<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">BECN1 Gene</th>
</tr>
<tr>
<td class="label">Symbol</td>
<td><strong>BECLIN1</strong></td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>BECN1</td>
</tr>
<tr>
<td class="label">Type</td>
<td>Gene</td>
</tr>
<tr>
<td class="label">NCBI</td>
<td><a href="https://www.ncbi.nlm.nih.gov/gene/?term=BECLIN1" target="_blank">Search NCBI</a></td>
</tr>
</table>
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">BECN1 Gene</th>
</tr>
<tr>
<td class="label">Symbol</td>
<td><strong>BECLIN1</strong></td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>BECN1</td>
</tr>
<tr>
<td class="label">Type</td>
<td>Gene</td>
</tr>
<tr>
<td class="label">NCBI</td>
<td><a href="https://www.ncbi.nlm.nih.gov/gene/?term=BECLIN1" target="_blank">Search NCBI</a></td>
</tr>
</table>
Becn1 Gene is an important component in the neurobiology of neurodegenerative diseases. This page provides detailed information about its structure, function, and role in disease processes.
:: infobox .infobox-gene [@hegdekar2023]
Symbol: BECN1 [@yao2021]
Full Name: Beclin 1 [@rusmini2019]
Chromosomal Location: 17q21.31 [@chen2021]
NCBI Gene ID: [9277](https://www.ncbi.nlm.nih.gov/gene/9277) [@yi2024]
OMIM: [604378](https://www.omim.org/entry/604378) [@luo2020]
Ensembl ID: [ENSG00000126581](https://www.ensembl.org/Homo_sapiens/Gene/Summary?g=ENSG00000126581) [@beccari2023]
UniProt: [Q14457](https://www.uniprot.org/uniprot/Q14457)
Proteins: [Beclin-1](/proteins/beclin-1)
Associated Diseases: [Alzheimer's Disease](/diseases/alzheimers-disease), [Parkinson's Disease](/diseases/parkinsons-disease), [Breast Cancer](/diseases/breast-cancer), [Neurodegeneration](/diseases/neurodegeneration)
::
BECN1 is a gene/protein encoding a key neuronal protein involved in synaptic function, signal transduction, and cellular homeostasis. Dysfunction of BECN1 is associated with neurodegenerative diseases including [Alzheimer's disease](/diseases/alzheimers-disease), [Parkinson's disease](/diseases/parkinsons-disease), and related disorders.
BECN1 encodes Beclin-1, a key regulator of [autophagy](/entities/autophagy) and [apoptosis](/entities/apoptosis). Beclin-1 is part of the PI3K complex that initiates autophagosome formation. It plays a dual role in cell survival (via autophagy) and cell death (via apoptosis). In neurodegenerative diseases, impaired autophagy leads to accumulation of protein aggregates, and Beclin-1 expression is often reduced.
Beclin-1 is widely expressed in:
The study of Becn1 Gene has evolved significantly over the past decades. Research in this area has revealed important insights into the underlying mechanisms of neurodegeneration and continues to drive therapeutic development.
Historical context and key discoveries in this field have shaped our current understanding and will continue to guide future research directions.
The following diagram shows the key molecular relationships involving BECN1 Gene discovered through SciDEX knowledge graph analysis: