Gene Gene information from NCBI Gene database.
Entrez ID 7462
Gene name Linker for activation of T cells family member 2
Gene symbol LAT2
Synonyms (NCBI Gene)
HSPC046LABNTALWBSCR15WBSCR5WSCR5
Chromosome 7
Chromosome location 7q11.23
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 p
miRNA miRNA information provided by mirtarbase database.
87
miRTarBase ID miRNA Experiments Reference
MIRT005092 hsa-miR-155-5p Microarray 19193853
MIRT644203 hsa-miR-3127-3p HITS-CLIP 23824327
MIRT644202 hsa-miR-6756-3p HITS-CLIP 23824327
MIRT644201 hsa-miR-5193 HITS-CLIP 23824327
MIRT644200 hsa-miR-660-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
23
GO ID Ontology Definition Evidence Reference
GO:0002250 Process Adaptive immune response IEA
GO:0002376 Process Immune system process IEA
GO:0002764 Process Immune response-regulating signaling pathway IEA
GO:0005515 Function Protein binding IPI 14722116
GO:0005886 Component Plasma membrane IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605719 12749 ENSG00000086730
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9GZY6
Protein name Linker for activation of T-cells family member 2 (Linker for activation of B-cells) (Membrane-associated adapter molecule) (Non-T-cell activation linker) (Williams-Beuren syndrome chromosomal region 15 protein) (Williams-Beuren syndrome chromosomal region
Protein function Involved in FCER1 (high affinity immunoglobulin epsilon receptor)-mediated signaling in mast cells. May also be involved in BCR (B-cell antigen receptor)-mediated signaling in B-cells and FCGR1 (high affinity immunoglobulin gamma Fc receptor I)-
PDB 3MAZ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15703 LAT2 28 238 Linker for activation of T-cells family member 2 Family
Tissue specificity TISSUE SPECIFICITY: Highly expressed in spleen, peripheral blood lymphocytes, and germinal centers of lymph nodes. Also expressed in placenta, lung, pancreas and small intestine. Present in B-cells, NK cells and monocytes. Absent from T-cells (at protein
Sequence
Sequence length 243
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Natural killer cell mediated cytotoxicity   Role of LAT2/NTAL/LAB on calcium mobilization
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
LEUKEMIA, PROMYELOCYTIC, ACUTE CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MOYAMOYA DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SYSTEMIC LUPUS ERYTHEMATOSUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
WILLIAMS SYNDROME Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Arthritis Rheumatoid Associate 36902005
★☆☆☆☆
Found in Text Mining only
Autoimmune Diseases Associate 36902005
★☆☆☆☆
Found in Text Mining only
Carcinoma Embryonal Associate 32741077
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Associate 39778021
★☆☆☆☆
Found in Text Mining only
Carcinoma Renal Cell Associate 24168110
★☆☆☆☆
Found in Text Mining only
Fetal Growth Retardation Associate 33004923
★☆☆☆☆
Found in Text Mining only
Gliosis Associate 27469356
★☆☆☆☆
Found in Text Mining only
Leukemia Associate 22269118, 23001822
★☆☆☆☆
Found in Text Mining only
Leukemia Myeloid Acute Associate 24456692
★☆☆☆☆
Found in Text Mining only
Leukemia T Cell Associate 21488857
★☆☆☆☆
Found in Text Mining only