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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 71226 - 71250 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:2841 asthma HGNC:20823 Homo sapiens (human) 57628 DPP10
  • MGI:6194238
  • PMID:14566338
  • PMID:19672052
  • PMID:21103062
DOID:2841 asthma MGI:105367 Mus musculus (house mouse) 16190 Il4ra
  • MGI:6194238
  • PMID:14557412
  • PMID:19770271
DOID:0060740 methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency MGI:97239 Mus musculus (house mouse) 17850 Mmut
  • MGI:6194238
  • PMID:14555645
  • PMID:17937813
  • PMID:23898205
  • PMID:27519416
  • PMID:34901307
DOID:10763 hypertension RGD:2961 Rattus norvegicus (Norway rat) 29747 Kcnmb1
  • MGI:6194238
  • PMID:14551242
  • PMID:16814121
DOID:1612 breast cancer HGNC:952 Homo sapiens (human) 580 BARD1
  • MGI:6194238
  • PMID:14550946
  • PMID:16152612
  • PMID:16333312
  • PMID:16768547
  • PMID:17028982
  • PMID:17333333
  • PMID:17972171
  • RGD:7240710
DOID:0050990 episodic ataxia type 2 HGNC:1388 Homo sapiens (human) 773 CACNA1A
  • MGI:6194238
  • PMID:14530926
  • RGD:7240710
DOID:9970 obesity MGI:104963 Mus musculus (house mouse) 18166 Npy1r
  • MGI:6194238
  • PMID:14525913
DOID:0111269 autosomal dominant hyaline body myopathy HGNC:7577 Homo sapiens (human) 4625 MYH7
  • MGI:6194238
  • PMID:14520662
  • RGD:7240710
DOID:1935 Bardet-Biedl syndrome HGNC:20087 Homo sapiens (human) 123016 TTC8
  • MGI:6194238
  • PMID:14520415
DOID:6000 congestive heart failure HGNC:285 Homo sapiens (human) 153 ADRB1
  • MGI:6194238
  • PMID:14502278
DOID:10754 otitis media RGD:2886 Rattus norvegicus (Norway rat) 25325 Il10
  • MGI:6194238
  • PMID:14500471
  • PMID:18524391
DOID:2671 transitional cell carcinoma HGNC:9599 Homo sapiens (human) 9536 PTGES
  • MGI:6194238
  • PMID:14499677
DOID:0050811 congenital adrenal hyperplasia HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • MGI:6194238
  • PMID:1430088
  • PMID:8964882
DOID:11247 disseminated intravascular coagulation RGD:3342 Rattus norvegicus (Norway rat) 25692 Plat
  • MGI:6194238
  • PMID:1425827
DOID:83 cataract RGD:2413 Rattus norvegicus (Norway rat) 24273 Cryaa
  • MGI:6194238
  • PMID:1424724
  • PMID:15042443
  • PMID:19120020
DOID:4674 androgen insensitivity syndrome HGNC:644 Homo sapiens (human) 367 AR
  • MGI:6194238
  • PMID:1424203
  • PMID:1487249
  • PMID:20888558
  • PMID:3186717
  • PMID:7970939
  • PMID:8325950
  • RGD:7240710
DOID:1793 pancreatic cancer HGNC:11765 Homo sapiens (human) 7039 TGFA
  • MGI:6194238
  • PMID:1401070
DOID:10763 hypertension HGNC:333 Homo sapiens (human) 183 AGT
  • MGI:6194238
  • PMID:1394429
  • PMID:16514903
  • PMID:16739866
  • PMID:17161775
  • PMID:17334527
  • PMID:21312059
DOID:3082 interstitial lung disease RGD:3645 Rattus norvegicus (Norway rat) 24770 Ccl2
  • MGI:6194238
  • PMID:1387671
DOID:552 pneumonia RGD:621159 Rattus norvegicus (Norway rat) 60582 Il1rn
  • MGI:6194238
  • PMID:1385928
DOID:3263 piebaldism HGNC:6342 Homo sapiens (human) 3815 KIT
  • MGI:6194238
  • PMID:1370874
  • PMID:1717985
  • RGD:7240710
DOID:11247 disseminated intravascular coagulation HGNC:3535 Homo sapiens (human) 2147 F2
  • MGI:6194238
  • PMID:1336986
  • PMID:19682336
DOID:9970 obesity HGNC:4922 Homo sapiens (human) 3098 HK1
  • MGI:6194238
  • PMID:131232
DOID:0110637 muscular dystrophy-dystroglycanopathy type B6 HGNC:6511 Homo sapiens (human) 9215 LARGE1
  • MGI:6194238
  • PMID:12966029
  • RGD:7240710
DOID:2217 Bernard-Soulier syndrome HGNC:4440 Homo sapiens (human) 2812 GP1BB
  • MGI:6194238
  • PMID:12945881
  • PMID:28131619
  • PMID:9116284
  • RGD:7240710

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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