SLC35G5 (solute carrier family 35 member G5)

2014-11-01  

Identity

HGNC
LOCATION
8p23.1
LOCUSID
ALIAS
AMAC,AMAC1L2

Other Information

Locus ID:

NCBI: 83650
MIM: 615199
HGNC: 15546
Ensembl: ENSG00000177710

Variants:

dbSNP: 83650
ClinVar: 83650
TCGA: ENSG00000177710
COSMIC: SLC35G5

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000177710ENST00000382435Q96KT7

Expression (GTEx)

0
1
2
3
4
5
6

References

Pubmed IDYearTitleCitations
190609062009Common variants at 30 loci contribute to polygenic dyslipidemia.552
205717542010Evaluating the discriminative power of multi-trait genetic risk scores for type 2 diabetes in a northern Swedish population.26
209722502011Genetic loci associated with lipid concentrations and cardiovascular risk factors in the Korean population.20
201601932010Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples.16

Citation

Dessen P

SLC35G5 (solute carrier family 35 member G5)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/73417/slc35g5