| SLC19A2 |
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| Identifiers |
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| Aliases | SLC19A2, TC1, THMD1, THT1, THTR1, TRMA, solute carrier family 19 member 2 |
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| External IDs | OMIM: 603941; MGI: 1928761; HomoloGene: 38258; GeneCards: SLC19A2; OMA:SLC19A2 - orthologs |
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| Gene location (Mouse) |
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| | Chr. | Chromosome 1 (mouse) |
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| | Band | 1 H2.2|1 71.56 cM | Start | 164,076,615 bp |
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| End | 164,092,954 bp |
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| RNA expression pattern |
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| Bgee | | Human | Mouse (ortholog) |
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| Top expressed in | - secondary oocyte
- gastrocnemius muscle
- tibialis anterior muscle
- Skeletal muscle tissue of rectus abdominis
- biceps brachii
- deltoid muscle
- muscle of thigh
- gastric mucosa
- buccal mucosa cell
- body of tongue
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| | Top expressed in | - retinal pigment epithelium
- left lobe of liver
- facial motor nucleus
- medullary collecting duct
- cornea
- endothelial cell of lymphatic vessel
- interventricular septum
- motor neuron
- cumulus cell
- spermatocyte
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| | More reference expression data |
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| BioGPS | |
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| Wikidata |
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Thiamine transporter 1, also known as thiamine carrier 1 (TC1) or solute carrier family 19 member 2 (SLC19A2) is a protein that in humans is encoded by the SLC19A2 gene. SLC19A2 is a thiamine transporter. Mutations in this gene cause thiamine-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness.
