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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 2651 - 2675 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10591 pre-eclampsia HGNC:2634 Homo sapiens (human) 1573 CYP2J2
  • MGI:6194238
  • PMID:23155181
DOID:0050848 obstructive sleep apnea HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:18606530
DOID:11204 allergic conjunctivitis HGNC:9031 Homo sapiens (human) 5320 PLA2G2A
  • PMID:21042565
DOID:12930 dilated cardiomyopathy HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:19926600
DOID:1793 pancreatic cancer HGNC:251 Homo sapiens (human) 126 ADH1C
  • PMID:19068087
DOID:2377 multiple sclerosis HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:10417663
DOID:1287 cardiovascular system disease HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:15331559
DOID:635 acquired immunodeficiency syndrome HGNC:1641 Homo sapiens (human) 30835 CD209
  • PMID:17530998
DOID:0080599 Coronavirus infectious disease HGNC:10803 Homo sapiens (human) 6441 SFTPD
  • MGI:6194238
DOID:162 cancer HGNC:9640 Homo sapiens (human) 201562 HACD2
  • MGI:6194238
DOID:1184 nephrotic syndrome HGNC:25223 Homo sapiens (human) 27235 COQ2
  • MGI:6194238
DOID:1612 breast cancer HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:15285606
  • PMID:17429315
  • PMID:17507616
  • PMID:17562079
DOID:684 hepatocellular carcinoma HGNC:9989 Homo sapiens (human) 9104 RGN
  • MGI:6194238
DOID:0112250 Gaucher's disease type IIIC HGNC:4177 Homo sapiens (human) 2629 GBA1
  • RGD:7240710
DOID:6000 congestive heart failure HGNC:9060 Homo sapiens (human) 5333 PLCD1
  • MGI:6194238
DOID:0070218 familial hyperinsulinemic hypoglycemia 2 HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • RGD:7240710
DOID:11612 polycystic ovary syndrome HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:17535988
DOID:9538 multiple myeloma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:22345095
DOID:9074 systemic lupus erythematosus HGNC:23792 Homo sapiens (human) 122618 PLD4
  • MGI:6194238
DOID:10923 sickle cell anemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:8140855
DOID:4306 radiculopathy HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • MGI:6194238
DOID:1596 depressive disorder HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma HGNC:391 Homo sapiens (human) 207 AKT1
  • PMID:23632475
  • PMID:32276600
DOID:0110728 neuronal ceroid lipofuscinosis 5 HGNC:2076 Homo sapiens (human) 1203 CLN5
  • MGI:6194238
  • RGD:7240710

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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