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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 69701 - 69725 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:8398 osteoarthritis HGNC:5956 Homo sapiens (human) 3549 IHH
  • MGI:6194238
  • PMID:24786088
DOID:0050848 obstructive sleep apnea RGD:2493 Rattus norvegicus (Norway rat) 24310 Ace
  • MGI:6194238
  • PMID:24775918
DOID:0060041 autism spectrum disorder RGD:621119 Rattus norvegicus (Norway rat) 171297 Nlgn3
  • MGI:6194238
  • PMID:24773431
  • PMID:28958035
DOID:0060887 ossification of the posterior longitudinal ligament of spine MGI:97370 Mus musculus (house mouse) 18605 Enpp1
  • MGI:6194238
  • PMID:24770645
  • PMID:9359030
  • PMID:9662402
DOID:0050741 alcohol dependence HGNC:2345 Homo sapiens (human) 1385 CREB1
  • MGI:6194238
  • PMID:24704376
DOID:9976 heroin dependence HGNC:2345 Homo sapiens (human) 1385 CREB1
  • MGI:6194238
  • PMID:24704376
DOID:224 transient cerebral ischemia HGNC:3415 Homo sapiens (human) 2056 EPO
  • MGI:6194238
  • PMID:24702327
DOID:0080450 developmental and epileptic encephalopathy 17 MGI:95775 Mus musculus (house mouse) 14681 Gnao1
  • MGI:6194238
  • PMID:24700286
  • PMID:30682176
DOID:11758 iron deficiency anemia HGNC:4553 Homo sapiens (human) 2876 GPX1
  • MGI:6194238
  • PMID:24691014
DOID:14693 Clouston syndrome MGI:107588 Mus musculus (house mouse) 14623 Gjb6
  • MGI:6194238
  • PMID:24685692
DOID:10652 Alzheimer's disease HGNC:5466 Homo sapiens (human) 3481 IGF2
  • MGI:6194238
  • PMID:24685003
DOID:9352 type 2 diabetes mellitus RGD:69247 Rattus norvegicus (Norway rat) 83535 Kcnj11
  • MGI:6194238
  • PMID:24681897
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:11180 Homo sapiens (human) 6648 SOD2
  • MGI:6194238
  • PMID:24649902
DOID:0060473 Kabuki syndrome HGNC:7133 Homo sapiens (human) 8085 KMT2D
  • MGI:6194238
  • PMID:24633898
  • PMID:26300940
  • RGD:7240710
DOID:3261 hyper IgE recurrent infection syndrome 1 MGI:103038 Mus musculus (house mouse) 20848 Stat3
  • MGI:6194238
  • PMID:24632714
DOID:206 hereditary multiple exostoses ZFIN:ZDB-GENE-041124-3 Danio rerio (zebrafish) 493780 ext2
  • MGI:6194238
  • PMID:24628984
DOID:898 autosomal dominant polycystic kidney disease ZFIN:ZDB-GENE-040827-4 Danio rerio (zebrafish) 432387 pkd2
  • MGI:6194238
  • PMID:24627348
  • PMID:26432887
  • PMID:28769124
  • PMID:31183407
  • PMID:31330507
  • PMID:31919453
  • PMID:34551202
DOID:4481 allergic rhinitis RGD:2898 Rattus norvegicus (Norway rat) 287287 Il4
  • MGI:6194238
  • PMID:24620662
DOID:9352 type 2 diabetes mellitus RGD:69051 Rattus norvegicus (Norway rat) 59086 Tgfb1
  • MGI:6194238
  • PMID:24613393
DOID:0111862 congenital bilateral absence of vas deferens RGD:2332 Rattus norvegicus (Norway rat) 24255 Cftr
  • MGI:6194238
  • PMID:24608905
DOID:1485 cystic fibrosis RGD:2332 Rattus norvegicus (Norway rat) 24255 Cftr
  • MGI:6194238
  • PMID:24608905
  • PMID:31942562
DOID:684 hepatocellular carcinoma HGNC:7562 Homo sapiens (human) 4615 MYD88
  • MGI:6194238
  • PMID:24603331
  • PMID:26985932
  • PMID:28370778
  • PMID:29022910
  • PMID:32144747
DOID:0110864 congenital stationary night blindness 1F MGI:2685267 Mus musculus (house mouse) 242235 Lrit3
  • MGI:6194238
  • PMID:24598786
DOID:0050884 triosephosphate isomerase deficiency SGD:S000002457 Saccharomyces cerevisiae S288C 851620 TPI1
  • MGI:6194238
  • PMID:24598263
DOID:0050574 L-2-hydroxyglutaric aciduria HGNC:20499 Homo sapiens (human) 79944 L2HGDH
  • MGI:6194238
  • PMID:24573090
  • RGD:7240710

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Last updated: December 9, 2024