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 (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
GOUT GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SLC25A43-related disorder Likely benign; Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Breast Carcinoma Breast Carcinoma BEFREE 22430806, 23354756, 28781661
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Breast neoplasm Pubtator 22430806, 22883974, 23354756 Associate
★☆☆☆☆
Found in Text Mining only
Carcinoma Carcinoma BEFREE 28781661
★☆☆☆☆
Found in Text Mining only
Carcinoma, Basal Cell Carcinoma BEFREE 28781661
★☆☆☆☆
Found in Text Mining only
Hereditary Breast and Ovarian Cancer Syndrome Hereditary breast and ovarian cancer syndrome Pubtator 22430806 Associate
★☆☆☆☆
Found in Text Mining only
Lung Diseases Lung disease Pubtator 22883974 Inhibit
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of breast Breast Cancer BEFREE 22430806, 23354756, 28781661
★☆☆☆☆
Found in Text Mining only
Malignant Neoplasms Malignant Neoplasm BEFREE 22883974, 23354756
★☆☆☆☆
Found in Text Mining only
Mammary Neoplasms Mammary Neoplasms BEFREE 22430806, 22883974
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 22430806, 22883974
★☆☆☆☆
Found in Text Mining only