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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 11801 - 11825 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▼ Evidence Code Names References
DOID:3525 middle cerebral artery infarction FB:FBgn0001092 Drosophila melanogaster (fruit fly) 32545 Gapdh2
  • MGI:6194238
DOID:13088 periventricular leukomalacia HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:8652010
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
  • PMID:18308829
DOID:5016 hepatocellular clear cell carcinoma MGI:104663 Mus musculus (house mouse) 16846 Lep
  • MGI:6194238
DOID:9256 colorectal cancer HGNC:8977 Homo sapiens (human) 5293 PIK3CD
  • PMID:25366420
DOID:9256 colorectal cancer HGNC:2602 Homo sapiens (human) 1591 CYP24A1
  • PMID:20398751
  • PMID:23463632
  • PMID:24213465
  • PMID:24562971
  • PMID:26260259
  • PMID:26997443
  • PMID:28821819
  • PMID:31802707
  • PMID:32803502
  • PMID:33504116
DOID:10652 Alzheimer's disease HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:12498973
DOID:0070352 stress-induced childhood-onset neurodegeneration with variable ataxia and seizures HGNC:8605 Homo sapiens (human) 8505 PARG
  • MGI:6194238
DOID:2349 arteriosclerosis HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • PMID:17664290
DOID:3407 carotid artery disease HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:22499993
DOID:0112298 spondylometaphyseal dysplasia Sedaghatian type SGD:S000001509 Saccharomyces cerevisiae S288C 853842 GPX1
  • MGI:6194238
DOID:12798 mucopolysaccharidosis HGNC:24102 Homo sapiens (human) 22901 ARSG
  • MGI:6194238
DOID:10591 pre-eclampsia HGNC:2602 Homo sapiens (human) 1591 CYP24A1
  • PMID:22871339
  • PMID:36477942
DOID:3146 lipid metabolism disorder HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • MGI:6194238
DOID:0110645 long QT syndrome 2 RGD:708500 Rattus norvegicus (Norway rat) 245960 Alg10
  • MGI:6194238
DOID:0080855 Parkinsonism SGD:S000005920 Saccharomyces cerevisiae S288C 854575 ERR1
  • MGI:6194238
DOID:4079 heart valve disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation ZFIN:ZDB-GENE-061013-84 Danio rerio (zebrafish) 768123 b4galt1l
  • MGI:6194238
DOID:8893 psoriasis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:12165738
  • PMID:12602965
DOID:1574 alcohol use disorder RGD:3676 Rattus norvegicus (Norway rat) 25197 St6gal1
  • MGI:6194238
DOID:11400 pyelonephritis RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • MGI:6194238
DOID:0080561 congenital disorder of glycosylation Ii ZFIN:ZDB-GENE-060502-2 Danio rerio (zebrafish) 403068 alg2
  • MGI:6194238
DOID:905 Zellweger syndrome HGNC:10606 Homo sapiens (human) 6342 SCP2
  • PMID:3555624
DOID:684 hepatocellular carcinoma HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
  • PMID:19422879

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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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