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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 5876 - 5900 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:0111530 linear nevus sebaceous syndrome HGNC:5173 Homo sapiens (human) 3265 HRAS inference by association of genotype from phenotype used in manual assertion
  • PMID:22683711
  • RGD:7240710
DOID:2841 asthma HGNC:4938 Homo sapiens (human) 3113 HLA-DPA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21814517
DOID:2893 cervix carcinoma HGNC:15971 Homo sapiens (human) 7251 TSG101 direct assay evidence used in manual assertion
  • PMID:10505033
  • PMID:10600297
DOID:9352 type 2 diabetes mellitus HGNC:12828 Homo sapiens (human) 7515 XRCC1 inference by association of genotype from phenotype used in manual assertion
  • PMID:30472145
DOID:9261 nasopharynx carcinoma HGNC:25941 Homo sapiens (human) 54790 TET2 mutant phenotype evidence used in manual assertion
  • PMID:32774157
DOID:4450 renal cell carcinoma HGNC:8125 Homo sapiens (human) 4968 OGG1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10987279
  • RGD:7240710
DOID:0081101 nonautoimmune hyperthyroidism HGNC:12373 Homo sapiens (human) 7253 TSHR inference by association of genotype from phenotype used in manual assertion
  • PMID:18306976
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:1550 Homo sapiens (human) 875 CBS inference by association of genotype from phenotype used in manual assertion
  • PMID:12855221
DOID:850 lung disease HGNC:1884 Homo sapiens (human) 1080 CFTR inference by association of genotype from phenotype used in manual assertion
  • PMID:1381442
  • PMID:16678503
  • PMID:19843100
  • PMID:19952026
  • PMID:7521937
  • PMID:7539891
  • PMID:8535440
DOID:2349 arteriosclerosis HGNC:7376 Homo sapiens (human) 4481 MSR1 mutant phenotype evidence used in manual assertion
  • PMID:14664792
DOID:0050800 cerebral creatine deficiency syndrome 1 HGNC:11055 Homo sapiens (human) 6535 SLC6A8 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12858 Huntington's disease HGNC:23 Homo sapiens (human) 18 ABAT direct assay evidence used in manual assertion
  • PMID:6237280
DOID:0110972 brachydactyly type E1 HGNC:5136 Homo sapiens (human) 3239 HOXD13 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070097 oculocutaneous albinism type III HGNC:12450 Homo sapiens (human) 7306 TYRP1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8947 diabetic retinopathy HGNC:12711 Homo sapiens (human) 9559 VPS26A inference by association of genotype from phenotype used in manual assertion
  • PMID:28821857
DOID:12894 Sjogren's syndrome HGNC:2505 Homo sapiens (human) 1493 CTLA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:16869018
DOID:11723 Duchenne muscular dystrophy HGNC:6143 Homo sapiens (human) 3679 ITGA7 mutant phenotype evidence used in manual assertion
  • PMID:23319059
DOID:9352 type 2 diabetes mellitus HGNC:9237 Homo sapiens (human) 10891 PPARGC1A inference by association of genotype from phenotype used in manual assertion
  • PMID:18162502
  • PMID:18270681
  • PMID:23251491
DOID:14067 Plasmodium falciparum malaria HGNC:3616 Homo sapiens (human) 2212 FCGR2A inference by association of genotype from phenotype used in manual assertion
  • PMID:18194515
DOID:0110728 neuronal ceroid lipofuscinosis 5 HGNC:2076 Homo sapiens (human) 1203 CLN5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060733 junctional epidermolysis bullosa with pyloric atresia HGNC:6158 Homo sapiens (human) 3691 ITGB4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11656 cicatricial pemphigoid HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:9008223
  • PMID:9683867
DOID:9119 acute myeloid leukemia HGNC:15514 Homo sapiens (human) 8301 PICALM inference by association of genotype from phenotype used in manual assertion
  • PMID:12461747
  • RGD:7240710
DOID:1574 alcohol use disorder HGNC:11050 Homo sapiens (human) 6532 SLC6A4 direct assay evidence used in manual assertion
  • PMID:20838391
DOID:0050569 Seckel syndrome HGNC:18672 Homo sapiens (human) 55755 CDK5RAP2 inference by association of genotype from phenotype used in manual assertion
  • PMID:26436113
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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