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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **10301 - 10325** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:0090101	lethal congenital glycogen storage disease of heart Aliases: fatal congenital hypertrophic cardiomyopathy due to GSD fatal congenital hypertrophic cardiomyopathy due to glycogenosis fatal congenital nonlysosomal cardiac glycogenosis phosphorylase kinase deficiency of heart	Prkag2 Prkag3	108099 241113	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110312	hypertrophic cardiomyopathy 6 Aliases: CMH6 cardiomyopathy, familial hypertrophic 6	Prkag2	108099	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:397	restrictive cardiomyopathy Aliases: Cardiomyopathy, constrictive primary restrictive cardiomyopathy	Prkcd Tnni3 Tnnt2	170538 24837 29248	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110119	autoimmune lymphoproliferative syndrome type 3 Aliases: ALPS3 autoimmune lymphoproliferative syndrome type III	Prkcd	170538	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050964	spinocerebellar ataxia type 14	Prkcg	18752	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050964	spinocerebellar ataxia type 14	Prkcg	24681	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0090048	dystonia 16	Prkra	23992	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050547	familial medullary thyroid carcinoma Aliases: THYROID CARCINOMA, FAMILIAL MEDULLARY	Prlr Ret	19116 19713	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050547	familial medullary thyroid carcinoma Aliases: THYROID CARCINOMA, FAMILIAL MEDULLARY	Prlr Ret	24684 24716	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:648	kuru Aliases: kuru encephalopathy	Prnp	19122	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5434	scrapie	Prnp	19122	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4249	Gerstmann-Straussler-Scheinker syndrome Aliases: Gerstmann-Straussler-Scheinker disease PRION DEMENTIA	Prnp	19122	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090103	Huntington's disease-like 1 Aliases: HDL1 HLN1 Huntington disease-like 1 Huntington-like neurodegenerative disorder 1 autosomal dominant Huntington-like neurodegenerative disorder early-onset prion disease with prominent psychiatric features	Prnp	19122	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:648	kuru Aliases: kuru encephalopathy	Prnp	24686	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0090103	Huntington's disease-like 1 Aliases: HDL1 HLN1 Huntington disease-like 1 Huntington-like neurodegenerative disorder 1 autosomal dominant Huntington-like neurodegenerative disorder early-onset prion disease with prominent psychiatric features	Prnp	24686	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:4249	Gerstmann-Straussler-Scheinker syndrome Aliases: Gerstmann-Straussler-Scheinker disease PRION DEMENTIA	Prnp	24686	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:5434	scrapie	Prnp	24686	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2450	central retinal vein occlusion	Proc Serpinf1	19123 20317	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9667	placental abruption Aliases: abruptio placenta abruptio placentae	Proc	19123	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111904	autosomal recessive thrombophilia due to protein C deficiency Aliases: THPH4 autosomal recessive PROC deficiency autosomal recessive protein C deficiency	Proc	19123	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111909	autosomal dominant thrombophilia due to protein C deficiency Aliases: THPH3 autosomal dominant PROC deficiency autosomal dominant protein C deficiency	Proc	19123	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3756	protein C deficiency	Proc	19123	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:10772	thrombotic thrombocytopenic purpura Aliases: Moschcowitz's syndrome	Proc Tfpi	25268 29436	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9667	placental abruption Aliases: abruptio placenta abruptio placentae	Proc	25268	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2450	central retinal vein occlusion	Proc	25268	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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