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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 376 - 400 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:784 chronic kidney disease HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • MGI:6194238
  • PMID:21111939
DOID:784 chronic kidney disease HGNC:6344 Homo sapiens (human) 9365 KL
  • MGI:6194238
  • PMID:21115613
DOID:898 autosomal dominant polycystic kidney disease HGNC:9009 Homo sapiens (human) 5311 PKD2
  • MGI:6194238
  • PMID:21115670
  • PMID:22863349
DOID:898 autosomal dominant polycystic kidney disease HGNC:9008 Homo sapiens (human) 5310 PKD1
  • MGI:6194238
  • PMID:21115670
  • PMID:8554072
DOID:3969 thyroid gland papillary carcinoma MGI:88190 Mus musculus (house mouse) 109880 Braf
  • MGI:6194238
  • PMID:21220306
  • PMID:21512141
DOID:11612 polycystic ovary syndrome HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • MGI:6194238
  • PMID:21282199
DOID:83 cataract HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
  • PMID:21329682
  • PMID:24360973
DOID:5844 myocardial infarction RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • MGI:6194238
  • PMID:21329947
DOID:12466 secondary hyperparathyroidism HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
  • PMID:21335517
DOID:10763 hypertension RGD:3546 Rattus norvegicus (Norway rat) 25703 Rbp4
  • MGI:6194238
  • PMID:21365528
DOID:0080208 metabolic dysfunction-associated steatotic liver disease RGD:620925 Rattus norvegicus (Norway rat) 83516 Ppargc1a
  • MGI:6194238
  • PMID:21373642
  • PMID:26394137
DOID:14330 Parkinson's disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:21376232
  • PMID:21595954
DOID:0060233 cardiofaciocutaneous syndrome MGI:88190 Mus musculus (house mouse) 109880 Braf
  • MGI:6194238
  • PMID:21383153
  • PMID:25035421
  • PMID:26472072
DOID:8677 perinatal necrotizing enterocolitis RGD:2053 Rattus norvegicus (Norway rat) 25591 Parp1
  • MGI:6194238
  • PMID:21399558
DOID:8677 perinatal necrotizing enterocolitis HGNC:270 Homo sapiens (human) 142 PARP1
  • MGI:6194238
  • PMID:21399558
DOID:3323 Sandhoff disease HGNC:4879 Homo sapiens (human) 3074 HEXB
  • MGI:6194238
  • PMID:2147027
  • RGD:7240710
DOID:12858 Huntington's disease RGD:620925 Rattus norvegicus (Norway rat) 83516 Ppargc1a
  • MGI:6194238
  • PMID:21493629
  • PMID:22813864
DOID:3770 pulmonary fibrosis HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
  • PMID:21681100
DOID:684 hepatocellular carcinoma RGD:2092 Rattus norvegicus (Norway rat) 24192 Akr1b1
  • MGI:6194238
  • PMID:21683810
DOID:0111182 familial hemiplegic migraine 2 MGI:88106 Mus musculus (house mouse) 98660 Atp1a2
  • MGI:6194238
  • PMID:21731499
  • PMID:26911348
DOID:13482 Proteus syndrome HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
  • PMID:21793738
  • RGD:7240710
DOID:0060563 Char syndrome MGI:104672 Mus musculus (house mouse) 21419 Tfap2b
  • MGI:6194238
  • PMID:21829553
DOID:1115 sarcoma RGD:3889 Rattus norvegicus (Norway rat) 24842 Tp53
  • MGI:6194238
  • PMID:21854749
DOID:127 leiomyoma RGD:3269 Rattus norvegicus (Norway rat) 25737 Pcna
  • MGI:6194238
  • PMID:21896544
DOID:10763 hypertension HGNC:4555 Homo sapiens (human) 2878 GPX3
  • MGI:6194238
  • PMID:21933611
  • PMID:32034489

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024