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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 10001 - 10025 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:0050426 Stevens-Johnson syndrome HGNC:4932 Homo sapiens (human) 3106 HLA-B inference by association of genotype from phenotype used in manual assertion
  • PMID:19018717
  • PMID:23692434
DOID:13608 biliary atresia HGNC:11255 Homo sapiens (human) 6696 SPP1 direct assay evidence used in manual assertion
  • PMID:15845635
DOID:1749 squamous cell carcinoma HGNC:11364 Homo sapiens (human) 6774 STAT3 direct assay evidence used in manual assertion
  • PMID:16043897
DOID:3996 urinary system cancer HGNC:12780 Homo sapiens (human) 7472 WNT2 inference by association of genotype from phenotype used in manual assertion
  • PMID:8064891
DOID:2394 ovarian cancer HGNC:6770 Homo sapiens (human) 4089 SMAD4 inference by association of genotype from phenotype used in manual assertion
  • PMID:10451707
DOID:10123 pigmentation disease HGNC:10978 Homo sapiens (human) 123041 SLC24A4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080737 Ehlers-Danlos syndrome musculocontractural type 2 HGNC:21144 Homo sapiens (human) 29940 DSE inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050585 congenital generalized lipodystrophy HGNC:8754 Homo sapiens (human) 5130 PCYT1A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:6307 Homo sapiens (human) 3791 KDR direct assay evidence used in manual assertion
  • PMID:16698275
DOID:1324 lung cancer HGNC:6919 Homo sapiens (human) 8930 MBD4 inference by association of genotype from phenotype used in manual assertion
  • PMID:18495292
DOID:7148 rheumatoid arthritis HGNC:5981 Homo sapiens (human) 3605 IL17A mutant phenotype evidence used in manual assertion
  • PMID:20926833
DOID:0111902 thrombophilia due to activated protein C resistance HGNC:9451 Homo sapiens (human) 5624 PROC direct assay evidence used in manual assertion
  • PMID:25196808
DOID:10652 Alzheimer's disease HGNC:336 Homo sapiens (human) 185 AGTR1 mutant phenotype evidence used in manual assertion
  • PMID:21929736
DOID:11265 trachoma HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:11023480
  • PMID:15789056
  • PMID:17947295
DOID:0080517 Meier-Gorlin syndrome 6 HGNC:17493 Homo sapiens (human) 51053 GMNN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16331578
DOID:5844 myocardial infarction HGNC:7943 Homo sapiens (human) 4881 NPR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:14646971
DOID:418 systemic scleroderma HGNC:5438 Homo sapiens (human) 3458 IFNG direct assay evidence used in manual assertion
  • PMID:1418004
DOID:6543 acne HGNC:11848 Homo sapiens (human) 7097 TLR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:20861605
DOID:0110401 retinitis pigmentosa 74 HGNC:967 Homo sapiens (human) 583 BBS2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111938 immunodeficiency 24 HGNC:2519 Homo sapiens (human) 1503 CTPS1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:7474 malignant pleural mesothelioma HGNC:11119 Homo sapiens (human) 6608 SMO inference by association of genotype from phenotype used in manual assertion
  • PMID:33209614
DOID:14694 Johanson-Blizzard syndrome HGNC:16808 Homo sapiens (human) 197131 UBR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:19006206
  • PMID:21711208
  • RGD:7240710
DOID:0060161 Kennedy's disease HGNC:644 Homo sapiens (human) 367 AR mutant phenotype evidence used in manual assertion
  • PMID:26942099
DOID:2987 familial Mediterranean fever HGNC:5331 Homo sapiens (human) 64127 NOD2 inference by association of genotype from phenotype used in manual assertion
  • PMID:22244368
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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