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GlyCosmos Diseases

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

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **3601 - 3625** of **7942** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism
DOID:5419	schizophrenia Aliases: schizophrenia-1	CG31637 CG9550 GlcAT-I Idgf1 Idgf2 Idgf3 Idgf4 Idgf5 Idgf6 alpha-Man-IIa fw sgg	251900 31248 31926 32162 33913 33914 34978 34979 34981 36868 37104 41126	Drosophila melanogaster (fruit fly)
DOID:2565	macular corneal dystrophy Aliases: Fehr corneal dystrophy MACULAR DYSTROPHY, CORNEAL, 1	CG31637 CG9550	33913 33914	Drosophila melanogaster (fruit fly)
DOID:0112315	brain small vessel disease 3 Aliases: BSVD3	CG31915	319025	Drosophila melanogaster (fruit fly)
DOID:0111238	congenital muscular dystrophy-dystroglycanopathy type A13 Aliases: MDDGA13 Walker-Warburg syndrome or muscle-eye-brain disease, B3GNT1-related Walker-Warburg syndrome or muscle-eye-brain disease, B4GNT1-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A13	CG3253	37861	Drosophila melanogaster (fruit fly)
DOID:0110798	hereditary spastic paraplegia 46 Aliases: SPG46 autosomal recessive spastic paraplegia 46 autosomal recessive spastic paraplegia type 46	CG33090	34835	Drosophila melanogaster (fruit fly)
DOID:0080520	Tn polyagglutination syndrome Aliases: galactosyltransferase deficiency	CG34057	3885645	Drosophila melanogaster (fruit fly)
DOID:12554	hemolytic-uremic syndrome Aliases: haemolytic-uraemic syndrome hemolytic uremic syndrome	CG34057	3885645	Drosophila melanogaster (fruit fly)
DOID:0080558	congenital disorder of glycosylation If Aliases: congenital disorder of glycosylation 1f	CG3792	33717	Drosophila melanogaster (fruit fly)
DOID:0111156	spermatogenic failure 9 Aliases: globozoospermia male infertility due to round-headed spermatozoa	CG6659	32854	Drosophila melanogaster (fruit fly)
DOID:2747	glycogen storage disease Aliases: glycogenosis	CG7766 Glyp Glys Gyg Pfk	31839 33386 36060 37419 41823	Drosophila melanogaster (fruit fly)
DOID:1459	hypothyroidism Aliases: Thyroid deficiency Thyroid insufficiency	CG7766 Plod kdn	31579 31839 39265	Drosophila melanogaster (fruit fly)
DOID:0111040	glycogen storage disease IXd Aliases: GSD IXd GSD due to muscle phosphorylase kinase deficiency GSD type 9D GSD type 9E GSD type IXd GSD type IXe GSD9D X-linked muscke glycogenosis glycogen storage disease due to muscle phosphorylase kinase deficiency glycogen storage disease type 9D glycogen storage disease type 9E glycogen storage disease type IXd glycogen storage disease type IXe glycogenosis due to muscle phosphorylase kinase deficiency glycogenosis type 9D glycogenosis type 9E glycogenosis type IXd glycogenosis type IXe muscle phosphorylase kinase deficiency	CG7766	31839	Drosophila melanogaster (fruit fly)
DOID:0050545	visceral heterotaxy Aliases: heterotaxia situs ambiguus	CG7766	31839	Drosophila melanogaster (fruit fly)
DOID:0111042	glycogen storage disease IXa Aliases: GSD type 9A GSD type IXa GSD9A glycogen storage disease type 9A glycogen storage disease type IXa glycogenosis type 9A glycogenosis type IXa	CG7766	31839	Drosophila melanogaster (fruit fly)
DOID:0080201	Peters plus syndrome Aliases: Krause-Kivlin syndrome Peters anomaly-short limb dwarfism syndrome Peters-plus syndrome	CG9109	33844	Drosophila melanogaster (fruit fly)
DOID:2256	osteochondrodysplasia Aliases: Cartilage Development disorder Congenital anomaly of cartilage Osteochondrodysplasia syndrome chondrodystrophy skeletal dysplasia	CG9550 Tsp trol	33913 33941 45320	Drosophila melanogaster (fruit fly)
DOID:0050813	spondyloepiphyseal dysplasia with congenital joint dislocations Aliases: CHONDRODYSPLASIA WITH MULTIPLE DISLOCATIONS CHST3-Related Skeletal Dysplasia Humero-spinal dysostosis with congenital heart disease Kozlowski Celermajer Tink syndrome Omani Type Spondyloepiphyseal Dysplasia humero-spinal dysostosis humerospinal dysostosis	CG9550	33913	Drosophila melanogaster (fruit fly)
DOID:11260	rabies Aliases: Lyssa	CH25H CYP1A2 CYP2C9 CYP3A4 ENOSF1 FUT2 GAS1 HPSE MTM1 PIK3CA PIK3CB PIK3CD PIK3CG PIP5K1C SOAT1	10855 1544 1559 1576 23396 2524 2619 4534 5290 5291 5293 5294 55556 6646 9023	Homo sapiens (human)
DOID:9786	bulbar polio Aliases: bulbar poliomyelitis	CHAT ICAM1 MMUT MRC1 PIK3CA	1103 3383 4360 4594 5290	Homo sapiens (human)
DOID:4953	poliomyelitis	CHAT ICAM1 MMUT MRC1 PIK3CA	1103 3383 4360 4594 5290	Homo sapiens (human)
DOID:14784	olivopontocerebellar atrophy Aliases: Dejerine-Thomas syndrome Thomas' syndrome WADIA-SWAMI SYNDROME	CHAT PMM2	1103 5373	Homo sapiens (human)
DOID:0070318	dry beriberi	CHAT SLC35F3 TKT	1103 148641 7086	Homo sapiens (human)
DOID:8457	pellagra Aliases: Niacin deficiency Niacin-tryptophan deficiency	CHAT SLC35F3 TKT	1103 148641 7086	Homo sapiens (human)
DOID:0110671	congenital myasthenic syndrome 6 Aliases: CMS Ia2 CMS1A2 CMS6 CMSEA FIM FIMG2 congenital myasthenic syndrome 6, presynaptic congenital myasthenic syndrome type Ia2 congenital presynaptic myasthenic syndrome associated with episodic apnea familial infantile myasthenia familial infantile myasthenia gravis 2	CHAT	1103	Homo sapiens (human)
DOID:4160	differentiating neuroblastoma	CHAT	1103	Homo sapiens (human)

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