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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 201 - 225 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:0050776 non-syndromic X-linked intellectual disability HGNC:3570 Homo sapiens (human) 2181 ACSL3
  • MGI:6194238
DOID:0112050 non-syndromic X-linked intellectual disability 63 HGNC:3571 Homo sapiens (human) 2182 ACSL4
  • MGI:6194238
  • RGD:7240710
DOID:1059 intellectual disability HGNC:3571 Homo sapiens (human) 2182 ACSL4
  • PMID:11889465
DOID:14501 Sjogren-Larsson syndrome HGNC:3571 Homo sapiens (human) 2182 ACSL4
  • MGI:6194238
DOID:0050776 non-syndromic X-linked intellectual disability HGNC:3571 Homo sapiens (human) 2182 ACSL4
  • MGI:6194238
DOID:0060774 congenital diarrhea HGNC:16526 Homo sapiens (human) 51703 ACSL5
  • RGD:7240710
DOID:1240 leukemia HGNC:16496 Homo sapiens (human) 23305 ACSL6
  • PMID:10502316
DOID:9119 acute myeloid leukemia HGNC:16496 Homo sapiens (human) 23305 ACSL6
  • PMID:10502316
DOID:10825 essential hypertension HGNC:10522 Homo sapiens (human) 6296 ACSM3
  • PMID:11592044
DOID:2986 IgA glomerulonephritis HGNC:10522 Homo sapiens (human) 6296 ACSM3
  • PMID:12484505
DOID:10763 hypertension HGNC:10522 Homo sapiens (human) 6296 ACSM3
  • MGI:6194238
DOID:9282 ocular hypertension HGNC:10522 Homo sapiens (human) 6296 ACSM3
  • MGI:6194238
DOID:8577 ulcerative colitis HGNC:10522 Homo sapiens (human) 6296 ACSM3
  • PMID:21987487
DOID:0050567 orofacial cleft HGNC:15814 Homo sapiens (human) 55902 ACSS2
  • PMID:27229527
  • PMID:28543373
DOID:1574 alcohol use disorder HGNC:15814 Homo sapiens (human) 55902 ACSS2
  • MGI:6194238
DOID:3319 lymphangioleiomyomatosis HGNC:15814 Homo sapiens (human) 55902 ACSS2
  • PMID:29885404
DOID:11981 morbid obesity HGNC:15814 Homo sapiens (human) 55902 ACSS2
  • PMID:22384010
DOID:684 hepatocellular carcinoma SGD:S000004915 Saccharomyces cerevisiae S288C 855346 ADE4
  • MGI:6194238
DOID:4450 renal cell carcinoma SGD:S000004915 Saccharomyces cerevisiae S288C 855346 ADE4
  • MGI:6194238
DOID:0050741 alcohol dependence HGNC:250 Homo sapiens (human) 125 ADH1B
  • RGD:7240710
DOID:1793 pancreatic cancer HGNC:251 Homo sapiens (human) 126 ADH1C
  • PMID:19068087
DOID:0060892 late onset Parkinson's disease HGNC:251 Homo sapiens (human) 126 ADH1C
  • RGD:7240710
DOID:0050741 alcohol dependence HGNC:251 Homo sapiens (human) 126 ADH1C
  • RGD:7240710
DOID:0050741 alcohol dependence HGNC:252 Homo sapiens (human) 127 ADH4
  • PMID:20077761
DOID:2841 asthma HGNC:253 Homo sapiens (human) 128 ADH5
  • PMID:17543375
  • PMID:19395503
  • PMID:19514054

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024