POMT1 (NM_001077366) Human 3' UTR Clone

Specifications

Product Data
Product Name	POMT1 (NM_001077366) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	LGMD2K; LGMDR11; MDDGA1; MDDGB1; MDDGC1; RT
ACCN	NM_001077366
Insert Size	723 bp
Sequence Data	Insert Sequence (showhide) >SC209058 3’UTR clone of NM_001077366 The sequence shown below is from the reference sequence of NM_001077366. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AGCTGGGACATCTTGATCCGAAAACACTAGAACAAGAGTGTGGCAAAGAACACCCGTGCTGGGGTCGGG ATGAGGTTGAAGGGTCTTGGTCAATGTACGTAATGAGCAGGGTGGGCCCCACGCTGGGAGGACACGGGC TGGGCTGAGCAGGGCCTCTAGTGGAACACATGGGGGTCTCATTGAAAAGCTCTCTGATGAGCACCTCCT TTTGTGCAAAGTTAATTTTTTCTCGACAATAAAGATATTCCGTGTCTTTACCCCTGAACTAAGACACAG GGAGTATTTCAGAGGCCAGCGTAGGAGTCATTGACAACAAAAAGCCGAGAACCCAGGGCCAGCAGTGGA GCCTCAGCAGACCAGGGCCTGGTCCTTGCTAACTGCTGCAGGGTGGAGTTTGATCTGGCAGACCCGATC CTCCTTCATGAACACCCAGCAACCTGAGCAAGTCCCGGCCCTGCCCTCAGCGAGCCCGGCAGGCGTCCT GGGACAGCTCAGTGTTGGAGGGCCACCTGAACCACGAGCCAGGGCTGGGGCTTGCATGTCATTGTCTAT GACAGCGTCAAGACTGGCCCTTGGCACCGTGCTGTGTGGAAACCCTCCCCTCTGAGACTCCACTGAGAC GTGGCTGAGTGAAATCTTCCTCGTCAGTGGTCAAGGTGTGTCATCCATACAGCTCCATGCCTTTGTCTT TTTTAAATGTAATTAAAAAAGGAACCAACTGGC 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_001077366.2
Synonyms	LGMD2K; LGMDR11; MDDGA1; MDDGB1; MDDGC1; RT
Summary	The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT2 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome (WWS) and limb-girdle muscular dystrophy type 2K (LGMD2K). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2008]
Locus ID	10585
MW	26.8

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