KCNJ16

potassium inwardly rectifying channel subfamily J member 16

Associated Studies

Identification of novel reproducible combinatorial genetic risk factors for myalgic encephalomyelitis in the DecodeME patient cohort and commonalities with long COVID

2026 | Sardell et al.

Phenotype: ME/CFS
Development and validation of blood-based diagnostic biomarkers for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) using EpiSwitch® 3-dimensional genomic regulatory immuno-genetic profiling

2025 | Hunter et al.

Phenotype: ME/CFS

Details

HGNC: 6262
GeneCards: KCNJ16
NCBI: 3773
Ensembl: ENSG00000153822
UniProt: Q9NPI9
OMIM: 605722
UCSC: uc031reh.2
VEGA: OTTHUMG00000180349
ENA: AF153815
Alias Symbols: Kir5.1, BIR9
Previous Symbols: None
Alias Names: None
Previous Names: "potassium inwardly-rectifying channel, subfamily J, member 16"