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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 **14551 - 14575** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲	Source
DOID:1024	leprosy	SMF3	850721	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060770	dextro-looped transposition of the great arteries Aliases: D-TGA DTGA1 congenitally uncorrected transposition of the great arteries congenitally uncorrected transposition of the great vessels isolated ventriculoarterial discordance ventriculoarterial discordance with atrioventricular concordance	SSN2	852053	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1749	squamous cell carcinoma Aliases: epidermoid carcinoma malignant squamous cell tumor squamous carcinoma squamous cell Epithelioma squamous cell cancer	ENV9	854420	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:2741	bilirubin metabolic disorder Aliases: hereditary hyperbilirubinemia hyperbilirubinemia	ATG26 BPT1	850645 850886	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:8398	osteoarthritis Aliases: Osteoarthrosis and allied disorder degenerative arthritis degenerative joint disease hypertrophic arthritis osteoarthrosis	NPP1 NPP2 SNT1	850391 850399 856699	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9282	ocular hypertension	TPI1	851620	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0050570	congenital disorder of glycosylation type I	ALG12 ALG1 ALG5 ALG6 ALG8 ALG9 DPM1 PMI40 RFT1 SEC53	850499 852261 852407 854163 854233 855502 855764 855874 856313 856720	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060475	myoclonic-atonic epilepsy Aliases: EEOC childhood onset epileptic encephalopathy	CHD1	856911	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:2349	arteriosclerosis Aliases: Arteriosclerotic vascular disease	CTS2 GCY1 KEX2 LRO1 PHO8 YOL075C YPR1	851974 851977 852092 854080 854287 855483 855742	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:3803	Crigler-Najjar syndrome Aliases: Bilirubin UDP glucuronyl transferase deficiency Crigler Najjar syndrome Crigler-Najjar syndrome, type I	ATG26	850886	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0002116	pterygium Aliases: surfer's eye	OGG1	854942	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060466	gingival fibromatosis Aliases: hereditary gingival fibromatosis hereditary gingival hyperplasia	CDC25	851019	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:5022	aflatoxins-related hepatocellular carcinoma	ECM38	851006	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:655	inherited metabolic disorder Aliases: Inborn Errors of Metabolism Metabolic hereditary disorder inborn metabolism disorder	GIT1	850462	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060326	myelomeningocele	VVS1	852543	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111743	cerebellar ataxia type 47 Aliases: SCA47	PUF3	850647	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1240	leukemia	GCY1 YPR1	851974 854287	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111446	progressive myoclonus epilepsy 3 Aliases: CLN14 disease EPM3 PME type 3 Progressive myoclonic epilepsy due to KCTD7 deficiency Progressive myoclonus epilepsy type 3 neuronal ceroid lipofuscinosis 14	WHI2	854208	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:4362	cervical cancer Aliases: cervical neoplasm cervix cancer cervix uteri cancer neoplasm of uterine cervix tumor of the Cervix Uteri uterine cervical neoplasm	CDC25 PBS2 PCM1	851019 853313 856652	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9255	frontotemporal dementia Aliases: Wilhemsen-Lynch disease frontotemporal lobar degeneration multiple system tauopathy with presenile dementia pallidopontonigral degeneration	YPS3 YPS7	850812 851950	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:83	cataract	FAB1 GCY1 GLR1 HSF1 OGG1 SOR1 SOR2 VVS1 XYL2 YPR1 ZWF1	850574 850759 851351 851974 852543 852806 853624 854287 854942 855480 856014	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:10595	Charcot-Marie-Tooth disease Aliases: CMT - Charcot-Marie-Tooth disease	CSG2 DPL1 FIG4	851888 852324 855392	Saccharomyces cerevisiae S288C	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:0070214	familial hyperinsulinemic hypoglycemia 7 Aliases: EIHI HHF7 exercise-induced hyperinsulinemic hypoglycemia exercise-induced hyperinsulinism hyperinsulinism due to SLC16A1 deficiency hyperinsulinism due to monocarboxylate transporter 1 deficiency	ERS1 ESBP6	850438 855598	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:14250	Down syndrome Aliases: Complete trisomy 21 syndrome Down's syndrome Down's syndrome - trisomy 21 Downs syndrome G Trisomy trisomy 21 syndrome	INP53	854276	Saccharomyces cerevisiae S288C	Alliance of Genome Resources

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