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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 71401 - 71425 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:5409 lung small cell carcinoma WB:WBGene00006897 Caenorhabditis elegans 186632 ver-4
  • MGI:6194238
DOID:2999 granulosa cell tumor WB:WBGene00006897 Caenorhabditis elegans 186632 ver-4
  • MGI:6194238
DOID:4450 renal cell carcinoma WB:WBGene00006897 Caenorhabditis elegans 186632 ver-4
  • MGI:6194238
DOID:962 neurofibroma WB:WBGene00006897 Caenorhabditis elegans 186632 ver-4
  • MGI:6194238
DOID:684 hepatocellular carcinoma WB:WBGene00006897 Caenorhabditis elegans 186632 ver-4
  • MGI:6194238
DOID:0060669 cerebral cavernous malformation WB:WBGene00006897 Caenorhabditis elegans 186632 ver-4
  • MGI:6194238
DOID:13207 proliferative diabetic retinopathy WB:WBGene00006897 Caenorhabditis elegans 186632 ver-4
  • MGI:6194238
DOID:2154 nephroblastoma WB:WBGene00006897 Caenorhabditis elegans 186632 ver-4
  • MGI:6194238
DOID:1115 sarcoma WB:WBGene00006897 Caenorhabditis elegans 186632 ver-4
  • MGI:6194238
DOID:11132 prostatic hypertrophy WB:WBGene00006897 Caenorhabditis elegans 186632 ver-4
  • MGI:6194238
DOID:1289 neurodegenerative disease WB:WBGene00010755 Caenorhabditis elegans 176441 vglu-2
  • MGI:6194238
DOID:11446 sciatic neuropathy WB:WBGene00010755 Caenorhabditis elegans 176441 vglu-2
  • MGI:6194238
DOID:0110555 autosomal dominant nonsyndromic deafness 25 WB:WBGene00010755 Caenorhabditis elegans 176441 vglu-2
  • MGI:6194238
DOID:14330 Parkinson's disease WB:WBGene00010755 Caenorhabditis elegans 176441 vglu-2
  • MGI:6194238
DOID:224 transient cerebral ischemia WB:WBGene00010755 Caenorhabditis elegans 176441 vglu-2
  • MGI:6194238
DOID:1289 neurodegenerative disease WB:WBGene00011556 Caenorhabditis elegans 176442 vglu-3
  • MGI:6194238
DOID:0110555 autosomal dominant nonsyndromic deafness 25 WB:WBGene00011556 Caenorhabditis elegans 176442 vglu-3
  • MGI:6194238
DOID:11446 sciatic neuropathy WB:WBGene00011556 Caenorhabditis elegans 176442 vglu-3
  • MGI:6194238
DOID:14330 Parkinson's disease WB:WBGene00011556 Caenorhabditis elegans 176442 vglu-3
  • MGI:6194238
DOID:224 transient cerebral ischemia WB:WBGene00011556 Caenorhabditis elegans 176442 vglu-3
  • MGI:6194238
DOID:0112002 immunodeficiency 47 WB:WBGene00021952 Caenorhabditis elegans 177103 vha-19
  • MGI:6194238
DOID:0070134 autosomal recessive cutis laxa type IIA WB:WBGene00006914 Caenorhabditis elegans 177626 vha-5
  • MGI:6194238
DOID:14219 renal tubular acidosis WB:WBGene00006914 Caenorhabditis elegans 177626 vha-5
  • MGI:6194238
DOID:0112171 wrinkly skin syndrome WB:WBGene00006914 Caenorhabditis elegans 177626 vha-5
  • MGI:6194238
DOID:0110942 autosomal recessive osteopetrosis 1 WB:WBGene00006914 Caenorhabditis elegans 177626 vha-5
  • MGI:6194238

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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