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Alliance of Genome Resources

Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.

Source Last Updated
Alliance of Genome Resources January 28, 2025
Displaying entries 176 - 200 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▼ References
DOID:0070004 myeloid neoplasm HGNC:3688 Homo sapiens (human) 2260 FGFR1 mutant phenotype evidence used in manual assertion
  • PMID:12969958
  • PMID:15448205
DOID:9256 colorectal cancer HGNC:2745 Homo sapiens (human) 1654 DDX3X mutant phenotype evidence used in manual assertion
  • PMID:31391454
DOID:5844 myocardial infarction HGNC:7876 Homo sapiens (human) 4846 NOS3 mutant phenotype evidence used in manual assertion
  • PMID:17637430
DOID:684 hepatocellular carcinoma HGNC:4056 Homo sapiens (human) 2538 G6PC1 mutant phenotype evidence used in manual assertion
  • PMID:28096054
DOID:0080066 autosomal recessive spinocerebellar ataxia 20 SGD:S000004572 Saccharomyces cerevisiae S288C 854867 MDM1 mutant phenotype evidence used in manual assertion
  • PMID:26283797
  • PMID:33740659
DOID:83 cataract RGD:69062 Rattus norvegicus (Norway rat) 83571 Cdkn1b mutant phenotype evidence used in manual assertion
  • PMID:30893315
DOID:10808 gastric ulcer RGD:3434 Rattus norvegicus (Norway rat) 25637 Ptger1 mutant phenotype evidence used in manual assertion
  • PMID:10807413
DOID:303 substance-related disorder RGD:2848 Rattus norvegicus (Norway rat) 25187 Htr2c mutant phenotype evidence used in manual assertion
  • PMID:16474401
DOID:3345 xanthomatosis RGD:2998 Rattus norvegicus (Norway rat) 300438 Ldlr mutant phenotype evidence used in manual assertion
  • PMID:22293196
DOID:1824 status epilepticus RGD:2143 Rattus norvegicus (Norway rat) 25293 Aqp4 mutant phenotype evidence used in manual assertion
  • PMID:20886625
DOID:4483 rhinitis HGNC:1030 Homo sapiens (human) 624 BDKRB2 mutant phenotype evidence used in manual assertion
  • PMID:11149999
DOID:4074 pancreatic adenocarcinoma HGNC:9829 Homo sapiens (human) 5894 RAF1 mutant phenotype evidence used in manual assertion
  • PMID:15014358
DOID:10534 stomach cancer HGNC:2731 Homo sapiens (human) 4921 DDR2 mutant phenotype evidence used in manual assertion
  • PMID:26934957
DOID:7614 meninges sarcoma RGD:3889 Rattus norvegicus (Norway rat) 24842 Tp53 mutant phenotype evidence used in manual assertion
  • PMID:27528400
DOID:10763 hypertension RGD:620600 Rattus norvegicus (Norway rat) 85431 Nox4 mutant phenotype evidence used in manual assertion
  • PMID:26644237
DOID:14330 Parkinson's disease HGNC:11179 Homo sapiens (human) 6647 SOD1 mutant phenotype evidence used in manual assertion
  • PMID:16353238
DOID:684 hepatocellular carcinoma HGNC:1066 Homo sapiens (human) 648 BMI1 mutant phenotype evidence used in manual assertion
  • PMID:26919246
DOID:0080552 congenital disorder of glycosylation Ia SGD:S000001849 Saccharomyces cerevisiae S288C 850499 SEC53 mutant phenotype evidence used in manual assertion
  • PMID:36214454
DOID:1289 neurodegenerative disease WB:WBGene00010775 Caenorhabditis elegans 187297 poml-1 mutant phenotype evidence used in manual assertion
  • PMID:26941331
DOID:3526 cerebral infarction HGNC:6293 Homo sapiens (human) 3783 KCNN4 mutant phenotype evidence used in manual assertion
  • PMID:29037241
DOID:14227 azoospermia RGD:1308135 Rattus norvegicus (Norway rat) 361722 Bscl2 mutant phenotype evidence used in manual assertion
  • PMID:25934999
DOID:2841 asthma RGD:2070 Rattus norvegicus (Norway rat) 24180 Agtr1a mutant phenotype evidence used in manual assertion
  • PMID:19080339
DOID:3827 congenital diaphragmatic hernia RGD:2072 Rattus norvegicus (Norway rat) 24182 Agtr2 mutant phenotype evidence used in manual assertion
  • PMID:22113494
DOID:83 cataract RGD:2092 Rattus norvegicus (Norway rat) 24192 Akr1b1 mutant phenotype evidence used in manual assertion
  • PMID:18452283
DOID:8398 osteoarthritis HGNC:9201 Homo sapiens (human) 5443 POMC mutant phenotype evidence used in manual assertion
  • PMID:21378032
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 8, 2025