人 NF2 (NM_181830) cDNA克隆

Accession: NM_181830
基因名称: NF2
基因别名: ACN; SCH; BANF
基因描述: Homo sapiens neurofibromin 2 (merlin) (NF2), transcript variant 7, mRNA.
种属: Human
CDS区长度: 1524 (查看编码区序列)
翻译后氨基酸长度: 507 (查看氨基酸序列)
Transcript Variant: This variant (7) lacks two alternate in-frame exons in the 5' coding region and includes an alternate exon in the 3' coding region, compared to variant 1. The resulting protein (isoform 7, also referred to as isoform delE2/3) is shorter and has a distinct C-terminus, compared to isoform 1.
产品编号 产品名称 载体 规格 价格
G102746 人 NF2 (NM_181830) cDNA克隆 pDONR223 2ug质粒 点击询价
人 NF2 (NM_000268) cDNA克隆 transcript variant 1
人 NF2 (NM_181825) cDNA克隆 transcript variant 12
人 NF2 (NM_181831) cDNA克隆 transcript variant 13
人 NF2 (NM_016418) cDNA克隆 transcript variant 2
人 NF2 (NM_181828) cDNA克隆 transcript variant 5
人 NF2 (NM_181829) cDNA克隆 transcript variant 6
人 NF2 (NM_181830) cDNA克隆 transcript variant 7
人 NF2 (NM_181832) cDNA克隆 transcript variant 8
人 NF2 (NM_181833) cDNA克隆 transcript variant 9

This gene encodes a protein that is similar to some members of the ERM (ezrin, radixin, moesin) family of proteins that are thought to link cytoskeletal components with proteins in the cell membrane. This gene product has been shown to interact with cell-surface proteins, proteins involved in cytoskeletal dynamics and proteins involved in regulating ion transport. This gene is expressed at high levels during embryonic development; in adults, significant expression is found in Schwann cells, meningeal cells, lens and nerve. Mutations in this gene are associated with neurofibromatosis type II which is characterized by nervous system and skin tumors and ocular abnormalities. Two predominant isoforms and a number of minor isoforms are produced by alternatively spliced transcripts. [provided by RefSeq, Jul 2008]