linker for activation of T-cells family member 2
Alias
HSPC046 | LAB | NTAL | WBSCR15 | WBSCR5 | WSCR5
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].