Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 9379
MIM: 600566
HGNC: 8009
Ensembl: ENSG00000110076
Variants:
dbSNP: 9379
ClinVar: 9379
TCGA: ENSG00000110076
COSMIC: NRXN2
RNA/Proteins
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36242655 | 2022 | Neurexin 2 p.G849D variant, implicated in Parkinson's disease, increases reactive oxygen species, and reduces cell viability and mitochondrial membrane potential in SH-SY5Y cells. | 1 |
| 36242655 | 2022 | Neurexin 2 p.G849D variant, implicated in Parkinson's disease, increases reactive oxygen species, and reduces cell viability and mitochondrial membrane potential in SH-SY5Y cells. | 1 |
| 34126933 | 2021 | A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study. | 4 |
| 34777568 | 2021 | NRXN2 Possesses a Tumor Suppressor Potential via Inhibiting the Growth of Thyroid Cancer Cells. | 0 |
| 34126933 | 2021 | A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study. | 4 |
| 34777568 | 2021 | NRXN2 Possesses a Tumor Suppressor Potential via Inhibiting the Growth of Thyroid Cancer Cells. | 0 |
| 32099033 | 2020 | Translational Inhibition of α-Neurexin 2. | 6 |
| 32099033 | 2020 | Translational Inhibition of α-Neurexin 2. | 6 |
| 30709877 | 2019 | Mutations in NRXN1 and NRXN2 in a patient with early-onset epileptic encephalopathy and respiratory depression. | 11 |
| 30709877 | 2019 | Mutations in NRXN1 and NRXN2 in a patient with early-onset epileptic encephalopathy and respiratory depression. | 11 |
| 29045040 | 2018 | Neurexin gene family variants as risk factors for autism spectrum disorder. | 31 |
| 29654904 | 2018 | A de novo 921 Kb microdeletion at 11q13.1 including neurexin 2 in a boy with developmental delay, deficits in speech and language without autistic behaviors. | 2 |
| 29045040 | 2018 | Neurexin gene family variants as risk factors for autism spectrum disorder. | 31 |
| 29654904 | 2018 | A de novo 921 Kb microdeletion at 11q13.1 including neurexin 2 in a boy with developmental delay, deficits in speech and language without autistic behaviors. | 2 |
| 28013231 | 2017 | Neurexins 1-3 Each Have a Distinct Pattern of Expression in the Early Developing Human Cerebral Cortex. | 24 |
Citation
Dessen P
NRXN2 (neurexin 2)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/70978/nrxn2-(neurexin-2)
