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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 70976 - 71000 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0111051 platelet-type bleeding disorder 18 HGNC:9879 Homo sapiens (human) 10235 RASGRP2
  • RGD:7240710
DOID:0110912 leukocyte adhesion deficiency 3 HGNC:9879 Homo sapiens (human) 10235 RASGRP2
  • MGI:6194238
DOID:4608 common bile duct neoplasm HGNC:7371 Homo sapiens (human) 10232 MSLN
  • PMID:16416732
DOID:3587 pancreatic ductal carcinoma HGNC:7371 Homo sapiens (human) 10232 MSLN
  • PMID:12874021
  • PMID:19818733
DOID:1793 pancreatic cancer HGNC:7371 Homo sapiens (human) 10232 MSLN
  • PMID:17019794
  • PMID:17785569
  • PMID:18281514
  • PMID:19843662
DOID:4897 bile duct carcinoma HGNC:7371 Homo sapiens (human) 10232 MSLN
  • PMID:17276942
DOID:2394 ovarian cancer HGNC:7371 Homo sapiens (human) 10232 MSLN
  • PMID:17581599
  • PMID:17785569
DOID:26 pancreas disease HGNC:7371 Homo sapiens (human) 10232 MSLN
  • PMID:19843662
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:16893 Homo sapiens (human) 10226 PLIN3
  • MGI:6194238
DOID:9970 obesity HGNC:16893 Homo sapiens (human) 10226 PLIN3
  • MGI:6194238
DOID:0111581 C syndrome HGNC:16892 Homo sapiens (human) 10225 CD96
  • RGD:7240710
DOID:0070418 vertebral hypersegmentation and orofacial anomalies HGNC:4216 Homo sapiens (human) 10220 GDF11
  • MGI:6194238
  • RGD:7240710
DOID:9993 hypoglycemia HGNC:1778 Homo sapiens (human) 1022 CDK7
  • MGI:6194238
DOID:0050593 primary congenital glaucoma HGNC:1778 Homo sapiens (human) 1022 CDK7
  • MGI:6194238
DOID:0110965 brachydactyly type A2 HGNC:1778 Homo sapiens (human) 1022 CDK7
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:1778 Homo sapiens (human) 1022 CDK7
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:1778 Homo sapiens (human) 1022 CDK7
  • PMID:11124424
DOID:1612 breast cancer HGNC:1778 Homo sapiens (human) 1022 CDK7
  • MGI:6194238
DOID:10825 essential hypertension HGNC:1778 Homo sapiens (human) 1022 CDK7
  • MGI:6194238
DOID:1787 pericarditis HGNC:9364 Homo sapiens (human) 10216 PRG4
  • PMID:16429407
DOID:0090127 camptodactyly-arthropathy-coxa vara-pericarditis syndrome HGNC:9364 Homo sapiens (human) 10216 PRG4
  • RGD:7240710
DOID:1824 status epilepticus HGNC:9398 Homo sapiens (human) 10215 OLIG2
  • MGI:6194238
DOID:219 colon cancer MGI:2142572 Mus musculus (house mouse) 102103 Mtus1
  • MGI:6194238
DOID:3459 breast carcinoma MGI:2142572 Mus musculus (house mouse) 102103 Mtus1
  • MGI:6194238
DOID:4001 ovarian carcinoma MGI:2142572 Mus musculus (house mouse) 102103 Mtus1
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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