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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 8101 - 8125 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▼ Evidence Code Names References
DOID:3770 pulmonary fibrosis HGNC:5988 Homo sapiens (human) 8809 IL18R1
  • PMID:15308504
DOID:4988 alcoholic pancreatitis HGNC:12539 Homo sapiens (human) 54577 UGT1A7
  • PMID:12806614
DOID:3312 bipolar disorder HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:22137759
DOID:11949 Creutzfeldt-Jakob disease WB:WBGene00016207 Caenorhabditis elegans 183002 C29E4.10
  • MGI:6194238
DOID:0050861 colorectal adenocarcinoma MGI:1861437 Mus musculus (house mouse) 56637 Gsk3b
  • MGI:6194238
DOID:9870 galactosemia WB:WBGene00008132 Caenorhabditis elegans 173171 gale-1
  • MGI:6194238
  • PMID:25298520
DOID:0050524 maturity-onset diabetes of the young RGD:2916 Rattus norvegicus (Norway rat) 24506 Ins2
  • MGI:6194238
DOID:0080470 developmental and epileptic encephalopathy 36 RGD:1359416 Rattus norvegicus (Norway rat) 300284 Alg13l1
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I HGNC:37258 Homo sapiens (human) 644974 ALG1L2
  • MGI:6194238
DOID:10534 stomach cancer RGD:620045 Rattus norvegicus (Norway rat) 170841 Mutyh
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:92 Homo sapiens (human) 37 ACADVL
  • PMID:25260493
DOID:10534 stomach cancer HGNC:8729 Homo sapiens (human) 5111 PCNA
  • PMID:26432329
DOID:0080555 congenital disorder of glycosylation Ic Xenbase:XB-GENE-17342009 Xenopus laevis (African clawed frog) 446684 alg6.S
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome SGD:S000000021 Saccharomyces cerevisiae S288C 851210 PMT2
  • MGI:6194238
DOID:8893 psoriasis RGD:70997 Rattus norvegicus (Norway rat) 140868 Fabp5
  • MGI:6194238
DOID:684 hepatocellular carcinoma MGI:97503 Mus musculus (house mouse) 18538 Pcna
  • MGI:6194238
DOID:7998 hyperthyroidism FB:FBgn0032713 Drosophila melanogaster (fruit fly) 35138 Ugt36D1
  • MGI:6194238
DOID:2043 hepatitis B WB:WBGene00018206 Caenorhabditis elegans 185500 ugt-61
  • MGI:6194238
DOID:4947 cholangiocarcinoma FB:FBgn0027070 Drosophila melanogaster (fruit fly) 35139 Ugt36E1
  • MGI:6194238
DOID:12365 malaria FB:FBgn0267385 Drosophila melanogaster (fruit fly) 42620 Pyk
  • MGI:6194238
DOID:0050156 idiopathic pulmonary fibrosis HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:31874165
DOID:0080753 keratosis follicularis spinulosa decalvans HGNC:19980 Homo sapiens (human) 64841 GNPNAT1
  • MGI:6194238
DOID:2729 dyskeratosis congenita HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:491 Homo sapiens (human) 27329 ANGPTL3
  • MGI:6194238
DOID:13241 Behcet's disease RGD:3870 Rattus norvegicus (Norway rat) 29260 Tlr4
  • 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