Mitochondrial glycine transporter
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| solute carrier family 25, member 38 | |
|---|---|
| Identifiers | |
| Symbol | SLC25A38 |
| NCBI gene | 54977 |
| HGNC | 26054 |
| OMIM | 610819 |
| RefSeq | NM_017875 |
| Other data | |
| Locus | Chr. 3 p22.1 |
Mitochondrial glycine transporter is a protein that in humans is encoded by the SLC25A38 gene. SLC25A38 is involved in mitochondrial handling of glycine and is needed for the first step in heme synthesis. Mutations in this gene can lead to an autosomal recessive form of sideroblastic anemia.
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see also solute carrier disorders | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
 | This article on a gene on human chromosome 3 is a stub. You can help Wikipedia by expanding it. |