PREY

TNFRSF10C

CD263, DCR1, DCR1-TNFR, LIT, TRAIL-R3, TRAILR3, TRID, UNQ321/PRO366
tumor necrosis factor receptor superfamily, member 10c, decoy without an intracellular domain
GO Process (1)
GO Function (1)
GO Component (1)

Gene Ontology Biological Process

Gene Ontology Molecular Function

Gene Ontology Cellular Component

Homo sapiens

Two-hybrid

Bait protein expressed as a DNA binding domain (DBD) fusion and prey expressed as a transcriptional activation domain (TAD) fusion and interaction measured by reporter gene activation.

Publication

Systematic identification of pathological lamin A interactors.

Dittmer TA, Sahni N, Kubben N, Hill DE, Vidal M, Burgess RC, Roukos V, Misteli T

Laminopathies are a collection of phenotypically diverse diseases that include muscular dystrophies, cardiomyopathies, lipodystrophies, and premature aging syndromes. Laminopathies are caused by >300 distinct mutations in the LMNA gene, which encodes the nuclear intermediate filament proteins lamin A and C, two major architectural elements of the mammalian cell nucleus. The genotype-phenotype relationship and the basis for the pronounced tissue specificity ... [more]

Mol. Biol. Cell May. 01, 2014; 25(9);1493-510 [Pubmed: 24623722]

Throughput

  • High Throughput

Curated By

  • BioGRID