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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 **9201 - 9225** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:850	lung disease	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9563	bronchiectasis Aliases: Polynesian bronchiectasis	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:13258	typhoid fever Aliases: Typhoid	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:5733	salpingitis	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:693	dental enamel hypoplasia Aliases: enamel hypoplasia	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111862	congenital bilateral absence of vas deferens Aliases: CAVD CBAVD congenital bilateral agenesis of vas deferens congenital bilateral aplasia of vas deferens	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110861	autosomal recessive polycystic kidney disease Aliases: Arpkd Pkhd1 Polycystic Kidney Disease, Infantile, Type I Polycystic Kidney and Hepatic Disease 1	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:13316	exocrine pancreatic insufficiency Aliases: EPI	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:13166	allergic bronchopulmonary aspergillosis Aliases: pulmonary aspergillus disease	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111864	autosomal recessive congenital bilateral absence of vas deferens	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:10808	gastric ulcer Aliases: acute gastric ulcer with haemorrhage and perforation acute gastric ulcer with hemorrhage AND with perforation but without obstruction acute gastric ulcer with hemorrhage and obstruction acute gastric ulcer with hemorrhage and perforation acute gastric ulcer with hemorrhage and perforation, with obstruction acute gastric ulcer with hemorrhage and perforation, without mention of obstruction acute gastric ulcer with hemorrhage, with obstruction acute gastric ulcer with hemorrhage, with perforation AND with obstruction acute gastric ulcer with perforation acute gastric ulcer with perforation AND obstruction acute gastric ulcer with perforation, with obstruction acute gastric ulcer without hemorrhage and without perforation acute gastric ulcer without hemorrhage, without perforation AND without obstruction acute gastric ulcer without mention of hemorrhage or perforation, without mention of obstruction bleeding acute gastric ulcer chronic gastric ulcer without hemorrhage AND without perforation chronic gastric ulcer without hemorrhage AND without perforation but with obstruction chronic gastric ulcer without mention of hemorrhage or perforation, with obstruction	NFT1	853978	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080133	multiple mitochondrial dysfunctions syndrome 1 Aliases: NFU1 deficiency	NFU1	27247	Homo sapiens (human)	Alliance of Genome Resources
DOID:431	myofascial pain syndrome	NGF NTRK1	4803 4914	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070145	hereditary sensory and autonomic neuropathy type 5 Aliases: HSAN5 hereditary sensory and autonomic neuropathy type V	NGF	4803	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080809	chronic asthma	NGF	4803	Homo sapiens (human)	Alliance of Genome Resources
DOID:10685	separation anxiety disorder	NGF	4803	Homo sapiens (human)	Alliance of Genome Resources
DOID:12143	neurogenic bladder Aliases: Neuropathic bladder neurogenic dysfunction of the urinary bladder neurogenic urinary bladder disorder	NGF	4803	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060728	NGLY1-deficiency Aliases: NGLY1-CDDG congenital disorder of deglycosylation congenital disorder of glycosylation type Iv deficiency of N-glycanase 1	NGLY1	55768	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110272	cataract 40 Aliases: CTRCT40 cataract 40 X-linked cataract 40 with or without microcornea	NHS	4810	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060599	Nance-Horan syndrome	NHS	4810	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111844	X-linked intellectual developmental disorder 108 Aliases: MRX108	NHX1	852066	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060825	Christianson syndrome Aliases: MRXSCH X-linked Angelman-like syndrome X-linked intellectual disability, South African type X-linked intellectual disability-craniofacial dysmorphism-epilepsy-ophthalmoplegia-cerebellar atrophy syndrome mental retardation, X-linked syndromic, Christianson type mental retardation, microcephaly, epilepsy, and ataxia syndrome	NHX1	852066	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070011	Seckel syndrome 7 Aliases: SCKL7	NIN	51199	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060715	autosomal recessive congenital ichthyosis 6 Aliases: ARCI6	NIPAL4	348938	Homo sapiens (human)	Alliance of Genome Resources
DOID:11725	Cornelia de Lange syndrome Aliases: Brachmann de Lange syndrome De Lange syndrome	NIPBL PDS5A SMC1A SMC3	23244 25836 8243 9126	Homo sapiens (human)	Alliance of Genome Resources

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