Identity
HGNC
LOCATION
9p13.3
LOCUSID
ALIAS
MUNC13,UNC13,Unc13h2,munc13-2
FUSION GENES
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: 10497
MIM: 605836
HGNC: 12566
Ensembl: ENSG00000198722
Variants:
dbSNP: 10497
ClinVar: 10497
TCGA: ENSG00000198722
COSMIC: UNC13B
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35135883 | 2022 | Munc13 structural transitions and oligomers that may choreograph successive stages in vesicle priming for neurotransmitter release. | 24 |
| 35135883 | 2022 | Munc13 structural transitions and oligomers that may choreograph successive stages in vesicle priming for neurotransmitter release. | 24 |
| 33876820 | 2021 | UNC13B variants associated with partial epilepsy with favourable outcome. | 19 |
| 33876820 | 2021 | UNC13B variants associated with partial epilepsy with favourable outcome. | 19 |
| 32134975 | 2020 | Munc13 mediates klotho-inhibitable diacylglycerol-stimulated exocytotic insertion of pre-docked TRPC6 vesicles. | 4 |
| 32134975 | 2020 | Munc13 mediates klotho-inhibitable diacylglycerol-stimulated exocytotic insertion of pre-docked TRPC6 vesicles. | 4 |
| 31713534 | 2019 | The Association of UNC13B Gene Polymorphisms and Diabetic Kidney Disease in a Chinese Han Population. | 4 |
| 31713534 | 2019 | The Association of UNC13B Gene Polymorphisms and Diabetic Kidney Disease in a Chinese Han Population. | 4 |
| 29485200 | 2018 | Tomosyn guides SNARE complex formation in coordination with Munc18 and Munc13. | 12 |
| 30117296 | 2018 | De novo UNC13B mutation identified in a bipolar disorder patient increases a rare exon-skipping variant. | 5 |
| 29485200 | 2018 | Tomosyn guides SNARE complex formation in coordination with Munc18 and Munc13. | 12 |
| 30117296 | 2018 | De novo UNC13B mutation identified in a bipolar disorder patient increases a rare exon-skipping variant. | 5 |
| 26990377 | 2016 | Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study. | 13 |
| 26990377 | 2016 | Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study. | 13 |
| 24854537 | 2014 | Structural insights into calmodulin/Munc13 interaction. | 3 |
Citation
Dessen P
UNC13B (unc-13 homolog B)
Atlas Genet Cytogenet Oncol Haematol. 2014-08-01
Online version: http://atlasgeneticsoncology.org/gene/54755/unc13b-(unc-13-homolog-b)
