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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 6826 - 6850 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:8577 ulcerative colitis HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:7679252
DOID:11664 nephrosclerosis HGNC:9592 Homo sapiens (human) 5730 PTGDS
  • PMID:11882588
DOID:9256 colorectal cancer HGNC:4922 Homo sapiens (human) 3098 HK1
  • MGI:6194238
DOID:0080600 COVID-19 HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:31986264
  • PMID:32345579
  • PMID:32365221
  • PMID:32427582
  • PMID:32696007
DOID:4194 glucose metabolism disease HGNC:4925 Homo sapiens (human) 3101 HK3
  • MGI:6194238
DOID:783 end stage renal disease HGNC:93 Homo sapiens (human) 38 ACAT1
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:6677 Homo sapiens (human) 4023 LPL
  • PMID:8641022
DOID:0081122 Catel Manzke syndrome HGNC:20324 Homo sapiens (human) 23483 TGDS
  • RGD:7240710
DOID:874 bacterial pneumonia HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:9351 diabetes mellitus HGNC:6081 Homo sapiens (human) 3630 INS
  • PMID:17855560
  • PMID:18451997
  • PMID:19537357
  • PMID:20034470
DOID:13603 obstructive jaundice HGNC:1628 Homo sapiens (human) 929 CD14
  • MGI:6194238
DOID:303 substance-related disorder HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
DOID:11650 bronchopulmonary dysplasia HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:22882323
DOID:10762 portal hypertension HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:2154 nephroblastoma HGNC:8729 Homo sapiens (human) 5111 PCNA
  • PMID:11869017
DOID:1574 alcohol use disorder HGNC:10852 Homo sapiens (human) 6472 SHMT2
  • MGI:6194238
DOID:418 systemic scleroderma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:32630589
DOID:0112152 CHIME syndrome HGNC:8966 Homo sapiens (human) 9487 PIGL
  • PMID:22444671
  • RGD:7240710
DOID:3492 mixed connective tissue disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:19684145
DOID:13252 mesenteric vascular occlusion HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
DOID:14213 hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:8406453
DOID:3371 chondrosarcoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:12598313
DOID:10159 osteonecrosis HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
DOID:9253 gastrointestinal stromal tumor HGNC:10681 Homo sapiens (human) 6390 SDHB
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:8896 Homo sapiens (human) 5230 PGK1
  • 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