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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 **10851 - 10875** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:2957	pulmonary tuberculosis	Egfr Jra Mdr49 Mdr65 Mvl Snmp2 Tl	36057 36428 37455 38726 38868 42490 43222	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:8567	Hodgkin's lymphoma Aliases: HL Hodgkin disease Hodgkin lymphoma Hodgkin's sarcoma Hodgkins lymphoma stage I Subdiaphragmatic Hodgkin Lymphoma stage II Subdiaphragmatic Hodgkin Lymphoma	Jra Sdc	36057 37447	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0050865	tongue squamous cell carcinoma	Egfr Jra	36057 37455	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:3121	gallbladder cancer Aliases: gallbladder Ca gallbladder neoplasm localized malignant gallbladder neoplasm malignant neoplasm of gallbladder malignant tumor of the gallbladder malignant tumour of gallbladder tumor of the gallbladder	Axn Calr Jra	36057 41166 43565	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0050744	anaplastic large cell lymphoma	Jra	36057	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:13139	crescentic glomerulonephritis	Jra	36057	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:4451	renal carcinoma Aliases: carcinoma of kidney kidney carcinoma	Jra	36057	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0014667	disease of metabolism Aliases: metabolic disease	Hsc70-4 Ldh Octbeta2R Pfk PyK	36060 41549 41840 42620 45880	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:11721	glycogen storage disease VII Aliases: Glycogen storage disease 7 Glycogen storage disease, type VII Muscle phosphofructokinase deficiency glycogen storage disease type VII phosphofructokinase myopathy	Pfk	36060	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0070311	oligoasthenoteratozoospermia Aliases: OAT oligoasthenoteratospermia	Agfg1 Spata20	360604 363266	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110344	osteogenesis imperfecta type 5 Aliases: OI5 osteogenesis imperfecta type V	Suco	360863	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050730	coenzyme Q10 deficiency disease Aliases: COENZYME Q10 DEFICIENCY, PRIMARY	Coq2 Coq8a	360887 498332	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080391	nephrotic syndrome type 9	Coq8a	360887	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070241	primary coenzyme Q10 deficiency 4 Aliases: COQ10D4 SCAR9 coenzyme Q10 deficiency, primary, 4 spinocerebellar ataxia, autosomal recessive 9	Coq8a	360887	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050460	Wolf-Hirschhorn syndrome Aliases: 4p deletion syndrome PITT SYNDROME Pitt-Rogers-Danks Syndrome chromosome 4p16.3 deletion syndrome	Fgfrl1	360903	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070468	Yoon-Bellen neurodevelopmental syndrome Aliases: YOBELN	Ogdh	360975	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0081326	oxoglutarate dehydrogenase deficiency Aliases: Oxoglutaric aciduria alpha-ketoglutarate dehydrogenase deficiency	Ogdh	360975	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3275	thymoma	AQP4	361	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080122	Alpers-Huttenlocher syndrome Aliases: Alper's syndrome Alpers disease Alpers progressive infantile poliodystrophy Alpers syndrome Alpers' disease or gray-matter degeneration Diffuse Cerebral Sclerosis of Schilder mitochondrial DNA depletion syndrome 4a progressive sclerosing poliodystrophy	AQP4	361	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080124	mitochondrial DNA depletion syndrome 5 Aliases: succinate-CoA ligase deficiency	Sucla2	361071	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080567	congenital disorder of glycosylation Ip Aliases: congenital disorder of glycosylation 1p	Alg11	361174	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0081221	autosomal recessive intellectual developmental disorder 59	IMPA1	3612	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110170	Charcot-Marie-Tooth disease axonal type 2Q Aliases: CMT2Q Charcot-Marie-Tooth neuropathy type 2Q autosomal dominant Charcot-Marie-Tooth disease type 2Q autosomal dominant axonal Charcot-Marie-Tooth disease type 2Q	Dhtkd1	361272	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111453	2-aminoadipic 2-oxoadipic aciduria Aliases: AMOXAD alpha-aminoadipic aciduria	Dhtkd1	361272	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:11727	facioscapulohumeral muscular dystrophy Aliases: Landouzy Dejerine muscular dystrophy Landouzy-Dejerine muscular dystrophy Muscular dystrophy, Landouzy-Dejerine	Large1 Slc25a4	361368 85333	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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