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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 69376 - 69400 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1432 blindness SGD:S000005875 Saccharomyces cerevisiae S288C 854530 PUT4
  • MGI:6194238
DOID:0080855 Parkinsonism SGD:S000005920 Saccharomyces cerevisiae S288C 854575 ERR1
  • MGI:6194238
DOID:11832 visual epilepsy SGD:S000005920 Saccharomyces cerevisiae S288C 854575 ERR1
  • MGI:6194238
DOID:14115 toxic shock syndrome SGD:S000005920 Saccharomyces cerevisiae S288C 854575 ERR1
  • MGI:6194238
DOID:1712 aortic valve stenosis SGD:S000005920 Saccharomyces cerevisiae S288C 854575 ERR1
  • MGI:6194238
DOID:10763 hypertension SGD:S000005920 Saccharomyces cerevisiae S288C 854575 ERR1
  • MGI:6194238
DOID:10652 Alzheimer's disease SGD:S000005920 Saccharomyces cerevisiae S288C 854575 ERR1
  • MGI:6194238
DOID:1227 neutropenia HGNC:566 Homo sapiens (human) 8546 AP3B1
  • PMID:12125811
DOID:3082 interstitial lung disease HGNC:566 Homo sapiens (human) 8546 AP3B1
  • PMID:22009278
DOID:3770 pulmonary fibrosis HGNC:566 Homo sapiens (human) 8546 AP3B1
  • PMID:12125811
DOID:3753 Hermansky-Pudlak syndrome HGNC:566 Homo sapiens (human) 8546 AP3B1
  • PMID:12125811
DOID:0060540 Hermansky-Pudlak syndrome 2 HGNC:566 Homo sapiens (human) 8546 AP3B1
  • MGI:6194238
  • RGD:7240710
DOID:2223 platelet storage pool deficiency HGNC:566 Homo sapiens (human) 8546 AP3B1
  • MGI:6194238
DOID:0081430 intellectual developmental disorder with autistic features and language delay, with or without seizures HGNC:29364 Homo sapiens (human) 85461 TANC1
  • MGI:6194238
DOID:7693 abdominal aortic aneurysm SGD:S000001435 Saccharomyces cerevisiae S288C 854634 VTH1
  • MGI:6194238
DOID:10652 Alzheimer's disease SGD:S000001435 Saccharomyces cerevisiae S288C 854634 VTH1
  • MGI:6194238
DOID:9266 cystinuria SGD:S000001434 Saccharomyces cerevisiae S288C 854635 IMA3
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:30580 Homo sapiens (human) 85464 SSH2
  • MGI:6194238
DOID:0112349 hereditary spastic paraplegia 81 HGNC:29361 Homo sapiens (human) 85465 SELENOI
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus SGD:S000001417 Saccharomyces cerevisiae S288C 854651 GUT2
  • MGI:6194238
DOID:1324 lung cancer SGD:S000001411 Saccharomyces cerevisiae S288C 854657 MLP2
  • PMID:34793452
DOID:0060308 autosomal recessive intellectual developmental disorder SGD:S000001411 Saccharomyces cerevisiae S288C 854657 MLP2
  • MGI:6194238
DOID:14330 Parkinson's disease SGD:S000001357 Saccharomyces cerevisiae S288C 854713 PRK1
  • MGI:6194238
DOID:0070185 X-linked spermatogenic failure 2 SGD:S000001335 Saccharomyces cerevisiae S288C 854737 SPO22
  • MGI:6194238
DOID:0111474 combined oxidative phosphorylation deficiency 1 HGNC:13780 Homo sapiens (human) 85476 GFM1
  • RGD:7240710

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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