| SLC23A2 |
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| Identifiers |
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| Aliases | SLC23A2, NBTL1, SLC23A1, SVCT2, YSPL2, hSVCT2, solute carrier family 23 member 2 |
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| External IDs | OMIM: 603791; MGI: 1859682; HomoloGene: 68440; GeneCards: SLC23A2; OMA:SLC23A2 - orthologs |
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| Gene location (Mouse) |
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| | Chr. | Chromosome 2 (mouse) |
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| | Band | 2|2 F2 | Start | 131,894,416 bp |
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| End | 131,987,028 bp |
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| RNA expression pattern |
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| Bgee | | Human | Mouse (ortholog) |
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| Top expressed in | - right adrenal cortex
- left adrenal cortex
- lateral nuclear group of thalamus
- Brodmann area 10
- Epithelium of choroid plexus
- paraflocculus of cerebellum
- cerebellar vermis
- pars compacta
- right lobe of liver
- subthalamic nucleus
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| | Top expressed in | - choroid plexus of fourth ventricle
- secondary oocyte
- gastrula
- zygote
- primary visual cortex
- perirhinal cortex
- CA3 field
- entorhinal cortex
- Epithelium of choroid plexus
- superior frontal gyrus
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| | More reference expression data |
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| BioGPS | |
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| Wikidata |
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Solute carrier family 23 member 2 is a protein that in humans is encoded by the SLC23A2 gene.
The absorption of vitamin C into the body and its distribution to organs requires two sodium-dependent vitamin C transporters. This gene encodes one of the two required transporters and the encoded protein accounts for tissue-specific uptake of vitamin C. Previously, this gene had an official symbol of SLC23A1.