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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 1201 - 1225 of 12216 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0060639 permanent neonatal diabetes mellitus HGNC:4195 Homo sapiens (human) 2645 GCK
  • RGD:7240710
DOID:0060639 permanent neonatal diabetes mellitus SGD:S000002924 Saccharomyces cerevisiae S288C 852128 EMI2
  • MGI:6194238
DOID:0060639 permanent neonatal diabetes mellitus MGI:1270854 Mus musculus (house mouse) 103988 Gck
  • MGI:6194238
DOID:0060639 permanent neonatal diabetes mellitus Xenbase:XB-GENE-864803 Xenopus laevis (African clawed frog) 378695 ins.L
  • MGI:6194238
DOID:0060639 permanent neonatal diabetes mellitus Xenbase:XB-GENE-6252363 Xenopus laevis (African clawed frog) 378696 ins.S
  • MGI:6194238
DOID:0060639 permanent neonatal diabetes mellitus ZFIN:ZDB-GENE-980526-110 Danio rerio (zebrafish) 30262 ins
  • MGI:6194238
DOID:0060639 permanent neonatal diabetes mellitus RGD:2915 Rattus norvegicus (Norway rat) 24505 Ins1
  • MGI:6194238
DOID:0060643 primary sclerosing cholangitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:9047083
DOID:0060643 primary sclerosing cholangitis MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:0060643 primary sclerosing cholangitis RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:0060644 chondrodysplasia-pseudohermaphroditism syndrome SGD:S000003052 Saccharomyces cerevisiae S288C 852796 GUP1
  • MGI:6194238
DOID:0060645 chronic recurrent multifocal osteomyelitis MGI:96545 Mus musculus (house mouse) 16177 Il1r1
  • MGI:6194238
DOID:0060645 chronic recurrent multifocal osteomyelitis HGNC:5993 Homo sapiens (human) 3554 IL1R1
  • RGD:7240710
DOID:0060653 lethal congenital contracture syndrome 3 HGNC:8996 Homo sapiens (human) 23396 PIP5K1C
  • RGD:7240710
DOID:0060668 anencephaly HGNC:3225 Homo sapiens (human) 1946 EFNA5
  • MGI:6194238
DOID:0060669 cerebral cavernous malformation MGI:1206581 Mus musculus (house mouse) 18706 Pik3ca
  • MGI:6194238
DOID:0060669 cerebral cavernous malformation RGD:620916 Rattus norvegicus (Norway rat) 170911 Pik3ca
  • MGI:6194238
DOID:0060669 cerebral cavernous malformation HGNC:8975 Homo sapiens (human) 5290 PIK3CA
  • RGD:7240710
DOID:0060669 cerebral cavernous malformation HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:19061355
DOID:0060673 Peters anomaly HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • PMID:15621878
DOID:0060680 pigment dispersion syndrome HGNC:4462 Homo sapiens (human) 10457 GPNMB
  • MGI:6194238
DOID:0060704 lymphoproliferative syndrome HGNC:18788 Homo sapiens (human) 22914 KLRK1
  • PMID:22105417
DOID:0060710 autosomal recessive congenital ichthyosis 2 HGNC:430 Homo sapiens (human) 242 ALOX12B
  • RGD:7240710
DOID:0060713 autosomal recessive congenital ichthyosis 4B HGNC:8957 Homo sapiens (human) 5277 PIGA
  • MGI:6194238
DOID:0060713 autosomal recessive congenital ichthyosis 4B WB:WBGene00008431 Caenorhabditis elegans 174386 piga-1
  • 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: August 19, 2024