Gene Symbol | C12orf57 |
Entrez Gene ID | 113246 |
Full Name | chromosome 12 open reading frame 57 |
Synonyms | C10,GRCC10 |
General protein information |
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Gene Type | protein-coding |
Organism | Homo sapiens(human) |
Genome | |
Summary | This gene is ubiquitously expressed in human tissues. It is required for development of the human corpus callosum. Mutations in this gene are associated with Temtamy syndrome (TEMTYS). Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2014]. |
Disorder MIM: | |
Disorder Html: | Temtamy syndrome, 218340 (3) |