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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 10901 - 10925 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:10591 pre-eclampsia HGNC:2602 Homo sapiens (human) 1591 CYP24A1
  • PMID:22871339
  • PMID:36477942
DOID:1793 pancreatic cancer HGNC:1097 Homo sapiens (human) 673 BRAF
  • PMID:22871572
DOID:1184 nephrotic syndrome RGD:620925 Rattus norvegicus (Norway rat) 83516 Ppargc1a
  • PMID:22874759
DOID:7147 ankylosing spondylitis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:22876137
DOID:11650 bronchopulmonary dysplasia HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:22882323
DOID:11506 suppurative otitis media HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:22883581
DOID:11506 suppurative otitis media HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:22883581
DOID:869 cholesteatoma HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:22883581
DOID:869 cholesteatoma HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:22883581
DOID:10952 nephritis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:22895845
DOID:8398 osteoarthritis HGNC:6081 Homo sapiens (human) 3630 INS
  • PMID:2290165
DOID:13141 uveitis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:229083
DOID:14566 disease of cellular proliferation RGD:3889 Rattus norvegicus (Norway rat) 24842 Tp53
  • PMID:22917926
DOID:9452 steatotic liver disease RGD:2670 Rattus norvegicus (Norway rat) 24385 Gck
  • PMID:22925001
DOID:9119 acute myeloid leukemia HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:22930375
  • PMID:26823947
  • PMID:26950655
DOID:11723 Duchenne muscular dystrophy HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • PMID:22934738
DOID:9120 amyloidosis HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:22935190
DOID:5082 liver cirrhosis RGD:619868 Rattus norvegicus (Norway rat) 25283 Gclc
  • PMID:22942279
DOID:10603 glucose intolerance RGD:3000 Rattus norvegicus (Norway rat) 25608 Lep
  • PMID:22948215
DOID:2018 hyperinsulinism RGD:3000 Rattus norvegicus (Norway rat) 25608 Lep
  • PMID:22948215
DOID:0050866 oral squamous cell carcinoma HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:22954124
DOID:10534 stomach cancer HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:22957075
DOID:2043 hepatitis B HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • PMID:22963605
DOID:1070 primary open angle glaucoma HGNC:4341 Homo sapiens (human) 2752 GLUL
  • PMID:22974818
DOID:10763 hypertension RGD:70982 Rattus norvegicus (Norway rat) 84027 Gsk3b
  • PMID:22982863

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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