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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 10601 - 10625 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:8778 Crohn's disease HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:7679252
DOID:10652 Alzheimer's disease HGNC:433 Homo sapiens (human) 246 ALOX15
  • PMID:15111312
DOID:0080208 metabolic dysfunction-associated steatotic liver disease RGD:3336 Rattus norvegicus (Norway rat) 24651 Pklr
  • PMID:26394137
DOID:0050912 colon adenoma HGNC:1937 Homo sapiens (human) 1119 CHKA
  • PMID:10363580
DOID:0050426 Stevens-Johnson syndrome HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:9852250
DOID:824 periodontitis RGD:631365 Rattus norvegicus (Norway rat) 297508 Nampt
  • PMID:26456152
DOID:9452 steatotic liver disease HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:19670414
DOID:4467 clear cell renal cell carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:28551630
DOID:526 human immunodeficiency virus infectious disease HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:22156911
DOID:5844 myocardial infarction HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:18480670
DOID:9352 type 2 diabetes mellitus HGNC:2705 Homo sapiens (human) 1634 DCN
  • PMID:18414424
DOID:9452 steatotic liver disease HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:16197789
DOID:9408 acute myocardial infarction RGD:2894 Rattus norvegicus (Norway rat) 25556 Il1rl1
  • PMID:24837094
DOID:5844 myocardial infarction RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • PMID:21362018
DOID:0050850 diabetic encephalopathy RGD:70982 Rattus norvegicus (Norway rat) 84027 Gsk3b
  • PMID:26970304
DOID:9471 meningitis HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:7521338
DOID:14330 Parkinson's disease HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:19474411
DOID:13241 Behcet's disease HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:21044750
DOID:898 autosomal dominant polycystic kidney disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:20555320
DOID:12858 Huntington's disease HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:18588971
DOID:0050848 obstructive sleep apnea HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:21698055
DOID:11656 cicatricial pemphigoid HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:7750940
DOID:12351 alcoholic hepatitis RGD:3369 Rattus norvegicus (Norway rat) 25747 Ppara
  • PMID:27939985
DOID:10223 dermatomyositis HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:19953283
DOID:1459 hypothyroidism RGD:3932 Rattus norvegicus (Norway rat) 54315 Ucp2
  • PMID:21190599

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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