SNX29 (sorting nexin 29)

2014-11-01  

Identity

HGNC
LOCATION
16p13.13
LOCUSID
ALIAS
A-388D4.1,RUNDC2A
FUSION GENES

Other Information

Locus ID:

NCBI: 92017
HGNC: 30542
Ensembl: ENSG00000048471

Variants:

dbSNP: 92017
ClinVar: 92017
TCGA: ENSG00000048471
COSMIC: SNX29

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000048471ENST00000562510H3BPI1
ENSG00000048471ENST00000563308H3BQF0
ENSG00000048471ENST00000564791A0A0C4DGM3
ENSG00000048471ENST00000566228Q8TEQ0
ENSG00000048471ENST00000569801H3BT98

Expression (GTEx)

0
5
10
15
20
25
30

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
331434982021SNX29, a new susceptibility gene shared with major mental disorders in Han Chinese population.7
331434982021SNX29, a new susceptibility gene shared with major mental disorders in Han Chinese population.7
233581602014Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci.86
233581602014Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci.86
197732792009Association between genetic variants in VEGF, ERCC3 and occupational benzene haematotoxicity.9
197732792009Association between genetic variants in VEGF, ERCC3 and occupational benzene haematotoxicity.9

Citation

Dessen P

SNX29 (sorting nexin 29)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/55065/gene-explorer/gene-fusions-explorer/deep-insight-explorer/