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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 66001 - 66025 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:9352 type 2 diabetes mellitus HGNC:11621 Homo sapiens (human) 6927 HNF1A
  • MGI:6194238
  • PMID:17828387
  • PMID:18003757
  • PMID:18332101
  • PMID:20716378
  • PMID:21208426
  • PMID:27087001
  • PMID:8945470
  • RGD:7240710
DOID:9074 systemic lupus erythematosus HGNC:2956 Homo sapiens (human) 1773 DNASE1
  • MGI:6194238
  • RGD:7240710
DOID:0060900 Parkinson's disease 14 HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • MGI:6194238
  • RGD:7240710
DOID:0070247 autosomal dominant Emery-Dreifuss muscular dystrophy 2 HGNC:6636 Homo sapiens (human) 4000 LMNA
  • MGI:6194238
  • PMID:10080180
  • PMID:10814726
  • PMID:17701980
  • RGD:7240710
DOID:0110497 autosomal recessive nonsyndromic deafness 39 HGNC:4893 Homo sapiens (human) 3082 HGF
  • MGI:6194238
  • PMID:19576567
  • RGD:7240710
DOID:10763 hypertension HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • MGI:6194238
  • PMID:10024332
DOID:12803 Sly syndrome HGNC:4696 Homo sapiens (human) 2990 GUSB
  • MGI:6194238
  • RGD:7240710
DOID:2962 Cockayne syndrome HGNC:3438 Homo sapiens (human) 2074 ERCC6
  • MGI:6194238
  • PMID:18446857
  • PMID:23599700
  • PMID:25463447
DOID:0060688 arteriovenous malformations of the brain HGNC:3349 Homo sapiens (human) 2022 ENG
  • MGI:6194238
  • PMID:16179574
  • PMID:24876084
DOID:2908 Treacher Collins syndrome HGNC:11654 Homo sapiens (human) 6949 TCOF1
  • MGI:6194238
  • PMID:9096354
DOID:0080552 congenital disorder of glycosylation Ia HGNC:9115 Homo sapiens (human) 5373 PMM2
  • MGI:6194238
  • RGD:7240710
DOID:0110156 Charcot-Marie-Tooth disease type 2B1 HGNC:6636 Homo sapiens (human) 4000 LMNA
  • MGI:6194238
  • PMID:14607793
  • RGD:7240710
DOID:0111066 congenital bile acid synthesis defect 5 HGNC:67 Homo sapiens (human) 5825 ABCD3
  • MGI:6194238
  • RGD:7240710
DOID:0110334 osteogenesis imperfecta type 1 HGNC:2197 Homo sapiens (human) 1277 COL1A1
  • MGI:6194238
  • RGD:7240710
DOID:0060810 syndromic X-linked intellectual disability type 10 HGNC:4800 Homo sapiens (human) 3028 HSD17B10
  • MGI:6194238
  • RGD:7240710
DOID:0050629 Aicardi-Goutieres syndrome HGNC:15925 Homo sapiens (human) 25939 SAMHD1
  • MGI:6194238
  • RGD:7240710
DOID:0060903 thrombosis HGNC:775 Homo sapiens (human) 462 SERPINC1
  • MGI:6194238
  • PMID:12595305
DOID:3650 lactic acidosis RGD:620687 Rattus norvegicus (Norway rat) 64035 Pygl
  • MGI:6194238
  • PMID:17705025
DOID:14504 Niemann-Pick disease HGNC:11120 Homo sapiens (human) 6609 SMPD1
  • MGI:6194238
  • PMID:12556236
DOID:0060733 junctional epidermolysis bullosa with pyloric atresia HGNC:6158 Homo sapiens (human) 3691 ITGB4
  • MGI:6194238
  • RGD:7240710
DOID:594 panic disorder HGNC:5286 Homo sapiens (human) 3350 HTR1A
  • MGI:6194238
  • PMID:20817074
DOID:0080154 short chain acyl-CoA dehydrogenase deficiency HGNC:90 Homo sapiens (human) 35 ACADS
  • MGI:6194238
  • RGD:7240710
DOID:1287 cardiovascular system disease HGNC:320 Homo sapiens (human) 177 AGER
  • MGI:6194238
  • PMID:12606536
  • PMID:20040351
DOID:14451 hyperkalemic periodic paralysis HGNC:10591 Homo sapiens (human) 6329 SCN4A
  • MGI:6194238
  • PMID:12933953
  • RGD:7240710
DOID:0111194 autosomal dominant adult-onset proximal spinal muscular atrophy HGNC:12649 Homo sapiens (human) 9217 VAPB
  • MGI:6194238
  • RGD:7240710

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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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