MP:0000841 | abnormal hindbrain morphology | "malformed caudal region of the brain; includes cerebellum, pons and medulla oblongata" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:45302] |
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Allelic Composition: Cptm1b(KOMP)Wtsi/Cptm1b(KOMP)Wtsi Genetic Background: C57BL/6N-Cptm1b(KOMP)Wtsi/J
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MP:0001362 | abnormal anxiety-related response | "altered emotional response related to anticipation of a non-specific threat" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, CFG:Center for Functional Genomics, Northwestern University] |
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Allelic Composition: Gabra1tm1.1Mjga/Gabra1+ Genetic Background: B6J.Cg-Gabra1tm1.1Mjga
Allelic Composition: Cyfip2tm1(KOMP)Vlcg/Cyfip2+,Fmr1tm1Cgr/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NTac
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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: Gabra1tm1.1Mjga/Gabra1+ Genetic Background: B6J.Cg-Gabra1tm1.1Mjga
Allelic Composition: Cyfip2tm1(KOMP)Vlcg/Cyfip2+,Fmr1tm1Cgr/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NTac
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MP:0001409 | increased stereotypic behavior | "more frequent incidence of repetitive, invariant, perseverative motor patterns that do not appear to be purposeful" [What s Wrong With My Mouse?:ISBN 0-471-31639-3, MGI:CLS, J:57125] |
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Allelic Composition: Cyfip2tm1(KOMP)Vlcg/Cyfip2+,Fmr1tm1Cgr/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NTac
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MP:0001489 | decreased startle reflex | "greater threshold or less severe reflex response to variable stimuli, often auditory; usually measured by amplitude of whole body flinch" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, What s Wrong With My Mouse?:ISBN 0-471-31639-3] |
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Allelic Composition: Gabra1tm1.1Mjga/Gabra1+ Genetic Background: B6J.Cg-Gabra1tm1.1Mjga
Allelic Composition: Cyfip2tm1(KOMP)Vlcg/Cyfip2+,Fmr1tm1Cgr/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NTac
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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: Cptm1b(KOMP)Wtsi/Cptm1b(KOMP)Wtsi Genetic Background: C57BL/6N-Cptm1b(KOMP)Wtsi/J
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MP:0003584 | bifid ureter | "cleft of the ureter into two parts or branches" [ncbi:Matthew Mailman, NCBI request] |
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Allelic Composition: Cptm1b(KOMP)Wtsi/Cptm1b(KOMP)Wtsi Genetic Background: C57BL/6N-Cptm1b(KOMP)Wtsi/J
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MP:0003586 | ureter dilation | "abnormal distention of the ureter due to accumulation of fluid" [ncbi:Matthew Mailman, NCBI request] |
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Allelic Composition: Cptm1b(KOMP)Wtsi/Cptm1b(KOMP)Wtsi Genetic Background: C57BL/6N-Cptm1b(KOMP)Wtsi/J
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MP:0004017 | duplex kidney | "a kidney that is split into two separate collecting systems; there may be a duplex ureter or a single ureter; may present unilaterally or bilaterally" [rbabiuk:Randall Babiuk, Mouse Genome Informatics Curator] |
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Allelic Composition: Cptm1b(KOMP)Wtsi/Cptm1b(KOMP)Wtsi Genetic Background: C57BL/6N-Cptm1b(KOMP)Wtsi/J
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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: Prkntm1Shn/Prkntm1Shn,Park7tm1Shn/Park7tm1Shn Genetic Background: B6.Cg-Park7tm1Shn Prkntm1Shn
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MP:0005627 | increased circulating potassium level | "greater than the normal concentration in the blood of this alkaline metallic element, the most abundant intracellular ion; anomalies in the extracellular (circulating) concentration have important implications for the function of excitable tissues, such as nerve and muscle" [RGD:Rat Genome Database submission] |
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Allelic Composition: Crb2tm1a(KOMP)Wtsi/Crb2+ Genetic Background: C57BL/6N-Crb2tm1a(KOMP)Wtsi/Wtsi
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MP:0005628 | decreased circulating potassium level | "less than the normal concentration in the blood of this alkaline metallic element, the most abundant intracellular ion; anomalies in the extracellular (circulating) concentration have important implications for the function of excitable tissues, such as nerve and muscle" [RGD:Rat Genome Database submission] |
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Allelic Composition: Crb2tm1a(KOMP)Wtsi/Crb2+ Genetic Background: C57BL/6N-Crb2tm1a(KOMP)Wtsi/Wtsi
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MP:0009141 | increased prepulse inhibition | "increase in the ability of a relatively mild stimulus to suppress the response to a strong, startle-eliciting stimulus" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Gabra1tm1.1Mjga/Gabra1+ Genetic Background: B6J.Cg-Gabra1tm1.1Mjga
Allelic Composition: Cyfip2tm1(KOMP)Vlcg/Cyfip2+,Fmr1tm1Cgr/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NTac
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MP:0009754 | enhanced behavioral response to cocaine | "increased sensitivity to cocaine resulting in a behavioral response, such as induced hyperactivity or stereotypic behavior, or decreased dosage threshold for the appearance of the behavioral response" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Prkntm1Shn/Prkntm1Shn,Park7tm1Shn/Park7tm1Shn Genetic Background: B6.Cg-Park7tm1Shn Prkntm1Shn
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MP:0009758 | impaired behavioral response to cocaine | "decreased sensitivity to cocaine resulting in a behavioral response, such as induced hyperactivity or stereotypic behavior, or increased dosage threshold for the appearance of the behavioral response" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Prkntm1Shn/Prkntm1Shn,Park7tm1Shn/Park7tm1Shn Genetic Background: B6.Cg-Park7tm1Shn Prkntm1Shn
Allelic Composition: Cyfip2M1N/Cyfip2+ Genetic Background: (C57BL/6N x C57BL/6J)F1
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MP:0009936 | abnormal dendritic spine morphology | "any structural anomaly of the small membranous protrusion from the dendrite of a neuron that is involved in synaptic transmission; it typically receives input from a single synapse of an axon" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
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Allelic Composition: Prkntm1Shn/Prkntm1Shn,Park7tm1Shn/Park7tm1Shn Genetic Background: B6.Cg-Park7tm1Shn Prkntm1Shn
Allelic Composition: Cyfip2tm1(KOMP)Vlcg/Cyfip2+ Genetic Background: involves: C57BL/6J * C57BL/6NTac
Allelic Composition: Cyfip2tm1(KOMP)Vlcg/Cyfip2+,Fmr1tm1Cgr/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NTac
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MP:0010484 | bicuspid aortic valve | "the presence of two cusps in the aortic valve instead of three" [http://emedicine.medscape.com] |
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Allelic Composition: Cptm1b(KOMP)Wtsi/Cptm1b(KOMP)Wtsi Genetic Background: C57BL/6N-Cptm1b(KOMP)Wtsi/J
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MP:0010490 | abnormal inferior vena cava valve morphology | "any structural anomaly of the semicircular fold of endocardium located on the right atrium at the point of attachment of the inferior vena cava" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Cptm1b(KOMP)Wtsi/Cptm1b(KOMP)Wtsi Genetic Background: C57BL/6N-Cptm1b(KOMP)Wtsi/J
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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: Gabra1tm1.1Mjga/Gabra1+ Genetic Background: B6J.Cg-Gabra1tm1.1Mjga
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MP:0011087 | complete neonatal lethality | "death of all organisms of a given genotype in a population within the neonatal period after birth (Mus: P0)" [MGI:csmith] |
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Allelic Composition: Prkntm1Shn/Prkntm1Shn,Park7tm1Shn/Park7tm1Shn Genetic Background: B6.Cg-Park7tm1Shn Prkntm1Shn
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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: Cptm1b(KOMP)Wtsi/Cptm1b(KOMP)Wtsi Genetic Background: C57BL/6N-Cptm1b(KOMP)Wtsi/J
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MP:0013848 | subcutaneous edema | "accumulation of watery or serous fluid in the subcutaneous region below the skin" [MGI:csmith] |
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Allelic Composition: Cptm1b(KOMP)Wtsi/Cptm1b(KOMP)Wtsi Genetic Background: C57BL/6N-Cptm1b(KOMP)Wtsi/J
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