2w2j | pdb_00002w2j
From Proteopedia
Structural highlights
DiseaseCAH8_HUMAN Defects in CA8 are the cause of cerebellar ataxia mental retardation and dysequilibrium syndrome type 3 (CMARQ3) [MIM:613227. CMARQ3 is a congenital cerebellar ataxia associated with dysarthia, quadrupedal gait and mild mental retardation. FunctionCAH8_HUMAN Does not have a carbonic anhydrase catalytic activity. Evolutionary Conservation![]() Check, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf. | ||||||||||||||||||||
This page was last modified 15:41, 13 December 2023.