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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 October 9, 2024
Displaying entries 71276 - 71300 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:1184 nephrotic syndrome HGNC:4555 Homo sapiens (human) 2878 GPX3
  • MGI:6194238
  • PMID:12824952
  • PMID:20685819
DOID:10652 Alzheimer's disease HGNC:933 Homo sapiens (human) 23621 BACE1
  • MGI:6194238
  • PMID:12824768
DOID:13141 uveitis RGD:621237 Rattus norvegicus (Norway rat) 25625 Tnfrsf1a
  • MGI:6194238
  • PMID:12824249
DOID:0080311 X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance HGNC:8148 Homo sapiens (human) 4983 OPHN1
  • MGI:6194238
  • PMID:12807966
  • PMID:16158428
  • PMID:18261018
  • PMID:20528889
  • PMID:24105372
  • RGD:7240710
DOID:4481 allergic rhinitis HGNC:5438 Homo sapiens (human) 3458 IFNG
  • MGI:6194238
  • PMID:12787306
DOID:9884 muscular dystrophy WB:WBGene00002248 Caenorhabditis elegans 172952 lam-3
  • MGI:6194238
  • PMID:12783803
DOID:0111128 focal segmental glomerulosclerosis 1 MGI:1890773 Mus musculus (house mouse) 60595 Actn4
  • MGI:6194238
  • PMID:12782671
DOID:0110832 Usher syndrome type 1F MGI:1891428 Mus musculus (house mouse) 11994 Pcdh15
  • MGI:6194238
  • PMID:12782354
  • PMID:15537665
  • PMID:24044941
DOID:13628 favism MGI:105979 Mus musculus (house mouse) 14381 G6pdx
  • MGI:6194238
  • PMID:12777375
  • PMID:14751857
  • PMID:3377761
DOID:12365 malaria MGI:96392 Mus musculus (house mouse) 15894 Icam1
  • MGI:6194238
  • PMID:12769195
DOID:9253 gastrointestinal stromal tumor MGI:96677 Mus musculus (house mouse) 16590 Kit
  • MGI:6194238
  • PMID:12754375
  • PMID:16061643
  • PMID:18098338
  • PMID:22652566
DOID:3911 progeria MGI:96794 Mus musculus (house mouse) 16905 Lmna
  • MGI:6194238
  • PMID:12748643
  • PMID:16862216
  • PMID:20421363
  • PMID:21088111
  • PMID:21464947
  • PMID:21875900
  • PMID:22030750
  • PMID:23690466
  • PMID:26999604
  • PMID:29703891
  • PMID:32128409
  • PMID:36583724
DOID:4154 dentinogenesis imperfecta MGI:109172 Mus musculus (house mouse) 666279 Dspp
  • MGI:6194238
  • PMID:12721295
DOID:0050458 juvenile myelomonocytic leukemia HGNC:9644 Homo sapiens (human) 5781 PTPN11
  • MGI:6194238
  • PMID:12717436
  • RGD:7240710
DOID:4450 renal cell carcinoma RGD:620349 Rattus norvegicus (Norway rat) 29527 Ptgs2
  • MGI:6194238
  • PMID:12708469
DOID:3911 progeria HGNC:6636 Homo sapiens (human) 4000 LMNA
  • MGI:6194238
  • PMID:12702809
  • PMID:12768443
  • PMID:15286156
  • PMID:19875478
  • RGD:7240710
DOID:3827 congenital diaphragmatic hernia MGI:1315202 Mus musculus (house mouse) 20564 Slit3
  • MGI:6194238
  • PMID:12702769
  • PMID:14550534
  • PMID:24355925
DOID:13580 cholestasis RGD:2366 Rattus norvegicus (Norway rat) 25303 Abcc2
  • MGI:6194238
  • PMID:12702498
  • PMID:15057744
  • PMID:16037978
  • PMID:17009103
  • PMID:27090119
DOID:783 end stage renal disease HGNC:7876 Homo sapiens (human) 4846 NOS3
  • MGI:6194238
  • PMID:12701818
DOID:1073 renal hypertension HGNC:7940 Homo sapiens (human) 4879 NPPB
  • MGI:6194238
  • PMID:12697975
DOID:1073 renal hypertension HGNC:7939 Homo sapiens (human) 4878 NPPA
  • MGI:6194238
  • PMID:12697975
  • PMID:15241786
DOID:0111103 maturity-onset diabetes of the young type 4 MGI:102851 Mus musculus (house mouse) 18609 Pdx1
  • MGI:6194238
  • PMID:12697734
DOID:8717 decubitus ulcer HGNC:12680 Homo sapiens (human) 7422 VEGFA
  • MGI:6194238
  • PMID:12692851
DOID:0060591 WHIM syndrome HGNC:2561 Homo sapiens (human) 7852 CXCR4
  • MGI:6194238
  • PMID:12692554
  • RGD:7240710
DOID:1826 epilepsy HGNC:40 Homo sapiens (human) 5243 ABCB1
  • MGI:6194238
  • PMID:12686700

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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: December 9, 2024