NSUN5 (NM_148956) Human 3' UTR Clone

Specifications

Product Data
Product Name	NSUN5 (NM_148956) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	NOL1; NOL1R; NSUN5A; p120; p120(NOL1); WBSCR20; WBSCR20A
ACCN	NM_148956
Insert Size	929 bp
Sequence Data	Insert Sequence (showhide) >SC210949 3’UTR clone of NM_148956 The sequence shown below is from the reference sequence of NM_148956. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GCCGGTGCTTGCACACCGCCTTGCACATAGCAGAGGCTCCGGGCTGACTCCTTCCTGGTGGGAAAGGAA GATGCCTGTCCTCTCCGTGGAGGACCCTGGGCCCTCACCGCAGGAAGCAGTTTGGGTTTTGAAAGGTTA TTGGGTCCCTTCCTTGGGCTGTGTTCTTGCTGGTGAGCAAAGTGTTGCCTGCAAAAATAAAATGCAGAA CGTACTCTACGATAGATCACAGTTTTTTATTCTTAATGTCACAAGCAGGAGAAAAATCTCACATTCATA CTAAAAGTTCCAACTAGACTCAACAGGAATGAAGTCTCTATTTGTAATGGAAAGTCCCAGCCTCCCGCT GCCGTCCAGTGCGTGTACTGTACACATCCACACTCACACTCACTCAGGGTTCCCGGACCGGCTGTCCTG CCTGCGGAACTGAGGTAAACTAGCTCAGGTGCTGACACTAGGAGGGTCTACCTTACATAAGGTACAGGT AGAAGCTTGATTGCTAGGCCCAGGCCCACCCAGACCCTCCAATCCTAACAGGTATTTAGGCTTGAGGTT CACTCCCTCCTCAGCTGCACACGCAGCCAGGTATTAACGAGGATCAGAGCTGTTCTGAGGGGTGGGAAG GAGCAGCCCCACCACCACTCACTCACCCTCAGTCACATCGGGGAGGGGGCACCAGTTACATTTACATCA CATTATTTATAAAATAAGAATTACATTTCATATAACATGGCCAGAAGGAGCTCTAGTCCCCCAGGAAAG CTGCCGGGGACAGCATTTGAGCCTCTTCTTTGCACAGGCATAACTTAACTATACAGCTAATTCCTAGTT AATAGCATTTATACTTAACCACCTCAATGAACCAAGCTTGAAGGAATTTAAAAGGCAATTTAGCTTAAA TACAAAAATAAATTTTTGTTAAAAAACGTTTA 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_148956.4
Synonyms	NOL1; NOL1R; NSUN5A; p120; p120(NOL1); WBSCR20; WBSCR20A
Summary	This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]
Locus ID	55695
MW	34.2

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