- accession:NM_003030
- 基因别名:SHOX2
- 基因描述:Homo sapiens short stature homeobox 2 (SHOX2), transcript variant 1, mRNA.
- 载体: 现货载体
- CDS区长度:1068
- 翻译后氨基酸长度:355
- TranscriptVariant:This variant (1) represents the longest transcript and encodes the longest isoform (b).
- 基因简介:This gene is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeobox genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeobox genes. This locus represents a pseudoautosomal homeobox gene that is thought to be responsible for idiopathic short stature, and it is implicated in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009]
- 载体信息:自有图片地址
- 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