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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 65901 - 65925 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:12361 Graves' disease HGNC:10986 Homo sapiens (human) 8034 SLC25A16
  • MGI:6194238
DOID:0110782 hereditary spastic paraplegia 31 HGNC:26176 Homo sapiens (human) 80346 REEP4
  • MGI:6194238
DOID:0080690 RASopathy HGNC:15454 Homo sapiens (human) 8036 SHOC2
  • MGI:6194238
DOID:3310 atopic dermatitis HGNC:15454 Homo sapiens (human) 8036 SHOC2
  • PMID:20882035
DOID:0080692 Noonan syndrome-like disorder with loose anagen hair 1 HGNC:15454 Homo sapiens (human) 8036 SHOC2
  • PMID:20882035
  • PMID:23918763
  • PMID:35348676
  • RGD:7240710
DOID:0080691 Noonan syndrome-like disorder with loose anagen hair HGNC:15454 Homo sapiens (human) 8036 SHOC2
  • MGI:6194238
DOID:8398 osteoarthritis HGNC:190 Homo sapiens (human) 8038 ADAM12
  • PMID:15334463
DOID:2957 pulmonary tuberculosis HGNC:18731 Homo sapiens (human) 80380 PDCD1LG2
  • PMID:23661793
DOID:1115 sarcoma HGNC:21350 Homo sapiens (human) 8050 PDHX
  • PMID:31089155
DOID:3649 pyruvate decarboxylase deficiency HGNC:21350 Homo sapiens (human) 8050 PDHX
  • RGD:7240710
DOID:0050659 biotin-responsive basal ganglia disease HGNC:16266 Homo sapiens (human) 80704 SLC19A3
  • MGI:6194238
  • RGD:7240710
DOID:784 chronic kidney disease HGNC:16266 Homo sapiens (human) 80704 SLC19A3
  • MGI:6194238
DOID:0050659 biotin-responsive basal ganglia disease MGI:1931307 Mus musculus (house mouse) 80721 Slc19a3
  • MGI:6194238
  • PMID:28665968
DOID:784 chronic kidney disease MGI:1931307 Mus musculus (house mouse) 80721 Slc19a3
  • MGI:6194238
DOID:0060251 sclerosteosis RGD:69358 Rattus norvegicus (Norway rat) 80722 Sost
  • MGI:6194238
DOID:0080036 SOST-related sclerosing bone dysplasia RGD:69358 Rattus norvegicus (Norway rat) 80722 Sost
  • MGI:6194238
DOID:0060756 sclerosteosis 1 RGD:69358 Rattus norvegicus (Norway rat) 80722 Sost
  • MGI:6194238
DOID:0080807 autosomal dominant craniodiaphyseal dysplasia RGD:69358 Rattus norvegicus (Norway rat) 80722 Sost
  • MGI:6194238
DOID:0080268 autosomal dominant nonsyndromic deafness 72 HGNC:13941 Homo sapiens (human) 80736 SLC44A4
  • RGD:7240710
DOID:10003 sensorineural hearing loss HGNC:13941 Homo sapiens (human) 80736 SLC44A4
  • MGI:6194238
DOID:784 chronic kidney disease HGNC:3680 Homo sapiens (human) 8074 FGF23
  • MGI:6194238
DOID:0050589 inflammatory bowel disease HGNC:3680 Homo sapiens (human) 8074 FGF23
  • PMID:22551310
DOID:0050948 autosomal dominant hypophosphatemic rickets HGNC:3680 Homo sapiens (human) 8074 FGF23
  • MGI:6194238
  • PMID:11062477
  • PMID:19655082
  • RGD:7240710
DOID:4676 uremia HGNC:3680 Homo sapiens (human) 8074 FGF23
  • MGI:6194238
DOID:2187 amelogenesis imperfecta MGI:2136853 Mus musculus (house mouse) 80752 Fam20c
  • MGI:6194238

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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