- accession:NM_001244735
- 基因别名:OPA7
- 基因描述:Homo sapiens transmembrane protein 126A (TMEM126A), transcript variant 2, mRNA.
- 载体:现货载体
- CDS区长度:378
- 翻译后氨基酸长度:125
- TranscriptVariant:This variant (2) differs in the 5' UTR and coding sequence compared to variant 1 by lacking the exon containing the translation start site. The resulting isoform (2) is shorter at the N-terminus compared to isoform 1.
- 基因简介:The protein encoded by this gene is a mitochondrial membrane protein of unknown function. Defects in this gene are a cause of optic atrophy type 7 (OPA7). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]
- 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