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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 71726 - 71750 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:5408 Paget's disease of bone HGNC:11908 Homo sapiens (human) 8792 TNFRSF11A
  • MGI:6194238
  • PMID:10615125
DOID:0090118 congenital amegakaryocytic thrombocytopenia MGI:97076 Mus musculus (house mouse) 17480 Mpl
  • MGI:6194238
  • PMID:10611229
DOID:0110340 osteogenesis imperfecta type 4 MGI:88467 Mus musculus (house mouse) 12842 Col1a1
  • MGI:6194238
  • PMID:10608859
  • PMID:24443344
  • PMID:26277094
DOID:0110341 osteogenesis imperfecta type 2 MGI:88467 Mus musculus (house mouse) 12842 Col1a1
  • MGI:6194238
  • PMID:10608859
  • PMID:18248096
DOID:0110381 retinitis pigmentosa 14 MGI:109571 Mus musculus (house mouse) 22157 Tulp1
  • MGI:6194238
  • PMID:10607826
DOID:2236 congenital afibrinogenemia HGNC:3661 Homo sapiens (human) 2243 FGA
  • MGI:6194238
  • PMID:10602365
  • PMID:15795544
  • RGD:7240710
DOID:14219 renal tubular acidosis RGD:3710 Rattus norvegicus (Norway rat) 24779 Slc4a1
  • MGI:6194238
  • PMID:10600930
DOID:9256 colorectal cancer HGNC:7127 Homo sapiens (human) 4292 MLH1
  • MGI:6194238
  • PMID:10598809
DOID:0050477 Liddle syndrome MGI:104696 Mus musculus (house mouse) 20277 Scnn1b
  • MGI:6194238
  • PMID:10589691
DOID:12801 mucopolysaccharidosis III MGI:1351641 Mus musculus (house mouse) 27419 Naglu
  • MGI:6194238
  • PMID:10588735
  • PMID:12576554
  • PMID:17712420
DOID:0050433 fatal familial insomnia MGI:97769 Mus musculus (house mouse) 19122 Prnp
  • MGI:6194238
  • PMID:10581259
  • PMID:19709627
  • PMID:23959875
  • PMID:9462739
DOID:4249 Gerstmann-Straussler-Scheinker syndrome MGI:97769 Mus musculus (house mouse) 19122 Prnp
  • MGI:6194238
  • PMID:10581259
  • PMID:1373228
  • PMID:19675240
  • PMID:1980379
  • PMID:8698234
  • PMID:9462739
DOID:11949 Creutzfeldt-Jakob disease MGI:97769 Mus musculus (house mouse) 19122 Prnp
  • MGI:6194238
  • PMID:10581259
  • PMID:1373228
  • PMID:19038218
  • PMID:22072968
  • PMID:23959875
  • PMID:7494265
  • PMID:9462739
DOID:3659 sialuria HGNC:10933 Homo sapiens (human) 26503 SLC17A5
  • MGI:6194238
  • PMID:10581036
  • RGD:7240710
DOID:11726 Emery-Dreifuss muscular dystrophy MGI:96794 Mus musculus (house mouse) 16905 Lmna
  • MGI:6194238
  • PMID:10579712
  • PMID:15548545
DOID:0060193 amyotrophic lateral sclerosis type 1 MGI:98351 Mus musculus (house mouse) 20655 Sod1
  • MGI:6194238
  • PMID:10578106
  • PMID:15263088
  • PMID:25468678
  • PMID:7846037
DOID:10763 hypertension HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • MGI:6194238
  • PMID:10577996
  • PMID:12372404
  • PMID:17070428
DOID:0080301 atypical hemolytic-uremic syndrome HGNC:4883 Homo sapiens (human) 3075 CFH
  • MGI:6194238
  • PMID:10577907
  • PMID:17517971
  • PMID:20513133
  • PMID:23243267
  • PMID:9811382
  • RGD:7240710
DOID:1485 cystic fibrosis MGI:88388 Mus musculus (house mouse) 12638 Cftr
  • MGI:6194238
  • PMID:10570187
  • PMID:11823443
  • PMID:1355249
  • PMID:1380723
  • PMID:1382232
  • PMID:15246977
  • PMID:22711878
  • PMID:29924856
  • PMID:35392567
  • PMID:7482032
  • PMID:7540910
  • PMID:7545494
  • PMID:7556083
  • PMID:7560099
  • PMID:8589719
  • PMID:8605891
DOID:12801 mucopolysaccharidosis III MGI:1350341 Mus musculus (house mouse) 27029 Sgsh
  • MGI:6194238
  • PMID:10561464
DOID:10652 Alzheimer's disease HGNC:9604 Homo sapiens (human) 5742 PTGS1
  • MGI:6194238
  • PMID:10560656
DOID:2513 basal cell carcinoma MGI:105373 Mus musculus (house mouse) 19206 Ptch1
  • MGI:6194238
  • PMID:10545995
  • PMID:20233865
  • PMID:23404854
DOID:14219 renal tubular acidosis HGNC:11030 Homo sapiens (human) 8671 SLC4A4
  • MGI:6194238
  • PMID:10545938
DOID:9352 type 2 diabetes mellitus HGNC:6107 Homo sapiens (human) 3651 PDX1
  • MGI:6194238
  • PMID:10545531
  • PMID:15170499
  • PMID:15734849
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:7876 Homo sapiens (human) 4846 NOS3
  • MGI:6194238
  • PMID:10531147
  • PMID:11903359
  • PMID:12362496
  • PMID:17637430

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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

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Last updated: December 9, 2024