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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 9926 - 9950 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:9849 Meniere's disease HGNC:4932 Homo sapiens (human) 3106 HLA-B inference by association of genotype from phenotype used in manual assertion
  • PMID:12542204
DOID:9975 cocaine dependence HGNC:29349 Homo sapiens (human) 401145 CCSER1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18438686
DOID:0111969 immunodeficiency 39 HGNC:6122 Homo sapiens (human) 3665 IRF7 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110315 hypertrophic cardiomyopathy 9 HGNC:12403 Homo sapiens (human) 7273 TTN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:399 tuberculosis HGNC:3443 Homo sapiens (human) 2069 EREG inference by association of genotype from phenotype used in manual assertion
  • PMID:22170233
DOID:0070456 hereditary spastic paraplegia 87 HGNC:23787 Homo sapiens (human) 57156 TMEM63C inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:6677 Homo sapiens (human) 4023 LPL inference by association of genotype from phenotype used in manual assertion
  • PMID:18985010
  • PMID:8641022
DOID:8947 diabetic retinopathy HGNC:9204 Homo sapiens (human) 5444 PON1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15270786
  • PMID:16949520
  • PMID:24100645
DOID:0111405 Fraser syndrome 1 HGNC:19185 Homo sapiens (human) 80144 FRAS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12766769
  • RGD:7240710
DOID:0112004 immunodeficiency 71 HGNC:704 Homo sapiens (human) 10095 ARPC1B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112143 retinitis pigmentosa 86 HGNC:22219 Homo sapiens (human) 57670 KIAA1549 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5419 schizophrenia HGNC:3033 Homo sapiens (human) 1822 ATN1 inference by association of genotype from phenotype used in manual assertion
  • PMID:9184318
DOID:11396 pulmonary edema HGNC:10798 Homo sapiens (human) 653509 SFTPA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16162765
DOID:3393 coronary artery disease HGNC:8133 Homo sapiens (human) 4973 OLR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12810610
  • PMID:15562935
DOID:219 colon cancer HGNC:11283 Homo sapiens (human) 6714 SRC inference by association of genotype from phenotype used in manual assertion
  • PMID:9988270
DOID:8692 myeloid leukemia HGNC:7180 Homo sapiens (human) 4330 MN1 inference by association of genotype from phenotype used in manual assertion
  • PMID:7731705
DOID:12134 factor VIII deficiency HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:9157572
DOID:2841 asthma HGNC:11608 Homo sapiens (human) 6915 TBXA2R inference by association of genotype from phenotype used in manual assertion
  • PMID:12000493
  • PMID:15805995
DOID:0060903 thrombosis HGNC:7155 Homo sapiens (human) 4312 MMP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:20616161
DOID:684 hepatocellular carcinoma HGNC:3689 Homo sapiens (human) 2263 FGFR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:30952770
DOID:0060170 generalized epilepsy with febrile seizures plus HGNC:11018 Homo sapiens (human) 140679 SLC32A1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2988 antiphospholipid syndrome HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11157139
DOID:1380 endometrial cancer HGNC:936 Homo sapiens (human) 572 BAD inference by association of genotype from phenotype used in manual assertion
  • PMID:24645842
DOID:2377 multiple sclerosis HGNC:4951 Homo sapiens (human) 3125 HLA-DRB3 inference by association of genotype from phenotype used in manual assertion
  • PMID:15201511
DOID:0112233 lissencephaly 8 HGNC:26899 Homo sapiens (human) 160418 TMTC3 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