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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 5501 - 5525 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:0080633 developmental cardiac valvular defect HGNC:9067 Homo sapiens (human) 5337 PLD1
  • MGI:6194238
  • RGD:7240710
DOID:0070174 spermatogenic failure 17 HGNC:19218 Homo sapiens (human) 89869 PLCZ1
  • RGD:7240710
DOID:4621 holoprosencephaly HGNC:29185 Homo sapiens (human) 23007 PLCH1
  • RGD:7240710
DOID:0090064 familial cold autoinflammatory syndrome 3 HGNC:9066 Homo sapiens (human) 5336 PLCG2
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:8534418
DOID:3459 breast carcinoma HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:1683701
DOID:684 hepatocellular carcinoma HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:30623526
DOID:3908 lung non-small cell carcinoma HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:33928024
DOID:3910 lung adenocarcinoma HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:33077911
DOID:9408 acute myocardial infarction HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • MGI:6194238
DOID:0050866 oral squamous cell carcinoma HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:25085076
  • PMID:26464646
DOID:219 colon cancer HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • MGI:6194238
DOID:2876 laryngeal squamous cell carcinoma HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:33466212
DOID:1612 breast cancer HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:9703922
DOID:9256 colorectal cancer HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:8275435
DOID:0050424 familial adenomatous polyposis HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:8174133
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
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:8466 retinal degeneration HGNC:9059 Homo sapiens (human) 5332 PLCB4
  • MGI:6194238

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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