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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 12301 - 12325 of 71927 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0081354 congenital myopathy 22A MGI:98250 Mus musculus (house mouse) 110880 Scn4a
  • MGI:6194238
DOID:0081354 congenital myopathy 22A ZFIN:ZDB-GENE-051201-2 Danio rerio (zebrafish) 572442 scn4aa
  • MGI:6194238
DOID:0081354 congenital myopathy 22A FB:FBgn0285944 Drosophila melanogaster (fruit fly) 32619 para
  • MGI:6194238
DOID:0081354 congenital myopathy 22A ZFIN:ZDB-GENE-051201-1 Danio rerio (zebrafish) 564977 scn4ab
  • MGI:6194238
DOID:0081355 congenital myopathy 22B ZFIN:ZDB-GENE-051201-1 Danio rerio (zebrafish) 564977 scn4ab
  • MGI:6194238
DOID:0081355 congenital myopathy 22B ZFIN:ZDB-GENE-051201-2 Danio rerio (zebrafish) 572442 scn4aa
  • MGI:6194238
DOID:0081355 congenital myopathy 22B MGI:98250 Mus musculus (house mouse) 110880 Scn4a
  • MGI:6194238
DOID:0081355 congenital myopathy 22B HGNC:10591 Homo sapiens (human) 6329 SCN4A
  • RGD:7240710
DOID:0081355 congenital myopathy 22B FB:FBgn0285944 Drosophila melanogaster (fruit fly) 32619 para
  • MGI:6194238
DOID:0081355 congenital myopathy 22B RGD:3636 Rattus norvegicus (Norway rat) 25722 Scn4a
  • MGI:6194238
DOID:0081356 spinal muscular atrophy, Jokela type MGI:1261428 Mus musculus (house mouse) 14004 Chchd2
  • MGI:6194238
DOID:0081358 epidermolytic hyperkeratosis 1 HGNC:6412 Homo sapiens (human) 3848 KRT1
  • RGD:7240710
DOID:0081358 epidermolytic hyperkeratosis 1 MGI:96698 Mus musculus (house mouse) 16678 Krt1
  • MGI:6194238
DOID:0081359 epidermolytic hyperkeratosis 2 HGNC:6413 Homo sapiens (human) 3858 KRT10
  • RGD:7240710
DOID:0081360 spastic quadriplegic cerebral palsy 2 HGNC:19309 Homo sapiens (human) 23189 KANK1
  • RGD:7240710
DOID:0081361 spastic quadriplegic cerebral palsy 3 RGD:2041 Rattus norvegicus (Norway rat) 24170 Add1
  • MGI:6194238
DOID:0081361 spastic quadriplegic cerebral palsy 3 HGNC:245 Homo sapiens (human) 120 ADD3
  • MGI:6194238
  • RGD:7240710
DOID:0081361 spastic quadriplegic cerebral palsy 3 MGI:87918 Mus musculus (house mouse) 11518 Add1
  • MGI:6194238
DOID:0081361 spastic quadriplegic cerebral palsy 3 HGNC:243 Homo sapiens (human) 118 ADD1
  • MGI:6194238
DOID:0081361 spastic quadriplegic cerebral palsy 3 HGNC:244 Homo sapiens (human) 119 ADD2
  • MGI:6194238
DOID:0081363 distal myopathy with rimmed vacuoles HGNC:11280 Homo sapiens (human) 8878 SQSTM1
  • RGD:7240710
DOID:0081363 distal myopathy with rimmed vacuoles MGI:107931 Mus musculus (house mouse) 18412 Sqstm1
  • MGI:6194238
DOID:0081364 neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset HGNC:11280 Homo sapiens (human) 8878 SQSTM1
  • MGI:6194238
  • RGD:7240710
DOID:0081364 neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset MGI:107931 Mus musculus (house mouse) 18412 Sqstm1
  • MGI:6194238
DOID:0081365 Paget's disease of bone 2 HGNC:11908 Homo sapiens (human) 8792 TNFRSF11A
  • 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: August 19, 2024