Mitochondrial glycine transporter: Difference between revisions
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'''SLC25A38''' is a human gene. |
'''SLC25A38''' is a human gene. |
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* 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]]. |
* 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== |
==See also== |
Revision as of 22:15, 17 April 2016
solute carrier family 25, member 38 | |
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Identifiers | |
Symbol | SLC25A38 |
NCBI gene | 54977 |
HGNC | 26054 |
OMIM | 610819 |
RefSeq | NM_017875 |
Other data | |
Locus | Chr. 3 p22.1 |
SLC25A38 is a human 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. ;)