HGD (NM_000187) Human 3' UTR Clone

Specifications

Product Data
Product Name	HGD (NM_000187) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	AKU; HGO
ACCN	NM_000187
Insert Size	238 bp
Sequence Data	Insert Sequence (showhide) >SC202423 3’UTR clone of NM_000187 The sequence shown below is from the reference sequence of NM_000187. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AACTCCAGGAACCCAGCAGAACCTAATTGAGACTGGAACATTGCTACCATAATTAAGAGTAGATTTGTG AAGATTTCTTCAGAATCTCATGCTTTCTGGTAGTATTGGAGGAGGGGGTTGGTTAAAATGAAAATTCAC TTTTCATAGTCAAGTAACTCAGAACTTTTATGGAAACGCATTTGCAAAGTTCTATGGCTGTCACCTTAA TTACTCAATAAACTTGCTGGTGTTCTGTGGA 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_000187.4
Synonyms	AKU; HGO
Summary	This gene encodes the enzyme homogentisate 1,2 dioxygenase. This enzyme is involved in the catabolism of the amino acids tyrosine and phenylalanine. Mutations in this gene are the cause of the autosomal recessive metabolism disorder alkaptonuria.[provided by RefSeq, May 2010]
Locus ID	3081
MW	9.3

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