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: Cacna1atm1Kano/Cacna1atm1Kano,Grid2tm1(cre)Mwa/Grid2+ Genetic Background: involves: C57BL/6 * C57BL/6N
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MP:0001999 | photosensitivity | "alterations in the response to sunlight or UV irradiation, especially sensitivity of the eyes" [cwg:Carroll W. Goldsmith, Mouse Genome Informatics Curator, Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Srftm1Rjs/Srftm2.1Nor,Tg(Myh6-cre)2182Mds/0 Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * FVB/N
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MP:0004021 | abnormal rod electrophysiology | "anomaly in the function of dark adapted vision mediated by the rods" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Apoa1tm1Unc/Apoa1tm1Unc,Tg(APOA2)3Rub/0 Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Gngt1tm1Ogk/Gngt1tm1Ogk Genetic Background: involves: 129
Allelic Composition: Gngt1tm1Ogk/Gngt1+ Genetic Background: involves: 129
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MP:0005551 | abnormal eye electrophysiology | "abnormal function of the eye as determined through electrophysiological recordings from single cells or summary recordings from multiple cells (e.g. electroretinogram)" [NMF:Stephanie Pretel, Neuroscience Mutagenesis Facility Curator] |
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Allelic Composition: Apoa1tm1Unc/Apoa1tm1Unc,Tg(APOA2)3Rub/0 Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Gngt1tm1Ogk/Gngt1tm1Ogk Genetic Background: involves: 129
Allelic Composition: Gngt1tm1Ogk/Gngt1+ Genetic Background: involves: 129
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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: Apoa1tm1Unc/Apoa1tm1Unc,Tg(APOA2)3Rub/0 Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Gnat1tm1Clma/Gnat1tm1Clma,Gngt1tm1Dgen/Gngt1tm1Dgen Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6
Allelic Composition: Gngt1tm1Dgen/Gngt1tm1Dgen,Pdctm1Vya/Pdctm1Vya Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6
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MP:0008451 | retinal rod cell degeneration | "a retrogressive impairment of function or destruction of one of the photoreceptor cell types of the vertebrate retina, in which the photopigment is in stacks of membranous disks separate from the outer cell membrane" [MESH:A08.663.650.650.670.650] |
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Allelic Composition: Apoa1tm1Unc/Apoa1tm1Unc,Tg(APOA2)3Rub/0 Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0008518 | retinal outer nuclear layer degeneration | "a retrogressive impairment or destruction of the retinal layer that contains the nuclei and cell bodies of rods and cones" [MGI:monikat "Monika Tomczuk, Mouse Genome Informatics Curator"] |
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Allelic Composition: Gngt1tm1Ogk/Gngt1tm1Ogk Genetic Background: involves: 129
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MP:0008587 | short photoreceptor outer segment | "decreased length of the photoreceptor region that is rich in the visual pigment rhodopsin" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Apoa1tm1Unc/Apoa1tm1Unc,Tg(APOA2)3Rub/0 Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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