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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 2126 - 2150 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:2671 transitional cell carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:18270948
DOID:8515 Cor pulmonale HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:20669672
DOID:9970 obesity HGNC:1473 Homo sapiens (human) 821 CANX
  • PMID:18567819
DOID:12930 dilated cardiomyopathy RGD:3889 Rattus norvegicus (Norway rat) 24842 Tp53
  • PMID:26004897
DOID:11204 allergic conjunctivitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:16023216
DOID:1073 renal hypertension RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • PMID:22188107
DOID:12554 hemolytic-uremic syndrome HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • PMID:30467800
DOID:2224 essential thrombocythemia HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:24434346
DOID:10376 amblyopia RGD:620925 Rattus norvegicus (Norway rat) 83516 Ppargc1a
  • PMID:20438809
DOID:5844 myocardial infarction HGNC:10661 Homo sapiens (human) 6385 SDC4
  • PMID:11372670
DOID:7148 rheumatoid arthritis HGNC:8638 Homo sapiens (human) 8850 KAT2B
  • PMID:36104638
DOID:14330 Parkinson's disease HGNC:8125 Homo sapiens (human) 4968 OGG1
  • PMID:15841414
DOID:0080199 colorectal carcinoma HGNC:4554 Homo sapiens (human) 2877 GPX2
  • PMID:30469315
DOID:10605 short bowel syndrome RGD:3001 Rattus norvegicus (Norway rat) 24536 Lepr
  • PMID:19730157
DOID:13636 Fanconi anemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:24021704
  • PMID:8438880
DOID:3458 breast adenocarcinoma HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:25050522
DOID:9563 bronchiectasis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:18221721
DOID:0081267 graft-versus-host disease HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:16393253
DOID:10286 prostate carcinoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:16372331
DOID:10534 stomach cancer HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:19050968
  • PMID:31725767
DOID:7148 rheumatoid arthritis HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:17326817
DOID:2797 idiopathic interstitial pneumonia HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:19218648
DOID:3571 liver cancer RGD:3269 Rattus norvegicus (Norway rat) 25737 Pcna
  • PMID:11797828
DOID:0050860 colorectal adenoma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:30469315
DOID:9352 type 2 diabetes mellitus HGNC:5209 Homo sapiens (human) 3291 HSD11B2
  • PMID:17519316

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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