GALNS (NM_000512) Human 3' UTR Clone

Specifications

Product Data
Product Name	GALNS (NM_000512) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	GalN6S; GALNAC6S; GAS; MPS4A
ACCN	NM_000512
Insert Size	735 bp
Sequence Data	Insert Sequence (showhide) >SC209273 3’UTR clone of NM_000512 The sequence shown below is from the reference sequence of NM_000512. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ATTCCCAAGAAGTGCCTCTGGTCCCACTAGCACCTGCGCAGACTCAGGCCAGGCCTAGAATCTCCGGTT GGCCCTGCAAGTGCCTGGAGGAAGGATGGCTCTGGCCTCGGTCCTCCCCCAACCCTGCCCAAGCCAGAC AGACAGCACCTGCAGACGCAGGGGGACTGCACAATTCCACCTGCCCAGGACCTGACCCTGGCGTGTGCT TGGCCCTCCTCCTCGCCCACGGCGCCTCAGATTTCAGGACCCTCCTCCTCGCCCACGGCGCCTCAGACC TCAGGACCCTGCCGTCTCACGCCTTTGTGAACCCCAAATATCTGAGACCAGTCTCAGTTTATTTTGCCA AGGTTAAGGATGCACCTGTGACAGCCTCAGGAGGTCCTGACAACAGGTGCCTGAGGTGGCTGGGGATAC AGTTTGCCTTTATACATCTTAGGGAGACACAAGATCAGTATGTGTATGGCGTACATTGGTTCAGTCAGC CTTCCACTGAATACACGATTGAGTCTGGCCCAGTGAATCCGCATTTTTATGTAAACAGTAAGGGAACGG GGCAATCATATAAGCGTTTGTCTCAGGGGAGCCCCAGAGGGATGACTTCCAGTTCCGTCTGTCCTTTGT CCACAAGGAATTTCCCTGGACGCTAATTATGAGGGAGGCGTGTAGCTTCTTATCATTGTAACTATGTTA TTTAGAAATAAAACGGGAGGCAGGTTTGCCTAATTCCCAGCTTGA 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_000512.5
Synonyms	GalN6S; GALNAC6S; GAS; MPS4A
Summary	This gene encodes N-acetylgalactosamine-6-sulfatase which is a lysosomal exohydrolase required for the degradation of the glycosaminoglycans, keratan sulfate, and chondroitin 6-sulfate. Sequence alterations including point, missense and nonsense mutations, as well as those that affect splicing, result in a deficiency of this enzyme. Deficiencies of this enzyme lead to Morquio A syndrome, a lysosomal storage disorder. [provided by RefSeq, Jul 2008]
Locus ID	2588
MW	26.4

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