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9469 CHST3

9469

CHST3

carbohydrate sulfotransferase 3

protein-coding

Homo sapiens

基因描述

Type Description
Definition carbohydrate sulfotransferase 3

研究结论

Date Results Publications
2021-01-09 13:33:00 Lysophosphatidic acid receptor 5 transactivation of TGFBR1 stimulates the mRNA expression of proteoglycan synthesizing genes XYLT1 and CHST3. 32920014
2020-10-03 12:51:00 Abnormal expression of chondroitin sulfate sulfotransferases in the articular cartilage of pediatric patients with Kashin-Beck disease. 31845005
2019-04-13 10:43:00 We show that the CHST3 and CHST13 alleles are significantly more frequent in pulmonary arterial hypertension patients with elevated aminotransferases during therapy with bosentan than those in patients without liver injury. This is the first pharmacogenomics study linking proteoglycan sulfating genes to drug-induced liver dysfunction. 30118797
2017-10-21 11:47:00 We describe three consanguineous Indian families with a distinct form of spondyloepiphyseal dysplasia (SED Omani type). It is an autosomal recessive disorder due to mutation in CHST3 gene. 27753269
2017-05-27 11:34:00 A novel CHST3 allele associated with spondyloepiphyseal dysplasia and hearing loss has been described in a consanguineous Pakistani pedigree. 26572954

名称对应

Type IDs
Synonymous C6ST, C6ST1, HSD
Gene
UniProtKB-ID: CHST3_HUMAN
UniprotKB: Q7LGC8
UniParc: UPI000013CB04
EMBL: AB012192, BC093690, AB017915, BC104856
Ensembl: ENSG00000122863
KO: hsa:9469
Nucleutide sequences
EMBL-CDS: BAA36348.1, AAI04857.1, AAH93690.1, BAA32576.1
Ensembl_TRS: ENST00000373115
Protein sequencees
Ensembl_PRO: ENSP00000362207
RefSeq: NP_004264.2, XP_006718138.1, XP_011538671.1
Others
UniRef100: UniRef100_Q7LGC8
UniRef90: UniRef90_Q7LGC8
UniRef50: UniRef50_Q7LGC8
UniGene: Hs.158304
CCDS: CCDS7312.1

全选

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