MP:0000832 | abnormal thalamus morphology | "malformation or absence of the large ovoid mass of paired bodies containing mostly gray matter and forming part of the lateral wall of the third ventricle of the brain" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Fzd5tm1Nat/Fzd5tm2Nat,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL
Allelic Composition: Fzd5tm1Nat/Fzd5tm2Nat,Gt(ROSA)26Sortm1(cre/ERT)Nat/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL
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MP:0001262 | decreased body weight | "lower than normal average weight " [J:61295] |
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Allelic Composition: Fzd5tm1Nat/Fzd5tm2Nat,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL
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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: Fzd5tm1Nat/Fzd5tm1Nat Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0001326 | retinal degeneration | "pathological change in the thin layer of neural tissue lining the back of the eyeball, which contains visual receptors and can result in the impairment or cessation of retinal neural function" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, NMF:Stephanie Pretel, Neuroscience Mutagenesis Facility Curator] |
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Allelic Composition: Fzd5tm1Nat/Fzd5tm2Nat,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL
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MP:0001405 | impaired coordination | "reduced ability to execute integrated movements of muscle" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Fzd5tm1Nat/Fzd5tm2Nat,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL
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MP:0001718 | abnormal yolk sac | "malformed extraembryonic tissue which contributes to hematopoietic circulation" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:12623] |
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Allelic Composition: Engtm1Hma/Engtm1Hma Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
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MP:0001722 | pale yolk sac | "bloodless yolk sac" [J:62571] |
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Allelic Composition: Engtm1Hma/Engtm1Hma Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
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MP:0001723 | disorganized vascular plexus | |
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Allelic Composition: Engtm1Hma/Engtm1Hma Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
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MP:0001914 | hemorrhage | "loss of blood from the vascular compartment to the exterior or into nonvascular body space as a result of rupture or severance of the blood vessels" [Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Engtm1Hma/Engtm1Hma Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
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MP:0004076 | abnormal vitelline vascular remodelling | "anomaly in the conversion of the primary (honeycomb-like) vascular plexus of the yolk sac into a mature vascular network" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Engtm1Hma/Engtm1Hma Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
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MP:0008803 | abnormal placental labyrinth vasculature morphology | "any structural anomaly in blood vessels of the layer of the placenta where embryonic and maternal blood vessels interdigitate" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Engtm1Hma/Engtm1Hma Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
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MP:0011091 | complete prenatal lethality | "death of all organisms of a given genotype in a population between fertilization and birth (Mus: approximately E18.5)" [MGI:csmith] |
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Allelic Composition: Engtm1Hma/Engtm1Hma Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Allelic Composition: Fzd5tm1Nat/Fzd5tm1Nat Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0014077 | ectopic Paneth cells | "abnormal position of the large secretory cells containing coarse granules normally confined to the base of the crypts of Lieberkuhn in the small intestine" [MGI:Anna] |
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Allelic Composition: Dvl1tm1Awb/Dvl1tm1Awb,Dvl2tm1Awb/Dvl2tm1Awb,Tg(Dvl2*K446M/EGFP)5Awb/? Genetic Background: involves: 129S6/SvEvTac
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