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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 69751 - 69775 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:636 central pontine myelinolysis HGNC:637 Homo sapiens (human) 361 AQP4
  • PMID:24252214
DOID:1727 retinal vein occlusion HGNC:637 Homo sapiens (human) 361 AQP4
  • MGI:6194238
DOID:2316 brain ischemia HGNC:637 Homo sapiens (human) 361 AQP4
  • MGI:6194238
DOID:0080122 Alpers-Huttenlocher syndrome HGNC:637 Homo sapiens (human) 361 AQP4
  • PMID:20680636
DOID:224 transient cerebral ischemia HGNC:637 Homo sapiens (human) 361 AQP4
  • MGI:6194238
DOID:1459 hypothyroidism HGNC:636 Homo sapiens (human) 360 AQP3
  • MGI:6194238
DOID:2316 brain ischemia HGNC:636 Homo sapiens (human) 360 AQP3
  • MGI:6194238
DOID:12387 nephrogenic diabetes insipidus HGNC:636 Homo sapiens (human) 360 AQP3
  • MGI:6194238
DOID:4724 brain edema HGNC:636 Homo sapiens (human) 360 AQP3
  • PMID:27487831
DOID:0081061 nephrogenic diabetes insipidus type 2 HGNC:634 Homo sapiens (human) 359 AQP2
  • RGD:7240710
DOID:10763 hypertension HGNC:634 Homo sapiens (human) 359 AQP2
  • MGI:6194238
DOID:9409 diabetes insipidus HGNC:634 Homo sapiens (human) 359 AQP2
  • MGI:6194238
DOID:1837 diabetic ketoacidosis HGNC:634 Homo sapiens (human) 359 AQP2
  • PMID:12021537
DOID:12387 nephrogenic diabetes insipidus HGNC:634 Homo sapiens (human) 359 AQP2
  • MGI:6194238
  • PMID:12191971
  • PMID:16845277
  • PMID:18653713
  • PMID:19147915
  • PMID:19293543
  • PMID:19458121
  • PMID:19461158
  • PMID:19585583
  • PMID:19701945
DOID:10763 hypertension HGNC:633 Homo sapiens (human) 358 AQP1
  • MGI:6194238
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:633 Homo sapiens (human) 358 AQP1
  • MGI:6194238
DOID:13141 uveitis HGNC:633 Homo sapiens (human) 358 AQP1
  • MGI:6194238
DOID:636 central pontine myelinolysis HGNC:633 Homo sapiens (human) 358 AQP1
  • PMID:24252214
DOID:4724 brain edema HGNC:633 Homo sapiens (human) 358 AQP1
  • MGI:6194238
  • PMID:27487831
DOID:1727 retinal vein occlusion HGNC:633 Homo sapiens (human) 358 AQP1
  • MGI:6194238
DOID:10908 hydrocephalus HGNC:633 Homo sapiens (human) 358 AQP1
  • MGI:6194238
DOID:9351 diabetes mellitus HGNC:633 Homo sapiens (human) 358 AQP1
  • MGI:6194238
DOID:9428 intracranial hypertension HGNC:633 Homo sapiens (human) 358 AQP1
  • PMID:27487831
DOID:1824 status epilepticus HGNC:633 Homo sapiens (human) 358 AQP1
  • MGI:6194238
DOID:14784 olivopontocerebellar atrophy HGNC:15984 Homo sapiens (human) 54840 APTX
  • PMID:21465257

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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