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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 2926 - 2950 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:11832 visual epilepsy HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • MGI:6194238
DOID:10825 essential hypertension HGNC:2638 Homo sapiens (human) 1577 CYP3A5
  • RGD:7240710
DOID:0080550 Noonan syndrome with multiple lentigines 3 HGNC:1097 Homo sapiens (human) 673 BRAF
  • RGD:7240710
DOID:3454 brain infarction HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • MGI:6194238
DOID:0111626 D-glyceric aciduria HGNC:24247 Homo sapiens (human) 132158 GLYCTK
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:20727007
  • PMID:22213409
DOID:9352 type 2 diabetes mellitus HGNC:10720 Homo sapiens (human) 6402 SELL
  • PMID:22119815
DOID:1064 cystinosis HGNC:2518 Homo sapiens (human) 1497 CTNS
  • MGI:6194238
  • PMID:10068513
  • PMID:11565547
  • PMID:18578013
  • PMID:9537412
  • PMID:9792862
  • RGD:7240710
DOID:0110914 infantile hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL
  • MGI:6194238
  • RGD:7240710
DOID:0060060 non-Hodgkin lymphoma HGNC:5467 Homo sapiens (human) 3482 IGF2R
  • PMID:29940770
DOID:5844 myocardial infarction HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • MGI:6194238
DOID:1307 dementia HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:22213409
DOID:74 hematopoietic system disease HGNC:12530 Homo sapiens (human) 54658 UGT1A1
  • PMID:23827973
DOID:7941 Barrett's adenocarcinoma HGNC:4559 Homo sapiens (human) 2882 GPX7
  • PMID:18664505
DOID:1749 squamous cell carcinoma HGNC:6710 Homo sapiens (human) 4048 LTA4H
  • MGI:6194238
DOID:1184 nephrotic syndrome HGNC:10817 Homo sapiens (human) 8879 SGPL1
  • MGI:6194238
DOID:0060903 thrombosis HGNC:11609 Homo sapiens (human) 6916 TBXAS1
  • MGI:6194238
DOID:2297 leptospirosis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19330263
DOID:14330 Parkinson's disease HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:17362997
  • PMID:21767974
DOID:1793 pancreatic cancer HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:12499913
DOID:0080433 developmental and epileptic encephalopathy 51 HGNC:6971 Homo sapiens (human) 4191 MDH2
  • MGI:6194238
  • RGD:7240710
DOID:0112263 hypoinsulinemic hypoglycemia with hemihypertrophy HGNC:392 Homo sapiens (human) 208 AKT2
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
DOID:0070341 neonatal-onset type II citrullinemia HGNC:10983 Homo sapiens (human) 10165 SLC25A13
  • RGD:7240710

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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