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
209722502011Genetic loci associated with lipid concentrations and cardiovascular risk factors in the Korean population.25
209722502011Genetic loci associated with lipid concentrations and cardiovascular risk factors in the Korean population.25
201601932010Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples.21
205717542010Evaluating the discriminative power of multi-trait genetic risk scores for type 2 diabetes in a northern Swedish population.31
201601932010Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples.21
205717542010Evaluating the discriminative power of multi-trait genetic risk scores for type 2 diabetes in a northern Swedish population.31
190609062009Common variants at 30 loci contribute to polygenic dyslipidemia.659
190609062009Common variants at 30 loci contribute to polygenic dyslipidemia.659

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-(solute-carrier-family-35-member-g5)