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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 July 29, 2024
Displaying entries 901 - 925 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:13580 cholestasis RGD:3387 Rattus norvegicus (Norway rat) 65248 Prkaa1
  • PMID:27090119
DOID:0070004 myeloid neoplasm HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:27077777
DOID:2559 opiate dependence HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:27061230
  • PMID:32407152
DOID:2871 endometrial carcinoma HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • PMID:27050373
DOID:10534 stomach cancer HGNC:8975 Homo sapiens (human) 5290 PIK3CA
  • PMID:26980034
  • PMID:30747208
  • PMID:30952761
  • RGD:7240710
DOID:0050850 diabetic encephalopathy RGD:70982 Rattus norvegicus (Norway rat) 84027 Gsk3b
  • PMID:26970304
DOID:264 hemangiopericytoma HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:26951238
DOID:3742 bladder squamous cell carcinoma HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:26916953
DOID:9256 colorectal cancer HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:26913609
DOID:0050083 Keshan disease HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:26893848
DOID:0050083 Keshan disease HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:26893848
DOID:12930 dilated cardiomyopathy HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:26893848
DOID:12930 dilated cardiomyopathy HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:26893848
DOID:684 hepatocellular carcinoma HGNC:5988 Homo sapiens (human) 8809 IL18R1
  • PMID:26893476
DOID:684 hepatocellular carcinoma HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:26890368
DOID:10652 Alzheimer's disease RGD:61800 Rattus norvegicus (Norway rat) 29595 Htr2a
  • PMID:26889223
DOID:635 acquired immunodeficiency syndrome HGNC:1119 Homo sapiens (human) 684 BST2
  • PMID:26885809
DOID:0050073 invasive aspergillosis HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:26861072
DOID:3908 lung non-small cell carcinoma HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:26842877
  • PMID:29228584
DOID:3748 esophagus squamous cell carcinoma HGNC:1119 Homo sapiens (human) 684 BST2
  • PMID:26832883
DOID:10534 stomach cancer HGNC:1119 Homo sapiens (human) 684 BST2
  • PMID:26832883
DOID:0050827 rheumatic heart disease RGD:2661 Rattus norvegicus (Norway rat) 24383 Gapdh
  • PMID:26823728
DOID:1612 breast cancer HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:26799162
DOID:0080491 cerebral cavernous malformation 1 HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • PMID:26795600
DOID:10579 leukodystrophy SGD:S000000387 Saccharomyces cerevisiae S288C 852481 YPC1
  • PMID:26792856

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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: August 19, 2024