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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 426 - 450 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:5419 schizophrenia RGD:61800 Rattus norvegicus (Norway rat) 29595 Htr2a
  • MGI:6194238
  • PMID:23291154
  • PMID:28265857
DOID:11832 visual epilepsy RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
  • PMID:23333565
DOID:11832 visual epilepsy HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:23333565
DOID:0050777 Joubert syndrome HGNC:21474 Homo sapiens (human) 56623 INPP5E
  • MGI:6194238
  • PMID:23386033
DOID:3347 osteosarcoma MGI:98834 Mus musculus (house mouse) 22059 Trp53
  • MGI:6194238
  • PMID:23486187
DOID:783 end stage renal disease HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • MGI:6194238
  • PMID:23619522
DOID:9655 oral mucosa leukoplakia HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
  • PMID:23776093
DOID:0050644 arterial calcification of infancy MGI:97370 Mus musculus (house mouse) 18605 Enpp1
  • MGI:6194238
  • PMID:23798568
  • PMID:25479107
DOID:4928 intrahepatic cholangiocarcinoma HGNC:1097 Homo sapiens (human) 673 BRAF
  • MGI:6194238
  • PMID:24139215
DOID:0080208 metabolic dysfunction-associated steatotic liver disease RGD:620329 Rattus norvegicus (Norway rat) 252900 Dgat2
  • MGI:6194238
  • PMID:24166662
  • PMID:26394137
DOID:6000 congestive heart failure RGD:2802 Rattus norvegicus (Norway rat) 25459 Hmgb1
  • MGI:6194238
  • PMID:24204700
DOID:224 transient cerebral ischemia HGNC:4432 Homo sapiens (human) 2805 GOT1
  • MGI:6194238
  • PMID:24407245
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • MGI:6194238
  • PMID:24477042
  • PMID:24831885
  • PMID:26740948
DOID:9870 galactosemia MGI:95638 Mus musculus (house mouse) 14430 Galt
  • MGI:6194238
  • PMID:24549051
DOID:5082 liver cirrhosis HGNC:4606 Homo sapiens (human) 2923 PDIA3
  • MGI:6194238
  • PMID:24562544
DOID:0050574 L-2-hydroxyglutaric aciduria HGNC:20499 Homo sapiens (human) 79944 L2HGDH
  • MGI:6194238
  • PMID:24573090
  • RGD:7240710
DOID:0050884 triosephosphate isomerase deficiency SGD:S000002457 Saccharomyces cerevisiae S288C 851620 TPI1
  • MGI:6194238
  • PMID:24598263
DOID:206 hereditary multiple exostoses ZFIN:ZDB-GENE-041124-3 Danio rerio (zebrafish) 493780 ext2
  • MGI:6194238
  • PMID:24628984
DOID:9352 type 2 diabetes mellitus RGD:69247 Rattus norvegicus (Norway rat) 83535 Kcnj11
  • MGI:6194238
  • PMID:24681897
DOID:10652 Alzheimer's disease HGNC:5466 Homo sapiens (human) 3481 IGF2
  • MGI:6194238
  • PMID:24685003
DOID:11758 iron deficiency anemia HGNC:4553 Homo sapiens (human) 2876 GPX1
  • MGI:6194238
  • PMID:24691014
DOID:0050770 polycystic liver disease HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:24706814
  • RGD:7240710
DOID:0060887 ossification of the posterior longitudinal ligament of spine MGI:97370 Mus musculus (house mouse) 18605 Enpp1
  • MGI:6194238
  • PMID:24770645
  • PMID:9359030
  • PMID:9662402
DOID:8577 ulcerative colitis RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
  • PMID:24812904
DOID:12894 Sjogren's syndrome RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
  • PMID:24941846

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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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