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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 11876 - 11900 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:2957 pulmonary tuberculosis HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:20141546
DOID:3312 bipolar disorder HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:20214684
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:0111069 congenital bile acid synthesis defect 2 HGNC:388 Homo sapiens (human) 6718 AKR1D1
  • RGD:7240710
DOID:0111773 46,XY sex reversal 8 HGNC:387 Homo sapiens (human) 1109 AKR1C4
  • RGD:7240710
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:0111773 46,XY sex reversal 8 HGNC:385 Homo sapiens (human) 1646 AKR1C2
  • RGD:7240710
DOID:9970 obesity HGNC:385 Homo sapiens (human) 1646 AKR1C2
  • PMID:15494612
DOID:9970 obesity HGNC:384 Homo sapiens (human) 1645 AKR1C1
  • PMID:15494612
DOID:2349 arteriosclerosis HGNC:381 Homo sapiens (human) 231 AKR1B1
  • PMID:16127462
DOID:4500 hypokalemia HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
DOID:1205 allergic disease HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
DOID:10534 stomach cancer HGNC:381 Homo sapiens (human) 231 AKR1B1
  • PMID:23808167
DOID:9743 diabetic neuropathy HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
  • PMID:9489533
DOID:9870 galactosemia HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
DOID:4195 hyperglycemia HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
DOID:83 cataract HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
  • PMID:21329682
  • PMID:24360973

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Supported by JST NBDC Grant Number JPMJND2204

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


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