FMN2 (NM_020066) Human 3' UTR Clone

Specifications

Product Data
Product Name	FMN2 (NM_020066) Human 3' UTR Clone
Vector	pMirTarget
ACCN	NM_020066
Insert Size	1063 bp
Sequence Data	Insert Sequence (showhide) >SC212048 3’UTR clone of NM_020066 The sequence shown below is from the reference sequence of NM_020066. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ATTAAAGCAAAGATAAGCATGAAAACTTGAACAATGAAAAGCAGAATGAAAATGAGTCATTGCAACGAC TTTCACAAAATTCAGCTGACCTGAGAGTGGGAGGGAAACTACCGTCATTCTGCTCATGTTTCTTCTTGA CCTCTTGCATAATCTTTTTGTTTTCTAGACAGTTCACTAATTGTTGAATTTTACTGTATATTCATATAA AAATGCAAACGTACTAGACCAGTGGAGAATTTGACACCTTTTCTTTTTGTAAAAGTTTATGGTATTATA CCGATAGACCAAAACAGCATGTGTAAGAGGCAGTATCTGCACTAATTCTCAACATGCTAAACATTAACT ACAATTCACTGTTGTGAGAATATTCCTCGTCACAGCAAAAACACTTTCCTTTCTACTGACAACCAGTCC TCCACATCACAGCATTTAGACATATGGGTAAAATGTTATTTCTAGTGAATTGTTTGTATCAGTTTCATG TCTAAGTATAAATTTTCTATTTTAAAATTTAAGAACCGTTTATAATCAGTGCTTTCCCAACTCTTGGGT TGCTCTCCATAACTATGTATTTGTGAAAGAAAATGGTCATTTTTTTTACTGAAGTCATATAATGACTTG GGTCAGCTCGTAATGCATTGTGATGGTTTTGTATGAGCTGGGTGTTTTTTTCCATTACTTTTAATGATC TTCGTTGCAAGTTATAGTTGTGGATAAAGGGGAGAATTTATTGCTCTTGCAAACCAATTATGGAAAGCA ACTTAAGAAAACCAATGTTCTAAATCATAATTGTTTGTATTTATGTAAAGTATGGTCTCTTACTTTTTA GTTTGTAGTTTAAGTGCAAAGAAACAGTAGTGGTTTTTTTTCTATTGTTTTGTAGTCTTCCTGTCCCCT TCAGTCCCTCCAGTGTGTATATTACCATTCTCCAATGAAATAATAGGGCATTTAACAAAGATCGCTATG TGCAATACTGTATTTAGTGTTTCTATTTCAATTTTTCTAGGATGTTAATTTATATGAAAATAAAATGAA TAATAAAAGAATAAAGATACTTGCAAAA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG
Restriction Sites	SgfI-MluI
OTI Disclaimer	Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs).
Reference Data
RefSeq	NM_020066.5
Summary	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]
Locus ID	56776
MW	40.9

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