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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 5076 - 5100 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:3650 lactic acidosis HGNC:9725 Homo sapiens (human) 5836 PYGL
  • MGI:6194238
  • PMID:17705025
DOID:2747 glycogen storage disease HGNC:9725 Homo sapiens (human) 5836 PYGL
  • PMID:9536091
DOID:2754 glycogen storage disease VI HGNC:9725 Homo sapiens (human) 5836 PYGL
  • MGI:6194238
  • PMID:17705025
  • PMID:21646031
  • RGD:7240710
DOID:3651 pyruvate carboxylase deficiency disease SGD:S000000422 Saccharomyces cerevisiae S288C 852519 PYC2
  • MGI:6194238
DOID:3651 pyruvate carboxylase deficiency disease SGD:S000003030 Saccharomyces cerevisiae S288C 852818 PYC1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:3083 chronic obstructive pulmonary disease HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:15949313
  • PMID:21655952
DOID:4947 cholangiocarcinoma HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:19621664
DOID:684 hepatocellular carcinoma HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
  • PMID:15800977
  • PMID:24720952
  • PMID:24759835
DOID:1824 status epilepticus HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:3213 demyelinating disease HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:14694045
DOID:332 amyotrophic lateral sclerosis HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:14511332
DOID:12466 secondary hyperparathyroidism HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
  • PMID:21335517
DOID:8634 prostate carcinoma in situ HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:18468781
DOID:1679 cystitis HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:5394 prolactinoma HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:22580984
DOID:0080322 polycystic kidney disease HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:5419 schizophrenia HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:5082 liver cirrhosis HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:29109031
DOID:6255 growth hormone secreting pituitary adenoma HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:22580984
DOID:2349 arteriosclerosis HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:16458279
DOID:4029 gastritis HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:2999 granulosa cell tumor HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:11994539
DOID:11963 esophagitis HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:20811626
DOID:10652 Alzheimer's disease HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
  • PMID:8892355
  • PMID:9740394

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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