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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 6076 - 6100 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:11382 corneal neovascularization HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:10359324
DOID:6432 pulmonary hypertension HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:7946395
DOID:11476 osteoporosis HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:8182127
DOID:13139 crescentic glomerulonephritis HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:7637259
DOID:10126 keratoconus HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:23462747
DOID:1407 anterior uveitis HGNC:6000 Homo sapiens (human) 3557 IL1RN mutant phenotype evidence used in manual assertion
  • PMID:19693263
DOID:11713 diabetic angiopathy HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10763 hypertension HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:11840488
DOID:5199 ureteral obstruction HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:21975862
DOID:1184 nephrotic syndrome HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:14758530
DOID:9744 type 1 diabetes mellitus HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:9158104
DOID:3908 lung non-small cell carcinoma HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:16126303
DOID:2841 asthma HGNC:6000 Homo sapiens (human) 3557 IL1RN mutant phenotype evidence used in manual assertion
  • PMID:16724092
DOID:3525 middle cerebral artery infarction HGNC:6000 Homo sapiens (human) 3557 IL1RN mutant phenotype evidence used in manual assertion
  • PMID:7790404
DOID:10534 stomach cancer HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:106 pleural tuberculosis HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:10377182
DOID:9074 systemic lupus erythematosus HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:17176440
DOID:0050854 Muckle-Wells syndrome HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:22146561
DOID:0080998 acute necrotizing pancreatitis HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:7736749
DOID:1909 melanoma HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:8168095
DOID:8577 ulcerative colitis HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:8119534
DOID:8927 learning disability HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:10751560
DOID:0081120 Graves ophthalmopathy HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:19702713
DOID:2841 asthma HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:15020290
  • PMID:16409203
  • PMID:17107994
  • PMID:18763028
  • PMID:18926055
DOID:0081267 graft-versus-host disease HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:8049450
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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: April 7, 2025