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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 July 29, 2024
Displaying entries 9151 - 9175 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1612 breast cancer HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:23828384
DOID:0050861 colorectal adenocarcinoma HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • PMID:21609933
DOID:10487 Hirschsprung's disease HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:21991983
DOID:9744 type 1 diabetes mellitus HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:16489975
DOID:5804 discrete subaortic stenosis HGNC:3575 Homo sapiens (human) 9415 FADS2
  • MGI:6194238
DOID:850 lung disease HGNC:10798 Homo sapiens (human) 653509 SFTPA1
  • MGI:6194238
  • PMID:16429424
  • PMID:9230741
DOID:5419 schizophrenia HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
  • PMID:14745448
  • PMID:17825267
  • PMID:20214684
  • PMID:20921115
  • PMID:21049487
DOID:2527 nephrosis HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • MGI:6194238
DOID:2841 asthma HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:20514434
DOID:784 chronic kidney disease HGNC:6554 Homo sapiens (human) 3953 LEPR
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:29482350
DOID:9675 pulmonary emphysema HGNC:4311 Homo sapiens (human) 2729 GCLC
  • MGI:6194238
DOID:3649 pyruvate decarboxylase deficiency HGNC:21350 Homo sapiens (human) 8050 PDHX
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:8275435
DOID:10763 hypertension HGNC:9592 Homo sapiens (human) 5730 PTGDS
  • PMID:11882588
DOID:1459 hypothyroidism HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • MGI:6194238
DOID:6364 migraine HGNC:11892 Homo sapiens (human) 7124 TNF
  • RGD:7240710
DOID:0060448 Fleck corneal dystrophy HGNC:23785 Homo sapiens (human) 200576 PIKFYVE
  • RGD:7240710
DOID:0060180 colitis HGNC:288 Homo sapiens (human) 155 ADRB3
  • MGI:6194238
DOID:10763 hypertension HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:17283861
DOID:5844 myocardial infarction HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:10534 stomach cancer HGNC:1637 Homo sapiens (human) 912 CD1D
  • PMID:26119195
DOID:2349 arteriosclerosis HGNC:435 Homo sapiens (human) 240 ALOX5
  • PMID:14702425
DOID:13603 obstructive jaundice HGNC:8729 Homo sapiens (human) 5111 PCNA
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:21679057

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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: August 19, 2024