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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 69376 - 69400 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:8778 Crohn's disease HGNC:3685 Homo sapiens (human) 2252 FGF7
  • PMID:9358773
DOID:8577 ulcerative colitis HGNC:3685 Homo sapiens (human) 2252 FGF7
  • PMID:9358773
DOID:10003 sensorineural hearing loss HGNC:2876 Homo sapiens (human) 1729 DIAPH1
  • PMID:9360932
DOID:10763 hypertension HGNC:9075 Homo sapiens (human) 5345 SERPINF2
  • PMID:9361364
DOID:9675 pulmonary emphysema MGI:1101771 Mus musculus (house mouse) 16591 Kl
  • PMID:9363890
DOID:11054 urinary bladder cancer HGNC:11772 Homo sapiens (human) 7046 TGFBR1
  • PMID:9363992
DOID:6419 tetralogy of Fallot MGI:103248 Mus musculus (house mouse) 13619 Phc1
  • PMID:9367423
DOID:2671 transitional cell carcinoma HGNC:11763 Homo sapiens (human) 7037 TFRC
  • PMID:9373912
DOID:418 systemic scleroderma HGNC:3535 Homo sapiens (human) 2147 F2
  • PMID:9374919
DOID:5082 liver cirrhosis HGNC:8931 Homo sapiens (human) 5261 PHKG2
  • PMID:9384616
DOID:9252 amino acid metabolic disorder HGNC:8653 Homo sapiens (human) 5095 PCCA
  • PMID:9385377
DOID:0050458 juvenile myelomonocytic leukemia HGNC:2434 Homo sapiens (human) 1437 CSF2
  • PMID:9389708
DOID:3310 atopic dermatitis HGNC:6015 Homo sapiens (human) 3566 IL4R
  • PMID:9392697
DOID:0080199 colorectal carcinoma HGNC:7329 Homo sapiens (human) 2956 MSH6
  • PMID:9401011
DOID:10652 Alzheimer's disease HGNC:2961 Homo sapiens (human) 1778 DYNC1H1
  • PMID:9402150
DOID:0081267 graft-versus-host disease HGNC:11920 Homo sapiens (human) 355 FAS
  • PMID:9404931
DOID:8432 polycythemia RGD:3249 Rattus norvegicus (Norway rat) 24617 Serpine1
  • PMID:9405184
DOID:1612 breast cancer HGNC:6134 Homo sapiens (human) 3672 ITGA1
  • PMID:9408292
DOID:2581 chondrodysplasia punctata HGNC:719 Homo sapiens (human) 415 ARSL
  • PMID:9409863
DOID:0060903 thrombosis HGNC:5181 Homo sapiens (human) 3273 HRG
  • PMID:9414276
DOID:0111151 Prinzmetal angina HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:9415270
DOID:3525 middle cerebral artery infarction RGD:3704 Rattus norvegicus (Norway rat) 24778 Slc2a1
  • PMID:9419067
DOID:898 autosomal dominant polycystic kidney disease MGI:97250 Mus musculus (house mouse) 17869 Myc
  • PMID:9422539
DOID:12554 hemolytic-uremic syndrome HGNC:3535 Homo sapiens (human) 2147 F2
  • PMID:9423793
DOID:13359 Ehlers-Danlos syndrome HGNC:2210 Homo sapiens (human) 1290 COL5A2
  • PMID:9425231

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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