| LAT2 |
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| Identifiers |
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| Aliases | LAT2, LAB, NTAL, WBSCR15, WBSCR5, WSCR5, HSPC046, linker for activation of T-cells family member 2, linker for activation of T cells family member 2 |
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| External IDs | OMIM: 605719; MGI: 1926479; HomoloGene: 11297; GeneCards: LAT2; OMA:LAT2 - orthologs |
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| Gene location (Mouse) |
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| | Chr. | Chromosome 5 (mouse) |
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| | Band | 5|5 G2 | Start | 134,628,876 bp |
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| End | 134,643,879 bp |
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| Wikidata |
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Linker for activation of T-cells family member 2 is a protein that in humans is encoded by the LAT2 gene.
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.