SLC25A27 (solute carrier family 25 member 27)
Gene | |
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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9481 |
Gene name
Gene Name - the full gene name approved by the HGNC.
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Solute carrier family 25 member 27 |
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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SLC25A27 |
Synonyms (NCBI Gene)
Gene synonyms aliases
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UCP4 |
Chromosome
Chromosome number
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6 |
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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6p12.3 |
Summary
Summary of gene provided in NCBI Entrez Gene.
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Mitochondrial uncoupling proteins (UCP) are members of the larger family of mitochondrial anion carrier proteins (MACP). UCPs separate oxidative phosphorylation from ATP synthesis with energy dissipated as heat, also referred to as the mitochondrial proto |
miRNA
miRNA information provided by mirtarbase database.
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Transcription factors | ||||||||||
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein | |||||||||||||||||||||
UniProt ID | O95847 | ||||||||||||||||||||
Protein name | Mitochondrial uncoupling protein 4 (UCP 4) (Solute carrier family 25 member 27) | ||||||||||||||||||||
Protein function | Facilitates proton transport across the inner mitochondrial membrane and may dissipate excessive proton gradient associated with oxidative and metabolic stress at neuronal synapses. Regulates glutamate-induced proton conductance in astrocytes, s | ||||||||||||||||||||
Family and domains |
Pfam
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Tissue specificity | TISSUE SPECIFICITY: Found in adult and fetal brain. Present in most of the brain tissues, with low levels in spinal cord, corpus callosum and substantia nigra. {ECO:0000269|PubMed:10025957}. | ||||||||||||||||||||
Sequence | |||||||||||||||||||||
Sequence length | 323 | ||||||||||||||||||||
Interactions | View interactions |
Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease information provided by ClinVar, GenCC, and GWAS databases.
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