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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 9926 - 9950 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:8552 chronic myeloid leukemia HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17387388
  • PMID:17893434
DOID:0050679 blue cone monochromacy HGNC:4206 Homo sapiens (human) 2652 OPN1MW inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060936 dystonia 28, childhood-onset HGNC:15840 Homo sapiens (human) 9757 KMT2B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111133 focal segmental glomerulosclerosis 8 HGNC:14082 Homo sapiens (human) 54443 ANLN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:7876 Homo sapiens (human) 4846 NOS3 mutant phenotype evidence used in manual assertion
  • PMID:17413318
DOID:4483 rhinitis HGNC:16711 Homo sapiens (human) 10333 TLR6 inference by association of genotype from phenotype used in manual assertion
  • PMID:20815312
DOID:8725 vascular dementia HGNC:5232 Homo sapiens (human) 3303 HSPA1A inference by association of genotype from phenotype used in manual assertion
  • PMID:15832029
DOID:0060366 Hennekam syndrome HGNC:219 Homo sapiens (human) 9508 ADAMTS3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:11005 Homo sapiens (human) 6513 SLC2A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18613291
DOID:4450 renal cell carcinoma HGNC:6720 Homo sapiens (human) 4057 LTF direct assay evidence used in manual assertion
  • PMID:23201854
DOID:10595 Charcot-Marie-Tooth disease HGNC:9118 Homo sapiens (human) 5376 PMP22 inference by association of genotype from phenotype used in manual assertion
  • PMID:9040744
  • RGD:7240710
DOID:0111730 familial episodic pain syndrome 2 HGNC:10582 Homo sapiens (human) 6336 SCN10A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11105 fundus albipunctatus HGNC:10024 Homo sapiens (human) 6017 RLBP1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111187 distal myopathy with anterior tibial onset HGNC:3097 Homo sapiens (human) 8291 DYSF inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2154 nephroblastoma HGNC:9966 Homo sapiens (human) 5978 REST inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12849 autistic disorder HGNC:4078 Homo sapiens (human) 2557 GABRA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:16770606
DOID:8778 Crohn's disease HGNC:7107 Homo sapiens (human) 4288 MKI67 direct assay evidence used in manual assertion
  • PMID:21364546
DOID:0111275 speech-language disorder-1 HGNC:13875 Homo sapiens (human) 93986 FOXP2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11586359
  • PMID:15877281
  • PMID:16984964
  • PMID:17033973
  • RGD:7240710
DOID:0080533 Carney-Stratakis syndrome HGNC:10683 Homo sapiens (human) 6392 SDHD inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:784 chronic kidney disease HGNC:610 Homo sapiens (human) 345 APOC3 direct assay evidence used in manual assertion
  • PMID:21297177
DOID:1324 lung cancer HGNC:20754 Homo sapiens (human) 57113 TRPC7 inference by association of genotype from phenotype used in manual assertion
  • PMID:27617218
DOID:0060227 Adams-Oliver syndrome HGNC:7881 Homo sapiens (human) 4851 NOTCH1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2043 hepatitis B HGNC:5423 Homo sapiens (human) 3440 IFNA2 direct assay evidence used in manual assertion
  • PMID:8509638
DOID:1588 thrombocytopenia HGNC:7217 Homo sapiens (human) 4352 MPL inference by association of genotype from phenotype used in manual assertion
  • PMID:10077649
DOID:0080226 autosomal dominant intellectual developmental disorder 56 HGNC:2092 Homo sapiens (human) 1213 CLTC inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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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