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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 10251 - 10275 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:11650 bronchopulmonary dysplasia RGD:3889 Rattus norvegicus (Norway rat) 24842 Tp53
  • PMID:26431790
DOID:219 colon cancer HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:21868509
DOID:10534 stomach cancer HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:29408335
  • PMID:32106377
DOID:635 acquired immunodeficiency syndrome HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:8548330
DOID:1206 Rett syndrome HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:18710461
DOID:0080600 COVID-19 HGNC:10718 Homo sapiens (human) 6401 SELE
  • PMID:32458111
DOID:7998 hyperthyroidism RGD:620925 Rattus norvegicus (Norway rat) 83516 Ppargc1a
  • PMID:18669938
DOID:3908 lung non-small cell carcinoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:20564116
DOID:0060074 ductal carcinoma in situ HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:17119686
DOID:11247 disseminated intravascular coagulation HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:16518755
DOID:0080379 nephrotic syndrome type 2 HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:17999093
DOID:11981 morbid obesity HGNC:13345 Homo sapiens (human) 23175 LPIN1
  • PMID:17563064
DOID:10320 asbestosis HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:20514434
DOID:783 end stage renal disease HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:20729266
DOID:0060704 lymphoproliferative syndrome HGNC:18788 Homo sapiens (human) 22914 KLRK1
  • PMID:22105417
DOID:8947 diabetic retinopathy HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:19237221
DOID:1485 cystic fibrosis HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:18353734
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:2605 Homo sapiens (human) 1593 CYP27A1
  • PMID:28774887
DOID:3070 high grade glioma RGD:620103 Rattus norvegicus (Norway rat) 64639 Bad
  • PMID:16944316
DOID:2316 brain ischemia HGNC:9604 Homo sapiens (human) 5742 PTGS1
  • PMID:10867793
DOID:9352 type 2 diabetes mellitus HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:18619052
DOID:2377 multiple sclerosis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:18644848
DOID:10652 Alzheimer's disease HGNC:389 Homo sapiens (human) 8574 AKR7A2
  • PMID:11597610
DOID:12930 dilated cardiomyopathy HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:26893848
DOID:0060669 cerebral cavernous malformation HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:19061355

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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