TCTN3 (NM_015631) Human 3' UTR Clone

Specifications

Product Data
Product Name	TCTN3 (NM_015631) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	C10orf61; JBTS18; OFD4; TECT3
ACCN	NM_015631
Insert Size	696 bp
Sequence Data	Insert Sequence (showhide) >SC208752 3’UTR clone of NM_015631 The sequence shown below is from the reference sequence of NM_015631. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTTGGAGTTCTCAACCTAGAGACTATGTGAAGAAAAGAAAATAATCAGATTTCAGTTTTCCCTATGAGA AACTCTGAGGCAGCCACTTATCTTGGCTAAATAGAACCTCACCTGCTCATGACCAGAGAGCATTTAGGA TAATAGAGGACCTAACTGAAGGAATCCTTGTATATGAAAGGAGTTATTTTAGAAAAGCAATAAAAATAT TTTATTCATCATAGCTCTCTGCTTTGGGCTCTGCAGGCCACCAGATACACATGAGGCCCCTACTTCTCA AGCTGGGAAGGCCAAGAGCCTTCCTTCAGCCTTTCTGGTTATGTTACACCTAGCTGAATGTTTACAAGG TCTGGATCCATCAGCCCTCAGGCACAGTTGGGCCAAGCAGAAAGAGAGAAACACTTCTGCTGTCACCTT GAATGAACTCAGGAATAGCTTCCCTCTGGACTGTAGAGGAGCTAACTGTTTGGAACAGAAAACTGCTGG CTGTTGATTTTGTCTGGTTCCTTTGCCAACATCTGGGCACACCCTTTGCCCAGACACGAGTGGGGAAAG CAGTTCTTTCTCCTCAGTTTCCAAAGTAAATGGGGAATCCCAGCTTTCTTTTCTACTAGCAAATGACCC TACCATTTATTTCTGCCTTTTTCTTCCGTTCATTGTGAGGAAAAATAAAACTGGTTGAGAGCTTTGTTG TACTAA 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_015631.6
Synonyms	C10orf61; JBTS18; OFD4; TECT3
Summary	This gene encodes a member of the tectonic gene family which functions in Hedgehog signal transduction and development of the neural tube. Mutations in this gene have been associated with Orofaciodigital Syndrome IV and Joubert Syndrom 18. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2012]
Locus ID	26123
MW	26.7

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