Gene Gene information from NCBI Gene database.
Entrez ID 203427
Gene name Solute carrier family 25 member 43
Gene symbol SLC25A43
Synonyms (NCBI Gene)
-
Chromosome X
Chromosome location Xq24
Summary This gene encodes a member of the mitochondrial carrier family of proteins.[provided by RefSeq, Dec 2009]
miRNA miRNA information provided by mirtarbase database.
324
miRTarBase ID miRNA Experiments Reference
MIRT540964 hsa-miR-548ac PAR-CLIP 21572407
MIRT540963 hsa-miR-548bb-3p PAR-CLIP 21572407
MIRT540962 hsa-miR-548d-3p PAR-CLIP 21572407
MIRT540961 hsa-miR-548h-3p PAR-CLIP 21572407
MIRT540960 hsa-miR-548z PAR-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
GO ID Ontology Definition Evidence Reference
GO:0005739 Component Mitochondrion IEA
GO:0005743 Component Mitochondrial inner membrane IEA
GO:0016020 Component Membrane IEA
GO:0055085 Process Transmembrane transport IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
300641 30557 ENSG00000077713
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8WUT9
Protein name Solute carrier family 25 member 43
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00153 Mito_carr 8 101 Mitochondrial carrier protein Family
PF00153 Mito_carr 102 195 Mitochondrial carrier protein Family
PF00153 Mito_carr 197 298 Mitochondrial carrier protein Family
Sequence
Sequence length 341
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
3
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
SLC25A43-related disorder Likely benign; Benign rs142240806, rs5957164, rs141488181 RCV003912095
RCV003964469
RCV003963824
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 22430806, 22883974, 23354756
Hereditary Breast and Ovarian Cancer Syndrome Associate 22430806
Lung Diseases Inhibit 22883974
Neoplasms Associate 22430806, 22883974
Uterine Cervicitis Inhibit 22883974