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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 68951 - 68975 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:12849 autistic disorder HGNC:5173 Homo sapiens (human) 3265 HRAS
  • PMID:8098541
DOID:8549 chronic ulcer of skin HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:8099861
DOID:4248 coronary stenosis RGD:2869 Rattus norvegicus (Norway rat) 25718 Igf1r
  • PMID:8102103
DOID:3008 invasive ductal carcinoma HGNC:8729 Homo sapiens (human) 5111 PCNA
  • PMID:8102204
DOID:1289 neurodegenerative disease WB:WBGene00003168 Caenorhabditis elegans 181728 mec-4
  • PMID:8107806
DOID:783 end stage renal disease HGNC:7941 Homo sapiens (human) 4880 NPPC
  • PMID:8117275
  • PMID:8743538
DOID:14115 toxic shock syndrome HGNC:7941 Homo sapiens (human) 4880 NPPC
  • PMID:8117275
DOID:8577 ulcerative colitis HGNC:6000 Homo sapiens (human) 3557 IL1RN
  • PMID:8119534
DOID:8805 intermediate coronary syndrome HGNC:775 Homo sapiens (human) 462 SERPINC1
  • PMID:8122184
DOID:627 severe combined immunodeficiency HGNC:12858 Homo sapiens (human) 7535 ZAP70
  • PMID:8124727
DOID:13141 uveitis RGD:2890 Rattus norvegicus (Norway rat) 24493 Il1a
  • PMID:8125721
DOID:2876 laryngeal squamous cell carcinoma HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:8138195
DOID:783 end stage renal disease HGNC:609 Homo sapiens (human) 344 APOC2
  • PMID:8139482
DOID:10923 sickle cell anemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:8140855
DOID:4608 common bile duct neoplasm HGNC:7514 Homo sapiens (human) 4585 MUC4
  • PMID:8143972
DOID:4608 common bile duct neoplasm HGNC:7515 Homo sapiens (human) 4586 MUC5AC
  • PMID:8143972
DOID:2583 agammaglobulinemia HGNC:1133 Homo sapiens (human) 695 BTK
  • PMID:8162018
DOID:9383 iridocyclitis HGNC:5991 Homo sapiens (human) 3552 IL1A
  • PMID:8162643
DOID:676 juvenile rheumatoid arthritis HGNC:5991 Homo sapiens (human) 3552 IL1A
  • PMID:8162643
DOID:13241 Behcet's disease HGNC:6018 Homo sapiens (human) 3569 IL6
  • PMID:8164212
DOID:1618 breast fibroadenoma HGNC:12787 Homo sapiens (human) 7477 WNT7B
  • PMID:8168088
DOID:1909 melanoma HGNC:6000 Homo sapiens (human) 3557 IL1RN
  • PMID:8168095
DOID:14115 toxic shock syndrome HGNC:1228 Homo sapiens (human) 710 SERPING1
  • PMID:8172580
DOID:0050424 familial adenomatous polyposis HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:8174133
DOID:10652 Alzheimer's disease HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:8179300

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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