MP:0001004 | abnormal photoreceptor morphology | "structural or developmental anomaly of the receptors sensitive to light " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Gt(ROSA)26Sortm2(ITK/Syk)Hjum/Gt(ROSA)26Sor+,Tg(Lck-cre)I57Jxm/0 Genetic Background: involves: 129S6/SvEvTac * ICR
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MP:0001325 | abnormal retina morphology | "structural or developmental anomaly of the thin layer of neural tissue lining the back of the eyeball which contains visual receptors " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Gt(ROSA)26Sortm2(ITK/Syk)Hjum/Gt(ROSA)26Sor+,Tg(Lck-cre)I57Jxm/0 Genetic Background: involves: 129S6/SvEvTac * ICR
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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: Gt(ROSA)26Sortm2(ITK/Syk)Hjum/Gt(ROSA)26Sor+,Tg(Lck-cre)I57Jxm/0 Genetic Background: involves: 129S6/SvEvTac * ICR
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MP:0001934 | increased litter size | "greater numbers of live born pups in a litter compared to average" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: MafOfl/MafOfl Genetic Background: either: 102/ElH or C3H/HeH
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MP:0003731 | abnormal outer nuclear layer morphology | "malformation/anomalous structure of the retinal layer that contains the nuclei and cell bodies of rods and cones" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator] |
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Allelic Composition: Gt(ROSA)26Sortm2(ITK/Syk)Hjum/Gt(ROSA)26Sor+,Tg(Lck-cre)I57Jxm/0 Genetic Background: involves: 129S6/SvEvTac * ICR
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MP:0005098 | abnormal choroid morphology | "anomalous structure of the thin, highly vascularized membrane covering most of the posterior of the eye between the retina and the sclera" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Gt(ROSA)26Sortm2(ITK/Syk)Hjum/Gt(ROSA)26Sor+,Tg(Lck-cre)I57Jxm/0 Genetic Background: involves: 129S6/SvEvTac * ICR
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MP:0005201 | abnormal retinal pigment epithelium morphology | "anomaly in the epithelial layer of the retina composed of cells containing pigment granules " [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Gt(ROSA)26Sortm2(ITK/Syk)Hjum/Gt(ROSA)26Sor+,Tg(Lck-cre)I57Jxm/0 Genetic Background: involves: 129S6/SvEvTac * ICR
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MP:0005239 | abnormal Bruch membrane morphology | "anomalous structure of the transparent, nearly structureless inner layer of the choroid in contact with the pigmented layer of the retina" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Gt(ROSA)26Sortm2(ITK/Syk)Hjum/Gt(ROSA)26Sor+,Tg(Lck-cre)I57Jxm/0 Genetic Background: involves: 129S6/SvEvTac * ICR
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MP:0005410 | abnormal fertilization | "anomaly in the process beginning with penetration of the secondary oocyte by the spermatozoon and completed by fusion of the male and female pronucei" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, cwg:Carroll W. Goldsmith , Mouse Genome Informatics Curator] |
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Allelic Composition: MafOfl/MafOfl Genetic Background: either: 102/ElH or C3H/HeH
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MP:0006238 | abnormal choriocapillaris morphology | "malformation of the capillaries forming the inner vascular layer of the choroid of the eye" [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Gt(ROSA)26Sortm2(ITK/Syk)Hjum/Gt(ROSA)26Sor+,Tg(Lck-cre)I57Jxm/0 Genetic Background: involves: 129S6/SvEvTac * ICR
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MP:0008450 | retinal photoreceptor degeneration | "a retrogressive impairment of function or destruction of a cell specialized to detect and transduce light, including rods and cones of the retina" [MESH:A08.663.650.650, MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Gt(ROSA)26Sortm2(ITK/Syk)Hjum/Gt(ROSA)26Sor+,Tg(Lck-cre)I57Jxm/0 Genetic Background: involves: 129S6/SvEvTac * ICR
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MP:0011557 | increased susceptibility to induced choroid neovascularization | "increased rate or amount of new growth of new, abnormal blood vessels that originate in the choroid through a break in the Bruch membrane into the sub-retinal pigment epithelium or subretinal space and may result in visual loss as a result of chemical or mechanical manipulation (e.g. laser-induced trauma)" [MGI:anna, MGI:mnk] |
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Allelic Composition: Gt(ROSA)26Sortm2(ITK/Syk)Hjum/Gt(ROSA)26Sor+,Tg(Lck-cre)I57Jxm/0 Genetic Background: involves: 129S6/SvEvTac * ICR
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