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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 **12726 - 12750** of **15957** in total

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Disease ID ▼	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0080006	bone development disease	gcy-28	172051	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080005	bone remodeling disease	IDH2	3418	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080005	bone remodeling disease	Idh2	269951	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080005	bone remodeling disease	Idh2	361596	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080005	bone remodeling disease	IDP2 IDP3	850871 855723	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080001	bone disease	poml-1 poml-2	171999 187297	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080001	bone disease	fgfr1 pon2	448598 548648	Xenopus tropicalis (tropical clawed frog)	Alliance of Genome Resources
DOID:0080001	bone disease	PHO8	852092	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080001	bone disease	btl htl	39564 42160	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080001	bone disease	CCN2 FGFR1 FGFR2 FGFR3 FGFR4 NPR3 PON1	1490 2260 2261 2263 2264 4883 5444	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080001	bone disease	Fgfr1 Fgfr2 Fgfr4 Npr3 Pon1	25022 25114 25339 79114 84024	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080001	bone disease	Ephx1 Fgfr1 Fgfr2 Fgfr4 Npr3 Pon1	13849 14182 14183 14186 18162 18979	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080001	bone disease	fgfr1a fgfr2 fgfr4 pon1	100000160 30705 352940 447803	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0080000	muscular disease	ina-1	176296	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080000	muscular disease	hmgcr.L	397750	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0080000	muscular disease	Clu Cpt2 Fasn Hmgcr Itga7 Lpl Prkcd	170538 24539 24854 25413 25675 50671 81008	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080000	muscular disease	ACACA ACACB CLU CPT2 FASN HMGCR ITGA7 LPL	1191 1376 2194 31 3156 32 3679 4023	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080000	muscular disease	Acaca Acacb Clu Cpt2 Fasn Hmgcr Itga7 Lpl Nmt1	100705 107476 12759 12896 14104 15357 16404 16956 18107	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080000	muscular disease	CPT2 Hmgcr mew	32275 38355 42803	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080000	muscular disease	HFA1 HMG1 HMG2	851171 854900 855247	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070539	Halperin-Birk syndrome Aliases: HLBKS NEDSOSB NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA, OPTIC ATROPHY, SEIZURES, AND STRUCTURAL BRAIN ANOMALIES	SEC31	851332	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070539	Halperin-Birk syndrome Aliases: HLBKS NEDSOSB NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA, OPTIC ATROPHY, SEIZURES, AND STRUCTURAL BRAIN ANOMALIES	SEC31A	22872	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070539	Halperin-Birk syndrome Aliases: HLBKS NEDSOSB NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA, OPTIC ATROPHY, SEIZURES, AND STRUCTURAL BRAIN ANOMALIES	Sec31a Sec31b	240667 69162	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070538	syndromic X-linked intellectual developmental disorder bain type Aliases: HNRNPH2-RNDD HNRNPH2-related neurodevelopmental disorder MRXSB Mental Retardation, X-linked, Syndrome, Bain Type	Hnrnph2	56258	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070538	syndromic X-linked intellectual developmental disorder bain type Aliases: HNRNPH2-RNDD HNRNPH2-related neurodevelopmental disorder MRXSB Mental Retardation, X-linked, Syndrome, Bain Type	HNRNPH2	3188	Homo sapiens (human)	Alliance of Genome Resources

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