TTC8 (NM_198309) Human 3' UTR Clone

Specifications

Product Data
Product Name	TTC8 (NM_198309) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	BBS8; RP51
ACCN	NM_198309
Insert Size	633 bp
Sequence Data	Insert Sequence (showhide) >SC208249 3’UTR clone of NM_198309 The sequence shown below is from the reference sequence of NM_198309. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CAATTAAGGCAGCATTTTGCTATGCTCTGATTGTTCCTTAGACCACATATGTTCTTATGAAGCAGCATT ATGCAAGGGGAAAAAAGCACTATGTCTGTGTATGTATGTATATAGTGTAATACGTATATTTTAACAAAC CTGTCCTTGATATTAGTTAAGGTGACACATAAGGGTGACACAGAATGTGTAATGCAAATTTCATAGTAA TAGTAACTTTATAAAATAATATTATAAAATACAGGATTTAAACCTTTCTAAATAGATCCTGAAACTGTC TCTCACATTATATAGTAGATGTTTGTTTATAATGTTTACAAAACATTTTGGTGAATTTCCTCAATGTTT TATAAATGTACATTTTTTAAGTCCTTAAGCTGACTCTTAGCCATCATGTAGCTTAAGGAGTCTGAAATC TGCCATTAAAACTGCACCTTTAAGCCAGGTGTGGTAGCATGTGCCTATAGTCCCAGCTACTTGGGAGGT GGAGGTGGGAGGATTATAAATAGAGACTTTCCTTAAGACTTTAAAAATGTATTTAAAACTATTTTTTAT TAAATACTTTGTGATTTCCTATTAAGCTTTAAAATAAATCATTGTGTAAAACACCATCATTTCAAAAAA AAAAAAAAAAAA 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_198309.3
Synonyms	BBS8; RP51
Summary	This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is involved in the formation of cilia. A mutation in this gene has also been implicated in nonsyndromic retinitis pigmentosa. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]
Locus ID	123016
MW	24.6

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