| Homo sapiens Gene: LAT2 | |||||||||||||||||||
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| Summary | |||||||||||||||||||
| InnateDB Gene | IDBG-21069.6 | ||||||||||||||||||
| Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
| Gene Symbol | LAT2 | ||||||||||||||||||
| Gene Name | linker for activation of T cells family, member 2 | ||||||||||||||||||
| Synonyms | LAB; NTAL; WBSCR15; WBSCR5; WSCR5 | ||||||||||||||||||
| Species | Homo sapiens | ||||||||||||||||||
| Ensembl Gene | ENSG00000086730 | ||||||||||||||||||
| Encoded Proteins |
linker for activation of T cells family, member 2
linker for activation of T cells family, member 2
linker for activation of T cells family, member 2
linker for activation of T cells family, member 2
linker for activation of T cells family, member 2
linker for activation of T cells family, member 2
linker for activation of T cells family, member 2
linker for activation of T cells family, member 2
linker for activation of T cells family, member 2
linker for activation of T cells family, member 2
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| Protein Structure |
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| Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||||
| Entrez 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, Jul 2008] |
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| Gene Information | |||||||||||||||||||
| Type | Protein coding | ||||||||||||||||||
| Genomic Location | Chromosome 7:74199652-74229834 | ||||||||||||||||||
| Strand | Forward strand | ||||||||||||||||||
| Band | q11.23 | ||||||||||||||||||
| Transcripts | |||||||||||||||||||
| Interactions | |||||||||||||||||||
| Number of Interactions |
This gene and/or its encoded proteins are associated with 8 experimentally validated interaction(s) in this database.
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| Gene Ontology | |||||||||||||||||||
Molecular Function |
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| Biological Process |
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| Cellular Component |
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| Orthologs | |||||||||||||||||||
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Species
Mus musculus
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Gene ID
Gene Order
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| Pathways | |||||||||||||||||||
| NETPATH |
BCR pathway
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| REACTOME |
Role of LAT2/NTAL/LAB on calcium mobilization pathway
Innate Immune System pathway
Fc epsilon receptor (FCERI) signaling pathway
Immune System pathway
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| KEGG | |||||||||||||||||||
| INOH | |||||||||||||||||||
| PID NCI |
Fc-epsilon receptor I signaling in mast cells
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| Cross-References | |||||||||||||||||||
| SwissProt | Q9GZY6 | ||||||||||||||||||
| TrEMBL | C9JA24 C9JDY7 F8W947 | ||||||||||||||||||
| UniProt Splice Variant | |||||||||||||||||||
| Entrez Gene | 7462 | ||||||||||||||||||
| UniGene | |||||||||||||||||||
| RefSeq | XM_005250562 NM_014146 NM_032463 NM_032464 | ||||||||||||||||||
| HUGO | HGNC:12749 | ||||||||||||||||||
| OMIM | 605719 | ||||||||||||||||||
| CCDS | CCDS5566 | ||||||||||||||||||
| HPRD | 09304 | ||||||||||||||||||
| IMGT | |||||||||||||||||||
| EMBL | AC005081 AF045555 AF161531 AF252611 AF252612 AF252613 AF252614 AF257135 AK002099 AK092904 AK290074 AK290916 AY190023 BC001609 BC009204 CH471200 | ||||||||||||||||||
| GenPept | AAF29018 AAF74978 AAF91352 AAH01609 AAH09204 AAK37429 AAK37430 AAK37431 AAK37633 AAO63155 AAS07404 AAS07405 BAA92084 BAF82763 BAF83605 BAG52627 EAW69610 EAW69611 EAW69612 EAW69613 | ||||||||||||||||||
| RNA Seq Atlas | 7462 | ||||||||||||||||||