenosis | "abnormal narrowing or constriction of the trachea" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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MP:0010890 | decreased alveolar lamellar body number | "reduced number of the specialized secretory organelles found in the cytoplasm of type II pneumocytes and involved in the synthesis, secretion, and reutilization of pulmonary surfactant" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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MP:0010902 | abnormal pulmonary alveolar sac morphology | "any structural anomaly of the small terminal dilation of the alveolar ducts around which the alveoli form pocket-like clusters" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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MP:0010975 | abnormal lung lobe morphology | "any structural anomaly of any of the anatomically and functionally distinct subunits (lobes) comprising the left or right lung, where each lobe receives air from its own secondary bronchus and is separated from it neighbors by one or more fissures (walls of connective tissue)" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
Allelic Composition: Fstl1tm2.1(cre/ERT2)Mvdh/Fstl1tm2.1(cre/ERT2)Mvdh Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0010993 | decreased surfactant secretion | "decreased production or release from pneumocytes of surfactant, a phospholipid present in the lungs that controls surface tension in the alveoli" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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MP:0011087 | complete neonatal lethality | "death of all organisms of a given genotype in a population within the neonatal period after birth (Mus: P0)" [MGI:csmith] |
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Allelic Composition: Otoftm1.1Erei/Otoftm1.1Erei Genetic Background: involves: 129P2/OlaHsd
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MP:0011089 | complete perinatal lethality | "death of all organisms of a given genotype in a population within the perinatal period (Mus: E18.5 through postnatal day 1)" [MGI:csmith] |
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Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
Allelic Composition: Fstl1tm2.1(cre/ERT2)Mvdh/Fstl1tm2.1(cre/ERT2)Mvdh Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0011304 | kidney papillary atrophy | "acquired diminution of the size of the apex (tip) of a renal pyramid 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: Fstl1tm1.1Nju/Fstl1tm1.1Nju Genetic Background: involves: 129 * C57BL/6 * FVB/N
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MP:0011484 | abnormal ureter urothelium morphology | "any structural anomaly of the epithelial lining of the luminal space of the ureter" [MGI:csmith] |
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Allelic Composition: Fstl1tm1.1Nju/Fstl1tm1.1Nju Genetic Background: involves: 129 * C57BL/6 * FVB/N
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MP:0011505 | camptomelia | "a skeletal dysplasia characterized by the bending of the long bones of the extremities" [ISBN:0-683-40008-8] |
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Allelic Composition: Fstl1tm2.1(cre/ERT2)Mvdh/Fstl1tm2.1(cre/ERT2)Mvdh Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0020040 | decreased bone ossification | "decrease in the formation of bone or of a bony substance, or the conversion of fibrous tissue or of cartilage into bone or a bony substance" [ORCID: orcid.org/0000-0003-4606-0597] |
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Allelic Composition: Fstl1tm1.2Mvdh/Fstl1tm1.2Mvdh Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB
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