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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 October 9, 2024
Displaying entries 69601 - 69625 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:11981 morbid obesity RGD:3057 Rattus norvegicus (Norway rat) 25635 Mc4r
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:5244 Homo sapiens (human) 3313 HSPA9
  • MGI:6194238
  • PMID:16565515
  • PMID:18219256
  • PMID:19657588
  • PMID:20817635
DOID:2671 transitional cell carcinoma HGNC:1383 Homo sapiens (human) 768 CA9
  • PMID:15069539
DOID:10763 hypertension HGNC:7978 Homo sapiens (human) 2908 NR3C1
  • MGI:6194238
DOID:11400 pyelonephritis ZFIN:ZDB-GENE-030131-1826 Danio rerio (zebrafish) 565980 ace
  • MGI:6194238
DOID:0080957 primary hypoalphalipoproteinemia 1 MGI:99607 Mus musculus (house mouse) 11303 Abca1
  • MGI:6194238
DOID:9065 leishmaniasis MGI:96285 Mus musculus (house mouse) 15567 Slc6a4
  • MGI:6194238
DOID:5844 myocardial infarction MGI:891982 Mus musculus (house mouse) 16615 Klk1b16
  • MGI:6194238
DOID:0110165 Charcot-Marie-Tooth disease type 2E HGNC:7739 Homo sapiens (human) 4747 NEFL
  • MGI:6194238
  • RGD:7240710
DOID:1824 status epilepticus HGNC:3942 Homo sapiens (human) 2475 MTOR
  • MGI:6194238
DOID:3652 Leigh disease HGNC:11180 Homo sapiens (human) 6648 SOD2
  • MGI:6194238
DOID:4481 allergic rhinitis RGD:3644 Rattus norvegicus (Norway rat) 29397 Ccl11
  • PMID:23089405
DOID:0060558 lethal congenital contracture syndrome MGI:1916151 Mus musculus (house mouse) 215798 Adgrg6
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I RGD:1305468 Rattus norvegicus (Norway rat) 293129 Alg8
  • MGI:6194238
DOID:8893 psoriasis HGNC:4177 Homo sapiens (human) 2629 GBA1
  • PMID:15610510
DOID:1312 focal segmental glomerulosclerosis RGD:2072 Rattus norvegicus (Norway rat) 24182 Agtr2
  • PMID:21357516
DOID:9778 irritable bowel syndrome HGNC:3393 Homo sapiens (human) 2048 EPHB2
  • MGI:6194238
DOID:0050700 cardiomyopathy HGNC:6206 Homo sapiens (human) 3727 JUND
  • PMID:30629164
DOID:0080855 Parkinsonism MGI:98735 Mus musculus (house mouse) 21823 Th
  • MGI:6194238
DOID:0070517 retinal macular dystrophy 2 HGNC:9454 Homo sapiens (human) 8842 PROM1
  • RGD:7240710
DOID:1826 epilepsy HGNC:11444 Homo sapiens (human) 6812 STXBP1
  • MGI:6194238
DOID:5082 liver cirrhosis FB:FBgn0011828 Drosophila melanogaster (fruit fly) 38326 Pxn
  • MGI:6194238
DOID:12858 Huntington's disease HGNC:14929 Homo sapiens (human) 23411 SIRT1
  • PMID:18538940
  • PMID:9949199
DOID:11832 visual epilepsy HGNC:12828 Homo sapiens (human) 7515 XRCC1
  • MGI:6194238
DOID:9952 acute lymphoblastic leukemia HGNC:2348 Homo sapiens (human) 1387 CREBBP
  • PMID:25917266

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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: December 9, 2024