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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 11401 - 11425 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:9352 type 2 diabetes mellitus HGNC:9235 Homo sapiens (human) 5467 PPARD
  • MGI:6194238
  • PMID:16804087
DOID:0111395 mucopolysaccharidosis type IIIA HGNC:10818 Homo sapiens (human) 6448 SGSH
  • MGI:6194238
  • RGD:7240710
DOID:0110913 adult hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL
  • MGI:6194238
  • RGD:7240710
DOID:10325 silicosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:11264025
DOID:3650 lactic acidosis RGD:620687 Rattus norvegicus (Norway rat) 64035 Pygl
  • MGI:6194238
  • PMID:17705025
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 HGNC:9202 Homo sapiens (human) 10585 POMT1
  • MGI:6194238
  • RGD:7240710
DOID:1115 sarcoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
  • PMID:31089155
DOID:0080153 medium chain acyl-CoA dehydrogenase deficiency HGNC:89 Homo sapiens (human) 34 ACADM
  • MGI:6194238
  • RGD:7240710
DOID:5082 liver cirrhosis HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
  • PMID:18233990
DOID:83 cataract HGNC:6708 Homo sapiens (human) 4047 LSS
  • MGI:6194238
  • PMID:26200341
DOID:0080154 short chain acyl-CoA dehydrogenase deficiency HGNC:90 Homo sapiens (human) 35 ACADS
  • MGI:6194238
  • RGD:7240710
DOID:0070253 congenital disorder of glycosylation type IIa HGNC:7045 Homo sapiens (human) 4247 MGAT2
  • MGI:6194238
  • RGD:7240710
DOID:10763 hypertension HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • MGI:6194238
  • PMID:10024332
DOID:0050773 paraganglioma HGNC:10680 Homo sapiens (human) 6389 SDHA
  • MGI:6194238
  • RGD:7240710
DOID:0110644 long QT syndrome 1 HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • MGI:6194238
  • RGD:7240710
DOID:0060887 ossification of the posterior longitudinal ligament of spine HGNC:3356 Homo sapiens (human) 5167 ENPP1
  • MGI:6194238
  • PMID:15834329
DOID:9266 cystinuria HGNC:11025 Homo sapiens (human) 6519 SLC3A1
  • MGI:6194238
  • PMID:8054986
  • RGD:7240710
DOID:11476 osteoporosis HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:17002564
DOID:9268 glycine encephalopathy HGNC:4313 Homo sapiens (human) 2731 GLDC
  • MGI:6194238
  • PMID:15851735
  • PMID:17361008
  • RGD:7240710
DOID:5813 purine nucleoside phosphorylase deficiency HGNC:7892 Homo sapiens (human) 4860 PNP
  • MGI:6194238
  • RGD:7240710
DOID:14701 propionic acidemia HGNC:8653 Homo sapiens (human) 5095 PCCA
  • MGI:6194238
  • RGD:7240710
DOID:10763 hypertension HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • MGI:6194238
  • PMID:10577996
  • PMID:12372404
  • PMID:17070428
DOID:0080886 vitamin D-dependent rickets type 1A HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • MGI:6194238
  • RGD:7240710
DOID:0060537 mitochondrial complex II deficiency HGNC:10683 Homo sapiens (human) 6392 SDHD
  • MGI:6194238
  • RGD:7240710
DOID:0050560 Walker-Warburg syndrome HGNC:9202 Homo sapiens (human) 10585 POMT1
  • MGI:6194238
  • PMID:12369018
  • PMID:15637732
  • PMID:16575835

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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Supported by JST NBDC Grant Number JPMJND2204

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


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