Identity
HGNC
LOCATION
1p35.2
LOCUSID
ALIAS
FKSG84,PRO0899,TDE2,TDE2L
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: 347735
MIM: 614549
HGNC: 23231
Ensembl: ENSG00000168528
Variants:
dbSNP: 347735
ClinVar: 347735
TCGA: ENSG00000168528
COSMIC: SERINC2
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000168528 | ENST00000373709 | Q96SA4 |
| ENSG00000168528 | ENST00000373710 | Q96SA4 |
| ENSG00000168528 | ENST00000536384 | Q96SA4 |
| ENSG00000168528 | ENST00000536859 | Q96SA4 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 34288243 | 2021 | SERINC2 increases the risk of bipolar disorder in the Chinese population. | 0 |
| 34288243 | 2021 | SERINC2 increases the risk of bipolar disorder in the Chinese population. | 0 |
| 29268082 | 2018 | Localization to detergent-resistant membranes and HIV-1 core entry inhibition correlate with HIV-1 restriction by SERINC5. | 32 |
| 29268082 | 2018 | Localization to detergent-resistant membranes and HIV-1 core entry inhibition correlate with HIV-1 restriction by SERINC5. | 32 |
| 28935972 | 2017 | Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder. | 15 |
| 28935972 | 2017 | Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder. | 15 |
| 24424505 | 2014 | siRNA-mediated knockdown of hTDE2 retards cell cycle progression through transcriptional activation of p21. | 3 |
| 24424505 | 2014 | siRNA-mediated knockdown of hTDE2 retards cell cycle progression through transcriptional activation of p21. | 3 |
| 23455491 | 2013 | NKAIN1-SERINC2 is a functional, replicable and genome-wide significant risk gene region specific for alcohol dependence in subjects of European descent. | 19 |
| 23778322 | 2013 | Rare SERINC2 variants are specific for alcohol dependence in individuals of European descent. | 11 |
| 23455491 | 2013 | NKAIN1-SERINC2 is a functional, replicable and genome-wide significant risk gene region specific for alcohol dependence in subjects of European descent. | 19 |
| 23778322 | 2013 | Rare SERINC2 variants are specific for alcohol dependence in individuals of European descent. | 11 |
| 21752829 | 2011 | Characterization of the CLEAR network reveals an integrated control of cellular clearance pathways. | 522 |
| 21752829 | 2011 | Characterization of the CLEAR network reveals an integrated control of cellular clearance pathways. | 522 |
Citation
Dessen P
SERINC2 (serine incorporator 2)
Atlas Genet Cytogenet Oncol Haematol. 2003-11-01
Online version: http://atlasgeneticsoncology.org/gene/42504/serinc2-(serine-incorporator-2)
