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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 71576 - 71600 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:13580 cholestasis HGNC:1681 Homo sapiens (human) 960 CD44
  • MGI:6194238
DOID:4450 renal cell carcinoma HGNC:1681 Homo sapiens (human) 960 CD44
  • PMID:12833185
  • PMID:17284111
DOID:5154 borna disease HGNC:1681 Homo sapiens (human) 960 CD44
  • MGI:6194238
DOID:3457 invasive lobular carcinoma HGNC:1681 Homo sapiens (human) 960 CD44
  • PMID:11245336
DOID:0050861 colorectal adenocarcinoma HGNC:1681 Homo sapiens (human) 960 CD44
  • PMID:16425351
DOID:1459 hypothyroidism HGNC:7672 Homo sapiens (human) 9611 NCOR1
  • MGI:6194238
DOID:0060037 developmental disorder of mental health HGNC:7672 Homo sapiens (human) 9611 NCOR1
  • MGI:6194238
DOID:11612 polycystic ovary syndrome HGNC:7672 Homo sapiens (human) 9611 NCOR1
  • MGI:6194238
DOID:12858 Huntington's disease HGNC:7672 Homo sapiens (human) 9611 NCOR1
  • PMID:10441327
DOID:2030 anxiety disorder HGNC:7672 Homo sapiens (human) 9611 NCOR1
  • MGI:6194238
DOID:8398 osteoarthritis HGNC:7673 Homo sapiens (human) 9612 NCOR2
  • PMID:15334463
DOID:4971 myelofibrosis HGNC:7673 Homo sapiens (human) 9612 NCOR2
  • MGI:6194238
DOID:0060037 developmental disorder of mental health HGNC:7673 Homo sapiens (human) 9612 NCOR2
  • MGI:6194238
DOID:1612 breast cancer HGNC:7673 Homo sapiens (human) 9612 NCOR2
  • PMID:19904269
DOID:2871 endometrial carcinoma HGNC:7673 Homo sapiens (human) 9612 NCOR2
  • PMID:14751175
DOID:10534 stomach cancer HGNC:4212 Homo sapiens (human) 9615 GDA
  • PMID:8076377
DOID:783 end stage renal disease HGNC:73 Homo sapiens (human) 9619 ABCG1
  • MGI:6194238
DOID:0050580 hereditary lymphedema HGNC:1850 Homo sapiens (human) 9620 CELSR1
  • RGD:7240710
DOID:10283 prostate cancer HGNC:6365 Homo sapiens (human) 9622 KLK4
  • PMID:12370833
  • PMID:17545602
DOID:0110057 amelogenesis imperfecta type 2A1 HGNC:6365 Homo sapiens (human) 9622 KLK4
  • RGD:7240710
DOID:2394 ovarian cancer HGNC:6365 Homo sapiens (human) 9622 KLK4
  • PMID:15262123
DOID:1612 breast cancer HGNC:6365 Homo sapiens (human) 9622 KLK4
  • PMID:18687310
  • PMID:19190825
DOID:162 cancer HGNC:1686 Homo sapiens (human) 963 CD53
  • MGI:6194238
DOID:0050650 familial atrial fibrillation HGNC:8063 Homo sapiens (human) 9631 NUP155
  • RGD:7240710
DOID:0111723 Jacobsen Syndrome HGNC:3660 Homo sapiens (human) 9637 FEZ2
  • 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