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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 10076 - 10100 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:0050589 inflammatory bowel disease HGNC:3236 Homo sapiens (human) 1956 EGFR inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8398 osteoarthritis HGNC:190 Homo sapiens (human) 8038 ADAM12 inference by association of genotype from phenotype used in manual assertion
  • PMID:15334463
DOID:9256 colorectal cancer HGNC:11772 Homo sapiens (human) 7046 TGFBR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:24880985
DOID:0110639 congenital muscular dystrophy due to integrin alpha-7 deficiency HGNC:6143 Homo sapiens (human) 3679 ITGA7 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060903 thrombosis HGNC:12724 Homo sapiens (human) 7448 VTN direct assay evidence used in manual assertion
  • PMID:15069014
DOID:1588 thrombocytopenia HGNC:6922 Homo sapiens (human) 4153 MBL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:18361938
DOID:9976 heroin dependence HGNC:7978 Homo sapiens (human) 2908 NR3C1 inference by association of genotype from phenotype used in manual assertion
  • PMID:29465008
DOID:0080845 omodysplasia 2 HGNC:4040 Homo sapiens (human) 2535 FZD2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110727 neuronal ceroid lipofuscinosis 13 HGNC:2531 Homo sapiens (human) 8722 CTSF inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2841 asthma HGNC:1604 Homo sapiens (human) 1232 CCR3 inference by association of genotype from phenotype used in manual assertion
  • PMID:20220260
DOID:10534 stomach cancer HGNC:11726 Homo sapiens (human) 7011 TEP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:27305982
DOID:9119 acute myeloid leukemia HGNC:10830 Homo sapiens (human) 6455 SH3GL1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3068 glioblastoma HGNC:6973 Homo sapiens (human) 4193 MDM2 inference by association of genotype from phenotype used in manual assertion
  • PMID:23796897
DOID:0060482 oculoauricular syndrome HGNC:5017 Homo sapiens (human) 3166 HMX1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060058 lymphoma HGNC:8575 Homo sapiens (human) 5049 PAFAH1B2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11983068
DOID:0050941 spastic ataxia 2 HGNC:6317 Homo sapiens (human) 10749 KIF1C inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:83 cataract HGNC:8125 Homo sapiens (human) 4968 OGG1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22306120
DOID:0060987 preaxial polydactyly I HGNC:4317 Homo sapiens (human) 2735 GLI1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5517 stomach carcinoma HGNC:270 Homo sapiens (human) 142 PARP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18716896
DOID:1059 intellectual disability HGNC:24502 Homo sapiens (human) 284403 WDR62 inference by association of genotype from phenotype used in manual assertion
  • PMID:24479948
DOID:10016 multiple endocrine neoplasia type 2B HGNC:9967 Homo sapiens (human) 5979 RET inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111943 immunodeficiency 48 HGNC:12858 Homo sapiens (human) 7535 ZAP70 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:13922 eosinophilic esophagitis HGNC:11766 Homo sapiens (human) 7040 TGFB1 direct assay evidence used in manual assertion
  • PMID:24486052
DOID:1470 major depressive disorder HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:30734130
DOID:9351 diabetes mellitus HGNC:11850 Homo sapiens (human) 7099 TLR4 inference by association of genotype from phenotype used in manual assertion
  • PMID:15632890
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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