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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 70251 - 70275 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:0110349 osteogenesis imperfecta type 9 MGI:97750 Mus musculus (house mouse) 19035 Ppib
  • MGI:6194238
  • PMID:19997487
  • PMID:24968150
DOID:9352 type 2 diabetes mellitus RGD:2922 Rattus norvegicus (Norway rat) 25467 Irs1
  • MGI:6194238
  • PMID:19996384
  • PMID:22001674
DOID:2861 congenital nonspherocytic hemolytic anemia HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
  • PMID:1999409
  • PMID:24923766
DOID:0080322 polycystic kidney disease ZFIN:ZDB-GENE-040827-4 Danio rerio (zebrafish) 432387 pkd2
  • MGI:6194238
  • PMID:19966229
  • PMID:32159259
DOID:12365 malaria HGNC:3616 Homo sapiens (human) 2212 FCGR2A
  • MGI:6194238
  • PMID:19965803
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:281 Homo sapiens (human) 150 ADRA2A
  • MGI:6194238
  • PMID:19965390
DOID:9352 type 2 diabetes mellitus RGD:2056 Rattus norvegicus (Norway rat) 25083 Adra2a
  • MGI:6194238
  • PMID:19965390
DOID:10584 retinitis pigmentosa HGNC:10012 Homo sapiens (human) 6010 RHO
  • MGI:6194238
  • PMID:19960070
  • PMID:21268285
  • PMID:2215617
  • PMID:22419850
  • PMID:23288993
  • PMID:23402891
  • PMID:23470535
  • PMID:9810568
DOID:3529 congenital myopathy 1A MGI:99659 Mus musculus (house mouse) 20190 Ryr1
  • MGI:6194238
  • PMID:19959667
  • PMID:25564733
  • PMID:7515481
DOID:6432 pulmonary hypertension HGNC:10647 Homo sapiens (human) 6376 CX3CL1
  • MGI:6194238
  • PMID:19948918
  • PMID:20869263
DOID:14330 Parkinson's disease HGNC:4177 Homo sapiens (human) 2629 GBA1
  • MGI:6194238
  • PMID:19945510
  • PMID:20528910
  • PMID:20947659
  • PMID:21242499
  • PMID:24126159
  • PMID:25639775
  • PMID:26223426
DOID:3827 congenital diaphragmatic hernia RGD:69311 Rattus norvegicus (Norway rat) 83467 Slit3
  • MGI:6194238
  • PMID:19944214
DOID:9976 heroin dependence RGD:621531 Rattus norvegicus (Norway rat) 50592 Gria1
  • MGI:6194238
  • PMID:19940171
DOID:2219 Glanzmann's thrombasthenia MGI:96612 Mus musculus (house mouse) 16416 Itgb3
  • MGI:6194238
  • PMID:19933310
DOID:10763 hypertension RGD:2411 Rattus norvegicus (Norway rat) 25419 Crp
  • MGI:6194238
  • PMID:19905982
DOID:9675 pulmonary emphysema RGD:621320 Rattus norvegicus (Norway rat) 81687 Mmp9
  • MGI:6194238
  • PMID:19897563
DOID:850 lung disease HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
  • PMID:19897513
DOID:0060352 Kleefstra syndrome 1 MGI:1924933 Mus musculus (house mouse) 77683 Ehmt1
  • MGI:6194238
  • PMID:19896504
  • PMID:20005824
  • PMID:23175442
DOID:11832 visual epilepsy HGNC:13830 Homo sapiens (human) 26047 CNTNAP2
  • MGI:6194238
  • PMID:19896112
DOID:0050741 alcohol dependence HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:19884906
  • PMID:29912265
DOID:5419 schizophrenia RGD:2369 Rattus norvegicus (Norway rat) 25248 Cnr1
  • MGI:6194238
  • PMID:19854030
DOID:0080070 mucolipidosis II alpha/beta ZFIN:ZDB-GENE-030131-4714 Danio rerio (zebrafish) 553365 gnptab
  • MGI:6194238
  • PMID:19834066
  • PMID:22046029
  • PMID:26404503
  • PMID:29539424
DOID:8677 perinatal necrotizing enterocolitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:19824106
DOID:8677 perinatal necrotizing enterocolitis RGD:620588 Rattus norvegicus (Norway rat) 60350 Cd14
  • MGI:6194238
  • PMID:19824106
DOID:8677 perinatal necrotizing enterocolitis HGNC:1628 Homo sapiens (human) 929 CD14
  • MGI:6194238
  • PMID:19824106

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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