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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 68926 - 68950 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:684 hepatocellular carcinoma MGI:97569 Mus musculus (house mouse) 18670 Abcb4
  • PMID:7977654
DOID:2256 osteochondrodysplasia HGNC:2185 Homo sapiens (human) 1300 COL10A1
  • PMID:8004099
DOID:9268 glycine encephalopathy HGNC:473 Homo sapiens (human) 275 AMT
  • PMID:8005589
  • PMID:9600239
  • PMID:9621520
  • RGD:7240710
DOID:3209 junctional epidermolysis bullosa HGNC:6493 Homo sapiens (human) 3918 LAMC2
  • PMID:8012393
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:4392 Homo sapiens (human) 2778 GNAS
  • PMID:8012802
DOID:3904 bronchus carcinoma HGNC:5962 Homo sapiens (human) 3586 IL10
  • PMID:8030748
DOID:3904 bronchus carcinoma HGNC:6000 Homo sapiens (human) 3557 IL1RN
  • PMID:8030748
DOID:9146 visceral leishmaniasis HGNC:2434 Homo sapiens (human) 1437 CSF2
  • PMID:8035028
DOID:479 angiokeratoma HGNC:7631 Homo sapiens (human) 4668 NAGA
  • PMID:8040340
DOID:10123 pigmentation disease HGNC:3327 Homo sapiens (human) 2006 ELN
  • PMID:8040608
DOID:8645 subacute delirium HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:8043620
DOID:769 neuroblastoma HGNC:7849 Homo sapiens (human) 4830 NME1
  • PMID:8047138
DOID:2855 hyperthyroxinemia HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:8048949
DOID:0081267 graft-versus-host disease HGNC:6000 Homo sapiens (human) 3557 IL1RN
  • PMID:8049450
DOID:11656 cicatricial pemphigoid HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1
  • PMID:8052655
  • PMID:9683867
DOID:11054 urinary bladder cancer RGD:3322 Rattus norvegicus (Norway rat) 25344 Phb1
  • PMID:8062216
DOID:3996 urinary system cancer HGNC:12780 Homo sapiens (human) 7472 WNT2
  • PMID:8064891
DOID:9884 muscular dystrophy HGNC:10805 Homo sapiens (human) 6442 SGCA
  • PMID:8069911
  • PMID:9192266
DOID:3883 Lynch syndrome HGNC:9121 Homo sapiens (human) 5378 PMS1
  • PMID:8072530
DOID:11832 visual epilepsy RGD:620713 Rattus norvegicus (Norway rat) 79114 Fgfr1
  • PMID:8072686
DOID:0060903 thrombosis HGNC:9451 Homo sapiens (human) 5624 PROC
  • PMID:8073406
DOID:1923 disorder of sexual development HGNC:5212 Homo sapiens (human) 3293 HSD17B3
  • PMID:8075637
DOID:10534 stomach cancer HGNC:4212 Homo sapiens (human) 9615 GDA
  • PMID:8076377
DOID:2394 ovarian cancer HGNC:7029 Homo sapiens (human) 4233 MET
  • PMID:8077049
DOID:986 alopecia areata HGNC:6000 Homo sapiens (human) 3557 IL1RN
  • PMID:8077705

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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