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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 71651 - 71675 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:10763 hypertension HGNC:7876 Homo sapiens (human) 4846 NOS3
  • MGI:6194238
  • PMID:10981549
  • PMID:9674630
DOID:6000 congestive heart failure HGNC:3176 Homo sapiens (human) 1906 EDN1
  • MGI:6194238
  • PMID:10973842
  • PMID:8149524
DOID:3343 glycoproteinosis HGNC:13356 Homo sapiens (human) 57192 MCOLN1
  • MGI:6194238
  • PMID:10973263
DOID:14219 renal tubular acidosis HGNC:866 Homo sapiens (human) 50617 ATP6V0A4
  • MGI:6194238
  • PMID:10973252
DOID:0050437 Danon disease MGI:96748 Mus musculus (house mouse) 16784 Lamp2
  • MGI:6194238
  • PMID:10972293
  • PMID:28526246
  • PMID:34459252
DOID:9970 obesity MGI:96929 Mus musculus (house mouse) 17201 Mc3r
  • MGI:6194238
  • PMID:10965927
DOID:0060682 autosomal dominant nocturnal frontal lobe epilepsy 1 MGI:87888 Mus musculus (house mouse) 11438 Chrna4
  • MGI:6194238
  • PMID:10964949
  • PMID:12623222
DOID:0060574 von Willebrand's disease 2 HGNC:12726 Homo sapiens (human) 7450 VWF
  • MGI:6194238
  • PMID:10959688
  • PMID:16409463
  • PMID:20589313
  • PMID:26019279
  • PMID:8839848
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus MGI:95484 Mus musculus (house mouse) 14102 Fas
  • MGI:6194238
  • PMID:10946317
DOID:0060691 platelet-type bleeding disorder 16 MGI:96601 Mus musculus (house mouse) 16399 Itga2b
  • MGI:6194238
  • PMID:10942384
DOID:0090060 Wolcott-Rallison syndrome HGNC:3255 Homo sapiens (human) 9451 EIF2AK3
  • MGI:6194238
  • PMID:10932183
  • RGD:7240710
DOID:9409 diabetes insipidus RGD:2184 Rattus norvegicus (Norway rat) 24221 Avp
  • MGI:6194238
  • PMID:10919858
  • PMID:13995944
  • PMID:5692127
  • PMID:6717565
  • PMID:9396613
DOID:3083 chronic obstructive pulmonary disease HGNC:7218 Homo sapiens (human) 4353 MPO
  • MGI:6194238
  • PMID:10917466
DOID:0111095 Fanconi anemia complementation group A MGI:1341823 Mus musculus (house mouse) 14087 Fanca
  • MGI:6194238
  • PMID:10915769
  • PMID:12913077
DOID:10763 hypertension HGNC:1030 Homo sapiens (human) 624 BDKRB2
  • MGI:6194238
  • PMID:10904024
DOID:9970 obesity RGD:3001 Rattus norvegicus (Norway rat) 24536 Lepr
  • MGI:6194238
  • PMID:10901178
  • PMID:11500530
  • PMID:20159938
  • PMID:22693203
  • PMID:27225180
  • PMID:27465994
  • PMID:28746409
  • PMID:32710530
  • PMID:33568522
  • PMID:8702432
  • PMID:8841178
  • PMID:9843879
DOID:9352 type 2 diabetes mellitus RGD:3342 Rattus norvegicus (Norway rat) 25692 Plat
  • MGI:6194238
  • PMID:10899350
  • PMID:14693179
DOID:1270 hereditary hemorrhagic telangiectasia HGNC:3349 Homo sapiens (human) 2022 ENG
  • MGI:6194238
  • PMID:10899246
  • PMID:15024723
  • PMID:15375013
  • PMID:15907823
  • PMID:16542389
  • PMID:16752392
  • PMID:7894484
  • PMID:9245986
  • RGD:7240710
DOID:1094 attention deficit hyperactivity disorder HGNC:3025 Homo sapiens (human) 1815 DRD4
  • MGI:6194238
  • PMID:10898895
  • PMID:11431226
  • PMID:11449395
  • PMID:12960764
  • PMID:14699430
  • PMID:15389764
  • PMID:15909295
  • PMID:17171658
  • PMID:17679637
  • PMID:21906006
  • PMID:23083021
  • PMID:9118321
  • RGD:7240710
DOID:2908 Treacher Collins syndrome MGI:892003 Mus musculus (house mouse) 21453 Tcof1
  • MGI:6194238
  • PMID:10888597
  • PMID:16938878
DOID:3310 atopic dermatitis HGNC:5973 Homo sapiens (human) 3596 IL13
  • MGI:6194238
  • PMID:10887320
  • PMID:16672002
  • PMID:21913997
  • PMID:23317483
DOID:9352 type 2 diabetes mellitus HGNC:4056 Homo sapiens (human) 2538 G6PC1
  • MGI:6194238
  • PMID:10866049
DOID:8947 diabetic retinopathy HGNC:333 Homo sapiens (human) 183 AGT
  • MGI:6194238
  • PMID:10862638
DOID:14264 benign neonatal seizures MGI:1309503 Mus musculus (house mouse) 16536 Kcnq2
  • MGI:6194238
  • PMID:10854243
  • PMID:18483067
DOID:14264 benign neonatal seizures HGNC:6297 Homo sapiens (human) 3786 KCNQ3
  • MGI:6194238
  • PMID:10852552
  • PMID:9425900
  • RGD:7240710

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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