MP:0001005 | abnormal rod morphology | "structural or developmental anomaly of the photoreceptors that contain rhodopsin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Tpmttm1Rlng/Tpmt+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * NMRI
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MP:0001262 | decreased body weight | "lower than normal average weight " [J:61295] |
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Allelic Composition: Tpmttm1Rlng/Tpmt+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * NMRI
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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: Tpmttm1Rlng/Tpmt+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * NMRI
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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: Tpmttm1Rlng/Tpmt+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * NMRI
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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: Tpmttm1Rlng/Tpmt+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * NMRI
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MP:0004022 | abnormal cone electrophysiology | "anomaly in the function of light adapted vision mediated by the cones" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Tpmttm1Rlng/Tpmt+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * NMRI
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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: Tpmttm1Rlng/Tpmt+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * NMRI
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MP:0008446 | decreased retinal cone cell number | "reduced number of one of the photoreceptor cell types in the retina, in which the photopigment is in invaginations of the cell membrane of the outer segment" [MESH:A08.663.650.650.670.100, MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Tpmttm1Rlng/Tpmt+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * NMRI
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MP:0008456 | abnormal retinal rod cell outer segment morphology | "any strucutral anomaly of the retinal rod cell region which contains stacks of membranous discs separate from the outer cell membrane that are rich in the visual pigment rhodopsin" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Tpmttm1Rlng/Tpmt+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * NMRI
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MP:0008515 | thin retinal outer nuclear layer | "reduced thickness 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: Tpmttm1Rlng/Tpmt+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * NMRI
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