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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 976 - 1000 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0050579 glycogen storage disease XV HGNC:4699 Homo sapiens (human) 2992 GYG1
  • MGI:6194238
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:5208 Homo sapiens (human) 3290 HSD11B1
  • MGI:6194238
  • PMID:28750217
DOID:1742 drug psychosis HGNC:4092 Homo sapiens (human) 2571 GAD1
  • MGI:6194238
  • PMID:27967329
DOID:10763 hypertension HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:19204185
DOID:898 autosomal dominant polycystic kidney disease HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:25920554
DOID:3827 congenital diaphragmatic hernia HGNC:23399 Homo sapiens (human) 158326 FREM1
  • MGI:6194238
  • PMID:23221805
DOID:5419 schizophrenia HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • MGI:6194238
  • RGD:7240710
DOID:2861 congenital nonspherocytic hemolytic anemia HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
  • PMID:1999409
  • PMID:24923766
DOID:684 hepatocellular carcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
  • PMID:29749584
  • RGD:7240710
DOID:3320 Tay-Sachs disease HGNC:4878 Homo sapiens (human) 3073 HEXA
  • MGI:6194238
  • RGD:7240710
DOID:898 autosomal dominant polycystic kidney disease HGNC:9008 Homo sapiens (human) 5310 PKD1
  • MGI:6194238
  • PMID:21115670
  • PMID:8554072
DOID:9269 maple syrup urine disease HGNC:987 Homo sapiens (human) 594 BCKDHB
  • MGI:6194238
  • PMID:2022752
DOID:0060062 familial juvenile hyperuricemic nephropathy HGNC:12559 Homo sapiens (human) 7369 UMOD
  • MGI:6194238
  • PMID:12471200
  • RGD:7240710
DOID:13482 Proteus syndrome HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
  • PMID:21793738
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:4177 Homo sapiens (human) 2629 GBA1
  • MGI:6194238
  • PMID:19945510
  • PMID:20528910
  • PMID:20947659
  • PMID:21242499
  • PMID:24126159
  • PMID:25639775
  • PMID:26223426
DOID:0050461 aspartylglucosaminuria HGNC:318 Homo sapiens (human) 175 AGA
  • MGI:6194238
  • RGD:7240710
DOID:0050560 Walker-Warburg syndrome HGNC:19139 Homo sapiens (human) 55624 POMGNT1
  • MGI:6194238
  • PMID:11709191
  • PMID:15236414
  • PMID:22554691
  • PMID:23689641
DOID:0050574 L-2-hydroxyglutaric aciduria HGNC:20499 Homo sapiens (human) 79944 L2HGDH
  • MGI:6194238
  • PMID:24573090
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:8975 Homo sapiens (human) 5290 PIK3CA
  • MGI:6194238
  • PMID:16331247
  • PMID:24673525
  • PMID:26823876
  • RGD:7240710
DOID:10591 pre-eclampsia HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:15901845
DOID:0050848 obstructive sleep apnea HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:19482546
  • PMID:20182789
DOID:8947 diabetic retinopathy HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
  • PMID:16701918
  • PMID:19587357
  • PMID:21067572
DOID:11949 Creutzfeldt-Jakob disease HGNC:9449 Homo sapiens (human) 5621 PRNP
  • MGI:6194238
  • PMID:1684755
  • RGD:7240710
DOID:0080562 congenital disorder of glycosylation Ij HGNC:2995 Homo sapiens (human) 1798 DPAGT1
  • MGI:6194238
  • RGD:7240710
DOID:2748 glycogen storage disease III HGNC:321 Homo sapiens (human) 178 AGL
  • MGI:6194238
  • PMID:16705713
  • RGD:7240710

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Last updated: August 19, 2024