CHST5 information

CHST5
Identifiers
Aliases	CHST5, I-GlcNAc-6-ST, I-GlcNAc6ST, glcNAc6ST-3, gn6st-3, hIGn6ST, carbohydrate sulfotransferase 5
External IDs	OMIM: 604817; HomoloGene: 69379; GeneCards: CHST5; OMA:CHST5 - orthologs
Gene location (Human)
Chr.	Chromosome 16 (human)
End	75,536,108 bp
RNA expression pattern
	Top expressed in
	duodenum; ; rectum; ; mucosa of transverse colon; ; right uterine tube; ; ventricular zone; ; gonad; ; cerebellum; ; cerebellar cortex; ; cerebellar hemisphere; ; right hemisphere of cerebellum;
	n/a
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	transferase activity; sulfotransferase activity; N-acetylglucosamine 6-O-sulfotransferase activity;
Cellular component	Golgi membrane; Golgi apparatus; intrinsic component of Golgi membrane; membrane; integral component of membrane; trans-Golgi network;
Biological process	sulfur compound metabolic process; protein sulfation; keratan sulfate biosynthetic process; N-acetylglucosamine metabolic process; carbohydrate metabolic process;
	Sources:Amigo / QuickGO
Orthologs
	23563
	n/a
	ENSG00000135702
	n/a
	Q9GZS9
	n/a
	NM_024533; NM_012126
	n/a
	NP_078809
	n/a
	Wikidata
View/Edit Human

Carbohydrate sulfotransferase 5 is an enzyme that in humans is encoded by the CHST5 gene.^[3]^[4]^[5]

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000135702 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Lee JK, Bhakta S, Rosen SD, Hemmerich S (Sep 1999). "Cloning and characterization of a mammalian N-acetylglucosamine-6-sulfotransferase that is highly restricted to intestinal tissue". Biochemical and Biophysical Research Communications. 263 (2): 543–9. doi:10.1006/bbrc.1999.1324. PMID 10491328.
^ Akama TO, Nishida K, Nakayama J, Watanabe H, Ozaki K, Nakamura T, Dota A, Kawasaki S, Inoue Y, Maeda N, Yamamoto S, Fujiwara T, Thonar EJ, Shimomura Y, Kinoshita S, Tanigami A, Fukuda MN (Oct 2000). "Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene". Nature Genetics. 26 (2): 237–41. doi:10.1038/79987. PMID 11017086. S2CID 25547752.
^ "Entrez Gene: CHST5 carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 5".

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