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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 10801 - 10825 of 12216 in total
Disease ID ▼ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0070467 carpal tunnel syndrome 2 FB:FBgn0031850 Drosophila melanogaster (fruit fly) 33941 Tsp CG11326
  • MGI:6194238
DOID:0070460 hereditary spastic paraplegia 90B HGNC:20361 Homo sapiens (human) 171546 SPTSSA
  • RGD:7240710
DOID:0070459 hereditary spastic paraplegia 90A HGNC:20361 Homo sapiens (human) 171546 SPTSSA
  • RGD:7240710
DOID:0070450 mitochondrial DNA depletion syndrome 19 HGNC:10980 Homo sapiens (human) 1468 SLC25A10
  • RGD:7240710
DOID:0070450 mitochondrial DNA depletion syndrome 19 MGI:1353497 Mus musculus (house mouse) 27376 Slc25a10
  • MGI:6194238
DOID:0070437 hyperphosphatasia with impaired intellectual development syndrome 6 HGNC:28213 Homo sapiens (human) 84992 PIGY
  • RGD:7240710
DOID:0070436 hyperphosphatasia with impaired intellectual development syndrome 4 FB:FBgn0033088 Drosophila melanogaster (fruit fly) 35570 PGAP3
  • MGI:6194238
DOID:0070436 hyperphosphatasia with impaired intellectual development syndrome 4 HGNC:23719 Homo sapiens (human) 93210 PGAP3
  • RGD:7240710
DOID:0070435 hyperphosphatasia with impaired intellectual development syndrome 3 FB:FBgn0031284 Drosophila melanogaster (fruit fly) 33258 PGAP2
  • MGI:6194238
DOID:0070435 hyperphosphatasia with impaired intellectual development syndrome 3 HGNC:17893 Homo sapiens (human) 27315 PGAP2
  • RGD:7240710
DOID:0070434 hyperphosphatasia with impaired intellectual development syndrome 2 HGNC:23215 Homo sapiens (human) 84720 PIGO
  • RGD:7240710
DOID:0070433 hyperphosphatasia with impaired intellectual development syndrome 1 SGD:S000000208 Saccharomyces cerevisiae S288C 852289 GPI18
  • MGI:6194238
DOID:0070433 hyperphosphatasia with impaired intellectual development syndrome 1 WB:WBGene00020375 Caenorhabditis elegans 172305 pigv-1
  • MGI:6194238
DOID:0070433 hyperphosphatasia with impaired intellectual development syndrome 1 Xenbase:XB-GENE-965986 Xenopus tropicalis (tropical clawed frog) 100380028 pigv
  • MGI:6194238
DOID:0070433 hyperphosphatasia with impaired intellectual development syndrome 1 MGI:2442480 Mus musculus (house mouse) 230801 Pigv
  • MGI:6194238
DOID:0070433 hyperphosphatasia with impaired intellectual development syndrome 1 FB:FBgn0265174 Drosophila melanogaster (fruit fly) 19835383 PIG-V
  • MGI:6194238
DOID:0070433 hyperphosphatasia with impaired intellectual development syndrome 1 ZFIN:ZDB-GENE-121116-1 Danio rerio (zebrafish) 100148642 pigv
  • MGI:6194238
DOID:0070433 hyperphosphatasia with impaired intellectual development syndrome 1 HGNC:26031 Homo sapiens (human) 55650 PIGV
  • PMID:20802478
  • RGD:7240710
DOID:0070433 hyperphosphatasia with impaired intellectual development syndrome 1 RGD:1309526 Rattus norvegicus (Norway rat) 366478 Pigv
  • MGI:6194238
DOID:0070432 hyperphosphatasia with impaired intellectual development syndrome 5 HGNC:23213 Homo sapiens (human) 284098 PIGW
  • RGD:7240710
DOID:0070430 combined oxidative phosphorylation deficiency 57 HGNC:16148 Homo sapiens (human) 54675 CRLS1
  • RGD:7240710
DOID:0070403 hypomyelinating leukodystrophy 26 HGNC:16872 Homo sapiens (human) 347734 SLC35B2
  • RGD:7240710
DOID:0070403 hypomyelinating leukodystrophy 26 FB:FBgn0038524 Drosophila melanogaster (fruit fly) 42115 sll CG7623
  • MGI:6194238
DOID:0070399 hypomyelinating leukodystrophy 18 HGNC:13709 Homo sapiens (human) 8560 DEGS1
  • RGD:7240710
DOID:0070395 developmental and epileptic encephalopathy 110 HGNC:1399 Homo sapiens (human) 781 CACNA2D1
  • RGD:7240710

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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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Last updated: August 19, 2024