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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 October 9, 2024
Displaying entries 62776 - 62800 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0111144 preterm premature rupture of the membranes HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:19012190
DOID:14115 toxic shock syndrome HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:11776329
DOID:3770 pulmonary fibrosis HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:16338226
DOID:12134 factor VIII deficiency HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:24263002
  • PMID:24687919
DOID:5425 ovarian hyperstimulation syndrome HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:12695751
DOID:14566 disease of cellular proliferation HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:11864704
DOID:1184 nephrotic syndrome HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:22319062
DOID:2451 protein S deficiency HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:20002538
  • PMID:23079294
DOID:9074 systemic lupus erythematosus HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:11709459
DOID:1168 familial hyperlipidemia HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:8914465
DOID:10591 pre-eclampsia HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:10078579
DOID:9351 diabetes mellitus HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:8914465
DOID:10772 thrombotic thrombocytopenic purpura HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:7740478
DOID:5082 liver cirrhosis HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:23841464
DOID:0111030 hemochromatosis type 3 HGNC:11762 Homo sapiens (human) 7036 TFR2
  • MGI:6194238
  • RGD:7240710
DOID:9119 acute myeloid leukemia HGNC:11762 Homo sapiens (human) 7036 TFR2
  • PMID:15015967
DOID:2352 hemochromatosis HGNC:11762 Homo sapiens (human) 7036 TFR2
  • PMID:10802645
DOID:2216 factor V deficiency MGI:1917611 Mus musculus (house mouse) 70361 Lman1
  • MGI:6194238
DOID:2211 factor XIII deficiency MGI:1917611 Mus musculus (house mouse) 70361 Lman1
  • MGI:6194238
DOID:9538 multiple myeloma HGNC:11763 Homo sapiens (human) 7037 TFRC
  • PMID:21654517
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:11763 Homo sapiens (human) 7037 TFRC
  • MGI:6194238
DOID:10283 prostate cancer HGNC:11763 Homo sapiens (human) 7037 TFRC
  • PMID:15514585
DOID:0111948 immunodeficiency 46 HGNC:11763 Homo sapiens (human) 7037 TFRC
  • RGD:7240710
DOID:767 muscular atrophy HGNC:11763 Homo sapiens (human) 7037 TFRC
  • MGI:6194238
DOID:2394 ovarian cancer HGNC:11763 Homo sapiens (human) 7037 TFRC
  • PMID:3493065

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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: December 9, 2024