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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 10501 - 10525 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:0070259 congenital disorder of glycosylation type IIg HGNC:6545 Homo sapiens (human) 9382 COG1
  • RGD:7240710
DOID:3070 high grade glioma HGNC:2172 Homo sapiens (human) 6900 CNTN2
  • PMID:11280781
DOID:850 lung disease HGNC:2172 Homo sapiens (human) 6900 CNTN2
  • PMID:24292748
DOID:0111691 familial adult myoclonic epilepsy 5 HGNC:2172 Homo sapiens (human) 6900 CNTN2
  • RGD:7240710
DOID:0080101 Compton-North congenital myopathy HGNC:2171 Homo sapiens (human) 1272 CNTN1
  • MGI:6194238
  • RGD:7240710
DOID:1312 focal segmental glomerulosclerosis HGNC:18290 Homo sapiens (human) 55907 CMAS
  • MGI:6194238
DOID:0110728 neuronal ceroid lipofuscinosis 5 HGNC:2076 Homo sapiens (human) 1203 CLN5
  • MGI:6194238
  • RGD:7240710
DOID:13564 aspergillosis HGNC:14558 Homo sapiens (human) 64581 CLEC7A
  • RGD:7240710
DOID:2058 chronic mucocutaneous candidiasis HGNC:14558 Homo sapiens (human) 64581 CLEC7A
  • RGD:7240710
DOID:13564 aspergillosis HGNC:24355 Homo sapiens (human) 51267 CLEC1A
  • RGD:7240710
DOID:2377 multiple sclerosis HGNC:29013 Homo sapiens (human) 23274 CLEC16A
  • PMID:21653641
DOID:9744 type 1 diabetes mellitus HGNC:29013 Homo sapiens (human) 23274 CLEC16A
  • PMID:18946483
  • PMID:19221398
DOID:13774 Addison's disease HGNC:29013 Homo sapiens (human) 23274 CLEC16A
  • PMID:18593762
DOID:7148 rheumatoid arthritis HGNC:29013 Homo sapiens (human) 23274 CLEC16A
  • PMID:19221398
DOID:1289 neurodegenerative disease HGNC:29013 Homo sapiens (human) 23274 CLEC16A
  • MGI:6194238
DOID:7998 hyperthyroidism SGD:S000006205 Saccharomyces cerevisiae S288C 856107 CIT3
  • MGI:6194238
DOID:3312 bipolar disorder SGD:S000006205 Saccharomyces cerevisiae S288C 856107 CIT3
  • MGI:6194238
DOID:12930 dilated cardiomyopathy SGD:S000006205 Saccharomyces cerevisiae S288C 856107 CIT3
  • MGI:6194238
DOID:5844 myocardial infarction SGD:S000006205 Saccharomyces cerevisiae S288C 856107 CIT3
  • MGI:6194238
DOID:8466 retinal degeneration SGD:S000006205 Saccharomyces cerevisiae S288C 856107 CIT3
  • MGI:6194238
DOID:6000 congestive heart failure SGD:S000006205 Saccharomyces cerevisiae S288C 856107 CIT3
  • MGI:6194238
DOID:1459 hypothyroidism SGD:S000006205 Saccharomyces cerevisiae S288C 856107 CIT3
  • MGI:6194238
DOID:11984 hypertrophic cardiomyopathy SGD:S000006205 Saccharomyces cerevisiae S288C 856107 CIT3
  • MGI:6194238
DOID:0050852 limb ischemia SGD:S000006205 Saccharomyces cerevisiae S288C 856107 CIT3
  • MGI:6194238
DOID:7998 hyperthyroidism SGD:S000000598 Saccharomyces cerevisiae S288C 850361 CIT2
  • 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: August 19, 2024