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NGN2 (Neurogenin-2)

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wiki page Created: 2026-04-02T07:19:30 By: crosslink-migration Quality: 50% ✓ SciDEX ID: wiki-genes-ngn2
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NGN2 (Neurogenin-2)

<div class="infobox infobox-gene">

| Property | Value |
|----------|-------|
| Gene Symbol | NGN2 (NEUROG2) |
| Full Name | Neurogenin-2 |
| Chromosomal Location | 4q21.1 |
| NCBI Gene ID | 63973 |
| OMIM ID | 607574 |
| Ensembl ID | ENSG00000174348 |
| UniProt ID | Q9HSY5 |
| Encoded Protein | Ngn2 (Neurogenin-2) |
| Associated Diseases | Alzheimer's Disease, Parkinson's Disease, Autism, Intellectual Disability, Schizophrenia |

</div>

Overview

NGN2 encodes neurogenin-2, a Class A basic helix-loop-helix (bHLH) transcription factor that functions as a master regulator of excitatory neuronal fate determination in the developing nervous system. As part of the neurogenin family (NGN1, NGN2), this gene plays critical roles in neurogenesis, neuronal subtype specification, and cortical layer formation[@bertrand2002].

NGN2 is expressed transiently during development, where it directs neural progenitor cells toward excitatory glutamatergic neuron differentiation while suppressing alternative cell fates such as astrocyte and oligodendrocyte differentiation. Its expression is tightly regulated by Notch signaling and environmental cues, creating a well-controlled window for neurogenesis.

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NGN2
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kg_node_idNGN2
entity_typegene
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wiki_page_idwp-3b5e74fc4fce
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📊 Evidence Profile Foundational
Evidence Balance
+0%
Certainty
55%
Debates
0
Incoming
11
Outgoing
15
0 supporting 0 contradicting 0 neutral
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