Identity
HGNC
LOCATION
16p13.13
LOCUSID
ALIAS
A-388D4.1,RUNDC2A
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: 92017
HGNC: 30542
Ensembl: ENSG00000048471
Variants:
dbSNP: 92017
ClinVar: 92017
TCGA: ENSG00000048471
COSMIC: SNX29
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 33143498 | 2021 | SNX29, a new susceptibility gene shared with major mental disorders in Han Chinese population. | 7 |
| 33143498 | 2021 | SNX29, a new susceptibility gene shared with major mental disorders in Han Chinese population. | 7 |
| 23358160 | 2014 | Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci. | 86 |
| 23358160 | 2014 | Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci. | 86 |
| 19773279 | 2009 | Association between genetic variants in VEGF, ERCC3 and occupational benzene haematotoxicity. | 9 |
| 19773279 | 2009 | Association 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/snx29-(sorting-nexin-29)
