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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 11326 - 11350 of 12216 in total
Disease ID Disease Name ▼ Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:5408 Paget's disease of bone HGNC:6079 Homo sapiens (human) 3635 INPP5D
  • MGI:6194238
DOID:0111843 Paganini-Miozzo syndrome HGNC:19133 Homo sapiens (human) 90161 HS6ST2
  • RGD:7240710
DOID:0111843 Paganini-Miozzo syndrome Xenbase:XB-GENE-6039291 Xenopus tropicalis (tropical clawed frog) 100496603 hs6st2
  • MGI:6194238
DOID:0111843 Paganini-Miozzo syndrome FB:FBgn0038755 Drosophila melanogaster (fruit fly) 42380 Hs6st CG4451
  • MGI:6194238
DOID:0111843 Paganini-Miozzo syndrome RGD:1564397 Rattus norvegicus (Norway rat) 302489 Hs6st2
  • MGI:6194238
DOID:0111843 Paganini-Miozzo syndrome MGI:1354959 Mus musculus (house mouse) 50786 Hs6st2
  • MGI:6194238
DOID:0111843 Paganini-Miozzo syndrome ZFIN:ZDB-GENE-030909-14 Danio rerio (zebrafish) 378450 hs6st2
  • MGI:6194238
DOID:0080191 PTEN hamartoma tumor syndrome HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:16773562
  • PMID:17341483
  • PMID:24102544
  • PMID:9140396
DOID:0111271 Oliver-McFarlane syndrome HGNC:16268 Homo sapiens (human) 10908 PNPLA6
  • RGD:7240710
DOID:1391 Norum disease HGNC:6522 Homo sapiens (human) 3931 LCAT
  • MGI:6194238
  • PMID:16061733
  • RGD:7240710
DOID:0080693 Noonan syndrome-like disorder with loose anagen hair 2 SGD:S000000935 Saccharomyces cerevisiae S288C 856870 GLC7
  • MGI:6194238
DOID:0080693 Noonan syndrome-like disorder with loose anagen hair 2 MGI:104871 Mus musculus (house mouse) 19046 Ppp1cb
  • MGI:6194238
DOID:0080693 Noonan syndrome-like disorder with loose anagen hair 2 Xenbase:XB-GENE-961670 Xenopus tropicalis (tropical clawed frog) 496958 ppp1cb
  • MGI:6194238
DOID:0080693 Noonan syndrome-like disorder with loose anagen hair 2 Xenbase:XB-GENE-17344746 Xenopus laevis (African clawed frog) 108717671 ppp1cb.S
  • MGI:6194238
DOID:0080693 Noonan syndrome-like disorder with loose anagen hair 2 RGD:3376 Rattus norvegicus (Norway rat) 25594 Ppp1cb
  • MGI:6194238
DOID:0080693 Noonan syndrome-like disorder with loose anagen hair 2 Xenbase:XB-GENE-961676 Xenopus laevis (African clawed frog) 443852 ppp1cb.L
  • MGI:6194238
DOID:0080693 Noonan syndrome-like disorder with loose anagen hair 2 HGNC:9282 Homo sapiens (human) 5500 PPP1CB
  • RGD:7240710
DOID:0080550 Noonan syndrome with multiple lentigines 3 HGNC:1097 Homo sapiens (human) 673 BRAF
  • RGD:7240710
DOID:0080550 Noonan syndrome with multiple lentigines 3 MGI:88190 Mus musculus (house mouse) 109880 Braf
  • MGI:6194238
DOID:0060585 Noonan syndrome 7 MGI:88190 Mus musculus (house mouse) 109880 Braf
  • MGI:6194238
DOID:0060585 Noonan syndrome 7 HGNC:1097 Homo sapiens (human) 673 BRAF
  • RGD:7240710
DOID:0070113 Niemann-Pick disease type C1 MGI:1097712 Mus musculus (house mouse) 18145 Npc1
  • MGI:6194238
  • PMID:28167839
DOID:0070113 Niemann-Pick disease type C1 HGNC:7897 Homo sapiens (human) 4864 NPC1
  • MGI:6194238
  • RGD:7240710
DOID:0070112 Niemann-Pick disease type B HGNC:11120 Homo sapiens (human) 6609 SMPD1
  • RGD:7240710
DOID:0070112 Niemann-Pick disease type B WB:WBGene00000211 Caenorhabditis elegans 174131 asm-1
  • 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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