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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 6176 - 6200 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:2256 osteochondrodysplasia HGNC:2218 Homo sapiens (human) 1298 COL9A2
  • PMID:8528240
DOID:4928 intrahepatic cholangiocarcinoma HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:24796583
DOID:2355 anemia HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • PMID:18974656
DOID:783 end stage renal disease HGNC:12518 Homo sapiens (human) 7351 UCP2
  • PMID:18242170
  • PMID:19406964
DOID:1926 Gaucher's disease HGNC:9020 Homo sapiens (human) 5313 PKLR
  • PMID:9677056
DOID:0070300 multiple epiphyseal dysplasia 4 HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:24598000
  • RGD:7240710
DOID:9408 acute myocardial infarction HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:10763 hypertension HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • MGI:6194238
DOID:0111225 centronuclear myopathy X-linked HGNC:16825 Homo sapiens (human) 55613 MTMR8
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
DOID:2841 asthma HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:22512728
  • PMID:22674410
DOID:9970 obesity HGNC:4341 Homo sapiens (human) 2752 GLUL
  • MGI:6194238
DOID:0060673 Peters anomaly HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • PMID:15621878
DOID:9744 type 1 diabetes mellitus HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:1336356
  • PMID:9025006
DOID:0110735 neurodegeneration with brain iron accumulation 2a HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • MGI:6194238
  • PMID:22934738
  • RGD:7240710
DOID:0050635 alternating hemiplegia of childhood HGNC:800 Homo sapiens (human) 477 ATP1A2
  • RGD:7240710
DOID:3534 Lafora disease HGNC:21576 Homo sapiens (human) 378884 NHLRC1
  • MGI:6194238
DOID:0050742 nicotine dependence HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • MGI:6194238
  • PMID:25366721
  • PMID:28900078
DOID:0050865 tongue squamous cell carcinoma HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • PMID:23181352
DOID:1574 alcohol use disorder HGNC:4093 Homo sapiens (human) 2572 GAD2
  • MGI:6194238
DOID:1485 cystic fibrosis HGNC:10802 Homo sapiens (human) 6440 SFTPC
  • PMID:15271694
DOID:7941 Barrett's adenocarcinoma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:16229808
  • PMID:18664505
DOID:5844 myocardial infarction HGNC:9952 Homo sapiens (human) 5968 REG1B
  • MGI:6194238
DOID:1094 attention deficit hyperactivity disorder HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • MGI:6194238
DOID:0080572 congenital disorder of glycosylation Iw HGNC:6172 Homo sapiens (human) 3703 STT3A
  • MGI:6194238
  • RGD:7240710

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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