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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 October 9, 2024
Displaying entries 67001 - 67025 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:0111693 familial adult myoclonic epilepsy 4 HGNC:25489 Homo sapiens (human) 55689 YEATS2
  • MGI:6194238
  • RGD:7240710
DOID:11446 sciatic neuropathy HGNC:11179 Homo sapiens (human) 6647 SOD1
  • MGI:6194238
  • PMID:21489258
DOID:0080109 infantile myofibromatosis HGNC:8804 Homo sapiens (human) 5159 PDGFRB
  • MGI:6194238
  • RGD:7240710
DOID:0060929 non-syndromic X-linked intellectual developmental disorder 111 HGNC:13449 Homo sapiens (human) 84631 SLITRK2
  • MGI:6194238
  • RGD:7240710
DOID:0112341 hereditary spastic paraplegia 80 HGNC:12461 Homo sapiens (human) 51271 UBAP1
  • MGI:6194238
  • RGD:7240710
DOID:0110490 autosomal recessive nonsyndromic deafness 31 HGNC:16361 Homo sapiens (human) 25861 WHRN
  • MGI:6194238
  • RGD:7240710
DOID:0110703 hypotrichosis 6 HGNC:21307 Homo sapiens (human) 147409 DSG4
  • MGI:6194238
  • RGD:7240710
DOID:0080240 non-syndromic X-linked intellectual disability 106 HGNC:8127 Homo sapiens (human) 8473 OGT
  • MGI:6194238
  • RGD:7240710
DOID:0111072 myostatin-related muscle hypertrophy HGNC:4223 Homo sapiens (human) 2660 MSTN
  • MGI:6194238
  • RGD:7240710
DOID:0090030 corticosteroid-binding globulin deficiency HGNC:1540 Homo sapiens (human) 866 SERPINA6
  • MGI:6194238
  • RGD:7240710
DOID:9976 heroin dependence HGNC:8154 Homo sapiens (human) 4986 OPRK1
  • MGI:6194238
  • PMID:31940240
DOID:2843 long QT syndrome RGD:621503 Rattus norvegicus (Norway rat) 84020 Kcnq1
  • MGI:6194238
  • PMID:16368876
DOID:10763 hypertension HGNC:5209 Homo sapiens (human) 3291 HSD11B2
  • MGI:6194238
  • PMID:9683587
DOID:14219 renal tubular acidosis HGNC:11027 Homo sapiens (human) 6521 SLC4A1
  • MGI:6194238
  • PMID:22126643
  • PMID:22919024
DOID:0090132 complex cortical dysplasia with other brain malformations 7 HGNC:30829 Homo sapiens (human) 347733 TUBB2B
  • MGI:6194238
  • RGD:7240710
DOID:6000 congestive heart failure HGNC:285 Homo sapiens (human) 153 ADRB1
  • MGI:6194238
  • PMID:14502278
DOID:0080991 congenital myopathy 1B HGNC:10483 Homo sapiens (human) 6261 RYR1
  • MGI:6194238
  • RGD:7240710
DOID:0060812 syndromic X-linked intellectual disability Siderius type HGNC:20672 Homo sapiens (human) 23133 PHF8
  • MGI:6194238
  • RGD:7240710
DOID:1742 drug psychosis HGNC:4092 Homo sapiens (human) 2571 GAD1
  • MGI:6194238
  • PMID:27967329
DOID:0070253 congenital disorder of glycosylation type IIa HGNC:7045 Homo sapiens (human) 4247 MGAT2
  • MGI:6194238
  • RGD:7240710
DOID:0110766 hereditary spastic paraplegia 13 HGNC:5261 Homo sapiens (human) 3329 HSPD1
  • MGI:6194238
  • RGD:7240710
DOID:988 mitral valve prolapse HGNC:20908 Homo sapiens (human) 22873 DZIP1
  • MGI:6194238
  • RGD:7240710
DOID:1919 Lesch-Nyhan syndrome HGNC:5157 Homo sapiens (human) 3251 HPRT1
  • MGI:6194238
  • PMID:20638392
  • PMID:24940672
  • RGD:7240710
DOID:0111628 high myopia-sensorineural deafness syndrome HGNC:23503 Homo sapiens (human) 84189 SLITRK6
  • MGI:6194238
  • RGD:7240710
DOID:0111128 focal segmental glomerulosclerosis 1 HGNC:166 Homo sapiens (human) 81 ACTN4
  • MGI:6194238
  • RGD:7240710

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

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: December 9, 2024