MP:0000351 | increased cell proliferation | "greater than the normal growth and reproduction of similar cells" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: KitW-27H/KitW-27H Genetic Background: CBA/H-KitW-27H
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MP:0000604 | amyloidosis | "an accumulation of extracellular amyloid in tissues of the body" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Mapk14tm1Nbr/Mapk14tm1Nbr Genetic Background: either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)
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MP:0000745 | tremors | "repetitive, cyclical movements of the body or a body part; usually involuntary, but can also manifest in response to an attempt at movement" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Notch1tm2Agt/Notch1tm2Agt Genetic Background: involves: 129/Sv * C57BL/6
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MP:0000774 | reduced brain size | "smaller appearance of the brain" [J:35802] |
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Allelic Composition: Bdnftm1Yab/Bdnftm1Yab,Mapttm1(cre)Nagy/Mapt+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0000812 | abnormal dentate gyrus morphology | "absence or malformation of one of two interlocking gyri of the hippocampus that contains granule cells, which project to the pyramidal cells and interneurons of the CA3 region of the ammon gyrus" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:38857] |
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Allelic Composition: Mapttm3(Hdac2)Jae/Mapttm3(Hdac2)Jae Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0000846 | abnormal medulla oblongata | "anomaly in the most caudal region of the brainstem that lies directly rostral to the spinal cord; includes regions responsible for autonomic functions such as digestion, breathing and control of heart rate" [Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3] |
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Allelic Composition: Kif3atm2Gsn/Kif3atm2Gsn,Tg(Col2a1-cre)1Bhr/? Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
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MP:0000859 | abnormal somatosensory cortex morphology | "any malformation or absence of the area of the parietal lobe that lies posterior to the central sulcus and is concerned with receiving and processing general sensations from the body surface" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Pclotm3.3Sud/Pclotm3.3Sud Genetic Background: involves: 129S1/Sv * 129X1/SvJ
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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: Sf3b1tm1.1Mdf/Sf3b1+,Tet2tm1.1Iaai/Tet2tm1.1Iaai,Tg(Mx1-cre)1Cgn/? Genetic Background: involves: 129S/SvEv * 129S4/SvJae * C57BL/6 * CBA/J
Allelic Composition: Mapttm2.1(FUS)Neas/Mapt+ Genetic Background: B6J.129P2(129S)-Mapttm2.1(FUS)Neas
Allelic Composition: Chattm2(cre)Lowl/Chat+,Mapttm3(FUS)Neas/Mapt+ Genetic Background: B6.129-Mapttm3(FUS)Neas Chattm2(cre)Lowl
Allelic Composition: Mapttm3.1(FUS)Neas/Mapt+ Genetic Background: B6J.129P2(129S)-Mapttm3.1(FUS)Neas
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MP:0000940 | abnormal motor neuron innervation | "misprojection or failure to bundle motor axons to an effector tissue" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:60159] |
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Allelic Composition: Rasgrf1tm1Toc/Rasgrf1tm1Toc Genetic Background: involves: 129/Sv
Allelic Composition: Mapttm2.1(FUS)Neas/Mapt+ Genetic Background: B6J.129P2(129S)-Mapttm2.1(FUS)Neas
Allelic Composition: Mapttm3.1(FUS)Neas/Mapt+ Genetic Background: B6J.129P2(129S)-Mapttm3.1(FUS)Neas
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MP:0000955 | abnormal spinal cord morphology | "malformation or disorganization of the cylindrical tissue of the vertebral canal that extends from the medulla oblongata to the conus medullaris" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Ctla4tm1All/Ctla4tm1All,Tg(TcraBDC2.5,TcrbBDC2.5)1Doi/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * NOD * SJL
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MP:0000961 | abnormal dorsal root ganglia morphology | "malformed group of nerve cell bodies of each segmental nerve projecting from the spinal cord " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:60159] |
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Allelic Composition: Etv1tm2Tmj/Etv1tm2Tmj Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6
Allelic Composition: Mapttm2Arbr/Mapt+,Pvalbtm1(cre)Arbr/Pvalb+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0000965 | abnormal sensory neuron morphology | "malformation or absence of cells that innervate an effector (muscle or glandular) tissue; responsible for transmission of sensory impulses" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:60159] |
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Allelic Composition: Etv1tm2Tmj/Etv1tm2Tmj Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6
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MP:0000968 | abnormal sensory neuron innervation | "defective or incomplete supply of nerve fibers to sensory termini or to spinal cord" [J:31622] |
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Allelic Composition: Etv1tm2Tmj/Etv1tm2Tmj Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6
Allelic Composition: Mapttm1(Sema3e)Yuyo/Mapt+,Olig2tm1(cre)Tmj/Olig2+ Genetic Background: Not Specified
Allelic Composition: Cbfbtm2.1Ddg/Cbfbtm2.1Ddg,Mapttm2Arbr/?,H2afvTg(Wnt1-cre)11Rth/? Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * CBA/J
Allelic Composition: Mapttm2Arbr/?,Runx1tm3Spe/Runx1tm3Spe,H2afvTg(Wnt1-cre)11Rth/? Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J * CBA/J
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MP:0000969 | abnormal nociceptor morphology | "anomalous structure of any of the peripheral receptors for pain, including receptors sensitive to painful mechanical stimuli, extreme heat or cold, and chemical stimuli" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Cbfbtm2.1Ddg/Cbfbtm2.1Ddg,Mapttm2Arbr/?,H2afvTg(Wnt1-cre)11Rth/? Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * CBA/J
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MP:0000972 | abnormal mechanoreceptor morphology | "anomaly in the receptors of the body, usually nerve termini, that respond to mechanical pressure or distortion" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:34172] |
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Allelic Composition: Cbfbtm2.1Ddg/Cbfbtm2.1Ddg,H2afvTg(Wnt1-cre)11Rth/? Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * CBA/J
Allelic Composition: Mapttm2Arbr/?,Runx1tm3Spe/Runx1tm1(cre/Esr1*)Ims Genetic Background: involves: 129S4/SvJae * C57BL/6NCrlj * CBA/JNCrlj
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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: Chattm2(cre)Lowl/Chat+,Mapttm2(FUS)Neas/Mapt+ Genetic Background: B6.129-Mapttm2(FUS)Neas Chattm2(cre)Lowl
Allelic Composition: Mapttm2.1(FUS)Neas/Mapt+ Genetic Background: B6J.129P2(129S)-Mapttm2.1(FUS)Neas
Allelic Composition: Chattm2(cre)Lowl/Chat+,Mapttm3(FUS)Neas/Mapt+ Genetic Background: B6.129-Mapttm3(FUS)Neas Chattm2(cre)Lowl
Allelic Composition: Mapttm3.1(FUS)Neas/Mapt+ Genetic Background: B6J.129P2(129S)-Mapttm3.1(FUS)Neas
Allelic Composition: Mapttm3.1(FUS)Neas/Mapttm3.1(FUS)Neas Genetic Background: B6J.129P2(129S)-Mapttm3.1(FUS)Neas
Allelic Composition: Fustm1a(EUCOMM)Wtsi/Fustm1c(EUCOMM)Wtsi,Mapttm3.1(FUS)Neas/Mapt+,Ndor1Tg(UBC-cre/ERT2)1Ejb/0 Genetic Background: involves: 129 * C3H * C57BL/6 * C57BL/6N
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MP:0001260 | increased body weight | "greater than normal average weight " [J:33400] |
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Allelic Composition: Bdnftm1Yab/Bdnftm1Yab,Mapttm1(cre)Nagy/Mapt+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0001262 | decreased body weight | "lower than normal average weight " [J:61295] |
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Allelic Composition: Bdnftm1Yab/Bdnftm1Yab,Mapttm1(cre)Nagy/Mapt+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Allelic Composition: Mapttm1(Mecp2)Jae/Mapttm1(Mecp2)Jae Genetic Background: B6.Cg-Mapttm1(Mecp2)Jae
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MP:0001289 | persistence of hyaloid capillary system | "failure of the degeneration of the transient vascular system of the eye during development" [J:49840] |
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Allelic Composition: Mapkap1tm1b(EUCOMM)Wtsi/Mapkap1tm1b(EUCOMM)Wtsi Genetic Background: C57BL/6N-Mapkap1tm1b(EUCOMM)Wtsi/Bay
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MP:0001304 | cataracts | "complete or partial opacity of the lens" [J:65031] |
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Allelic Composition: Notch1tm2Agt/Notch1tm2Agt Genetic Background: involves: 129/Sv * C57BL/6
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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: Mapkap1tm1b(EUCOMM)Wtsi/Mapkap1tm1b(EUCOMM)Wtsi Genetic Background: C57BL/6N-Mapkap1tm1b(EUCOMM)Wtsi/Bay
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MP:0001330 | abnormal optic nerve morphology | "malformation, misprojection or atrophy in the second cranial nerve which is responsible for conveying visual information from the retina to the brain" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Bdnftm1Yab/Bdnftm1Yab,Mapttm1(cre)Nagy/Mapt+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0001363 | increased anxiety-related response | "when compared to controls, subjects exhibit more responses thought to be indicative of anxiety in behavioral tests" [cwg:Carroll-Ann W. Goldsmith, Mouse Genome Informatics curator, J:49752, J:53060] |
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Allelic Composition: Dok2tm1Ppp/Dok2+ Genetic Background: 129S1/Sv-Dok2tm1Ppp
Allelic Composition: Mapttm1(Mecp2)Jae/Mapttm1(Mecp2)Jae Genetic Background: B6.Cg-Mapttm1(Mecp2)Jae
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MP:0001364 | decreased anxiety-related response | "when compared to controls, subjects exhibit fewer responses thought to be indicative of anxiety in behavioral tests" [cwg:Carroll-Ann W. Goldsmith, Mouse Genome Informatics curator, J:86626, J:85438, J:64043] |
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Allelic Composition: KitW-27H/KitW-27H Genetic Background: CBA/H-KitW-27H
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MP:0001393 | ataxia | "inability to coordinate voluntary muscular movements" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:67231] |
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Allelic Composition: Notch1tm2Agt/Notch1tm2Agt Genetic Background: involves: 129/Sv * C57BL/6
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MP:0001399 | hyperactivity | "general restlessness or excessive movement; more frequent movement from one place to another" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409, J:57125] |
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Allelic Composition: Arntltm1.1Ljm/Arntltm1.1Ljm,Tmem163Tg(ACTB-cre)2Mrt/0 Genetic Background: involves: C57BL/6 * FVB/N
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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: Ctla4tm1All/Ctla4tm1All,Tg(TcraBDC2.5,TcrbBDC2.5)1Doi/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * NOD * SJL
Allelic Composition: Mapttm1(Setdb1)Akba/Mapt+,Mecp2tm1Jae/Y,Tg(Nes-cre)1Atp/0 Genetic Background: involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6 * FVB/N
Allelic Composition: Mapttm1(Setdb1)Akba/Mapttm1(Setdb1)Akba,Mecp2tm1Jae/Y,Tg(Nes-cre)1Atp/0 Genetic Background: involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6 * FVB/N
Allelic Composition: Mapttm1(Mecp2)Jae/Mapttm1(Mecp2)Jae Genetic Background: B6.Cg-Mapttm1(Mecp2)Jae
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MP:0001412 | excessive scratching | "compulsive scraping of the skin, usually with the nails" [J:61340] |
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Allelic Composition: Notch1tm2Agt/Notch1tm2Agt Genetic Background: involves: 129/Sv * C57BL/6
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MP:0001454 | abnormal cued conditioning behavior | "defect in the ability of an animal to learn and remember an association between an an aversive experience (the unconditioned stimulus (US), ususally a shock) and a neutral stimulus (the conditioned stimulus (CS), usually an auditory cue or light)" [CFG:Center for Functional Genomics , Northwestern University] |
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Allelic Composition: Mapttm1(Mecp2)Jae/Mapttm1(Mecp2)Jae Genetic Background: B6.Cg-Mapttm1(Mecp2)Jae
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MP:0001458 | abnormal object recognition memory | "defects in the ability to recognize objects that the animal has previously encountered; recognition is measured by relative amount of time exploring objects, which should decrease upon subsequent or multiple presentations of the same object when presented with novel objects at the same time" [CFG:Center for Functional Genomics , Northwestern University] |
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Allelic Composition: Mapttm1(Mecp2)Jae/Mapttm1(Mecp2)Jae Genetic Background: B6.Cg-Mapttm1(Mecp2)Jae
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MP:0001463 | abnormal spatial learning | "defects in the abilibity to navigate using behavioraly meaningful locations" [CFG:Center for Functional Genomics , Northwestern University] |
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Allelic Composition: Mapttm1Hnd/Mapt+,Zbtb20Tg(PDGFB-APPSwInd)20Lms/0 Genetic Background: involves: 129X1/SvJ * C57BL/6 * DBA/2
Allelic Composition: Mapttm3(Hdac2)Jae/Mapttm3(Hdac2)Jae Genetic Background: involves: 129S4/SvJae * C57BL/6
Allelic Composition: Mapttm1(EGFP)Klt/Mapttm1(EGFP)Klt,Tg(MAPT)8cPdav/0 Genetic Background: B6.Cg-Mapttm1(EGFP)Klt Tg(MAPT)8cPdav/J
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MP:0001469 | abnormal contextual conditioning | "defect in the ability of an animal to learn and remember an association between an an aversive experience (the unconditioned stimulus (US), ususally a shock) and a neutral stimulus (the conditioned stimulus (CS), or the environmental context in this case)" [CFG:Center for Functional Genomics , Northwestern University] |
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Allelic Composition: Mapttm1(Mecp2)Jae/Mapttm1(Mecp2)Jae Genetic Background: B6.Cg-Mapttm1(Mecp2)Jae
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MP:0001473 | reduced long term potentiation | "less than the normal persistent robust synaptic response induced by synchronous stimulation of pre- and postsynaptic cells " [Principles of Neural Science:ISBN 0-8385-8034-3] |
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Allelic Composition: Bdnftm1Msd/Bdnftm1Msd,Mapttm1(cre)Nagy/Mapt+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Allelic Composition: Mapttm3(Hdac2)Jae/Mapttm3(Hdac2)Jae Genetic Background: involves: 129S4/SvJae * C57BL/6
Allelic Composition: Mapttm1(Mecp2)Jae/Mapttm1(Mecp2)Jae Genetic Background: B6.Cg-Mapttm1(Mecp2)Jae
Allelic Composition: Mapttm1(EGFP)Klt/Mapttm1(EGFP)Klt Genetic Background: B6.129S4-Mapttm1(EGFP)Klt
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MP:0001511 | disheveled coat | "coat that looks generally unkempt" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Notch1tm2Agt/Notch1tm2Agt Genetic Background: involves: 129/Sv * C57BL/6
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MP:0001513 | limb grasping | "mice clasp front and/or hind feet almost immediately upon being lifted by tail" [cml:Cathleen M. Lutz , Mouse Genome Informatics Curator] |
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Allelic Composition: Bdnftm1Yab/Bdnftm1Yab,Mapttm1(cre)Nagy/Mapt+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0001516 | abnormal motor coordination/ balance | "altered ability of an animal to maintain skillful and effective interaction of movements or maintenance of equilibrium" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Rps6kb1tm1Gtho/Rps6kb1tm1Gtho Genetic Background: involves: 129P2/OlaHsd
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MP:0001525 | impaired balance | "reduced ability of an animal to maintain equilibrium" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:64962, J:17123] |
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Allelic Composition: Notch1tm2Agt/Notch1tm2Agt Genetic Background: involves: 129/Sv * C57BL/6
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MP:0001732 | postnatal growth retardation | "slow or limited development after birth " [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Notch1tm2Agt/Notch1tm2Agt Genetic Background: involves: 129/Sv * C57BL/6
Allelic Composition: Bdnftm1Yab/Bdnftm1Yab,Mapttm1(cre)Nagy/Mapt+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0002062 | abnormal conditioning behavior | "inability to change the frequency or form of a behavior as a result of the influence of the environment " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Dido1tm1Cmar/Dido1tm2Cmar Genetic Background: involves: 129S1/Sv * 129X1/SvJ
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MP:0002081 | perinatal lethality | "death anytime between E18.5 and postnatal day 1 " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Gt(ROSA)26Sortm2.1(CAG-EGFP,-DTA*G128D)Pjen/Gt(ROSA)26Sortm2.1(CAG-EGFP,-DTA*G128D)Pjen Genetic Background: B6.Cg-Gt(ROSA)26Sortm2.1(CAG-EGFP,-DTA*G128D)Pjen/J
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MP:0002083 | premature death | "death after 3 weeks of age, but before normal life span" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Ctla4tm1All/Ctla4tm1All,Tg(TcraBDC2.5,TcrbBDC2.5)1Doi/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * NOD * SJL
Allelic Composition: Mapttm1(Setdb1)Akba/Mapt+,Mecp2tm1Jae/Y,Tg(Nes-cre)1Atp/0 Genetic Background: involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6 * FVB/N
Allelic Composition: Mapttm1(Setdb1)Akba/Mapttm1(Setdb1)Akba,Mecp2tm1Jae/Y,Tg(Nes-cre)1Atp/0 Genetic Background: involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6 * FVB/N
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MP:0002152 | abnormal brain morphology | "anomalous structure of or abnormal development of the brain, one of the two components of the central nervous system and the center of thought and emotion; controls coordination, bodily activities and the interpretation of information from the senses (sight, hearing, smell, etc.)" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, http://cancerweb.ncl.ac.uk] |
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Allelic Composition: Ctla4tm1All/Ctla4tm1All,Tg(TcraBDC2.5,TcrbBDC2.5)1Doi/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * NOD * SJL
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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: Pafah1b1tm1Awb/Pafah1b1+,Ywhaetm1Awb/Ywhae+ Genetic Background: either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * NIH Black Swiss)
Allelic Composition: Mapttm1(Mecp2)Jae/Mapt+ Genetic Background: involves: 129/Sv * C57BL/6
Allelic Composition: Mapttm3(cre/PGR)Aha/Mapttm3(cre/PGR)Aha Genetic Background: Not Specified
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MP:0002175 | low brain weight | "lower than average weight of the brain" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Bdnftm1Yab/Bdnftm1Yab,Mapttm1(cre)Nagy/Mapt+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0002356 | abnormal spleen red pulp morphology | "anomalous structure of the area of the spleen that screens and eliminates defective or foreign cells" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Pathology:ISBN 0-397-51047-0] |
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Allelic Composition: Mapk14tm1Nbr/Mapk14tm1Nbr Genetic Background: either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)
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MP:0002566 | abnormal sexual interaction | "altered initiation, failure of initiation or incomplete mating behavior" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Notch1tm2Agt/Notch1tm2Agt Genetic Background: involves: 129/Sv * C57BL/6
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MP:0002651 | abnormal sciatic nerve | "malformation, absence or misprojection of the nerve which originates in the lumbar and sacral spinal cord (L4 to S3) and supplies motor and sensory innervation to the lower extremity" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Ctla4tm1All/Ctla4tm1All,Tg(TcraBDC2.5,TcrbBDC2.5)1Doi/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * NOD * SJL
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MP:0002792 | abnormal retinal vascularization | "malformation or disorganization of the blood vessels supplying the retina" [cml:Cathleen M. Lutz , Mouse Genome Informatics Curator] |
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Allelic Composition: Mapkap1tm1b(EUCOMM)Wtsi/Mapkap1tm1b(EUCOMM)Wtsi Genetic Background: C57BL/6N-Mapkap1tm1b(EUCOMM)Wtsi/Bay
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MP:0002801 | abnormal long-term recognition memory | "defects in long-term memory for objects that is consolidated over hours and days after training." [CFG:Center for Functional Genomics , Northwestern University] |
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Allelic Composition: KitW-27H/KitW-27H Genetic Background: CBA/H-KitW-27H
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MP:0002804 | abnormal motor learning | "defects in the ability to repeat a motor task requiring well coordinated movements and balance; measures cerebellar dependent learning" [CFG:Center for Functional Genomics , Northwestern University] |
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Allelic Composition: Mapttm1(EGFP)Klt/Mapttm1(EGFP)Klt Genetic Background: B6.129S4-Mapttm1(EGFP)Klt
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MP:0002882 | abnormal neuron | "anomaly in the functional cells of the nervous system that receive, conduct, and transmit impulses " [MeSH:National Library of Medicine - Medical Subject Headings, 2003] |
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Allelic Composition: Mapk14tm1Nbr/Mapk14tm1Nbr Genetic Background: either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)
Allelic Composition: Lbx1tm2Cbm/Lbx1tm3.1(cre)Cbm,Mapttm2Arbr/Mapt+ Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: Mapttm1Hnd/Mapttm1Hnd,Zbtb20Tg(PDGFB-APPSwInd)20Lms/0 Genetic Background: involves: 129X1/SvJ * C57BL/6 * DBA/2
Allelic Composition: Mapttm1Hnd/Mapt+,Zbtb20Tg(PDGFB-APPSwInd)20Lms/0 Genetic Background: involves: 129X1/SvJ * C57BL/6 * DBA/2
Allelic Composition: Bdnftm1Yab/Bdnftm1Yab,Mapttm1(cre)Nagy/Mapt+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0002887 | resistance to pharmacologically induced seizures | "ability to withstand doses of pharmacological drugs that induce seizure activity in normal animals" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, J:77284] |
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Allelic Composition: Mapttm1Hnd/Mapttm1Hnd,Zbtb20Tg(PDGFB-APPSwInd)20Lms/0 Genetic Background: involves: 129X1/SvJ * C57BL/6 * DBA/2
Allelic Composition: Mapttm1Hnd/Mapt+,Zbtb20Tg(PDGFB-APPSwInd)20Lms/0 Genetic Background: involves: 129X1/SvJ * C57BL/6 * DBA/2
Allelic Composition: Mapttm1Hnd/Mapt+ Genetic Background: involves: 129X1/SvJ * C57BL/6
Allelic Composition: Mapttm1Hnd/Mapttm1Hnd Genetic Background: involves: 129X1/SvJ * C57BL/6
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MP:0002912 | abnormal excitatory postsynaptic potential | "defect in the potential detected in postsynaptic cells when an excitatory impulse arrives at the synapse causing depolarization" [Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3] |
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Allelic Composition: Mapttm1(Sema3e)Yuyo/Mapt+,Olig2tm1(cre)Tmj/Olig2+ Genetic Background: Not Specified
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MP:0002915 | abnormal synaptic depression | "changes in the duration of the reduction of effectiveness of synaptic connections between neurons and target after repetitive stimulation" [Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3] |
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Allelic Composition: Mapttm3.1(FUS)Neas/Mapt+ Genetic Background: B6J.129P2(129S)-Mapttm3.1(FUS)Neas
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MP:0002919 | enhanced paired-pulse facilitation | "increase in the response of central synapses when activated twice in rapid succession; indicative of defects in short-term plasticity due to greater increase of neurotransmitter release at the second stimulus" [Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3] |
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Allelic Composition: Mapttm1(Mecp2)Jae/Mapttm1(Mecp2)Jae Genetic Background: B6.Cg-Mapttm1(Mecp2)Jae
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MP:0002948 | abnormal neuronal specification | "defects in the developmental patterning of neurons resulting in ectopic placement, decreased numbers or absence of mature neurons" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, J:87948] |
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Allelic Composition: Lbx1tm2Cbm/Lbx1tm3.1(cre)Cbm,Mapttm2Arbr/Mapt+ Genetic Background: involves: 129P2/OlaHsd
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MP:0003083 | abnormal tibialis anterior morphology | "anomaly in the the muscle of the shin that is responsible for dorsiflexion and inversion of the foot" [smb:Susan M. Bello, Mouse Genome Informatics Curator, Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Mapttm3.1(FUS)Neas/Mapt+ Genetic Background: B6J.129P2(129S)-Mapttm3.1(FUS)Neas
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MP:0003204 | decreased neuron apoptosis | "decrease in the number of neurons undergoing programmed cell death" [RGD:Rat Genome Database submission] |
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Allelic Composition: Pclotm3.3Sud/Pclotm3.3Sud Genetic Background: involves: 129S1/Sv * 129X1/SvJ
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MP:0003214 | neurofibrillary tangles | "dense intraneuronal accumulations of helical filaments (neurofilaments and microtubules) that assume twisted contorted patterns; found in subclasses of cells of the neocortex, hippocampus, brain stem, and diencephalon in individuals with Alzheimer disease" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, MeSH:National Library of Medicine - Medical Subject Headings , 2003, RGD:Rat Genome Database submission] |
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Allelic Composition: Ctla4tm1All/Ctla4tm1All,Tg(TcraBDC2.5,TcrbBDC2.5)1Doi/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * NOD * SJL
Allelic Composition: Mapttm1(EGFP)Klt/Mapttm1(EGFP)Klt,Tg(MAPT)8cPdav/0 Genetic Background: B6.Cg-Mapttm1(EGFP)Klt Tg(MAPT)8cPdav/J
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MP:0003313 | abnormal locomotor activation | "altered ability or desire of an animal to initiate locomotor activity" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Bdnftm1Yab/Bdnftm1Yab,Mapttm1(cre)Nagy/Mapt+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0003329 | amyloid beta deposits | |
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Allelic Composition: Mapttm1Hnd/Mapttm1Hnd,Zbtb20Tg(PDGFB-APPSwInd)20Lms/0 Genetic Background: involves: 129X1/SvJ * C57BL/6 * DBA/2
Allelic Composition: Mapttm1Hnd/Mapt+,Zbtb20Tg(PDGFB-APPSwInd)20Lms/0 Genetic Background: involves: 129X1/SvJ * C57BL/6 * DBA/2
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MP:0003354 | astrocytosis | "a proliferation or spread of astrocytes in the area of a degenerative lesion or damaged tissue" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Mapttm2.1(FUS)Neas/Mapt+ Genetic Background: B6J.129P2(129S)-Mapttm2.1(FUS)Neas
Allelic Composition: Mapttm3.1(FUS)Neas/Mapt+ Genetic Background: B6J.129P2(129S)-Mapttm3.1(FUS)Neas
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MP:0003633 | abnormal nervous system physiology | |
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Allelic Composition: Mapttm2Arbr/Mapt+,Shox2tm1.1(cre)Oki/Shox2+,Slc17a6tm1.1Thna/Slc17a6tm1.2Edw Genetic Background: involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6J
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MP:0003635 | abnormal synaptic transmission | "defect in the communication from a neuron to a target across a synapse " [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Mapttm3.1(FUS)Neas/Mapt+ Genetic Background: B6J.129P2(129S)-Mapttm3.1(FUS)Neas
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MP:0003651 | abnormal axon outgrowth | "defect/abnormality in the ability of an axon to extend from a neuron cell body" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator, J:96121] |
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Allelic Composition: Baxtm1Sjk/Baxtm1Sjk Genetic Background: involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6
Allelic Composition: Mapttm1Hnd/Mapttm1Hnd Genetic Background: involves: 129X1/SvJ * C57BL/6
Allelic Composition: Mapttm1(MAPT)Vln/Mapttm1(MAPT)Vln Genetic Background: involves: FVB/N
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MP:0003935 | abnormal craniofacial development | "anomaly in the process of forming the face and/or cranium" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Cbfbtm2.1Ddg/Cbfbtm2.1Ddg,Mapttm2Arbr/?,H2afvTg(Wnt1-cre)11Rth/? Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * CBA/J
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MP:0003960 | increased lean body mass | "more than average fat-free physical bulk or volume of the body including all its components except adipose tissue" [honda:Hiraoki Onda, Mouse GEnome Informatics Curator] |
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Allelic Composition: Mapkap1tm1b(EUCOMM)Wtsi/Mapkap1tm1b(EUCOMM)Wtsi Genetic Background: C57BL/6N-Mapkap1tm1b(EUCOMM)Wtsi/Bay
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MP:0004090 | abnormal sarcomere morphology | "any structural abnormality in the segment of a myofibril between two Z lines comprised of multi-protein complexes composed of three different filament systems; these systems work together to contract and relax muscle" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator] |
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Allelic Composition: Mapttm3.1(FUS)Neas/Mapt+ Genetic Background: B6J.129P2(129S)-Mapttm3.1(FUS)Neas
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MP:0004250 | tau protein deposits | "formation of self-assembled tangles of paired helical filaments and straight filaments due to hyperphosphorylation of the tau protein; often seen in neuronal tissues of individuals with neurodegenerative disorders" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Mapk14tm1Nbr/Mapk14tm1Nbr Genetic Background: either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)
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MP:0004753 | abnormal miniature excitatory postsynaptic currents | "defect in the size or duration of spontaneous currents detected in postsynaptic cells that occur in the absence of an excitatory impulse" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Mapttm1(Mecp2)Jae/Mapttm1(Mecp2)Jae Genetic Background: B6.Cg-Mapttm1(Mecp2)Jae
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MP:0004768 | abnormal axonal transport | "any functional anomaly of the directed movement of organelles or vesicles along microtubules in nerve cell axons" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Arntltm1.1Ljm/Arntltm1.1Ljm,Tmem163Tg(ACTB-cre)2Mrt/0 Genetic Background: involves: C57BL/6 * FVB/N
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MP:0004924 | abnormal behavior | "anomalies in the actions, reactions, or performance of an organism in response to external or internal stimuli compared to controls" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Mapkap1tm1b(EUCOMM)Wtsi/Mapkap1tm1b(EUCOMM)Wtsi Genetic Background: C57BL/6N-Mapkap1tm1b(EUCOMM)Wtsi/Bay
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MP:0005150 | cachexia | "general weight loss and wasting occurring in the course of chronic disease" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Notch1tm2Agt/Notch1tm2Agt Genetic Background: involves: 129/Sv * C57BL/6
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MP:0005277 | abnormal brainstem morphology | "anomalous structure of the midbrain, pons, or medulla" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:82670] |
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Allelic Composition: Kif3atm2Gsn/Kif3atm2Gsn,Tg(Col2a1-cre)1Bhr/? Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
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MP:0005325 | abnormal glomerulus | "anomalous structure of the capillary loops of the kidney that normally function as a filtration unit" [J:57971, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Mapk14tm1Nbr/Mapk14tm1Nbr Genetic Background: either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)
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MP:0005404 | abnormal axon morphology | "anomaly in the structure of the single process of a nerve cell that normally conducts impulses away from the cell body" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Irs1tm1Tka/Irs1tm1Tka Genetic Background: Not Specified
Allelic Composition: Mapttm1Aha/Mapttm1Aha Genetic Background: Not Specified
Allelic Composition: Cbfbtm2.1Ddg/Cbfbtm2.1Ddg,Mapttm2Arbr/?,H2afvTg(Wnt1-cre)11Rth/? Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * CBA/J
Allelic Composition: Mapttm2Arbr/?,Runx1tm3Spe/Runx1tm3Spe,H2afvTg(Wnt1-cre)11Rth/? Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J * CBA/J
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MP:0006006 | increased sensory neuron number | "greater than normal numbers of cells that innervate an effector (muscle or glandular) tissue" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Lbx1tm2Cbm/Lbx1tm3.1(cre)Cbm,Mapttm2Arbr/Mapt+ Genetic Background: involves: 129P2/OlaHsd
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MP:0008143 | abnormal dendrite morphology | "any structural anomaly of the highly branched tree-like process of a neuron that serves as a receptive field and conducts impulses toward the cell body" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", MGI:rbabiuk "Randall Babiuk, Mouse Genome Informatics Curator"] |
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Allelic Composition: Mapttm1Hnd/Mapttm1Hnd Genetic Background: involves: 129X1/SvJ * C57BL/6
Allelic Composition: Mapttm1(MAPT)Vln/Mapttm1(MAPT)Vln Genetic Background: involves: FVB/N
Allelic Composition: Bdnftm1Yab/Bdnftm1Yab,Mapttm1(cre)Nagy/Mapt+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0008263 | abnormal hippocampus CA1 region morphology | |
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Allelic Composition: Mapttm3(Hdac2)Jae/Mapttm3(Hdac2)Jae Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0008282 | enlarged hippocampus | "increased size of the deep lying structure of the cerebrum involved with memory storage and spatial navigation" [ISBN:0-12-402035-6 "Kaufman, MH The Atlas of Mouse Development", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Mapttm1(MAPT)Vln/Mapttm1(MAPT)Vln Genetic Background: involves: FVB/N
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MP:0008428 | abnormal spatial working memory | "anomaly in the ability to spontaneously process spatial location information in order to naviagate or perform other behavior using such locational cues, without previous encounters or training at that location" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Mapttm3(Hdac2)Jae/Mapttm3(Hdac2)Jae Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0008470 | abnormal spleen B cell follicle morphology | "any structural anomaly of the area of the white pulp where the affinity maturation of B cells and the generation of memory B cells and plasma cells occur" [PMID:17495967] |
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Allelic Composition: Mapk14tm1Nbr/Mapk14tm1Nbr Genetic Background: either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)
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MP:0008486 | decreased muscle spindle number | "reduced number of the sensory organs in muscle that are involved in the stretch reflex" [ISBN:0838580343 "Kandel ER, et al. Principles of Neural Science, 3rd edition"] |
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Allelic Composition: Etv1tm2Tmj/Etv1tm2Tmj Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6
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MP:0008528 | polycystic kidney | "the development of innumerable cysts in the kidneys filled with fluid replacing much of the mass of the kidneys leading to reduction in kidney function and frequently kidney failure" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
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Allelic Composition: Mapkap1tm1b(EUCOMM)Wtsi/Mapkap1tm1b(EUCOMM)Wtsi Genetic Background: C57BL/6N-Mapkap1tm1b(EUCOMM)Wtsi/Bay
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MP:0008571 | abnormal synaptic bouton morphology | "any structural anomaly of the knoblike enlargements along the course of axons, or more commonly at the distal terminations of axons which are specialized for the release of neurotransmitters" [MESH:A08.663.542.145.750] |
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Allelic Composition: Mapttm1(Sema3e)Yuyo/Mapt+,Olig2tm1(cre)Tmj/Olig2+ Genetic Background: Not Specified
Allelic Composition: Mapttm3.1(FUS)Neas/Mapt+ Genetic Background: B6J.129P2(129S)-Mapttm3.1(FUS)Neas
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MP:0008918 | microgliosis | "a proliferation or spread of microglia in the area of a degenerative lesion or damaged tissue" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Mapttm2.1(FUS)Neas/Mapt+ Genetic Background: B6J.129P2(129S)-Mapttm2.1(FUS)Neas
Allelic Composition: Mapttm3.1(FUS)Neas/Mapt+ Genetic Background: B6J.129P2(129S)-Mapttm3.1(FUS)Neas
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MP:0008947 | increased neuron number | "greater than normal numbers of the cells of the nervous system that receive, conduct, and transmit impulses" [MESH:A08.663] |
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Allelic Composition: Pclotm3.3Sud/Pclotm3.3Sud Genetic Background: involves: 129S1/Sv * 129X1/SvJ
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MP:0009317 | follicular lymphoma | "malignant lymphoma arising from lymphoid follicular B cells which may be small or large" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Mapk14tm1Nbr/Mapk14tm1Nbr Genetic Background: either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)
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MP:0009434 | paraparesis | "a weakness affecting lower limbs" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
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Allelic Composition: Mapttm3.1(FUS)Neas/Mapt+ Genetic Background: B6J.129P2(129S)-Mapttm3.1(FUS)Neas
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MP:0009454 | impaired contextual conditioning | "decrease in the ability of an animal to learn and remember an association between an aversive experience (the unconditioned stimulus (US), usually a shock) and the neutral, unchanging environment (the conditioned stimulus (CS), or the environmental context in this case)" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Mapttm3(Hdac2)Jae/Mapttm3(Hdac2)Jae Genetic Background: involves: 129S4/SvJae * C57BL/6
Allelic Composition: Mapttm1(EGFP)Klt/Mapttm1(EGFP)Klt Genetic Background: B6.129S4-Mapttm1(EGFP)Klt
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MP:0009456 | impaired cued conditioning behavior | "decrease in the ability of an animal to learn and remember an association between an aversive experience (the unconditioned stimulus (US), usually a shock) and a neutral stimulus (the conditioned stimulus (CS), usually an auditory cue or light flash)" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Mapttm1(EGFP)Klt/Mapttm1(EGFP)Klt Genetic Background: B6.129S4-Mapttm1(EGFP)Klt
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MP:0009937 | abnormal neuron differentiation | "abnormal growth or development of the cells of the nervous system that receive, conduct, and transmit impulses" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Lbx1tm2Cbm/Lbx1tm3.1(cre)Cbm,Mapttm2Arbr/Mapt+ Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: Mapttm1Hnd/Mapttm1Hnd,Zbtb20Tg(PDGFB-APPSwInd)20Lms/0 Genetic Background: involves: 129X1/SvJ * C57BL/6 * DBA/2
Allelic Composition: Mapttm1Hnd/Mapt+,Zbtb20Tg(PDGFB-APPSwInd)20Lms/0 Genetic Background: involves: 129X1/SvJ * C57BL/6 * DBA/2
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MP:0009940 | abnormal hippocampus pyramidal cell morphology | "any structural anomaly of the projection neuron in the pyramidal layer of the hippocampus" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Mapttm1(MAPT)Vln/Mapttm1(MAPT)Vln Genetic Background: involves: FVB/N
Allelic Composition: Mapttm2(Hdac1)Jae/Mapttm2(Hdac1)Jae Genetic Background: involves: 129S4/SvJae * C57BL/6
Allelic Composition: Mapttm3(Hdac2)Jae/Mapttm3(Hdac2)Jae Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0010097 | abnormal retinal blood vessel morphology | "any structural anomaly of the blood vessels supplying the retina" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Mapkap1tm1b(EUCOMM)Wtsi/Mapkap1tm1b(EUCOMM)Wtsi Genetic Background: C57BL/6N-Mapkap1tm1b(EUCOMM)Wtsi/Bay
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MP:0011085 | complete postnatal lethality | "premature death anytime between the neonatal period and weaning age of all organisms of a given genotype in a population (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith] |
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Allelic Composition: Bdnftm1Yab/Bdnftm1Yab,Mapttm1(cre)Nagy/Mapt+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0011965 | decreased total retina thickness | "decreased width of the retina through the center plane" [MGI:csmith] |
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Allelic Composition: Mapkap1tm1b(EUCOMM)Wtsi/Mapkap1tm1b(EUCOMM)Wtsi Genetic Background: C57BL/6N-Mapkap1tm1b(EUCOMM)Wtsi/Bay
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MP:0012306 | enhanced spatial learning | "enhanced ability to ascertain or acquire spatial location information in order to improve navigation or other behavior using such location cues" [MGI:csmith] |
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Allelic Composition: Mapttm1(EGFP)Klt/Mapttm1(EGFP)Klt Genetic Background: B6.129S4-Mapttm1(EGFP)Klt
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MP:0012431 | increased lymphoma incidence | "greater than the expected number of neoplasms characterized by a proliferation of malignant lymphocytes in lymphoid tissue in a specific population in a given time period" [http://orcid.org/0000-0001-5208-3432, MGI:csmith] |
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Allelic Composition: Mapk14tm1Nbr/Mapk14tm1Nbr Genetic Background: either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)
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MP:0012468 | decreased striatum area | "reduced size of a large cluster of dopaminergic nerve cells, consisting of the caudate nucleus and the putamen, that controls movement, balance, and walking" [ISBN:0838580343, MGI:csmith] |
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Allelic Composition: Bdnftm1Yab/Bdnftm1Yab,Mapttm1(cre)Nagy/Mapt+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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