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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 826 - 850 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:2754 glycogen storage disease VI RGD:620687 Rattus norvegicus (Norway rat) 64035 Pygl
  • MGI:6194238
  • PMID:17705025
  • PMID:21646031
DOID:0080201 Peters plus syndrome HGNC:20207 Homo sapiens (human) 145173 B3GLCT
  • MGI:6194238
  • RGD:7240710
DOID:0070263 congenital disorder of glycosylation type IIk HGNC:30760 Homo sapiens (human) 55858 TMEM165
  • MGI:6194238
  • RGD:7240710
DOID:0050770 polycystic liver disease HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:24706814
  • RGD:7240710
DOID:14499 Fabry disease HGNC:4296 Homo sapiens (human) 2717 GLA
  • MGI:6194238
  • PMID:2539398
  • RGD:7240710
DOID:0111100 maturity-onset diabetes of the young type 2 HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
  • RGD:7240710
DOID:0060001 withdrawal disorder HGNC:4092 Homo sapiens (human) 2571 GAD1
  • MGI:6194238
  • PMID:19111404
DOID:12716 newborn respiratory distress syndrome HGNC:10799 Homo sapiens (human) 729238 SFTPA2
  • MGI:6194238
  • PMID:9475280
DOID:0080101 Compton-North congenital myopathy HGNC:2171 Homo sapiens (human) 1272 CNTN1
  • MGI:6194238
  • RGD:7240710
DOID:0111042 glycogen storage disease IXa HGNC:8926 Homo sapiens (human) 5256 PHKA2
  • MGI:6194238
  • PMID:28283841
  • PMID:28627441
  • PMID:8733134
  • RGD:7240710
DOID:12801 mucopolysaccharidosis III HGNC:4422 Homo sapiens (human) 2799 GNS
  • MGI:6194238
  • PMID:12573255
DOID:0050453 lissencephaly HGNC:8574 Homo sapiens (human) 5048 PAFAH1B1
  • MGI:6194238
  • PMID:11115846
DOID:0050773 paraganglioma HGNC:10683 Homo sapiens (human) 6392 SDHD
  • MGI:6194238
  • PMID:10657297
  • RGD:7240710
DOID:0090032 Silverman-Handmaker type dyssegmental dysplasia HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • MGI:6194238
  • RGD:7240710
DOID:14501 Sjogren-Larsson syndrome HGNC:403 Homo sapiens (human) 224 ALDH3A2
  • MGI:6194238
  • RGD:7240710
DOID:0050741 alcohol dependence HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • MGI:6194238
  • PMID:19060480
  • PMID:19328219
  • PMID:21930285
  • PMID:23321485
  • RGD:7240710
DOID:0111135 congenital generalized lipodystrophy type 1 HGNC:325 Homo sapiens (human) 10555 AGPAT2
  • MGI:6194238
  • RGD:7240710
DOID:0111182 familial hemiplegic migraine 2 HGNC:800 Homo sapiens (human) 477 ATP1A2
  • MGI:6194238
  • RGD:7240710
DOID:12716 newborn respiratory distress syndrome HGNC:10798 Homo sapiens (human) 653509 SFTPA1
  • MGI:6194238
  • PMID:11063734
DOID:3649 pyruvate decarboxylase deficiency HGNC:8806 Homo sapiens (human) 5160 PDHA1
  • MGI:6194238
  • PMID:10679936
  • PMID:20002461
  • RGD:7240710
DOID:0112248 17-beta hydroxysteroid dehydrogenase 3 deficiency HGNC:5212 Homo sapiens (human) 3293 HSD17B3
  • MGI:6194238
  • RGD:7240710
DOID:0050464 Farber lipogranulomatosis HGNC:735 Homo sapiens (human) 427 ASAH1
  • MGI:6194238
  • RGD:7240710
DOID:10763 hypertension HGNC:2642 Homo sapiens (human) 1579 CYP4A11
  • MGI:6194238
  • PMID:16144986
DOID:0060728 NGLY1-deficiency HGNC:17646 Homo sapiens (human) 55768 NGLY1
  • MGI:6194238
  • RGD:7240710
DOID:9452 steatotic liver disease HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
  • PMID:14606109

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Last updated: August 19, 2024