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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 1951 - 1975 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
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
DOID:1073 renal hypertension HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:3827 congenital diaphragmatic hernia HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:633 myositis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:10399751
DOID:3770 pulmonary fibrosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:12030733
DOID:0050700 cardiomyopathy HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:12449 aplastic anemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:12941546
DOID:11832 visual epilepsy HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:23333565
DOID:13452 scleritis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:23177360
DOID:9884 muscular dystrophy HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:10235436
DOID:2841 asthma HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:12530118
  • PMID:16728705
  • PMID:18711258
  • PMID:18763028
  • PMID:18811622
  • PMID:19196817
  • PMID:20465535
  • RGD:7240710
DOID:850 lung disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:9462189
DOID:10283 prostate cancer HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:19851870
DOID:8515 Cor pulmonale HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:20669672
DOID:13636 Fanconi anemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:24021704
  • PMID:8438880

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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: August 19, 2024