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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 3951 - 3975 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050453 lissencephaly HGNC:8574 Homo sapiens (human) 5048 PAFAH1B1
  • MGI:6194238
  • PMID:11115846
DOID:0112237 lissencephaly 1 HGNC:8574 Homo sapiens (human) 5048 PAFAH1B1
  • RGD:7240710
DOID:11832 visual epilepsy HGNC:8574 Homo sapiens (human) 5048 PAFAH1B1
  • MGI:6194238
DOID:1508 candidiasis ZFIN:ZDB-GENE-050309-15 Danio rerio (zebrafish) 503885 fut9d
  • MGI:6194238
DOID:2978 carbohydrate metabolic disorder HGNC:8527 Homo sapiens (human) 5019 OXCT1
  • PMID:8844009
DOID:9352 type 2 diabetes mellitus HGNC:8527 Homo sapiens (human) 5019 OXCT1
  • MGI:6194238
DOID:9970 obesity HGNC:8527 Homo sapiens (human) 5019 OXCT1
  • MGI:6194238
DOID:1826 epilepsy HGNC:877 Homo sapiens (human) 501 ALDH7A1
  • MGI:6194238
DOID:0080768 pyridoxine-dependent epilepsy HGNC:877 Homo sapiens (human) 501 ALDH7A1
  • MGI:6194238
DOID:0070519 early-onset vitamin B6-dependent epilepsy 4 HGNC:877 Homo sapiens (human) 501 ALDH7A1
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:877 Homo sapiens (human) 501 ALDH7A1
  • PMID:30901224
DOID:0080572 congenital disorder of glycosylation Iw RGD:1565793 Rattus norvegicus (Norway rat) 500972 Stt3a
  • MGI:6194238
DOID:331 central nervous system disease HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
DOID:0111442 optic atrophy 9 HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
DOID:0050883 infantile cerebellar-retinal degeneration HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
  • RGD:7240710
DOID:1891 optic nerve disease HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
DOID:0081097 Rafiq syndrome RGD:1563595 Rattus norvegicus (Norway rat) 499751 Man1b1
  • MGI:6194238
DOID:4752 multiple system atrophy RGD:1306722 Rattus norvegicus (Norway rat) 498332 Coq2
  • MGI:6194238
DOID:0050730 coenzyme Q10 deficiency disease RGD:1306722 Rattus norvegicus (Norway rat) 498332 Coq2
  • MGI:6194238
DOID:0070238 primary coenzyme Q10 deficiency 1 RGD:1306722 Rattus norvegicus (Norway rat) 498332 Coq2
  • MGI:6194238
DOID:1184 nephrotic syndrome RGD:1306722 Rattus norvegicus (Norway rat) 498332 Coq2
  • MGI:6194238
DOID:10603 glucose intolerance RGD:1306722 Rattus norvegicus (Norway rat) 498332 Coq2
  • PMID:26296322
DOID:2394 ovarian cancer HGNC:8143 Homo sapiens (human) 4978 OPCML
  • 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: August 19, 2024