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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 6676 - 6700 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:2957 pulmonary tuberculosis HGNC:9053 Homo sapiens (human) 5329 PLAUR
  • PMID:18359089
DOID:9471 meningitis HGNC:9053 Homo sapiens (human) 5329 PLAUR
  • PMID:21971819
DOID:10652 Alzheimer's disease HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • MGI:6194238
  • PMID:8534418
DOID:5844 myocardial infarction HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • MGI:6194238
DOID:0050908 myelodysplastic syndrome HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • PMID:16820933
  • PMID:21109771
DOID:0080459 developmental and epileptic encephalopathy 12 HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • RGD:7240710
DOID:5419 schizophrenia HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • MGI:6194238
DOID:9970 obesity HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • MGI:6194238
DOID:9119 acute myeloid leukemia HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • PMID:20516454
DOID:9970 obesity HGNC:9055 Homo sapiens (human) 5330 PLCB2
  • MGI:6194238
DOID:1682 congenital heart disease HGNC:9055 Homo sapiens (human) 5330 PLCB2
  • MGI:6194238
DOID:0112303 spondylometaphyseal dysplasia with corneal dystrophy HGNC:9056 Homo sapiens (human) 5331 PLCB3
  • RGD:7240710
DOID:9970 obesity HGNC:9056 Homo sapiens (human) 5331 PLCB3
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:9056 Homo sapiens (human) 5331 PLCB3
  • MGI:6194238
DOID:8466 retinal degeneration HGNC:9059 Homo sapiens (human) 5332 PLCB4
  • MGI:6194238
DOID:0050742 nicotine dependence HGNC:9059 Homo sapiens (human) 5332 PLCB4
  • MGI:6194238
DOID:5679 retinal disease HGNC:9059 Homo sapiens (human) 5332 PLCB4
  • MGI:6194238
DOID:6000 congestive heart failure HGNC:9060 Homo sapiens (human) 5333 PLCD1
  • MGI:6194238
DOID:10763 hypertension HGNC:9060 Homo sapiens (human) 5333 PLCD1
  • MGI:6194238
DOID:0080081 nonsyndromic congenital nail disorder 3 HGNC:9060 Homo sapiens (human) 5333 PLCD1
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:9060 Homo sapiens (human) 5333 PLCD1
  • PMID:8534418
DOID:0080379 nephrotic syndrome type 2 HGNC:17175 Homo sapiens (human) 51196 PLCE1
  • PMID:20591883
DOID:0080382 nephrotic syndrome type 3 HGNC:17175 Homo sapiens (human) 51196 PLCE1
  • RGD:7240710
DOID:1184 nephrotic syndrome HGNC:17175 Homo sapiens (human) 51196 PLCE1
  • PMID:17086182
DOID:3717 gastric adenocarcinoma HGNC:17175 Homo sapiens (human) 51196 PLCE1
  • PMID:24796667

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

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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