D2HGDH (NM_152783) Human 3' UTR Clone

Specifications

Product Data
Product Name	D2HGDH (NM_152783) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	D2HGD
ACCN	NM_152783
Insert Size	872 bp
Sequence Data	Insert Sequence (showhide) >SC210585 3’UTR clone of NM_152783 The sequence shown below is from the reference sequence of NM_152783. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CCCTACAAGACGCTGCCCAGCCAGGCCTGACGGCCACTCCTGCTGCTGCCAAGGCCCACTGGGGGTCGG CGGGTGGCTCTCGGGCGGGGGTGTTGCGGTGGCTCTGAGGGATGAGCCGGCAGTGGGCAGGGGACCAGG CACCTGGTTGAAGGGACTGGGAGCCCGCACTGGGGAACTGCCGGACGCAGGCCCTCGGGCAGGAGCATC TGGCAGAGTGGGGGGCGTGGCAGGCACCCTCCTTTGCAGGGCGAGGTGGGGCCTCTGCAGCCATCCTGG ACAGGCCGGGGTGGCGGCAGCTTTGCCCACGTGGAAGCGGGGTGGGTCTCACTTGCGTGGTGGCCCCTG GCCCCATCTTGCCTGCTGCGGCCTGGGGAGCAGGCGCTGGGTGGTGGTTCTGCCTGCTTGCTGCTCGTT CCCCGGGCATGCGTGGGCAGCGGGGGGCATGCGTGGGCAGCAGGGGGCGTGGGCAGCGGGGGCACGGGC AGGACCACGTGGGCCGTGATCGTGGGTTGCCGAGAGGACCTGAGCGCTGCGGCTCTGCTGAATGGAGCC GGGTCCCTCAGGCCGTGGACGCCCTCGGGAGGGGGGTGACTGTGGCTTGTGTCTGGACAGGAATGTGTC ATTTCCCACATCTTCTAGAGGGCTGCCAGCTGGGAAGACAGTTATCAGGGCAAGCTGTGCTCTGAGTTT CGGGTTCTGCTCCTACAAAGAACGTGCGGTGCTGCGGGCGAGGGCCCCGGCACGGACAAGGGCCACTGC AGAGTGTGTTTCTGCTCGTCAGCTGCCCTGGGCAGCGGATGGGCTGGGCGATGCAGCTGGATGCACATC TCATTCTGTCATGAATGTCCAGTAAAAATCTGAATTGGTTGCAA 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_152783.5
Synonyms	D2HGD
Summary	This gene encodes D-2hydroxyglutarate dehydrogenase, a mitochondrial enzyme belonging to the FAD-binding oxidoreductase/transferase type 4 family. This enzyme, which is most active in liver and kidney but also active in heart and brain, converts D-2-hydroxyglutarate to 2-ketoglutarate. Mutations in this gene are present in D-2-hydroxyglutaric aciduria, a rare recessive neurometabolic disorder causing developmental delay, epilepsy, hypotonia, and dysmorphic features. [provided by RefSeq, Jul 2008]
Locus ID	728294
MW	29.9

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