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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 8926 - 8950 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9256 colorectal cancer HGNC:4092 Homo sapiens (human) 2571 GAD1
  • PMID:26549033
DOID:0050745 diffuse large B-cell lymphoma HGNC:1643 Homo sapiens (human) 933 CD22
  • PMID:25708834
DOID:7148 rheumatoid arthritis HGNC:319 Homo sapiens (human) 176 ACAN
  • PMID:16507130
DOID:10283 prostate cancer HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:15239127
DOID:9810 polyarteritis nodosa HGNC:4243 Homo sapiens (human) 2674 GFRA1
  • PMID:9853108
DOID:0050650 familial atrial fibrillation HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • RGD:7240710
DOID:3910 lung adenocarcinoma HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:18245558
DOID:0111271 Oliver-McFarlane syndrome HGNC:16268 Homo sapiens (human) 10908 PNPLA6
  • RGD:7240710
DOID:0112219 developmental and epileptic encephalopathy 84 HGNC:12525 Homo sapiens (human) 7358 UGDH
  • RGD:7240710
DOID:5199 ureteral obstruction HGNC:2634 Homo sapiens (human) 1573 CYP2J2
  • MGI:6194238
DOID:11949 Creutzfeldt-Jakob disease HGNC:9449 Homo sapiens (human) 5621 PRNP
  • MGI:6194238
  • PMID:1684755
  • RGD:7240710
DOID:0050770 polycystic liver disease HGNC:4138 Homo sapiens (human) 23193 GANAB
  • PMID:27259053
  • PMID:31462075
DOID:13207 proliferative diabetic retinopathy HGNC:3357 Homo sapiens (human) 5168 ENPP2
  • PMID:22864860
DOID:824 periodontitis HGNC:9232 Homo sapiens (human) 5465 PPARA
  • MGI:6194238
DOID:8567 Hodgkin's lymphoma HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:7686390
DOID:10283 prostate cancer HGNC:429 Homo sapiens (human) 239 ALOX12
  • PMID:7624992
DOID:3042 allergic contact dermatitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:20711192
DOID:2921 glomerulonephritis HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:18574676
DOID:1459 hypothyroidism HGNC:2422 Homo sapiens (human) 1431 CS
  • MGI:6194238
DOID:9256 colorectal cancer HGNC:6470 Homo sapiens (human) 3897 L1CAM
  • PMID:17873897
DOID:4752 multiple system atrophy HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:20683839
DOID:0050868 hepatocellular adenoma HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
DOID:9976 heroin dependence HGNC:4092 Homo sapiens (human) 2571 GAD1
  • PMID:19500151
  • PMID:22564729
  • PMID:31866536
DOID:2129 atypical teratoid rhabdoid tumor HGNC:4451 Homo sapiens (human) 2719 GPC3
  • PMID:23530909
DOID:0080562 congenital disorder of glycosylation Ij HGNC:2995 Homo sapiens (human) 1798 DPAGT1
  • MGI:6194238
  • 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