MP:0000753 | paralysis | "loss of power of voluntary movement in a muscle through injury or disease of its nerve supply" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Dctn1tm1.1Cai/Dctn1tm1.1Cai Genetic Background: involves: 129X1/SvJ * C57BL/6 * FVB/N
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MP:0000938 | motor neuron degeneration | "retrogressive impairment of function or destruction of the cells that innervate an effector (muscle or glandular) tissue" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Reltm1Grd/Rel+ Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0001053 | abnormal neuromuscular synapse | "malformed or absent membrane to membrane contact of a motor axon and a muscle myofiber resulting in aberrant transmission of nerve impulses" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:60159, J:47439] |
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Allelic Composition: Reltm1Grd/Rel+ Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0001407 | short stride length | "reduced average distance between steps" [J:34193] |
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Allelic Composition: Reltm1Grd/Rel+ Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0001539 | decreased number of caudal vertebrae | "reduced number of the bony segments of the tail" [Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Dbn1tm1a(KOMP)Wtsi/Dbn1+ Genetic Background: C57BL/6N-Dbn1tm1a(KOMP)Wtsi/Wtsi
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MP:0001695 | abnormal gastrulation | "anomalous development and invagination of the embryonic germ layers" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Reltm1Grd/Rel+ Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0001730 | embryonic growth arrest | "the cessation of development beyond a particular stage" [J:17509] |
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Allelic Composition: Reltm1Grd/Rel+ Genetic Background: involves: 129S1/Sv * C57BL/6
Allelic Composition: Dctn1tm1.1Cai/Dctn1tm1.1Cai Genetic Background: involves: 129X1/SvJ * C57BL/6 * FVB/N
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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: Reltm1Grd/Rel+ Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0005553 | increased circulating creatinine level | "greater than the normal blood concentration of this product of creatine catabolism; abnormal levels indicative of renal dysfunction" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, RGD:Rat Genome Database submission] |
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Allelic Composition: Dbn1tm1a(KOMP)Wtsi/Dbn1+ Genetic Background: C57BL/6N-Dbn1tm1a(KOMP)Wtsi/Wtsi
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MP:0006042 | increased apoptosis | "greater than normal programmed cell death" [RGD:Rat Genome Database submission, smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Reltm1Grd/Rel+ Genetic Background: involves: 129S1/Sv * C57BL/6
Allelic Composition: Dctn1tm1.1Cai/Dctn1tm1.1Cai Genetic Background: involves: 129X1/SvJ * C57BL/6 * FVB/N
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MP:0006386 | absent somites | "missing all somites" [MGI:rbabiuk "Randall Babiuk, Mouse Genome Informatics Curator"] |
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Allelic Composition: Reltm1Grd/Rel+ Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0010845 | decreased effector memory CD4-positive, alpha-beta T cell number | "reduced number of CD4-positive, alpha-beta memory T cells with the phenotype CCR7-negative, CD127-positive, CD45RO-positive, and CD25-negative" [CL:0000905, GO_REF:0000031, GOC:add, GOC:pam, GOC:tfm] |
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Allelic Composition: Dbn1tm1a(KOMP)Wtsi/Dbn1+ Genetic Background: C57BL/6N-Dbn1tm1a(KOMP)Wtsi/Wtsi
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MP:0011092 | complete embryonic lethality | "death of all organisms of a given genotype in a population within the embryonic period prior to organogenesis (Mus: prior to E14)" [MGI:csmith] |
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Allelic Composition: Reltm1Grd/Rel+ Genetic Background: involves: 129S1/Sv * C57BL/6
Allelic Composition: Dctn1tm1.1Cai/Dctn1tm1.1Cai Genetic Background: involves: 129X1/SvJ * C57BL/6 * FVB/N
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MP:0011100 | complete preweaning lethality | "death of all organisms of a given genotype in a population between fertilization and weaning age (Mus: approximately 3-4 weeks of age)" [MGI:csmith] |
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Allelic Composition: Dbn1tm1b(KOMP)Wtsi/Dbn1tm1b(KOMP)Wtsi Genetic Background: C57BL/6N-Dbn1tm1b(KOMP)Wtsi/Wtsi
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