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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 70926 - 70950 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:0060688 arteriovenous malformations of the brain HGNC:3349 Homo sapiens (human) 2022 ENG
  • MGI:6194238
  • PMID:16179574
  • PMID:24876084
DOID:1094 attention deficit hyperactivity disorder HGNC:17938 Homo sapiens (human) 50632 CALY
  • MGI:6194238
  • PMID:16172615
DOID:0050469 Costello syndrome HGNC:5173 Homo sapiens (human) 3265 HRAS
  • MGI:6194238
  • PMID:16170316
  • PMID:16881968
  • PMID:25914166
  • RGD:7240710
DOID:6000 congestive heart failure HGNC:7166 Homo sapiens (human) 4313 MMP2
  • MGI:6194238
  • PMID:16169329
  • PMID:20606426
DOID:0090129 carnitine palmitoyltransferase I deficiency MGI:1098296 Mus musculus (house mouse) 12894 Cpt1a
  • MGI:6194238
  • PMID:16169268
DOID:1612 breast cancer MGI:98834 Mus musculus (house mouse) 22059 Trp53
  • MGI:6194238
  • PMID:16166291
  • PMID:9519874
DOID:1596 depressive disorder HGNC:12008 Homo sapiens (human) 7166 TPH1
  • MGI:6194238
  • PMID:16165107
  • PMID:17134762
DOID:10763 hypertension RGD:2535 Rattus norvegicus (Norway rat) 24326 Ednra
  • MGI:6194238
  • PMID:16157796
  • PMID:20144075
DOID:0060291 oculodentodigital dysplasia MGI:95713 Mus musculus (house mouse) 14609 Gja1
  • MGI:6194238
  • PMID:16155213
  • PMID:17311295
  • PMID:18003637
  • PMID:18077386
DOID:0110871 congenital stationary night blindness 2A MGI:1859639 Mus musculus (house mouse) 54652 Cacna1f
  • MGI:6194238
  • PMID:16155113
  • PMID:16597347
  • PMID:24163243
  • PMID:24466230
  • PMID:30445045
DOID:10763 hypertension HGNC:2642 Homo sapiens (human) 1579 CYP4A11
  • MGI:6194238
  • PMID:16144986
DOID:1826 epilepsy HGNC:4571 Homo sapiens (human) 2890 GRIA1
  • MGI:6194238
  • PMID:16142284
DOID:10907 microcephaly HGNC:19048 Homo sapiens (human) 259266 ASPM
  • MGI:6194238
  • PMID:16141009
  • PMID:19808985
  • PMID:20823249
DOID:10763 hypertension HGNC:9958 Homo sapiens (human) 5972 REN
  • MGI:6194238
  • PMID:16138564
DOID:1574 alcohol use disorder HGNC:2689 Homo sapiens (human) 1621 DBH
  • MGI:6194238
  • PMID:16133787
  • PMID:16252068
DOID:289 endometriosis HGNC:8910 Homo sapiens (human) 5241 PGR
  • MGI:6194238
  • PMID:16126772
DOID:0080153 medium chain acyl-CoA dehydrogenase deficiency MGI:87867 Mus musculus (house mouse) 11364 Acadm
  • MGI:6194238
  • PMID:16121256
DOID:12387 nephrogenic diabetes insipidus MGI:1096865 Mus musculus (house mouse) 11827 Aqp2
  • MGI:6194238
  • PMID:16121255
  • PMID:16641094
  • PMID:17229678
DOID:4483 rhinitis HGNC:10610 Homo sapiens (human) 6356 CCL11
  • MGI:6194238
  • PMID:16120080
  • PMID:17999785
DOID:5844 myocardial infarction HGNC:10618 Homo sapiens (human) 6347 CCL2
  • MGI:6194238
  • PMID:16116069
DOID:9452 steatotic liver disease HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • MGI:6194238
  • PMID:16115302
  • PMID:20714777
DOID:13515 tuberous sclerosis HGNC:12363 Homo sapiens (human) 7249 TSC2
  • MGI:6194238
  • PMID:16114042
  • PMID:9007104
DOID:13515 tuberous sclerosis HGNC:12362 Homo sapiens (human) 7248 TSC1
  • MGI:6194238
  • PMID:16114042
  • PMID:25900779
  • PMID:9242607
DOID:9744 type 1 diabetes mellitus HGNC:6081 Homo sapiens (human) 3630 INS
  • MGI:6194238
  • PMID:16113600
  • PMID:16382177
  • PMID:16552513
  • PMID:17284223
  • PMID:17284779
  • PMID:18824271
  • PMID:20535137
  • PMID:21765853
  • PMID:26783749
DOID:0050861 colorectal adenocarcinoma HGNC:40 Homo sapiens (human) 5243 ABCB1
  • MGI:6194238
  • PMID:16107775

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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: December 9, 2024