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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 6126 - 6150 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▼ References
DOID:10534 stomach cancer HGNC:3438 Homo sapiens (human) 2074 ERCC6 inference by association of genotype from phenotype used in manual assertion
  • PMID:27340861
DOID:9952 acute lymphoblastic leukemia HGNC:8064 Homo sapiens (human) 8021 NUP214 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9409 diabetes insipidus HGNC:894 Homo sapiens (human) 551 AVP inference by association of genotype from phenotype used in manual assertion
  • PMID:8945633
DOID:0060297 complement component 4a deficiency HGNC:1323 Homo sapiens (human) 720 C4A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110844 xeroderma pigmentosum group C HGNC:12816 Homo sapiens (human) 7508 XPC inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110242 cataract 13 with adult i phenotype HGNC:4204 Homo sapiens (human) 2651 GCNT2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11054 urinary bladder cancer HGNC:6407 Homo sapiens (human) 3845 KRAS inference by association of genotype from phenotype used in manual assertion
  • PMID:1553789
  • RGD:7240710
DOID:7188 autoimmune thyroiditis HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12126634
  • PMID:20825955
DOID:0080137 multiple endocrine neoplasia type 4 HGNC:1785 Homo sapiens (human) 1027 CDKN1B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11054 urinary bladder cancer HGNC:11904 Homo sapiens (human) 8797 TNFRSF10A inference by association of genotype from phenotype used in manual assertion
  • PMID:16217763
DOID:1883 hepatitis C HGNC:6340 Homo sapiens (human) 3813 KIR3DS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15942906
  • PMID:31977279
DOID:0060688 arteriovenous malformations of the brain HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050908 myelodysplastic syndrome HGNC:1785 Homo sapiens (human) 1027 CDKN1B inference by association of genotype from phenotype used in manual assertion
  • PMID:9171997
DOID:0111580 Behr syndrome HGNC:8140 Homo sapiens (human) 4976 OPA1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3407 carotid artery disease HGNC:9236 Homo sapiens (human) 5468 PPARG inference by association of genotype from phenotype used in manual assertion
  • PMID:15284449
DOID:9256 colorectal cancer HGNC:4886 Homo sapiens (human) 3077 HFE inference by association of genotype from phenotype used in manual assertion
  • PMID:10383894
DOID:10223 dermatomyositis HGNC:11365 Homo sapiens (human) 6775 STAT4 inference by association of genotype from phenotype used in manual assertion
  • PMID:22402141
DOID:11165 common wart HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15257408
DOID:14330 Parkinson's disease HGNC:18618 Homo sapiens (human) 120892 LRRK2 inference by association of genotype from phenotype used in manual assertion
  • PMID:20669305
  • PMID:20721916
  • PMID:21159540
  • PMID:21167764
  • PMID:21954089
  • PMID:21989859
  • PMID:25639775
  • PMID:26223426
DOID:3307 teratoma HGNC:7850 Homo sapiens (human) 4831 NME2 inference by association of genotype from phenotype used in manual assertion
  • PMID:7518576
DOID:2986 IgA glomerulonephritis HGNC:8784 Homo sapiens (human) 8654 PDE5A inference by association of genotype from phenotype used in manual assertion
  • PMID:20563733
DOID:0110081 arrhythmogenic right ventricular dysplasia 10 HGNC:3049 Homo sapiens (human) 1829 DSG2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1727 retinal vein occlusion HGNC:9204 Homo sapiens (human) 5444 PON1 inference by association of genotype from phenotype used in manual assertion
  • PMID:23441121
DOID:14067 Plasmodium falciparum malaria HGNC:79 Homo sapiens (human) 28 ABO inference by association of genotype from phenotype used in manual assertion
  • PMID:18003641
DOID:0080291 developmental and epileptic encephalopathy 59 HGNC:4507 Homo sapiens (human) 9568 GABBR2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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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