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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 January 28, 2025
Displaying entries 2576 - 2600 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence References
DOID:0060296 congenital secretory chloride diarrhea 1 HGNC:3018 Homo sapiens (human) 1811 SLC26A3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:13250 diarrhea HGNC:3018 Homo sapiens (human) 1811 SLC26A3 inference by association of genotype from phenotype used in manual assertion
  • PMID:8896562
DOID:0080055 achondrogenesis type IB HGNC:10994 Homo sapiens (human) 1836 SLC26A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:8528239
  • RGD:7240710
DOID:0050648 atelosteogenesis HGNC:10994 Homo sapiens (human) 1836 SLC26A2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070300 multiple epiphyseal dysplasia 4 HGNC:10994 Homo sapiens (human) 1836 SLC26A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:24598000
  • RGD:7240710
DOID:14687 diastrophic dysplasia HGNC:10994 Homo sapiens (human) 1836 SLC26A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:10482955
  • RGD:7240710
DOID:676 juvenile rheumatoid arthritis HGNC:10994 Homo sapiens (human) 1836 SLC26A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:17393463
DOID:2300 spondylolysis HGNC:10994 Homo sapiens (human) 1836 SLC26A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:26077908
DOID:2256 osteochondrodysplasia HGNC:10994 Homo sapiens (human) 1836 SLC26A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:8571951
DOID:0050581 brachydactyly HGNC:10994 Homo sapiens (human) 1836 SLC26A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21155763
DOID:0080652 calcium oxalate nephrolithiasis HGNC:10993 Homo sapiens (human) 10861 SLC26A1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112330 pontocerebellar hypoplasia type 1E HGNC:25198 Homo sapiens (human) 91137 SLC25A46 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:655 inherited metabolic disorder HGNC:14409 Homo sapiens (human) 60386 SLC25A19 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10907 microcephaly HGNC:14409 Homo sapiens (human) 60386 SLC25A19 inference by association of genotype from phenotype used in manual assertion
  • PMID:12185364
DOID:0070342 adult-onset type II citrullinemia HGNC:10983 Homo sapiens (human) 10165 SLC25A13 inference by association of genotype from phenotype used in manual assertion
  • PMID:10369257
  • PMID:11153906
  • RGD:7240710
DOID:0070341 neonatal-onset type II citrullinemia HGNC:10983 Homo sapiens (human) 10165 SLC25A13 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12849 autistic disorder HGNC:10982 Homo sapiens (human) 8604 SLC25A12 inference by association of genotype from phenotype used in manual assertion
  • PMID:15056512
DOID:0080349 developmental and epileptic encephalopathy 39 HGNC:10982 Homo sapiens (human) 8604 SLC25A12 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050432 Asperger syndrome HGNC:10982 Homo sapiens (human) 8604 SLC25A12 inference by association of genotype from phenotype used in manual assertion
  • PMID:24679184
DOID:0050773 paraganglioma HGNC:10981 Homo sapiens (human) 8402 SLC25A11 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070450 mitochondrial DNA depletion syndrome 19 HGNC:10980 Homo sapiens (human) 1468 SLC25A10 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10123 pigmentation disease HGNC:10978 Homo sapiens (human) 123041 SLC24A4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110063 amelogenesis imperfecta hypomaturation type 2A5 HGNC:10978 Homo sapiens (human) 123041 SLC24A4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110868 congenital stationary night blindness 1D HGNC:10975 Homo sapiens (human) 9187 SLC24A1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3883 Lynch syndrome HGNC:16261 Homo sapiens (human) 114571 SLC22A9 inference by association of genotype from phenotype used in manual assertion
  • PMID:28218421
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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: April 7, 2025