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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 66176 - 66200 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0081215 autosomal recessive intellectual developmental disorder 52 HGNC:19263 Homo sapiens (human) 81562 LMAN2L
  • RGD:7240710
DOID:0060170 generalized epilepsy with febrile seizures plus RGD:69364 Rattus norvegicus (Norway rat) 81574 Scn1a
  • MGI:6194238
DOID:0060041 autism spectrum disorder RGD:69364 Rattus norvegicus (Norway rat) 81574 Scn1a
  • MGI:6194238
DOID:1826 epilepsy RGD:69364 Rattus norvegicus (Norway rat) 81574 Scn1a
  • MGI:6194238
DOID:0070379 developmental and epileptic encephalopathy 6B RGD:69364 Rattus norvegicus (Norway rat) 81574 Scn1a
  • MGI:6194238
DOID:0080422 Dravet syndrome RGD:69364 Rattus norvegicus (Norway rat) 81574 Scn1a
  • MGI:6194238
DOID:0111294 generalized epilepsy with febrile seizures plus 2 RGD:69364 Rattus norvegicus (Norway rat) 81574 Scn1a
  • MGI:6194238
DOID:0111183 familial hemiplegic migraine 3 RGD:69364 Rattus norvegicus (Norway rat) 81574 Scn1a
  • MGI:6194238
DOID:2030 anxiety disorder RGD:69364 Rattus norvegicus (Norway rat) 81574 Scn1a
  • MGI:6194238
DOID:9975 cocaine dependence HGNC:17025 Homo sapiens (human) 81578 COL21A1
  • PMID:18438686
DOID:10273 heart conduction disease HGNC:1461 Homo sapiens (human) 816 CAMK2B
  • MGI:6194238
DOID:0080230 autosomal dominant intellectual developmental disorder 54 HGNC:1461 Homo sapiens (human) 816 CAMK2B
  • RGD:7240710
DOID:12053 cryptococcosis MGI:1932052 Mus musculus (house mouse) 81600 Chia1
  • MGI:6194238
DOID:10325 silicosis MGI:1932052 Mus musculus (house mouse) 81600 Chia1
  • MGI:6194238
DOID:0050127 sinusitis MGI:1932052 Mus musculus (house mouse) 81600 Chia1
  • MGI:6194238
DOID:2841 asthma MGI:1932052 Mus musculus (house mouse) 81600 Chia1
  • MGI:6194238
DOID:1508 candidiasis HGNC:16673 Homo sapiens (human) 81611 ANP32E
  • MGI:6194238
DOID:10588 adrenoleukodystrophy HGNC:24174 Homo sapiens (human) 81616 ACSBG2
  • MGI:6194238
DOID:162 cancer HGNC:23303 Homo sapiens (human) 81619 TSPAN14
  • MGI:6194238
DOID:936 brain disease HGNC:13481 Homo sapiens (human) 81622 UNC93B1
  • RGD:7240710
DOID:1338 congenital dyserythropoietic anemia HGNC:15480 Homo sapiens (human) 81624 DIAPH3
  • MGI:6194238
DOID:0060690 autosomal dominant auditory neuropathy 1 HGNC:15480 Homo sapiens (human) 81624 DIAPH3
  • MGI:6194238
  • RGD:7240710
DOID:1682 congenital heart disease RGD:619965 Rattus norvegicus (Norway rat) 81636 Adcy2
  • MGI:6194238
DOID:12858 Huntington's disease RGD:2071 Rattus norvegicus (Norway rat) 81638 Agtr1b
  • MGI:6194238
DOID:4450 renal cell carcinoma RGD:2071 Rattus norvegicus (Norway rat) 81638 Agtr1b
  • MGI:6194238

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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