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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Htt
huntingtin
MGI:96067
189 phenotypes from multigenic genotypes
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Cnr1tm1Map/Cnr1tm1Map
Tg(HD82Gln)81Gschi/0
involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6 * CD-1
abnormal postnatal growth J:172874
abnormal striatum morphology J:172874
decreased body weight J:172874
impaired coordination J:172874
premature death J:172874
Emx1tm1(cre)Ito/Emx1+
Rgs9tm1(cre)Yql/Rgs9+
Tg(HTT*97Q)IXwy/0
involves: 129P2/OlaHsd * FVB
normal behavior/neurological phenotype J:208675
normal nervous system phenotype J:208675
Emx1tm1(cre)Ito/Emx1+
Tg(HTT*97Q)IXwy/0
involves: 129P2/OlaHsd * FVB
normal behavior/neurological phenotype J:208675
hypoactivity J:208675
impaired coordination J:208675
normal nervous system phenotype J:208675
Emx1tm1(cre)Ito/?
Gt(ROSA)26Sortm1(HD*103Q)Xwy/?
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
normal nervous system phenotype J:99759
Gt(ROSA)26Sortm1(HD*103Q)Xwy/?
Tg(Nes-cre)1Kln/?
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
abnormal cerebral cortex pyramidal cell morphology J:99759
abnormal inhibitory postsynaptic currents J:99759
cerebral cortex pyramidal cell degeneration J:99759
gliosis J:99759
hypoactivity J:99759
neurodegeneration J:99759
Hap1tm1Id/Hap1+
Htttm1Szi/Htttm1Szi
involves: 129S/SvEv * 129S1/Sv * C57BL/6
absent neural folds J:94581
absent somites J:94581
decreased embryo size J:94581
Hap1tm1Id/Hap1tm1Id
Htttm1Szi/Htttm1Szi
involves: 129S/SvEv * 129S1/Sv * C57BL/6
absent neural folds J:94581
absent somites J:94581
decreased embryo size J:94581
Htttm1Hay/Htt+
Tg(YAC72)2511Hay/0
involves: FVB/N
testicular atrophy J:67366
Htttm1Hay/Htttm1Hay
Tg(HTT*97Q)IXwy/0
Tg(YAC18)18Hay/Tg(YAC18)18Hay
FVB.Cg-Htttm1Hay Tg(HTT*97Q)IXwy Tg(YAC18)18Hay
abnormal action potential J:215223
abnormal CNS synaptic transmission J:215223
abnormal corpus callosum morphology J:191147
abnormal depression-related behavior J:191147
abnormal excitatory postsynaptic currents J:215223
abnormal forebrain morphology J:191147
abnormal motor capabilities/coordination/movement J:191147
abnormal motor learning J:191147
abnormal object recognition memory J:191147
abnormal striatum morphology J:191147
decreased excitatory postsynaptic current amplitude J:215223
decreased paired-pulse facilitation J:215223
impaired coordination J:191147
impaired spatial learning J:191147
impaired synaptic plasticity J:215223
increased body weight J:191147
increased stereotypic behavior J:191147
increased thigmotaxis J:191147
reduced long term potentiation J:215223
Htttm1Hay/Htttm1Hay
Tg(YAC18)18Hay/0
involves: FVB/N
normal mortality/aging J:67366
normal reproductive system phenotype J:67366
Htttm1Hay/Htttm1Hay
Tg(YAC46)668Hay/0
involves: FVB/N
male infertility J:67366
normal mortality/aging J:67366
normal reproductive system phenotype J:67366
Htttm1Hay/Htttm1Hay
Tg(YAC72)2511Hay/0
involves: FVB/N
abnormal male germ cell apoptosis J:67366
abnormal spermatid morphology J:67366
male infertility J:67366
normal mortality/aging J:67366
multinucleated giant male germ cells J:67366
oligozoospermia J:67366
normal reproductive system phenotype J:67366
testicular atrophy J:67366
Htttm1Hay/Htttm1Hay
Tg(YAC128)53Hay/0
involves: C57BL/6J * FVB
normal mortality/aging J:120991
Htttm1Hay/Htttm1Hay
Tg(YAC353G6)W7Hay/0
involves: C57BL/6J * FVB/NJ
normal mortality/aging J:120991
Htttm1Mfc/Htt+
Ppargc1atm1Dpk/Ppargc1a+
involves: 129S1/Sv * 129X1/SvJ
abnormal striatum morphology J:116058
impaired coordination J:116058
neuron degeneration J:116058
Htttm1Szi/Htttm1Szi
Tg(HTT*)1Xwy/0
involves: 129S/SvEv * FVB
normal mortality/aging J:157723
Htttm1Szi/Htttm1Szi
Tg(HTT*)BXwy/0
involves: 129S/SvEv * FVB
normal mortality/aging J:157723
normal nervous system phenotype J:157723
Htttm5Mem/Htt+
Msh2tm1Htr/Msh2tm1Htr
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * CD-1 * FVB/N
neuronal intranuclear inclusions J:81666
Neil1tm1Bjor/Neil1tm1Bjor
Tg(HDexon1)61Gpb/0
involves: C57BL/6 * C57BL/6J * CBA
abnormal cell physiology J:188338
Rgs9tm1(cre)Yql/Rgs9+
Tg(HTT*97Q)IXwy/0
involves: FVB
behavioral despair J:208675
forebrain atrophy J:208675
hypoactivity J:208675
impaired coordination J:208675
increased anxiety-related response J:208675
normal nervous system phenotype J:208675
Sirt2tm1Gdon/Sirt2tm1Gdon
Tg(HDexon1)62Gpb/0
involves: 129P2/OlaHsd * C57BL/6 * CBA
decreased brain weight J:193012
decreased grip strength J:193012
impaired coordination J:193012
Supt4atm1Yty/Supt4a+
Tg(HDexon1)62Gpb/0
involves: 129S6/SvEvTac * C57BL/6 * CBA
decreased body weight J:224237
impaired coordination J:224237
premature death J:224237
Tg(Camk2a-tTA)1Mmay/0
Tg(tetO-HTT*94Q,-lacZ)1Rhn/0
involves: C57BL/6 * CBA
abnormal dorsal striatum morphology J:61490
astrocytosis J:61490
decreased brain size J:61490
decreased grooming behavior J:61490
decreased striatum area J:61490
dystonia J:61490
enlarged brain ventricles J:61490
gliosis J:61490
hypoactivity J:61490
limb grasping J:61490
neuronal intranuclear inclusions J:61490
premature death J:61490
prenatal lethality, incomplete penetrance J:61490
tremors J:61490
Tg(CMV-HTT*48Q)BTag/0
involves: FVB/N
abnormal sensory capabilities/reflexes/nociception J:50173
akinesia J:50173
astrocytosis J:50173
gliosis J:50173
hyperactivity J:50173
hypoactivity J:50173
increased grooming behavior J:50173
increased stereotypic behavior J:50173
limb grasping J:50173
neuron degeneration J:50173
neuronal intranuclear inclusions J:50173
slow postnatal weight gain J:50173
unidirectional circling J:50173
urinary incontinence J:50173
Tg(CMV-HTT*48Q)BTag/Tg(CMV-HTT*48Q)BTag
involves: FVB/N
hyperactivity J:50173
increased grooming behavior J:50173
increased stereotypic behavior J:50173
neuron degeneration J:50173
unidirectional circling J:50173
Tg(CMV-HTT*89Q)ATag/0
involves: FVB/N
abnormal sensory capabilities/reflexes/nociception J:50173
akinesia J:50173
astrocytosis J:50173
gliosis J:50173
hyperactivity J:50173
hypoactivity J:50173
increased grooming behavior J:50173
increased stereotypic behavior J:50173
limb grasping J:50173
neuron degeneration J:50173
neuronal intranuclear inclusions J:50173
slow postnatal weight gain J:50173
unidirectional circling J:50173
urinary incontinence J:50173
Tg(CMV-HTT*89Q)ATag/Tg(CMV-HTT*89Q)ATag
involves: FVB/N
hyperactivity J:50173
increased grooming behavior J:50173
increased stereotypic behavior J:50173
neuron degeneration J:50173
unidirectional circling J:50173
Tg(GFAP-HTT*160Q)1Xjl/0
either: (involves: FVB/NCrl) or (involves: C3H * C57BL/6 * FVB/NCrl)
abnormal behavior J:156460
gliosis J:156460
hunched posture J:156460
impaired coordination J:156460
lethargy J:156460
limb grasping J:156460
neurodegeneration J:156460
poor grooming J:156460
premature death J:156460
weight loss J:156460
Tg(GFAP-HTT*160Q)31Xjl/0
either: (involves: FVB/NCrl) or (involves: C3H * C57BL/6 * FVB/NCrl)
abnormal behavior J:156460
gliosis J:156460
hunched posture J:156460
impaired coordination J:156460
limb grasping J:156460
neurodegeneration J:156460
premature death J:156460
weight loss J:156460
Tg(HD82Gln)81Gschi/0
involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6 * CD-1
abnormal postnatal growth J:172874
abnormal striatum morphology J:172874
decreased body weight J:172874
impaired coordination J:172874
premature death J:172874
Tg(HD82Gln)81Gschi/0
involves: C3H/HeJ * C57BL/6
abnormal gait J:53797
abnormal hypothalamus morphology J:84682
bradykinesia J:53797
decreased body size J:53797
decreased body weight J:53797
impaired coordination J:53797
limb grasping J:53797
neurodegeneration J:84682
neuronal intranuclear inclusions J:53797
poor grooming J:53797
premature death J:53797
tremors J:53797
Tg(HD)63Aron/?
involves: C57BL/6 * SJL
abnormal cerebral cortex morphology J:72772
abnormal dendrite morphology J:72772
abnormal excitatory postsynaptic potential J:72772
abnormal gait J:72772
abnormal locomotor activation J:72772
abnormal medium spiny neuron morphology J:72772
abnormal neuron morphology J:72772
abnormal striatum morphology J:72772
enhanced NMDA-mediated synaptic currents J:72772
impaired coordination J:72772
limb grasping J:72772
neuronal intranuclear inclusions J:72772
Tg(HDexon1)61Gpb/0
involves: C57BL/6 * C57BL/6J * CBA
abnormal cell physiology J:188338
Tg(HDexon1)61Gpb/?
involves: C57BL/6 * CBA
abnormal heart rate J:203027
abnormal impulse conducting system conduction J:203027
abnormal long term spatial reference memory J:130936
abnormal motor capabilities/coordination/movement J:203027
abnormal neuron morphology J:42085
abnormal RR interval J:203027
abnormal short term spatial reference memory J:130936
abnormal sinus arrhythmia J:203027
abnormal spatial learning J:130936
abnormal striatum morphology J:42085
atrial fibrillation J:203027
decreased body weight J:203027
decreased exploration in new environment J:130936
decreased noradrenaline level J:203027
decreased systemic arterial blood pressure J:203027
impaired coordination J:130936
increased circulating noradrenaline level J:203027
increased neuron number J:203027
irregular heartbeat J:203027
limb grasping J:203027
neuronal intranuclear inclusions J:42085
premature death J:203027
small myocardial fiber J:203027
ventricular premature beat J:203027
ventricular tachycardia J:203027
Tg(HDexon1)61Gpb/0
involves: C57BL/6 * CBA/J
abnormal cone electrophysiology J:80810
abnormal eye electrophysiology J:80810
abnormal photoreceptor inner segment morphology J:80810
abnormal photoreceptor outer segment morphology J:80810
abnormal retina morphology J:80810
abnormal retinal outer nuclear layer morphology J:80810
abnormal retinal outer plexiform layer morphology J:80810
abnormal retinal photoreceptor morphology J:80810
abnormal rod electrophysiology J:80810
disorganized photoreceptor inner segment J:80810
disorganized photoreceptor outer segment J:80810
neuronal intranuclear inclusions J:80810
retinal photoreceptor degeneration J:80810
retinal spots J:80810
Tg(HDexon1)62Gpb/0
B6.Cg-Tg(HDexon1)62Gpb/240
abnormal gait J:185262
decreased body weight J:185262
decreased grip strength J:185262
decreased prepulse inhibition J:185262
decreased startle reflex J:185262
decreased vertical activity J:185262
hypoactivity J:185262
impaired coordination J:185262
increased anxiety-related response J:185262
premature death J:185262
short stride length J:185262
Tg(HDexon1)62Gpb/0
B6CBA-Tg(HDexon1)62Gpb/1J
abnormal cerebellum morphology J:111237
abnormal cerebral cortex morphology J:111237
abnormal diastolic filling velocity J:116660
abnormal myocardial fiber morphology J:116660
abnormal nervous system physiology J:99425
abnormal neuron physiology J:76018
abnormal striatum morphology J:111237
abnormal voluntary movement J:99425
decreased cardiac output J:116660
decreased cardiac stroke volume J:116660
decreased heart weight J:116660
decreased left ventricle systolic pressure J:116660
decreased ventricle muscle contractility J:116660
dilated heart left ventricle J:116660
limb grasping J:99425
slow postnatal weight gain J:116660
weight loss J:99425
Tg(HDexon1)62Gpb/0
B6CBA-Tg(HDexon1)62Gpb/3J
abnormal gait J:185262
decreased body weight J:185262
decreased grip strength J:185262
decreased prepulse inhibition J:185262
decreased startle reflex J:185262
decreased vertical activity J:185262
hypoactivity J:185262
impaired coordination J:185262
increased anxiety-related response J:185262
premature death J:185262
short stride length J:185262
Tg(HDexon1)62Gpb/0
involves: C57BL/6 * C57BL/6JOlaHsd * CBA * CBA/CaOlaHsd
decreased brain weight J:193012
decreased grip strength J:193012
impaired coordination J:193012
Tg(HDexon1)62Gpb/0
involves: C57BL/6 * CBA
abnormal cerebral cortex morphology J:42085
abnormal neuron morphology J:42085
abnormal striatum morphology J:42085
decreased body weight J:42085
decreased brain weight J:42085
neuronal intranuclear inclusions J:42085
Tg(HDexon1)62Gpb/0
involves: C57BL/6 * CBA/J
abnormal photoreceptor inner segment morphology J:80810
abnormal photoreceptor outer segment morphology J:80810
abnormal retina morphology J:80810
abnormal retinal outer nuclear layer morphology J:80810
abnormal retinal outer plexiform layer morphology J:80810
abnormal retinal photoreceptor morphology J:80810
disorganized photoreceptor inner segment J:80810
disorganized photoreceptor outer segment J:80810
neuronal intranuclear inclusions J:80810
retinal photoreceptor degeneration J:80810
Tg(HDexon1)62Gpb/0
involves: C57BL/6J * CBA/J
abnormal female reproductive system morphology J:36689
abnormal glucose homeostasis J:96353
abnormal pancreatic alpha cell morphology J:96353
abnormal pancreatic beta cell morphology J:96353
abnormal pancreatic delta cell morphology J:96353
abnormal vocalization J:36689
decreased body weight J:96353
decreased brain size J:36689
decreased circulating insulin level J:96353
decreased pancreatic beta cell number J:96353
female infertility J:36689
impaired balance J:36689
impaired glucose tolerance J:96353
limb grasping J:36689
polyuria J:36689
premature death J:36689
seizures J:36689
small ovary J:36689
small seminal vesicle J:36689
small testis J:36689
small uterus J:36689
stereotypic behavior J:36689
tremors J:36689
weight loss J:36689
Tg(HTT*97Q)IXwy/0
FVB-Tg(HTT*97Q)IXwy
abnormal cerebral cortex morphology J:137345
abnormal depression-related behavior J:157723
abnormal excitatory postsynaptic currents J:208675
abnormal forebrain morphology J:157723
abnormal gait J:185262
abnormal inhibitory postsynaptic currents J:208675
abnormal nervous system electrophysiology J:137345
abnormal neuron morphology J:157723
normal behavior/neurological phenotype J:185262
behavioral despair J:208675
brain atrophy J:137345
decreased brain weight J:137345
decreased forebrain size J:208675
decreased prepulse inhibition J:185262
decreased startle reflex J:185262
decreased striatum area J:137345
decreased vertical activity J:185262
forebrain atrophy J:208675
hypoactivity J:185262
impaired coordination J:137345, J:157723, J:185262, J:208675
increased anxiety-related response J:157723, J:185262, J:208675
increased body weight J:137345, J:185262
normal nervous system phenotype J:208675
neurodegeneration J:137345
neuron degeneration J:137345, J:157723
neuronal intranuclear inclusions J:137345
reduced NMDA-mediated synaptic currents J:208675
short stride length J:185262
Tg(HTT*97Q)LXwy/0
FVB-Tg(HTT*97Q)LXwy
abnormal brain morphology J:137345
abnormal neuron morphology J:157723
impaired coordination J:157723
increased body weight J:137345
Tg(HTT*)1Xwy/0
FVB-Tg(HTT*)1Xwy
abnormal cerebral cortex morphology J:157723
abnormal depression-related behavior J:157723
abnormal forebrain morphology J:157723
abnormal neuron morphology J:157723
decreased striatum area J:157723
impaired coordination J:157723
increased anxiety-related response J:157723
neuron degeneration J:157723
Tg(HTT*)AXwy/0
involves: FVB/NJ
abnormal head movements J:219890
brain atrophy J:219890
dystonia J:219890
neuronal intranuclear inclusions J:219890
weight loss J:219890
Tg(HTT*)BXwy/0
FVB-Tg(HTT*)BXwy
normal behavior/neurological phenotype J:157723
normal nervous system phenotype J:157723
Tg(HTT*)LXwy/0
involves: FVB/NJ
abnormal forebrain morphology J:219890
abnormal head movements J:219890
dystonia J:219890
neuronal intranuclear inclusions J:219890
premature death J:219890
weight loss J:219890
Tg(HTT*)NXwy/0
involves: FVB/NJ
abnormal cerebral cortex morphology J:219890
abnormal depression-related behavior J:219890
abnormal forebrain morphology J:219890
abnormal gait J:219890
abnormal head movements J:219890
abnormal medium spiny neuron morphology J:219890
abnormal nervous system electrophysiology J:219890
astasia J:219890
astrocytosis J:219890
brain atrophy J:219890
CNS inflammation J:219890
decreased striatum area J:219890
decreased vertical activity J:219890
dystonia J:219890
hypoactivity J:219890
impaired coordination J:219890
increased body weight J:219890
male infertility J:219890
neurodegeneration J:219890
neuronal intranuclear inclusions J:219890
poor grooming J:219890
skeletal muscle fiber atrophy J:219890
testicular atrophy J:219890
weight loss J:219890
Tg(HTT*/EGFP)150Nn/0
involves: C57BL/6 * DBA/2
abnormal cerebral cortex morphology J:174269
abnormal hippocampus morphology J:174269
abnormal involuntary movement J:174269
abnormal nervous system morphology J:174269
abnormal striatum morphology J:174269
ataxia J:174269
limb grasping J:174269
neuronal intranuclear inclusions J:174269
premature death J:174269
tremors J:174269
Tg(HTT*/EGFP)190Nn/0
involves: C57BL/6 * DBA/2
abnormal involuntary movement J:174269
abnormal nervous system morphology J:174269
ataxia J:174269
limb grasping J:174269
premature death J:174269
tremors J:174269
Tg(Plp1-HTT*150Q)4aXjl/0
Not Specified
abnormal motor capabilities/coordination/movement J:221608
axon degeneration J:221608
demyelination J:221608
hypoactivity J:221608
impaired coordination J:221608
increased susceptibility to pharmacologically induced seizures J:221608
limb grasping J:221608
premature death J:221608
tremors J:221608
weight loss J:221608
Tg(Ppp1r1b-HTT*)1Meeh/0
C57BL/6J-Tg(Ppp1r1b-HTT*)1Meeh
decreased brain weight J:139807
hypoactivity J:139807
impaired coordination J:139807
neuronal intranuclear inclusions J:139807
slow postnatal weight gain J:139807
small lateral ventricles J:139807
Tg(Prnp-HTT*82Q)8AGschi/0
involves: C3H/HeJ * C57BL/6J
hunched posture J:91795
hypoactivity J:91795
impaired coordination J:91795
limb grasping J:91795
neuronal intranuclear inclusions J:91795
poor grooming J:91795
premature death J:91795
weight loss J:91795
Tg(Prnp-HTT*82Q)52Caro/0
involves: C3H * C57BL/6
abnormal associative learning J:179364
decreased body size J:179364
decreased brain size J:179364
hunched posture J:179364
hyperactivity J:179364
hypoactivity J:179364
impaired contextual conditioning behavior J:179364
impaired coordination J:179364
impaired cued conditioning behavior J:179364
limb grasping J:179364
poor grooming J:179364
premature death J:179364
weight loss J:179364
Tg(Prnp-HTT*82Q)61Gschi/0
involves: C3H/HeJ * C57BL/6J
hunched posture J:91795
limb grasping J:91795
neuronal intranuclear inclusions J:91795
poor grooming J:91795
premature death J:91795
weight loss J:91795
Tg(Prnp-HTT*82Q,KRT14-EGFP)C63Dbo/0
Not Specified
abnormal cerebellar granule cell morphology J:173756
abnormal hippocampus morphology J:173756
abnormal motor capabilities/coordination/movement J:173756
abnormal striatum morphology J:173756
astrocytosis J:173756
ataxia J:173756
decreased body weight J:173756
decreased brain size J:173756
decreased brain weight J:173756
decreased cerebellar granule cell number J:173756
dehydration J:173756
impaired coordination J:173756
premature death J:173756
Tg(Prnp-SNAP25/HTT*150Q)8Xjl/0
involves: FVB
astrocytosis J:201806
decreased paired-pulse facilitation J:201806
decreased startle reflex J:201806
decreased synaptic glutamate release J:201806
impaired coordination J:201806
increased anxiety-related response J:201806
kyphosis J:201806
limb grasping J:201806
premature death J:201806
reduced long term potentiation J:201806
weight loss J:201806
Tg(tetO-HTT*94Q,-lacZ)1Rhn/0
involves: C57BL/6 * CBA
no abnormal phenotype detected J:61490
Tg(UBC-GFP/HTT*84Q)22Shya/0
involves: FVB
abnormal gait J:209055
decreased grip strength J:209055
decreased survivor rate J:209055
impaired coordination J:209055
limb grasping J:209055
neuronal intranuclear inclusions J:209055
premature death J:209055
short stride length J:209055
Tg(YAC18)18Hay/?
involves: FVB/N
normal behavior/neurological phenotype J:55405
normal nervous system phenotype J:55405
Tg(YAC18)18Hay/0
involves: FVB/N
decreased susceptibility to neuronal excitotoxicity J:144917
Tg(YAC46)668Hay/?
involves: FVB/N
abnormal long term potentiation J:55405
normal behavior/neurological phenotype J:55405
decreased post-tetanic potentiation J:55405
normal nervous system phenotype J:55405
Tg(YAC72)2511Hay/?
involves: FVB/N
abnormal excitatory postsynaptic potential J:55405
abnormal long term potentiation J:55405
abnormal striatum morphology J:55405
enhanced NMDA-mediated synaptic currents J:55405
hyperactivity J:55405
neuron degeneration J:55405
reduced long term potentiation J:55405
unidirectional circling J:55405
Tg(YAC72)2511Hay/0
involves: FVB/N
increased susceptibility to neuronal excitotoxicity J:144917
normal reproductive system phenotype J:67366
Tg(YAC72)2511Hay/Tg(YAC72)2511Hay
FVB/N-Tg(YAC72)2511Hay
increased neuron apoptosis J:105728
increased susceptibility to neuronal excitotoxicity J:105728
Tg(YAC128)53Hay/0
B6.FVB-Tg(YAC128)53Hay
normal behavior/neurological phenotype J:185262
decreased prepulse inhibition J:185262
hypoactivity J:185262
impaired coordination J:185262
increased body weight J:185262
normal nervous system phenotype J:185262
Tg(YAC128)53Hay/0
FVB-Tg(YAC128)53Hay/J
normal behavior/neurological phenotype J:185262
decreased vertical activity J:185262
hyperactivity J:185262
hypoactivity J:185262
impaired coordination J:185262
increased anxiety-related response J:185262
increased body weight J:185262
increased vertical activity J:185262
normal nervous system phenotype J:185262
Tg(YAC128)53Hay/0
FVB/N-Tg(YAC128)53Hay
abnormal basal ganglion morphology J:84453
abnormal cerebral cortex morphology J:84453, J:111237
abnormal learning/memory/conditioning J:105723
abnormal medium spiny neuron morphology J:84453
abnormal motor capabilities/coordination/movement J:105723
abnormal motor learning J:105723
abnormal striatum morphology J:105723, J:111237, J:120991
bradykinesia J:120991
decreased brain weight J:84453, J:120991
hyperactivity J:84453, J:105723
hypoactivity J:84453, J:105723
impaired coordination J:84453, J:105723, J:120991
increased body weight J:84453
increased susceptibility to neuronal excitotoxicity J:105723
loss of basal ganglia neurons J:84453
neuronal intranuclear inclusions J:84453, J:105723
Tg(YAC128)55Hay/0
FVB/N-Tg(YAC128)55Hay
abnormal striatum morphology J:105723
impaired coordination J:105723
increased susceptibility to neuronal excitotoxicity J:105723
normal nervous system phenotype J:105723
Tg(YAC128)55Hay/Tg(YAC128)55Hay
FVB/N-Tg(YAC128)55Hay
abnormal striatum morphology J:105723
hypoactivity J:105723
impaired coordination J:105723
increased neuron apoptosis J:105728
increased susceptibility to neuronal excitotoxicity J:105723, J:105728
neuronal intranuclear inclusions J:105723
Tg(YAC128)#Hay/0
FVB/N-Tg(YAC128)#Hay
abnormal habituation J:98736
abnormal habituation to a new environment J:98736
abnormal learning/memory/conditioning J:98736
abnormal motor learning J:98736
abnormal startle reflex J:98736
decreased prepulse inhibition J:98736
impaired coordination J:98736
impaired spatial learning J:98736
impaired swimming J:98736
reduced sensorimotor gating J:98736
Tg(YAC353G6)W7Hay/0
FVB/NJ-Tg(YAC353G6)W7Hay
abnormal striatum morphology J:120991
increased brain weight J:120991
normal nervous system phenotype J:120991
Tg(YAC353G6)W7Hay/Tg(YAC353G6)W7Hay
FVB/NJ-Tg(YAC353G6)W7Hay
decreased susceptibility to neuronal excitotoxicity J:120991
Tgm2tm1.1Rmgr/Tgm2+
Tg(HDexon1)62Gpb/0
involves: 129X1/SvJ * C57BL/6 * CBA
abnormal cerebral cortex morphology J:95452
abnormal striatum morphology J:95452
Tgm2tm1.1Rmgr/Tgm2tm1.1Rmgr
Tg(HDexon1)62Gpb/0
involves: 129X1/SvJ * C57BL/6 * CBA
abnormal cerebral cortex morphology J:95452
abnormal striatum morphology J:95452
extended life span J:95452
impaired coordination J:95452

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
10/08/2019
MGI 6.14
The Jackson Laboratory