SLC25A46 (NM_138773) Human 3' UTR Clone

Specifications

Product Data
Product Name	SLC25A46 (NM_138773) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	HMSN6B; PCH1E
ACCN	NM_138773
Insert Size	1014 bp
Sequence Data	Insert Sequence (showhide) >SC211973 3' UTR clone of NM_138773 The sequence shown below is from the reference sequence of NM_138773. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC TATTTACTCTACACTTCTTCAAAATAACATTTGAGATTTAGGTTCCTTCACTGAGTAGTCTGGAAGATAT AATCTGGATAATTTGCTATGAAGTTATGAGGGATACAAGTGAAATACTGGGGAAGAAAATGGATTGGAAA GTAAAATTGGTACTAAAGCCCATACTGATTATCTTGACTTTGTTTTTTAAGGCATAGGTATATATTTTGG ATCAAAATCCTTCCAAATTTGAAAACTCAATAAAAATAACACTTATTAAATTCTAGTTAGTGTAGCACTC ATGCTGAAGTAAACATGATCGTAGGCAGAAGCAAAATTTTATTATAAAATCTAAAACAAAACTTTATAGA GTTGAATCTATTCCATCTGACTTCAATATTTGCCAAACGTTTATTTTACCTCCTAGATTGATGTTGGTAT AGTATCCTTAATACAGTGTAGTATATTAATGTCCTTAATACAATCAGGAGGTTTTTACCTTTAAGCAAAT AAATTATGTCATTATTGAAAAAGACTTAAGGGATGATTAGACTTGGCAATCTGTAAGCAGGAGTATAAAT GTTTTAAATTGCATTGTCCCTATGTAACTATCTTAATGGCTATATATATGTATTTTATAAAGCCATTTAT GTATACACATGTAACTTGGAATTTCCTTCATCCCTACACATTTTCTACACTTACATCACCTTATTGCATA AAACAAAGTCACGCGCTTTCTGCTTGAACATCAAAATATCAAAAACCAAGGTACCCAAAAGATACAAGTC AGAGACAACATCCTTGTCCATATCCAAACCCAGTGTTTCAGTGCTAGCAACTTAATTTCTCATACATTTA TAGAGTTTGGTTTGCTTTGCTAGTTGTGTGAATCATTGGGCTGTTTTTAGAGCCACTGTTAAGAGAGAAT ATAAAATAATCATGACAATTACTACTGTTTCCACATTTACAAATTGTGTACTTAAATGAACCTCATTTCC CTTTTATTTCTGAATGGCTTGTCTGAGAGGAAAC ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG
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_138773.1
Synonyms	HMSN6B; PCH1E
Summary	This gene encodes a mitochondrial solute carrier protein family member. It functions in promoting mitochondrial fission, and prevents the formation of hyperfilamentous mitochondria. Mutation of this gene results in neuropathy and optic atrophy. [provided by RefSeq, Aug 2016]
Locus ID	91137

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