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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 64726 - 64750 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0080634 nanophthalmos HGNC:1181 Homo sapiens (human) 745 MYRF
  • PMID:31048900
DOID:5614 eye disease HGNC:1181 Homo sapiens (human) 745 MYRF
  • MGI:6194238
DOID:9834 hyperopia HGNC:1181 Homo sapiens (human) 745 MYRF
  • PMID:36129575
DOID:1312 focal segmental glomerulosclerosis HGNC:12726 Homo sapiens (human) 7450 VWF
  • PMID:22295953
DOID:2217 Bernard-Soulier syndrome HGNC:12726 Homo sapiens (human) 7450 VWF
  • PMID:14717981
DOID:783 end stage renal disease HGNC:12726 Homo sapiens (human) 7450 VWF
  • PMID:21378155
  • PMID:22091998
  • PMID:22189209
DOID:0060573 von Willebrand's disease 1 HGNC:12726 Homo sapiens (human) 7450 VWF
  • PMID:15226188
  • PMID:8839833
  • RGD:7240710
DOID:0060224 atrial fibrillation HGNC:12726 Homo sapiens (human) 7450 VWF
  • PMID:21497043
DOID:10159 osteonecrosis HGNC:12726 Homo sapiens (human) 7450 VWF
  • PMID:16547717
DOID:0060574 von Willebrand's disease 2 HGNC:12726 Homo sapiens (human) 7450 VWF
  • MGI:6194238
  • PMID:10959688
  • PMID:16409463
  • PMID:20589313
  • PMID:26019279
  • PMID:8839848
  • RGD:7240710
DOID:5419 schizophrenia HGNC:12726 Homo sapiens (human) 7450 VWF
  • PMID:19839997
DOID:4450 renal cell carcinoma HGNC:12726 Homo sapiens (human) 7450 VWF
  • PMID:21953673
DOID:6432 pulmonary hypertension HGNC:12726 Homo sapiens (human) 7450 VWF
  • PMID:14507115
DOID:3407 carotid artery disease HGNC:12726 Homo sapiens (human) 7450 VWF
  • PMID:20439183
DOID:224 transient cerebral ischemia HGNC:12726 Homo sapiens (human) 7450 VWF
  • MGI:6194238
DOID:8947 diabetic retinopathy HGNC:12726 Homo sapiens (human) 7450 VWF
  • PMID:10077454
DOID:5844 myocardial infarction HGNC:12726 Homo sapiens (human) 7450 VWF
  • MGI:6194238
DOID:10763 hypertension HGNC:12726 Homo sapiens (human) 7450 VWF
  • MGI:6194238
DOID:418 systemic scleroderma HGNC:12726 Homo sapiens (human) 7450 VWF
  • PMID:22596213
DOID:2224 essential thrombocythemia HGNC:12726 Homo sapiens (human) 7450 VWF
  • PMID:25876231
DOID:9970 obesity HGNC:12726 Homo sapiens (human) 7450 VWF
  • PMID:16631442
  • PMID:16739871
DOID:12531 von Willebrand's disease HGNC:12726 Homo sapiens (human) 7450 VWF
  • MGI:6194238
  • PMID:26239086
DOID:13241 Behcet's disease HGNC:12726 Homo sapiens (human) 7450 VWF
  • PMID:15849757
DOID:13809 familial combined hyperlipidemia HGNC:12726 Homo sapiens (human) 7450 VWF
  • PMID:18417194
DOID:9744 type 1 diabetes mellitus HGNC:12726 Homo sapiens (human) 7450 VWF
  • MGI:6194238

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International Collaboration

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