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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 70201 - 70225 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:2841 asthma HGNC:10632 Homo sapiens (human) 6352 CCL5
  • MGI:6194238
  • PMID:20430255
DOID:224 transient cerebral ischemia HGNC:6000 Homo sapiens (human) 3557 IL1RN
  • MGI:6194238
  • PMID:20412072
DOID:10763 hypertension RGD:3932 Rattus norvegicus (Norway rat) 54315 Ucp2
  • MGI:6194238
  • PMID:20404217
DOID:10763 hypertension HGNC:285 Homo sapiens (human) 153 ADRB1
  • MGI:6194238
  • PMID:20398560
DOID:1826 epilepsy MGI:96654 Mus musculus (house mouse) 16485 Kcna1
  • MGI:6194238
  • PMID:20392939
DOID:9352 type 2 diabetes mellitus RGD:2857 Rattus norvegicus (Norway rat) 25464 Icam1
  • MGI:6194238
  • PMID:20388520
DOID:784 chronic kidney disease HGNC:11019 Homo sapiens (human) 6569 SLC34A1
  • MGI:6194238
  • PMID:20383146
DOID:12365 malaria HGNC:9020 Homo sapiens (human) 5313 PKLR
  • MGI:6194238
  • PMID:20377593
DOID:0110336 osteogenesis imperfecta type 8 MGI:1888921 Mus musculus (house mouse) 56401 P3h1
  • MGI:6194238
  • PMID:20363744
DOID:4483 rhinitis HGNC:5973 Homo sapiens (human) 3596 IL13
  • MGI:6194238
  • PMID:20358028
  • PMID:20484924
DOID:5844 myocardial infarction RGD:2081 Rattus norvegicus (Norway rat) 24185 Akt1
  • MGI:6194238
  • PMID:20352476
DOID:12259 hemophilia B HGNC:3551 Homo sapiens (human) 2158 F9
  • MGI:6194238
  • PMID:20351275
  • PMID:2041805
  • PMID:21122306
  • PMID:2714791
  • PMID:2752145
  • RGD:7240710
DOID:850 lung disease HGNC:7176 Homo sapiens (human) 4318 MMP9
  • MGI:6194238
  • PMID:20335295
DOID:1184 nephrotic syndrome WB:WBGene00006365 Caenorhabditis elegans 180555 syg-1
  • MGI:6194238
  • PMID:20233749
DOID:1184 nephrotic syndrome WB:WBGene00007750 Caenorhabditis elegans 181561 syg-2
  • MGI:6194238
  • PMID:20233749
DOID:2841 asthma RGD:2886 Rattus norvegicus (Norway rat) 25325 Il10
  • MGI:6194238
  • PMID:20230687
  • PMID:20560982
DOID:13949 interstitial cystitis HGNC:7808 Homo sapiens (human) 4803 NGF
  • MGI:6194238
  • PMID:20227820
  • PMID:23028581
DOID:9269 maple syrup urine disease HGNC:987 Homo sapiens (human) 594 BCKDHB
  • MGI:6194238
  • PMID:2022752
  • RGD:7240710
DOID:1596 depressive disorder HGNC:1033 Homo sapiens (human) 627 BDNF
  • MGI:6194238
  • PMID:20227453
DOID:2987 familial mediterranean fever HGNC:6998 Homo sapiens (human) 4210 MEFV
  • MGI:6194238
  • PMID:20217092
  • PMID:23038988
  • PMID:23862117
  • RGD:7240710
DOID:2048 autoimmune hepatitis HGNC:4606 Homo sapiens (human) 2923 PDIA3
  • MGI:6194238
  • PMID:20208391
DOID:2841 asthma HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
  • PMID:20205697
DOID:0110033 autosomal recessive Alport syndrome MGI:104688 Mus musculus (house mouse) 12828 Col4a3
  • MGI:6194238
  • PMID:20197625
  • PMID:24262794
  • PMID:8947561
  • PMID:8956999
  • PMID:9682811
DOID:3770 pulmonary fibrosis HGNC:5981 Homo sapiens (human) 3605 IL17A
  • MGI:6194238
  • PMID:20176803
DOID:0111196 X-linked distal spinal muscular atrophy 3 HGNC:869 Homo sapiens (human) 538 ATP7A
  • MGI:6194238
  • PMID:20170900
  • RGD:7240710

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Last updated: December 9, 2024