Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
9481
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 25 member 27
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC25A27
Synonyms (NCBI Gene) Gene synonyms aliases
UCP4
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p12.3
Summary Summary of gene provided in NCBI Entrez Gene.
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.
miRTarBase ID miRNA Experiments Reference
MIRT509160 hsa-miR-369-3p HITS-CLIP 21572407
MIRT509159 hsa-miR-5692b HITS-CLIP 21572407
MIRT509158 hsa-miR-5692c HITS-CLIP 21572407
MIRT509157 hsa-miR-410-3p HITS-CLIP 21572407
MIRT509156 hsa-miR-5011-5p HITS-CLIP 21572407
Transcription factors
Transcription factor Regulation Reference
NFKB1 Activation 20385226
RELA Activation 20385226
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005739 Component Mitochondrion IDA 10025957
GO:0005743 Component Mitochondrial inner membrane TAS
GO:0008284 Process Positive regulation of cell population proliferation IEA
GO:0009409 Process Response to cold IBA 21873635
GO:0010917 Process Negative regulation of mitochondrial membrane potential IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
613725 21065 ENSG00000153291
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

Accession ID Position in sequence Description Type
PF00153 Mito_carr 16 120 Mitochondrial carrier protein Family
PF00153 Mito_carr 123 222 Mitochondrial carrier protein Family
PF00153 Mito_carr 225 320 Mitochondrial carrier protein Family
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.
  Reactome
    The fatty acid cycling model
The proton buffering model
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
21332312, 17066476
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 36877954
Alzheimer Disease Associate 30425186
Frontotemporal Dementia Associate 30425186
Lung Neoplasms Associate 36877954
Mitochondrial complex I deficiency Inhibit 22427795
Neoplasms Associate 25154973, 32053908
Neuroblastoma Associate 22427795
Neurodegenerative Diseases Associate 30425186