GSDME (NM_001127453) Human 3' UTR Clone

Specifications

Product Data
Product Name	GSDME (NM_001127453) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	DFNA5; ICERE-1
ACCN	NM_001127453
Insert Size	701 bp
Sequence Data	Insert Sequence (showhide) >SC209020 3’UTR clone of NM_001127453 The sequence shown below is from the reference sequence of NM_001127453. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTCTGTGCTTTAGGCAGAGAACATTCATGATGTCATATGTGAACTAGAAGTACGTGTTACTGGCCAAGG CTATTTTTCAGAACTGTTAAAGGTCATATGCACGTTAAAAGTTGACCAATGAAATGAATTTACAGAACA GTTTAAGAAGTGGTGACATTTTGCATGATGAATGACCTGACTTTTAGCCACCAGGTACTCTTTAAACAG TTTTCCTTATCAGAGGCCCTCCTGTGCTGGTGACCCAGCATCTGAGTTAGGTTCCAGCATGTAAAGAGC TGGGAGGGCGGAGAATTCTTAGCATACATTCAGACGTTTTTTCTGCACAATAATAAGTCCATCTGTCAC TTGCATTCCACTTTTTGTTACATAGAAAGAGTCTGACCCTTTAATCCAAAAGGTCTTTTTACATTGTGA ATGCTGTGGGAAGGCAATTTCTCTGCACACAAGAGGCTACGTTTTGGAAGTGATGTATGTTATTTGATG ACTGAAAATGAACTGTAAATGCTCCTAGAGTATATTCCTCTGCTGAACAAAATTAAACTTCAAAAAAAT CTAACAGTAACACACCCCTGCTTGGGACCCTAGCTATATGCATTTTATGTGACCTTGCCATGCTTCAGT GAACATACTAATTCTATGTCTAGCACATGTTGATTTCCTATGTATTCTGGGTATTCTATTAAAGGAAAC TTTGAACTATG 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_001127453.2
Synonyms	DFNA5; ICERE-1
Summary	Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Locus ID	1687
MW	27.3

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