Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 23539
MIM: 610409
HGNC: 16270
Ensembl: ENSG00000100156
Variants:
dbSNP: 23539
ClinVar: 23539
TCGA: ENSG00000100156
COSMIC: SLC16A8
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000100156 | ENST00000320521 | O95907 |
| ENSG00000100156 | ENST00000427592 | B0QYL4 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 33477551 | 2021 | A Splice Variant in SLC16A8 Gene Leads to Lactate Transport Deficit in Human iPS Cell-Derived Retinal Pigment Epithelial Cells. | 7 |
| 33477551 | 2021 | A Splice Variant in SLC16A8 Gene Leads to Lactate Transport Deficit in Human iPS Cell-Derived Retinal Pigment Epithelial Cells. | 7 |
| 27966779 | 2017 | Serum Levels of TIMP-3, LIPC, IER3, and SLC16A8 in CFH-Negative AMD Cases. | 8 |
| 27966779 | 2017 | Serum Levels of TIMP-3, LIPC, IER3, and SLC16A8 in CFH-Negative AMD Cases. | 8 |
| 20424473 | 2010 | L-type voltage-dependent calcium channel alpha subunit 1C is a novel candidate gene associated with secondary hyperparathyroidism: an application of haplotype-based analysis for multiple linked single nucleotide polymorphisms. | 0 |
| 20424473 | 2010 | L-type voltage-dependent calcium channel alpha subunit 1C is a novel candidate gene associated with secondary hyperparathyroidism: an application of haplotype-based analysis for multiple linked single nucleotide polymorphisms. | 0 |
Citation
Dessen P
SLC16A8 (solute carrier family 16 member 8)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/73298/slc16a8-(solute-carrier-family-16-member-8)
