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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 July 29, 2024
Displaying entries 7726 - 7750 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:11400 pyelonephritis HGNC:11847 Homo sapiens (human) 7096 TLR1
  • PMID:19543401
DOID:10320 asbestosis HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:20514434
DOID:13628 favism RGD:2645 Rattus norvegicus (Norway rat) 24377 G6pd
  • MGI:6194238
DOID:3393 coronary artery disease FB:FBgn0262473 Drosophila melanogaster (fruit fly) 43222 Tl
  • MGI:6194238
DOID:9119 acute myeloid leukemia SGD:S000000400 Saccharomyces cerevisiae S288C 852495 PGI1
  • MGI:6194238
DOID:0110853 rhizomelic chondrodysplasia punctata type 3 HGNC:327 Homo sapiens (human) 8540 AGPS
  • MGI:6194238
  • RGD:7240710
DOID:3672 rhabdoid cancer RGD:3130 Rattus norvegicus (Norway rat) 24577 Myc
  • MGI:6194238
DOID:783 end stage renal disease HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:20729266
DOID:1793 pancreatic cancer HGNC:5195 Homo sapiens (human) 9956 HS3ST2
  • PMID:12527896
DOID:0060704 lymphoproliferative syndrome HGNC:18788 Homo sapiens (human) 22914 KLRK1
  • PMID:22105417
DOID:8947 diabetic retinopathy SGD:S000003769 Saccharomyces cerevisiae S288C 853465 TDH2
  • MGI:6194238
DOID:3393 coronary artery disease SGD:S000003222 Saccharomyces cerevisiae S288C 852639 HXK2
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:21376232
  • PMID:21595954
DOID:8947 diabetic retinopathy HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:19237221
DOID:5327 retinal detachment HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:10763 hypertension MGI:104874 Mus musculus (house mouse) 11652 Akt2
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:10681 Homo sapiens (human) 6390 SDHB
  • MGI:6194238
DOID:1485 cystic fibrosis HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:18353734
DOID:10652 Alzheimer's disease RGD:2053 Rattus norvegicus (Norway rat) 25591 Parp1
  • MGI:6194238
DOID:9675 pulmonary emphysema RGD:620396 Rattus norvegicus (Norway rat) 83504 Kl
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus FB:FBgn0064237 Drosophila melanogaster (fruit fly) 37104 Idgf5
  • MGI:6194238
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:2605 Homo sapiens (human) 1593 CYP27A1
  • PMID:28774887
DOID:5419 schizophrenia HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • MGI:6194238
DOID:417 autoimmune disease RGD:2053 Rattus norvegicus (Norway rat) 25591 Parp1
  • MGI:6194238
DOID:224 transient cerebral ischemia WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238

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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: August 19, 2024