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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 1976 - 2000 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:9974 drug dependence HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:18828801
DOID:5844 myocardial infarction HGNC:6677 Homo sapiens (human) 4023 LPL
  • PMID:18823627
DOID:8986 narcolepsy HGNC:1938 Homo sapiens (human) 1120 CHKB
  • PMID:18820697
DOID:783 end stage renal disease HGNC:18129 Homo sapiens (human) 51738 GHRL
  • PMID:18809976
DOID:0080855 Parkinsonism RGD:620351 Rattus norvegicus (Norway rat) 50686 Gsk3a
  • PMID:18805403
DOID:13580 cholestasis RGD:2645 Rattus norvegicus (Norway rat) 24377 G6pd
  • PMID:18802767
DOID:9744 type 1 diabetes mellitus HGNC:10718 Homo sapiens (human) 6401 SELE
  • PMID:18791689
DOID:0060071 pre-malignant neoplasm HGNC:10803 Homo sapiens (human) 6441 SFTPD
  • PMID:18779194
DOID:6000 congestive heart failure HGNC:11009 Homo sapiens (human) 6517 SLC2A4
  • PMID:18778861
DOID:5844 myocardial infarction RGD:620330 Rattus norvegicus (Norway rat) 170587 Cs
  • PMID:1877670
DOID:1793 pancreatic cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:18772397
DOID:9352 type 2 diabetes mellitus HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • PMID:18771471
DOID:783 end stage renal disease HGNC:2622 Homo sapiens (human) 1558 CYP2C8
  • PMID:18769365
DOID:3904 bronchus carcinoma HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:18764914
DOID:83 cataract MGI:98266 Mus musculus (house mouse) 20322 Sord
  • PMID:18760274
DOID:2526 prostate adenocarcinoma HGNC:8976 Homo sapiens (human) 5291 PIK3CB
  • PMID:18755892
DOID:10608 celiac disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:18728522
DOID:1612 breast cancer HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:18719053
DOID:5517 stomach carcinoma HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:18716896
DOID:674 cleft palate HGNC:10659 Homo sapiens (human) 6383 SDC2
  • PMID:18716610
DOID:9296 cleft lip HGNC:10659 Homo sapiens (human) 6383 SDC2
  • PMID:18716610
DOID:11758 iron deficiency anemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:18716131
DOID:9452 steatotic liver disease HGNC:6081 Homo sapiens (human) 3630 INS
  • PMID:18713300
DOID:5844 myocardial infarction HGNC:587 Homo sapiens (human) 328 APEX1
  • PMID:18712175
DOID:1485 cystic fibrosis HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:18711055
  • PMID:20720307

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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