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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 6501 - 6525 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:162 cancer FB:FBgn0266438 Drosophila melanogaster (fruit fly) 19835548 PIG-Z
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus SGD:S000004263 Saccharomyces cerevisiae S288C 850979 PIG1
  • MGI:6194238
DOID:1574 alcohol use disorder SGD:S000004263 Saccharomyces cerevisiae S288C 850979 PIG1
  • MGI:6194238
DOID:0080139 multiple congenital anomalies-hypotonia-seizures syndrome 2 HGNC:8957 Homo sapiens (human) 5277 PIGA
  • RGD:7240710
DOID:0060713 autosomal recessive congenital ichthyosis 4B HGNC:8957 Homo sapiens (human) 5277 PIGA
  • MGI:6194238
DOID:0060284 paroxysmal nocturnal hemoglobinuria HGNC:8957 Homo sapiens (human) 5277 PIGA
  • MGI:6194238
  • PMID:12424196
  • RGD:7240710
DOID:0112216 developmental and epileptic encephalopathy 80 HGNC:8959 Homo sapiens (human) 9488 PIGB
  • RGD:7240710
DOID:10112 sleeping sickness HGNC:8959 Homo sapiens (human) 9488 PIGB
  • MGI:6194238
DOID:0081223 glycosylphosphatidylinositol biosynthesis defect 16 HGNC:8960 Homo sapiens (human) 5279 PIGC
  • RGD:7240710
DOID:0112152 CHIME syndrome HGNC:8966 Homo sapiens (human) 9487 PIGL
  • PMID:22444671
  • RGD:7240710
DOID:0080138 multiple congenital anomalies-hypotonia-seizures syndrome 1 HGNC:8967 Homo sapiens (human) 23556 PIGN
  • RGD:7240710
DOID:4621 holoprosencephaly HGNC:8967 Homo sapiens (human) 23556 PIGN
  • MGI:6194238
DOID:0070434 hyperphosphatasia with impaired intellectual development syndrome 2 HGNC:23215 Homo sapiens (human) 84720 PIGO
  • RGD:7240710
DOID:0080283 developmental and epileptic encephalopathy 55 HGNC:3046 Homo sapiens (human) 51227 PIGP
  • RGD:7240710
DOID:0112213 multiple congenital anomalies-hypotonia-seizures syndrome 4 HGNC:14135 Homo sapiens (human) 9091 PIGQ
  • RGD:7240710
DOID:0070382 developmental and epileptic encephalopathy 95 HGNC:14937 Homo sapiens (human) 94005 PIGS
  • RGD:7240710
DOID:0080140 multiple congenital anomalies-hypotonia-seizures syndrome 3 HGNC:14938 Homo sapiens (human) 51604 PIGT
  • RGD:7240710
DOID:0060284 paroxysmal nocturnal hemoglobinuria HGNC:14938 Homo sapiens (human) 51604 PIGT
  • RGD:7240710
DOID:0070433 hyperphosphatasia with impaired intellectual development syndrome 1 HGNC:26031 Homo sapiens (human) 55650 PIGV
  • PMID:20802478
  • RGD:7240710
DOID:0070432 hyperphosphatasia with impaired intellectual development syndrome 5 HGNC:23213 Homo sapiens (human) 284098 PIGW
  • RGD:7240710
DOID:0070437 hyperphosphatasia with impaired intellectual development syndrome 6 HGNC:28213 Homo sapiens (human) 84992 PIGY
  • RGD:7240710
DOID:162 cancer HGNC:30596 Homo sapiens (human) 80235 PIGZ
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:8971 Homo sapiens (human) 5286 PIK3C2A
  • PMID:21127054
DOID:83 cataract HGNC:8971 Homo sapiens (human) 5286 PIK3C2A
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:8973 Homo sapiens (human) 5288 PIK3C2G
  • PMID:17991425

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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