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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	January 28, 2025
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **4276 - 4300** of **5716** in total

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Disease ID ▲	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:14018	alcoholic liver cirrhosis Aliases: Alcoholic Cirrhosis Alcoholic cirrhosis of liver Laennec's cirrhosis Laennec's cirrhosis, alcoholic Portal cirrhosis	ALDH2 CYP2E1 GABRG2 LEP SERPINE1 SOD2 TG	1571 217 2566 3952 5054 6648 7038	Homo sapiens (human)	Alliance of Genome Resources
DOID:14018	alcoholic liver cirrhosis Aliases: Alcoholic Cirrhosis Alcoholic cirrhosis of liver Laennec's cirrhosis Laennec's cirrhosis, alcoholic Portal cirrhosis	Lep	25608	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:14021	Tietze's syndrome Aliases: Costalchondritis Costochondral junction syndrome Costochondritis Slipping rib syndrome Tietze's disease	MITF	4286	Homo sapiens (human)	Alliance of Genome Resources
DOID:14040	autoimmune polyendocrine syndrome Aliases: Autoimmune polyglandular failure Lloyd's syndrome autoimmune polyendocrinopathy	HLA-DQA1 HLA-DQB1 HLA-DRB1	3117 3119 3123	Homo sapiens (human)	Alliance of Genome Resources
DOID:1405	primary angle-closure glaucoma Aliases: primary Angle Closure Glaucoma	ACVR1 COL18A1 MYRF	745 80781 90	Homo sapiens (human)	Alliance of Genome Resources
DOID:14067	Plasmodium falciparum malaria Aliases: Malaria fever, subtertian falciparum malaria malignant tertian fever	ABO CYP2C19 FCGR2A G6PD HLA-DQB1 HP MBL2	1557 2212 2539 28 3119 3240 4153	Homo sapiens (human)	Alliance of Genome Resources
DOID:14069	cerebral malaria Aliases: Malarial encephalitis	ACE2 NRG1	3084 59272	Homo sapiens (human)	Alliance of Genome Resources
DOID:1407	anterior uveitis	Cd59b	25407	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1407	anterior uveitis	CCL2 CFB CFH HLA-B IL1RN TLR2 TLR4 TNF	3075 3106 3557 629 6347 7097 7099 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:14080	glucocorticoid-remediable aldosteronism Aliases: GRA GRS familial hyperaldosteronism type I glucocorticoid-suppressible hyperaldosteronism	CYP11B1	1584	Homo sapiens (human)	Alliance of Genome Resources
DOID:14115	toxic shock syndrome Aliases: TSS toxic shock	ACE ADRB2 HSPA1B IL10 IL1RN MBL2 PROC SERPINC1 SERPINE1 SERPING1 SFTPB TFPI	154 1636 3304 3557 3586 4153 462 5054 5624 6439 7035 710	Homo sapiens (human)	Alliance of Genome Resources
DOID:14115	toxic shock syndrome Aliases: TSS toxic shock	A2m Tbxa2r	24153 24816	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:14118	familial lipoprotein lipase deficiency Aliases: Fredrickson type I hyperlipoproteinemia Fredrickson type I lipaemia familial LPL deficiency familial hyperlipoproteinemia type I hypercholesterinaemic xanthomatosis hyperchylomicronemia mixed hyperglyceridemia	LPL	4023	Homo sapiens (human)	Alliance of Genome Resources
DOID:14118	familial lipoprotein lipase deficiency Aliases: Fredrickson type I hyperlipoproteinemia Fredrickson type I lipaemia familial LPL deficiency familial hyperlipoproteinemia type I hypercholesterinaemic xanthomatosis hyperchylomicronemia mixed hyperglyceridemia	Lpl	16956	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1415	gyrate atrophy Aliases: Gyrate atrophy of the choroid and/or retina Ornithinemia with gyrate atrophy gyrate atrophy of the retina	OAT	4942	Homo sapiens (human)	Alliance of Genome Resources
DOID:14159	obstructive hydrocephalus	Myo9a	270163	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1417	choroid disease	IL10	3586	Homo sapiens (human)	Alliance of Genome Resources
DOID:14175	von Hippel-Lindau disease Aliases: Hippel Lindau syndrome von Hippel-Lindau syndrome	MMP3	4314	Homo sapiens (human)	Alliance of Genome Resources
DOID:14179	X-linked agammaglobulinemia Aliases: BTK deficiency Bruton agammaglobulinemia tyrosine kinase deficiency Bruton disease Bruton's Sex-Linked Agammaglobulinemia Bruton's agammaglobulinaemia Bruton's type agammaglobulinemia Bruton-type agammaglobulinemia	Btk Pik3r1	12229 18708	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14179	X-linked agammaglobulinemia Aliases: BTK deficiency Bruton agammaglobulinemia tyrosine kinase deficiency Bruton disease Bruton's Sex-Linked Agammaglobulinemia Bruton's agammaglobulinaemia Bruton's type agammaglobulinemia Bruton-type agammaglobulinemia	BTK	695	Homo sapiens (human)	Alliance of Genome Resources
DOID:14184	polyneuropathy due to drug	ERCC6	2074	Homo sapiens (human)	Alliance of Genome Resources
DOID:14213	hypophosphatasia Aliases: deficiency of alkaline phosphatase	PHO8	852092	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:14213	hypophosphatasia Aliases: deficiency of alkaline phosphatase	ALPL	249	Homo sapiens (human)	Alliance of Genome Resources
DOID:14218	dihydropyrimidine dehydrogenase deficiency Aliases: Dihydrouracil Dehydrogenase deficiency familial pyrimidinaemia thymine-uracilurea	DPYD	1806	Homo sapiens (human)	Alliance of Genome Resources
DOID:14219	renal tubular acidosis	Slc4a1 Slc4a4	20533 54403	Mus musculus (house mouse)	Alliance of Genome Resources

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