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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 70601 - 70625 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:0060041 autism spectrum disorder MGI:2444609 Mus musculus (house mouse) 245537 Nlgn3
  • MGI:6194238
  • PMID:17823315
  • PMID:19243448
  • PMID:22983708
  • PMID:24995986
DOID:3021 acute kidney failure HGNC:11784 Homo sapiens (human) 7056 THBD
  • MGI:6194238
  • PMID:17804460
DOID:9970 obesity HGNC:10618 Homo sapiens (human) 6347 CCL2
  • MGI:6194238
  • PMID:17803693
DOID:1793 pancreatic cancer RGD:3849 Rattus norvegicus (Norway rat) 24827 Tgfa
  • MGI:6194238
  • PMID:17785207
DOID:9352 type 2 diabetes mellitus RGD:62387 Rattus norvegicus (Norway rat) 29535 Pdx1
  • MGI:6194238
  • PMID:17764693
DOID:11054 urinary bladder cancer HGNC:1748 Homo sapiens (human) 999 CDH1
  • MGI:6194238
  • PMID:17760743
DOID:0080050 acromesomelic dysplasia, Maroteaux type MGI:97372 Mus musculus (house mouse) 230103 Npr2
  • MGI:6194238
  • PMID:17728275
DOID:9744 type 1 diabetes mellitus MGI:1346060 Mus musculus (house mouse) 24088 Tlr2
  • MGI:6194238
  • PMID:17707128
DOID:3650 lactic acidosis HGNC:9725 Homo sapiens (human) 5836 PYGL
  • MGI:6194238
  • PMID:17705025
DOID:3650 lactic acidosis RGD:620687 Rattus norvegicus (Norway rat) 64035 Pygl
  • MGI:6194238
  • PMID:17705025
DOID:2754 glycogen storage disease VI RGD:620687 Rattus norvegicus (Norway rat) 64035 Pygl
  • MGI:6194238
  • PMID:17705025
  • PMID:21646031
DOID:2754 glycogen storage disease VI HGNC:9725 Homo sapiens (human) 5836 PYGL
  • MGI:6194238
  • PMID:17705025
  • PMID:21646031
  • RGD:7240710
DOID:2841 asthma HGNC:7515 Homo sapiens (human) 4586 MUC5AC
  • MGI:6194238
  • PMID:17698377
DOID:3261 hyper IgE recurrent infection syndrome 1 HGNC:11364 Homo sapiens (human) 6774 STAT3
  • MGI:6194238
  • PMID:17676033
  • RGD:7240710
DOID:9206 Barrett's esophagus RGD:620349 Rattus norvegicus (Norway rat) 29527 Ptgs2
  • MGI:6194238
  • PMID:17675820
DOID:2841 asthma HGNC:11766 Homo sapiens (human) 7040 TGFB1
  • MGI:6194238
  • PMID:17673695
  • PMID:18711258
  • PMID:19046298
  • PMID:19096005
  • PMID:19136038
  • PMID:19222424
  • PMID:19317336
  • PMID:19533439
DOID:0060745 Doyne honeycomb retinal dystrophy MGI:1339998 Mus musculus (house mouse) 216616 Efemp1
  • MGI:6194238
  • PMID:17664227
  • PMID:17666404
DOID:12714 Ellis-Van Creveld syndrome MGI:1890596 Mus musculus (house mouse) 59056 Evc
  • MGI:6194238
  • PMID:17660199
DOID:8398 osteoarthritis MGI:95688 Mus musculus (house mouse) 14563 Gdf5
  • MGI:6194238
  • PMID:17656374
DOID:10763 hypertension HGNC:895 Homo sapiens (human) 552 AVPR1A
  • MGI:6194238
  • PMID:17653244
DOID:0110278 autosomal recessive limb-girdle muscular dystrophy type 2D HGNC:10805 Homo sapiens (human) 6442 SGCA
  • MGI:6194238
  • PMID:17653106
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:9052 Homo sapiens (human) 5328 PLAU
  • MGI:6194238
  • PMID:17653104
  • PMID:20518747
DOID:3083 chronic obstructive pulmonary disease RGD:3249 Rattus norvegicus (Norway rat) 24617 Serpine1
  • MGI:6194238
  • PMID:17651644
DOID:5844 myocardial infarction HGNC:7940 Homo sapiens (human) 4879 NPPB
  • MGI:6194238
  • PMID:17639095
DOID:3083 chronic obstructive pulmonary disease HGNC:7515 Homo sapiens (human) 4586 MUC5AC
  • MGI:6194238
  • PMID:17637221
  • PMID:19723147

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Last updated: December 9, 2024