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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 2851 - 2875 of 12216 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0111949 immunodeficiency 36 MGI:97583 Mus musculus (house mouse) 18708 Pik3r1
  • MGI:6194238
DOID:0111949 immunodeficiency 36 RGD:3329 Rattus norvegicus (Norway rat) 25513 Pik3r1
  • MGI:6194238
DOID:0111953 immunodeficiency 23 MGI:97566 Mus musculus (house mouse) 109785 Pgm3
  • MGI:6194238
DOID:0111953 immunodeficiency 23 HGNC:8907 Homo sapiens (human) 5238 PGM3
  • RGD:7240710
DOID:0111953 immunodeficiency 23 SGD:S000000784 Saccharomyces cerevisiae S288C 856652 PCM1
  • MGI:6194238
DOID:0112002 immunodeficiency 47 HGNC:868 Homo sapiens (human) 537 ATP6AP1
  • RGD:7240710
DOID:0112022 non-syndromic X-linked intellectual disability 21 RGD:727891 Rattus norvegicus (Norway rat) 317553 Il1rapl1
  • MGI:6194238
DOID:0112022 non-syndromic X-linked intellectual disability 21 HGNC:5996 Homo sapiens (human) 11141 IL1RAPL1
  • RGD:7240710
DOID:0112022 non-syndromic X-linked intellectual disability 21 ZFIN:ZDB-GENE-061013-249 Danio rerio (zebrafish) 568868 il1rapl1a
  • MGI:6194238
DOID:0112022 non-syndromic X-linked intellectual disability 21 ZFIN:ZDB-GENE-090109-2 Danio rerio (zebrafish) 557801 il1rapl1b
  • MGI:6194238
DOID:0112050 non-syndromic X-linked intellectual disability 63 HGNC:3571 Homo sapiens (human) 2182 ACSL4
  • MGI:6194238
  • RGD:7240710
DOID:0112050 non-syndromic X-linked intellectual disability 63 HGNC:3570 Homo sapiens (human) 2181 ACSL3
  • MGI:6194238
DOID:0112072 nuclear type mitochondrial complex I deficiency 20 HGNC:88 Homo sapiens (human) 33 ACADL
  • MGI:6194238
DOID:0112105 X-linked parkinsonism-spasticity syndrome HGNC:18305 Homo sapiens (human) 10159 ATP6AP2
  • RGD:7240710
DOID:0112105 X-linked parkinsonism-spasticity syndrome FB:FBgn0037671 Drosophila melanogaster (fruit fly) 41104 ATP6AP2
  • MGI:6194238
DOID:0112127 HRPT-related hyperuricemia RGD:2826 Rattus norvegicus (Norway rat) 24465 Hprt1
  • MGI:6194238
DOID:0112127 HRPT-related hyperuricemia MGI:96217 Mus musculus (house mouse) 15452 Hprt1
  • MGI:6194238
DOID:0112127 HRPT-related hyperuricemia HGNC:5157 Homo sapiens (human) 3251 HPRT1
  • RGD:7240710
DOID:0112136 severe congenital neutropenia 4 HGNC:24861 Homo sapiens (human) 92579 G6PC3
  • RGD:7240710
DOID:0112136 severe congenital neutropenia 4 MGI:1915651 Mus musculus (house mouse) 68401 G6pc3
  • MGI:6194238
DOID:0112136 severe congenital neutropenia 4 ZFIN:ZDB-GENE-061215-19 Danio rerio (zebrafish) 790919 g6pc3
  • MGI:6194238
DOID:0112136 severe congenital neutropenia 4 RGD:727875 Rattus norvegicus (Norway rat) 303565 G6pc3
  • MGI:6194238
DOID:0112147 retinitis pigmentosa 90 HGNC:5384 Homo sapiens (human) 3419 IDH3A
  • RGD:7240710
DOID:0112147 retinitis pigmentosa 90 SGD:S000005662 Saccharomyces cerevisiae S288C 854303 IDH2
  • MGI:6194238
DOID:0112152 CHIME syndrome HGNC:8966 Homo sapiens (human) 9487 PIGL
  • PMID:22444671
  • RGD:7240710

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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: August 19, 2024