Identity
HGNC
LOCATION
15q13.3
LOCUSID
ALIAS
7B2,P7B2,SGNE1,SgV
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: 6447
MIM: 173120
HGNC: 10816
Ensembl: ENSG00000166922
Variants:
dbSNP: 6447
ClinVar: 6447
TCGA: ENSG00000166922
COSMIC: SCG5
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 27984123 | 2017 | Clinicopathological features of a kindred with SCG5-GREM1-associated hereditary mixed polyposis syndrome. | 5 |
| 27984123 | 2017 | Clinicopathological features of a kindred with SCG5-GREM1-associated hereditary mixed polyposis syndrome. | 5 |
| 25811241 | 2015 | Phosphorylation and Alternative Splicing of 7B2 Reduce Prohormone Convertase 2 Activation. | 6 |
| 25811241 | 2015 | Phosphorylation and Alternative Splicing of 7B2 Reduce Prohormone Convertase 2 Activation. | 6 |
| 23172224 | 2013 | The neuroendocrine protein 7B2 suppresses the aggregation of neurodegenerative disease-related proteins. | 28 |
| 24042052 | 2013 | Blockade of islet amyloid polypeptide fibrillation and cytotoxicity by the secretory chaperones 7B2 and proSAAS. | 18 |
| 23172224 | 2013 | The neuroendocrine protein 7B2 suppresses the aggregation of neurodegenerative disease-related proteins. | 28 |
| 24042052 | 2013 | Blockade of islet amyloid polypeptide fibrillation and cytotoxicity by the secretory chaperones 7B2 and proSAAS. | 18 |
| 21901745 | 2012 | Frequent epigenetic inactivation of the chaperone SGNE1/7B2 in human gliomas. | 3 |
| 22947085 | 2012 | The neuroendocrine protein 7B2 is intrinsically disordered. | 8 |
| 21901745 | 2012 | Frequent epigenetic inactivation of the chaperone SGNE1/7B2 in human gliomas. | 3 |
| 22947085 | 2012 | The neuroendocrine protein 7B2 is intrinsically disordered. | 8 |
| 19058789 | 2009 | A common variant in DRD3 receptor is associated with autism spectrum disorder. | 31 |
| 19058789 | 2009 | A common variant in DRD3 receptor is associated with autism spectrum disorder. | 31 |
| 18448176 | 2008 | Measurements of secretogranins II, III, V and proconvertases 1/3 and 2 in plasma from patients with neuroendocrine tumours. | 13 |
Citation
Dessen P
SCG5 (secretogranin V)
Atlas Genet Cytogenet Oncol Haematol. 2007-10-01
Online version: http://atlasgeneticsoncology.org/gene/49757/scg5
