Inosine triphosphate pyrophosphatase (ITPA) (NM_181493) Human 3' UTR Clone

Specifications

Product Data
Product Name	Inosine triphosphate pyrophosphatase (ITPA) (NM_181493) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	C20orf37; DEE35; dJ794I6.3; HLC14-06-P; ITPase; My049; NTPase
ACCN	NM_181493
Insert Size	428 bp
Sequence Data	Insert Sequence (showhide) >SC206479 3’UTR clone of NM_181493 The sequence shown below is from the reference sequence of NM_181493. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CAGGAGTACTTTGGCAGTTTGGCAGCTTGACTTCTGCAGCTGGAGGAGGCCCCTCAGGCCGGGGATCTG GGGAGGGCTAGCCCAAAACCTCCCGCATCGGGCAGGCACCCCCTGAAGTACTTCCTTCAGGGTTTCCCC TTTGTGAGGGTGTCGAGTAGCCTCACCGGCCTGTCTGGAGGAGCAGCTGGCTCTGCTCTGAGAAACTCT GGCAAGTGGACGCCATTCTCTTGCCCTTAGGATTCACTGCTCTCTCCTACAGCCGCCAGGCCTGGGGTC CTGAAAGGACCTTGGGTGGTAAAGCTGTACTTGGTGGGAGTGAGGGCGTGGGGAGGAACCATGCAAATC GCCTTCCATGGTTTTTAAATGCAGTAAATAACATTTCTGGATGAGACTTGTTTCCAAAATAAACCAGCT ATATCTGTTTTGAA 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_181493.4
Synonyms	C20orf37; DEE35; dJ794I6.3; HLC14-06-P; ITPase; My049; NTPase
Summary	This gene encodes an inosine triphosphate pyrophosphohydrolase. The encoded protein hydrolyzes inosine triphosphate and deoxyinosine triphosphate to the monophosphate nucleotide and diphosphate. This protein, which is a member of the HAM1 NTPase protein family, is found in the cytoplasm and acts as a homodimer. Defects in the encoded protein can result in inosine triphosphate pyrophosphorylase deficiency which causes an accumulation of ITP in red blood cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]
Locus ID	3704
MW	15.2

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