SLC16A9 (solute carrier family 16 member 9)

2014-11-01  

Identity

HGNC
LOCATION
10q21.2
LOCUSID
ALIAS
C10orf36,MCT9
FUSION GENES

Other Information

Locus ID:

NCBI: 220963
MIM: 614242
HGNC: 23520
Ensembl: ENSG00000165449

Variants:

dbSNP: 220963
ClinVar: 220963
TCGA: ENSG00000165449
COSMIC: SLC16A9

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000165449ENST00000395347Q7RTY1
ENSG00000165449ENST00000395348Q7RTY1

Expression (GTEx)

0
50
100
150

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
200375892010A genome-wide perspective of genetic variation in human metabolism.252
195035972009Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.228
163854512006A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.69
198903912009Common polymorphisms influencing serum uric acid levels contribute to susceptibility to gout, but not to coronary artery disease.34
198614892010Replication of the five novel loci for uric acid concentrations and potential mediating mechanisms.33
239901052013Common missense variant of monocarboxylate transporter 9 (MCT9/SLC16A9) gene is associated with renal overload gout, but not with all gout susceptibility.17
201627422010Predictive value of 8 genetic loci for serum uric acid concentration.6
201627432010Common variants in SLC17A3 gene affect intra-personal variation in serum uric acid levels in longitudinal time series.3
248242782014HBsAg loss in patients treated with peginterferon alfa-2a and adefovir is associated with SLC16A9 gene variation and lower plasma carnitine levels.2

Citation

Dessen P

SLC16A9 (solute carrier family 16 member 9)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/73299/slc16a9