6m22 | pdb_00006m22
From Proteopedia
Structural highlights
Disease[S12A6_HUMAN] Corpus callosum agenesis-neuronopathy syndrome. The disease is caused by mutations affecting the gene represented in this entry. Function[S12A6_HUMAN] Mediates electroneutral potassium-chloride cotransport. May be activated by cell swelling. May contribute to cell volume homeostasis in single cells. Contents | ||||||||||||||||||||
This page was last modified 10:14, 19 May 2021.