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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 64101 - 64125 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10591 pre-eclampsia HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:15901845
DOID:12800 mucopolysaccharidosis VI HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:12849 autistic disorder HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:26418275
DOID:9970 obesity HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:28843383
DOID:13406 pulmonary sarcoidosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15653992
  • PMID:20070603
DOID:5844 myocardial infarction HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:9743 diabetic neuropathy HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:4692 endophthalmitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:1407 anterior uveitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15851552
DOID:3070 high grade glioma HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:11810046
DOID:0050685 small cell carcinoma HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:8624296
DOID:9744 type 1 diabetes mellitus HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:19120272
DOID:3310 atopic dermatitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:22533231
DOID:5082 liver cirrhosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:19695831
DOID:0060643 primary sclerosing cholangitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:9047083
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:25894568
DOID:8725 vascular dementia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:11273064
DOID:12449 aplastic anemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:12941546
DOID:0110429 dilated cardiomyopathy 1H HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:14676433
DOID:0050426 Stevens-Johnson syndrome HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:9852250
DOID:12306 vitiligo HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:16911396
DOID:614 lymphopenia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:2324681
DOID:1588 thrombocytopenia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:16987073
  • PMID:25128199
DOID:1875 impotence HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:13976 peptic esophagitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238

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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