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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 October 9, 2024
Displaying entries 66001 - 66025 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:1682 congenital heart disease HGNC:4173 Homo sapiens (human) 2626 GATA4
  • MGI:6194238
  • PMID:12845333
DOID:0110087 asphyxiating thoracic dystrophy 3 HGNC:2962 Homo sapiens (human) 79659 DYNC2H1
  • MGI:6194238
  • RGD:7240710
DOID:0110175 Charcot-Marie-Tooth disease axonal type 2O HGNC:2961 Homo sapiens (human) 1778 DYNC1H1
  • MGI:6194238
  • RGD:7240710
DOID:1056 oculocerebrorenal syndrome HGNC:8108 Homo sapiens (human) 4952 OCRL
  • MGI:6194238
  • RGD:7240710
DOID:2129 atypical teratoid rhabdoid tumor HGNC:11103 Homo sapiens (human) 6598 SMARCB1
  • MGI:6194238
  • RGD:7240710
DOID:10629 microphthalmia HGNC:4837 Homo sapiens (human) 3052 HCCS
  • MGI:6194238
  • PMID:17033964
DOID:10584 retinitis pigmentosa HGNC:17340 Homo sapiens (human) 10594 PRPF8
  • MGI:6194238
  • PMID:11468273
DOID:0060569 hypertrichotic osteochondrodysplasia Cantu type HGNC:60 Homo sapiens (human) 10060 ABCC9
  • MGI:6194238
  • RGD:7240710
DOID:4483 rhinitis HGNC:1033 Homo sapiens (human) 627 BDNF
  • MGI:6194238
  • PMID:21723144
DOID:0110867 congenital stationary night blindness 1C HGNC:7146 Homo sapiens (human) 4308 TRPM1
  • MGI:6194238
  • RGD:7240710
DOID:0081126 DeSanto-Shinawi syndrome HGNC:17327 Homo sapiens (human) 51322 WAC
  • MGI:6194238
  • RGD:7240710
DOID:0110659 congenital myasthenic syndrome 7 HGNC:11510 Homo sapiens (human) 127833 SYT2
  • MGI:6194238
  • RGD:7240710
DOID:1572 normal pressure hydrocephalus HGNC:26684 Homo sapiens (human) 80217 CFAP43
  • MGI:6194238
  • RGD:7240710
DOID:0050773 paraganglioma HGNC:10681 Homo sapiens (human) 6390 SDHB
  • MGI:6194238
  • PMID:11404820
  • RGD:7240710
DOID:0070248 autosomal recessive Emery-Dreifuss muscular dystrophy 3 HGNC:6636 Homo sapiens (human) 4000 LMNA
  • MGI:6194238
  • RGD:7240710
DOID:10588 adrenoleukodystrophy HGNC:61 Homo sapiens (human) 215 ABCD1
  • MGI:6194238
  • PMID:8048932
  • RGD:7240710
DOID:0060545 Hermansky-Pudlak syndrome 7 HGNC:17328 Homo sapiens (human) 84062 DTNBP1
  • MGI:6194238
  • RGD:7240710
DOID:11476 osteoporosis HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:17002564
DOID:9074 systemic lupus erythematosus HGNC:1324 Homo sapiens (human) 721 C4B
  • MGI:6194238
  • PMID:17503323
DOID:0090078 hypogonadotropic hypogonadism 7 with or without anosmia HGNC:4421 Homo sapiens (human) 2798 GNRHR
  • MGI:6194238
  • PMID:17235395
  • RGD:7240710
DOID:9452 steatotic liver disease HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
  • PMID:14606109
DOID:1929 supravalvular aortic stenosis HGNC:3327 Homo sapiens (human) 2006 ELN
  • MGI:6194238
  • PMID:8132745
  • RGD:7240710
DOID:14264 benign neonatal seizures HGNC:6296 Homo sapiens (human) 3785 KCNQ2
  • MGI:6194238
  • RGD:7240710
DOID:0090144 Donnai-Barrow syndrome HGNC:6694 Homo sapiens (human) 4036 LRP2
  • MGI:6194238
  • RGD:7240710
DOID:5813 purine nucleoside phosphorylase deficiency HGNC:7892 Homo sapiens (human) 4860 PNP
  • MGI:6194238
  • 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: December 9, 2024