MP:0001263 | weight loss | "progressive reduction of body weight below normal average for age" [J:45400] |
Show
Allelic Composition: Draxintm1Htnk/Draxin+ Genetic Background: involves: C57BL/6NCrj * CBA/JNCrj
|
MP:0001388 | abnormal stationary movement | "altered ability or inability to change body posture or shift a body part" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Plxna3tm1Matl/Y,Plxna4tm1Matl/Plxna4tm1Matl Genetic Background: either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1)
|
MP:0001402 | hypoactivity | "reduced movement from one place to another" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, J:64289] |
Show
Allelic Composition: Wnt3avt/Wnt3avt Genetic Background: B6EiC3Sn a/A-Egfrwa2 Wnt3avt/J
Allelic Composition: Park7tm1Cai/Park7tm1Cai Genetic Background: involves: 129X1/SvJ * C57BL/6
|
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] |
Show
Allelic Composition: Fbn1Tsk/Fbn1+ Genetic Background: B6.Cg-Fbn1Tsk +/+ Bloc1s6pa/JKcc
Allelic Composition: Gpx1tm1Ysh/Gpx1tm1Ysh,Prkntm1Shn/Prkntm1Shn,Park7tm1Shn/Park7tm1Shn Genetic Background: B6.Cg-Park7tm1Shn Gpx1tm1Ysh Prkntm1Shn
Allelic Composition: Prkntm1Shn/Prkntm1Shn,Park7tm1Shn/Park7tm1Shn Genetic Background: B6.Cg-Park7tm1Shn Prkntm1Shn
|
MP:0001406 | abnormal gait | "unusual or distinctive way of walking" [J:65038] |
Show
Allelic Composition: Park7tm1Cai/Park7tm1Cai Genetic Background: involves: 129X1/SvJ * C57BL/6
|
MP:0001407 | short stride length | "reduced average distance between steps" [J:34193] |
Show
Allelic Composition: Park7tm1Cai/Park7tm1Cai Genetic Background: involves: 129X1/SvJ * C57BL/6
|
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] |
Show
Allelic Composition: Airetm1.1Doi/Airetm1.1Doi Genetic Background: involves: 129S2/SvPas * C57BL/6 * NOD
|
MP:0001524 | impaired limb coordination | "reduced ability to organize limb movements to execute complex maneuvers, such as walking" [J:64962, MGI:CLS, J:17123] |
Show
Allelic Composition: Wnt3avt/Wnt3avt Genetic Background: B6EiC3Sn a/A-Egfrwa2 Wnt3avt/J
|
MP:0001899 | absent long term depression | "lack of the normal, persistent activity-dependent decrease in synaptic efficacy between neurons, often following slow, weak stimulation of CA1 neurons" [Principles of Neural Science:ISBN 0-8385-8034-3, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Plxna3tm1Matl/Y,Plxna4tm1Matl/Plxna4tm1Matl Genetic Background: either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1)
|
MP:0001905 | abnormal dopamine level | "greater or less than the normal concentration of this catecholamine neurotransmitter, dervied from tyrosine and the precursor to norepinephrine and epinephrine" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
Show
Allelic Composition: Airetm1.1Doi/Airetm1.1Doi Genetic Background: involves: 129S2/SvPas * C57BL/6 * NOD
|
MP:0001906 | increased dopamine level | "greater than the normal concentration of this catecholamine neurotransmitter, dervied from tyrosine and the precursor to norepinephrine and epinephrine" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
Show
Allelic Composition: Wnt3avt/Wnt3avt Genetic Background: B6EiC3Sn a/A-Egfrwa2 Wnt3avt/J
Allelic Composition: Gpx1tm1Ysh/Gpx1tm1Ysh,Prkntm1Shn/Prkntm1Shn,Park7tm1Shn/Park7tm1Shn Genetic Background: B6.Cg-Park7tm1Shn Gpx1tm1Ysh Prkntm1Shn
|
MP:0002066 | abnormal motor capabilities/coordination/movement | "altered ability to coordinate voluntary movement or repetitive, compulsive movements" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Cyp27b1tm1Hfd/Cyp27b1tm1Hfd Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
MP:0002757 | reduced vertical activity | "lesser than average time spent jumping or rearing" [J:82829, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Plxna3tm1Matl/Y,Plxna4tm1Matl/Plxna4tm1Matl Genetic Background: either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1)
Allelic Composition: Park7tm1Xz/Park7tm1Xz Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
|
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] |
Show
Allelic Composition: Park7tm1Cai/Park7tm1Cai Genetic Background: involves: 129X1/SvJ * C57BL/6
|
MP:0003224 | neuron degeneration | "a retrogressive impairment of function or destruction of the functional cells of the nervous system that receive, conduct, and transmit impulses " [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
Show
Allelic Composition: Cyp27b1tm1Hfd/Cyp27b1tm1Hfd Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
MP:0003244 | loss of dopaminergic neurons | "loss of the neurons that utilize dopamine as a neurotransmitter, commonly due to an apoptotic event" [RGD:Rat Genome Database submission] |
Show
Allelic Composition: Cyp27b1tm1Hfd/Cyp27b1tm1Hfd Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
MP:0003313 | abnormal locomotor activation | "altered ability or desire of an animal to initiate locomotor activity" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Plxna3tm1Matl/Y,Plxna4tm1Matl/Plxna4tm1Matl Genetic Background: either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1)
|
MP:0003444 | abnormal neurotransmitter uptake | "aberration in the reabsorbtion of endogenous signaling molecules normally taken in by neurons that alter the behavior of neurons or effector cells" [J:95639, smb:Susan M Bello, Mouse Genome Informatics Curator] |
Show
Allelic Composition: Plxna3tm1Matl/Y,Plxna4tm1Matl/Plxna4tm1Matl Genetic Background: either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1)
|
MP:0003661 | abnormal locus ceruleus | "anomaly in a dense cluster of neurons within the dorsorostral pons; it is the major location of neurons that release norepinephrine throughout the brain, and is responsible for physiological responses to stress and panic" [J:96328, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3] |
Show
Allelic Composition: Cyp27b1tm1Hfd/Cyp27b1tm1Hfd Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
MP:0004077 | abnormal striatum morphology | "malformation of a large cluster of dopaminergic nerve cells, consisting of the caudate nucleus and the putamen, that controls movement, balance, and walking" [Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3] |
Show
Allelic Composition: Cyp27b1tm1Hfd/Cyp27b1tm1Hfd Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
MP:0005156 | bradykinesia | "decreased spontaneity and movement" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:83301] |
Show
Allelic Composition: Plxna3tm1Matl/Y,Plxna4tm1Matl/Plxna4tm1Matl Genetic Background: either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1)
|
MP:0005402 | abnormal action potential | "change in the electric response of a nerve or other excitable tissue to its stimulation" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Plxna3tm1Matl/Y,Plxna4tm1Matl/Plxna4tm1Matl Genetic Background: either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1)
|
MP:0005621 | abnormal cell physiology | "aberration in the vital processes of the cell " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, hdene:Howard Dene , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Rrn3tm1.1Igt/Rrn3tm1.1Igt,Tg(Slc6a3-icre)9190Gsc/0 Genetic Background: involves: 129/Sv * C57BL/6 * FVB/N
|
MP:0008830 | abnormal nucleolus morphology | "any structural anomaly of the small rounded nuclear substructure that produces ribonucleoprotein" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
Show
Allelic Composition: Park7Gt(XE726)Byg/Park7Gt(XE726)Byg,Pink1tm1.1Wrst/Pink1tm1.1Wrst,Rrn3tm1.1Igt/Rrn3tm1.1Igt,Tg(Slc6a3-cre/ERT2)1Span/0 Genetic Background: involves: 129 * 129P2/OlaHsd * 129S2/SvPas * C57BL/6J
|
MP:0008872 | abnormal response to xenobiotics | "any anomaly in the physiological or morphological changes induced by a foreign compound, such as changes in blood pressure, changes in hormone or protein levels or hypertrophy or hypotrophy of an organ" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Cyp27b1tm1Hfd/Cyp27b1tm1Hfd Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
MP:0009745 | abnormal behavioral response to xenobiotic | "any anomaly in the behavioral response induced by a foreign compound, such as consumption preference, induced hyperactivity or stereotypic behavior" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Cyp27b1tm1Hfd/Cyp27b1tm1Hfd Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|
MP:0010053 | decreased grip strength | "reduced ability to grasp and hold objects, often measured as time spent hanging from an object or wire" [ISBN:0471316393 "Crawley, JN, What s Wrong with my Mouse: Behavioral Phenotyping of Transgenic and Knockout Mice"] |
Show
Allelic Composition: Cyp27b1tm1Hfd/Cyp27b1tm1Hfd Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
Allelic Composition: Park7tm1Cai/Park7tm1Cai Genetic Background: involves: 129X1/SvJ * C57BL/6
|
MP:0010069 | increased serotonin concentration | "increase in the amount per unit of biochemical messenger and regulator, found in the CNS, gastrointestinal tract, and produced by platelets that mediates neurotransmission, gastrointestinal motility, hemostasis, and cardiovascular integrity" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
Show
Allelic Composition: Gpx1tm1Ysh/Gpx1tm1Ysh,Prkntm1Shn/Prkntm1Shn,Park7tm1Shn/Park7tm1Shn Genetic Background: B6.Cg-Park7tm1Shn Gpx1tm1Ysh Prkntm1Shn
Allelic Composition: Prkntm1Shn/Prkntm1Shn,Park7tm1Shn/Park7tm1Shn Genetic Background: B6.Cg-Park7tm1Shn Prkntm1Shn
|
MP:0010954 | abnormal cellular respiration | "anomaly in the enzymatic release of energy from organic compounds (especially carbohydrates and fats) which either requires oxygen (aerobic respiration) or does not (anaerobic respiration)" [GO:0045333] |
Show
Allelic Composition: C1galt1ptl1/C1galt1ptl1,Rag1tm1Bal/Rag1tm1Bal Genetic Background: involves: 129S4/SvJae * C57BL/6
|
MP:0010958 | abnormal tricarboxylic acid cycle | "any anomaly in the universal metabolic pathway in which the acetyl group of acetyl coenzyme A is effectively oxidized to two CO2 and four pairs of electrons are transferred to coenzymes; the acetyl group combines with oxaloacetate to form citrate, which undergoes successive transformations to isocitrate, 2-oxoglutarate, succinyl-CoA, succinate, fumarate, malate, and oxaloacetate again, thus completing the cycle" [GO:0006099] |
Show
Allelic Composition: C1galt1ptl1/C1galt1ptl1,Rag1tm1Bal/Rag1tm1Bal Genetic Background: involves: 129S4/SvJae * C57BL/6
|
MP:0011451 | increased susceptibility to dopaminergic neuron neurotoxicity | "greater than normal amount of dopaminergic neuronal cell death following exposure to a neurotoxic compound, such as MPTP-induced cell death occurring through interference in mitochondrial metabolism" [MGI:csmith] |
Show
Allelic Composition: Airetm1.1Doi/Airetm1.1Doi Genetic Background: involves: 129S2/SvPas * C57BL/6 * NOD
|
MP:0013219 | abnormal substantia nigra pars compacta morphology | "any structural anomaly of the posterior (dorsal) part of grey matter of the substantia nigra which contains large, polygonal, and densely packed dopamine-producing cells; pars compacta neurons are pigmented in many species" [MGI:anna] |
Show
Allelic Composition: Cyp27b1tm1Hfd/Cyp27b1tm1Hfd Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
|