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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 5926 - 5950 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0110632 megaconial type congenital muscular dystrophy HGNC:1938 Homo sapiens (human) 1120 CHKB
  • MGI:6194238
  • RGD:7240710
DOID:2986 IgA glomerulonephritis HGNC:11847 Homo sapiens (human) 7096 TLR1
  • PMID:21108742
DOID:1289 neurodegenerative disease HGNC:9386 Homo sapiens (human) 51422 PRKAG2
  • MGI:6194238
DOID:10907 microcephaly HGNC:1937 Homo sapiens (human) 1119 CHKA
  • MGI:6194238
DOID:1059 intellectual disability HGNC:20779 Homo sapiens (human) 64579 NDST4
  • MGI:6194238
DOID:12800 mucopolysaccharidosis VI HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:783 end stage renal disease HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • MGI:6194238
  • PMID:23619522
DOID:14330 Parkinson's disease HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • PMID:23691265
DOID:9256 colorectal cancer HGNC:8976 Homo sapiens (human) 5291 PIK3CB
  • PMID:30789971
DOID:3393 coronary artery disease HGNC:11009 Homo sapiens (human) 6517 SLC2A4
  • PMID:21645024
DOID:1909 melanoma HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • PMID:23416000
DOID:5679 retinal disease HGNC:9059 Homo sapiens (human) 5332 PLCB4
  • MGI:6194238
DOID:2527 nephrosis HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:20685819
DOID:2030 anxiety disorder HGNC:21072 Homo sapiens (human) 79694 MANEA
  • PMID:24473444
DOID:1070 primary open angle glaucoma HGNC:4341 Homo sapiens (human) 2752 GLUL
  • PMID:22974818
DOID:3070 high grade glioma HGNC:11240 Homo sapiens (human) 8877 SPHK1
  • MGI:6194238
DOID:0111394 mucopolysaccharidosis type IIIB HGNC:7632 Homo sapiens (human) 4669 NAGLU
  • RGD:7240710
DOID:0110942 autosomal recessive osteopetrosis 1 HGNC:18481 Homo sapiens (human) 23545 ATP6V0A2
  • MGI:6194238
DOID:0060000 infective endocarditis HGNC:16711 Homo sapiens (human) 10333 TLR6
  • PMID:25213166
DOID:0111865 MEND syndrome HGNC:3133 Homo sapiens (human) 10682 EBP
  • RGD:7240710
DOID:1936 atherosclerosis HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:12590019
DOID:409 liver disease HGNC:4341 Homo sapiens (human) 2752 GLUL
  • PMID:23362937
  • PMID:31335486
DOID:14250 Down syndrome HGNC:11504 Homo sapiens (human) 8871 SYNJ2
  • MGI:6194238
DOID:1824 status epilepticus HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:4448 macular degeneration HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • PMID:23335958

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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: August 19, 2024