Identity
HGNC
LOCATION
7q31.2
LOCUSID
ALIAS
ETS7q,FAM4A,FAM4A1,HELG,RAY1,SEN4,TSG7
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: 7982
MIM: 600833
HGNC: 11351
Ensembl: ENSG00000004866
Variants:
dbSNP: 7982
ClinVar: 7982
TCGA: ENSG00000004866
COSMIC: ST7
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 30945288 | 2019 | Inflammation-dependent overexpression of c-Myc enhances CRL4(DCAF4) E3 ligase activity and promotes ubiquitination of ST7 in colitis-associated cancer. | 17 |
| 30945288 | 2019 | Inflammation-dependent overexpression of c-Myc enhances CRL4(DCAF4) E3 ligase activity and promotes ubiquitination of ST7 in colitis-associated cancer. | 17 |
| 24453002 | 2014 | Genetic validation of the protein arginine methyltransferase PRMT5 as a candidate therapeutic target in glioblastoma. | 80 |
| 24453002 | 2014 | Genetic validation of the protein arginine methyltransferase PRMT5 as a candidate therapeutic target in glioblastoma. | 80 |
| 20238225 | 2011 | Localization and characterization of ST7 in cancer. | 7 |
| 20238225 | 2011 | Localization and characterization of ST7 in cancer. | 7 |
| 20379614 | 2010 | Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. | 78 |
| 20628086 | 2010 | Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study. | 15 |
| 20379614 | 2010 | Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. | 78 |
| 20628086 | 2010 | Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study. | 15 |
| 19058789 | 2009 | A common variant in DRD3 receptor is associated with autism spectrum disorder. | 31 |
| 19736351 | 2009 | Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation. | 176 |
| 19913121 | 2009 | Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip. | 105 |
| 19058789 | 2009 | A common variant in DRD3 receptor is associated with autism spectrum disorder. | 31 |
| 19736351 | 2009 | Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation. | 176 |
Citation
Dessen P
ST7 (suppression of tumorigenicity 7)
Atlas Genet Cytogenet Oncol Haematol. 2004-08-01
Online version: http://atlasgeneticsoncology.org/gene/42919/st7-(suppression-of-tumorigenicity-7)
