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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 11776 - 11800 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:10762 portal hypertension RGD:3329 Rattus norvegicus (Norway rat) 25513 Pik3r1
  • PMID:11826414
DOID:11394 adult respiratory distress syndrome HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:21317313
DOID:418 systemic scleroderma HGNC:5993 Homo sapiens (human) 3554 IL1R1
  • PMID:1375465
DOID:5844 myocardial infarction RGD:619719 Rattus norvegicus (Norway rat) 81829 Mdh2
  • PMID:9753871
DOID:12858 Huntington's disease HGNC:4341 Homo sapiens (human) 2752 GLUL
  • PMID:3159462
  • PMID:6237280
DOID:3525 middle cerebral artery infarction RGD:620103 Rattus norvegicus (Norway rat) 64639 Bad
  • PMID:21891976
  • PMID:22200499
DOID:1459 hypothyroidism RGD:620330 Rattus norvegicus (Norway rat) 170587 Cs
  • PMID:15817832
  • PMID:29748131
DOID:9206 Barrett's esophagus HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:18664505
DOID:9120 amyloidosis HGNC:4432 Homo sapiens (human) 2805 GOT1
  • PMID:28390893
DOID:9351 diabetes mellitus HGNC:4057 Homo sapiens (human) 2539 G6PD
  • PMID:24865682
DOID:332 amyotrophic lateral sclerosis HGNC:4432 Homo sapiens (human) 2805 GOT1
  • PMID:26113413
DOID:3042 allergic contact dermatitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:20711192
DOID:0110861 autosomal recessive polycystic kidney disease RGD:2081 Rattus norvegicus (Norway rat) 24185 Akt1
  • PMID:24498161
DOID:0060060 non-Hodgkin lymphoma HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:25016003
DOID:2841 asthma HGNC:3570 Homo sapiens (human) 2181 ACSL3
  • PMID:19221603
DOID:1324 lung cancer HGNC:5195 Homo sapiens (human) 9956 HS3ST2
  • PMID:12527896
DOID:2378 relapsing-remitting multiple sclerosis HGNC:2466 Homo sapiens (human) 1464 CSPG4
  • PMID:10976643
DOID:6432 pulmonary hypertension HGNC:2634 Homo sapiens (human) 1573 CYP2J2
  • PMID:20118222
DOID:1407 anterior uveitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:17389503
DOID:5041 esophageal cancer HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:33292587
DOID:7998 hyperthyroidism RGD:620330 Rattus norvegicus (Norway rat) 170587 Cs
  • PMID:15817832
DOID:10283 prostate cancer HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:18387661
DOID:9538 multiple myeloma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:23699600
DOID:3457 invasive lobular carcinoma HGNC:1681 Homo sapiens (human) 960 CD44
  • PMID:11245336
DOID:1907 malignant fibrous histiocytoma HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • PMID:23166610

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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