SLC25A38
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.
See also
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| SLC1–10 |
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| | SLC11–20 |
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- proton coupled metal ion transporter
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- human Na+-sulfate/carboxylate cotransporter
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- proton oligopeptide cotransporter
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- monocarboxylate transporter
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| | SLC21–30 |
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- Na+-dependent ascorbic acid transporter
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- multifunctional anion exchanger
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- Na+-coupled nucleoside transport (SLC28A1
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- facilitative nucleoside transporter
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| | SLC31–40 |
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- type II Na+-phosphate cotransporter
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- nucleoside-sugar transporter
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- SLC35E1
- SLC35E2
- SLC35E3
- SLC35E4
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- proton-coupled amino-acid transporter
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- sugar-phosphate/phosphate exchanger
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- System A & N, sodium-coupled neutral amino-acid transporter
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- basolateral iron transporter
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| | SLC41–48 |
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- Na+-independent, system-L like amino-acid transporter
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- Putative sugar transporter
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see also solute carrier disorders |