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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 5876 - 5900 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:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:27049718
  • PMID:28442395
DOID:0050431 arrhythmogenic right ventricular cardiomyopathy HGNC:9024 Homo sapiens (human) 5318 PKP2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15489853
  • PMID:16567567
DOID:93 language disorder HGNC:13875 Homo sapiens (human) 93986 FOXP2 inference by association of genotype from phenotype used in manual assertion
  • PMID:20649982
DOID:1793 pancreatic cancer HGNC:11998 Homo sapiens (human) 7157 TP53 inference by association of genotype from phenotype used in manual assertion
  • PMID:18772397
DOID:0090091 hypogonadotropic hypogonadism 23 with or without anosmia HGNC:6584 Homo sapiens (human) 3972 LHB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3347 osteosarcoma HGNC:16627 Homo sapiens (human) 11200 CHEK2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8924 autoimmune thrombocytopenic purpura HGNC:3616 Homo sapiens (human) 2212 FCGR2A inference by association of genotype from phenotype used in manual assertion
  • PMID:22123287
DOID:2377 multiple sclerosis HGNC:7158 Homo sapiens (human) 4321 MMP12 inference by association of genotype from phenotype used in manual assertion
  • PMID:19628284
DOID:12361 Graves' disease HGNC:11998 Homo sapiens (human) 7157 TP53 inference by association of genotype from phenotype used in manual assertion
  • PMID:17980001
DOID:0070025 X-linked dyskeratosis congenita HGNC:2890 Homo sapiens (human) 1736 DKC1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10211 cholelithiasis HGNC:12530 Homo sapiens (human) 54658 UGT1A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10498597
  • PMID:17593033
  • PMID:18081723
DOID:3908 lung non-small cell carcinoma HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A inference by association of genotype from phenotype used in manual assertion
  • PMID:20422457
DOID:0112193 tetraamelia syndrome 2 HGNC:28583 Homo sapiens (human) 340419 RSPO2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:13250 diarrhea HGNC:3018 Homo sapiens (human) 1811 SLC26A3 inference by association of genotype from phenotype used in manual assertion
  • PMID:8896562
DOID:3008 invasive ductal carcinoma HGNC:391 Homo sapiens (human) 207 AKT1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18392055
DOID:13809 familial combined hyperlipidemia HGNC:610 Homo sapiens (human) 345 APOC3 inference by association of genotype from phenotype used in manual assertion
  • PMID:9062353
DOID:1405 primary angle-closure glaucoma HGNC:1181 Homo sapiens (human) 745 MYRF inference by association of genotype from phenotype used in manual assertion
  • PMID:36129575
DOID:418 systemic scleroderma HGNC:1705 Homo sapiens (human) 942 CD86 inference by association of genotype from phenotype used in manual assertion
  • PMID:16790753
DOID:11335 sarcoidosis HGNC:10907 Homo sapiens (human) 6556 SLC11A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22160516
DOID:2349 arteriosclerosis HGNC:7173 Homo sapiens (human) 4314 MMP3 inference by association of genotype from phenotype used in manual assertion
  • PMID:15823277
DOID:0050426 Stevens-Johnson syndrome HGNC:4931 Homo sapiens (human) 3105 HLA-A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0090019 sitosterolemia 1 HGNC:13886 Homo sapiens (human) 64240 ABCG5 inference by association of genotype from phenotype used in manual assertion
  • PMID:11452359
DOID:14175 von Hippel-Lindau disease HGNC:7173 Homo sapiens (human) 4314 MMP3 inference by association of genotype from phenotype used in manual assertion
  • PMID:19551141
DOID:0080058 autosomal recessive spinocerebellar ataxia 14 HGNC:11276 Homo sapiens (human) 6712 SPTBN2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:7693 abdominal aortic aneurysm HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16879749
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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