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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 65251 - 65275 of 71927 in total
Disease ID ▼ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0060668 anencephaly HGNC:29558 Homo sapiens (human) 81788 NUAK2
  • RGD:7240710
DOID:0060668 anencephaly SGD:S000002529 Saccharomyces cerevisiae S288C 851700 KIN1
  • MGI:6194238
DOID:0060668 anencephaly WB:WBGene00001165 Caenorhabditis elegans 176882 efn-4
  • MGI:6194238
DOID:0060668 anencephaly HGNC:3225 Homo sapiens (human) 1946 EFNA5
  • MGI:6194238
DOID:0060668 anencephaly SGD:S000004086 Saccharomyces cerevisiae S288C 850785 KIN2
  • MGI:6194238
DOID:0060668 anencephaly RGD:620391 Rattus norvegicus (Norway rat) 116683 Efna5
  • MGI:6194238
DOID:0060668 anencephaly ZFIN:ZDB-GENE-980526-186 Danio rerio (zebrafish) 30223 efna5b
  • MGI:6194238
DOID:0060656 autosomal recessive congenital ichthyosis 1 HGNC:14637 Homo sapiens (human) 26154 ABCA12
  • PMID:12915478
DOID:0060656 autosomal recessive congenital ichthyosis 1 WB:WBGene00000020 Caenorhabditis elegans 171782 abt-2
  • MGI:6194238
DOID:0060656 autosomal recessive congenital ichthyosis 1 MGI:2676312 Mus musculus (house mouse) 74591 Abca12
  • MGI:6194238
DOID:0060654 lethal congenital contracture syndrome 4 HGNC:7549 Homo sapiens (human) 4604 MYBPC1
  • RGD:7240710
DOID:0060653 lethal congenital contracture syndrome 3 HGNC:8996 Homo sapiens (human) 23396 PIP5K1C
  • RGD:7240710
DOID:0060653 lethal congenital contracture syndrome 3 MGI:1298224 Mus musculus (house mouse) 18717 Pip5k1c
  • MGI:6194238
DOID:0060652 familial erythrocytosis 1 HGNC:3416 Homo sapiens (human) 2057 EPOR
  • PMID:11929803
  • PMID:20700488
  • PMID:8506290
  • PMID:9192789
  • PMID:9394420
  • RGD:7240710
DOID:0060652 familial erythrocytosis 1 MGI:95408 Mus musculus (house mouse) 13857 Epor
  • MGI:6194238
DOID:0060652 familial erythrocytosis 1 Xenbase:XB-GENE-6251686 Xenopus laevis (African clawed frog) 734211 epor.L
  • MGI:6194238
DOID:0060651 MYH-9 related disease MGI:107717 Mus musculus (house mouse) 17886 Myh9
  • MGI:6194238
  • PMID:21908426
DOID:0060651 MYH-9 related disease HGNC:7579 Homo sapiens (human) 4627 MYH9
  • MGI:6194238
  • PMID:11752022
  • PMID:11935325
  • PMID:16806139
  • RGD:7240710
DOID:0060650 dicarboxylic aminoaciduria RGD:3696 Rattus norvegicus (Norway rat) 25550 Slc1a1
  • MGI:6194238
DOID:0060650 dicarboxylic aminoaciduria MGI:105083 Mus musculus (house mouse) 20510 Slc1a1
  • MGI:6194238
  • PMID:9233792
DOID:0060650 dicarboxylic aminoaciduria WB:WBGene00001622 Caenorhabditis elegans 188744 glt-4
  • MGI:6194238
DOID:0060650 dicarboxylic aminoaciduria HGNC:10939 Homo sapiens (human) 6505 SLC1A1
  • MGI:6194238
  • RGD:7240710
DOID:0060649 congenital hereditary endothelial dystrophy of cornea MGI:2138987 Mus musculus (house mouse) 269356 Slc4a11
  • MGI:6194238
  • PMID:23942972
DOID:0060649 congenital hereditary endothelial dystrophy of cornea HGNC:16438 Homo sapiens (human) 83959 SLC4A11
  • MGI:6194238
  • RGD:7240710
DOID:0060648 anterior segment dysgenesis MGI:1929183 Mus musculus (house mouse) 64930 Tsc1
  • PMID:28250050

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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