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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 1351 - 1375 of 12216 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0070263 congenital disorder of glycosylation type IIk HGNC:30760 Homo sapiens (human) 55858 TMEM165
  • MGI:6194238
  • RGD:7240710
DOID:0070264 congenital disorder of glycosylation type IIl HGNC:18621 Homo sapiens (human) 57511 COG6
  • RGD:7240710
DOID:0070264 congenital disorder of glycosylation type IIl SGD:S000004986 Saccharomyces cerevisiae S288C 855687 COG6
  • MGI:6194238
DOID:0070265 congenital disorder of glycosylation type IIm HGNC:11022 Homo sapiens (human) 7355 SLC35A2
  • RGD:7240710
DOID:0070265 congenital disorder of glycosylation type IIm FB:FBgn0024994 Drosophila melanogaster (fruit fly) 31255 Ugalt CG2675
  • MGI:6194238
DOID:0070266 congenital disorder of glycosylation type IIn HGNC:20862 Homo sapiens (human) 64116 SLC39A8
  • RGD:7240710
DOID:0070267 congenital disorder of glycosylation type IIo HGNC:28178 Homo sapiens (human) 84317 CCDC115
  • RGD:7240710
DOID:0070268 congenital disorder of glycosylation type IIp HGNC:18085 Homo sapiens (human) 147007 TMEM199
  • RGD:7240710
DOID:0070269 congenital disorder of glycosylation type IIq HGNC:6546 Homo sapiens (human) 22796 COG2
  • RGD:7240710
DOID:0070295 primary autosomal dominant microcephaly 18 MGI:1096875 Mus musculus (house mouse) 72145 Wdfy3
  • MGI:6194238
DOID:0070298 multiple epiphyseal dysplasia 2 HGNC:2218 Homo sapiens (human) 1298 COL9A2
  • RGD:7240710
DOID:0070300 multiple epiphyseal dysplasia 4 HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:24598000
  • RGD:7240710
DOID:0070303 multiple epiphyseal dysplasia 1 FB:FBgn0031850 Drosophila melanogaster (fruit fly) 33941 Tsp CG11326
  • MGI:6194238
DOID:0070311 oligoasthenoteratozoospermia HGNC:26125 Homo sapiens (human) 64847 SPATA20
  • MGI:6194238
DOID:0070311 oligoasthenoteratozoospermia MGI:2183449 Mus musculus (house mouse) 217116 Spata20
  • PMID:29247744
DOID:0070311 oligoasthenoteratozoospermia RGD:735087 Rattus norvegicus (Norway rat) 360604 Spata20
  • MGI:6194238
DOID:0070311 oligoasthenoteratozoospermia WB:WBGene00015204 Caenorhabditis elegans 174243 B0495.5
  • MGI:6194238
DOID:0070329 mitochondrial DNA depletion syndrome HGNC:10980 Homo sapiens (human) 1468 SLC25A10
  • MGI:6194238
DOID:0070329 mitochondrial DNA depletion syndrome MGI:1353497 Mus musculus (house mouse) 27376 Slc25a10
  • MGI:6194238
DOID:0070330 multiple mitochondrial dysfunctions syndrome HGNC:4208 Homo sapiens (human) 2653 GCSH
  • RGD:7240710
DOID:0070341 neonatal-onset type II citrullinemia FB:FBgn0028646 Drosophila melanogaster (fruit fly) 43616 aralar1
  • MGI:6194238
DOID:0070341 neonatal-onset type II citrullinemia HGNC:10983 Homo sapiens (human) 10165 SLC25A13
  • RGD:7240710
DOID:0070341 neonatal-onset type II citrullinemia MGI:1354721 Mus musculus (house mouse) 50799 Slc25a13
  • MGI:6194238
DOID:0070342 adult-onset type II citrullinemia MGI:1354721 Mus musculus (house mouse) 50799 Slc25a13
  • MGI:6194238
DOID:0070342 adult-onset type II citrullinemia FB:FBgn0028646 Drosophila melanogaster (fruit fly) 43616 aralar1
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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