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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 69326 - 69350 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:1799 islet cell tumor HGNC:886 Homo sapiens (human) 546 ATRX
  • PMID:24148618
DOID:0112125 alpha-thalassemia myelodysplasia syndrome HGNC:886 Homo sapiens (human) 546 ATRX
  • RGD:7240710
DOID:0080982 X-linked mental retardation-hypotonic facies syndrome-1 HGNC:886 Homo sapiens (human) 546 ATRX
  • PMID:10632111
  • PMID:26997013
  • PMID:8630485
  • RGD:7240710
DOID:3910 lung adenocarcinoma HGNC:886 Homo sapiens (human) 546 ATRX
  • PMID:31374064
DOID:3907 lung squamous cell carcinoma HGNC:886 Homo sapiens (human) 546 ATRX
  • PMID:31374064
DOID:3070 high grade glioma HGNC:886 Homo sapiens (human) 546 ATRX
  • PMID:23104868
DOID:3069 malignant astrocytoma HGNC:886 Homo sapiens (human) 546 ATRX
  • PMID:23765250
  • PMID:24810474
DOID:1909 melanoma HGNC:886 Homo sapiens (human) 546 ATRX
  • PMID:24468746
DOID:3068 glioblastoma HGNC:886 Homo sapiens (human) 546 ATRX
  • PMID:27478330
DOID:0050569 Seckel syndrome HGNC:33499 Homo sapiens (human) 84126 ATRIP
  • MGI:6194238
DOID:12704 ataxia telangiectasia HGNC:882 Homo sapiens (human) 545 ATR
  • MGI:6194238
DOID:219 colon cancer HGNC:882 Homo sapiens (human) 545 ATR
  • MGI:6194238
  • PMID:17879369
DOID:10652 Alzheimer's disease HGNC:882 Homo sapiens (human) 545 ATR
  • PMID:23861893
DOID:1612 breast cancer HGNC:882 Homo sapiens (human) 545 ATR
  • MGI:6194238
DOID:0080202 adenoid cystic carcinoma HGNC:882 Homo sapiens (human) 545 ATR
  • PMID:32001675
DOID:1380 endometrial cancer HGNC:882 Homo sapiens (human) 545 ATR
  • MGI:6194238
DOID:0070007 Seckel syndrome 1 HGNC:882 Homo sapiens (human) 545 ATR
  • PMID:12640452
  • RGD:7240710
DOID:0060060 non-Hodgkin lymphoma HGNC:882 Homo sapiens (human) 545 ATR
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:882 Homo sapiens (human) 545 ATR
  • PMID:18381943
DOID:9261 nasopharynx carcinoma HGNC:882 Homo sapiens (human) 545 ATR
  • PMID:28820634
DOID:1324 lung cancer HGNC:882 Homo sapiens (human) 545 ATR
  • PMID:25010037
DOID:0050569 Seckel syndrome HGNC:882 Homo sapiens (human) 545 ATR
  • MGI:6194238
DOID:0050768 mitochondrial complex V (ATP synthase) deficiency nuclear type 1 HGNC:18802 Homo sapiens (human) 91647 ATPAF2
  • MGI:6194238
  • RGD:7240710
DOID:686 liver carcinoma HGNC:870 Homo sapiens (human) 540 ATP7B
  • MGI:6194238
DOID:2697 renal adenoma HGNC:870 Homo sapiens (human) 540 ATP7B
  • 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