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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 8876 - 8900 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:440 neuromuscular disease HGNC:4458 Homo sapiens (human) 2821 GPI
  • PMID:9856489
DOID:114 heart disease HGNC:4458 Homo sapiens (human) 2821 GPI
  • MGI:6194238
DOID:1059 intellectual disability HGNC:4458 Homo sapiens (human) 2821 GPI
  • PMID:9856489
DOID:13580 cholestasis SGD:S000006364 Saccharomyces cerevisiae S288C 856289 GPH1
  • MGI:6194238
DOID:3650 lactic acidosis SGD:S000006364 Saccharomyces cerevisiae S288C 856289 GPH1
  • MGI:6194238
DOID:2747 glycogen storage disease SGD:S000006364 Saccharomyces cerevisiae S288C 856289 GPH1
  • MGI:6194238
DOID:2746 glycogen storage disease V SGD:S000006364 Saccharomyces cerevisiae S288C 856289 GPH1
  • MGI:6194238
DOID:2754 glycogen storage disease VI SGD:S000006364 Saccharomyces cerevisiae S288C 856289 GPH1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:4456 Homo sapiens (human) 2820 GPD2
  • RGD:7240710
DOID:0110219 Brugada syndrome 2 SGD:S000005420 Saccharomyces cerevisiae S288C 854095 GPD2
  • MGI:6194238
DOID:0110219 Brugada syndrome 2 HGNC:28956 Homo sapiens (human) 23171 GPD1L
  • RGD:7240710
DOID:0110219 Brugada syndrome 2 SGD:S000002180 Saccharomyces cerevisiae S288C 851539 GPD1
  • MGI:6194238
DOID:0080844 omodysplasia 1 HGNC:4454 Homo sapiens (human) 10082 GPC6
  • RGD:7240710
DOID:0060248 Simpson-Golabi-Behmel syndrome type 1 HGNC:4451 Homo sapiens (human) 2719 GPC3
  • MGI:6194238
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:4451 Homo sapiens (human) 2719 GPC3
  • MGI:6194238
  • PMID:19496787
  • PMID:21438004
  • PMID:22883669
  • PMID:23558072
  • PMID:25449037
  • PMID:28801286
DOID:2154 nephroblastoma HGNC:4451 Homo sapiens (human) 2719 GPC3
  • RGD:7240710
DOID:5082 liver cirrhosis HGNC:4451 Homo sapiens (human) 2719 GPC3
  • PMID:28801286
DOID:2129 atypical teratoid rhabdoid tumor HGNC:4451 Homo sapiens (human) 2719 GPC3
  • PMID:23530909
DOID:3596 placental site trophoblastic tumor HGNC:4451 Homo sapiens (human) 2719 GPC3
  • PMID:20868507
DOID:687 hepatoblastoma HGNC:4451 Homo sapiens (human) 2719 GPC3
  • PMID:23530909
DOID:684 hepatocellular carcinoma HGNC:4449 Homo sapiens (human) 2817 GPC1
  • PMID:35693827
DOID:1184 nephrotic syndrome HGNC:24865 Homo sapiens (human) 57678 GPAM
  • MGI:6194238
DOID:9970 obesity HGNC:24865 Homo sapiens (human) 57678 GPAM
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:24865 Homo sapiens (human) 57678 GPAM
  • MGI:6194238
DOID:3498 pancreatic ductal adenocarcinoma HGNC:4432 Homo sapiens (human) 2805 GOT1
  • PMID:23535601

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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