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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 676 - 700 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:5419 schizophrenia HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • RGD:7240710
DOID:3770 pulmonary fibrosis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:20888745
DOID:1612 breast cancer HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:12889595
DOID:3068 glioblastoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:11161003
DOID:10763 hypertension HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • MGI:6194238
DOID:9470 bacterial meningitis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:11986266
DOID:2394 ovarian cancer HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:12883737
DOID:9744 type 1 diabetes mellitus HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:18957531
DOID:3393 coronary artery disease HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:17627189
DOID:9352 type 2 diabetes mellitus HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:21143859
DOID:10286 prostate carcinoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:16372331
DOID:10591 pre-eclampsia HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:18054022
DOID:3908 lung non-small cell carcinoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:20564116
DOID:9538 multiple myeloma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:16930142
DOID:418 systemic scleroderma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:16195162
DOID:13375 temporal arteritis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:10616010
DOID:9119 acute myeloid leukemia HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:16361549
DOID:2841 asthma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:18003958
  • PMID:19414556
  • PMID:19568425
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:18480670
DOID:7148 rheumatoid arthritis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:10461474
DOID:1380 endometrial cancer HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:17023034
DOID:3371 chondrosarcoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:12598313
DOID:1826 epilepsy HGNC:1937 Homo sapiens (human) 1119 CHKA
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:1937 Homo sapiens (human) 1119 CHKA
  • MGI:6194238
DOID:219 colon cancer HGNC:1937 Homo sapiens (human) 1119 CHKA
  • MGI:6194238

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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: August 19, 2024