Inversin (INVS) (NM_183245) Human 3' UTR Clone

Specifications

Product Data
Product Name	Inversin (INVS) (NM_183245) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	INV; NPH2; NPHP2
ACCN	NM_183245
Insert Size	500 bp
Sequence Data	Insert Sequence (showhide) >SC206372 3’UTR clone of NM_183245 The sequence shown below is from the reference sequence of NM_183245. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ACTCAGCCAAAAAACAAAACAAAACCTTGACTGCCTATGGAGGAAGACTGTGTTCGGGGGAGCTGGCAT AGCTAGTGCAGAGTTCAGATTTTCTGCTGATAATCTTTTACACCTTGGGAAAACTTTAATATCCGTACC TGAAGGCTGATTCACCTAAAAATGTGTTAACTGAAAGAAAATGTCAGAATGTTTCCTTTCTGCTCTTAC ACAGCATTGTTTTGTCAATCAACACAGCCTGCACTGAAAGGACCTGCATAGACTATGTCTGTGCAAAGT GCCTGAGTGTCTGCTTTCACCTCAGTCTGTACAGTTGGAAATGAGAATTCATAATTAACAGCAAAATCT AAGGAAAACTACGGCTGCTGGGTTGGGATTTCTGCCAGCTAGCTGGTACTGGCTTCTTGTTTCAAGAGA TGAACCTAAATGAGATAGGAAGCCTGTCCCATAGCAGCCTTCCTCTCACTACTTTCCTGGCATCTAATG CAACAAACTTATCACAC 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_183245.2
Synonyms	INV; NPH2; NPHP2
Summary	This gene encodes a protein containing multiple ankyrin domains and two IQ calmodulin-binding domains. The encoded protein may function in renal tubular development and function, and in left-right axis determination. This protein interacts with nephrocystin and infers a connection between primary cilia function and left-right axis determination. A similar protein in mice interacts with calmodulin. Mutations in this gene have been associated with nephronophthisis type 2. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, May 2012]
Locus ID	27130
MW	18.8

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