Gene Details



CHST6 and homologs in 1 species are found in 94 GeneSets:


- Entrez   - Ensembl   - GeneNetwork   - STRING   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 158 Genes GS200257: GO:0006022 aminoglycan metabolic process
Expand Tier I Human GO 1762 Genes GS196284: GO:0012505 endomembrane system
Expand Tier I Human GO 1718 Genes GS208734: GO:0016740 transferase activity
Expand Tier I Human CTD 2 Genes GS122199: poly-N-acetyllactosamine interacting genes (MeSH:C037199) in CTD
Expand Tier I Human GO 149 Genes GS197282: GO:0030203 glycosaminoglycan metabolic process
Expand Tier I Human GO 25 Genes GS193780: GO:0006044 N-acetylglucosamine metabolic process
Expand Tier I Human GO 1682 Genes GS204629: GO:1901564 organonitrogen compound metabolic process
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human GO 60 Genes GS208038: GO:0016782 transferase activity, transferring sulfur-containing groups
Expand Tier I Human GO 32 Genes GS194985: GO:1901071 glucosamine-containing compound metabolic process
Expand Tier I Human GO 5120 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human 97 Genes GS175976: HP:0003621 Juvenile onset
Expand Tier I Human CTD 23 Genes GS124314: apple polyphenol extract interacting genes (MeSH:C526219) in CTD
Expand Tier I Human GO 5 Genes GS206103: GO:0001517 N-acetylglucosamine 6-O-sulfotransferase activity
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human 38 Genes GS175272: HP:0200020 Corneal erosions
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 1202 Genes GS194505: GO:1901135 carbohydrate derivative metabolic process
Expand Tier I Human GO 2509 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human GO 6256 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human CTD 916 Genes GS121965: Amiodarone interacting genes (MeSH:D000638) in CTD
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human GO 5359 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human GO 547 Genes GS205302: GO:0000139 Golgi membrane
Expand Tier I Human GO 5243 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 129 Genes GS173247: HP:0007957 Reduction of corneal clarity
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human GO 100 Genes GS200263: GO:0006024 glycosaminoglycan biosynthetic process
Expand Tier I Human 9 Genes GS173080: HP:0000495 Recurrent corneal erosions
Expand Tier I Human 105 Genes GS175571: HP:0011492 Abnormality of corneal stroma
Expand Tier I Human 4 Genes GS176387: HP:0007856 Punctate opacification of the cornea
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 646 Genes GS204631: GO:1901566 organonitrogen compound biosynthetic process
Expand Tier I Human GO 37 Genes GS209566: GO:0006040 amino sugar metabolic process
Expand Tier I Human GO 2361 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 33 Genes GS174652: HP:0001131 Corneal dystrophy
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 101 Genes GS200258: GO:0006023 aminoglycan biosynthetic process
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 4245 Genes GS207858: GO:0009059 macromolecule biosynthetic process
Expand Tier I Human CTD 1593 Genes GS124695: arsenic trioxide interacting genes (MeSH:C006632) in CTD
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human GO 6073 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 113 Genes GS204687: GO:0044272 sulfur compound biosynthetic process
Expand Tier I Human GO 549 Genes GS194503: GO:1901137 carbohydrate derivative biosynthetic process
Expand Tier I Human GO 32 Genes GS201065: GO:0042339 keratan sulfate metabolic process
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human GO 786 Genes GS199922: GO:0005975 carbohydrate metabolic process
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human GO 970 Genes GS210163: GO:0006082 organic acid metabolic process
Expand Tier I Human GO 27 Genes GS210234: GO:0018146 keratan sulfate biosynthetic process
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 469 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human GO 5190 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Human GO 5280 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 1166 Genes GS201075: GO:0005794 Golgi apparatus
Expand Tier I Human 51 Genes GS174243: HP:0011495 Abnormality of corneal epithelium
Expand Tier I Human 323 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human GO 51 Genes GS201288: GO:0008146 sulfotransferase activity
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 234 Genes GS209234: GO:0006790 sulfur compound metabolic process
Expand Tier I Human 120 Genes GS171657: HP:0000613 Photophobia
Expand Tier I Human GO 665 Genes GS205609: GO:0044431 Golgi apparatus part
Expand Tier I Human 104 Genes GS175835: HP:0007759 Opacification of the corneal stroma
Expand Tier I Human CTD 1454 Genes GS121893: Vitamin E interacting genes (MeSH:D014810) in CTD
Expand Tier I Human GO 5928 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 5014 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human GO 952 Genes GS202555: GO:0043436 oxoacid metabolic process
Expand Tier I Human CTD 1523 Genes GS124579: Selenium interacting genes (MeSH:D012643) in CTD
Expand Tier I Human CTD 4 Genes GS123340: Keratan Sulfate interacting genes (MeSH:D007632) in CTD