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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 63551 - 63575 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:841 extrinsic allergic alveolitis HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:15929959
DOID:13141 uveitis HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • MGI:6194238
  • PMID:15746567
  • PMID:19440225
DOID:2316 brain ischemia HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • MGI:6194238
DOID:0050848 obstructive sleep apnea HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:19148690
DOID:0050157 cryptogenic organizing pneumonia HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:21144722
DOID:8893 psoriasis HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:15998370
DOID:0090018 autosomal dominant familial periodic fever HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • MGI:6194238
  • RGD:7240710
DOID:5199 ureteral obstruction HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • MGI:6194238
DOID:557 kidney disease HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:14613268
DOID:9352 type 2 diabetes mellitus HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • MGI:6194238
DOID:9074 systemic lupus erythematosus HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:8393677
DOID:13166 allergic bronchopulmonary aspergillosis HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:20646338
DOID:2355 anemia HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:14613268
DOID:2377 multiple sclerosis HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:22801493
  • RGD:7240710
DOID:6543 acne HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:20556591
DOID:4450 renal cell carcinoma HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:7912320
DOID:224 transient cerebral ischemia HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • MGI:6194238
DOID:326 ischemia HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • MGI:6194238
DOID:8778 Crohn's disease HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • MGI:6194238
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

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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