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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 5251 - 5275 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:76 stomach disease HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
DOID:0080191 PTEN hamartoma tumor syndrome HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:16773562
  • PMID:17341483
  • PMID:24102544
  • PMID:9140396
DOID:10584 retinitis pigmentosa HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
DOID:3742 bladder squamous cell carcinoma HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:26916953
DOID:6457 Cowden syndrome HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
DOID:8719 in situ carcinoma HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:17349568
DOID:3070 high grade glioma HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:9090379
  • RGD:7240710
DOID:1612 breast cancer HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:12055674
  • PMID:9345101
  • PMID:9399897
DOID:2394 ovarian cancer HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:18347155
DOID:9256 colorectal cancer HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:27661110
DOID:2938 Epstein-Barr virus infectious disease HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:19339266
DOID:303 substance-related disorder HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
DOID:10534 stomach cancer HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:27572739
DOID:13042 persistent fetal circulation syndrome HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
DOID:264 hemangiopericytoma HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:26951238
DOID:0111507 Lenz-Majewski hyperostotic dwarfism HGNC:9587 Homo sapiens (human) 9791 PTDSS1
  • RGD:7240710
DOID:3211 lysosomal storage disease HGNC:9498 Homo sapiens (human) 5660 PSAP
  • MGI:6194238
DOID:9455 lipid storage disease HGNC:9498 Homo sapiens (human) 5660 PSAP
  • MGI:6194238
DOID:0110961 atypical Gaucher's disease due to saposin c deficiency HGNC:9498 Homo sapiens (human) 5660 PSAP
  • RGD:7240710
DOID:10587 Krabbe disease HGNC:9498 Homo sapiens (human) 5660 PSAP
  • MGI:6194238
DOID:0060892 late onset Parkinson's disease HGNC:9498 Homo sapiens (human) 5660 PSAP
  • RGD:7240710
DOID:0111330 combined saposin deficiency HGNC:9498 Homo sapiens (human) 5660 PSAP
  • MGI:6194238
  • RGD:7240710
DOID:10581 metachromatic leukodystrophy HGNC:9498 Homo sapiens (human) 5660 PSAP
  • MGI:6194238
DOID:987 alopecia HGNC:9491 Homo sapiens (human) 5652 PRSS8
  • MGI:6194238
DOID:8634 prostate carcinoma in situ HGNC:9491 Homo sapiens (human) 5652 PRSS8
  • PMID:12518323

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

Acknowledgements

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