This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene, alpha 5 type IV collagen, so that the gene pair shares a common promoter. Deletions in the alpha 5 gene that extend into the alpha 6 gene result in diffuse leiomyomatosis accompanying the X-linked Alport syndrome caused by the deletion in the alpha 5 gene. Two splice variants have been identified for this gene. [provided by RefSeq, Jul 2008].
Hu, Sleeman, Miyashita, Linton, Allan, He, Larsson, Tu, Sandoval, Jung, Mapar, Machida, Murakami, Nakajima, Ploug, Fong, Young, Beigneux: "Monoclonal antibodies that bind to the Ly6 domain of GPIHBP1 abolish the binding of LPL." in: Journal of lipid research, Vol. 58, Issue 1, pp. 208-215, (2016) (PubMed).
Zhang, Zhou, Reeders, Tryggvason: "Structure of the human type IV collagen COL4A6 gene, which is mutated in Alport syndrome-associated leiomyomatosis." in: Genomics, Vol. 33, Issue 3, pp. 473-9, (1996) (PubMed).
Aliases for COL4a6 抗体
collagen type IV alpha 6 chain (COL4A6) 抗体 collagen, type IV, alpha 6 (Col4a6) 抗体 collagen, type IV, alpha 6 (col4a6) 抗体 collagen, type IV, alpha 6 (COL4A6) 抗体 collagen type IV alpha 6 chain (col4a6) 抗体 collagen type IV alpha 6 chain (Col4a6) 抗体 BB116301 抗体 CXDELq22.3 抗体 DELXq22.3 抗体