- accession:NM_000216
- 基因别名:KAL1
- 基因描述:Homo sapiens Kallmann syndrome 1 sequence (KAL1), mRNA.
- 载体:现货载体
- CDS区长度:2043
- 翻译后氨基酸长度:680
- 基因简介: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]
- 规格:10ul 质粒
CDS区参考序列: 点击查看序列翻译后氨基酸参数序列: 点击查看序列