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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 3076 - 3100 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:8947 diabetic retinopathy HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:11106834
  • PMID:2157294
  • PMID:23065222
  • PMID:7729604
DOID:11650 bronchopulmonary dysplasia HGNC:10798 Homo sapiens (human) 653509 SFTPA1
  • PMID:11105614
  • PMID:17264398
DOID:1324 lung cancer HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:11103801
  • PMID:15192016
  • PMID:16615267
  • PMID:23516596
  • PMID:32850411
DOID:2256 osteochondrodysplasia HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • PMID:11101850
DOID:14179 X-linked agammaglobulinemia MGI:97583 Mus musculus (house mouse) 18708 Pik3r1
  • PMID:11062485
  • PMID:9888854
  • PMID:9888855
DOID:8499 night blindness HGNC:8082 Homo sapiens (human) 60506 NYX
  • PMID:11062471
  • RGD:7240710
DOID:0050773 paraganglioma HGNC:10682 Homo sapiens (human) 6391 SDHC
  • PMID:11062460
  • RGD:7240710
DOID:2861 congenital nonspherocytic hemolytic anemia HGNC:9020 Homo sapiens (human) 5313 PKLR
  • PMID:11054094
  • PMID:1536957
  • PMID:7949104
  • PMID:8161798
DOID:14018 alcoholic liver cirrhosis HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:11051375
  • PMID:23550892
  • PMID:29779728
DOID:684 hepatocellular carcinoma HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:11021356
DOID:4398 pustulosis of palm and sole HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:11019918
  • PMID:12691703
DOID:0080821 exercise-induced bronchoconstriction HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:10984370
DOID:10763 hypertension HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:10981554
DOID:2378 relapsing-remitting multiple sclerosis HGNC:2466 Homo sapiens (human) 1464 CSPG4
  • PMID:10976643
DOID:10487 Hirschsprung's disease HGNC:11005 Homo sapiens (human) 6513 SLC2A1
  • PMID:10975929
DOID:8584 Burkitt lymphoma HGNC:1455 Homo sapiens (human) 811 CALR
  • PMID:10961892
  • PMID:9858521
DOID:10112 sleeping sickness SGD:S000003110 Saccharomyces cerevisiae S288C 852735 GPI10
  • PMID:10954751
DOID:1168 familial hyperlipidemia RGD:620396 Rattus norvegicus (Norway rat) 83504 Kl
  • PMID:10892340
DOID:1074 kidney failure RGD:620396 Rattus norvegicus (Norway rat) 83504 Kl
  • PMID:10892340
DOID:10763 hypertension RGD:620396 Rattus norvegicus (Norway rat) 83504 Kl
  • PMID:10892340
  • PMID:21051829
DOID:4440 seminoma HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:10886088
DOID:3307 teratoma HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:10886088
DOID:12554 hemolytic-uremic syndrome HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:10873870
DOID:0080000 muscular disease HGNC:2330 Homo sapiens (human) 1376 CPT2
  • PMID:10873395
DOID:2316 brain ischemia HGNC:9604 Homo sapiens (human) 5742 PTGS1
  • PMID:10867793

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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