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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 9951 - 9975 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:0050700 cardiomyopathy HGNC:7871 Homo sapiens (human) 4841 NONO inference by association of genotype from phenotype used in manual assertion
  • PMID:31883306
DOID:10652 Alzheimer's disease HGNC:7872 Homo sapiens (human) 4842 NOS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17418914
  • PMID:21098972
DOID:14330 Parkinson's disease HGNC:7872 Homo sapiens (human) 4842 NOS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11809160
DOID:1485 cystic fibrosis HGNC:7872 Homo sapiens (human) 4842 NOS1 direct assay evidence used in manual assertion
  • PMID:11890749
DOID:1485 cystic fibrosis HGNC:7872 Homo sapiens (human) 4842 NOS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:14760158
DOID:2841 asthma HGNC:7872 Homo sapiens (human) 4842 NOS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10673365
  • PMID:10833424
  • PMID:14767694
  • PMID:20609134
DOID:9352 type 2 diabetes mellitus HGNC:7873 Homo sapiens (human) 4843 NOS2 inference by association of genotype from phenotype used in manual assertion
  • PMID:19395279
DOID:10763 hypertension HGNC:7873 Homo sapiens (human) 4843 NOS2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11702222
DOID:12365 malaria HGNC:7873 Homo sapiens (human) 4843 NOS2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1307 dementia HGNC:7873 Homo sapiens (human) 4843 NOS2 direct assay evidence used in manual assertion
  • PMID:10674474
DOID:2841 asthma HGNC:7873 Homo sapiens (human) 4843 NOS2 inference by association of genotype from phenotype used in manual assertion
  • PMID:17177683
  • PMID:17189532
  • PMID:18714530
DOID:6432 pulmonary hypertension HGNC:7873 Homo sapiens (human) 4843 NOS2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16813666
DOID:2957 pulmonary tuberculosis HGNC:7873 Homo sapiens (human) 4843 NOS2 inference by association of genotype from phenotype used in manual assertion
  • PMID:19575238
DOID:12217 Lewy body dementia HGNC:7873 Homo sapiens (human) 4843 NOS2 direct assay evidence used in manual assertion
  • PMID:10674474
DOID:1070 primary open angle glaucoma HGNC:7876 Homo sapiens (human) 4846 NOS3 inference by association of genotype from phenotype used in manual assertion
  • PMID:19815736
  • PMID:20069064
  • PMID:21245953
  • PMID:21670344
  • PMID:22561696
  • PMID:9493554
DOID:4914 esophagus adenocarcinoma HGNC:7876 Homo sapiens (human) 4846 NOS3 inference by association of genotype from phenotype used in manual assertion
  • PMID:21472143
DOID:10873 Kuhnt-Junius degeneration HGNC:7876 Homo sapiens (human) 4846 NOS3 inference by association of genotype from phenotype used in manual assertion
  • PMID:23276910
DOID:5844 myocardial infarction HGNC:7876 Homo sapiens (human) 4846 NOS3 inference by association of genotype from phenotype used in manual assertion
  • PMID:10531147
  • PMID:11903359
  • PMID:12362496
DOID:10923 sickle cell anemia HGNC:7876 Homo sapiens (human) 4846 NOS3 inference by association of genotype from phenotype used in manual assertion
  • PMID:24088668
DOID:1272 telangiectasis HGNC:7876 Homo sapiens (human) 4846 NOS3 inference by association of genotype from phenotype used in manual assertion
  • PMID:18027873
DOID:10763 hypertension HGNC:7876 Homo sapiens (human) 4846 NOS3 inference by association of genotype from phenotype used in manual assertion
  • PMID:9674630
DOID:8947 diabetic retinopathy HGNC:7876 Homo sapiens (human) 4846 NOS3 inference by association of genotype from phenotype used in manual assertion
  • PMID:11918626
  • PMID:15890549
  • PMID:17973941
  • PMID:23776381
DOID:0050848 obstructive sleep apnea HGNC:7876 Homo sapiens (human) 4846 NOS3 inference by association of genotype from phenotype used in manual assertion
  • PMID:18651156
DOID:9119 acute myeloid leukemia HGNC:7876 Homo sapiens (human) 4846 NOS3 inference by association of genotype from phenotype used in manual assertion
  • PMID:24684492
DOID:9952 acute lymphoblastic leukemia HGNC:7876 Homo sapiens (human) 4846 NOS3 inference by association of genotype from phenotype used in manual assertion
  • PMID:20510681
  • PMID:23922896

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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