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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 July 29, 2024
Displaying entries 5351 - 5375 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050812 spondyloepimetaphyseal dysplasia, Pakistani type HGNC:8604 Homo sapiens (human) 9060 PAPSS2
  • MGI:6194238
  • RGD:7240710
DOID:3321 GM2 gangliosidosis HGNC:4367 Homo sapiens (human) 2760 GM2A
  • PMID:10364519
DOID:162 cancer HGNC:10852 Homo sapiens (human) 6472 SHMT2
  • MGI:6194238
DOID:331 central nervous system disease HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
DOID:10584 retinitis pigmentosa HGNC:23059 Homo sapiens (human) 63827 BCAN
  • PMID:29150673
DOID:0080630 B-lymphoblastic leukemia/lymphoma HGNC:2638 Homo sapiens (human) 1577 CYP3A5
  • PMID:21225912
DOID:4608 common bile duct neoplasm HGNC:7371 Homo sapiens (human) 10232 MSLN
  • PMID:16416732
DOID:4989 pancreatitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:10283 prostate cancer HGNC:1681 Homo sapiens (human) 960 CD44
  • PMID:17998819
DOID:341 peripheral vascular disease HGNC:10720 Homo sapiens (human) 6402 SELL
  • MGI:6194238
DOID:114 heart disease HGNC:404 Homo sapiens (human) 217 ALDH2
  • MGI:6194238
DOID:0111232 congenital muscular dystrophy-dystroglycanopathy type A9 HGNC:2666 Homo sapiens (human) 1605 DAG1
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:4001 ovarian carcinoma HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:9066601
DOID:2377 multiple sclerosis HGNC:29013 Homo sapiens (human) 23274 CLEC16A
  • PMID:21653641
DOID:4195 hyperglycemia HGNC:9035 Homo sapiens (human) 5321 PLA2G4A
  • MGI:6194238
DOID:10763 hypertension HGNC:6344 Homo sapiens (human) 9365 KL
  • MGI:6194238
DOID:0090141 cortisone reductase deficiency 1 HGNC:4795 Homo sapiens (human) 9563 H6PD
  • RGD:7240710
DOID:0080070 mucolipidosis II alpha/beta HGNC:29670 Homo sapiens (human) 79158 GNPTAB
  • MGI:6194238
  • RGD:7240710
DOID:1380 endometrial cancer HGNC:936 Homo sapiens (human) 572 BAD
  • PMID:24645842
DOID:3083 chronic obstructive pulmonary disease HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:15949313
  • PMID:21655952
DOID:3347 osteosarcoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
  • RGD:7240710
DOID:13129 severe pre-eclampsia HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:8476834
DOID:1883 hepatitis C HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19703233
  • PMID:20570631
DOID:5419 schizophrenia HGNC:1971 Homo sapiens (human) 9469 CHST3
  • MGI:6194238

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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