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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 11676 - 11700 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:5844 myocardial infarction HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
  • PMID:12200370
  • PMID:16025836
  • PMID:8814351
DOID:12217 Lewy body dementia HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:23576984
DOID:3587 pancreatic ductal carcinoma HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:19488907
DOID:1574 alcohol use disorder HGNC:491 Homo sapiens (human) 27329 ANGPTL3
  • MGI:6194238
DOID:0111061 familial hypobetalipoproteinemia 2 HGNC:491 Homo sapiens (human) 27329 ANGPTL3
  • RGD:7240710
DOID:9268 glycine encephalopathy HGNC:473 Homo sapiens (human) 275 AMT
  • PMID:8005589
  • PMID:9600239
  • PMID:9621520
  • RGD:7240710
DOID:11054 urinary bladder cancer HGNC:451 Homo sapiens (human) 23600 AMACR
  • PMID:18648853
DOID:3459 breast carcinoma HGNC:451 Homo sapiens (human) 23600 AMACR
  • PMID:15941950
DOID:0060602 alpha-methylacyl-CoA racemase deficiency HGNC:451 Homo sapiens (human) 23600 AMACR
  • MGI:6194238
  • RGD:7240710
DOID:8634 prostate carcinoma in situ HGNC:451 Homo sapiens (human) 23600 AMACR
  • PMID:18343427
DOID:0111068 congenital bile acid synthesis defect 4 HGNC:451 Homo sapiens (human) 23600 AMACR
  • RGD:7240710
DOID:4450 renal cell carcinoma HGNC:451 Homo sapiens (human) 23600 AMACR
  • PMID:14707866
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:2316 brain ischemia HGNC:435 Homo sapiens (human) 240 ALOX5
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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