PCDH15 (NM_001142766) Human 3' UTR Clone

Specifications

Product Data
Product Name	PCDH15 (NM_001142766) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CDHR15; DFNB23; USH1F
ACCN	NM_001142766
Insert Size	789 bp
Sequence Data	Insert Sequence (showhide) >SC209613 3’UTR clone of NM_001142766 The sequence shown below is from the reference sequence of NM_001142766. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CAATCTCACAGTCAATCTACTTCACTGTAATGTTGCTTTTCTTATTTTAGTCGGGCAAACCTCTTGTTG ATCATAGTCTTCAAGTTGAACATCAAATTTGAACGTCAAAGAAGACTCTATTATTTTACCCCAAATTCA ATGAAATGCAGTTTTTTTTCTCGTTTTTAATTTAAAAAGATATTAACCTCATCACTACTAACTCACTCA TATAATAGATTTACCTTACTTTTTAAAAACTACAAAGTAGCATAATTTGTTCTACATTTATTTGAAAAG TAAGTAATTTTAATCTCTTTTTTAGTGGGAATATGTGGGCATGAAAATTAGATACCCAACTTAAACCAA AGGCATGTCTATCATGTGGATGCAGTAACATTTACATTTAGTTTTTGATCGTAGTTTTATATGAATGTT CCAAGAAAAAAGCAGACTGTTACAAATAAGTTAAAACTGATATGATTGATAGGTTCTGTTTTTTCTTGA AGCCTATGTATTTGGTAAGAAGAAATACTACCGAAGTAAAATATAATGTACCTAGATTGTAGGAGATGA CAGACATAAGGTATTTCAAAATAAATCTCAGGTGCTATAACATGTAGTCATCTGTTTTCTGATAAGAAC ATCTTTTACTCTGACTTGCTTTTATCTTAGTAGTATGCTTATGGATTTAGTAGTATGCTTATGGATTTG ATAAATCTTATACTTTTTCAGTTGCTGTCTTATTCTCTTTATTTCTCATTGTGCTTTCCCTTCCCTTCT TTATAATGAAAATAAATCTTGAGTCGTTGA 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_001142766.2
Synonyms	CDHR15; DFNB23; USH1F
Summary	This gene is a member of the cadherin superfamily. Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. It plays an essential role in maintenance of normal retinal and cochlear function. Mutations in this gene result in hearing loss and Usher Syndrome Type IF (USH1F). Extensive alternative splicing resulting in multiple isoforms has been observed in the mouse ortholog. Similar alternatively spliced transcripts are inferred to occur in human, and additional variants are likely to occur. [provided by RefSeq, Dec 2008]
Locus ID	65217
MW	30.7

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