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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 69526 - 69550 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3393 coronary artery disease HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:17627189
DOID:5844 myocardial infarction HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:18480670
DOID:1612 breast cancer HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:12889595
DOID:2841 asthma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:18003958
  • PMID:19414556
  • PMID:19568425
  • RGD:7240710
DOID:10286 prostate carcinoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:16372331
DOID:2349 arteriosclerosis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:10073974
DOID:9352 type 2 diabetes mellitus HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:21143859
DOID:13406 pulmonary sarcoidosis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:15763444
DOID:9744 type 1 diabetes mellitus HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:18957531
DOID:418 systemic scleroderma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:16195162
DOID:9538 multiple myeloma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:16930142
DOID:3371 chondrosarcoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:12598313
DOID:5419 schizophrenia HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • RGD:7240710
DOID:3908 lung non-small cell carcinoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:20564116
DOID:0050700 cardiomyopathy HGNC:15710 Homo sapiens (human) 11155 LDB3
  • MGI:6194238
DOID:11720 distal myopathy HGNC:15710 Homo sapiens (human) 11155 LDB3
  • PMID:17337483
DOID:423 myopathy HGNC:15710 Homo sapiens (human) 11155 LDB3
  • MGI:6194238
DOID:0080095 myofibrillar myopathy 4 HGNC:15710 Homo sapiens (human) 11155 LDB3
  • MGI:6194238
  • RGD:7240710
DOID:0081337 congenital myopathy HGNC:15710 Homo sapiens (human) 11155 LDB3
  • MGI:6194238
DOID:0110423 dilated cardiomyopathy 1C HGNC:15710 Homo sapiens (human) 11155 LDB3
  • MGI:6194238
  • RGD:7240710
DOID:11722 myotonic dystrophy type 1 HGNC:15710 Homo sapiens (human) 11155 LDB3
  • PMID:24878509
DOID:0080092 myofibrillar myopathy 1 HGNC:15710 Homo sapiens (human) 11155 LDB3
  • MGI:6194238
DOID:12930 dilated cardiomyopathy HGNC:15710 Homo sapiens (human) 11155 LDB3
  • PMID:14660611
  • PMID:20852297
  • PMID:26419279
DOID:0110739 neurodegeneration with brain iron accumulation 5 HGNC:28912 Homo sapiens (human) 11152 WDR45
  • MGI:6194238
  • RGD:7240710
DOID:0090014 severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive HGNC:2252 Homo sapiens (human) 11151 CORO1A
  • MGI:6194238

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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