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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 10226 - 10250 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:289 endometriosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:13141 uveitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:11586057
  • PMID:1318867
  • PMID:15209464
  • PMID:20673052
DOID:12549 hepatitis A HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:9047083
DOID:13241 Behcet's disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:12632436
  • PMID:12770792
  • PMID:14600787
  • PMID:15875188
  • PMID:20601837
  • PMID:21334264
DOID:684 hepatocellular carcinoma HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:26890368
DOID:5419 schizophrenia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15927374
DOID:4362 cervical cancer HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:19823053
DOID:1270 hereditary hemorrhagic telangiectasia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:16611101
DOID:12297 Vogt-Koyanagi-Harada disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:21334264
DOID:11168 anogenital venereal wart HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:23754510
DOID:4780 anti-basement membrane glomerulonephritis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:4450 renal cell carcinoma HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:19384924
  • PMID:19904265
DOID:13976 peptic esophagitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:13406 pulmonary sarcoidosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15653992
  • PMID:20070603
DOID:8677 perinatal necrotizing enterocolitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:19824106
DOID:0060319 cardiac arrest HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:614 lymphopenia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:2324681
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:25894568
DOID:10754 otitis media HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:3310 atopic dermatitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:22533231
DOID:11963 esophagitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:20811626
DOID:12783 migraine without aura HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:14718719
DOID:2355 anemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:14613268
  • PMID:2324681
DOID:0060224 atrial fibrillation HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:19169931

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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: August 19, 2024