SGCE (NM_003919) Human 3' UTR Clone

Specifications

Product Data
Product Name	SGCE (NM_003919) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	DYT11; epsilon-SG; ESG
ACCN	NM_003919
Insert Size	549 bp
Sequence Data	Insert Sequence (showhide) >SC203654 3’UTR clone of NM_003919 The sequence shown below is from the reference sequence of NM_003919. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CAGCAGACTACAGGTAAATGGTATCCCTGAAGAAAGAAAACTGACTGAAGCAATGAATTTATAATCAGA CAATATAGCAGTTACATCACATTTCTTTTCTCTTCCAATAATGCATGAGCTTTTCTGGCATATGTTATG CATGTTGGCAGTATTAAGTGTATACCAAATAATACAACATAACTTTCATTTTACTAATGTATTTTTTTG TACTTAAAGCATTTTTGACAATTTGTAAAACATTGATGACTTTATATTTGTTACAATAAAAGTTGATCT TTAAAATAAATATTATTAATGAAGCCTAATGACTGGTGAAATTTACTTCAGTAAACTATTTGCTTCCTA TTTAGTAGAAATCTTTTAATCGCTAGAAACAGGTTTATGTGTTCATTCTCATTCCACAAGACTTTAGTG CTTCCTATGAATATATAAAATGCCTGTGCCTCCGTGTTCCAGTTGAGCAACCCATTTAAATAATACTTT AACTCTTGTGGCCTGTAAATCCTGTTGTTTTATATACCACTTGGGAGTGTTTTCGAATAAACCTAG 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_003919.3
Synonyms	DYT11; epsilon-SG; ESG
Summary	This gene encodes the epsilon member of the sarcoglycan family. Sarcoglycans are transmembrane proteins that are components of the dystrophin-glycoprotein complex, which link the actin cytoskeleton to the extracellular matrix. Unlike other family members which are predominantly expressed in striated muscle, the epsilon sarcoglycan is more broadly expressed. Mutations in this gene are associated with myoclonus-dystonia syndrome. This gene is imprinted, with preferential expression from the paternal allele. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. A pseudogene associated with this gene is located on chromosome 2. [provided by RefSeq, Oct 2016]
Locus ID	8910
MW	21.4

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