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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 7526 - 7550 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9351 diabetes mellitus HGNC:6081 Homo sapiens (human) 3630 INS
  • PMID:17855560
  • PMID:18451997
  • PMID:19537357
  • PMID:20034470
DOID:1920 hyperuricemia HGNC:6081 Homo sapiens (human) 3630 INS
  • PMID:19033255
DOID:10763 hypertension HGNC:6080 Homo sapiens (human) 3636 INPPL1
  • PMID:15220217
DOID:9970 obesity HGNC:6080 Homo sapiens (human) 3636 INPPL1
  • PMID:15220217
DOID:9352 type 2 diabetes mellitus HGNC:6080 Homo sapiens (human) 3636 INPPL1
  • PMID:12086927
  • PMID:15220217
DOID:5408 Paget's disease of bone HGNC:6079 Homo sapiens (human) 3635 INPP5D
  • MGI:6194238
DOID:9074 systemic lupus erythematosus HGNC:6079 Homo sapiens (human) 3635 INPP5D
  • MGI:6194238
DOID:3312 bipolar disorder HGNC:6051 Homo sapiens (human) 3613 IMPA2
  • PMID:11673796
  • PMID:14699425
  • PMID:9322233
DOID:5419 schizophrenia HGNC:6051 Homo sapiens (human) 3613 IMPA2
  • PMID:11317223
DOID:1059 intellectual disability HGNC:6050 Homo sapiens (human) 3612 IMPA1
  • PMID:26416544
DOID:0081221 autosomal recessive intellectual developmental disorder 59 HGNC:6050 Homo sapiens (human) 3612 IMPA1
  • RGD:7240710
DOID:11832 visual epilepsy HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • MGI:6194238
DOID:0080596 hyper IgE recurrent infection syndrome 4 HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • PMID:10095017
DOID:10763 hypertension HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • PMID:11778537
DOID:7148 rheumatoid arthritis HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • MGI:6194238
DOID:612 primary immunodeficiency disease HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • RGD:7240710
DOID:11613 hyperandrogenism HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • PMID:12917504
DOID:10534 stomach cancer HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • MGI:6194238
DOID:2316 brain ischemia HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • MGI:6194238
DOID:1824 status epilepticus HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • MGI:6194238
DOID:2349 arteriosclerosis HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • PMID:17664290
DOID:3083 chronic obstructive pulmonary disease HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • PMID:19927353
DOID:12662 paracoccidioidomycosis HGNC:5998 Homo sapiens (human) 9173 IL1RL1
  • PMID:28992214

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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