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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 9001 - 9025 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0081326 oxoglutarate dehydrogenase deficiency HGNC:25590 Homo sapiens (human) 55753 OGDHL
  • MGI:6194238
DOID:0060050 autoimmune disease of blood ZFIN:ZDB-GENE-061013-303 Danio rerio (zebrafish) 557675 c1galt1la
  • MGI:6194238
DOID:0060728 NGLY1-deficiency HGNC:17646 Homo sapiens (human) 55768 NGLY1
  • MGI:6194238
  • RGD:7240710
DOID:1059 intellectual disability ZFIN:ZDB-GENE-090109-2 Danio rerio (zebrafish) 557801 il1rapl1b
  • MGI:6194238
DOID:0112022 non-syndromic X-linked intellectual disability 21 ZFIN:ZDB-GENE-090109-2 Danio rerio (zebrafish) 557801 il1rapl1b
  • MGI:6194238
DOID:10273 heart conduction disease HGNC:15460 Homo sapiens (human) 55799 CACNA2D3
  • MGI:6194238
DOID:0050589 inflammatory bowel disease HGNC:23614 Homo sapiens (human) 55808 ST6GALNAC1
  • MGI:6194238
DOID:0070263 congenital disorder of glycosylation type IIk HGNC:30760 Homo sapiens (human) 55858 TMEM165
  • MGI:6194238
  • RGD:7240710
DOID:0050571 congenital disorder of glycosylation type II HGNC:30760 Homo sapiens (human) 55858 TMEM165
  • MGI:6194238
DOID:0110777 hereditary spastic paraplegia 26 ZFIN:ZDB-GENE-070112-1462 Danio rerio (zebrafish) 558684 b4galnt1a
  • MGI:6194238
DOID:409 liver disease HGNC:9411 Homo sapiens (human) 5589 PRKCSH
  • PMID:12529853
DOID:0050770 polycystic liver disease HGNC:9411 Homo sapiens (human) 5589 PRKCSH
  • MGI:6194238
  • PMID:15057895
  • RGD:7240710
DOID:0050567 orofacial cleft HGNC:15814 Homo sapiens (human) 55902 ACSS2
  • PMID:27229527
  • PMID:28543373
DOID:1574 alcohol use disorder HGNC:15814 Homo sapiens (human) 55902 ACSS2
  • MGI:6194238
DOID:3319 lymphangioleiomyomatosis HGNC:15814 Homo sapiens (human) 55902 ACSS2
  • PMID:29885404
DOID:11981 morbid obesity HGNC:15814 Homo sapiens (human) 55902 ACSS2
  • PMID:22384010
DOID:1312 focal segmental glomerulosclerosis HGNC:18290 Homo sapiens (human) 55907 CMAS
  • MGI:6194238
DOID:4079 heart valve disease ZFIN:ZDB-GENE-030131-2360 Danio rerio (zebrafish) 559073 galnt1
  • MGI:6194238
DOID:5419 schizophrenia ZFIN:ZDB-GENE-090312-180 Danio rerio (zebrafish) 559721 chst3a
  • MGI:6194238
DOID:0050813 spondyloepiphyseal dysplasia with congenital joint dislocations ZFIN:ZDB-GENE-090312-180 Danio rerio (zebrafish) 559721 chst3a
  • MGI:6194238
DOID:2256 osteochondrodysplasia ZFIN:ZDB-GENE-090312-180 Danio rerio (zebrafish) 559721 chst3a
  • MGI:6194238
DOID:9256 colorectal cancer ZFIN:ZDB-GENE-060503-704 Danio rerio (zebrafish) 559736 galnt12
  • MGI:6194238
DOID:0112216 developmental and epileptic encephalopathy 80 MGI:1891825 Mus musculus (house mouse) 55981 Pigb
  • MGI:6194238
DOID:10112 sleeping sickness MGI:1891825 Mus musculus (house mouse) 55981 Pigb
  • MGI:6194238
DOID:0060770 dextro-looped transposition of the great arteries HGNC:18292 Homo sapiens (human) 55997 CFC1
  • MGI:6194238

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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