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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 2701 - 2725 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:10763 hypertension HGNC:6080 Homo sapiens (human) 3636 INPPL1
  • PMID:15220217
DOID:9970 obesity HGNC:6080 Homo sapiens (human) 3636 INPPL1
  • PMID:15220217
DOID:12361 Graves' disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15219383
  • PMID:17348243
  • PMID:19732761
DOID:0081120 Graves ophthalmopathy HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15219383
  • PMID:16191343
  • PMID:8444271
DOID:2256 osteochondrodysplasia HGNC:1971 Homo sapiens (human) 9469 CHST3
  • PMID:15215498
DOID:1485 cystic fibrosis SGD:S000001247 Saccharomyces cerevisiae S288C 856611 MNL1
  • PMID:15215312
DOID:3459 breast carcinoma HGNC:11284 Homo sapiens (human) 6715 SRD5A1
  • PMID:15212687
DOID:3459 breast carcinoma HGNC:11285 Homo sapiens (human) 6716 SRD5A2
  • PMID:15212687
DOID:3748 esophagus squamous cell carcinoma HGNC:6919 Homo sapiens (human) 8930 MBD4
  • PMID:15205355
  • PMID:25162968
DOID:824 periodontitis HGNC:3774 Homo sapiens (human) 2331 FMOD
  • PMID:15196146
DOID:3087 gingivitis HGNC:3774 Homo sapiens (human) 2331 FMOD
  • PMID:15196146
DOID:2841 asthma HGNC:17432 Homo sapiens (human) 27159 CHIA
  • PMID:15192232
  • PMID:16179638
  • PMID:20226308
DOID:1612 breast cancer HGNC:2637 Homo sapiens (human) 1576 CYP3A4
  • PMID:15180491
DOID:3393 coronary artery disease HGNC:4195 Homo sapiens (human) 2645 GCK
  • PMID:15173029
DOID:83 cataract HGNC:4204 Homo sapiens (human) 2651 GCNT2
  • PMID:15161861
DOID:0081120 Graves ophthalmopathy HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:15158621
  • PMID:20394549
DOID:0050570 congenital disorder of glycosylation type I SGD:S000005163 Saccharomyces cerevisiae S288C 855502 ALG9
  • PMID:15148656
  • PMID:15945070
DOID:13378 Kawasaki disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:15144709
DOID:3649 pyruvate decarboxylase deficiency HGNC:8808 Homo sapiens (human) 5162 PDHB
  • PMID:15138885
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:15138244
DOID:11132 prostatic hypertrophy HGNC:11284 Homo sapiens (human) 6715 SRD5A1
  • PMID:15136785
DOID:5844 myocardial infarction HGNC:6562 Homo sapiens (human) 3957 LGALS2
  • PMID:15129282
  • RGD:7240710
DOID:0050697 chorioamnionitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15128916
DOID:10652 Alzheimer's disease HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:15126281
DOID:9008 psoriatic arthritis HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:15124938

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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