CLDN19 (NM_148960) Human 3' UTR Clone

Specifications

Product Data
Product Name	CLDN19 (NM_148960) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	HOMG5
ACCN	NM_148960
Insert Size	2000 bp
Sequence Data	Insert Sequence (showhide) >SC217319 3’UTR clone of NM_148960 The sequence shown below is from the reference sequence of NM_148960. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GCCTCCGCCAAGGGCCCCCTGGGTGTGTAATGTCCAGTCCCCAGCCAGGCTCTGTCCCCTGCCATACCT AGACTGTGTGTTTCATATTTTTTTGGAAAGAGAAGTGAACATCCAGCCCCAATCATGGTATCATTCGGT CTGTCCTCAGCGTGGCTTGGACGGGGCCTGTGTCAGAGTGGTCAGTGCTGACCCCTGGGGCTCTTGGGC AGAAAGATGAGGAGACAGAGGTCCAGGGTGGGTTACATAGCACATCCAGGGCTAAGCAAGAAATAATTC AGAGGTCCTACCCTCTGTCTAGGGACCCCCCTCCCAAGCCTGGCCTTGGCCTTGGCACAAAGTCCTCCT TGATAGGAGATCCCACTCACTCCTGGAGGCTGCCCCTGAGGCTTGGCCCAGCTCTAGGAGCAGTCCCCA GGGTCAGGGAGCCCCTGGTGTGGAAAGAGGCCCCAAGGTAGTAAACCCTGCCCCTGTTACTGTGCTCCA GAGACCTCCTAAGGGAAGGGACAGTTCCTGGAAGGCCCTCCAGCTGGATGCTGGGGATCAGCGATAGGT GAGGGGACACAGTGTAGGAGCTCCCCATGTAGAAAAGGGAATGTGGGGAGGGCGTTAGGAGCTTGCAGG CATTAGGACTGTCCTGAGCAAGGTCTGCAGCCCCCAGCTCTGCTCACCCCGAATCCTGCCCCTTGTTTC CACACCTACCATTCCTCCTCTCCTGATCCCCAGCATCCAGCTGAGGTCCAAGGTCTTTGTCCTAGAATC AGAGTGGGGAGGGGACAGCCTGGGGCTGCCCAGAGACTGTGGGTGGAGCTGCCTGCTGCACTCAGCAGT GCGGTCAGAGAAGGGCTTTTGGTCTTGAAGTCCAGGTACCATCCCCCCTTAGCATACAGGGGGAAGGGC CTGAGAGGAATGTAAGGAAACCAGCCCAGATCAGTCCCAAGGCCAGAGTCCTTTGTCCTACATCTCCCT GAACCAGAGTGTGCCCTGCCCCTCATGCTCAGACCTCTCCCACCCCAAACCCTCTCCCGGGACTCAGTC TCCCTGGCCACTGCGTATCAGGCTTCTGGGGAAAGCATCCATCACAGAACCTCCCCTTCCCTGCCACGC ACCTTCCTTGGCCAGCTCCATTCTGGCCTCCTCCACCACCTGCCTTGTGACCACATCTCCCACCACGTC CCCAGATCTCAAGAACGCAGCTCAGCTTCTCCTTCGAGCTTGACTCTGAGAGGGAAAGTGACGGAAACC AAGTCAGATGAGATGACTGCCATGTACACTGCAGTCAAGGGCAGGGAGGGGAGGAATGACACAAATGGC AGGGAGCTGCTGGGGGACTGACCCCTCGGCGCCTGGCCTGGCCGGTGCTGCACATCCACCGGGGCACAA CAGGGACTTGTCCAGCCTCTGGTCAGAGGATGTGGCCACCTGACCCTAAATAGGTTCCCCAGAGTCCTG CCCCTCTAATGAATGAGAACTGCAGGAGTTTCTCCTCTGGGTGCCTGAAGCTATAGTGCAATGGTTCCC AACCCTGCATGCACATTCGAATCACCTGGGGGCACAATGCCTAGGCTCCAACCCCAGACACTCTTATTT CATTGGTCTGGGTGGACCTGGCATCAGAAGTCATGTAGCTCCTCAGGGGACTGTAGTGTGTGGTCAGCA CTGAGGGCTCCTCTATGAGGCCTCAAGCCCAGGTGACTCTGTGAGGTCTGCAGAGGGAGAAAAGAACCC ACAAGGGAAGAGGTGGAGGTCAGGCACGGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCCGAGG TGGGTAGATACCTGAAGTCAGGAGTTCGAGACTAGCCTGGCCAATATGGTAAAACCCCGTGTCTATTAA AAATACAAAAATTAGCTGGCTGTGGTGGTGGGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGG AGAATCGCTTGAACTCGGGAGGTGGAGGTTGCAGTCAGCCAAGATCGTGCCACTGCACACCATCCTGG 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_148960.3
Synonyms	HOMG5
Summary	The product of this gene belongs to the claudin family. It plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. Defects in this gene are the cause of hypomagnesemia renal with ocular involvement (HOMGO). HOMGO is a progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis associated with severe ocular abnormalities such as bilateral chorioretinal scars, macular colobomata, significant myopia and nystagmus. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jun 2010]
Locus ID	149461
MW	71.8

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