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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 9551 - 9575 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:0060074 ductal carcinoma in situ HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:15375487
DOID:1168 familial hyperlipidemia RGD:3560 Rattus norvegicus (Norway rat) 25106 Rgn
  • PMID:15375596
DOID:4440 seminoma HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • PMID:15389592
DOID:2870 endometrial adenocarcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:1540970
DOID:10763 hypertension HGNC:5208 Homo sapiens (human) 3290 HSD11B1
  • PMID:15452033
DOID:11832 visual epilepsy RGD:2554 Rattus norvegicus (Norway rat) 24334 Eno2
  • PMID:15464860
DOID:2513 basal cell carcinoma HGNC:8125 Homo sapiens (human) 4968 OGG1
  • PMID:15466987
  • PMID:22436579
DOID:3070 high grade glioma HGNC:2705 Homo sapiens (human) 1634 DCN
  • PMID:15475879
DOID:438 autoimmune disease of the nervous system HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:15486486
DOID:824 periodontitis HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:15491310
DOID:9970 obesity HGNC:384 Homo sapiens (human) 1645 AKR1C1
  • PMID:15494612
DOID:9970 obesity HGNC:385 Homo sapiens (human) 1646 AKR1C2
  • PMID:15494612
DOID:8566 herpes simplex HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:15498041
  • PMID:19480845
DOID:10652 Alzheimer's disease HGNC:24864 Homo sapiens (human) 26330 GAPDHS
  • PMID:15507493
DOID:1712 aortic valve stenosis HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • PMID:15520318
DOID:9744 type 1 diabetes mellitus HGNC:5467 Homo sapiens (human) 3482 IGF2R
  • PMID:15531531
DOID:9869 hereditary fructose intolerance syndrome HGNC:417 Homo sapiens (human) 229 ALDOB
  • PMID:15532022
  • PMID:8096362
  • RGD:7240710
DOID:1793 pancreatic cancer HGNC:7413 Homo sapiens (human) 4507 MTAP
  • PMID:15534104
DOID:0050685 small cell carcinoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:15541818
DOID:13544 low tension glaucoma HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15557444
DOID:1070 primary open angle glaucoma HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15557444
DOID:9352 type 2 diabetes mellitus HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:15563966
DOID:9352 type 2 diabetes mellitus HGNC:381 Homo sapiens (human) 231 AKR1B1
  • PMID:15569136
DOID:10591 pre-eclampsia HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • PMID:15569322
DOID:10892 hypospadias HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:15579657
  • PMID:21300689

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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