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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 5976 - 6000 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence References
DOID:1324 lung cancer HGNC:9896 Homo sapiens (human) 8241 RBM10 inference by association of genotype from phenotype used in manual assertion
  • PMID:33219256
DOID:9256 colorectal cancer HGNC:9896 Homo sapiens (human) 8241 RBM10 inference by association of genotype from phenotype used in manual assertion
  • PMID:33194656
DOID:3910 lung adenocarcinoma HGNC:9896 Homo sapiens (human) 8241 RBM10 inference by association of genotype from phenotype used in manual assertion
  • PMID:22980975
DOID:0112025 female-restricted syndromic X-linked intellectual disability 99 HGNC:12632 Homo sapiens (human) 8239 USP9X inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112026 non-syndromic X-linked intellectual disability 99 HGNC:12632 Homo sapiens (human) 8239 USP9X inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9119 acute myeloid leukemia HGNC:23019 Homo sapiens (human) 8233 ZRSR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:25550361
  • PMID:32027246
DOID:0050908 myelodysplastic syndrome HGNC:23019 Homo sapiens (human) 8233 ZRSR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:22343920
  • PMID:25586593
  • PMID:28220884
  • PMID:28942350
DOID:0080205 CAKUT HGNC:8001 Homo sapiens (human) 8204 NRIP1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11476 osteoporosis HGNC:8001 Homo sapiens (human) 8204 NRIP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16530497
DOID:9970 obesity HGNC:7670 Homo sapiens (human) 8202 NCOA3 inference by association of genotype from phenotype used in manual assertion
  • PMID:14557830
DOID:14330 Parkinson's disease HGNC:4220 Homo sapiens (human) 8200 GDF5 direct assay evidence used in manual assertion
  • PMID:22436046
DOID:8398 osteoarthritis HGNC:4220 Homo sapiens (human) 8200 GDF5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110964 brachydactyly type A1 HGNC:4220 Homo sapiens (human) 8200 GDF5 inference by association of genotype from phenotype used in manual assertion
  • PMID:20683927
DOID:0080788 proximal symphalangism 2 HGNC:4220 Homo sapiens (human) 8200 GDF5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110977 brachydactyly type A1C HGNC:4220 Homo sapiens (human) 8200 GDF5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050790 fibular hypoplasia and complex brachydactyly HGNC:4220 Homo sapiens (human) 8200 GDF5 inference by association of genotype from phenotype used in manual assertion
  • PMID:12121354
  • RGD:7240710
DOID:0080052 acromesomelic dysplasia, Grebe type HGNC:4220 Homo sapiens (human) 8200 GDF5 inference by association of genotype from phenotype used in manual assertion
  • PMID:18979166
  • PMID:19038017
  • PMID:23812741
  • RGD:7240710
DOID:0110970 brachydactyly type C HGNC:4220 Homo sapiens (human) 8200 GDF5 inference by association of genotype from phenotype used in manual assertion
  • PMID:14735582
  • PMID:23812741
  • PMID:25092592
  • RGD:7240710
DOID:0110965 brachydactyly type A2 HGNC:4220 Homo sapiens (human) 8200 GDF5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060931 developmental dysplasia of the hip 1 HGNC:4220 Homo sapiens (human) 8200 GDF5 inference by association of genotype from phenotype used in manual assertion
  • PMID:18947434
DOID:0081318 multiple synostoses syndrome 2 HGNC:4220 Homo sapiens (human) 8200 GDF5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0081317 multiple synostoses syndrome 1 HGNC:4220 Homo sapiens (human) 8200 GDF5 inference by association of genotype from phenotype used in manual assertion
  • PMID:16532400
DOID:0080051 acromesomelic dysplasia, Hunter-Thompson type HGNC:4220 Homo sapiens (human) 8200 GDF5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:219 colon cancer HGNC:11063 Homo sapiens (human) 8140 SLC7A5 mutant phenotype evidence used in manual assertion
  • PMID:19900191
DOID:3907 lung squamous cell carcinoma HGNC:11063 Homo sapiens (human) 8140 SLC7A5 genetic interaction evidence used in manual assertion
  • PMID:19068093
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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