SNX29

sorting nexin 29

Associated Studies

Identification of Novel Reproducible Combinatorial Genetic Risk Factors for Myalgic Encephalomyelitis in the DecodeME Patient Cohort and Commonalities with Long COVID

2025 | Sardell et al.

Phenotype: ME/CFS

Details

HGNC: 30542
GeneCards: SNX29
NCBI: 92017
Ensembl: ENSG00000048471
UniProt: Q8TEQ0
OMIM: None
UCSC: uc002dby.6
VEGA: OTTHUMG00000129827
ENA: AK074072
Alias Symbols: FLJ12363
Previous Symbols: RUNDC2A
Alias Names: None
Previous Names: "RUN domain containing 2A"