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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 **1 - 25** of **4115** in total

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Disease ID ▼	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:9993	hypoglycemia Aliases: Hypoglycaemia	AGTR2 AKT2 CYP2C9 GCK GLUD1 HNF4A PPP1R3A UCP3	1559 186 208 2645 2746 3172 5506 7352	Homo sapiens (human)	Alliance of Genome Resources
DOID:999	hypereosinophilic syndrome Aliases: Eosinophilic leukocytosis eosinophilia	F5 PDGFRA	2153 5156	Homo sapiens (human)	Alliance of Genome Resources
DOID:9976	heroin dependence	ABCB1 ACHE ADRA1A ALDH2 CHRM2 COMT CREB1 CYP2B6 CYP2C19 DRD2 DRD4 GABBR1 GABRB3 GABRG2 GAD1 GAD2 GDNF GRIN2A HTR3A NGF NPY1R NR3C1 NTRK2 OPRD1 OPRK1 OPRM1	1129 1312 1385 148 1555 1557 1813 1815 217 2550 2562 2566 2571 2572 2668 2903 2908 3359 43 4803 4886 4915 4985 4986 4988 5243	Homo sapiens (human)	Alliance of Genome Resources
DOID:9975	cocaine dependence	BDNF CAMK4 CCSER1 CHRNA3 CHRNB3 COL21A1 COMT DRD2 GABBR1 HTR2A HTR3A MANEA OPRD1 OPRK1 PER2 TENM3	1136 1142 1312 1813 2550 3356 3359 401145 4985 4986 55714 627 79694 814 81578 8864	Homo sapiens (human)	Alliance of Genome Resources
DOID:9974	drug dependence	ABCB1 ACHE COMT CYP2B6 NCAM1 OPRM1	1312 1555 43 4684 4988 5243	Homo sapiens (human)	Alliance of Genome Resources
DOID:9970	obesity	ABCA1 ABCG8 ADRB2 ADRB3 AGT APOD AR BBS2 CADM2 CAPN10 CCKAR CNR1 COMT CPE CRHR1 CYP27B1 CYP2R1 DRD2 EDN1 ENPP1 F7 FTO GFPT1 GHRL GHSR GIPR GLP1R GNAS HFE HK1 HK2 HSD11B2 HSPA1B HTR2A HTR2C IGFBP2 IGFBP6 IL6 IL6R INPPL1 LEPR MBL2 MC3R MC4R MIF NCOA3 NMB NMU NPPB NPY2R NPY5R NR1H3 NR3C1 OPRM1 PCSK1 PDP1 PGR PLIN1 POMC PPARG PPARGC1B SDC3 SERPINF1 SLC2A1 SLC6A14 SLC6A3 SOCS3 SORBS1 STAT3 UCP2 UCP3 WNT10B	10062 10580 10874 11132 11254 120227 1268 1312 133522 1363 1394 154 155 1594 1813 183 19 1906 2155 253559 2673 2693 2696 2740 2778 2908 3077 3098 3099 3291 3304 3356 3358 347 3485 3489 3569 3570 3636 367 3953 4153 4159 4160 4282 4828 4879 4887 4889 4988 5122 5167 51738 5176 5241 5346 5443 5468 54704 583 64241 6513 6531 6774 7351 7352 7480 79068 8202 886 9021 9672	Homo sapiens (human)	Alliance of Genome Resources
DOID:9955	hypoplastic left heart syndrome	MYH7	4625	Homo sapiens (human)	Alliance of Genome Resources
DOID:9953	acute biphenotypic leukemia Aliases: mixed phenotype acute leukemia	DOT1L	84444	Homo sapiens (human)	Alliance of Genome Resources
DOID:9952	acute lymphoblastic leukemia Aliases: ALL acute lymphoblastic leukaemia acute lymphocytic leukaemia precursor lymphoblastic lymphoma/leukemia	ABCB1 ABCC2 ABO BAX BCR CFB CREBBP CSF3 CYP1A1 CYP3A5 DPYD FLT3 GNB1 GPX1 HFE HK1 HLA-DQA1 HLA-DQB1 IFNG IKZF1 IRF4 KDM6A KRAS MEFV MTR NAT2 NBN NOS3 NRAS NUP214 PON1 TERT TYMS XRCC1	10 10320 1244 1387 1440 1543 1577 1806 2322 2782 28 2876 3077 3098 3117 3119 3458 3662 3845 4210 4548 4683 4846 4893 5243 5444 581 613 629 7015 7298 7403 7515 8021	Homo sapiens (human)	Alliance of Genome Resources
DOID:9938	dacryocystitis	IL1RN	3557	Homo sapiens (human)	Alliance of Genome Resources
DOID:9884	muscular dystrophy	CAPN3 CHKB COL6A3 DYSF FKRP FKTN LAMA2 POMGNT1 POMT1 POMT2 SGCA SGCB SGCD SYNE1	10585 1120 1293 2218 23345 29954 3908 55624 6442 6443 6444 79147 825 8291	Homo sapiens (human)	Alliance of Genome Resources
DOID:9883	Becker muscular dystrophy Aliases: Benign pseudohypertrophic muscular dystrophy benign congenital myopathy	DMD	1756	Homo sapiens (human)	Alliance of Genome Resources
DOID:988	mitral valve prolapse Aliases: Barlow's syndrome floppy mitral valve	ACE AGT DCHS1 DZIP1 FBN1 FLNA HLA-B PLAU TSHR	1636 183 2200 22873 2316 3106 5328 7253 8642	Homo sapiens (human)	Alliance of Genome Resources
DOID:987	alopecia	CDSN HLA-B	1041 3106	Homo sapiens (human)	Alliance of Genome Resources
DOID:9869	hereditary fructose intolerance syndrome Aliases: Fructosaemia Fructose-1,6-bisphosphate aldolase B deficiency Fructosemia	ALDOB	229	Homo sapiens (human)	Alliance of Genome Resources
DOID:986	alopecia areata Aliases: Circumscribed alopecia	CTLA4 HLA-DQA1 HLA-DQB1 IL1RN IL2 NOTCH4	1493 3117 3119 3557 3558 4855	Homo sapiens (human)	Alliance of Genome Resources
DOID:9849	Meniere's disease Aliases: Meniere disease Mnire's vertigo Otogenic vertigo	AQP4 HLA-B HLA-DRB1 HSPA1A	3106 3123 3303 361	Homo sapiens (human)	Alliance of Genome Resources
DOID:9834	hyperopia Aliases: Far-sightedness farsightedness hypermetropia	MYRF NOG	745 9241	Homo sapiens (human)	Alliance of Genome Resources
DOID:9828	neonatal abstinence syndrome Aliases: Drug withdrawal syndrome in newborn	COMT CYP2B6 OPRK1 OPRM1	1312 1555 4986 4988	Homo sapiens (human)	Alliance of Genome Resources
DOID:9827	radioulnar synostosis	HOXA11 SMAD6	3207 4091	Homo sapiens (human)	Alliance of Genome Resources
DOID:9821	choroideremia Aliases: progressive Choroidal Atrophy	CHM	1121	Homo sapiens (human)	Alliance of Genome Resources
DOID:9810	polyarteritis nodosa	ELN	2006	Homo sapiens (human)	Alliance of Genome Resources
DOID:980	choroidal sclerosis Aliases: Choroidal degenerations	GUCY2D PRPH2	3000 5961	Homo sapiens (human)	Alliance of Genome Resources
DOID:9778	irritable bowel syndrome Aliases: IBD Irritable colon	HTR3A RNF43	3359 54894	Homo sapiens (human)	Alliance of Genome Resources
DOID:9775	diastolic heart failure	ACE	1636	Homo sapiens (human)	Alliance of Genome Resources

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