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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 9876 - 9900 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:11247 disseminated intravascular coagulation HGNC:775 Homo sapiens (human) 462 SERPINC1 direct assay evidence used in manual assertion
  • PMID:2679067
DOID:8805 intermediate coronary syndrome HGNC:775 Homo sapiens (human) 462 SERPINC1 direct assay evidence used in manual assertion
  • PMID:8122184
DOID:0080488 mucolipidosis HGNC:7758 Homo sapiens (human) 4758 NEU1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:4992 optic nerve glioma HGNC:7765 Homo sapiens (human) 4763 NF1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21278392
DOID:3070 high grade glioma HGNC:7765 Homo sapiens (human) 4763 NF1 inference by association of genotype from phenotype used in manual assertion
  • PMID:26190195
DOID:0050458 juvenile myelomonocytic leukemia HGNC:7765 Homo sapiens (human) 4763 NF1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12849 autistic disorder HGNC:7765 Homo sapiens (human) 4763 NF1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15389774
DOID:0070482 spinal neurofibromatosis HGNC:7765 Homo sapiens (human) 4763 NF1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9119 acute myeloid leukemia HGNC:7765 Homo sapiens (human) 4763 NF1 inference by association of genotype from phenotype used in manual assertion
  • PMID:23460398
DOID:5151 plexiform neurofibroma HGNC:7765 Homo sapiens (human) 4763 NF1 mutant phenotype evidence used in manual assertion
  • PMID:17335073
DOID:0070483 Watson syndrome HGNC:7765 Homo sapiens (human) 4763 NF1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111253 neurofibromatosis 1 HGNC:7765 Homo sapiens (human) 4763 NF1 inference by association of genotype from phenotype used in manual assertion
  • PMID:2134734
  • PMID:32575496
  • RGD:7240710
DOID:0111683 neurofibromatosis-Noonan syndrome HGNC:7765 Homo sapiens (human) 4763 NF1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10283 prostate cancer HGNC:777 Homo sapiens (human) 463 ZFHX3 inference by association of genotype from phenotype used in manual assertion
  • PMID:15750593
  • PMID:16637072
  • RGD:7240710
DOID:3908 lung non-small cell carcinoma HGNC:777 Homo sapiens (human) 463 ZFHX3 inference by association of genotype from phenotype used in manual assertion
  • PMID:32653938
DOID:684 hepatocellular carcinoma HGNC:777 Homo sapiens (human) 463 ZFHX3 mutant phenotype evidence used in manual assertion
  • PMID:32277050
DOID:0050957 spinocerebellar ataxia type 4 HGNC:777 Homo sapiens (human) 463 ZFHX3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3910 lung adenocarcinoma HGNC:777 Homo sapiens (human) 463 ZFHX3 inference by association of genotype from phenotype used in manual assertion
  • PMID:32653938
DOID:0050650 familial atrial fibrillation HGNC:777 Homo sapiens (human) 463 ZFHX3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1657 ventricular septal defect HGNC:7775 Homo sapiens (human) 4772 NFATC1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21499900
  • PMID:23286482
DOID:1682 congenital heart disease HGNC:7775 Homo sapiens (human) 4772 NFATC1 inference by association of genotype from phenotype used in manual assertion
  • PMID:28829497
DOID:12930 dilated cardiomyopathy HGNC:7778 Homo sapiens (human) 4776 NFATC4 inference by association of genotype from phenotype used in manual assertion
  • PMID:12939651
DOID:10652 Alzheimer's disease HGNC:7782 Homo sapiens (human) 4780 NFE2L2 inference by association of genotype from phenotype used in manual assertion
  • PMID:20064547
DOID:10652 Alzheimer's disease HGNC:7782 Homo sapiens (human) 4780 NFE2L2 mutant phenotype evidence used in manual assertion
  • PMID:19805328
DOID:399 tuberculosis HGNC:7782 Homo sapiens (human) 4780 NFE2L2 inference by association of genotype from phenotype used in manual assertion
  • PMID:31586142

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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