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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 **5626 - 5650** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:305	carcinoma Aliases: epithelial cancer epithelioma malignant Epithelioma	ERS1 PHO8	850438 852092	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110934	nemaline myopathy 7 Aliases: NEM7 nemaline myopathy 7, autosomal recessive	ERS1	850438	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:299	adenocarcinoma	ERS1	850438	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1062	Fanconi syndrome Aliases: Congenital Fanconi syndrome De Toni-Fanconi syndrome Fanconi-de Toni syndrome Fanconi-de-Toni syndrome Infantile nephropathic cystinosis Lignac-Fanconi syndrome adult Fanconi Anemia adult Fanconi syndrome deToni Fanconi syndrome	ERS1	850438	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1064	cystinosis Aliases: cystine storage disease	ERS1	850438	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070353	cataract 47 Aliases: CTRCT47	ESBP6 MCH4 MCH5	854030 854483 855598	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:3319	lymphangioleiomyomatosis Aliases: lung lymphangioleiomyomatosis lymphangiomyomatosis pulmonary lymphangioleiomyomatosis	ESBP6 TDH1 TDH2 TDH3	853106 853395 853465 855598	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:5325	Roberts syndrome Aliases: LONG BONE DEFICIENCIES ASSOCIATED WITH CLEFT LIP-PALATE RBS Roberts-Sc Phocomelia Syndrome SC phocomelia syndrome	ESCO1 ESCO2 SEC23A SEC23B	10483 10484 114799 157570	Homo sapiens (human)	Alliance of Genome Resources
DOID:8029	sporadic breast cancer	ESR1 MLH1 PHB1 PTEN	2099 4292 5245 5728	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060358	multiple acyl-CoA dehydrogenase deficiency Aliases: MAD deficiency MADD electron transfer flavoprotein deficiency electron transfer flavoprotein ubiquinone oxidoreductase deficiency glutaric acidemia type 2 glutaric aciduria type 2	ETFB	2109	Homo sapiens (human)	Alliance of Genome Resources
DOID:6432	pulmonary hypertension	EUG1 HMG1 HMG2 HXK1 PDI1 RHO1 VVS1	850314 850614 851171 852130 852543 854900 856294	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:2055	post-traumatic stress disorder Aliases: PTSD traumatic neurosis	EUG1 KAR2 PDI1	850314 852130 853418	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060438	Cole-Carpenter syndrome	EUG1 PDI1	850314 852130	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:2048	autoimmune hepatitis Aliases: Autoimmune chronic active hepatitis autoimmune hepatitis with centrilobular necrosis	EUG1 PDI1	850314 852130	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9778	irritable bowel syndrome Aliases: IBD Irritable colon	EUG1 PDI1	850314 852130	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:11088	asphyxia neonatorum Aliases: Asphyxia - birth Asphyxia, in liveborn infant Birth asphyxia postnatal asphyxia	EUG1 PDI1	850314 852130	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:12714	Ellis-Van Creveld syndrome Aliases: Chondroectodermal dysplasia mesoectodermal dysplasia	EVC2 WDR35	132884 57539	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	132884	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060198	amyotrophic lateral sclerosis type 6 Aliases: ALS6 amyotrophic lateral sclerosis 6, with or without frontotemporal dementia autosomal recessive amyotrophic lateral sclerosis 6	EWSR1 FUS	2130 2521	Homo sapiens (human)	Alliance of Genome Resources
DOID:3369	Ewing sarcoma Aliases: Ewing's family localized tumor Ewing's sarcoma/peripheral primitive neuroectodermal tumor Ewing's tumor Ewings sarcoma Ewings sarcoma-primitive neuroectodermal tumor PNET of Thoracopulmonary Region localized Ewing sarcoma localized Ewing's sarcoma localized Ewing's sarcoma/peripheral primitive neuroectodermal tumor localized Ewing's tumor localized peripheral primitive neuroectodermal tumor peripheral primitive neuroectodermal tumor	EWSR1 KDM3A	2130 55818	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081175	short stature, hearing loss, retinitis pigmentosa, and distinctive facies	EXOSC2	23404	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112334	pontocerebellar hypoplasia type 1C Aliases: PCH1C	EXOSC8	11340	Homo sapiens (human)	Alliance of Genome Resources
DOID:206	hereditary multiple exostoses Aliases: Multiple congenital exostosis Multiple exostosis syndromes Osteochondromatosis syndrome hereditary multiple exostoses 1 hereditary multiple exostoses 2 hereditary multiple exostoses 3 multiple ostechondromas	EXT1 EXT2 EXTL1 EXTL3	2131 2132 2134 2137	Homo sapiens (human)	Alliance of Genome Resources
DOID:14702	branchiootorenal syndrome Aliases: Branchio-Oto-renal syndrome Branchio-otorenal dysplasia Melnick-Fraser syndrome branchiootorenal dysplasia	EYA3 EYA4 SIX1 SIX4 SIX5	147912 2070 2140 51804 6495	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110542	autosomal dominant nonsyndromic deafness 10 Aliases: DFNA10 autosomal dominant deafness 10	EYA4	2070	Homo sapiens (human)	Alliance of Genome Resources

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