Entrez gene ID | | 7462 |
Official gene symbol | | LAT2 |
Full name | | linker for activation of T cells family, member 2 |
Aliases | | ,HSPC046,LAB,NTAL,WBSCR15,WBSCR5,WSCR5, |
Gene 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] |
Location | | Chromosome: 7 Locus: 7q11.23 |
Gene position | | 73624087 - 73644164 Map Viewer |
Gene orientation | | plus |
Gene size | | 20078 bp |
Gene sequence |
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OMIM ID | | 605719 |
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