Gene Symbol | LAT2 |
Entrez Gene ID | 7462 |
Full Name | linker for activation of T cells family member 2 |
Synonyms | HSPC046,LAB,NTAL,WBSCR15,WBSCR5,WSCR5 |
General protein information |
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Gene Type | protein-coding |
Organism | Homo sapiens(human) |
Genome | |
Summary | This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein. [provided by RefSeq, Jul 2008]. |
Disorder MIM: |