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Symbol Name ID |
Becn1
beclin 1, autophagy related MGI:1891828 |
| Darker colors indicate more annotations |
| Human Phenotypes | Absent Achilles reflex |
Dysphagia |
Spasticity |
Gliosis |
Dilated fourth ventricle |
Cerebellar atrophy |
Spinocerebellar tract degeneration |
Ataxia |
Limb ataxia |
Progressive cerebellar ataxia |
Truncal ataxia |
Abnormality of extrapyramidal motor function |
Bradykinesia |
Parkinsonism |
Fasciculations |
Facial-lingual fasciculations |
Babinski sign |
Dysarthria |
Dementia |
Dystonia |
Postural instability |
Impaired vibratory sensation |
Abnormal autonomic nervous system physiology |
| Disease(s) Associated with BECN1 | |||||||||||||||||||||||
| Machado-Joseph disease |
| Mouse Phenotypes | abnormal brain development |
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| Availability | Mouse Genotype | |
| Becn1tm1Ebr/Becn1+ Tg(MMTV-cre)1Mam/? (conditional) |
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| Becn1tm1Ebr/Becn1+ Tg(EIIa-cre)C5379Lmgd/? (conditional) |
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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 04/23/2024 MGI 6.23 |
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