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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 64651 - 64675 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:8466 retinal degeneration HGNC:11761 Homo sapiens (human) 7980 TFPI2
  • PMID:15184935
DOID:9119 acute myeloid leukemia HGNC:11761 Homo sapiens (human) 7980 TFPI2
  • PMID:22052167
DOID:11247 disseminated intravascular coagulation HGNC:11760 Homo sapiens (human) 7035 TFPI
  • MGI:6194238
  • PMID:11074537
  • PMID:8292719
  • PMID:8914465
  • PMID:8929465
DOID:1240 leukemia HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:12206017
  • PMID:18549615
DOID:0081267 graft-versus-host disease HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:20037809
DOID:0050156 idiopathic pulmonary fibrosis HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:10946084
DOID:224 transient cerebral ischemia HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:18067952
DOID:10159 osteonecrosis HGNC:11760 Homo sapiens (human) 7035 TFPI
  • MGI:6194238
  • PMID:18695356
DOID:2216 factor V deficiency HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:18695002
DOID:0080630 B-lymphoblastic leukemia/lymphoma HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:19874310
DOID:0060224 atrial fibrillation HGNC:11760 Homo sapiens (human) 7035 TFPI
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:11760 Homo sapiens (human) 7035 TFPI
  • MGI:6194238
  • PMID:14656922
  • PMID:15630488
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

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International Collaboration

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