CHST5

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

CHST5
Identifiers
AliasesCHST5, I-GlcNAc-6-ST, I-GlcNAc6ST, glcNAc6ST-3, gn6st-3, hIGn6ST, carbohydrate sulfotransferase 5
External IDsOMIM: 604817 HomoloGene: 69379 GeneCards: CHST5
Gene location (Human)
Chr.Chromosome 16 (human)[1]
Band16q23.1Start75,528,535 bp[1]
End75,535,247 bp[1]
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez

23563

n/a

Ensembl

ENSG00000135702

n/a

UniProt

Q9GZS9

n/a

RefSeq (mRNA)

NM_024533
NM_012126

n/a

RefSeq (protein)

NP_078809

n/a

Location (UCSC)Chr 16: 75.53 – 75.54 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

References

  1. GRCh38: Ensembl release 89: ENSG00000135702 - Ensembl, May 2017
  2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. 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.
  4. 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.
  5. "Entrez Gene: CHST5 carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 5".

Further reading

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