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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 70951 - 70975 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:0060194 amyotrophic lateral sclerosis type 2 MGI:1921268 Mus musculus (house mouse) 74018 Als2
  • MGI:6194238
  • PMID:16107644
  • PMID:16321985
  • PMID:18558633
DOID:0060363 glycerol kinase deficiency MGI:106594 Mus musculus (house mouse) 14933 Gk
  • MGI:6194238
  • PMID:16105550
  • PMID:9302256
DOID:0090034 myoclonic dystonia 11 MGI:1329042 Mus musculus (house mouse) 20392 Sgce
  • MGI:6194238
  • PMID:16099459
  • PMID:22040906
DOID:10763 hypertension HGNC:11784 Homo sapiens (human) 7056 THBD
  • MGI:6194238
  • PMID:16095049
  • PMID:17401180
DOID:4947 cholangiocarcinoma HGNC:11766 Homo sapiens (human) 7040 TGFB1
  • MGI:6194238
  • PMID:16083599
DOID:0111027 hemochromatosis type 2A MGI:1916835 Mus musculus (house mouse) 69585 Hjv
  • MGI:6194238
  • PMID:16075058
  • PMID:16075059
DOID:1391 Norum disease HGNC:6522 Homo sapiens (human) 3931 LCAT
  • MGI:6194238
  • PMID:16061733
  • RGD:7240710
DOID:3070 high grade glioma HGNC:23059 Homo sapiens (human) 63827 BCAN
  • MGI:6194238
  • PMID:16061654
  • PMID:23253190
DOID:5844 myocardial infarction HGNC:336 Homo sapiens (human) 185 AGTR1
  • MGI:6194238
  • PMID:16061119
  • PMID:9857918
DOID:9744 type 1 diabetes mellitus HGNC:4114 Homo sapiens (human) 51083 GAL
  • MGI:6194238
  • PMID:16060906
DOID:0111028 hemochromatosis type 4 MGI:1315204 Mus musculus (house mouse) 53945 Slc40a1
  • MGI:6194238
  • PMID:16054062
  • PMID:17289807
  • PMID:25100063
DOID:5844 myocardial infarction RGD:3249 Rattus norvegicus (Norway rat) 24617 Serpine1
  • MGI:6194238
  • PMID:16053971
DOID:9352 type 2 diabetes mellitus HGNC:4910 Homo sapiens (human) 3091 HIF1A
  • MGI:6194238
  • PMID:16046581
  • PMID:23244125
DOID:850 lung disease HGNC:10801 Homo sapiens (human) 6439 SFTPB
  • MGI:6194238
  • PMID:16042774
  • PMID:16274485
  • PMID:8569184
DOID:9255 frontotemporal dementia HGNC:24537 Homo sapiens (human) 25978 CHMP2B
  • MGI:6194238
  • PMID:16041373
  • PMID:16979267
  • PMID:19202337
DOID:10763 hypertension HGNC:286 Homo sapiens (human) 154 ADRB2
  • MGI:6194238
  • PMID:16041242
  • PMID:16685203
  • PMID:17221209
  • PMID:20484896
  • PMID:20739939
DOID:14557 primary pulmonary hypertension MGI:1095407 Mus musculus (house mouse) 12168 Bmpr2
  • MGI:6194238
  • PMID:16027259
  • PMID:18663089
  • PMID:20562228
  • PMID:26076038
DOID:0090019 sitosterolemia RGD:620298 Rattus norvegicus (Norway rat) 114628 Abcg5
  • MGI:6194238
  • PMID:16026620
DOID:10283 prostate cancer HGNC:125 Homo sapiens (human) 55 ACP3
  • MGI:6194238
  • PMID:16024648
  • PMID:17991541
DOID:3803 Crigler-Najjar syndrome HGNC:12530 Homo sapiens (human) 54658 UGT1A1
  • MGI:6194238
  • PMID:16019265
  • PMID:16337205
  • PMID:22094718
  • PMID:24285217
  • PMID:9497253
  • RGD:7240710
DOID:4448 macular degeneration HGNC:8824 Homo sapiens (human) 5176 SERPINF1
  • MGI:6194238
  • PMID:16019000
DOID:0080855 Parkinsonism HGNC:4232 Homo sapiens (human) 2668 GDNF
  • MGI:6194238
  • PMID:16018990
  • PMID:27286696
  • PMID:29372975
DOID:2231 factor XII deficiency MGI:1891012 Mus musculus (house mouse) 58992 F12
  • MGI:6194238
  • PMID:16009717
DOID:5844 myocardial infarction HGNC:4910 Homo sapiens (human) 3091 HIF1A
  • MGI:6194238
  • PMID:15999059
DOID:0110544 autosomal dominant nonsyndromic deafness 12 MGI:109575 Mus musculus (house mouse) 21683 Tecta
  • MGI:6194238
  • PMID:15995703
  • PMID:24363064

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024