LAT2

LAT2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesLAT2, LAB, NTAL, WBSCR15, WBSCR5, WSCR5, HSPC046, linker for activation of T-cells family member 2, linker for activation of T cells family member 2
External IDsOMIM: 605719; MGI: 1926479; HomoloGene: 11297; GeneCards: LAT2; OMA:LAT2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

7462

56743

Ensembl

ENSG00000086730

ENSMUSG00000040751

UniProt

Q9GZY6

Q9JHL0

RefSeq (mRNA)

NM_014146
NM_032463
NM_032464

NM_020044
NM_022964

RefSeq (protein)

NP_054865
NP_115852
NP_115853

NP_064428
NP_075253

Location (UCSC)Chr 7: 74.2 – 74.23 MbChr 5: 134.63 – 134.64 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

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.