3-Methylcrotonyl-CoA carboxylase deficiency(3-甲基巴豆酰辅酶A羧化酶缺乏症)

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检测编号:NS0050015


基因 MCCC2 与疾病

3-甲基巴豆酰辅酶A羧化酶是亮氨酸中间代谢产物3-甲基巴豆酰辅酶A转化成3-甲基戊烯二酸单酰辅酶A的一个羧化酶,由6个α-β组合体形成一个功能性3-甲基巴豆酰辅酶A羧化酶,在线粒体中发挥作用,MCCC2编码其β亚基,已经发现40多种突变,大多是点突变。

基因名称基因全名基因位置外显子个数 CDS长度
MCCC2 methylcrotonoyl-CoA carboxylase 2 (beta) 5q12-q13 17 约3673 bp
基因摘要 This gene encodes the small subunit of 3-methylcrotonyl-CoA carboxylase. This enzyme functions as a heterodimer and catalyzes the carboxylation of 3-methylcrotonyl-CoA to form 3-methylglutaconyl-CoA. Mutations in this gene are associated with 3-Methylcrotonylglycinuria, an autosomal recessive disorder of leucine catabolism. [provided by RefSeq, Jul 2008].