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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 **3251 - 3275** of **4649** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▼
DOID:0080855	Parkinsonism	ABAT ABCC8 ABCC9 BAD BDNF CASP9 CNR1 COMT COX1 CSF2 CX3CL1 DRD2 DRD3 EGFR ENO2 ESR1 GBA1 GDNF GFRA1 GFRA2 GRM8 GSK3A HSPA1A HSPA9 KCNJ11 LRRK2 MAPT MMP3 NDUFS3 NFKB2 NGF NGFR NOS1 NTRK1 PARK7 PINK1 PTGS2 RELA RET SHH SLC11A2 SLC17A8 SLC6A3 SLC6A4 SRC TNFRSF1B VDAC1	10060 11315 120892 1268 1312 1437 18 1813 1814 1956 2026 2099 246213 2629 2668 2674 2675 2918 2931 3303 3313 3767 4137 4314 4512 4722 4791 4803 4804 4842 4891 4914 572 5743 5970 5979 627 6376 6469 65018 6531 6532 6714 6833 7133 7416 842	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080846	latent autoimmune diabetes in adults Aliases: LADA type 1.5 diabetes	CTLA4	1493	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080845	omodysplasia 2	FZD2	2535	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080844	omodysplasia 1	GPC6	10082	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080839	X-linked warfarin sensitivity	F9	2158	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080837	growth hormone insensitivity syndrome with immune dysregulation 2	STAT5B	6777	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080836	growth hormone insensitivity syndrome with immune dysregulation 1	STAT5A STAT5B	6776 6777	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080832	mild cognitive impairment	AGER NEFL SLC6A3	177 4747 6531	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080828	VEXAS syndrome Aliases: vacuoles, E1 enzyme, X-linked, autoinflammatory and somatic syndrome	UBA1	7317	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080827	human cytomegalovirus infection	KIR3DS1 REN	3813 5972	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080822	aspirin-induced respiratory disease Aliases: aspirin-sensitive asthma	CCR3 CYSLTR2 HLA-DQA1 HLA-DQB1 HLA-DRB1 HLA-DRB3 HLA-DRB4 IL4 PTGS2 TBXA2R	1232 3117 3119 3123 3125 3126 3565 57105 5743 6915	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080821	exercise-induced bronchoconstriction Aliases: exercise-induced asthma	ALOX5 CCL5 TACR1	240 6352 6869	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080820	occupational asthma	HLA-B HLA-DOA HLA-DPB1 HLA-E	3106 3111 3115 3133	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080809	chronic asthma	NGF	4803	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080807	autosomal dominant craniodiaphyseal dysplasia	SOST	50964	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080804	cranioectodermal dysplasia 2	WDR35	57539	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080799	sinonasal undifferentiated carcinoma	SMARCB1	6598	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080797	nasal type extranodal NK/T-cell lymphoma	ABCB1 CD274 FAS GPX3 PRDM1 STAT3	2878 29126 355 5243 639 6774	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080792	Treacher Collins syndrome 4	POLR1B	84172	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080789	Treacher Collins syndrome 1	TCOF1	6949	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080788	proximal symphalangism 2	GDF5	8200	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080787	proximal symphalangism 1	NOG	9241	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080786	Brown-Vialetto-Van Laere syndrome 2	SLC52A2	79581	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080785	Brown-Vialetto-Van Laere syndrome 1	SLC52A3	113278	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080784	urinary tract infection Aliases: UTI	CXCR1 HSPA1B IL1A LCN2 TLR2 TLR4	3304 3552 3577 3934 7097 7099	Homo sapiens (human)	Alliance of Genome Resources

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