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LTA lymphotoxin alpha

Gene ID: 4049, updated on 17-Jun-2024
Gene type: protein coding
Also known as: LT; TNFB; TNFSF1; TNLG1E

Summary

The encoded protein, a member of the tumor necrosis factor family, is a cytokine produced by lymphocytes. The protein is highly inducible, secreted, and forms heterotrimers with lymphotoxin-beta which anchor lymphotoxin-alpha to the cell surface. This protein also mediates a large variety of inflammatory, immunostimulatory, and antiviral responses, is involved in the formation of secondary lymphoid organs during development and plays a role in apoptosis. Genetic variations in this gene are associated with susceptibility to leprosy type 4, myocardial infarction, non-Hodgkin's lymphoma, and psoriatic arthritis. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]

Associated conditions

See all available tests in GTR for this gene

DescriptionTests
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.
GeneReviews: Not available
Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus.
GeneReviews: Not available
Leprosy, susceptibility to, 4
MedGen: C1970254OMIM: 610988GeneReviews: Not available
See labs
Myocardial infarction, susceptibility to
MedGen: C1832662OMIM: 608446GeneReviews: Not available
See labs
Psoriatic arthritis, susceptibility to
MedGen: C1835223OMIM: 607507GeneReviews: Not available
See labs

Genomic context

Location:
6p21.33
Sequence:
Chromosome: 6; NC_000006.12 (31560610..31574324)
Total number of exons:
6

Links

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