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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 8501 - 8525 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:607 paraplegia HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:0111156 spermatogenic failure 9 ZFIN:ZDB-GENE-030521-11 Danio rerio (zebrafish) 368327 dpy19l1l
  • MGI:6194238
DOID:0080162 lupus nephritis MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:12783 migraine without aura RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:10763 hypertension MGI:88470 Mus musculus (house mouse) 12846 Comt
  • MGI:6194238
DOID:3323 Sandhoff disease MGI:96074 Mus musculus (house mouse) 15212 Hexb
  • MGI:6194238
  • PMID:14722612
  • PMID:23028353
  • PMID:31547903
  • PMID:7550345
  • PMID:8789434
DOID:9970 obesity SGD:S000005646 Saccharomyces cerevisiae S288C 854287 GCY1
  • MGI:6194238
DOID:0050985 spinocerebellar ataxia type 38 HGNC:21308 Homo sapiens (human) 60481 ELOVL5
  • RGD:7240710
DOID:0080005 bone remodeling disease HGNC:5383 Homo sapiens (human) 3418 IDH2
  • MGI:6194238
DOID:3748 esophagus squamous cell carcinoma RGD:2081 Rattus norvegicus (Norway rat) 24185 Akt1
  • MGI:6194238
DOID:11476 osteoporosis HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:11459801
  • PMID:21376149
DOID:6432 pulmonary hypertension HGNC:4818 Homo sapiens (human) 3036 HAS1
  • MGI:6194238
DOID:10584 retinitis pigmentosa HGNC:4922 Homo sapiens (human) 3098 HK1
  • PMID:25190649
  • RGD:7240710
DOID:4450 renal cell carcinoma HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
  • PMID:17899436
DOID:0050719 cerebral folate receptor alpha deficiency HGNC:3791 Homo sapiens (human) 2348 FOLR1
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus MGI:2153588 Mus musculus (house mouse) 140491 Ppp1r3a
  • MGI:6194238
  • PMID:12606498
DOID:8466 retinal degeneration WB:WBGene00000833 Caenorhabditis elegans 176437 cts-1
  • MGI:6194238
DOID:12858 Huntington's disease WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:2580 rhizomelic chondrodysplasia punctata HGNC:327 Homo sapiens (human) 8540 AGPS
  • PMID:9553082
DOID:10534 stomach cancer WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • MGI:6194238
  • PMID:24477042
  • PMID:24831885
  • PMID:26740948
DOID:3534 Lafora disease RGD:1589798 Rattus norvegicus (Norway rat) 690987 Gys1
  • MGI:6194238
DOID:12053 cryptococcosis RGD:1303058 Rattus norvegicus (Norway rat) 113901 Chia
  • PMID:18482441
DOID:684 hepatocellular carcinoma SGD:S000000257 Saccharomyces cerevisiae S288C 852342 YBR053C
  • MGI:6194238
DOID:11832 visual epilepsy HGNC:587 Homo sapiens (human) 328 APEX1
  • MGI:6194238

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

Acknowledgements

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