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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 **13676 - 13700** of **15957** in total

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Disease ID	Disease Name ▼	Gene Symbol	Gene ID	Organism	Source
DOID:0070067	White-Sutton syndrome Aliases: MRD37 WHSUS autosomal dominant mental retardation 37	Pogz	310658	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070067	White-Sutton syndrome Aliases: MRD37 WHSUS autosomal dominant mental retardation 37	POGZ	23126	Homo sapiens (human)	Alliance of Genome Resources
DOID:8476	Whipple disease Aliases: Whipple's disease intestinal lipodystrophy	CD163	9332	Homo sapiens (human)	Alliance of Genome Resources
DOID:8476	Whipple disease Aliases: Whipple's disease intestinal lipodystrophy	Cd163	93671	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111571	Weyers acrofacial dysostosis Aliases: Curry-Hall syndrome WAD Weyers acrodental dysostosis acrofacial dysostosis, Weyers type	EVC2	132884	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111571	Weyers acrofacial dysostosis Aliases: Curry-Hall syndrome WAD Weyers acrodental dysostosis acrofacial dysostosis, Weyers type	Evc2 Evc	59056 68525	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050562	West syndrome	Cfl1 Mc2r Stxbp1	12631 17200 20910	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050562	West syndrome	ABAT CFL1 MC2R STXBP1	1072 18 4158 6812	Homo sapiens (human)	Alliance of Genome Resources
DOID:2366	West Nile fever	CCR5 KIR3DS1 RFC1	1234 3813 5981	Homo sapiens (human)	Alliance of Genome Resources
DOID:2366	West Nile fever	Ccr5	12774	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2366	West Nile fever	Ccr5 Kir3dl1	117029 353253	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2384	Wernicke encephalopathy Aliases: Wernicke's disease Wernicke's encephalopathy	FOS PTGS2	2353 5743	Homo sapiens (human)	Alliance of Genome Resources
DOID:2384	Wernicke encephalopathy Aliases: Wernicke's disease Wernicke's encephalopathy	Fos Ptgs2	14281 19225	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2384	Wernicke encephalopathy Aliases: Wernicke's disease Wernicke's encephalopathy	Ptgs2	29527	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:5688	Werner syndrome Aliases: WS Werner's syndrome adult premature ageing syndrome adult progeria	BLM LMNA	4000 641	Homo sapiens (human)	Alliance of Genome Resources
DOID:5688	Werner syndrome Aliases: WS Werner's syndrome adult premature ageing syndrome adult progeria	Lmna Wrn	16905 22427	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4258	Weissenbacher-Zweymuller syndrome Aliases: Piere-Robin syndrome Pierre Robin Malformation	TRE1 TRE2	854430 855927	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:4258	Weissenbacher-Zweymuller syndrome Aliases: Piere-Robin syndrome Pierre Robin Malformation	ACVR2A TFRC	7037 92	Homo sapiens (human)	Alliance of Genome Resources
DOID:4258	Weissenbacher-Zweymuller syndrome Aliases: Piere-Robin syndrome Pierre Robin Malformation	Acvr2a Tfrc	11480 22042	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4258	Weissenbacher-Zweymuller syndrome Aliases: Piere-Robin syndrome Pierre Robin Malformation	daf-4	175781	Caenorhabditis elegans	Alliance of Genome Resources
DOID:4258	Weissenbacher-Zweymuller syndrome Aliases: Piere-Robin syndrome Pierre Robin Malformation	Acvr2a Tfrc	29263 64678	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050475	Weill-Marchesani syndrome Aliases: GEMSS syndrome Marchesani-Weill Syndrome Mesodermal Dysmorphodystrophy, Congenital Spherophakia Brachymorphia Syndrome congenital mesodermal dystrophy	ADAMTS10 ADAMTS17 FBN1 LTBP2 TNF	170691 2200 4053 7124 81794	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050475	Weill-Marchesani syndrome Aliases: GEMSS syndrome Marchesani-Weill Syndrome Mesodermal Dysmorphodystrophy, Congenital Spherophakia Brachymorphia Syndrome congenital mesodermal dystrophy	Adamts10 Fbn1 Ltbp2 Tnf	14118 16997 21926 224697	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050475	Weill-Marchesani syndrome Aliases: GEMSS syndrome Marchesani-Weill Syndrome Mesodermal Dysmorphodystrophy, Congenital Spherophakia Brachymorphia Syndrome congenital mesodermal dystrophy	fbn-1	176076	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050475	Weill-Marchesani syndrome Aliases: GEMSS syndrome Marchesani-Weill Syndrome Mesodermal Dysmorphodystrophy, Congenital Spherophakia Brachymorphia Syndrome congenital mesodermal dystrophy	Ltbp2 Tnf	24835 59106	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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