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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 1251 - 1275 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▼ Evidence Code Names References
DOID:12351 alcoholic hepatitis RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • PMID:27939985
DOID:0110544 autosomal dominant nonsyndromic deafness 12 HGNC:11720 Homo sapiens (human) 7007 TECTA
  • MGI:6194238
  • RGD:7240710
DOID:162 cancer SGD:S000000233 Saccharomyces cerevisiae S288C 852317 CDS1
  • PMID:26354769
DOID:4362 cervical cancer HGNC:8907 Homo sapiens (human) 5238 PGM3
  • PMID:508567
DOID:1574 alcohol use disorder RGD:2379 Rattus norvegicus (Norway rat) 24267 Comt
  • MGI:6194238
DOID:7148 rheumatoid arthritis WB:WBGene00000503 Caenorhabditis elegans 180628 cht-1
  • MGI:6194238
DOID:4988 alcoholic pancreatitis WB:WBGene00018206 Caenorhabditis elegans 185500 ugt-61
  • MGI:6194238
DOID:0111063 hyperphosphatemic familial tumoral calcinosis HGNC:4125 Homo sapiens (human) 2591 GALNT3
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:29595 Homo sapiens (human) 130120 REG3G
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:11009 Homo sapiens (human) 6517 SLC2A4
  • MGI:6194238
  • PMID:1918382
DOID:4977 lymphedema RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • MGI:6194238
DOID:783 end stage renal disease HGNC:11178 Homo sapiens (human) 8435 SOAT2
  • MGI:6194238
DOID:783 end stage renal disease HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:9294834
DOID:0050560 Walker-Warburg syndrome Xenbase:XB-GENE-1006906 Xenopus tropicalis (tropical clawed frog) 100490100 pomt2
  • MGI:6194238
DOID:8947 diabetic retinopathy MGI:87986 Mus musculus (house mouse) 11651 Akt1
  • MGI:6194238
DOID:0050589 inflammatory bowel disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:0070459 hereditary spastic paraplegia 90A HGNC:20361 Homo sapiens (human) 171546 SPTSSA
  • RGD:7240710
DOID:0080558 congenital disorder of glycosylation If RGD:1307699 Rattus norvegicus (Norway rat) 303244 Mpdu1
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:17878891
  • PMID:27218147
DOID:0050474 Netherton syndrome HGNC:4177 Homo sapiens (human) 2629 GBA1
  • PMID:16601670
DOID:5744 ovary serous adenocarcinoma MGI:98834 Mus musculus (house mouse) 22059 Trp53
  • MGI:6194238
DOID:1612 breast cancer MGI:1929282 Mus musculus (house mouse) 56351 Ptges3
  • MGI:6194238
DOID:10763 hypertension HGNC:6623 Homo sapiens (human) 9388 LIPG
  • MGI:6194238
DOID:1591 renovascular hypertension RGD:2645 Rattus norvegicus (Norway rat) 24377 G6pd
  • PMID:22684021
DOID:2747 glycogen storage disease HGNC:8877 Homo sapiens (human) 5213 PFKM
  • MGI:6194238

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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