FTCD (NM_206965) Human 3' UTR Clone

Specifications

Product Data
Product Name	FTCD (NM_206965) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	LCHC1
ACCN	NM_206965
Insert Size	238 bp
Sequence Data	Insert Sequence (showhide) >SC202464 3’UTR clone of NM_206965 The sequence shown below is from the reference sequence of NM_206965. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTGGACTGCTTGGAGACCCGGCAGGAGTGACGGTGCGGGAGGCCTCTCCGGGCTCTGTGGCCCCTCCCT CGCCCATCCCCAGAGGGCAGAGCTGTGACCTCGGTGGGGACACAGCTTGTTCGTGTGGGGCCCGGAGGG TAGGTGGGCAGGCAGCGGGGCATCGCCTGGGAATGGAGGCGCTGGCAGGGACAGAAGGCCCCTAGTCCC ATGTGACCTCCAGTAAAGTTTTGGCACCAAA 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_206965.2
Synonyms	LCHC1
Summary	The protein encoded by this gene is a bifunctional enzyme that channels 1-carbon units from formiminoglutamate, a metabolite of the histidine degradation pathway, to the folate pool. Mutations in this gene are associated with glutamate formiminotransferase deficiency. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Dec 2009]
Locus ID	10841
MW	9

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