CHST3 | ENSG00000122863 | NCBI 9469

Details for: CHST3

Gene ID: 9469

Symbol: CHST3

Ensembl ID: ENSG00000122863

Description: carbohydrate sulfotransferase 3

Associated with

Chondroitin sulfate/dermatan sulfate metabolism
(R-HSA-1793185)
Chondroitin sulfate biosynthesis
(R-HSA-2022870)
Defective chst3 causes sedcjd
(R-HSA-3595172)
Disease
(R-HSA-1643685)
Diseases associated with glycosaminoglycan metabolism
(R-HSA-3560782)
Diseases of glycosylation
(R-HSA-3781865)
Diseases of metabolism
(R-HSA-5668914)
Glycosaminoglycan metabolism
(R-HSA-1630316)
Metabolism
(R-HSA-1430728)
Metabolism of carbohydrates
(R-HSA-71387)
Carbohydrate metabolic process
(GO:0005975)
Chondroitin 6-sulfotransferase activity
(GO:0008459)
Chondroitin sulfate biosynthetic process
(GO:0030206)
Golgi membrane
(GO:0000139)
N-acetylglucosamine 6-o-sulfotransferase activity
(GO:0001517)
N-acetylglucosamine metabolic process
(GO:0006044)
Proteoglycan sulfotransferase activity
(GO:0050698)
Sulfur compound metabolic process
(GO:0006790)
T cell homeostasis
(GO:0043029)
Trans-golgi network
(GO:0005802)

Other Information

Proteins

Chondroitin 6-O-sulfotransferase 1

Genular Protein ID: 1171865933

Symbol: CHST3_HUMAN

Name: Chondroitin 6-O-sulfotransferase 1

UniProtKB Accession Codes:

Q7LGC8 O75099 Q52M30

Database IDs:

Citations:

PubMed ID: 9714738

Title: Molecular cloning and expression of human chondroitin 6-sulfotransferase.

PubMed ID: 9714738

DOI: 10.1016/s0167-4781(98)00089-x

PubMed ID: 9883891

Title: Functional expression and genomic structure of human chondroitin 6-sulfotransferase.

PubMed ID: 9883891

DOI: 10.1016/s0014-5793(98)01532-4

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 15215498

Title: Loss of chondroitin 6-O-sulfotransferase-1 function results in severe human chondrodysplasia with progressive spinal involvement.

PubMed ID: 15215498

DOI: 10.1073/pnas.0400334101

PubMed ID: 18513679

Title: Congenital joint dislocations caused by carbohydrate sulfotransferase 3 deficiency in recessive Larsen syndrome and humero-spinal dysostosis.

PubMed ID: 18513679

DOI: 10.1016/j.ajhg.2008.05.006

Sequence Information:

Length: 479
Mass: 54706
Checksum: 7C290DC4970F66E0
Sequence:

MEKGLTLPQD CRDFVHSLKM RSKYALFLVF VVIVFVFIEK ENKIISRVSD KLKQIPQALA 
DANSTDPALI LAENASLLSL SELDSAFSQL QSRLRNLSLQ LGVEPAMEAA GEEEEEQRKE 
EEPPRPAVAG PRRHVLLMAT TRTGSSFVGE FFNQQGNIFY LFEPLWHIER TVSFEPGGAN 
AAGSALVYRD VLKQLFLCDL YVLEHFITPL PEDHLTQFMF RRGSSRSLCE DPVCTPFVKK 
VFEKYHCKNR RCGPLNVTLA AEACRRKEHM ALKAVRIRQL EFLQPLAEDP RLDLRVIQLV 
RDPRAVLASR MVAFAGKYKT WKKWLDDEGQ DGLREEEVQR LRGNCESIRL SAELGLRQPA 
WLRGRYMLVR YEDVARGPLQ KAREMYRFAG IPLTPQVEDW IQKNTQAAHD GSGIYSTQKN 
SSEQFEKWRF SMPFKLAQVV QAACGPAMRL FGYKLARDAA ALTNRSVSLL EERGTFWVT

The gene details are incomplete or unavailable at the moment.

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.

Details for: CHST3

Associated with

Other Information

Molecular cloning and expression of human chondroitin 6-sulfotransferase. PubMed ID: 9714738

Functional expression and genomic structure of human chondroitin 6-sulfotransferase. PubMed ID: 9883891

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). PubMed ID: 15489334