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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 3151 - 3175 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:12895 keratoconjunctivitis sicca HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:10487957
DOID:2977 primary hyperoxaluria HGNC:4570 Homo sapiens (human) 9380 GRHPR
  • PMID:10484776
DOID:14067 Plasmodium falciparum malaria HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:10471063
DOID:7148 rheumatoid arthritis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:10461474
DOID:10283 prostate cancer HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:10458410
  • PMID:16467092
DOID:0050700 cardiomyopathy HGNC:7150 Homo sapiens (human) 23417 MLYCD
  • PMID:10455107
DOID:9719 neovascular inflammatory vitreoretinopathy HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:10450379
DOID:1485 cystic fibrosis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:10449435
  • PMID:16879250
DOID:576 proteinuria HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:10430976
DOID:0110741 type 1 diabetes mellitus 2 MGI:1315197 Mus musculus (house mouse) 15277 Hk2
  • PMID:10428828
DOID:2377 multiple sclerosis HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:10417663
DOID:9719 neovascular inflammatory vitreoretinopathy HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:10413701
DOID:633 myositis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:10399751
DOID:1574 alcohol use disorder HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:10395222
  • PMID:32889058
DOID:2581 chondrodysplasia punctata HGNC:3133 Homo sapiens (human) 10682 EBP
  • PMID:10391218
DOID:1793 pancreatic cancer HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:10374842
  • PMID:11249065
DOID:1824 status epilepticus RGD:2137 Rattus norvegicus (Norway rat) 25239 Apod
  • PMID:10372566
DOID:2841 asthma HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:10369259
  • PMID:12911785
  • PMID:16364163
  • PMID:17394438
  • PMID:18204779
  • PMID:20128419
  • PMID:9642160
  • RGD:7240710
DOID:0070342 adult-onset type II citrullinemia HGNC:10983 Homo sapiens (human) 10165 SLC25A13
  • PMID:10369257
  • PMID:11153906
  • RGD:7240710
DOID:12365 malaria HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:10369255
  • RGD:7240710
DOID:3321 GM2 gangliosidosis HGNC:4367 Homo sapiens (human) 2760 GM2A
  • PMID:10364519
DOID:0050912 colon adenoma HGNC:1937 Homo sapiens (human) 1119 CHKA
  • PMID:10363580
DOID:0050570 congenital disorder of glycosylation type I SGD:S000006148 Saccharomyces cerevisiae S288C 855874 ALG5
  • PMID:10359825
DOID:0050570 congenital disorder of glycosylation type I SGD:S000005528 Saccharomyces cerevisiae S288C 854163 ALG6
  • PMID:10359825
  • PMID:10914684
  • PMID:10924277
DOID:11984 hypertrophic cardiomyopathy HGNC:2422 Homo sapiens (human) 1431 CS
  • PMID:10354207

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Supported by JST NBDC Grant Number JPMJND2204

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


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