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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 1426 - 1450 of 12216 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0070519 early-onset vitamin B6-dependent epilepsy 4 HGNC:877 Homo sapiens (human) 501 ALDH7A1
  • RGD:7240710
DOID:0080000 muscular disease HGNC:2330 Homo sapiens (human) 1376 CPT2
  • PMID:10873395
DOID:0080000 muscular disease FB:FBgn0035383 Drosophila melanogaster (fruit fly) 38355 CPT2
  • MGI:6194238
DOID:0080000 muscular disease HGNC:84 Homo sapiens (human) 31 ACACA
  • MGI:6194238
DOID:0080000 muscular disease HGNC:6677 Homo sapiens (human) 4023 LPL
  • PMID:7635990
DOID:0080000 muscular disease HGNC:3594 Homo sapiens (human) 2194 FASN
  • MGI:6194238
DOID:0080000 muscular disease HGNC:85 Homo sapiens (human) 32 ACACB
  • MGI:6194238
DOID:0080005 bone remodeling disease SGD:S000004954 Saccharomyces cerevisiae S288C 855723 IDP3
  • MGI:6194238
DOID:0080005 bone remodeling disease SGD:S000004164 Saccharomyces cerevisiae S288C 850871 IDP2
  • MGI:6194238
DOID:0080005 bone remodeling disease RGD:1597139 Rattus norvegicus (Norway rat) 361596 Idh2
  • MGI:6194238
DOID:0080005 bone remodeling disease HGNC:5383 Homo sapiens (human) 3418 IDH2
  • MGI:6194238
DOID:0080005 bone remodeling disease MGI:96414 Mus musculus (house mouse) 269951 Idh2
  • PMID:29527922
DOID:0080016 spina bifida HGNC:587 Homo sapiens (human) 328 APEX1
  • PMID:15887293
DOID:0080037 Worth syndrome MGI:1278315 Mus musculus (house mouse) 16973 Lrp5
  • MGI:6194238
DOID:0080037 Worth syndrome HGNC:6697 Homo sapiens (human) 4041 LRP5
  • RGD:7240710
DOID:0080046 Stickler syndrome HGNC:2218 Homo sapiens (human) 1298 COL9A2
  • RGD:7240710
DOID:0080047 pseudoachondroplasia FB:FBgn0031850 Drosophila melanogaster (fruit fly) 33941 Tsp CG11326
  • MGI:6194238
DOID:0080055 achondrogenesis type IB HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:8528239
  • RGD:7240710
DOID:0080070 mucolipidosis II alpha/beta HGNC:29670 Homo sapiens (human) 79158 GNPTAB
  • MGI:6194238
  • RGD:7240710
DOID:0080070 mucolipidosis II alpha/beta MGI:3643902 Mus musculus (house mouse) 432486 Gnptab
  • MGI:6194238
  • PMID:17962477
  • PMID:24127423
  • PMID:25107912
  • PMID:26857995
DOID:0080070 mucolipidosis II alpha/beta ZFIN:ZDB-GENE-030131-4714 Danio rerio (zebrafish) 553365 gnptab
  • MGI:6194238
  • PMID:19834066
  • PMID:22046029
  • PMID:26404503
  • PMID:29539424
DOID:0080071 mucolipidosis III alpha/beta MGI:3643902 Mus musculus (house mouse) 432486 Gnptab
  • MGI:6194238
DOID:0080071 mucolipidosis III alpha/beta ZFIN:ZDB-GENE-030131-4714 Danio rerio (zebrafish) 553365 gnptab
  • MGI:6194238
DOID:0080071 mucolipidosis III alpha/beta HGNC:29670 Homo sapiens (human) 79158 GNPTAB
  • RGD:7240710
DOID:0080072 intestinal pseudo-obstruction HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238

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Supported by JST NBDC Grant Number JPMJND2204

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