Car5a

ENCODES a protein that exhibits carbonate dehydratase activity; ASSOCIATED WITH 16Q24.3 Microdeletion Syndrome (ortholog); autosomal recessive chronic granulomatous disease 4 (ortholog); CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO (ortholog); FOUND IN mitochondrion (ortholog); INTERACTS WITH (+)-schisandrin B; 1-naphthyl isothiocyanate; 2,3,7,8-tetrachlorodibenzodioxine编码一种表现出碳酸酐酶活性的蛋白质；与16Q24.3微缺失综合征（同源）相关；常染色体隐性慢性肉芽肿病4型（同源）；碳酸酐酶VA缺乏症，因之引起的高氨血症（同源）；存在于线粒体中（同源）；与（+）五味子素B、1-萘基异硫氰酸酯、2,3,7,8-四氯二苯并-对-二噁英相互作用。