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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 69626 - 69650 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:1459 hypothyroidism HGNC:713 Homo sapiens (human) 410 ARSA
  • MGI:6194238
DOID:1470 major depressive disorder HGNC:711 Homo sapiens (human) 408 ARRB1
  • PMID:15514408
DOID:0060180 colitis HGNC:711 Homo sapiens (human) 408 ARRB1
  • MGI:6194238
DOID:6000 congestive heart failure HGNC:711 Homo sapiens (human) 408 ARRB1
  • MGI:6194238
DOID:1508 candidiasis HGNC:23366 Homo sapiens (human) 81873 ARPC5L
  • MGI:6194238
DOID:0050328 congenital hypothyroidism HGNC:708 Homo sapiens (human) 10092 ARPC5
  • MGI:6194238
DOID:612 primary immunodeficiency disease HGNC:708 Homo sapiens (human) 10092 ARPC5
  • RGD:7240710
DOID:1508 candidiasis HGNC:708 Homo sapiens (human) 10092 ARPC5
  • MGI:6194238
DOID:3907 lung squamous cell carcinoma HGNC:708 Homo sapiens (human) 10092 ARPC5
  • PMID:22089643
DOID:3908 lung non-small cell carcinoma HGNC:708 Homo sapiens (human) 10092 ARPC5
  • PMID:22089643
DOID:0050866 oral squamous cell carcinoma HGNC:704 Homo sapiens (human) 10095 ARPC1B
  • PMID:26138391
DOID:0112004 immunodeficiency 71 HGNC:704 Homo sapiens (human) 10095 ARPC1B
  • RGD:7240710
DOID:10534 stomach cancer HGNC:704 Homo sapiens (human) 10095 ARPC1B
  • PMID:15279900
DOID:0050908 myelodysplastic syndrome HGNC:704 Homo sapiens (human) 10095 ARPC1B
  • PMID:22608605
DOID:5419 schizophrenia HGNC:704 Homo sapiens (human) 10095 ARPC1B
  • PMID:15098003
DOID:4029 gastritis HGNC:704 Homo sapiens (human) 10095 ARPC1B
  • PMID:23292007
DOID:5419 schizophrenia HGNC:703 Homo sapiens (human) 10552 ARPC1A
  • PMID:15098003
DOID:1793 pancreatic cancer HGNC:703 Homo sapiens (human) 10552 ARPC1A
  • PMID:19145645
DOID:10763 hypertension HGNC:700 Homo sapiens (human) 405 ARNT
  • MGI:6194238
DOID:4450 renal cell carcinoma HGNC:700 Homo sapiens (human) 405 ARNT
  • PMID:27595394
DOID:9352 type 2 diabetes mellitus HGNC:700 Homo sapiens (human) 405 ARNT
  • PMID:16096055
DOID:12336 male infertility HGNC:23045 Homo sapiens (human) 84071 ARMC2
  • MGI:6194238
DOID:0111919 spermatogenic failure 38 HGNC:23045 Homo sapiens (human) 84071 ARMC2
  • RGD:7240710
DOID:0050777 Joubert syndrome HGNC:694 Homo sapiens (human) 403 ARL3
  • RGD:7240710
DOID:0110415 retinitis pigmentosa 2 HGNC:694 Homo sapiens (human) 403 ARL3
  • 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: December 9, 2024