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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 8801 - 8825 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:6432 pulmonary hypertension HGNC:14240 Homo sapiens (human) 55512 SMPD3
  • MGI:6194238
DOID:2977 primary hyperoxaluria HGNC:4570 Homo sapiens (human) 9380 GRHPR
  • PMID:10484776
DOID:0070255 congenital disorder of glycosylation type IIc HGNC:4369 Homo sapiens (human) 2762 GMDS
  • MGI:6194238
DOID:1891 optic nerve disease HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
DOID:4621 holoprosencephaly HGNC:29185 Homo sapiens (human) 23007 PLCH1
  • RGD:7240710
DOID:3827 congenital diaphragmatic hernia HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:12858 Huntington's disease HGNC:4341 Homo sapiens (human) 2752 GLUL
  • PMID:3159462
  • PMID:6237280
DOID:6457 Cowden syndrome HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
DOID:0070134 autosomal recessive cutis laxa type IIA HGNC:18481 Homo sapiens (human) 23545 ATP6V0A2
  • RGD:7240710
DOID:13482 Proteus syndrome HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
  • PMID:21793738
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:12452318
DOID:10603 glucose intolerance HGNC:6554 Homo sapiens (human) 3953 LEPR
  • MGI:6194238
DOID:9970 obesity HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
  • PMID:12843191
DOID:9675 pulmonary emphysema HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:10763 hypertension HGNC:8125 Homo sapiens (human) 4968 OGG1
  • PMID:25529925
DOID:11396 pulmonary edema HGNC:435 Homo sapiens (human) 240 ALOX5
  • MGI:6194238
DOID:11650 bronchopulmonary dysplasia HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:9020 Homo sapiens (human) 5313 PKLR
  • MGI:6194238
DOID:0112233 lissencephaly 8 HGNC:26899 Homo sapiens (human) 160418 TMTC3
  • RGD:7240710
DOID:552 pneumonia HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:15928955
DOID:1682 congenital heart disease HGNC:12757 Homo sapiens (human) 11091 WDR5
  • MGI:6194238
DOID:13375 temporal arteritis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:10616010
DOID:3407 carotid artery disease HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:15258789
DOID:14330 Parkinson's disease HGNC:4177 Homo sapiens (human) 2629 GBA1
  • MGI:6194238
  • PMID:19945510
  • PMID:20528910
  • PMID:20947659
  • PMID:21242499
  • PMID:24126159
  • PMID:25639775
  • PMID:26223426
DOID:5419 schizophrenia HGNC:4092 Homo sapiens (human) 2571 GAD1
  • PMID:17303389
  • PMID:18534564
  • PMID:21250934

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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