SNX19 (sorting nexin 19)

2014-11-01  

Identity

HGNC
SNX19
LOCATION
11q24.3
LOCUSID
399979
ALIAS
CHET8
FUSION GENES
Show Gene Fusions

Other Information

Locus ID:

NCBI: 399979
HGNC: 21532
Ensembl: ENSG00000255455

Variants:

dbSNP: 399979
ClinVar: 399979
TCGA: ENSG00000255455
COSMIC: SNX19

RNA/Proteins

References

Pubmed IDYearTitleCitations
179751192008Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study.65
197306832009The variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factors.59
180735812007Five common gene variants identify elevated genetic risk for coronary heart disease.43
190230992009Gene variants associated with ischemic stroke: the cardiovascular health study.16
197525512009Polymorphisms associated with both noncardioembolic stroke and coronary heart disease: vienna stroke registry.11

Citation

Dessen P

SNX19 (sorting nexin 19)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/74053/snx19