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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 8351 - 8375 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:4006 Homo sapiens (human) 2517 FUCA1
  • PMID:16176171
DOID:2945 severe acute respiratory syndrome HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:19635508
DOID:14330 Parkinson's disease HGNC:10680 Homo sapiens (human) 6389 SDHA
  • PMID:26605748
DOID:9970 obesity HGNC:10799 Homo sapiens (human) 729238 SFTPA2
  • MGI:6194238
DOID:526 human immunodeficiency virus infectious disease HGNC:1641 Homo sapiens (human) 30835 CD209
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:14573732
DOID:612 primary immunodeficiency disease HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • RGD:7240710
DOID:1508 candidiasis HGNC:4018 Homo sapiens (human) 2529 FUT7
  • MGI:6194238
DOID:9281 phenylketonuria HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:9351 diabetes mellitus HGNC:4006 Homo sapiens (human) 2517 FUCA1
  • PMID:3609421
DOID:684 hepatocellular carcinoma HGNC:9232 Homo sapiens (human) 5465 PPARA
  • MGI:6194238
  • PMID:19119483
DOID:9352 type 2 diabetes mellitus HGNC:9377 Homo sapiens (human) 5563 PRKAA2
  • PMID:16567511
DOID:11981 morbid obesity HGNC:18129 Homo sapiens (human) 51738 GHRL
  • PMID:19188925
DOID:526 human immunodeficiency virus infectious disease HGNC:9031 Homo sapiens (human) 5320 PLA2G2A
  • PMID:18096355
DOID:9775 diastolic heart failure HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:19021695
  • PMID:19752885
DOID:1574 alcohol use disorder HGNC:9293 Homo sapiens (human) 5507 PPP1R3C
  • MGI:6194238
DOID:12305 Bloch-Sulzberger syndrome HGNC:13398 Homo sapiens (human) 50814 NSDHL
  • MGI:6194238
DOID:14115 toxic shock syndrome HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:28336767
DOID:10247 pleurisy HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:3459 breast carcinoma HGNC:9491 Homo sapiens (human) 5652 PRSS8
  • PMID:11774283
DOID:10652 Alzheimer's disease HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
  • PMID:19154537
  • PMID:24101602
DOID:583 hemolytic anemia HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:3136561
DOID:0090064 familial cold autoinflammatory syndrome 3 HGNC:9066 Homo sapiens (human) 5336 PLCG2
  • RGD:7240710
DOID:0070435 hyperphosphatasia with impaired intellectual development syndrome 3 HGNC:17893 Homo sapiens (human) 27315 PGAP2
  • RGD:7240710
DOID:11832 visual epilepsy HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238

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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