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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 65151 - 65175 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:2738 pseudoxanthoma elasticum HGNC:15517 Homo sapiens (human) 64132 XYLT2
  • RGD:7240710
DOID:0081017 congenital fibrosis of the extraocular muscles 3A HGNC:20772 Homo sapiens (human) 10381 TUBB3
  • RGD:7240710
DOID:0110082 arrhythmogenic right ventricular dysplasia 11 HGNC:3036 Homo sapiens (human) 1824 DSC2
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:15138244
DOID:0110147 Bartter disease type 5 HGNC:16353 Homo sapiens (human) 10916 MAGED2
  • RGD:7240710
DOID:11336 rhinoscleroma HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1
  • PMID:17321882
DOID:0050591 tooth agenesis HGNC:17655 Homo sapiens (human) 64388 GREM2
  • RGD:7240710
DOID:13544 low tension glaucoma HGNC:7610 Homo sapiens (human) 4653 MYOC
  • PMID:16148883
DOID:0111479 combined oxidative phosphorylation deficiency 8 HGNC:21022 Homo sapiens (human) 57505 AARS2
  • RGD:7240710
DOID:0050585 congenital generalized lipodystrophy HGNC:8754 Homo sapiens (human) 5130 PCYT1A
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:29 Homo sapiens (human) 19 ABCA1
  • PMID:18003760
DOID:3181 oligodendroglioma HGNC:9884 Homo sapiens (human) 5925 RB1
  • PMID:15970925
DOID:4483 rhinitis HGNC:16711 Homo sapiens (human) 10333 TLR6
  • PMID:20815312
DOID:9256 colorectal cancer HGNC:6018 Homo sapiens (human) 3569 IL6
  • PMID:28349833
DOID:0080446 developmental and epileptic encephalopathy 66 HGNC:23794 Homo sapiens (human) 23241 PACS2
  • RGD:7240710
DOID:0060931 developmental dysplasia of the hip 1 HGNC:4220 Homo sapiens (human) 8200 GDF5
  • PMID:18947434
DOID:1485 cystic fibrosis HGNC:7876 Homo sapiens (human) 4846 NOS3
  • PMID:12406848
DOID:0110899 inflammatory bowel disease 28 HGNC:5964 Homo sapiens (human) 3587 IL10RA
  • RGD:7240710
DOID:0112142 retinitis pigmentosa 85 HGNC:348 Homo sapiens (human) 196 AHR
  • RGD:7240710
DOID:0080326 familial hypertrophic cardiomyopathy HGNC:7551 Homo sapiens (human) 4607 MYBPC3
  • PMID:12110947
  • PMID:16004897
  • PMID:9048664
  • PMID:9562578
DOID:10652 Alzheimer's disease HGNC:9205 Homo sapiens (human) 5445 PON2
  • PMID:11803456
  • PMID:16319130
DOID:3181 oligodendroglioma HGNC:7059 Homo sapiens (human) 4255 MGMT
  • PMID:15455350
DOID:9146 visceral leishmaniasis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:12438370
DOID:0080415 developmental and epileptic encephalopathy 23 HGNC:19190 Homo sapiens (human) 85440 DOCK7
  • RGD:7240710
DOID:3310 atopic dermatitis HGNC:15454 Homo sapiens (human) 8036 SHOC2
  • PMID:20882035

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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