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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 401 - 425 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9352 type 2 diabetes mellitus HGNC:6126 Homo sapiens (human) 8660 IRS2
  • MGI:6194238
  • PMID:11030756
  • RGD:7240710
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:6126 Homo sapiens (human) 8660 IRS2
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:6126 Homo sapiens (human) 8660 IRS2
  • PMID:18479783
DOID:10591 pre-eclampsia HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • MGI:6194238
  • PMID:19681734
DOID:5603 T-cell acute lymphoblastic leukemia HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • PMID:26116659
DOID:0080630 B-lymphoblastic leukemia/lymphoma HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • PMID:26116659
DOID:10283 prostate cancer HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • PMID:24571686
DOID:1240 leukemia HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • PMID:18339682
DOID:0080909 castration-resistant prostate carcinoma HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • PMID:23196782
DOID:0060074 ductal carcinoma in situ HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • PMID:16735089
DOID:11612 polycystic ovary syndrome HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • MGI:6194238
DOID:12849 autistic disorder HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • PMID:15056512
DOID:4137 common bile duct disease HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • MGI:6194238
DOID:0050432 Asperger syndrome HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • PMID:24679184
DOID:0060041 autism spectrum disorder HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • PMID:17151801
  • PMID:18180767
DOID:9273 citrullinemia HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • MGI:6194238
DOID:1852 intrahepatic cholestasis HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • MGI:6194238
DOID:0080349 developmental and epileptic encephalopathy 39 HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • MGI:6194238
  • RGD:7240710
DOID:3498 pancreatic ductal adenocarcinoma HGNC:389 Homo sapiens (human) 8574 AKR7A2
  • PMID:19077459
DOID:10652 Alzheimer's disease HGNC:389 Homo sapiens (human) 8574 AKR7A2
  • PMID:11597610
DOID:0050571 congenital disorder of glycosylation type II SGD:S000000959 Saccharomyces cerevisiae S288C 856901 COG3
  • MGI:6194238
DOID:0080693 Noonan syndrome-like disorder with loose anagen hair 2 SGD:S000000935 Saccharomyces cerevisiae S288C 856870 GLC7
  • MGI:6194238
DOID:6000 congestive heart failure SGD:S000000935 Saccharomyces cerevisiae S288C 856870 GLC7
  • MGI:6194238
DOID:162 cancer SGD:S000000935 Saccharomyces cerevisiae S288C 856870 GLC7
  • PMID:26354769
DOID:9352 type 2 diabetes mellitus SGD:S000000935 Saccharomyces cerevisiae S288C 856870 GLC7
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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