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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 70151 - 70175 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1749 squamous cell carcinoma HGNC:10019 Homo sapiens (human) 8737 RIPK1
  • PMID:19778795
DOID:0111952 immunodeficiency 57 HGNC:10019 Homo sapiens (human) 8737 RIPK1
  • RGD:7240710
DOID:9201 lichen planus HGNC:10019 Homo sapiens (human) 8737 RIPK1
  • PMID:20368033
DOID:1826 epilepsy HGNC:10019 Homo sapiens (human) 8737 RIPK1
  • MGI:6194238
DOID:2986 IgA glomerulonephritis HGNC:11930 Homo sapiens (human) 8740 TNFSF14
  • MGI:6194238
DOID:0080630 B-lymphoblastic leukemia/lymphoma HGNC:11928 Homo sapiens (human) 8741 TNFSF13
  • PMID:15488762
DOID:305 carcinoma HGNC:11927 Homo sapiens (human) 8742 TNFSF12
  • MGI:6194238
DOID:0080074 neural tube defect HGNC:1550 Homo sapiens (human) 875 CBS
  • PMID:12649066
DOID:3393 coronary artery disease HGNC:1550 Homo sapiens (human) 875 CBS
  • PMID:12855221
DOID:12365 malaria HGNC:1550 Homo sapiens (human) 875 CBS
  • PMID:27198213
DOID:14250 Down syndrome HGNC:1550 Homo sapiens (human) 875 CBS
  • MGI:6194238
DOID:3526 cerebral infarction HGNC:1550 Homo sapiens (human) 875 CBS
  • PMID:20458436
DOID:9263 homocystinuria HGNC:1550 Homo sapiens (human) 875 CBS
  • MGI:6194238
  • PMID:7506602
  • RGD:7240710
DOID:2394 ovarian cancer HGNC:1550 Homo sapiens (human) 875 CBS
  • MGI:6194238
DOID:219 colon cancer HGNC:1550 Homo sapiens (human) 875 CBS
  • MGI:6194238
DOID:9279 hyperhomocysteinemia HGNC:1550 Homo sapiens (human) 875 CBS
  • MGI:6194238
  • PMID:10704624
DOID:0050731 vitamin B12 deficiency HGNC:1550 Homo sapiens (human) 875 CBS
  • MGI:6194238
DOID:1612 breast cancer HGNC:1550 Homo sapiens (human) 875 CBS
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:193 Homo sapiens (human) 8751 ADAM15
  • PMID:17465204
DOID:1824 status epilepticus HGNC:216 Homo sapiens (human) 8754 ADAM9
  • MGI:6194238
DOID:0111020 cone-rod dystrophy 9 HGNC:216 Homo sapiens (human) 8754 ADAM9
  • MGI:6194238
  • RGD:7240710
DOID:8991 cervix uteri carcinoma in situ HGNC:216 Homo sapiens (human) 8754 ADAM9
  • PMID:19473694
DOID:1793 pancreatic cancer HGNC:216 Homo sapiens (human) 8754 ADAM9
  • PMID:17465204
DOID:10652 Alzheimer's disease HGNC:216 Homo sapiens (human) 8754 ADAM9
  • MGI:6194238
DOID:3587 pancreatic ductal carcinoma HGNC:216 Homo sapiens (human) 8754 ADAM9
  • PMID:14997207

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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