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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 October 9, 2024
Displaying entries 69576 - 69600 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:10534 stomach cancer HGNC:3689 Homo sapiens (human) 2263 FGFR2
  • PMID:9816310
  • RGD:7240710
DOID:2377 multiple sclerosis HGNC:5438 Homo sapiens (human) 3458 IFNG
  • PMID:9818947
DOID:0060870 isolated growth hormone deficiency RGD:621397 Rattus norvegicus (Norway rat) 84022 Ghsr
  • PMID:9822798
DOID:11573 listeriosis RGD:2887 Rattus norvegicus (Norway rat) 25670 Il15
  • PMID:9826341
DOID:13406 pulmonary sarcoidosis HGNC:4540 Homo sapiens (human) 2833 CXCR3
  • PMID:9834133
DOID:13241 Behcet's disease HGNC:11920 Homo sapiens (human) 355 FAS
  • PMID:9836498
DOID:9744 type 1 diabetes mellitus RGD:3935 Rattus norvegicus (Norway rat) 24861 Ugt1a1
  • PMID:9841869
DOID:627 severe combined immunodeficiency HGNC:6024 Homo sapiens (human) 3575 IL7R
  • PMID:9843216
DOID:2986 IgA glomerulonephritis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:9844059
DOID:11713 diabetic angiopathy HGNC:8583 Homo sapiens (human) 5054 SERPINE1
  • PMID:9844142
DOID:13375 temporal arteritis HGNC:2434 Homo sapiens (human) 1437 CSF2
  • PMID:9844760
DOID:7147 ankylosing spondylitis HGNC:5472 Homo sapiens (human) 3486 IGFBP3
  • PMID:9851264
DOID:0050426 Stevens-Johnson syndrome HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:9852250
DOID:1687 neovascular glaucoma HGNC:12680 Homo sapiens (human) 7422 VEGFA
  • PMID:9852717
DOID:3049 Churg-Strauss syndrome HGNC:4232 Homo sapiens (human) 2668 GDNF
  • PMID:9853108
DOID:12842 Guillain-Barre syndrome HGNC:4232 Homo sapiens (human) 2668 GDNF
  • PMID:9853108
DOID:9810 polyarteritis nodosa HGNC:4243 Homo sapiens (human) 2674 GFRA1
  • PMID:9853108
DOID:9810 polyarteritis nodosa HGNC:4232 Homo sapiens (human) 2668 GDNF
  • PMID:9853108
DOID:12894 Sjogren's syndrome HGNC:4232 Homo sapiens (human) 2668 GDNF
  • PMID:9853108
DOID:3049 Churg-Strauss syndrome HGNC:4243 Homo sapiens (human) 2674 GFRA1
  • PMID:9853108
DOID:0080379 nephrotic syndrome type 2 HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:9853251
DOID:0060859 salmonellosis HGNC:5970 Homo sapiens (human) 3593 IL12B
  • PMID:9854038
DOID:9667 placental abruption HGNC:9451 Homo sapiens (human) 5624 PROC
  • PMID:9855597
DOID:1059 intellectual disability HGNC:4458 Homo sapiens (human) 2821 GPI
  • PMID:9856489
DOID:440 neuromuscular disease HGNC:4458 Homo sapiens (human) 2821 GPI
  • PMID:9856489

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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 9, 2024