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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 71251 - 71275 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:5962 Homo sapiens (human) 3586 IL10
  • MGI:6194238
  • PMID:12938145
  • PMID:20121766
DOID:14451 hyperkalemic periodic paralysis HGNC:10591 Homo sapiens (human) 6329 SCN4A
  • MGI:6194238
  • PMID:12933953
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus MGI:96572 Mus musculus (house mouse) 16333 Ins1
  • MGI:6194238
  • PMID:12925730
DOID:9744 type 1 diabetes mellitus MGI:96573 Mus musculus (house mouse) 16334 Ins2
  • MGI:6194238
  • PMID:12925730
  • PMID:22297672
  • PMID:9836515
DOID:2512 nevoid basal cell carcinoma syndrome HGNC:9585 Homo sapiens (human) 5727 PTCH1
  • MGI:6194238
  • PMID:12925203
  • PMID:15308259
  • PMID:19557015
  • PMID:21514272
DOID:4989 pancreatitis HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
  • PMID:12923961
DOID:10763 hypertension HGNC:9236 Homo sapiens (human) 5468 PPARG
  • MGI:6194238
  • PMID:12923396
  • PMID:18316027
DOID:9266 cystinuria MGI:1195264 Mus musculus (house mouse) 20532 Slc3a1
  • MGI:6194238
  • PMID:12923163
  • PMID:19484501
  • PMID:25048459
  • PMID:28165480
DOID:1094 attention deficit hyperactivity disorder HGNC:11049 Homo sapiens (human) 6531 SLC6A3
  • MGI:6194238
  • PMID:12915833
DOID:0080199 colorectal carcinoma RGD:2311 Rattus norvegicus (Norway rat) 25407 Cd59b
  • MGI:6194238
  • PMID:12909127
DOID:0080199 colorectal carcinoma HGNC:1689 Homo sapiens (human) 966 CD59
  • MGI:6194238
  • PMID:12909127
DOID:6000 congestive heart failure HGNC:7155 Homo sapiens (human) 4312 MMP1
  • MGI:6194238
  • PMID:12892382
DOID:3328 temporal lobe epilepsy HGNC:4845 Homo sapiens (human) 348980 HCN1
  • MGI:6194238
  • PMID:12890777
DOID:3328 temporal lobe epilepsy RGD:620688 Rattus norvegicus (Norway rat) 84390 Hcn1
  • MGI:6194238
  • PMID:12890777
  • PMID:21905079
DOID:0050644 arterial calcification of infancy HGNC:3356 Homo sapiens (human) 5167 ENPP1
  • MGI:6194238
  • PMID:12881724
  • PMID:15940697
  • PMID:20016754
  • RGD:7240710
DOID:0111113 nephronophthisis 2 HGNC:17870 Homo sapiens (human) 27130 INVS
  • MGI:6194238
  • PMID:12872123
  • RGD:7240710
DOID:0111114 nephronophthisis 3 HGNC:7907 Homo sapiens (human) 27031 NPHP3
  • MGI:6194238
  • PMID:12872122
  • RGD:7240710
DOID:1067 open-angle glaucoma HGNC:7610 Homo sapiens (human) 4653 MYOC
  • MGI:6194238
  • PMID:12860809
DOID:3393 coronary artery disease HGNC:613 Homo sapiens (human) 348 APOE
  • MGI:6194238
  • PMID:12860263
  • PMID:14563588
  • PMID:15059615
DOID:14330 Parkinson's disease HGNC:16369 Homo sapiens (human) 11315 PARK7
  • MGI:6194238
  • PMID:12851414
  • PMID:23766857
DOID:1682 congenital heart disease HGNC:4173 Homo sapiens (human) 2626 GATA4
  • MGI:6194238
  • PMID:12845333
DOID:9970 obesity HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
  • PMID:12843191
DOID:0050831 familial encephalopathy with neuroserpin inclusion bodies MGI:1194506 Mus musculus (house mouse) 20713 Serpini1
  • MGI:6194238
  • PMID:12837630
DOID:10933 obsessive-compulsive disorder HGNC:1033 Homo sapiens (human) 627 BDNF
  • MGI:6194238
  • PMID:12836135
DOID:784 chronic kidney disease HGNC:336 Homo sapiens (human) 185 AGTR1
  • MGI:6194238
  • PMID:12832734

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Last updated: December 9, 2024