Gene Symbol | SLC16A12 |
Entrez Gene ID | 387700 |
Full Name | solute carrier family 16 member 12 |
Synonyms | CJMG,CRT2,CTRCT47,MCT12 |
General protein information |
|
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) |