MP:0001262 | decreased body weight | "lower than normal average weight " [J:61295] |
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Allelic Composition: Eportm1(EGFP/cre)Uk/Eportm1(EGFP/cre)Uk Genetic Background: involves: BALB/cJ
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MP:0001265 | reduced body size | "smaller than average body weight, height and/or length of an organism compared to controls" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:23170] |
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Allelic Composition: Casp9tm1Flv/Casp9tm1Flv Genetic Background: B6.129S1-Casp9tm1Flv
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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: Eportm1(EGFP/cre)Uk/Eportm1(EGFP/cre)Uk Genetic Background: involves: BALB/cJ
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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: Slc17a7tm1Edw/Slc17a7tm1Edw Genetic Background: involves: 129X1/SvJ
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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: Kcnn2bc-9J/Kcnn2bc-9J Genetic Background: C57BL/6J-bc9J/GrsrJ
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MP:0001488 | increased startle reflex | "reduced threshold or more severe reflex response to variable stimuli, often auditory; usually measured by amplitude of whole body flinch" [What s Wrong With My Mouse?:ISBN 0-471-31639-3, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Slc17a7tm1Edw/Slc17a7tm1Edw Genetic Background: involves: 129X1/SvJ
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MP:0001491 | unresponsive to tactile stimuli | "absence of reflex action normally induced by touch or pain" [J:43515, J:47439] |
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Allelic Composition: Eportm1(EGFP/cre)Uk/Eportm1(EGFP/cre)Uk Genetic Background: involves: BALB/cJ
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MP:0001505 | hunched posture | "stooped low with the limbs pulled in close to the body and arched back" [J:67231, J:30404] |
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Allelic Composition: Eportm1(EGFP/cre)Uk/Eportm1(EGFP/cre)Uk Genetic Background: involves: BALB/cJ
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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: Casp9tm1Flv/Casp9tm1Flv Genetic Background: B6.129S1-Casp9tm1Flv
Allelic Composition: Slc17a7tm1Rmnd/Slc17a7tm1Rmnd Genetic Background: involves: 129P2/OlaHsd
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MP:0002001 | blindness | "loss of the sense of sight" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Slc17a7tm1Edw/Slc17a7tm1Edw Genetic Background: involves: 129X1/SvJ
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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: Casp9tm1Flv/Casp9tm1Flv Genetic Background: B6.129S1-Casp9tm1Flv
Allelic Composition: Slc17a7tm1Edw/Slc17a7tm1Edw Genetic Background: involves: 129X1/SvJ
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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: Gt(ROSA)26Sortm1Red/Gt(ROSA)26Sor+,Foxg1tm1(cre)Skm/Foxg1+ Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ
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MP:0002206 | abnormal CNS synaptic transmission | "defect in the communication from a neuron to a target across a synapse in the central nervous system" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Slc17a7tm1Edw/Slc17a7tm1Edw Genetic Background: involves: 129X1/SvJ
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MP:0002573 | behavioral despair | "depression assayed by reduced escape attempts and/or immobility when placed in a stressful situation such as a forced swim test or a suspension test; or failure to seek pleasurable stimuli" [J:80395] |
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Allelic Composition: Eportm1(EGFP/cre)Uk/Eportm1(EGFP/cre)Uk Genetic Background: involves: BALB/cJ
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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: Eportm1(EGFP/cre)Uk/Eportm1(EGFP/cre)Uk Genetic Background: involves: BALB/cJ
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MP:0002910 | abnormal excitatory postsynaptic currents | "defect in the size or duration of currents 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: Slc17a7tm1Edw/Slc17a7tm1Edw Genetic Background: involves: 129X1/SvJ
Allelic Composition: Slc17a7tm1Rmnd/Slc17a7tm1Rmnd Genetic Background: involves: 129P2/OlaHsd
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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: Slc17a7tm1Edw/Slc17a7tm1Edw Genetic Background: involves: 129X1/SvJ
Allelic Composition: Slc17a7tm1Lex/Slc17a7+ Genetic Background: involves: 129S5/SvEvBrd * C57BL/6J
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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] |
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Allelic Composition: Slc17a7tm1Edw/Slc17a7tm1Edw Genetic Background: involves: 129X1/SvJ
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MP:0003463 | abnormal single cell response | "altered values from controls obtained upon extra- or intracellular recordings from single cells" [Nmice:Neuromice Consortium Submission] |
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Allelic Composition: Slc17a7tm1Edw/Slc17a7tm1Edw Genetic Background: involves: 129X1/SvJ
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MP:0003633 | abnormal nervous system physiology | |
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Allelic Composition: Eportm1(EGFP/cre)Uk/Eportm1(EGFP/cre)Uk Genetic Background: involves: BALB/cJ
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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: Slc17a7tm1Rmnd/Slc17a7tm1Rmnd Genetic Background: involves: 129P2/OlaHsd
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MP:0004792 | abnormal synaptic vesicle number | "anomaly in the number of the small, membrane bound sacs that contain various neurotransmitter molecules that are concentrated at pre-synaptic membranes and release the neurotransmitters by fusion of these vesicles with the presynaptic membrane, followed by exocytosis of their contents" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Slc17a7tm1Edw/Slc17a7tm1Edw Genetic Background: involves: 129X1/SvJ
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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: Slc17a7tm1Edw/Slc17a7tm1Edw Genetic Background: involves: 129X1/SvJ
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MP:0005449 | abnormal food intake | "anomalous total number of calories taken in daily when compared to the norm" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Slc17a7tm1Edw/Slc17a7tm1Edw Genetic Background: involves: 129X1/SvJ
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MP:0011083 | complete lethality at weaning | "premature death at weaning age of all organisms of a given genotype in a population, often due to the inability to make the transition to solid food" [MGI:csmith] |
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Allelic Composition: Slc17a7tm1Rmnd/Slc17a7tm1Rmnd Genetic Background: involves: 129P2/OlaHsd
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MP:0020340 | abnormal inhibitory learning | "anomaly in the process by which a subject learns to suppress a prior learned response" [http://cognitivedefusion.tumblr.com/post/90402024947/what-is-inhibitory-learning, ORCID: orcid.org/0000-0003-4606-0597, PMID:19321764] |
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Allelic Composition: Slc17a7tm1Lex/Slc17a7+ Genetic Background: involves: 129S5/SvEvBrd * C57BL/6J
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