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Symbol
Name
ID
Hap1
huntingtin-associated protein 1
MGI:1261831
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Gliosis
Cerebellar atrophy
Neuronal loss in central nervous system
Gait ataxia
Bradykinesia
Chorea
Depression
Personality changes
Dementia
Hyperreflexia
Seizure
Disease(s) Associated with HAP1
Huntington's disease

Mouse Phenotypes
impaired neuron differentiation
abnormal neuron proliferation
decreased brain weight
decreased brain size
abnormal hypothalamus morphology
abnormal paraventricular hypothalamic nucleus morphology
abnormal ventromedial hypothalamic nucleus morphology
abnormal cerebral cortex morphology
thin cerebral cortex
abnormal neurite morphology
neurodegeneration
Availability Mouse Genotype
Hap1tm1Hay/Hap1tm1Hay
Hap1tm1Xjl/Hap1tm1Xjl
Hap1tm2Xjl/Hap1tm2Xjl
Tg(HCRT-cre)1Stak/0  (conditional)
Hap1tm2Xjl/Hap1tm2Xjl
Tg(CAG-cre/Esr1*)5Amc/0  (conditional)
Hap1tm2Xjl/Hap1tm2Xjl
Tg(Camk2a-cre)159Kln/0  (conditional)

Contributing Projects:
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
04/23/2024
MGI 6.23
The Jackson Laboratory