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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 63851 - 63875 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:2986 IgA glomerulonephritis HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:16209246
  • PMID:9844059
DOID:14550 root resorption HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • MGI:6194238
DOID:7148 rheumatoid arthritis HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:25311255
DOID:1520 colon carcinoma HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:1655258
DOID:3083 chronic obstructive pulmonary disease HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:19643942
DOID:11394 adult respiratory distress syndrome HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:21283009
DOID:783 end stage renal disease HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:22266663
DOID:2921 glomerulonephritis HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:20525973
  • PMID:23400706
DOID:2394 ovarian cancer HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:19825522
DOID:13241 Behcet's disease HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:14600787
DOID:10652 Alzheimer's disease HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:20110607
  • PMID:21978728
DOID:0080745 polymyositis HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:11055823
DOID:635 acquired immunodeficiency syndrome HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:8548330
DOID:3393 coronary artery disease HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:19845893
DOID:0050860 colorectal adenoma HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:23082052
DOID:9120 amyloidosis HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:14613268
DOID:3525 middle cerebral artery infarction HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • MGI:6194238
DOID:11832 visual epilepsy HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • MGI:6194238
DOID:3355 fibrosarcoma HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:10753499
DOID:9970 obesity HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:12935365
DOID:1380 endometrial cancer HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:8920779
DOID:11446 sciatic neuropathy HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:20422457
  • PMID:20824709
DOID:3021 acute kidney failure HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:12500222
  • PMID:18074478
DOID:11168 anogenital venereal wart HGNC:11914 Homo sapiens (human) 8784 TNFRSF18
  • PMID:23754510

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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