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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 6026 - 6050 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence References
DOID:10534 stomach cancer HGNC:13718 Homo sapiens (human) 8061 FOSL1 inference by association of genotype from phenotype used in manual assertion
  • PMID:28169308
DOID:1115 sarcoma HGNC:21350 Homo sapiens (human) 8050 PDHX inference by association of genotype from phenotype used in manual assertion
  • PMID:31089155
DOID:3649 pyruvate decarboxylase deficiency HGNC:21350 Homo sapiens (human) 8050 PDHX inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8398 osteoarthritis HGNC:190 Homo sapiens (human) 8038 ADAM12 inference by association of genotype from phenotype used in manual assertion
  • PMID:15334463
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:3393 coronary artery disease HGNC:2548 Homo sapiens (human) 8029 CUBN inference by association of genotype from phenotype used in manual assertion
  • PMID:33004870
DOID:9119 acute myeloid leukemia HGNC:16063 Homo sapiens (human) 8028 MLLT10 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8864 acute monocytic leukemia HGNC:16063 Homo sapiens (human) 8028 MLLT10 inference by association of genotype from phenotype used in manual assertion
  • PMID:7662954
DOID:9952 acute lymphoblastic leukemia HGNC:8064 Homo sapiens (human) 8021 NUP214 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:936 brain disease HGNC:8064 Homo sapiens (human) 8021 NUP214 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9119 acute myeloid leukemia HGNC:8064 Homo sapiens (human) 8021 NUP214 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:4549 extraskeletal myxoid chondrosarcoma HGNC:7982 Homo sapiens (human) 8013 NR4A3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9119 acute myeloid leukemia HGNC:13013 Homo sapiens (human) 7994 KAT6A inference by association of genotype from phenotype used in manual assertion
  • PMID:12676584
DOID:0070062 Arboleda-Tham syndrome HGNC:13013 Homo sapiens (human) 7994 KAT6A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0081183 autosomal recessive intellectual developmental disorder 7 HGNC:30242 Homo sapiens (human) 7991 TUSC3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8466 retinal degeneration HGNC:11761 Homo sapiens (human) 7980 TFPI2 direct assay evidence used in manual assertion
  • PMID:15184935
DOID:9119 acute myeloid leukemia HGNC:11761 Homo sapiens (human) 7980 TFPI2 inference by association of genotype from phenotype used in manual assertion
  • PMID:22052167
DOID:1928 Williams-Beuren syndrome HGNC:4041 Homo sapiens (human) 7976 FZD3 inference by association of genotype from phenotype used in manual assertion
  • PMID:9147651
DOID:5419 schizophrenia HGNC:4041 Homo sapiens (human) 7976 FZD3 inference by association of genotype from phenotype used in manual assertion
  • PMID:14642436
  • PMID:15274031
DOID:891 progressive myoclonus epilepsy HGNC:3413 Homo sapiens (human) 7957 EPM2A inference by association of genotype from phenotype used in manual assertion
  • PMID:9771710
DOID:1936 atherosclerosis HGNC:9040 Homo sapiens (human) 7941 PLA2G7 inference by association of genotype from phenotype used in manual assertion
  • PMID:12590019
DOID:2841 asthma HGNC:9040 Homo sapiens (human) 7941 PLA2G7 inference by association of genotype from phenotype used in manual assertion
  • PMID:10733466
DOID:12554 hemolytic-uremic syndrome HGNC:9040 Homo sapiens (human) 7941 PLA2G7 inference by association of genotype from phenotype used in manual assertion
  • PMID:10873870
DOID:0080379 nephrotic syndrome type 2 HGNC:9040 Homo sapiens (human) 7941 PLA2G7 inference by association of genotype from phenotype used in manual assertion
  • PMID:9853251
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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