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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 70926 - 70950 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10976 membranous glomerulonephritis HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • MGI:6194238
DOID:8634 prostate carcinoma in situ HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • PMID:18691549
DOID:8991 cervix uteri carcinoma in situ HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • PMID:18301453
DOID:3829 pituitary adenoma HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • MGI:6194238
DOID:9669 senile cataract HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • PMID:21501079
DOID:4450 renal cell carcinoma HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • PMID:17924468
  • PMID:18425369
  • PMID:18495610
DOID:0080137 multiple endocrine neoplasia type 4 HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • RGD:7240710
DOID:1686 glaucoma HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • MGI:6194238
DOID:1324 lung cancer HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • MGI:6194238
DOID:6432 pulmonary hypertension HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • MGI:6194238
DOID:0050771 pheochromocytoma HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • MGI:6194238
DOID:9970 obesity HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • MGI:6194238
DOID:3125 multiple endocrine neoplasia HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • MGI:6194238
DOID:11054 urinary bladder cancer HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • PMID:18334837
DOID:5844 myocardial infarction HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • MGI:6194238
DOID:83 cataract HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • MGI:6194238
DOID:0050908 myelodysplastic syndrome HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • PMID:9171997
DOID:3021 acute kidney failure HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • MGI:6194238
DOID:4448 macular degeneration HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • PMID:20054800
DOID:0050773 paraganglioma HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • MGI:6194238
DOID:2154 nephroblastoma HGNC:1785 Homo sapiens (human) 1027 CDKN1B
  • PMID:14760081
DOID:12347 osteogenesis imperfecta MGI:2143230 Mus musculus (house mouse) 102693 Phldb1
  • MGI:6194238
DOID:9256 colorectal cancer HGNC:9845 Homo sapiens (human) 10268 RAMP3
  • PMID:21839130
DOID:6432 pulmonary hypertension HGNC:9844 Homo sapiens (human) 10266 RAMP2
  • MGI:6194238
DOID:11394 adult respiratory distress syndrome HGNC:9844 Homo sapiens (human) 10266 RAMP2
  • MGI:6194238

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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