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MIRAGE
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 January 28, 2025
Displaying entries 5926 - 5950 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence References
DOID:8893 psoriasis HGNC:6922 Homo sapiens (human) 4153 MBL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:23113841
DOID:2394 ovarian cancer HGNC:6922 Homo sapiens (human) 4153 MBL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:25038892
DOID:3770 pulmonary fibrosis HGNC:6922 Homo sapiens (human) 4153 MBL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:18637104
DOID:409 liver disease HGNC:6922 Homo sapiens (human) 4153 MBL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:19467940
DOID:0060041 autism spectrum disorder HGNC:20445 Homo sapiens (human) 114785 MBD6 inference by association of genotype from phenotype used in manual assertion
  • PMID:23055267
DOID:0060041 autism spectrum disorder HGNC:20444 Homo sapiens (human) 55777 MBD5 inference by association of genotype from phenotype used in manual assertion
  • PMID:23055267
  • PMID:23632792
DOID:0070031 autosomal dominant intellectual developmental disorder 1 HGNC:20444 Homo sapiens (human) 55777 MBD5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080199 colorectal carcinoma HGNC:6919 Homo sapiens (human) 8930 MBD4 inference by association of genotype from phenotype used in manual assertion
  • PMID:10637515
DOID:3748 esophagus squamous cell carcinoma HGNC:6919 Homo sapiens (human) 8930 MBD4 inference by association of genotype from phenotype used in manual assertion
  • PMID:15205355
  • PMID:25162968
DOID:1324 lung cancer HGNC:6919 Homo sapiens (human) 8930 MBD4 inference by association of genotype from phenotype used in manual assertion
  • PMID:18495292
DOID:7148 rheumatoid arthritis HGNC:6919 Homo sapiens (human) 8930 MBD4 inference by association of genotype from phenotype used in manual assertion
  • PMID:20676650
DOID:6039 uveal melanoma HGNC:6919 Homo sapiens (human) 8930 MBD4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060212 amyotrophic lateral sclerosis type 21 HGNC:6912 Homo sapiens (human) 9782 MATR3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2256 osteochondrodysplasia HGNC:6909 Homo sapiens (human) 4148 MATN3 inference by association of genotype from phenotype used in manual assertion
  • PMID:11479597
  • PMID:15121775
DOID:8398 osteoarthritis HGNC:6909 Homo sapiens (human) 4148 MATN3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070299 multiple epiphyseal dysplasia 5 HGNC:6909 Homo sapiens (human) 4148 MATN3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1324 lung cancer HGNC:6904 Homo sapiens (human) 4144 MAT2A direct assay evidence used in manual assertion
  • PMID:34258296
DOID:1588 thrombocytopenia HGNC:19042 Homo sapiens (human) 84930 MASTL inference by association of genotype from phenotype used in manual assertion
  • PMID:12890928
DOID:0070394 developmental and epileptic encephalopathy 108 HGNC:19036 Homo sapiens (human) 23031 MAST3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111403 mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations HGNC:19034 Homo sapiens (human) 22983 MAST1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050671 female breast cancer HGNC:19034 Homo sapiens (human) 22983 MAST1 inference by association of genotype from phenotype used in manual assertion
  • PMID:30303537
DOID:0060575 3MC syndrome 1 HGNC:6901 Homo sapiens (human) 5648 MASP1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111468 combined oxidative phosphorylation deficiency 25 HGNC:25133 Homo sapiens (human) 92935 MARS2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050942 spastic ataxia 3 HGNC:25133 Homo sapiens (human) 92935 MARS2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070454 hereditary spastic paraplegia 70 HGNC:6898 Homo sapiens (human) 4141 MARS1 inference by association of genotype from phenotype used in manual assertion
  • 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: April 7, 2025