WFS1 (NM_006005) Human 3' UTR Clone

Specifications

Product Data
Product Name	WFS1 (NM_006005) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CTRCT41; WFRS; WFS; WFSL
ACCN	NM_006005
Insert Size	827 bp
Sequence Data	Insert Sequence (showhide) >SC209978 3’UTR clone of NM_006005 The sequence shown below is from the reference sequence of NM_006005. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TTTTTCTTCCCATTCCTGTCGGCGGCCTGAGGATGGTCCGCCACGAGGAGCTTCCAGTGCATGTTGCCA TGAGGCCTTTCCCCAGTGTGGCCCCAGCCCGACAGGCATGCACCAGTGCCGCCTGTGCCCACGTGTGCA GACTGTGGCTGCAGAGACCTTGCGACCATGTGTAGATTGCGTGGACCCCGACAAAGGGAAGGCTGCTGT GTAGCTCTGTCCACTCTGAATACCAAGTGTGTTGGGAATTGCATGCCATCTCCACCCTGAGCCTGACCT TTCTGAGTGACATGGGTGTGCCAGGCTAGACTAGGAGGTTCCGGTGTCTGGAAAAGCACTTTACAGATG AGATTCCCTCTCCTCCCCCACCTTCAAGCACCCTGTTCCCTCTTTCTTTCTTTTGTGTTGGATTTGTTT AAAAACCAAATAAGCATCTGTGTAACCTCCACAGTAGCATTTCTTATTTGTTTGGTCACTGCTACACCT TAGCAGCTCTTCCCCTTTCCTGGGGGATGTGCACGGCAGCTTGAGCCTGTCACGTGGTCAAGGCCCGGC CCCATCAGAGGCTGGGGGAGGCGGCACATTGGCAGTGTGTCACACTGAGCTGGGCACCACAGGCTGCCT CATGACCCTCCTGTCCAGCAGGTAGTGGGTGAATGTGTGAAGGTCTTGCCTGAATCCATCAGGACTTGG GAAACAGAGAACCCTGTGGGGGCGGCTGTGGGGGAGGTCCCTGCCAGTGTTTAGAAGAGCCTGACTGTG TTCAGTGCCTTGGAGCAGAAAGCCAGGGTCCTGAGTGGCTGAAATAAAAGCCTCTGGTGGAACCTGCA 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_006005.3
Synonyms	CTRCT41; WFRS; WFS; WFSL
Summary	This gene encodes a transmembrane protein, which is located primarily in the endoplasmic reticulum and ubiquitously expressed with highest levels in brain, pancreas, heart, and insulinoma beta-cell lines. Mutations in this gene are associated with Wolfram syndrome, also called DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness), an autosomal recessive disorder. The disease affects the brain and central nervous system. Mutations in this gene can also cause autosomal dominant deafness 6 (DFNA6), also known as DFNA14 or DFNA38. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2009]
Locus ID	7466
MW	30.1

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