- accession:NM_002688
- 基因别名:SEPT5
- 基因描述:Homo sapiens septin 5 (SEPT5), transcript variant 1, mRNA.
- 载体:现货载体
- CDS区长度:1110
- 翻译后氨基酸长度:369
- TranscriptVariant:This variant (1) encodes the longer isoform (1).
- 基因简介:This gene is a member of the septin gene family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is mapped to 22q11, the region frequently deleted in DiGeorge and velocardiofacial syndromes. A translocation involving the MLL gene and this gene has also been reported in patients with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. The presence of a non-consensus polyA signal (AACAAT) in this gene also results in read-through transcription into the downstream neighboring gene (GP1BB; platelet glycoprotein Ib), whereby larger, non-coding transcripts are produced. [provided by RefSeq, Dec 2010]
- 规格:10ul 质粒
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