WDR81 (NM_001163809) Human 3' UTR Clone

Specifications

Product Data
Product Name	WDR81 (NM_001163809) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CAMRQ2; HYC3; PPP1R166; SORF-2
ACCN	NM_001163809
Insert Size	930 bp
Sequence Data	Insert Sequence (showhide) >SC211048 3’UTR clone of NM_001163809 The sequence shown below is from the reference sequence of NM_001163809. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GACAACGGGGTTATCCGCCTCCTGGCATAGACTGAGGCAGGAGCTGGCCGGGCAAGGGTGGGAAGACAT CTGCGGGCGCGTGTCCACTCACCCTGTTCCCTGAGCAGCAGCTCCCTCCAGGGAGGCCCTGGGTCCCAC GCCCTGGGTGCCCACATGGCCTGCCAACTAGGGCCTGCAAATGGAGTGGGGGAGTCCTGGCCCCTGAAT CACCAGAGCCACCAAGCCTGCCAGAGGGGTCTCATTCATGGCTTGGGGACACAGGGCTCCTAGCAAGCA GGAAGTTAAGAGCAGGAGGAAGCGTTGCTACCTTCACTTCTCCCCAGCTCTGCCCTCTGGGTCCACATG AGGACAGGGAAGCTCGGGAAGGGGAAGGGAGACTGGCCCTGCCCAGCCGGTCTCTAGCCCCTCAGCCCC CGCTGGGCACTCTCTGTCCCATCCCTCTAGGACAGGGAAGCTGGCCTGGTCCAGGGCACTGATGGTGCT TGGATTCCAGCCTAAGGAAGGCTGGCCGTGGTCCAGGAGTTAAGGGCTTGGGTCTGGGGTTTAAGTGGC CACCCATCCAGGCCCTGGCCAGTGTGGGACCGGGACGGGAAGGAAGAAGGAGGCTAGGAGCAGGGGGAA AAGGTGCACTTGGCCAGTGGCGCCTGCCAGGAGTGAGTCCATGCGTTGTCTGCCCACCCCTACCACAGT GTTTGTGCCTTCAGCTGAGGGGGCAGCCTCTGGGCCCTGAACCCCTGCTGGGGCTCCACGACCCTGAGA GAAGGGGTGAGAAGAATCATCTCTGCACCTCGGGTCTCTGCCAGAGGAAGACTTAAGCATCCCTGCGAC CTCACATTCTAGACAGAGATGAGGTCCAGGGGTTGGCCCCTGCTGCCTTCTCACAATTTGCAATAGATG TAAATAGGACCAATAAATCCTTTGGAAGAGCCA 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_001163809.2
Synonyms	CAMRQ2; HYC3; PPP1R166; SORF-2
Summary	This gene encodes a multi-domain transmembrane protein which is predominantly expressed in the brain and is thought to play a role in endolysosomal trafficking. Mutations in this gene are associated with an autosomal recessive form of a syndrome exhibiting cerebellar ataxia, cognitive disability, and disequilibrium (CAMRQ2). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]
Locus ID	124997
MW	33.2

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