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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 66026 - 66050 of 71927 in total
Disease ID ▼ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0060292 X-linked chondrodysplasia punctata 1 MGI:107822 Mus musculus (house mouse) 13595 Ebp
  • PMID:10391218
DOID:0060292 X-linked chondrodysplasia punctata 1 HGNC:13398 Homo sapiens (human) 50814 NSDHL
  • MGI:6194238
DOID:0060292 X-linked chondrodysplasia punctata 1 HGNC:3133 Homo sapiens (human) 10682 EBP
  • MGI:6194238
DOID:0060292 X-linked chondrodysplasia punctata 1 HGNC:719 Homo sapiens (human) 415 ARSL
  • RGD:7240710
DOID:0060291 oculodentodigital dysplasia MGI:95713 Mus musculus (house mouse) 14609 Gja1
  • MGI:6194238
  • PMID:16155213
  • PMID:17311295
  • PMID:18003637
  • PMID:18077386
DOID:0060290 Ohdo syndrome, SBBYS variant FB:FBgn0034975 Drosophila melanogaster (fruit fly) 37859 enok
  • MGI:6194238
DOID:0060290 Ohdo syndrome, SBBYS variant MGI:1858746 Mus musculus (house mouse) 54169 Kat6b
  • MGI:6194238
DOID:0060290 Ohdo syndrome, SBBYS variant HGNC:17582 Homo sapiens (human) 23522 KAT6B
  • PMID:22077973
  • RGD:7240710
DOID:0060287 cornea plana ZFIN:ZDB-GENE-041210-165 Danio rerio (zebrafish) 567017 kera
  • MGI:6194238
DOID:0060287 cornea plana MGI:1202398 Mus musculus (house mouse) 16545 Kera
  • MGI:6194238
  • PMID:12665512
DOID:0060287 cornea plana HGNC:6309 Homo sapiens (human) 11081 KERA
  • MGI:6194238
  • RGD:7240710
DOID:0060287 cornea plana WB:WBGene00008656 Caenorhabditis elegans 184307 lron-5
  • MGI:6194238
DOID:0060286 combined oxidative phosphorylation deficiency HGNC:26223 Homo sapiens (human) 79736 TEFM
  • RGD:7240710
DOID:0060286 combined oxidative phosphorylation deficiency MGI:1915541 Mus musculus (house mouse) 68291 Mto1
  • PMID:25506927
DOID:0060286 combined oxidative phosphorylation deficiency HGNC:19261 Homo sapiens (human) 25821 MTO1
  • MGI:6194238
DOID:0060285 parietal foramina HGNC:450 Homo sapiens (human) 60529 ALX4
  • MGI:6194238
  • RGD:7240710
DOID:0060284 paroxysmal nocturnal hemoglobinuria WB:WBGene00008918 Caenorhabditis elegans 179519 pigt-1
  • MGI:6194238
DOID:0060284 paroxysmal nocturnal hemoglobinuria RGD:2232 Rattus norvegicus (Norway rat) 24232 C3
  • MGI:6194238
DOID:0060284 paroxysmal nocturnal hemoglobinuria HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1
  • PMID:12070003
DOID:0060284 paroxysmal nocturnal hemoglobinuria SGD:S000006096 Saccharomyces cerevisiae S288C 855928 SPT14
  • MGI:6194238
  • PMID:7737116
DOID:0060284 paroxysmal nocturnal hemoglobinuria Xenbase:XB-GENE-489917 Xenopus tropicalis (tropical clawed frog) 100038176 cxcr4
  • MGI:6194238
DOID:0060284 paroxysmal nocturnal hemoglobinuria Xenbase:XB-GENE-489921 Xenopus laevis (African clawed frog) 100192360 cxcr4.L
  • MGI:6194238
DOID:0060284 paroxysmal nocturnal hemoglobinuria Xenbase:XB-GENE-6256540 Xenopus laevis (African clawed frog) 380373 cxcr4.S
  • MGI:6194238
DOID:0060284 paroxysmal nocturnal hemoglobinuria RGD:620465 Rattus norvegicus (Norway rat) 60628 Cxcr4
  • MGI:6194238
DOID:0060284 paroxysmal nocturnal hemoglobinuria MGI:99461 Mus musculus (house mouse) 18700 Piga
  • 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