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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 9926 - 9950 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:2957 pulmonary tuberculosis HGNC:11847 Homo sapiens (human) 7096 TLR1
  • PMID:16493059
DOID:2377 multiple sclerosis HGNC:319 Homo sapiens (human) 176 ACAN
  • PMID:11764092
DOID:1307 dementia HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:16278861
DOID:824 periodontitis RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • PMID:24586097
DOID:3969 thyroid gland papillary carcinoma HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:20204550
DOID:3459 breast carcinoma HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:16608642
DOID:11506 suppurative otitis media HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:22883581
DOID:12236 primary biliary cholangitis HGNC:6554 Homo sapiens (human) 3953 LEPR
  • PMID:16093869
DOID:0050559 Fukuyama congenital muscular dystrophy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • PMID:11445638
DOID:2870 endometrial adenocarcinoma HGNC:9599 Homo sapiens (human) 9536 PTGES
  • PMID:11592775
DOID:9970 obesity HGNC:6107 Homo sapiens (human) 3651 PDX1
  • PMID:15979049
DOID:526 human immunodeficiency virus infectious disease HGNC:6554 Homo sapiens (human) 3953 LEPR
  • PMID:12100031
DOID:0050912 colon adenoma HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:25712946
DOID:14330 Parkinson's disease HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:10584677
DOID:13378 Kawasaki disease HGNC:10721 Homo sapiens (human) 6403 SELP
  • PMID:20079717
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:16066 Homo sapiens (human) 55331 ACER3
  • PMID:31949129
DOID:4914 esophagus adenocarcinoma HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:12055587
DOID:1712 aortic valve stenosis HGNC:8127 Homo sapiens (human) 8473 OGT
  • PMID:22128088
DOID:11650 bronchopulmonary dysplasia HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:20050784
DOID:11132 prostatic hypertrophy HGNC:936 Homo sapiens (human) 572 BAD
  • PMID:11781193
DOID:607 paraplegia RGD:2081 Rattus norvegicus (Norway rat) 24185 Akt1
  • PMID:18236467
DOID:2945 severe acute respiratory syndrome HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:14514395
  • PMID:15888207
DOID:10763 hypertension RGD:1308214 Rattus norvegicus (Norway rat) 304322 Chst12
  • PMID:25001272
DOID:10964 cholesteatoma of middle ear HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:8562031
DOID:1936 atherosclerosis RGD:3546 Rattus norvegicus (Norway rat) 25703 Rbp4
  • PMID:33889291

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Supported by JST NBDC Grant Number JPMJND2204

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


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