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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 9901 - 9925 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:0111348 multiple epiphyseal dysplasia with myopia and deafness HGNC:2200 Homo sapiens (human) 1280 COL2A1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10892 hypospadias HGNC:2568 Homo sapiens (human) 10046 MAMLD1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:288 Homo sapiens (human) 155 ADRB3 inference by association of genotype from phenotype used in manual assertion
  • PMID:15318095
DOID:3310 atopic dermatitis HGNC:11892 Homo sapiens (human) 7124 TNF inference by association of genotype from phenotype used in manual assertion
  • PMID:22533231
DOID:0070248 autosomal recessive Emery-Dreifuss muscular dystrophy 3 HGNC:6636 Homo sapiens (human) 4000 LMNA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1115 sarcoma HGNC:6973 Homo sapiens (human) 4193 MDM2 inference by association of genotype from phenotype used in manual assertion
  • PMID:1614537
DOID:0081216 autosomal recessive intellectual developmental disorder 54 HGNC:30765 Homo sapiens (human) 23043 TNIK inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1686 glaucoma HGNC:21205 Homo sapiens (human) 84894 LINGO1 mutant phenotype evidence used in manual assertion
  • PMID:19422885
DOID:0110734 neurodegeneration with brain iron accumulation HGNC:15578 Homo sapiens (human) 85021 REPS1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9146 visceral leishmaniasis HGNC:6009 Homo sapiens (human) 3560 IL2RB inference by association of genotype from phenotype used in manual assertion
  • PMID:17108990
DOID:0070250 autosomal dominant Emery-Dreifuss muscular dystrophy 5 HGNC:17084 Homo sapiens (human) 23224 SYNE2 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
DOID:7693 abdominal aortic aneurysm HGNC:10937 Homo sapiens (human) 6573 SLC19A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18635682
DOID:0080526 bronchiectasis 1 HGNC:10600 Homo sapiens (human) 6338 SCNN1B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080743 transverse myelitis HGNC:637 Homo sapiens (human) 361 AQP4 direct assay evidence used in manual assertion
  • PMID:21771203
  • PMID:23999580
DOID:11204 allergic conjunctivitis HGNC:5973 Homo sapiens (human) 3596 IL13 inference by association of genotype from phenotype used in manual assertion
  • PMID:22023794
DOID:14018 alcoholic liver cirrhosis HGNC:11180 Homo sapiens (human) 6648 SOD2 inference by association of genotype from phenotype used in manual assertion
  • PMID:26873981
DOID:1040 chronic lymphocytic leukemia HGNC:1705 Homo sapiens (human) 942 CD86 direct assay evidence used in manual assertion
  • PMID:23154584
DOID:0050811 congenital adrenal hyperplasia HGNC:2591 Homo sapiens (human) 1584 CYP11B1 inference by association of genotype from phenotype used in manual assertion
  • PMID:1430088
  • PMID:8964882
DOID:0111815 low molecular weight proteinuria with hypercalciuric nephrocalcinosis HGNC:2023 Homo sapiens (human) 1184 CLCN5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:9204 Homo sapiens (human) 5444 PON1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10729395
  • PMID:11917194
DOID:1742 drug psychosis HGNC:4093 Homo sapiens (human) 2572 GAD2 inference by association of genotype from phenotype used in manual assertion
  • PMID:27967329
DOID:1485 cystic fibrosis HGNC:7872 Homo sapiens (human) 4842 NOS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:14760158
DOID:0070267 congenital disorder of glycosylation type IIo HGNC:28178 Homo sapiens (human) 84317 VMA22 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060203 amyotrophic lateral sclerosis type 12 HGNC:17142 Homo sapiens (human) 10133 OPTN 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