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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 2251 - 2275 of 12216 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0090129 carnitine palmitoyltransferase I deficiency HGNC:2328 Homo sapiens (human) 1374 CPT1A
  • MGI:6194238
  • RGD:7240710
DOID:0090129 carnitine palmitoyltransferase I deficiency RGD:2396 Rattus norvegicus (Norway rat) 25757 Cpt1a
  • MGI:6194238
DOID:0090129 carnitine palmitoyltransferase I deficiency MGI:1098296 Mus musculus (house mouse) 12894 Cpt1a
  • MGI:6194238
  • PMID:16169268
DOID:0090139 cortisone reductase deficiency MGI:2140356 Mus musculus (house mouse) 100198 H6pd
  • MGI:6194238
DOID:0090139 cortisone reductase deficiency HGNC:5208 Homo sapiens (human) 3290 HSD11B1
  • PMID:12858176
DOID:0090139 cortisone reductase deficiency HGNC:4795 Homo sapiens (human) 9563 H6PD
  • PMID:12858176
DOID:0090140 cortisone reductase deficiency 2 HGNC:5208 Homo sapiens (human) 3290 HSD11B1
  • MGI:6194238
  • RGD:7240710
DOID:0090141 cortisone reductase deficiency 1 HGNC:4795 Homo sapiens (human) 9563 H6PD
  • RGD:7240710
DOID:0090141 cortisone reductase deficiency 1 MGI:2140356 Mus musculus (house mouse) 100198 H6pd
  • MGI:6194238
DOID:0090145 dopamine beta-hydroxylase deficiency SGD:S000003571 Saccharomyces cerevisiae S288C 853418 KAR2
  • MGI:6194238
DOID:0110011 advanced sleep phase syndrome 1 RGD:61945 Rattus norvegicus (Norway rat) 63840 Per2
  • MGI:6194238
DOID:0110011 advanced sleep phase syndrome 1 MGI:1195265 Mus musculus (house mouse) 18627 Per2
  • MGI:6194238
  • MGI:6197761
DOID:0110011 advanced sleep phase syndrome 1 HGNC:8846 Homo sapiens (human) 8864 PER2
  • MGI:6194238
  • RGD:7240710
DOID:0110123 Bardet-Biedl syndrome 1 MGI:1927136 Mus musculus (house mouse) 56297 Arl6
  • MGI:6194238
DOID:0110125 Bardet-Biedl syndrome 3 MGI:1927136 Mus musculus (house mouse) 56297 Arl6
  • MGI:6194238
  • PMID:27170093
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q Xenbase:XB-GENE-980614 Xenopus laevis (African clawed frog) 403360 dhtkd1.L
  • MGI:6194238
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q FB:FBgn0039827 Drosophila melanogaster (fruit fly) 43689 CG1544
  • MGI:6194238
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q WB:WBGene00014098 Caenorhabditis elegans 179674 ogdh-2
  • MGI:6194238
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q ZFIN:ZDB-GENE-041212-44 Danio rerio (zebrafish) 494076 dhtkd1
  • MGI:6194238
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q MGI:2445096 Mus musculus (house mouse) 209692 Dhtkd1
  • MGI:6194238
  • PMID:29661920
  • PMID:32169121
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q HGNC:23537 Homo sapiens (human) 55526 DHTKD1
  • MGI:6194238
  • RGD:7240710
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q RGD:1308092 Rattus norvegicus (Norway rat) 361272 Dhtkd1
  • MGI:6194238
DOID:0110178 Charcot-Marie-Tooth disease axonal type 2V HGNC:7632 Homo sapiens (human) 4669 NAGLU
  • RGD:7240710
DOID:0110184 Charcot-Marie-Tooth disease type 4J SGD:S000005269 Saccharomyces cerevisiae S288C 855392 FIG4
  • MGI:6194238
  • PMID:17572665
DOID:0110184 Charcot-Marie-Tooth disease type 4J HGNC:16873 Homo sapiens (human) 9896 FIG4
  • MGI:6194238
  • 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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