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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 6601 - 6625 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:8778 Crohn's disease MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:6000 congestive heart failure HGNC:2596 Homo sapiens (human) 1544 CYP1A2
  • MGI:6194238
DOID:0110297 autosomal recessive limb-girdle muscular dystrophy type 2K SGD:S000003904 Saccharomyces cerevisiae S288C 853608 PMT4
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 ZFIN:ZDB-GENE-041010-195 Danio rerio (zebrafish) 450072 alg14
  • MGI:6194238
DOID:1040 chronic lymphocytic leukemia RGD:3130 Rattus norvegicus (Norway rat) 24577 Myc
  • MGI:6194238
DOID:5419 schizophrenia FB:FBgn0026415 Drosophila melanogaster (fruit fly) 31926 Idgf4 CG1780
  • MGI:6194238
DOID:8677 perinatal necrotizing enterocolitis HGNC:11847 Homo sapiens (human) 7096 TLR1
  • MGI:6194238
DOID:1035 aggressive NK-cell leukemia HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:1591 renovascular hypertension MGI:105977 Mus musculus (house mouse) 14380 G6pd2
  • MGI:6194238
DOID:0070253 congenital disorder of glycosylation type IIa Xenbase:XB-GENE-17345473 Xenopus laevis (African clawed frog) 444674 mgat2.S
  • MGI:6194238
DOID:0110339 osteogenesis imperfecta type 3 HGNC:14240 Homo sapiens (human) 55512 SMPD3
  • MGI:6194238
DOID:2043 hepatitis B RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:767 muscular atrophy HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:20575 Homo sapiens (human) 284541 CYP4A22
  • MGI:6194238
DOID:13359 Ehlers-Danlos syndrome FB:FBgn0033315 Drosophila melanogaster (fruit fly) 35848 beta3GalTII CG8734
  • MGI:6194238
DOID:8677 perinatal necrotizing enterocolitis HGNC:16711 Homo sapiens (human) 10333 TLR6
  • MGI:6194238
DOID:1793 pancreatic cancer MGI:1202879 Mus musculus (house mouse) 21416 Tcf7l2
  • MGI:6194238
DOID:0080565 congenital disorder of glycosylation Im FB:FBgn0034141 Drosophila melanogaster (fruit fly) 36856 Dolk CG8311
  • MGI:6194238
DOID:12053 cryptococcosis WB:WBGene00000503 Caenorhabditis elegans 180628 cht-1
  • MGI:6194238
DOID:10283 prostate cancer WB:WBGene00011884 Caenorhabditis elegans 174423 enol-1
  • MGI:6194238
DOID:0110429 dilated cardiomyopathy 1H RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:7148 rheumatoid arthritis MGI:105095 Mus musculus (house mouse) 18654 Pgf
  • MGI:6194238
DOID:5154 borna disease ZFIN:ZDB-GENE-030821-1 Danio rerio (zebrafish) 369193 aldocb
  • MGI:6194238
DOID:3319 lymphangioleiomyomatosis MGI:95640 Mus musculus (house mouse) 14433 Gapdh
  • MGI:6194238
DOID:11151 cholecystolithiasis RGD:3935 Rattus norvegicus (Norway rat) 24861 Ugt1a1
  • 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