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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 5301 - 5325 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10273 heart conduction disease HGNC:25575 Homo sapiens (human) 55224 ETNK2
  • MGI:6194238
DOID:2978 carbohydrate metabolic disorder HGNC:11559 Homo sapiens (human) 6888 TALDO1
  • PMID:11283793
DOID:0070460 hereditary spastic paraplegia 90B HGNC:20361 Homo sapiens (human) 171546 SPTSSA
  • RGD:7240710
DOID:5082 liver cirrhosis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:19456900
  • PMID:26681055
  • PMID:29085215
DOID:11984 hypertrophic cardiomyopathy HGNC:10683 Homo sapiens (human) 6392 SDHD
  • MGI:6194238
DOID:10763 hypertension HGNC:2623 Homo sapiens (human) 1559 CYP2C9
  • PMID:17305793
  • PMID:19669737
DOID:0060639 permanent neonatal diabetes mellitus HGNC:4195 Homo sapiens (human) 2645 GCK
  • RGD:7240710
DOID:0112002 immunodeficiency 47 HGNC:868 Homo sapiens (human) 537 ATP6AP1
  • RGD:7240710
DOID:9452 steatotic liver disease HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
DOID:1936 atherosclerosis HGNC:4555 Homo sapiens (human) 2878 GPX3
  • MGI:6194238
DOID:0111453 2-aminoadipic 2-oxoadipic aciduria HGNC:23537 Homo sapiens (human) 55526 DHTKD1
  • MGI:6194238
  • RGD:7240710
DOID:1574 alcohol use disorder HGNC:253 Homo sapiens (human) 128 ADH5
  • MGI:6194238
DOID:10140 dry eye syndrome HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:22025895
DOID:13641 exfoliation syndrome HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:22831837
DOID:332 amyotrophic lateral sclerosis HGNC:5467 Homo sapiens (human) 3482 IGF2R
  • MGI:6194238
DOID:3343 glycoproteinosis HGNC:7758 Homo sapiens (human) 4758 NEU1
  • MGI:6194238
DOID:14681 Silver-Russell syndrome HGNC:5466 Homo sapiens (human) 3481 IGF2
  • RGD:7240710
DOID:9976 heroin dependence HGNC:2615 Homo sapiens (human) 1555 CYP2B6
  • PMID:21790905
DOID:0060180 colitis HGNC:10720 Homo sapiens (human) 6402 SELL
  • MGI:6194238
DOID:0080533 Carney-Stratakis syndrome HGNC:10682 Homo sapiens (human) 6391 SDHC
  • RGD:7240710
DOID:6088 acute stress disorder HGNC:108 Homo sapiens (human) 43 ACHE
  • MGI:6194238
DOID:0090101 lethal congenital glycogen storage disease of heart HGNC:9387 Homo sapiens (human) 53632 PRKAG3
  • MGI:6194238
DOID:3713 ovary adenocarcinoma HGNC:2602 Homo sapiens (human) 1591 CYP24A1
  • PMID:16180015
DOID:13628 favism HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
  • RGD:7240710
DOID:0080124 mitochondrial DNA depletion syndrome 5 HGNC:11448 Homo sapiens (human) 8803 SUCLA2
  • 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