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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 101 - 125 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:0050855 renal fibrosis RGD:3870 Rattus norvegicus (Norway rat) 29260 Tlr4
  • PMID:22777483
DOID:1936 atherosclerosis HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:12451000
DOID:0081292 traumatic brain injury RGD:3889 Rattus norvegicus (Norway rat) 24842 Tp53
  • PMID:27553877
DOID:224 transient cerebral ischemia RGD:2645 Rattus norvegicus (Norway rat) 24377 G6pd
  • PMID:22580330
DOID:0080821 exercise-induced bronchoconstriction HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:10984370
DOID:3070 high grade glioma RGD:2802 Rattus norvegicus (Norway rat) 25459 Hmgb1
  • PMID:10830965
DOID:0080599 Coronavirus infectious disease HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:20864747
DOID:162 cancer SGD:S000001085 Saccharomyces cerevisiae S288C 856439 DOG2
  • PMID:31481524
DOID:11151 cholecystolithiasis HGNC:12530 Homo sapiens (human) 54658 UGT1A1
  • PMID:18392554
DOID:9351 diabetes mellitus HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • PMID:15292329
DOID:2247 spondylosis HGNC:6344 Homo sapiens (human) 9365 KL
  • PMID:12110410
DOID:10534 stomach cancer HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:19035188
DOID:0081419 childhood-onset dystonia with optic atrophy and basal ganglia abnormalities HGNC:19691 Homo sapiens (human) 51102 MECR
  • RGD:7240710
DOID:5082 liver cirrhosis HGNC:8931 Homo sapiens (human) 5261 PHKG2
  • PMID:9384616
DOID:676 juvenile rheumatoid arthritis HGNC:26789 Homo sapiens (human) 144811 LACC1
  • RGD:7240710
DOID:2394 ovarian cancer HGNC:8143 Homo sapiens (human) 4978 OPCML
  • RGD:7240710
DOID:2841 asthma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:19383228
  • PMID:19484664
DOID:0110429 dilated cardiomyopathy 1H HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • PMID:12031704
DOID:0080000 muscular disease HGNC:2330 Homo sapiens (human) 1376 CPT2
  • PMID:10873395
DOID:0080844 omodysplasia 1 HGNC:4454 Homo sapiens (human) 10082 GPC6
  • RGD:7240710
DOID:3321 GM2 gangliosidosis HGNC:4367 Homo sapiens (human) 2760 GM2A
  • PMID:10364519
DOID:0080630 B-lymphoblastic leukemia/lymphoma HGNC:2638 Homo sapiens (human) 1577 CYP3A5
  • PMID:21225912
DOID:0111232 congenital muscular dystrophy-dystroglycanopathy type A9 HGNC:2666 Homo sapiens (human) 1605 DAG1
  • RGD:7240710
DOID:2377 multiple sclerosis HGNC:29013 Homo sapiens (human) 23274 CLEC16A
  • PMID:21653641
DOID:0090141 cortisone reductase deficiency 1 HGNC:4795 Homo sapiens (human) 9563 H6PD
  • 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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Last updated: August 19, 2024