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 | |||||||||||||||||||
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 | |||||||||||||||||||
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 | ||||||||||||||||||