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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 8101 - 8125 of 12216 in total
Disease ID Disease Name ▲ Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0070329 mitochondrial DNA depletion syndrome HGNC:10980 Homo sapiens (human) 1468 SLC25A10
  • MGI:6194238
DOID:0070329 mitochondrial DNA depletion syndrome MGI:1353497 Mus musculus (house mouse) 27376 Slc25a10
  • MGI:6194238
DOID:0080119 mitochondrial DNA depletion syndrome 1 HGNC:3148 Homo sapiens (human) 1890 TYMP
  • RGD:7240710
DOID:0080119 mitochondrial DNA depletion syndrome 1 MGI:1920212 Mus musculus (house mouse) 72962 Tymp
  • MGI:6194238
  • PMID:12077348
DOID:0080119 mitochondrial DNA depletion syndrome 1 RGD:1305756 Rattus norvegicus (Norway rat) 315219 Tymp
  • MGI:6194238
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:0080124 mitochondrial DNA depletion syndrome 5 HGNC:11448 Homo sapiens (human) 8803 SUCLA2
  • MGI:6194238
  • RGD:7240710
DOID:0080128 mitochondrial DNA depletion syndrome 9 HGNC:11449 Homo sapiens (human) 8802 SUCLG1
  • RGD:7240710
DOID:0060536 mitochondrial complex I deficiency HGNC:10980 Homo sapiens (human) 1468 SLC25A10
  • MGI:6194238
DOID:0060536 mitochondrial complex I deficiency MGI:1353497 Mus musculus (house mouse) 27376 Slc25a10
  • MGI:6194238
DOID:0060537 mitochondrial complex II deficiency HGNC:10680 Homo sapiens (human) 6389 SDHA
  • MGI:6194238
  • RGD:7240710
DOID:0060537 mitochondrial complex II deficiency HGNC:10681 Homo sapiens (human) 6390 SDHB
  • MGI:6194238
  • RGD:7240710
DOID:0060537 mitochondrial complex II deficiency HGNC:10683 Homo sapiens (human) 6392 SDHD
  • MGI:6194238
  • RGD:7240710
DOID:890 mitochondrial encephalomyopathy HGNC:10681 Homo sapiens (human) 6390 SDHB
  • MGI:6194238
DOID:890 mitochondrial encephalomyopathy RGD:1305756 Rattus norvegicus (Norway rat) 315219 Tymp
  • MGI:6194238
DOID:890 mitochondrial encephalomyopathy MGI:1920212 Mus musculus (house mouse) 72962 Tymp
  • MGI:6194238
DOID:890 mitochondrial encephalomyopathy HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:9924029
DOID:700 mitochondrial metabolism disease HGNC:4803 Homo sapiens (human) 3032 HADHB
  • PMID:8651282
DOID:700 mitochondrial metabolism disease HGNC:10979 Homo sapiens (human) 6576 SLC25A1
  • MGI:6194238
DOID:0111277 mitochondrial trifunctional protein deficiency HGNC:4801 Homo sapiens (human) 3030 HADHA
  • RGD:7240710
DOID:0111277 mitochondrial trifunctional protein deficiency HGNC:4803 Homo sapiens (human) 3032 HADHB
  • MGI:6194238
  • RGD:7240710
DOID:61 mitral valve disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:14765837
DOID:988 mitral valve prolapse HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:17379330
DOID:3492 mixed connective tissue disease MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238

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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: August 19, 2024