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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 3026 - 3050 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:5419 schizophrenia HGNC:6470 Homo sapiens (human) 3897 L1CAM
  • PMID:11425011
DOID:224 transient cerebral ischemia RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • PMID:11412877
  • PMID:24053818
DOID:0050771 pheochromocytoma HGNC:10681 Homo sapiens (human) 6390 SDHB
  • PMID:11404820
DOID:1686 glaucoma HGNC:9604 Homo sapiens (human) 5742 PTGS1
  • PMID:11391707
DOID:3908 lung non-small cell carcinoma HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:11389090
DOID:3459 breast carcinoma HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:11389090
DOID:409 liver disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:11389006
DOID:2352 hemochromatosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:11389006
  • PMID:16793930
DOID:10283 prostate cancer HGNC:9156 Homo sapiens (human) 5407 PNLIPRP1
  • PMID:11384102
DOID:9970 obesity HGNC:12518 Homo sapiens (human) 7351 UCP2
  • PMID:11381268
  • PMID:17870627
DOID:10763 hypertension HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • PMID:11378836
  • PMID:15659047
DOID:5844 myocardial infarction HGNC:10661 Homo sapiens (human) 6385 SDC4
  • PMID:11372670
DOID:9351 diabetes mellitus HGNC:4195 Homo sapiens (human) 2645 GCK
  • PMID:11372010
DOID:4450 renal cell carcinoma HGNC:8729 Homo sapiens (human) 5111 PCNA
  • PMID:11369057
DOID:77 gastrointestinal system disease HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:11361181
DOID:12894 Sjogren's syndrome HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:11359451
DOID:6543 acne HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:11349462
  • PMID:16489259
  • PMID:23174057
DOID:2349 arteriosclerosis HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:11326751
DOID:9352 type 2 diabetes mellitus HGNC:4923 Homo sapiens (human) 3099 HK2
  • PMID:11319725
DOID:5419 schizophrenia HGNC:6051 Homo sapiens (human) 3613 IMPA2
  • PMID:11317223
DOID:9743 diabetic neuropathy HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:11311965
DOID:8947 diabetic retinopathy HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:11311965
DOID:8634 prostate carcinoma in situ HGNC:587 Homo sapiens (human) 328 APEX1
  • PMID:11309329
DOID:9744 type 1 diabetes mellitus RGD:2870 Rattus norvegicus (Norway rat) 24483 Igf2
  • PMID:11307180
DOID:10783 methemoglobinemia HGNC:2873 Homo sapiens (human) 1727 CYB5R3
  • PMID:11295830

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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