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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 8926 - 8950 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9261 nasopharynx carcinoma HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:26582733
DOID:9256 colorectal cancer HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:30489355
DOID:2044 drug-induced hepatitis HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
DOID:14018 alcoholic liver cirrhosis HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:29404441
DOID:684 hepatocellular carcinoma HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:20364586
  • PMID:29765251
DOID:3070 high grade glioma HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:12540498
DOID:8618 oral cavity cancer HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:16721740
DOID:841 extrinsic allergic alveolitis HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:20514434
DOID:409 liver disease HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
  • PMID:17950035
  • PMID:20392357
DOID:3021 acute kidney failure HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
DOID:1168 familial hyperlipidemia HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
DOID:10320 asbestosis HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:20514434
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
DOID:9970 obesity HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
DOID:0050868 hepatocellular adenoma HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
DOID:3083 chronic obstructive pulmonary disease HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:17442289
DOID:10534 stomach cancer HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:22957075
DOID:1596 depressive disorder HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
DOID:2841 asthma HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:20514434
DOID:552 pneumonia HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:15928955
DOID:0050866 oral squamous cell carcinoma HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:22954124
DOID:3525 middle cerebral artery infarction HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
DOID:10588 adrenoleukodystrophy HGNC:26292 Homo sapiens (human) 79993 ELOVL7
  • MGI:6194238
DOID:10908 hydrocephalus HGNC:26267 Homo sapiens (human) 84197 POMK
  • MGI:6194238
DOID:0111235 congenital muscular dystrophy-dystroglycanopathy type A12 HGNC:26267 Homo sapiens (human) 84197 POMK
  • RGD:7240710

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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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