N-acetylgalactosamine-4-O-sulfotransferase [Homo sapiens]

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The glycan-specific sulfotransferase (R77W)GalNAc-4-ST1 putatively responsible for peeling skin syndrome has normal properties consistent with a simple sequence polymorphisim. [Glycobiology. 2017]
The glycan-specific sulfotransferase (R77W)GalNAc-4-ST1 putatively responsible for peeling skin syndrome has normal properties consistent with a simple sequence polymorphisim.
Fiete D, Mi Y, Beranek M, Baenziger NL, Baenziger JU. Glycobiology. 2017 May 1; 27(5):450-456.
Whole-exome sequencing in a single proband reveals a mutation in the CHST8 gene in autosomal recessive peeling skin syndrome. [Genomics. 2012]
Whole-exome sequencing in a single proband reveals a mutation in the CHST8 gene in autosomal recessive peeling skin syndrome.
Cabral RM, Kurban M, Wajid M, Shimomura Y, Petukhova L, Christiano AM. Genomics. 2012 Apr; 99(4):202-8. Epub 2012 Jan 25.
Differential expression and enzymatic properties of GalNAc-4-sulfotransferase-1 and GalNAc-4-sulfotransferase-2. [Glycobiology. 2005]
Differential expression and enzymatic properties of GalNAc-4-sulfotransferase-1 and GalNAc-4-sulfotransferase-2.
Boregowda RK, Mi Y, Bu H, Baenziger JU. Glycobiology. 2005 Dec; 15(12):1349-58. Epub 2005 Aug 3.

RefSeq genomic sequence
See the genomic reference sequence for the CHST8 gene (NG_029857.2).
RefSeq protein isoforms
See 9 reference sequence protein isoforms for the CHST8 gene.

Nucleotide
Nucleotide sequence from coding region
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Transcript/Protein Information [PANTHER Classification System]
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reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

ym32a08.s1 Soares infant brain 1NIB Homo sapiens cDNA clone IMAGE:49632 3', mRNA...
ym32a08.s1 Soares infant brain 1NIB Homo sapiens cDNA clone IMAGE:49632 3', mRNA sequence
gi|900168|gnl|dbEST|289817|gb|H2925

Nucleotide

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Protein