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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 1351 - 1375 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:9352 type 2 diabetes mellitus HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:16444766
  • PMID:17727676
  • PMID:19659999
DOID:0080693 Noonan syndrome-like disorder with loose anagen hair 2 HGNC:9282 Homo sapiens (human) 5500 PPP1CB
  • RGD:7240710
DOID:0060222 Scheie syndrome HGNC:5391 Homo sapiens (human) 3425 IDUA
  • RGD:7240710
DOID:4195 hyperglycemia HGNC:2623 Homo sapiens (human) 1559 CYP2C9
  • PMID:17597710
DOID:2300 spondylolysis HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:26077908
DOID:3908 lung non-small cell carcinoma HGNC:10682 Homo sapiens (human) 6391 SDHC
  • PMID:25576295
DOID:4914 esophagus adenocarcinoma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:22715394
DOID:3393 coronary artery disease HGNC:9232 Homo sapiens (human) 5465 PPARA
  • PMID:16043164
DOID:2224 essential thrombocythemia HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:24496303
  • PMID:25860380
  • RGD:7240710
DOID:3748 esophagus squamous cell carcinoma HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:11860825
DOID:2799 bronchiolitis obliterans HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19104434
DOID:5844 myocardial infarction HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:15864121
  • PMID:18549840
DOID:10283 prostate cancer HGNC:8125 Homo sapiens (human) 4968 OGG1
  • PMID:19914098
  • PMID:24649009
DOID:2043 hepatitis B HGNC:12538 Homo sapiens (human) 54578 UGT1A6
  • PMID:29239247
DOID:0050560 Walker-Warburg syndrome HGNC:17997 Homo sapiens (human) 79147 FKRP
  • PMID:20236121
DOID:9111 cutaneous leishmaniasis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:16950634
DOID:8689 anorexia nervosa HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • RGD:7240710
DOID:2394 ovarian cancer HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • PMID:18497059
DOID:8893 psoriasis HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:12713578
DOID:1094 attention deficit hyperactivity disorder HGNC:17223 Homo sapiens (human) 10090 UST
  • PMID:35642741
DOID:10584 retinitis pigmentosa HGNC:23302 Homo sapiens (human) 80201 HKDC1
  • RGD:7240710
DOID:0080176 meningococcal meningitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:23691182
DOID:13378 Kawasaki disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:15144709
DOID:10283 prostate cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:18225585
DOID:9970 obesity HGNC:612 Homo sapiens (human) 347 APOD
  • PMID:7913935

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Supported by JST NBDC Grant Number JPMJND2204

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


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