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: 399979
HGNC: 21532
Ensembl: ENSG00000255455
Variants:
dbSNP: 399979
ClinVar: 399979
TCGA: ENSG00000255455
COSMIC: SNX19
RNA/Proteins
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 33649454 | 2021 | Single molecule in situ hybridization reveals distinct localizations of schizophrenia risk-related transcripts SNX19 and AS3MT in human brain. | 3 |
| 34315878 | 2021 | SNX19 restricts endolysosome motility through contacts with the endoplasmic reticulum. | 21 |
| 33649454 | 2021 | Single molecule in situ hybridization reveals distinct localizations of schizophrenia risk-related transcripts SNX19 and AS3MT in human brain. | 3 |
| 34315878 | 2021 | SNX19 restricts endolysosome motility through contacts with the endoplasmic reticulum. | 21 |
| 30635639 | 2020 | Schizophrenia risk variants influence multiple classes of transcripts of sorting nexin 19 (SNX19). | 19 |
| 30635639 | 2020 | Schizophrenia risk variants influence multiple classes of transcripts of sorting nexin 19 (SNX19). | 19 |
| 19023099 | 2009 | Gene variants associated with ischemic stroke: the cardiovascular health study. | 20 |
| 19730683 | 2009 | The variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factors. | 74 |
| 19752551 | 2009 | Polymorphisms associated with both noncardioembolic stroke and coronary heart disease: vienna stroke registry. | 13 |
| 19023099 | 2009 | Gene variants associated with ischemic stroke: the cardiovascular health study. | 20 |
| 19730683 | 2009 | The variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factors. | 74 |
| 19752551 | 2009 | Polymorphisms associated with both noncardioembolic stroke and coronary heart disease: vienna stroke registry. | 13 |
| 17975119 | 2008 | Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study. | 77 |
| 17975119 | 2008 | Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study. | 77 |
| 18073581 | 2007 | Five common gene variants identify elevated genetic risk for coronary heart disease. | 51 |
Citation
Dessen P
SNX19 (sorting nexin 19)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/74053/snx19-(sorting-nexin-19)
