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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 5751 - 5775 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:11721 glycogen storage disease VII WB:WBGene00022199 Caenorhabditis elegans 180583 pfk-1.1
  • MGI:6194238
DOID:13129 severe pre-eclampsia HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:19573524
  • PMID:27279411
  • PMID:31949674
DOID:8778 Crohn's disease MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:3748 esophagus squamous cell carcinoma HGNC:6919 Homo sapiens (human) 8930 MBD4
  • PMID:15205355
  • PMID:25162968
DOID:6000 congestive heart failure HGNC:2596 Homo sapiens (human) 1544 CYP1A2
  • MGI:6194238
DOID:0110297 autosomal recessive limb-girdle muscular dystrophy type 2K SGD:S000003904 Saccharomyces cerevisiae S288C 853608 PMT4
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 ZFIN:ZDB-GENE-041010-195 Danio rerio (zebrafish) 450072 alg14
  • MGI:6194238
DOID:1040 chronic lymphocytic leukemia RGD:3130 Rattus norvegicus (Norway rat) 24577 Myc
  • MGI:6194238
DOID:11832 visual epilepsy RGD:620103 Rattus norvegicus (Norway rat) 64639 Bad
  • PMID:15968425
DOID:8677 perinatal necrotizing enterocolitis HGNC:11847 Homo sapiens (human) 7096 TLR1
  • MGI:6194238
DOID:1035 aggressive NK-cell leukemia HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:0060227 Adams-Oliver syndrome HGNC:28526 Homo sapiens (human) 285203 EOGT
  • RGD:7240710
DOID:13406 pulmonary sarcoidosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15653992
  • PMID:20070603
DOID:1591 renovascular hypertension MGI:105977 Mus musculus (house mouse) 14380 G6pd2
  • MGI:6194238
DOID:0070253 congenital disorder of glycosylation type IIa Xenbase:XB-GENE-17345473 Xenopus laevis (African clawed frog) 444674 mgat2.S
  • MGI:6194238
DOID:0110339 osteogenesis imperfecta type 3 HGNC:14240 Homo sapiens (human) 55512 SMPD3
  • MGI:6194238
DOID:2043 hepatitis B RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:0060180 colitis RGD:3870 Rattus norvegicus (Norway rat) 29260 Tlr4
  • PMID:19002562
DOID:767 muscular atrophy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:20575 Homo sapiens (human) 284541 CYP4A22
  • MGI:6194238
DOID:0111277 mitochondrial trifunctional protein deficiency HGNC:4801 Homo sapiens (human) 3030 HADHA
  • RGD:7240710
DOID:8677 perinatal necrotizing enterocolitis HGNC:16711 Homo sapiens (human) 10333 TLR6
  • MGI:6194238
DOID:8677 perinatal necrotizing enterocolitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:19824106
DOID:1793 pancreatic cancer MGI:1202879 Mus musculus (house mouse) 21416 Tcf7l2
  • MGI:6194238
DOID:12053 cryptococcosis WB:WBGene00000503 Caenorhabditis elegans 180628 cht-1
  • MGI:6194238

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

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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