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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 7801 - 7825 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:4398 pustulosis of palm and sole HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:11019918
  • PMID:12691703
DOID:12306 vitiligo HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:16911396
DOID:0081120 Graves ophthalmopathy HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15219383
  • PMID:16191343
  • PMID:8444271
DOID:0050848 obstructive sleep apnea HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:14633242
  • PMID:19022640
  • PMID:20846669
DOID:3492 mixed connective tissue disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:19684145
DOID:0050156 idiopathic pulmonary fibrosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:9408 acute myocardial infarction HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:526 human immunodeficiency virus infectious disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:1768380
DOID:2755 Mycobacterium avium complex disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:7640175
DOID:9402 epididymitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:0050700 cardiomyopathy HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:874 bacterial pneumonia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:10650487
  • PMID:7546648
DOID:3525 middle cerebral artery infarction HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:8515 Cor pulmonale HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:20669672
DOID:9120 amyloidosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:14613268
DOID:841 extrinsic allergic alveolitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15653992
DOID:2048 autoimmune hepatitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:9047083
DOID:5082 liver cirrhosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:19695831
DOID:8893 psoriasis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:16821276
  • PMID:9326391
DOID:0050452 mevalonic aciduria HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:7780142
DOID:1407 anterior uveitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15851552
DOID:0080162 lupus nephritis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:7750940
DOID:1679 cystitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:9008 psoriatic arthritis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:9326391
DOID:2355 anemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:14613268
  • PMID:2324681

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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: February 17, 2025