| Gene Symbol | SLC16A12 |
| Entrez Gene ID | 387700 |
| Full Name | solute carrier family 16 member 12 |
| Synonyms | CJMG,CRT2,CTRCT47,MCT12 |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | This gene encodes a transmembrane transporter that likely plays a role in monocarboxylic acid transport. A mutation in this gene has been associated with juvenile cataracts with microcornea and renal glucosuria. [provided by RefSeq, Mar 2010]. |
| Disorder MIM: | |
| Disorder Html: | Cataract 47, juvenile, with microcornea, 612018 (3) |








































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