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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 January 28, 2025
Displaying entries 2676 - 2700 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence References
DOID:0080195 Marinesco-Sjogren syndrome SGD:S000005391 Saccharomyces cerevisiae S288C 854126 SIL1 mutant phenotype evidence used in manual assertion
  • PMID:28257000
DOID:9277 primary cerebellar degeneration HGNC:24624 Homo sapiens (human) 64374 SIL1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080195 Marinesco-Sjogren syndrome SGD:S000005391 Saccharomyces cerevisiae S288C 854126 SIL1 sequence similarity evidence used in manual assertion
  • PMID:28257000
DOID:0080465 developmental and epileptic encephalopathy 30 HGNC:11142 Homo sapiens (human) 150094 SIK1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:417 autoimmune disease HGNC:18187 Homo sapiens (human) 54414 SIAE inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111633 congenital sucrase-isomaltase deficiency HGNC:10856 Homo sapiens (human) 6476 SI inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080692 Noonan syndrome-like disorder with loose anagen hair 1 HGNC:15454 Homo sapiens (human) 8036 SHOC2 inference by association of genotype from phenotype used in manual assertion
  • PMID:20882035
  • PMID:23918763
  • PMID:35348676
  • RGD:7240710
DOID:3310 atopic dermatitis HGNC:15454 Homo sapiens (human) 8036 SHOC2 inference by association of genotype from phenotype used in manual assertion
  • PMID:20882035
DOID:0070543 neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities HGNC:10852 Homo sapiens (human) 6472 SHMT2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1612 breast cancer HGNC:10850 Homo sapiens (human) 6470 SHMT1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17896178
DOID:0110875 holoprosencephaly 3 HGNC:10848 Homo sapiens (human) 6469 SHH inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111564 hypoplastic or aplastic tibia with polydactyly HGNC:10848 Homo sapiens (human) 6469 SHH inference by association of genotype from phenotype used in manual assertion
  • PMID:19847792
DOID:2513 basal cell carcinoma HGNC:10848 Homo sapiens (human) 6469 SHH direct assay evidence used in manual assertion
  • PMID:23284750
DOID:4621 holoprosencephaly HGNC:10848 Homo sapiens (human) 6469 SHH inference by association of genotype from phenotype used in manual assertion
  • PMID:10441331
  • PMID:11919111
  • PMID:8896572
DOID:0111818 syndactyly type 4 HGNC:10848 Homo sapiens (human) 6469 SHH inference by association of genotype from phenotype used in manual assertion
  • PMID:18417549
DOID:10487 Hirschsprung's disease HGNC:10848 Homo sapiens (human) 6469 SHH inference by association of genotype from phenotype used in manual assertion
  • PMID:20972907
DOID:0060986 preaxial polydactyly II HGNC:10848 Homo sapiens (human) 6469 SHH inference by association of genotype from phenotype used in manual assertion
  • PMID:18463159
  • PMID:20569257
DOID:0111380 solitary median maxillary central incisor HGNC:10848 Homo sapiens (human) 6469 SHH inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1148 polydactyly HGNC:10848 Homo sapiens (human) 6469 SHH inference by association of genotype from phenotype used in manual assertion
  • PMID:22903933
DOID:3525 middle cerebral artery infarction HGNC:10848 Homo sapiens (human) 6469 SHH direct assay evidence used in manual assertion
  • PMID:22324418
DOID:1380 endometrial cancer HGNC:10839 Homo sapiens (human) 6462 SHBG inference by association of genotype from phenotype used in manual assertion
  • PMID:17315164
DOID:9352 type 2 diabetes mellitus HGNC:10839 Homo sapiens (human) 6462 SHBG inference by association of genotype from phenotype used in manual assertion
  • PMID:19657112
DOID:12849 autistic disorder HGNC:14295 Homo sapiens (human) 22941 SHANK2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111789 Frank-Ter Haar syndrome HGNC:29242 Homo sapiens (human) 285590 SH3PXD2B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111999 immunodeficiency 61 HGNC:13867 Homo sapiens (human) 30011 SH3KBP1 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