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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 8101 - 8125 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0111037 glycine N-methyltransferase deficiency HGNC:4415 Homo sapiens (human) 27232 GNMT
  • MGI:6194238
  • RGD:7240710
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
DOID:2349 arteriosclerosis HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:17010978
DOID:0110913 adult hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL
  • MGI:6194238
  • RGD:7240710
DOID:9452 steatotic liver disease HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:16197789
DOID:14213 hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL
  • PMID:8406453
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:1067 open-angle glaucoma HGNC:4369 Homo sapiens (human) 2762 GMDS
  • PMID:25173105
DOID:0070255 congenital disorder of glycosylation type IIc HGNC:4369 Homo sapiens (human) 2762 GMDS
  • MGI:6194238
DOID:3321 GM2 gangliosidosis HGNC:4367 Homo sapiens (human) 2760 GM2A
  • PMID:10364519
DOID:4795 GM2 gangliosidosis, AB variant HGNC:4367 Homo sapiens (human) 2760 GM2A
  • MGI:6194238
  • RGD:7240710
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

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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