SLC25A14 (solute carrier family 25 member 14)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 9016 |
| Gene name | Solute carrier family 25 member 14 |
| Gene symbol | SLC25A14 |
| Synonyms (NCBI Gene) |
BMCP1UCP5
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| Chromosome | X |
| Chromosome location | Xq26.1 |
| Summary | Mitochondrial uncoupling proteins (UCP) are members of the larger family of mitochondrial anion carrier proteins (MACP). Uncoupling proteins separate oxidative phosphorylation from ATP synthesis with energy dissipated as heat, also referred to as the mito |
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miRNA
miRNA information provided by mirtarbase database.
14
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
20
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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O95258 | ||||||||||||||||||||
| Protein name | Brain mitochondrial carrier protein 1 (BMCP-1) (Mitochondrial uncoupling protein 5) (UCP 5) (Solute carrier family 25 member 14) | ||||||||||||||||||||
| Protein function | Transports inorganic anions (sulfate, sulfite, thiosulfate and phosphate) and, to a lesser extent, a variety of dicarboxylates (e.g. malonate, malate and citramalate) and, even more so, aspartate and glutamate and tricarboxylates (PubMed:3135677 | ||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Mainly expressed in brain (PubMed:10928996). Some expression in testis and pituitary (PubMed:10928996). {ECO:0000269|PubMed:10928996}. | ||||||||||||||||||||
| Sequence |
MGIFPGIILIFLRVKFATAAVIVSGHQKSTTVSHEMSGLNWKPFVYGGLASIVAEFGTFP |
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| Sequence length | 325 | ||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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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)
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Related Genes
Genes most often co-reported with SLC25A14 across shared curated disease and pathway associations.
4
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to SLC25A14 (see Related Genes above), that are NOT already directly curated for SLC25A14 itself -- a lead worth checking, not a confirmed association.
5
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