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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 501 - 525 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:2316 brain ischemia HGNC:435 Homo sapiens (human) 240 ALOX5
  • MGI:6194238
DOID:4947 cholangiocarcinoma HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:18507031
DOID:1184 nephrotic syndrome HGNC:435 Homo sapiens (human) 240 ALOX5
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:12163367
  • PMID:12481414
DOID:2957 pulmonary tuberculosis HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:18174194
DOID:10247 pleurisy HGNC:435 Homo sapiens (human) 240 ALOX5
  • MGI:6194238
DOID:10459 common cold HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:11865407
DOID:8719 in situ carcinoma HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:16024599
DOID:10762 portal hypertension HGNC:435 Homo sapiens (human) 240 ALOX5
  • MGI:6194238
DOID:3770 pulmonary fibrosis HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:8621765
DOID:10763 hypertension HGNC:435 Homo sapiens (human) 240 ALOX5
  • MGI:6194238
DOID:6432 pulmonary hypertension HGNC:435 Homo sapiens (human) 240 ALOX5
  • MGI:6194238
  • PMID:31462075
  • PMID:9445303
DOID:11396 pulmonary edema HGNC:435 Homo sapiens (human) 240 ALOX5
  • MGI:6194238
DOID:2349 arteriosclerosis HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:14702425
DOID:3021 acute kidney failure HGNC:435 Homo sapiens (human) 240 ALOX5
  • MGI:6194238
DOID:2841 asthma HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:10369259
  • PMID:12911785
  • PMID:16364163
  • PMID:17394438
  • PMID:18204779
  • PMID:20128419
  • PMID:9642160
  • RGD:7240710
DOID:0080821 exercise-induced bronchoconstriction HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:10984370
DOID:8778 Crohn's disease HGNC:437 Homo sapiens (human) 248 ALPI
  • PMID:22783049
DOID:0050589 inflammatory bowel disease HGNC:437 Homo sapiens (human) 248 ALPI
  • PMID:29567797
DOID:8577 ulcerative colitis HGNC:437 Homo sapiens (human) 248 ALPI
  • PMID:22783049
DOID:0110914 infantile hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL
  • MGI:6194238
  • RGD:7240710
DOID:4676 uremia HGNC:438 Homo sapiens (human) 249 ALPL
  • MGI:6194238
DOID:8719 in situ carcinoma HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:10547581
DOID:0110915 childhood hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL
  • MGI:6194238
  • RGD:7240710
DOID:13809 familial combined hyperlipidemia HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:16336518

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Supported by JST NBDC Grant Number JPMJND2204

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


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