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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 576 - 600 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:2841 asthma HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:26205779
DOID:841 extrinsic allergic alveolitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15653992
DOID:6432 pulmonary hypertension HGNC:435 Homo sapiens (human) 240 ALOX5
  • MGI:6194238
  • PMID:31462075
  • PMID:9445303
DOID:10763 hypertension RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
  • PMID:16415373
  • PMID:25715999
  • PMID:9590569
DOID:10283 prostate cancer HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
  • PMID:16984224
  • PMID:17700571
  • PMID:18336616
  • RGD:7240710
DOID:7148 rheumatoid arthritis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:12563673
  • PMID:22660635
  • PMID:25311255
DOID:684 hepatocellular carcinoma HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
  • PMID:15800977
  • PMID:24720952
  • PMID:24759835
DOID:9352 type 2 diabetes mellitus HGNC:6081 Homo sapiens (human) 3630 INS
  • MGI:6194238
  • PMID:1569197
  • PMID:3322910
DOID:4450 renal cell carcinoma HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • MGI:6194238
  • PMID:22000673
  • PMID:22296350
  • PMID:9631944
DOID:684 hepatocellular carcinoma HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:18573568
  • PMID:28452232
DOID:684 hepatocellular carcinoma RGD:3000 Rattus norvegicus (Norway rat) 25608 Lep
  • MGI:6194238
  • PMID:18573568
  • PMID:28452232
DOID:0050559 Fukuyama congenital muscular dystrophy HGNC:3622 Homo sapiens (human) 2218 FKTN
  • MGI:6194238
  • PMID:11445638
  • RGD:7240710
DOID:11054 urinary bladder cancer HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
  • PMID:18190825
  • PMID:9671402
DOID:9352 type 2 diabetes mellitus HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:12606537
  • PMID:18162502
  • PMID:18270681
  • PMID:23210442
  • PMID:23251491
DOID:14330 Parkinson's disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:21376232
  • PMID:21595954
DOID:9352 type 2 diabetes mellitus HGNC:6677 Homo sapiens (human) 4023 LPL
  • MGI:6194238
  • PMID:18321693
  • PMID:18985010
  • PMID:8641022
DOID:5082 liver cirrhosis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:19456900
  • PMID:26681055
  • PMID:29085215
DOID:12858 Huntington's disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:17018277
  • PMID:19133136
  • PMID:21211002
  • PMID:21595933
  • PMID:21757867
  • PMID:22589246
  • PMID:24383721
DOID:8947 diabetic retinopathy HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
  • PMID:18834676
  • PMID:18942221
DOID:9256 colorectal cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
  • PMID:28910954
  • PMID:29286614
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:6107 Homo sapiens (human) 3651 PDX1
  • MGI:6194238
  • PMID:10545531
  • PMID:15170499
  • PMID:15734849
  • RGD:7240710
DOID:850 lung disease HGNC:10798 Homo sapiens (human) 653509 SFTPA1
  • MGI:6194238
  • PMID:16429424
  • PMID:9230741
DOID:5419 schizophrenia HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
  • PMID:14745448
  • PMID:17825267
  • PMID:20214684
  • PMID:20921115
  • PMID:21049487
DOID:5844 myocardial infarction HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
  • PMID:12200370
  • PMID:16025836
  • PMID:8814351
DOID:14330 Parkinson's disease HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
  • PMID:18395980
  • PMID:19800394
  • PMID:21741444

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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