Identity
HGNC
LOCATION
7q32.2
LOCUSID
ALIAS
2-COP,gamma-2-COP
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: 26958
MIM: 604355
HGNC: 2237
Ensembl: ENSG00000158623
Variants:
dbSNP: 26958
ClinVar: 26958
TCGA: ENSG00000158623
COSMIC: COPG2
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000158623 | ENST00000330992 | Q9UBF2 |
| ENSG00000158623 | ENST00000425248 | Q9UBF2 |
| ENSG00000158623 | ENST00000425248 | A0A140VK12 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 32583741 | 2020 | SCYL1 arginine methylation by PRMT1 is essential for neurite outgrowth via Golgi morphogenesis. | 8 |
| 32583741 | 2020 | SCYL1 arginine methylation by PRMT1 is essential for neurite outgrowth via Golgi morphogenesis. | 8 |
| 22456293 | 2012 | Methylation and expression analyses of the 7q autism susceptibility locus genes MEST , COPG2, and TSGA14 in human and anthropoid primate cortices. | 10 |
| 22456293 | 2012 | Methylation and expression analyses of the 7q autism susceptibility locus genes MEST , COPG2, and TSGA14 in human and anthropoid primate cortices. | 10 |
| 11920156 | 2002 | Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region. | 8 |
| 11920156 | 2002 | Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region. | 8 |
Citation
Dessen P
COPG2 (COPI coat complex subunit gamma 2)
Atlas Genet Cytogenet Oncol Haematol. 2003-02-01
Online version: http://atlasgeneticsoncology.org/gene/40132/copg2
