Gene Gene information from NCBI Gene database.
Entrez ID 283600
Gene name Solute carrier family 25 member 47
Gene symbol SLC25A47
Synonyms (NCBI Gene)
C14orf68HDCMPHDMCPHMFN1655
Chromosome 14
Chromosome location 14q32.2
Summary This gene encodes a member of a large family of mitochondrial transporters. The nuclear-encoded carrier protein is embedded in the inner mitochondrial membrane. This member of the family is thought to be an uncoupling protein that uncouples mitochondrial
miRNA miRNA information provided by mirtarbase database.
17
miRTarBase ID miRNA Experiments Reference
MIRT1357350 hsa-miR-1228 CLIP-seq
MIRT1357351 hsa-miR-329 CLIP-seq
MIRT1357352 hsa-miR-345 CLIP-seq
MIRT1357353 hsa-miR-3622a-3p CLIP-seq
MIRT1357354 hsa-miR-3622b-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
16
GO ID Ontology Definition Evidence Reference
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005739 Component Mitochondrion IBA
GO:0005739 Component Mitochondrion IEA
GO:0005741 Component Mitochondrial outer membrane IEA
GO:0005741 Component Mitochondrial outer membrane ISS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
609911 20115 ENSG00000140107
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6Q0C1
Protein name Solute carrier family 25 member 47 (Hepatocellular carcinoma down-regulated mitochondrial carrier protein) (Mitochondrial NAD(+) transporter SLC25A47)
Protein function Mitochondrial NAD(+) transporter that acts as a 'metabolic gate' in hepatic lipogenesis. Provides NAD(+) substrate to mitochondrial SIRT3 deacetylase and enables its NAD(+)-dependent activities in mitochondrial energy metabolism. This triggers d
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00153 Mito_carr 1 83 Mitochondrial carrier protein Family
PF00153 Mito_carr 94 210 Mitochondrial carrier protein Family
PF00153 Mito_carr 214 305 Mitochondrial carrier protein Family
Tissue specificity TISSUE SPECIFICITY: Specifically expressed in liver. {ECO:0000269|PubMed:15322095, ECO:0000269|PubMed:36804859}.
Sequence
Sequence length 308
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Prostate cancer Uncertain significance rs193920797 RCV000149395