Mus musculus Gene: Slc25a4 | |||||||||||||||||||||||
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Summary | |||||||||||||||||||||||
InnateDB Gene | IDBG-153787.6 | ||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||
Gene Symbol | Slc25a4 | ||||||||||||||||||||||
Gene Name | solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 | ||||||||||||||||||||||
Synonyms | Ant1; AU019225 | ||||||||||||||||||||||
Species | Mus musculus | ||||||||||||||||||||||
Ensembl Gene | ENSMUSG00000031633 | ||||||||||||||||||||||
Encoded Proteins |
solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4
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Protein Structure |
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Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||||||||
Entrez Gene | |||||||||||||||||||||||
Summary |
This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000151729:
This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the mitochondrial matrix into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Mutations in this gene have been shown to result in autosomal dominant progressive external opthalmoplegia and familial hypertrophic cardiomyopathy. [provided by RefSeq, Sep 2009] This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the cytoplasm into the mitochondrial matrix and ATP from the mitochondrial matrix into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Mutations in this gene have been shown to result in autosomal dominant progressive external opthalmoplegia and familial hypertrophic cardiomyopathy. [provided by RefSeq, Jun 2013] |
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Gene Information | |||||||||||||||||||||||
Type | Protein coding | ||||||||||||||||||||||
Genomic Location | Chromosome 8:46206797-46211284 | ||||||||||||||||||||||
Strand | Reverse strand | ||||||||||||||||||||||
Band | B1.1 | ||||||||||||||||||||||
Transcripts |
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Interactions | |||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 17 experimentally validated interaction(s) in this database.
They are also associated with 18 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||||||||||
Species
Homo sapiens
Bos taurus
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Gene ID
Gene Order
Not yet available
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Pathways | |||||||||||||||||||||||
NETPATH | |||||||||||||||||||||||
REACTOME |
Integration of energy metabolism pathway
Metabolism pathway
Metabolism of proteins pathway
Mitochondrial protein import pathway
Regulation of insulin secretion pathway
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KEGG |
Calcium signaling pathway pathway
Parkinson's disease pathway
Huntington's disease pathway
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INOH | |||||||||||||||||||||||
PID NCI | |||||||||||||||||||||||
Pathway Predictions based on Human Orthology Data | |||||||||||||||||||||||
NETPATH |
AndrogenReceptor pathway
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REACTOME |
Mitochondrial protein import pathway
Regulation of insulin secretion pathway
Integration of energy metabolism pathway
Vpr-mediated induction of apoptosis by mitochondrial outer membrane permeabilization pathway
Interactions of Vpr with host cellular proteins pathway
Metabolism of proteins pathway
HIV Infection pathway
Metabolism pathway
Host Interactions of HIV factors pathway
Disease pathway
Mitochondrial protein import pathway
Regulation of insulin secretion pathway
Integration of energy metabolism pathway
Metabolism of proteins pathway
Metabolism pathway
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KEGG |
Calcium signaling pathway pathway
Parkinson's disease pathway
Huntington's disease pathway
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INOH | |||||||||||||||||||||||
PID NCI | |||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||
SwissProt | P48962 | ||||||||||||||||||||||
TrEMBL | |||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||
Entrez Gene | 11739 | ||||||||||||||||||||||
UniGene | Mm.16228 Mm.393487 | ||||||||||||||||||||||
RefSeq | NM_007450 | ||||||||||||||||||||||
OMIM | |||||||||||||||||||||||
CCDS | CCDS40333 | ||||||||||||||||||||||
HPRD | |||||||||||||||||||||||
IMGT | |||||||||||||||||||||||
MGI ID | MGI:1353495 | ||||||||||||||||||||||
MGI Symbol | Slc25a4 | ||||||||||||||||||||||
EMBL | AF240002 BC003791 BC026925 U27315 X74510 | ||||||||||||||||||||||
GenPept | AAC52837 AAF64470 AAH03791 AAH26925 CAA52616 | ||||||||||||||||||||||
RNA Seq Atlas | 11739 | ||||||||||||||||||||||