solute carrier family 25 member 46
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrial fission | ||
| mitochondrial fission | ||
| mitochondrial fission | ||
| autophagy of mitochondrion | ||
| mitochondrial transport |
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrion | ||
| mitochondrion | ||
| mitochondrial outer membrane | ||
| mitochondrial outer membrane | ||
| mitochondrial outer membrane |
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| protein-containing complex binding |
| Gene Ontology |
|---|
| axon development |
| mitochondrial fission |
| mitochondrial membrane fission |
| InterPro |
|---|
| Mitochondrial carrier domain superfamily |
| Mitochondrial substrate/solute carrier |
| Solute carrier family 25 member 46 |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0112330 | pontocerebellar hypoplasia type 1E |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: April 6, 2026