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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 5801 - 5825 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▼ References
DOID:2876 laryngeal squamous cell carcinoma HGNC:4553 Homo sapiens (human) 2876 GPX1 inference by association of genotype from phenotype used in manual assertion
  • PMID:27188866
DOID:2987 familial Mediterranean fever HGNC:40 Homo sapiens (human) 5243 ABCB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17610314
  • PMID:24773260
DOID:0050711 aceruloplasminemia HGNC:2295 Homo sapiens (human) 1356 CP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3319 lymphangioleiomyomatosis HGNC:12362 Homo sapiens (human) 7248 TSC1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060275 pontocerebellar hypoplasia type 6 HGNC:21406 Homo sapiens (human) 57038 RARS2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080455 developmental and epileptic encephalopathy 52 HGNC:10586 Homo sapiens (human) 6324 SCN1B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3310 atopic dermatitis HGNC:11850 Homo sapiens (human) 7099 TLR4 inference by association of genotype from phenotype used in manual assertion
  • PMID:23821954
DOID:3312 bipolar disorder HGNC:17582 Homo sapiens (human) 23522 KAT6B inference by association of genotype from phenotype used in manual assertion
  • PMID:24444492
DOID:3748 esophagus squamous cell carcinoma HGNC:24308 Homo sapiens (human) 81037 CLPTM1L inference by association of genotype from phenotype used in manual assertion
  • PMID:25007268
  • PMID:26716642
DOID:10159 osteonecrosis HGNC:2200 Homo sapiens (human) 1280 COL2A1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12849 autistic disorder HGNC:13875 Homo sapiens (human) 93986 FOXP2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15108192
  • PMID:15737702
DOID:3070 high grade glioma HGNC:886 Homo sapiens (human) 546 ATRX inference by association of genotype from phenotype used in manual assertion
  • PMID:23104868
DOID:1996 rectum adenocarcinoma HGNC:11364 Homo sapiens (human) 6774 STAT3 inference by association of genotype from phenotype used in manual assertion
  • PMID:22121102
DOID:1612 breast cancer HGNC:11920 Homo sapiens (human) 355 FAS inference by association of genotype from phenotype used in manual assertion
  • PMID:17183065
DOID:5844 myocardial infarction HGNC:10618 Homo sapiens (human) 6347 CCL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16116069
DOID:1924 hypogonadism HGNC:4510 Homo sapiens (human) 84634 KISS1R inference by association of genotype from phenotype used in manual assertion
  • PMID:12944565
DOID:14705 Pfeiffer syndrome HGNC:3689 Homo sapiens (human) 2263 FGFR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:33074973
  • PMID:7795583
  • RGD:7240710
DOID:3312 bipolar disorder HGNC:8847 Homo sapiens (human) 8863 PER3 inference by association of genotype from phenotype used in manual assertion
  • PMID:30121446
DOID:768 retinoblastoma HGNC:9884 Homo sapiens (human) 5925 RB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12402348
  • RGD:7240710
DOID:104 bacterial infectious disease HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16987934
DOID:418 systemic scleroderma HGNC:10907 Homo sapiens (human) 6556 SLC11A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17876529
DOID:11054 urinary bladder cancer HGNC:6844 Homo sapiens (human) 6416 MAP2K4 inference by association of genotype from phenotype used in manual assertion
  • PMID:15665277
DOID:0111590 Cohen syndrome HGNC:2183 Homo sapiens (human) 157680 VPS13B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060712 autosomal recessive congenital ichthyosis 4A HGNC:14637 Homo sapiens (human) 26154 ABCA12 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8398 osteoarthritis HGNC:14872 Homo sapiens (human) 54829 ASPN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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International Collaboration

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: December 8, 2025