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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 5151 - 5175 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:11054 urinary bladder cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:18208803
DOID:0080562 congenital disorder of glycosylation Ij ZFIN:ZDB-GENE-060526-18 Danio rerio (zebrafish) 566539 dpagt1
  • MGI:6194238
DOID:479 angiokeratoma RGD:1306025 Rattus norvegicus (Norway rat) 315165 Naga
  • MGI:6194238
DOID:9111 cutaneous leishmaniasis MGI:96824 Mus musculus (house mouse) 21898 Tlr4
  • MGI:6194238
DOID:2316 brain ischemia SGD:S000001568 Saccharomyces cerevisiae S288C 853777 MDH1
  • MGI:6194238
DOID:9952 acute lymphoblastic leukemia HGNC:4458 Homo sapiens (human) 2821 GPI
  • PMID:6589021
DOID:2738 pseudoxanthoma elasticum HGNC:15516 Homo sapiens (human) 64131 XYLT1
  • RGD:7240710
DOID:417 autoimmune disease MGI:104803 Mus musculus (house mouse) 22619 Siae
  • MGI:6194238
DOID:10283 prostate cancer RGD:2554 Rattus norvegicus (Norway rat) 24334 Eno2
  • MGI:6194238
DOID:219 colon cancer HGNC:1937 Homo sapiens (human) 1119 CHKA
  • MGI:6194238
DOID:0112160 autosomal dominant nonsyndromic deafness 79 HGNC:21088 Homo sapiens (human) 79966 SCD5
  • RGD:7240710
DOID:1485 cystic fibrosis RGD:3000 Rattus norvegicus (Norway rat) 25608 Lep
  • MGI:6194238
DOID:0060806 syndromic X-linked intellectual disability Hedera type HGNC:18305 Homo sapiens (human) 10159 ATP6AP2
  • RGD:7240710
DOID:0050730 coenzyme Q10 deficiency disease HGNC:25223 Homo sapiens (human) 27235 COQ2
  • MGI:6194238
DOID:589 congenital hemolytic anemia HGNC:4458 Homo sapiens (human) 2821 GPI
  • PMID:8499925
  • PMID:9856489
DOID:9744 type 1 diabetes mellitus HGNC:10718 Homo sapiens (human) 6401 SELE
  • PMID:18791689
DOID:3594 choriocarcinoma HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:17556377
DOID:3454 brain infarction HGNC:11609 Homo sapiens (human) 6916 TBXAS1
  • MGI:6194238
DOID:13948 bladder neck obstruction HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • PMID:21356374
DOID:1312 focal segmental glomerulosclerosis HGNC:6677 Homo sapiens (human) 4023 LPL
  • MGI:6194238
DOID:5381 bile duct adenoma HGNC:1097 Homo sapiens (human) 673 BRAF
  • MGI:6194238
  • PMID:25704541
DOID:0050570 congenital disorder of glycosylation type I RGD:1304826 Rattus norvegicus (Norway rat) 315212 Alg12
  • MGI:6194238
DOID:10652 Alzheimer's disease WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:1287 cardiovascular system disease MGI:97370 Mus musculus (house mouse) 18605 Enpp1
  • MGI:6194238
DOID:12449 aplastic anemia RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • 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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Last updated: August 19, 2024