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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 5051 - 5075 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10754 otitis media HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:16750996
DOID:5082 liver cirrhosis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:20570631
  • PMID:26857650
DOID:13375 temporal arteritis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:12375325
DOID:14115 toxic shock syndrome HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:17202308
DOID:8566 herpes simplex HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:15498041
  • PMID:19480845
DOID:552 pneumonia HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:15249448
  • PMID:18988662
DOID:11394 adult respiratory distress syndrome HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:17133182
DOID:2799 bronchiolitis obliterans HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19104434
DOID:13378 Kawasaki disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:15144709
DOID:853 polymyalgia rheumatica HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:12375325
DOID:13450 coccidioidomycosis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19083122
DOID:2394 ovarian cancer HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:25038892
DOID:11650 bronchopulmonary dysplasia HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:22882323
DOID:2565 macular corneal dystrophy HGNC:6938 Homo sapiens (human) 4166 CHST6
  • RGD:7240710
DOID:0112222 developmental and epileptic encephalopathy 88 HGNC:6970 Homo sapiens (human) 4190 MDH1
  • RGD:7240710
DOID:0080433 developmental and epileptic encephalopathy 51 HGNC:6971 Homo sapiens (human) 4191 MDH2
  • MGI:6194238
  • RGD:7240710
DOID:6000 congestive heart failure HGNC:6971 Homo sapiens (human) 4191 MDH2
  • MGI:6194238
DOID:2316 brain ischemia HGNC:6971 Homo sapiens (human) 4191 MDH2
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:6971 Homo sapiens (human) 4191 MDH2
  • MGI:6194238
DOID:0070253 congenital disorder of glycosylation type IIa HGNC:7045 Homo sapiens (human) 4247 MGAT2
  • MGI:6194238
  • RGD:7240710
DOID:1793 pancreatic cancer HGNC:7047 Homo sapiens (human) 11320 MGAT4A
  • PMID:16434023
DOID:576 proteinuria HGNC:7049 Homo sapiens (human) 4249 MGAT5
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:7056 Homo sapiens (human) 10724 OGA
  • MGI:6194238
DOID:0112333 pontocerebellar hypoplasia type 16 HGNC:7102 Homo sapiens (human) 9562 MINPP1
  • RGD:7240710
DOID:3969 thyroid gland papillary carcinoma HGNC:7102 Homo sapiens (human) 9562 MINPP1
  • RGD:7240710

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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