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Proteintech
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Immunogen sequence: SVDYLTDVL ANVSLDFLDY KSNFEPFFMM IATPAPHSPW TAAPQYQKAF QNVFAPRNKN FNIHGTNKHW LIRQAKTPMT NSSIQFLDNA FRKRWQTLLS VDDLVEKLVK RLEFTGELNN TYIFYTSDNG YHTGQFSLPI DKRQLYEFDI KVPLLVRGPG IKPNQTSKML VANIDLGPTI LDIAGYDLNK TQMDGMSLLP ILRGASNLTW RSDVLVEYQG EGRNVTDPTC PSLSPGVSQC FPDCVCEDAY NNTYACVRTM SALWNLQYCE FDDQEVFVEV YNLTADPDQI TNIAKTIDPE LLGKMNYRLM MLQSCSGPTC RTPGVFDPGY RFDPRLMFSN RGSVRTRRFS KHLL (200-552 aa encoded by B C012482)
GNS is a lysosomal enzyme found in all cells. It is involved in the catabolism of heparin, heparan sulphate, and keratan sulphate. Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder mucopolysaccharidosis type IIID (Sanfilippo D syndrome). Mucopolysaccharidosis type IIID is the least common of the four subtypes of Sanfilippo syndrome.
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Protein Aliases: G6S; glucosamine -6-sulfatase; Glucosamine-6-sulfatase; N-acetylglucosamine-6-sulfatase
Gene Aliases: 2610016K11Rik; AU042285; C87209; G6S; GNS; N28088
UniProt ID: (Human) P15586, (Mouse) Q8BFR4
Entrez Gene ID: (Human) 2799, (Mouse) 75612, (Rat) 299825
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