SGK196 (POMK) (NM_032237) Human 3' UTR Clone

Specifications

Product Data
Product Name	SGK196 (POMK) (NM_032237) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	MDDGA12; MDDGC12; SGK196
ACCN	NM_032237
Insert Size	587 bp
Sequence Data	Insert Sequence (showhide) >SC203970 3’UTR clone of NM_032237 The sequence shown below is from the reference sequence of NM_032237. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ATGATGTCTCAGGCAAGAGAGATGCTGTGAAAACCAGTCCAGCCAATGAAGGTGGGATTGAAGGGCTGA ATGGAAGTTACAGCATTCTACTCTGATGGTGGAGTTTTTTGCCTGAGTTTCGTGTTTTATTGTTTTTTT TATGGCTTAGCCATGTGGTTCGTTGTCCACATCCACATGTACGTTTGTATGTAGTCCACATTGGTTGTT AGATTTTTTTTTTTTTCTTTGAGATGCGGTCTTGCTCTGTTGCTGAGGCTGGAGTGCAGTGATGTGATC TTGGCTCACTGCAGCCTCTGCCTCCCAGGTTCAAGCAATTCTCCCACCTCAGCCTCCTGAGTAGCTGGG ATTACAGGCACACCACCACGCCTGGCTAATTTTTGTATTTTTAGTGGAGGTGGGGTTTCACCATGTTGG CCAGGCTGGTCCCGAACTCCTGACTTCCTCGGCCTCCCAAAGTGTTGGGATTACAGGCATGGGCCACTA TGCCTGGCCAGTTGTTAGATTTCCATGGATTTGTAGTTTCCAAAGTTTCTCGTTATTGATTTCTACTTT TCTTCCATTGTGGTCTGAGAAGGTACTTGATATGA 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_032237.5
Synonyms	MDDGA12; MDDGC12; SGK196
Summary	This gene encodes a protein that may be involved in the presentation of the laminin-binding O-linked carbohydrate chain of alpha-dystroglycan (a-DG), which forms transmembrane linkages between the extracellular matrix and the exoskeleton. Some pathogens use this O-linked carbohydrate unit for host entry. Loss of function compound heterozygous mutations in this gene were found in a human patient affected by the Walker-Warburg syndrome (WWS) phenotype. Mice lacking this gene contain misplaced neurons (heterotopia) in some regions of the brain, possibly from defects in neuronal migration. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2013]
Locus ID	84197
MW	21.7

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