人 KAL1 (NM_000216) cDNA克隆

Accession: NM_000216
基因名称: KAL1
基因别名: HH1; HHA; KAL; KMS; ADMLX; WFDC19; KALIG-1
基因描述: Homo sapiens Kallmann syndrome 1 sequence (KAL1), mRNA.
种属: Human
CDS区长度: 2043 (查看编码区序列)
翻译后氨基酸长度: 680 (查看氨基酸序列)
产品编号 产品名称 载体 规格 价格
G150967 人 KAL1 (NM_000216) cDNA克隆 pDONR223 2ug质粒 点击询价

Mutations in this gene cause the X-linked Kallmann syndrome. The encoded protein is similar in sequence to proteins known to function in neural cell adhesion and axonal migration. In addition, this cell surface protein is N-glycosylated and may have anti-protease activity. [provided by RefSeq, Jul 2008]