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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 71301 - 71325 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050813 spondyloepiphyseal dysplasia with congenital joint dislocations HGNC:1971 Homo sapiens (human) 9469 CHST3
  • RGD:7240710
DOID:3963 thyroid gland carcinoma HGNC:1662 Homo sapiens (human) 947 CD34
  • PMID:32626543
DOID:8947 diabetic retinopathy HGNC:1662 Homo sapiens (human) 947 CD34
  • MGI:6194238
DOID:8689 anorexia nervosa HGNC:376 Homo sapiens (human) 9472 AKAP6
  • PMID:21079607
DOID:2152 ovary epithelial cancer HGNC:376 Homo sapiens (human) 9472 AKAP6
  • PMID:29979793
DOID:9352 type 2 diabetes mellitus HGNC:6882 Homo sapiens (human) 9479 MAPK8IP1
  • RGD:7240710
DOID:2378 relapsing-remitting multiple sclerosis HGNC:1663 Homo sapiens (human) 948 CD36
  • PMID:20855355
DOID:9352 type 2 diabetes mellitus HGNC:1663 Homo sapiens (human) 948 CD36
  • MGI:6194238
  • PMID:12479587
  • PMID:15221799
  • PMID:16911630
  • PMID:16952981
  • PMID:20134099
DOID:2957 pulmonary tuberculosis HGNC:1663 Homo sapiens (human) 948 CD36
  • PMID:28693442
DOID:2224 essential thrombocythemia HGNC:1663 Homo sapiens (human) 948 CD36
  • PMID:8555064
DOID:11984 hypertrophic cardiomyopathy HGNC:1663 Homo sapiens (human) 948 CD36
  • MGI:6194238
DOID:4448 macular degeneration HGNC:1663 Homo sapiens (human) 948 CD36
  • MGI:6194238
DOID:12554 hemolytic-uremic syndrome HGNC:1663 Homo sapiens (human) 948 CD36
  • PMID:16197457
DOID:0070004 myeloid neoplasm HGNC:1663 Homo sapiens (human) 948 CD36
  • PMID:12479587
DOID:12132 granulomatosis with polyangiitis HGNC:1663 Homo sapiens (human) 948 CD36
  • PMID:21412229
DOID:0050827 rheumatic heart disease HGNC:1663 Homo sapiens (human) 948 CD36
  • PMID:16741676
DOID:12365 malaria HGNC:1663 Homo sapiens (human) 948 CD36
  • RGD:7240710
DOID:10923 sickle cell anemia HGNC:1663 Homo sapiens (human) 948 CD36
  • PMID:18322255
DOID:9970 obesity HGNC:1663 Homo sapiens (human) 948 CD36
  • MGI:6194238
DOID:10772 thrombotic thrombocytopenic purpura HGNC:1663 Homo sapiens (human) 948 CD36
  • PMID:7529543
DOID:10763 hypertension HGNC:1663 Homo sapiens (human) 948 CD36
  • MGI:6194238
DOID:3429 inclusion body myositis HGNC:1663 Homo sapiens (human) 948 CD36
  • PMID:17572512
DOID:0060224 atrial fibrillation HGNC:1663 Homo sapiens (human) 948 CD36
  • PMID:21195211
DOID:1936 atherosclerosis HGNC:1663 Homo sapiens (human) 948 CD36
  • MGI:6194238
DOID:8398 osteoarthritis HGNC:1663 Homo sapiens (human) 948 CD36
  • PMID:15334463

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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: December 9, 2024