SLC35D3 (solute carrier family 35 member D3)

2014-11-01  

Identity

HGNC
LOCATION
6q23.3
LOCUSID
ALIAS
FRCL1

Other Information

Locus ID:

NCBI: 340146
MIM: 612519
HGNC: 15621
Ensembl: ENSG00000182747

Variants:

dbSNP: 340146
ClinVar: 340146
TCGA: ENSG00000182747
COSMIC: SLC35D3

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000182747ENST00000331858Q5M8T2

Expression (GTEx)

0
1
2
3
4
5
6

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
245507372014Mutation of SLC35D3 causes metabolic syndrome by impairing dopamine signaling in striatal D1 neurons.19
245507372014Mutation of SLC35D3 causes metabolic syndrome by impairing dopamine signaling in striatal D1 neurons.19

Citation

Dessen P

SLC35D3 (solute carrier family 35 member D3)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/73405/slc35d3-(solute-carrier-family-35-member-d3)