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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 63601 - 63625 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:4450 renal cell carcinoma HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:20566746
DOID:11394 adult respiratory distress syndrome HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:19916860
DOID:11832 visual epilepsy HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • MGI:6194238
DOID:3083 chronic obstructive pulmonary disease HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:21037022
DOID:8893 psoriasis HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • MGI:6194238
DOID:289 endometriosis HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:21481092
  • PMID:21741153
DOID:8778 Crohn's disease HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • MGI:6194238
DOID:635 acquired immunodeficiency syndrome HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:8548330
DOID:2986 IgA glomerulonephritis HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:16209246
  • PMID:9844059
DOID:841 extrinsic allergic alveolitis HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:15929959
DOID:0080162 lupus nephritis HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:22846145
DOID:1074 kidney failure HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:9650354
DOID:2394 ovarian cancer HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:19825522
DOID:0080745 polymyositis HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:11055823
DOID:399 tuberculosis HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:20007930
DOID:2921 glomerulonephritis HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:23400706
DOID:5844 myocardial infarction HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:20110607
  • PMID:21978728
DOID:783 end stage renal disease HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:22266663
DOID:10591 pre-eclampsia HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:21505354
DOID:3021 acute kidney failure HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:12500222
  • PMID:18074478
DOID:552 pneumonia HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:18664626
  • PMID:20811626
DOID:13406 pulmonary sarcoidosis HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:21508170
DOID:9074 systemic lupus erythematosus HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:11607787
  • PMID:8393677
DOID:0080855 Parkinsonism HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:21831964

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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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