KIRREL 3 (KIRREL3) (NM_001161707) Human 3' UTR Clone

Specifications

Product Data
Product Name	KIRREL 3 (KIRREL3) (NM_001161707) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	KIRRE; MRD4; NEPH2; PRO4502
ACCN	NM_001161707
Insert Size	402 bp
Sequence Data	Insert Sequence (showhide) >SC205013 3’UTR clone of NM_001161707 The sequence shown below is from the reference sequence of NM_001161707. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AAGCAGGAGTGCAATGAACAGGGGTCCTAACAGTGCTGTGAGCTCCTGGGGCAGGGAGTGGGTCTGATG CATCGGTGTATGTGAGCCTGGGCAACATGGCGCCTGGCAGAGTGGGCGCTAGGCTGAGGTTGACCTGGA CTAGACTGAACTTCATCTGCAGGGCAGCCAGCATTTTGGATTGAACACATAGCTCTTTCAGTCAGGAAC TGTACAGAAAGATAGGGGGAAAAGCGGTTTGTGGTTTGATCCTTGCTCTACAAGAGCTGTTAGTCTAGA GAGACCCCATCTCTACAACAAAATAAAAATAAAGAGCTGCTAGTCTCACCAGAAAAGCAGGTCACTCAC ACAGCTGTGGGGGAGTGGGTGGGGAAGCAATAAAGGAATTGCTTTGAGAAAACTTAA 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_001161707.1
Synonyms	KIRRE; MRD4; NEPH2; PRO4502
Summary	The protein encoded by this gene is a member of the nephrin-like protein family. These proteins are expressed in fetal and adult brain, and also in podocytes of kidney glomeruli. The cytoplasmic domains of these proteins interact with the C-terminus of podocin, also expressed in the podocytes, cells involved in ensuring size- and charge-selective ultrafiltration. The protein encoded by this gene is a synaptic cell adhesion molecule with multiple extracellular immunoglobulin-like domains and a cytoplasmic PDZ domain-binding motif. Mutations in this gene are associated with several neurological and cognitive disorders. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]
Locus ID	84623
MW	15

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