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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 70751 - 70775 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:10941 intracranial aneurysm HGNC:7166 Homo sapiens (human) 4313 MMP2
  • MGI:6194238
  • PMID:16961137
  • PMID:9724118
DOID:10941 intracranial aneurysm HGNC:7176 Homo sapiens (human) 4318 MMP9
  • MGI:6194238
  • PMID:16961137
  • PMID:32602008
  • PMID:9310982
DOID:11476 osteoporosis RGD:2582 Rattus norvegicus (Norway rat) 25149 Esr2
  • MGI:6194238
  • PMID:16955786
DOID:11476 osteoporosis RGD:2581 Rattus norvegicus (Norway rat) 24890 Esr1
  • MGI:6194238
  • PMID:16955786
DOID:0110957 Gaucher's disease type I MGI:95665 Mus musculus (house mouse) 14466 Gba1
  • MGI:6194238
  • PMID:16954197
  • PMID:17079175
  • PMID:20962279
  • PMID:35711931
DOID:6000 congestive heart failure HGNC:7176 Homo sapiens (human) 4318 MMP9
  • MGI:6194238
  • PMID:16952784
  • PMID:20606426
DOID:0060785 adult-onset autosomal dominant demyelinating leukodystrophy HGNC:6637 Homo sapiens (human) 4001 LMNB1
  • MGI:6194238
  • PMID:16951681
  • RGD:7240710
DOID:2841 asthma MGI:1341813 Mus musculus (house mouse) 110751 Adam33
  • MGI:6194238
  • PMID:16943435
DOID:0080322 polycystic kidney disease HGNC:9009 Homo sapiens (human) 5311 PKD2
  • MGI:6194238
  • PMID:16943309
DOID:0060676 catecholaminergic polymorphic ventricular tachycardia 2 MGI:1309469 Mus musculus (house mouse) 12373 Casq2
  • MGI:6194238
  • PMID:16932808
  • PMID:17607358
  • PMID:18583715
DOID:0080422 Dravet syndrome MGI:98246 Mus musculus (house mouse) 20265 Scn1a
  • MGI:6194238
  • PMID:16921370
  • PMID:17881658
  • PMID:22908258
  • PMID:22914087
  • PMID:23922229
  • PMID:24152123
  • PMID:29329111
DOID:9970 obesity HGNC:5208 Homo sapiens (human) 3290 HSD11B1
  • MGI:6194238
  • PMID:16914598
DOID:9743 diabetic neuropathy RGD:2092 Rattus norvegicus (Norway rat) 24192 Akr1b1
  • MGI:6194238
  • PMID:16900242
DOID:2741 bilirubin metabolic disorder RGD:2366 Rattus norvegicus (Norway rat) 25303 Abcc2
  • MGI:6194238
  • PMID:16899240
  • PMID:8662992
DOID:6432 pulmonary hypertension HGNC:7940 Homo sapiens (human) 4879 NPPB
  • MGI:6194238
  • PMID:16893710
DOID:8398 osteoarthritis MGI:1328350 Mus musculus (house mouse) 17182 Matn3
  • MGI:6194238
  • PMID:16877353
DOID:14686 Axenfeld-Rieger syndrome HGNC:9005 Homo sapiens (human) 5308 PITX2
  • MGI:6194238
  • PMID:16876867
  • PMID:19052653
DOID:9970 obesity RGD:3234 Rattus norvegicus (Norway rat) 25601 Oprm1
  • MGI:6194238
  • PMID:16876155
  • PMID:31258545
DOID:2349 arteriosclerosis HGNC:6307 Homo sapiens (human) 3791 KDR
  • MGI:6194238
  • PMID:16873710
DOID:6432 pulmonary hypertension HGNC:7176 Homo sapiens (human) 4318 MMP9
  • MGI:6194238
  • PMID:16867026
  • PMID:18355767
  • PMID:21063214
DOID:9255 frontotemporal dementia HGNC:4601 Homo sapiens (human) 2896 GRN
  • MGI:6194238
  • PMID:16862116
  • PMID:16983685
  • PMID:18855025
  • PMID:19012866
DOID:0080855 Parkinsonism HGNC:16369 Homo sapiens (human) 11315 PARK7
  • MGI:6194238
  • PMID:16860563
DOID:9352 type 2 diabetes mellitus HGNC:8583 Homo sapiens (human) 5054 SERPINE1
  • MGI:6194238
  • PMID:16855181
  • PMID:8236167
DOID:11949 Creutzfeldt-Jakob disease HGNC:9449 Homo sapiens (human) 5621 PRNP
  • MGI:6194238
  • PMID:1684755
  • RGD:7240710
DOID:5844 myocardial infarction RGD:621320 Rattus norvegicus (Norway rat) 81687 Mmp9
  • MGI:6194238
  • PMID:16845718
  • PMID:8531210

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024