SNX8 (sorting nexin 8)

2014-11-01  

Identity

HGNC
LOCATION
7p22.3
LOCUSID
ALIAS
Mvp1
FUSION GENES

Other Information

Locus ID:

NCBI: 29886
MIM: 614905
HGNC: 14972
Ensembl: ENSG00000106266

Variants:

dbSNP: 29886
ClinVar: 29886
TCGA: ENSG00000106266
COSMIC: SNX8

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000106266ENST00000222990Q9Y5X2
ENSG00000106266ENST00000419693C9IYC5
ENSG00000106266ENST00000435060C9J271
ENSG00000106266ENST00000435336C9J8E6
ENSG00000106266ENST00000447136C9JCB9
ENSG00000106266ENST00000457286C9J014

Expression (GTEx)

0
10
20
30
40
50
60

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
219730562012SNX-BAR-mediated endosome tubulation is co-ordinated with endosome maturation.54
291804172017SNX8 mediates IFNγ-triggered noncanonical signaling pathway and host defense against Listeria monocytogenes.6
243115142014SNX8: A candidate gene for 7p22 cardiac malformations including tetralogy of fallot.2

Citation

Dessen P

SNX8 (sorting nexin 8)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/74064/snx8