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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 69351 - 69375 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:6000 congestive heart failure HGNC:1953 Homo sapiens (human) 1132 CHRM4
  • MGI:6194238
DOID:0080736 Ehlers-Danlos syndrome musculocontractural type 1 HGNC:24464 Homo sapiens (human) 113189 CHST14
  • PMID:20004762
  • PMID:26373698
  • RGD:7240710
DOID:6432 pulmonary hypertension HGNC:13708 Homo sapiens (human) 11318 GPR182
  • MGI:6194238
DOID:0060370 Parkinson's disease 7 HGNC:16369 Homo sapiens (human) 11315 PARK7
  • MGI:6194238
  • RGD:7240710
DOID:8466 retinal degeneration HGNC:16369 Homo sapiens (human) 11315 PARK7
  • MGI:6194238
DOID:3526 cerebral infarction HGNC:16369 Homo sapiens (human) 11315 PARK7
  • PMID:18003894
DOID:14330 Parkinson's disease HGNC:16369 Homo sapiens (human) 11315 PARK7
  • MGI:6194238
  • PMID:12851414
  • PMID:23766857
DOID:0080855 Parkinsonism HGNC:16369 Homo sapiens (human) 11315 PARK7
  • MGI:6194238
  • PMID:16860563
DOID:0060894 early-onset Parkinson's disease HGNC:16369 Homo sapiens (human) 11315 PARK7
  • MGI:6194238
DOID:3525 middle cerebral artery infarction HGNC:16369 Homo sapiens (human) 11315 PARK7
  • PMID:17882163
DOID:2841 asthma HGNC:1952 Homo sapiens (human) 1131 CHRM3
  • PMID:20394512
DOID:3083 chronic obstructive pulmonary disease HGNC:1952 Homo sapiens (human) 1131 CHRM3
  • PMID:19281093
DOID:0060610 megacystis-microcolon-intestinal hypoperistalsis syndrome HGNC:1952 Homo sapiens (human) 1131 CHRM3
  • MGI:6194238
DOID:365 bladder disease HGNC:1952 Homo sapiens (human) 1131 CHRM3
  • PMID:17922784
DOID:0060889 prune belly syndrome HGNC:1952 Homo sapiens (human) 1131 CHRM3
  • RGD:7240710
DOID:0050685 small cell carcinoma HGNC:1952 Homo sapiens (human) 1131 CHRM3
  • PMID:20150622
DOID:3770 pulmonary fibrosis HGNC:1952 Homo sapiens (human) 1131 CHRM3
  • PMID:18480105
DOID:3571 liver cancer HGNC:10962 Homo sapiens (human) 11309 SLCO2B1
  • PMID:21625523
DOID:1793 pancreatic cancer HGNC:10962 Homo sapiens (human) 11309 SLCO2B1
  • PMID:21625523
DOID:0050817 Stargardt disease MGI:109424 Mus musculus (house mouse) 11304 Abca4
  • PMID:10412977
  • PMID:18515570
  • PMID:29145636
DOID:0110354 retinitis pigmentosa 19 MGI:109424 Mus musculus (house mouse) 11304 Abca4
  • MGI:6194238
  • PMID:18515570
DOID:0111013 cone-rod dystrophy 3 MGI:109424 Mus musculus (house mouse) 11304 Abca4
  • MGI:6194238
  • PMID:18515570
DOID:10584 retinitis pigmentosa MGI:109424 Mus musculus (house mouse) 11304 Abca4
  • MGI:6194238
DOID:8466 retinal degeneration MGI:109424 Mus musculus (house mouse) 11304 Abca4
  • MGI:6194238
DOID:8501 fundus dystrophy MGI:109424 Mus musculus (house mouse) 11304 Abca4
  • 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