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FMN2


Official Full Name
formin 2
Organism
Homo sapiens
Gene ID
56776
Background
This gene is a member of the formin homology protein family. The encoded protein is thought to have essential roles in organization of the actin cytoskeleton and in cell polarity. This protein mediates the formation of an actin mesh that positions the spindle during oogenesis and also regulates the formation of actin filaments in the nucleus. This protein also forms a perinuclear actin/focal-adhesion system that regulates the shape and position of the nucleus during cell migration. Mutations in this gene have been associated with infertility and also with an autosomal recessive form of intellectual disability (MRT47). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Jul 2017]
Synonyms
TM7SF1L2

Cat.No. Product Name Price
SHH063749 shRNA set against Human FMN2(NM_020066.4) Inquiry
SHH063751 shRNA set against Mouse Fmn2(NM_019445.2) Inquiry
SHH295853 shRNA set against Human FMN2 (NM_020066.4) Inquiry
SHH295857 shRNA set against Mouse FMN2 (NM_019445.2) Inquiry
Cat.No. Product Name Price
CDFG002448 Human FMN2 cDNA Clone(NM_020066.4) Inquiry
MiUTR1H-03776 FMN2 miRNA 3'UTR clone Inquiry
MiUTR1M-04743 FMN2 miRNA 3'UTR clone Inquiry
CDCB198160 Rabbit LOC100356313 ORF clone (XM_008268218.1) Inquiry
CDCB199881 Rabbit LOC100344261 ORF clone (XM_008272829.1) Inquiry
CDCL108845 Human FMN2 ORF clone (NM_020066.4) Inquiry
CDCL150800 Human Fmn2 ORF clone (NM_019445.2) Inquiry
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