SLC25A15 (solute carrier family 25 member 15)

2019-04-01  

Identity

HGNC
LOCATION
13q14.11
LOCUSID
ALIAS
D13S327,HHH,LNC-HC,ORC1,ORNT1
FUSION GENES

Other Information

Locus ID:

NCBI: 10166
MIM: 603861
HGNC: 10985
Ensembl: ENSG00000102743

Variants:

dbSNP: 10166
ClinVar: 10166
TCGA: ENSG00000102743
COSMIC: SLC25A15

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000102743ENST00000338625Q9Y619
ENSG00000102743ENST00000417731Q5VZD9
ENSG00000102743ENST00000470509F2Z354

Expression (GTEx)

0
5
10
15
20
25
30
35

Pathways

PathwaySourceExternal ID
MetabolismREACTOMER-HSA-1430728
Metabolism of amino acids and derivativesREACTOMER-HSA-71291
Urea cycleREACTOMER-HSA-70635
Metabolism of polyaminesREACTOMER-HSA-351202

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
384505982024Deficiency in SLC25A15, a hypoxia-responsive gene, promotes hepatocellular carcinoma by reprogramming glutamine metabolism.1
384505982024Deficiency in SLC25A15, a hypoxia-responsive gene, promotes hepatocellular carcinoma by reprogramming glutamine metabolism.1
301213012018Structure/function relationships of the human mitochondrial ornithine/citrulline carrier by Cys site-directed mutagenesis. Relevance to mercury toxicity.4
304031792018Overexpression of SLC25A15 is involved in the proliferation of cutaneous melanoma and leads to poor prognosis.3
301213012018Structure/function relationships of the human mitochondrial ornithine/citrulline carrier by Cys site-directed mutagenesis. Relevance to mercury toxicity.4
304031792018Overexpression of SLC25A15 is involved in the proliferation of cutaneous melanoma and leads to poor prognosis.3
232661872013The mitochondrial transporter family SLC25: identification, properties and physiopathology.0
232661872013The mitochondrial transporter family SLC25: identification, properties and physiopathology.0
222628512012Substrate specificity of the two mitochondrial ornithine carriers can be swapped by single mutation in substrate binding site.24
222920902012Insights into the mutation-induced HHH syndrome from modeling human mitochondrial ornithine transporter-1.12
224650822012Long-term follow-up of four patients affected by HHH syndrome.9
222628512012Substrate specificity of the two mitochondrial ornithine carriers can be swapped by single mutation in substrate binding site.24
222920902012Insights into the mutation-induced HHH syndrome from modeling human mitochondrial ornithine transporter-1.12
224650822012Long-term follow-up of four patients affected by HHH syndrome.9
208776242010Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression.20

Citation

Dessen P

SLC25A15 (solute carrier family 25 member 15)

Atlas Genet Cytogenet Oncol Haematol. 2019-04-01

Online version: http://atlasgeneticsoncology.org/gene/57802/slc25a15-(solute-carrier-family-25-member-15)