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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 5776 - 5800 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▼ References
DOID:1935 Bardet-Biedl syndrome HGNC:28396 Homo sapiens (human) 91147 TMEM67 inference by association of genotype from phenotype used in manual assertion
  • PMID:18327255
DOID:1909 melanoma HGNC:1071 Homo sapiens (human) 652 BMP4 inference by association of genotype from phenotype used in manual assertion
  • PMID:19557432
DOID:8947 diabetic retinopathy HGNC:6137 Homo sapiens (human) 3673 ITGA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:12540964
  • PMID:23776381
DOID:2962 Cockayne syndrome HGNC:3438 Homo sapiens (human) 2074 ERCC6 inference by association of genotype from phenotype used in manual assertion
  • PMID:18446857
  • PMID:23599700
  • PMID:25463447
DOID:0060875 isolated growth hormone deficiency type III HGNC:1133 Homo sapiens (human) 695 BTK inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:13406 pulmonary sarcoidosis HGNC:11766 Homo sapiens (human) 7040 TGFB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17785866
DOID:0080505 Cornelia de Lange syndrome 1 HGNC:28862 Homo sapiens (human) 25836 NIPBL inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12662 paracoccidioidomycosis HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17325942
DOID:1324 lung cancer HGNC:3438 Homo sapiens (human) 2074 ERCC6 inference by association of genotype from phenotype used in manual assertion
  • PMID:17854076
  • PMID:17855454
  • RGD:7240710
DOID:12306 vitiligo HGNC:11180 Homo sapiens (human) 6648 SOD2 inference by association of genotype from phenotype used in manual assertion
  • PMID:24036105
DOID:1790 malignant mesothelioma HGNC:7646 Homo sapiens (human) 10 NAT2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15993904
DOID:10763 hypertension HGNC:1402 Homo sapiens (human) 783 CACNB2 inference by association of genotype from phenotype used in manual assertion
  • PMID:24338417
DOID:3748 esophagus squamous cell carcinoma HGNC:1101 Homo sapiens (human) 675 BRCA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21279724
DOID:1059 intellectual disability HGNC:6050 Homo sapiens (human) 3612 IMPA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:26416544
DOID:0060573 von Willebrand's disease 1 HGNC:12726 Homo sapiens (human) 7450 VWF inference by association of genotype from phenotype used in manual assertion
  • PMID:8839833
  • RGD:7240710
DOID:417 autoimmune disease HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21744463
DOID:9743 diabetic neuropathy HGNC:12518 Homo sapiens (human) 7351 UCP2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16373902
DOID:11836 clubfoot HGNC:3755 Homo sapiens (human) 2317 FLNB inference by association of genotype from phenotype used in manual assertion
  • PMID:27395407
DOID:1574 alcohol use disorder HGNC:5287 Homo sapiens (human) 3351 HTR1B inference by association of genotype from phenotype used in manual assertion
  • PMID:28923721
  • PMID:30774345
DOID:0050650 familial atrial fibrillation HGNC:7939 Homo sapiens (human) 4878 NPPA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110015 age related macular degeneration 2 HGNC:34 Homo sapiens (human) 24 ABCA4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060558 lethal congenital contracture syndrome HGNC:8011 Homo sapiens (human) 8506 CNTNAP1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111437 optic atrophy 7 HGNC:25382 Homo sapiens (human) 84233 TMEM126A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9975 cocaine dependence HGNC:8846 Homo sapiens (human) 8864 PER2 inference by association of genotype from phenotype used in manual assertion
  • PMID:22832851
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
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International Collaboration

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