SCUBA

SLC25A11 — Solute carrier family 25 member 11

SLC25A11 belongs to a gene co-expression module in 4 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

SLC25A11's module in each cell type

Cell typeModuleShares the module with
CD8⁺ T cellsRho GTPase Cytoskeletal
Cytoskeletal
ARHGDIA, BUD31, CYB5B, MORF4L1, PIN1, POLR2G, PPP4C, PSMB7 +5 moreView in SCUBA
Gamma-delta T cellsCellular Homeostasis
Housekeeping
ANAPC11, BANF1, CALM3, CBX3, CBX5, COMMD4, DPM2, DUT +21 more
Innate lymphoid cellsMitochondrial Metabolism
Mitochondrial & OxPhos
ACTR10, ANP32A, APOL3, ATP6V1E1, ECHS1, ERCC1, ETFB, GLRX3 +12 moreView in SCUBA
MacrophagesMitochondrial Biogenesis
Mitochondrial & OxPhos
AIMP1, ATP5F1D, ATP5MC1, C1QBP, CCT2, CCT3, CCT7, CHCHD1 +38 moreView in SCUBA

About the gene

SynonymsOGC, SLC20A4
Chromosome17: 4937130-4940053
Predicted locationMembrane
Essential geneNo
Protein classDisease related genes, Human disease related genes, Metabolic proteins, Plasma proteins, Potential drug targets, Predicted membrane proteins, Transporters
Biological processAntiport, Lipid transport, Transport

Function

Catalyzes the transport of 2-oxoglutarate (alpha- oxoglutarate) across the inner mitochondrial membrane in an electroneutral exchange for malate. Can also exchange 2-oxoglutarate for other dicarboxylic acids such as malonate, succinate, maleate and oxaloacetate, although with lower affinity. Contributes to several metabolic processes, including the malate-aspartate shuttle, the oxoglutarate/isocitrate shuttle, in gluconeogenesis from lactate, and in nitrogen metabolism (By similarity). Maintains mitochondrial fusion and fission events, and the organization and morphology of cristae. Involved in the regulation of apoptosis (By similarity). Helps protect from cytotoxic-induced apoptosis by modulating glutathione levels in mitochondria (By similarity).

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.