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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 71376 - 71400 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:0060001 withdrawal disorder RGD:61800 Rattus norvegicus (Norway rat) 29595 Htr2a
  • MGI:6194238
  • PMID:12398913
  • PMID:18801381
  • PMID:26031442
DOID:10283 prostate cancer HGNC:644 Homo sapiens (human) 367 AR
  • MGI:6194238
  • PMID:12394768
  • PMID:15479493
  • PMID:17049844
  • PMID:18158066
DOID:0090117 thiamine-responsive megaloblastic anemia syndrome MGI:1928761 Mus musculus (house mouse) 116914 Slc19a2
  • MGI:6194238
  • PMID:12393806
  • PMID:14567973
DOID:5844 myocardial infarction HGNC:9053 Homo sapiens (human) 5329 PLAUR
  • MGI:6194238
  • PMID:12393744
DOID:10652 Alzheimer's disease HGNC:7873 Homo sapiens (human) 4843 NOS2
  • MGI:6194238
  • PMID:12384247
DOID:1064 cystinosis MGI:1932872 Mus musculus (house mouse) 83429 Ctns
  • MGI:6194238
  • PMID:12370309
DOID:0050560 Walker-Warburg syndrome HGNC:9202 Homo sapiens (human) 10585 POMT1
  • MGI:6194238
  • PMID:12369018
  • PMID:15637732
  • PMID:16575835
DOID:0090003 agenesis of the corpus callosum with peripheral neuropathy MGI:2135960 Mus musculus (house mouse) 107723 Slc12a6
  • MGI:6194238
  • PMID:12368912
  • PMID:14532115
  • PMID:22423107
DOID:12930 dilated cardiomyopathy HGNC:2928 Homo sapiens (human) 1756 DMD
  • MGI:6194238
  • PMID:12359139
  • PMID:19194174
  • PMID:20373002
DOID:0050868 hepatocellular adenoma HGNC:11621 Homo sapiens (human) 6927 HNF1A
  • MGI:6194238
  • PMID:12355088
  • PMID:14598263
  • PMID:17663417
DOID:9352 type 2 diabetes mellitus HGNC:1667 Homo sapiens (human) 952 CD38
  • MGI:6194238
  • PMID:12242463
  • PMID:9754820
DOID:0050676 Birt-Hogg-Dube syndrome HGNC:27310 Homo sapiens (human) 201163 FLCN
  • MGI:6194238
  • PMID:12204536
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
  • PMID:12200370
  • PMID:16025836
  • PMID:8814351
DOID:11726 Emery-Dreifuss muscular dystrophy HGNC:6636 Homo sapiens (human) 4000 LMNA
  • MGI:6194238
  • PMID:12196663
DOID:0050754 ataxia with oculomotor apraxia type 1 HGNC:15984 Homo sapiens (human) 54840 APTX
  • MGI:6194238
  • PMID:12196655
  • PMID:17572444
  • PMID:21465257
  • RGD:7240710
DOID:12387 nephrogenic diabetes insipidus HGNC:634 Homo sapiens (human) 359 AQP2
  • MGI:6194238
  • PMID:12191971
  • PMID:16845277
  • PMID:18653713
  • PMID:19147915
  • PMID:19293543
  • PMID:19458121
  • PMID:19461158
  • PMID:19585583
  • PMID:19701945
DOID:3144 cutis laxa HGNC:3602 Homo sapiens (human) 10516 FBLN5
  • MGI:6194238
  • PMID:12189163
DOID:13269 hereditary coproporphyria HGNC:2321 Homo sapiens (human) 1371 CPOX
  • MGI:6194238
  • PMID:12181641
  • PMID:15896662
  • PMID:30385147
  • PMID:9888388
  • RGD:7240710
DOID:2226 myeloproliferative neoplasm HGNC:8804 Homo sapiens (human) 5159 PDGFRB
  • MGI:6194238
  • PMID:12181402
DOID:0050852 limb ischemia HGNC:7876 Homo sapiens (human) 4846 NOS3
  • MGI:6194238
  • PMID:12171788
DOID:874 bacterial pneumonia RGD:621700 Rattus norvegicus (Norway rat) 192155 Sftpb
  • MGI:6194238
  • PMID:12169586
DOID:874 bacterial pneumonia RGD:3667 Rattus norvegicus (Norway rat) 25350 Sftpd
  • MGI:6194238
  • PMID:12169586
DOID:9655 oral mucosa leukoplakia RGD:3889 Rattus norvegicus (Norway rat) 24842 Tp53
  • MGI:6194238
  • PMID:12167434
DOID:5844 myocardial infarction HGNC:10721 Homo sapiens (human) 6403 SELP
  • MGI:6194238
  • PMID:12165563
  • PMID:17391113
  • PMID:21162967
DOID:0090114 Sorsby's fundus dystrophy MGI:98754 Mus musculus (house mouse) 21859 Timp3
  • MGI:6194238
  • PMID:12147610

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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: December 9, 2024