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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 61351 - 61375 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 HGNC:1552 Homo sapiens (human) 84733 CBX2
  • PMID:35693827
DOID:0050866 oral squamous cell carcinoma HGNC:1552 Homo sapiens (human) 84733 CBX2
  • PMID:24885002
DOID:162 cancer HGNC:1552 Homo sapiens (human) 84733 CBX2
  • MGI:6194238
DOID:14447 gonadal dysgenesis HGNC:1552 Homo sapiens (human) 84733 CBX2
  • PMID:23219007
DOID:0111776 46,XY sex reversal 5 HGNC:1552 Homo sapiens (human) 84733 CBX2
  • RGD:7240710
DOID:2738 pseudoxanthoma elasticum HGNC:15517 Homo sapiens (human) 64132 XYLT2
  • RGD:7240710
DOID:0080322 polycystic kidney disease HGNC:15517 Homo sapiens (human) 64132 XYLT2
  • MGI:6194238
DOID:2738 pseudoxanthoma elasticum HGNC:15516 Homo sapiens (human) 64131 XYLT1
  • RGD:7240710
DOID:557 kidney disease HGNC:15516 Homo sapiens (human) 64131 XYLT1
  • MGI:6194238
DOID:0060462 Desbuquois dysplasia HGNC:15516 Homo sapiens (human) 64131 XYLT1
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus HGNC:15516 Homo sapiens (human) 64131 XYLT1
  • PMID:16759312
DOID:9119 acute myeloid leukemia HGNC:15514 Homo sapiens (human) 8301 PICALM
  • PMID:12461747
  • RGD:7240710
DOID:10908 hydrocephalus HGNC:15505 Homo sapiens (human) 79143 MBOAT7
  • MGI:6194238
DOID:0081219 autosomal recessive intellectual developmental disorder 57 HGNC:15505 Homo sapiens (human) 79143 MBOAT7
  • RGD:7240710
DOID:0080074 neural tube defect HGNC:1550 Homo sapiens (human) 875 CBS
  • PMID:12649066
DOID:3393 coronary artery disease HGNC:1550 Homo sapiens (human) 875 CBS
  • PMID:12855221
DOID:12365 malaria HGNC:1550 Homo sapiens (human) 875 CBS
  • PMID:27198213
DOID:14250 Down syndrome HGNC:1550 Homo sapiens (human) 875 CBS
  • MGI:6194238
DOID:3526 cerebral infarction HGNC:1550 Homo sapiens (human) 875 CBS
  • PMID:20458436
DOID:9263 homocystinuria HGNC:1550 Homo sapiens (human) 875 CBS
  • MGI:6194238
  • PMID:7506602
  • RGD:7240710
DOID:2394 ovarian cancer HGNC:1550 Homo sapiens (human) 875 CBS
  • MGI:6194238
DOID:219 colon cancer HGNC:1550 Homo sapiens (human) 875 CBS
  • MGI:6194238
DOID:9279 hyperhomocysteinemia HGNC:1550 Homo sapiens (human) 875 CBS
  • MGI:6194238
  • PMID:10704624
DOID:0050731 vitamin B12 deficiency HGNC:1550 Homo sapiens (human) 875 CBS
  • MGI:6194238
DOID:1612 breast cancer HGNC:1550 Homo sapiens (human) 875 CBS
  • MGI:6194238

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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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Last updated: December 9, 2024