NTAL Products

Description

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]. Transcript Variant: This variant (2) differs in the 5' UTR compared to variant 1. All three variants encode the same protein. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

Bioinformatics

Product By Gene ID

7462

Alternate Names

LAB LABWilliams-Beuren syndrome chromosomal region 15 protein Linker for activation of B-cells linker for activation of T cells family, member 2 linker for activation of T-cells family member 2 Membrane-associated adapter molecule Non-T-cell activation linker NTAL NTALWilliams-Beuren syndrome chromosomal region 5 protein WBS15 WBSCR15 WBSCR5 WBSCR5HSPC046 Williams-Beuren syndrome chromosome region 5 WSCR5

Research Areas for NTAL

Find related products by research area and learn more about each of the different research areas below.

Adaptive Immunity
Cell Biology
Immunology
Innate Immunity
Signal Transduction
Transcription Factors and Regulators