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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 July 29, 2024
Displaying entries 851 - 875 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0060740 methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency HGNC:7526 Homo sapiens (human) 4594 MMUT
  • MGI:6194238
  • PMID:27167370
  • RGD:7240710
DOID:12365 malaria HGNC:9020 Homo sapiens (human) 5313 PKLR
  • MGI:6194238
  • PMID:20377593
DOID:9970 obesity HGNC:6554 Homo sapiens (human) 3953 LEPR
  • MGI:6194238
  • PMID:18204169
  • PMID:9545018
DOID:0110635 muscular dystrophy-dystroglycanopathy type B5 HGNC:17997 Homo sapiens (human) 79147 FKRP
  • MGI:6194238
  • PMID:14652796
  • RGD:7240710
DOID:0060284 paroxysmal nocturnal hemoglobinuria HGNC:8957 Homo sapiens (human) 5277 PIGA
  • MGI:6194238
  • PMID:12424196
  • RGD:7240710
DOID:0110295 autosomal recessive limb-girdle muscular dystrophy type 2U HGNC:37276 Homo sapiens (human) 729920 CRPPA
  • MGI:6194238
  • RGD:7240710
DOID:0110657 congenital myasthenic syndrome 8 HGNC:329 Homo sapiens (human) 375790 AGRN
  • MGI:6194238
  • RGD:7240710
DOID:0050833 orotic aciduria HGNC:12563 Homo sapiens (human) 7372 UMPS
  • MGI:6194238
  • RGD:7240710
DOID:2747 glycogen storage disease HGNC:8931 Homo sapiens (human) 5261 PHKG2
  • MGI:6194238
  • PMID:8896567
DOID:0070257 congenital disorder of glycosylation type IIe HGNC:18622 Homo sapiens (human) 91949 COG7
  • MGI:6194238
  • RGD:7240710
DOID:0050441 mucosulfatidosis HGNC:20376 Homo sapiens (human) 285362 SUMF1
  • MGI:6194238
  • RGD:7240710
DOID:10763 hypertension HGNC:6554 Homo sapiens (human) 3953 LEPR
  • MGI:6194238
  • PMID:10999797
DOID:0112050 non-syndromic X-linked intellectual disability 63 HGNC:3571 Homo sapiens (human) 2182 ACSL4
  • MGI:6194238
  • RGD:7240710
DOID:0110352 retinitis pigmentosa 59 HGNC:20603 Homo sapiens (human) 79947 DHDDS
  • MGI:6194238
  • RGD:7240710
DOID:0110184 Charcot-Marie-Tooth disease type 4J HGNC:16873 Homo sapiens (human) 9896 FIG4
  • MGI:6194238
  • RGD:7240710
DOID:3649 pyruvate decarboxylase deficiency HGNC:2896 Homo sapiens (human) 1737 DLAT
  • MGI:6194238
  • RGD:7240710
DOID:0070468 Yoon-Bellen neurodevelopmental syndrome HGNC:25590 Homo sapiens (human) 55753 OGDHL
  • MGI:6194238
  • RGD:7240710
DOID:0090140 cortisone reductase deficiency 2 HGNC:5208 Homo sapiens (human) 3290 HSD11B1
  • MGI:6194238
  • RGD:7240710
DOID:0111037 glycine N-methyltransferase deficiency HGNC:4415 Homo sapiens (human) 27232 GNMT
  • MGI:6194238
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
  • PMID:1570017
  • PMID:8200206
  • PMID:8314445
  • PMID:8325445
  • RGD:7240710
DOID:2752 glycogen storage disease II HGNC:4065 Homo sapiens (human) 2548 GAA
  • MGI:6194238
  • RGD:7240710
DOID:0050433 fatal familial insomnia HGNC:9449 Homo sapiens (human) 5621 PRNP
  • MGI:6194238
  • RGD:7240710
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:23269818
DOID:0081168 HMG-CoA synthase 2 deficiency HGNC:5008 Homo sapiens (human) 3158 HMGCS2
  • MGI:6194238
  • RGD:7240710
DOID:0080556 congenital disorder of glycosylation Id HGNC:23056 Homo sapiens (human) 10195 ALG3
  • MGI:6194238
  • RGD:7240710

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