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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 68851 - 68875 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:8505 dermatitis herpetiformis HGNC:12680 Homo sapiens (human) 7422 VEGFA
  • PMID:7738351
DOID:10772 thrombotic thrombocytopenic purpura HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:7740478
DOID:2373 hereditary elliptocytosis HGNC:11027 Homo sapiens (human) 6521 SLC4A1
  • PMID:7742553
DOID:934 viral infectious disease MGI:88373 Mus musculus (house mouse) 12608 Cebpb
  • PMID:7744000
DOID:627 severe combined immunodeficiency HGNC:9986 Homo sapiens (human) 5993 RFX5
  • PMID:7744245
  • PMID:9401005
DOID:8893 psoriasis HGNC:11180 Homo sapiens (human) 6648 SOD2
  • PMID:7744320
DOID:6196 reactive arthritis HGNC:43 Homo sapiens (human) 6890 TAP1
  • PMID:7748224
DOID:0080162 lupus nephritis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:7750940
DOID:11656 cicatricial pemphigoid HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:7750940
DOID:3627 aortic aneurysm HGNC:3603 Homo sapiens (human) 2200 FBN1
  • PMID:7762551
DOID:5204 fructose-1,6-bisphosphatase deficiency HGNC:3606 Homo sapiens (human) 2203 FBP1
  • PMID:7763253
  • RGD:7240710
DOID:3454 brain infarction RGD:2870 Rattus norvegicus (Norway rat) 24483 Igf2
  • PMID:7770004
DOID:10283 prostate cancer HGNC:7534 Homo sapiens (human) 4601 MXI1
  • PMID:7773287
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:4192 Homo sapiens (human) 2642 GCGR
  • PMID:7773293
DOID:5517 stomach carcinoma HGNC:6407 Homo sapiens (human) 3845 KRAS
  • PMID:7773929
DOID:13641 exfoliation syndrome HGNC:3327 Homo sapiens (human) 2006 ELN
  • PMID:7777294
DOID:0050452 mevalonic aciduria HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:7780142
DOID:1793 pancreatic cancer HGNC:5991 Homo sapiens (human) 3552 IL1A
  • PMID:7787209
DOID:3525 middle cerebral artery infarction HGNC:6000 Homo sapiens (human) 3557 IL1RN
  • PMID:7790404
DOID:4989 pancreatitis RGD:2201 Rattus norvegicus (Norway rat) 25245 Bdkrb2
  • PMID:7791078
DOID:4948 gallbladder carcinoma HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:7795450
DOID:10487 Hirschsprung's disease HGNC:7809 Homo sapiens (human) 4804 NGFR
  • PMID:7807351
DOID:2316 brain ischemia RGD:2708 Rattus norvegicus (Norway rat) 24399 Glud1
  • PMID:7808037
DOID:14115 toxic shock syndrome RGD:3825 Rattus norvegicus (Norway rat) 24816 Tbxa2r
  • PMID:7816742
DOID:0050328 congenital hypothyroidism RGD:2913 Rattus norvegicus (Norway rat) 25196 Inhbb
  • PMID:7819453

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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