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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 1476 - 1500 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:7147 ankylosing spondylitis HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:12880680
DOID:3132 porphyria cutanea tarda HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:14714565
DOID:1324 lung cancer HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:16696009
DOID:3748 esophagus squamous cell carcinoma HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:11860825
DOID:8893 psoriasis HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:12713578
DOID:824 periodontitis HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:15491310
DOID:11836 clubfoot HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:21254355
DOID:9008 psoriatic arthritis HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:15124938
DOID:9952 acute lymphoblastic leukemia HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:16676594
  • PMID:22964275
  • PMID:23725389
DOID:1380 endometrial cancer HGNC:2596 Homo sapiens (human) 1544 CYP1A2
  • PMID:18497059
DOID:1596 depressive disorder HGNC:2596 Homo sapiens (human) 1544 CYP1A2
  • MGI:6194238
DOID:3083 chronic obstructive pulmonary disease HGNC:2596 Homo sapiens (human) 1544 CYP1A2
  • PMID:20080081
DOID:6000 congestive heart failure HGNC:2596 Homo sapiens (human) 1544 CYP1A2
  • MGI:6194238
DOID:3132 porphyria cutanea tarda HGNC:2596 Homo sapiens (human) 1544 CYP1A2
  • PMID:20957336
DOID:1612 breast cancer HGNC:2596 Homo sapiens (human) 1544 CYP1A2
  • PMID:18497059
DOID:10763 hypertension HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • MGI:6194238
DOID:3907 lung squamous cell carcinoma HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • PMID:10739169
DOID:11054 urinary bladder cancer HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • PMID:21990318
DOID:0060673 Peters anomaly HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • PMID:15621878
DOID:3458 breast adenocarcinoma HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • MGI:6194238
DOID:11212 hydrophthalmos HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • PMID:9097971
DOID:11984 hypertrophic cardiomyopathy HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • MGI:6194238
DOID:3748 esophagus squamous cell carcinoma HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • MGI:6194238
DOID:1612 breast cancer HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • PMID:10739169

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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