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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 9176 - 9200 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:13406 pulmonary sarcoidosis ZFIN:ZDB-GENE-060531-71 Danio rerio (zebrafish) 566487 gbgt1l2
  • MGI:6194238
DOID:2945 severe acute respiratory syndrome ZFIN:ZDB-GENE-060531-71 Danio rerio (zebrafish) 566487 gbgt1l2
  • MGI:6194238
DOID:10763 hypertension ZFIN:ZDB-GENE-060531-71 Danio rerio (zebrafish) 566487 gbgt1l2
  • MGI:6194238
DOID:4948 gallbladder carcinoma ZFIN:ZDB-GENE-060531-71 Danio rerio (zebrafish) 566487 gbgt1l2
  • MGI:6194238
DOID:0110676 congenital myasthenic syndrome 13 ZFIN:ZDB-GENE-060526-18 Danio rerio (zebrafish) 566539 dpagt1
  • MGI:6194238
DOID:0080562 congenital disorder of glycosylation Ij ZFIN:ZDB-GENE-060526-18 Danio rerio (zebrafish) 566539 dpagt1
  • MGI:6194238
DOID:0110669 congenital myasthenic syndrome 14 MGI:1914731 Mus musculus (house mouse) 56737 Alg2
  • MGI:6194238
DOID:0080561 congenital disorder of glycosylation Ii MGI:1914731 Mus musculus (house mouse) 56737 Alg2
  • MGI:6194238
DOID:2565 macular corneal dystrophy MGI:1931825 Mus musculus (house mouse) 56773 Chst5
  • MGI:6194238
DOID:0112315 brain small vessel disease 3 ZFIN:ZDB-GENE-070424-114 Danio rerio (zebrafish) 567859 colgalt1b
  • MGI:6194238
DOID:206 hereditary multiple exostoses RGD:62065 Rattus norvegicus (Norway rat) 56819 Extl3
  • MGI:6194238
DOID:9970 obesity HGNC:18859 Homo sapiens (human) 56848 SPHK2
  • MGI:6194238
DOID:0050700 cardiomyopathy HGNC:18859 Homo sapiens (human) 56848 SPHK2
  • MGI:6194238
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:18859 Homo sapiens (human) 56848 SPHK2
  • MGI:6194238
DOID:1059 intellectual disability ZFIN:ZDB-GENE-061013-249 Danio rerio (zebrafish) 568868 il1rapl1a
  • MGI:6194238
DOID:0112022 non-syndromic X-linked intellectual disability 21 ZFIN:ZDB-GENE-061013-249 Danio rerio (zebrafish) 568868 il1rapl1a
  • MGI:6194238
DOID:10534 stomach cancer ZFIN:ZDB-GENE-060929-728 Danio rerio (zebrafish) 568888 fut11
  • MGI:6194238
DOID:0060050 autoimmune disease of blood HGNC:24337 Homo sapiens (human) 56913 C1GALT1
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I ZFIN:ZDB-GENE-041210-295 Danio rerio (zebrafish) 569494 alg12
  • MGI:6194238
DOID:0080559 congenital disorder of glycosylation Ig ZFIN:ZDB-GENE-041210-295 Danio rerio (zebrafish) 569494 alg12
  • MGI:6194238
DOID:2377 multiple sclerosis HGNC:30308 Homo sapiens (human) 56963 RGMA
  • PMID:20072140
DOID:3328 temporal lobe epilepsy HGNC:30308 Homo sapiens (human) 56963 RGMA
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:30308 Homo sapiens (human) 56963 RGMA
  • MGI:6194238
DOID:3525 middle cerebral artery infarction HGNC:30308 Homo sapiens (human) 56963 RGMA
  • MGI:6194238
DOID:0110297 autosomal recessive limb-girdle muscular dystrophy type 2K ZFIN:ZDB-GENE-060929-966 Danio rerio (zebrafish) 569769 pomt1
  • MGI:6194238

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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