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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 70676 - 70700 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9119 acute myeloid leukemia HGNC:7669 Homo sapiens (human) 10499 NCOA2
  • PMID:12676584
DOID:2526 prostate adenocarcinoma HGNC:7669 Homo sapiens (human) 10499 NCOA2
  • PMID:25664849
DOID:10283 prostate cancer HGNC:7669 Homo sapiens (human) 10499 NCOA2
  • PMID:20166126
DOID:0080199 colorectal carcinoma HGNC:7669 Homo sapiens (human) 10499 NCOA2
  • PMID:19277704
  • PMID:25823027
DOID:11612 polycystic ovary syndrome HGNC:7669 Homo sapiens (human) 10499 NCOA2
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:12566 Homo sapiens (human) 10497 UNC13B
  • MGI:6194238
DOID:1826 epilepsy HGNC:12566 Homo sapiens (human) 10497 UNC13B
  • MGI:6194238
DOID:0110337 osteogenesis imperfecta type 7 HGNC:2379 Homo sapiens (human) 10491 CRTAP
  • MGI:6194238
  • RGD:7240710
DOID:0050696 fetal alcohol spectrum disorder HGNC:51483 Homo sapiens (human) 104909134 LINC02210-CRHR1
  • MGI:6194238
DOID:9778 irritable bowel syndrome HGNC:51483 Homo sapiens (human) 104909134 LINC02210-CRHR1
  • MGI:6194238
DOID:12918 thromboangiitis obliterans HGNC:51483 Homo sapiens (human) 104909134 LINC02210-CRHR1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:51483 Homo sapiens (human) 104909134 LINC02210-CRHR1
  • MGI:6194238
DOID:3877 functional colonic disease HGNC:51483 Homo sapiens (human) 104909134 LINC02210-CRHR1
  • MGI:6194238
DOID:10763 hypertension HGNC:51483 Homo sapiens (human) 104909134 LINC02210-CRHR1
  • MGI:6194238
DOID:1596 depressive disorder HGNC:51483 Homo sapiens (human) 104909134 LINC02210-CRHR1
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:20040 Homo sapiens (human) 10487 CAP1
  • PMID:19188911
DOID:12930 dilated cardiomyopathy HGNC:20039 Homo sapiens (human) 10486 CAP2
  • MGI:6194238
  • RGD:7240710
DOID:5325 Roberts syndrome HGNC:10701 Homo sapiens (human) 10484 SEC23A
  • MGI:6194238
DOID:0111401 congenital dyserythropoietic anemia type II HGNC:10701 Homo sapiens (human) 10484 SEC23A
  • MGI:6194238
DOID:0070307 craniolenticulosutural dysplasia HGNC:10701 Homo sapiens (human) 10484 SEC23A
  • MGI:6194238
  • RGD:7240710
DOID:0081003 Cowden syndrome 7 HGNC:10702 Homo sapiens (human) 10483 SEC23B
  • RGD:7240710
DOID:0070307 craniolenticulosutural dysplasia HGNC:10702 Homo sapiens (human) 10483 SEC23B
  • MGI:6194238
DOID:0111401 congenital dyserythropoietic anemia type II HGNC:10702 Homo sapiens (human) 10483 SEC23B
  • MGI:6194238
  • RGD:7240710
DOID:5325 Roberts syndrome HGNC:10702 Homo sapiens (human) 10483 SEC23B
  • MGI:6194238
DOID:0060825 Christianson syndrome HGNC:11079 Homo sapiens (human) 10479 SLC9A6
  • MGI:6194238
  • RGD:7240710

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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