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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 **12701 - 12725** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:8283	peritonitis Aliases: Retractile mesenteritis acute generalized peritonitis primary bacterial peritonitis sclerosing mesenteritis	Y105E8B.9 aldo-1	173326 176788	Caenorhabditis elegans	Alliance of Genome Resources
DOID:12803	Sly syndrome Aliases: MPS VII - Sly syndrome beta-glucuronidase deficiency deficiency of beta-glucuronidase mucopolysaccharidosis VII	Y105E8B.9	173326	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0112300	spondylometaphyseal dysplasia with cone-rod dystrophy Aliases: SMD-CRD SMDCRD spondylometaphyseal dysplasia-cone-rod dystrophy syndrome	Y18H1A.11	353380	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050585	congenital generalized lipodystrophy	Y18H1A.11	353380	Caenorhabditis elegans	Alliance of Genome Resources
DOID:10286	prostate carcinoma Aliases: cancer of prostate carcinoma of prostate	Y43C5A.2 cht-1 daf-2 dbl-1 pkc-2	175410 177911 179068 180628 181166	Caenorhabditis elegans	Alliance of Genome Resources
DOID:14735	hereditary angioedema Aliases: HANE Hereditary angioneurotic edema	Y43C5A.2 hst-3.2	177911 3564879	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2236	congenital afibrinogenemia Aliases: Factor I deficiency Fibrinogen deficiency	Y43C5A.2	177911	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110337	osteogenesis imperfecta type 7 Aliases: OI7 osteogenesis imperfecta type VII	Y73F8A.26	178435	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110336	osteogenesis imperfecta type 8 Aliases: OI8 osteogenesis imperfecta type VIII	Y73F8A.26	178435	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111249	uveal coloboma-cleft lip and palate-intellectual disability Aliases: COB1 Uveal coloboma-cleft lip/palate-mental retardation syndrome coloboma-microphthalmos syndrome coloboma-microphthalmos syndrome associated with sensorineural hearing loss, hematuria, and cleft lip/palate ocular coloboma with or without hearing impairment, cleft lip/palate, and/or mental retardation	YAP1	10413	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050795	cone dystrophy Aliases: retinal cone dystrophy	YAP1	10413	Homo sapiens (human)	Alliance of Genome Resources
DOID:070355	multisystem proteinopathy	YARS1	8565	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110199	Charcot-Marie-Tooth disease dominant intermediate C Aliases: CMTDIC Charcot-Marie-Tooth neuropathy dominant intermediate C DI-CMTC autosomal dominant intermediate Charcot-Marie-Tooth disease type C	YARS1	8565	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111186	myopathy, lactic acidosis, and sideroblastic anemia 2 Aliases: MLASA2	YARS2	51067	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type Aliases: Cantu syndrome	YBT1	850678	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0112262	leucine-sensitive hypoglycemia of infancy Aliases: LIH leucine-induced hypoglycemia	YBT1	850678	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0050650	familial atrial fibrillation Aliases: ATFB	YBT1	850678	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110451	dilated cardiomyopathy 1O Aliases: CMD1O dilated cardiomyopathy with ventricular tachycardia	YBT1	850678	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070219	familial hyperinsulinemic hypoglycemia 1 Aliases: HHF1	YBT1	850678	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:3805	porokeratosis Aliases: disseminated superficial actinic porokeratosis	YCT1	850671	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9784	trichinosis Aliases: Trichinella spiralis infection	YCT1	850671	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:3659	sialuria	YCT1	850671	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110555	autosomal dominant nonsyndromic deafness 25 Aliases: DFNA25 autosomal dominant deafness 25	YCT1	850671	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:5463	cochlear disease	YCT1	850671	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:10579	leukodystrophy	YDC1 YPC1	852481 856018	Saccharomyces cerevisiae S288C	Alliance of Genome Resources

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