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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 71426 - 71450 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3007 breast ductal carcinoma HGNC:971 Homo sapiens (human) 9564 BCAR1
  • PMID:11605729
DOID:1612 breast cancer HGNC:971 Homo sapiens (human) 9564 BCAR1
  • PMID:15448007
DOID:0050742 nicotine dependence HGNC:4507 Homo sapiens (human) 9568 GABBR2
  • PMID:19763258
  • RGD:7240710
DOID:0080291 developmental and epileptic encephalopathy 59 HGNC:4507 Homo sapiens (human) 9568 GABBR2
  • RGD:7240710
DOID:1574 alcohol use disorder HGNC:4507 Homo sapiens (human) 9568 GABBR2
  • PMID:28118741
DOID:0110984 Joubert syndrome 15 HGNC:12370 Homo sapiens (human) 95681 CEP41
  • RGD:7240710
DOID:14018 alcoholic liver cirrhosis HGNC:7962 Homo sapiens (human) 9572 NR1D1
  • PMID:24497272
DOID:0112313 brain small vessel disease HGNC:7962 Homo sapiens (human) 9572 NR1D1
  • PMID:23083441
DOID:10762 portal hypertension HGNC:7962 Homo sapiens (human) 9572 NR1D1
  • MGI:6194238
DOID:1459 hypothyroidism HGNC:7962 Homo sapiens (human) 9572 NR1D1
  • MGI:6194238
DOID:7998 hyperthyroidism HGNC:7962 Homo sapiens (human) 9572 NR1D1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:7962 Homo sapiens (human) 9572 NR1D1
  • MGI:6194238
DOID:0060838 isolated microphthalmia 7 HGNC:4218 Homo sapiens (human) 9573 GDF3
  • RGD:7240710
DOID:0080591 Klippel-Feil syndrome 3 HGNC:4218 Homo sapiens (human) 9573 GDF3
  • RGD:7240710
DOID:535 sleep disorder HGNC:2082 Homo sapiens (human) 9575 CLOCK
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:2082 Homo sapiens (human) 9575 CLOCK
  • PMID:20554694
DOID:9351 diabetes mellitus HGNC:2082 Homo sapiens (human) 9575 CLOCK
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:2082 Homo sapiens (human) 9575 CLOCK
  • PMID:23357097
  • PMID:23781009
  • PMID:23912676
DOID:3312 bipolar disorder HGNC:2082 Homo sapiens (human) 9575 CLOCK
  • MGI:6194238
DOID:13580 cholestasis HGNC:2082 Homo sapiens (human) 9575 CLOCK
  • MGI:6194238
DOID:10763 hypertension HGNC:2082 Homo sapiens (human) 9575 CLOCK
  • MGI:6194238
DOID:0060669 cerebral cavernous malformation HGNC:1738 Homo sapiens (human) 9578 CDC42BPB
  • MGI:6194238
DOID:14227 azoospermia HGNC:1738 Homo sapiens (human) 9578 CDC42BPB
  • MGI:6194238
DOID:10976 membranous glomerulonephritis HGNC:11919 Homo sapiens (human) 958 CD40
  • MGI:6194238
DOID:8778 Crohn's disease HGNC:11919 Homo sapiens (human) 958 CD40
  • PMID:20133813
  • PMID:20634952

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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