NCIt definition : Human IL1RAPL1 wild-type allele is located within Xp22.1-p21.3 and is approximately
1369 kb in length. This allele, which encodes X-linked interleukin-1 receptor accessory
protein-like 1 protein, plays a role in the modulation of signaling. Mutation of the
gene is associated with mental retardation X-linked type 21.;
NCIt note : The IL1RAPL1 gene product may be involved in the regulation of learning and memory.
(Entrez Gene);