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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 October 9, 2024
Displaying entries 66251 - 66275 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0050816 urofacial syndrome HGNC:20889 Homo sapiens (human) 9860 LRIG2
  • RGD:7240710
DOID:0070466 carpal tunnel syndrome 1 HGNC:12405 Homo sapiens (human) 7276 TTR
  • RGD:7240710
DOID:10159 osteonecrosis HGNC:40 Homo sapiens (human) 5243 ABCB1
  • PMID:28422712
DOID:3125 multiple endocrine neoplasia RGD:69062 Rattus norvegicus (Norway rat) 83571 Cdkn1b
  • PMID:12036912
  • PMID:17030811
DOID:2566 corneal dystrophy HGNC:6309 Homo sapiens (human) 11081 KERA
  • PMID:10802664
DOID:13166 allergic bronchopulmonary aspergillosis HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1
  • PMID:23278646
DOID:9261 nasopharynx carcinoma HGNC:1959 Homo sapiens (human) 1138 CHRNA5
  • PMID:25329654
DOID:5683 hereditary breast ovarian cancer syndrome HGNC:26144 Homo sapiens (human) 79728 PALB2
  • RGD:7240710
DOID:9074 systemic lupus erythematosus HGNC:6120 Homo sapiens (human) 3663 IRF5
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:8805 Homo sapiens (human) 5157 PDGFRL
  • RGD:7240710
DOID:0060668 anencephaly HGNC:29558 Homo sapiens (human) 81788 NUAK2
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:9642 Homo sapiens (human) 5770 PTPN1
  • PMID:21676396
DOID:11830 myopia HGNC:29222 Homo sapiens (human) 84146 ZNF644
  • RGD:7240710
DOID:2893 cervix carcinoma HGNC:3690 Homo sapiens (human) 2261 FGFR3
  • PMID:10471491
  • PMID:11114733
DOID:676 juvenile rheumatoid arthritis HGNC:4886 Homo sapiens (human) 3077 HFE
  • PMID:16047841
DOID:0111337 Jackson-Weiss syndrome HGNC:3689 Homo sapiens (human) 2263 FGFR2
  • PMID:7874170
  • RGD:7240710
DOID:0111243 acromicric dysplasia HGNC:3603 Homo sapiens (human) 2200 FBN1
  • RGD:7240710
DOID:4586 familial meningioma HGNC:9588 Homo sapiens (human) 5728 PTEN
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:5969 Homo sapiens (human) 3592 IL12A
  • PMID:20521253
  • PMID:26631030
  • PMID:27819525
DOID:13641 exfoliation syndrome HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:22831837
DOID:0110021 age related macular degeneration 9 HGNC:1318 Homo sapiens (human) 718 C3
  • RGD:7240710
DOID:0050592 asphyxiating thoracic dystrophy HGNC:2962 Homo sapiens (human) 79659 DYNC2H1
  • PMID:22499340
DOID:5419 schizophrenia HGNC:13221 Homo sapiens (human) 53335 BCL11A
  • PMID:25938782
DOID:576 proteinuria HGNC:15633 Homo sapiens (human) 54106 TLR9
  • PMID:22787315
DOID:9884 muscular dystrophy HGNC:1938 Homo sapiens (human) 1120 CHKB
  • PMID:21665002

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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: December 9, 2024