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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:10652	Alzheimer's disease Aliases: Alzheimer disease Alzheimers dementia	A2M ABAT ABCA1 ACHE ADAM17 ADRA1A ADRB3 AGER AGTR1 ALDH2 APBB1 APOA1 APOA4 APOE APP BACE1 BACE2 BCHE BDNF C2 C3 CASP7 CDK5 CHAT CLOCK CTSD CYP19A1 CYP46A1 DLST ECE1 EIF2AK2 EIF2S1 ENO1 EPO ESR1 FAS GAPDH GAPDHS GCG GLUL GRIN2B GRN GSK3B GSTO1 GSTO2 HFE HLA-DRB1 HMGCR HSPA1A HSPA1B ICAM1 IGFBP3 IL10 IL1A IL2 IL4 IL6R IREB2 IRS1 KCNMA1 KLK6 LDLR LIPC LPL LRP1 LRP8 LRPAP1 MAOA MAPT MBL2 MCM2 MME NCSTN NECTIN2 NEFM NFE2L2 NGFR NOS1 NOS3 NTF3 NTRK1 NTRK2 PARP1 PCK1 PLAU PON1 PON2 PON3 PPARA PPARG SERPINE2 SNCA SOD2 SORL1 STAT3 TFAM TLR4 TNF TPH1 TTR UQCRC1 VEGFA VLDLR XRN1	1020 10858 1103 119391 142 148 1509 155 1588 1743 177 18 185 1889 19 1965 2 2023 2056 2099 217 23385 23621 25825 2597 26330 2641 2752 2896 2904 2932 3077 3123 3156 322 3303 3304 335 337 3383 348 3486 351 355 3552 3558 3565 3570 3586 3658 3667 3778 3949 3990 4023 4035 4043 4128 4137 4153 4171 43 4311 4741 4780 4804 4842 4846 4908 4914 4915 5105 5270 5328 5444 5445 5446 54464 5465 5468 5610 5653 5819 590 627 6622 6648 6653 6774 6868 7019 7099 7124 7166 717 718 7276 7384 7422 7436 7804 840 9446 9575	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080600	COVID-19 Aliases: 2019 Novel Coronavirus (2019-nCoV) 2019-nCoV infection COVID19 SARS-CoV-2 infection Wuhan coronavirus infection Wuhan seafood market pneumonia virus infection	A2M ABO ACE2 ACE AGTR1 C3 C4BPA C4BPB CFH F3 HLA-B HLA-C IFNB1 IFNL1 KIR3DS1 PLG SERPINF2 SERPING1 TLR7	1636 185 2 2152 28 282618 3075 3106 3107 3456 3813 51284 5340 5345 59272 710 718 722 725	Homo sapiens (human)	Alliance of Genome Resources
DOID:2377	multiple sclerosis Aliases: Generalized multiple sclerosis insular sclerosis	A2M AGER APOC2 CCL1 CCL2 CCL7 CCR5 CD24 CD28 CD40 CD46 CD86 CIITA CLEC16A CTLA4 FAS FASLG GABRA3 GC H6PD HLA-DPB1 HLA-DQA1 HLA-DQB1 HLA-DRA HLA-DRB1 HLA-DRB3 HSP90AB1 IFNB1 IFNG IL21R IL23R IL2RA IL4 IL4R IL6 IRF5 JAG1 KIF1B MBP MMP12 MMP9 MOG MPHOSPH9 NDUFS2 NECTIN2 NOTCH4 PDCD1 PHACTR2 PRF1 PTPRC RGMA SLC11A1 SPP1 TNF TNFRSF1A	100133941 10198 1234 149233 1493 177 182 2 23095 23274 2556 2638 3115 3117 3119 3122 3123 3125 3326 344 3456 3458 355 3559 356 3565 3566 3569 3663 4155 4179 4261 4318 4321 4340 4720 4855 50615 5133 5551 56963 5788 5819 6346 6347 6354 6556 6696 7124 7132 940 942 9563 958 9749	Homo sapiens (human)	Alliance of Genome Resources
DOID:14330	Parkinson's disease Aliases: Parkinson disease paralysis agitans	A2M AKT1 ATM ATP13A2 CASP9 CAST CHRNB3 CREB1 CYP1A1 DBH DNAJC13 EIF2AK2 EPO FBXO7 GBA1 GDF5 GIGYF2 GSTO1 GSTO2 HLA-DRA HLA-DRB1 HMGCR HSPA8 HSPA9 HTT KLK6 LRRK2 MAPT NAT2 ND3 NOS1 PARK7 PARP1 PHACTR2 PINK1 PLA2G6 PPARGC1A PTGIS SLC11A2 SLC18A2 SNCA SNCB SOD1 SYNJ1 TARDBP TFAM	10 10891 11315 1142 119391 120892 1385 142 1543 1621 2 2056 207 23317 23400 23435 25793 26058 2629 3064 3122 3123 3156 3312 3313 4137 4537 472 4842 4891 5610 5653 5740 65018 6571 6620 6622 6647 7019 8200 831 8398 842 8867 9446 9749	Homo sapiens (human)	Alliance of Genome Resources
DOID:2320	obstructive lung disease Aliases: respiratory airway obstruction	A2M MMP1	2 4312	Homo sapiens (human)	Alliance of Genome Resources
DOID:13208	background diabetic retinopathy Aliases: Non proliferative diabetic retinopathy Non-Proliferative Diabetic Retinopathy	A2M	2	Homo sapiens (human)	Alliance of Genome Resources
DOID:10754	otitis media	A2ML1 IL10 IL6 MBL2	144568 3569 3586 4153	Homo sapiens (human)	Alliance of Genome Resources
DOID:9164	achalasia Aliases: Lack of reflex relaxation of lower oesophageal sphincter achalasia of cardia achalasia of esophagus cardiospasm esophageal achalasia hypertensive lower esophageal sphincter	AAAS HLA-DQA1 HLA-DQB1 VIPR1	3117 3119 7433 8086	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050602	triple-A syndrome Aliases: AAAS Achalasia-Addisonianism-Alacrimia syndrome Allgrove Syndrome	AAAS	8086	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111866	trichothiodystrophy Aliases: TTD	AARS1 MARS1	16 4141	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080451	developmental and epileptic encephalopathy 29 Aliases: DEE29 early infantile epileptic encephalopathy 29	AARS1	16	Homo sapiens (human)	Alliance of Genome Resources
DOID:10579	leukodystrophy	AARS1	16	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110177	Charcot-Marie-Tooth disease axonal type 2N Aliases: CMT2N Charcot-Marie-Tooth neuropathy axonal type 2N autosomal dominant Charcot-Marie-Tooth disease type 2N autosomal dominant axonal Charcot-Marie-Tooth disease type 2N	AARS1	16	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111479	combined oxidative phosphorylation deficiency 8 Aliases: COXPD8	AARS2	57505	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070396	progressive leukoencephalopathy with ovarian failure	AARS2	57505	Homo sapiens (human)	Alliance of Genome Resources
DOID:12858	Huntington's disease Aliases: HD Huntington disease Huntington's chorea	ABAT BDNF EIF2AK2 GLUL GRIK2 GRIN2A GRIN2B HSF1 HTT IL6 IL6R NOG NPY2R NRF1 PPARGC1A PRKAA1 SIRT1 TFAM	10891 18 23411 2752 2898 2903 2904 3064 3297 3569 3570 4887 4899 5562 5610 627 7019 9241	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060174	GABA aminotransferase deficiency Aliases: Gamma-amino butyric acid transaminase deficiency gamma-aminobutyric acid transaminase deficiency	ABAT	18	Homo sapiens (human)	Alliance of Genome Resources
DOID:9352	type 2 diabetes mellitus Aliases: NIDDM insulin resistance non-insulin-dependent diabetes mellitus type 2 diabetes type II diabetes mellitus	ABCA1 ABCB1 ABCC8 ACE ADAM17 ADIPOQ ADRA2A ADRB3 AGER AHSG AKR1B1 AKT2 ALDH2 ALDOB APOA5 APOB APOD APOM AXL BCHE BTC CACNA1D CADM2 CAPN10 CASP9 CASQ1 CD36 CD38 CDKAL1 CEL CNR1 CPE CYB5R4 CYP11B2 CYP1A1 CYP2C9 DPP4 DRD2 ENPP1 ESR1 F7 FASLG FFAR1 FTO GCGR GCK GFPT2 GHR GHRL GLO1 GP6 GPD2 GPX3 HFE HIF1A HK2 HLA-DQA1 HMGCR HNF1A HNF4A HSD11B1 HSPA1B IFNG IGF2R IGFBP3 IKBKB IL10 IL1RN IL6 INPPL1 INS INSR IRS1 IRS2 ITGA2 KCNJ11 KCNQ1 LEP LEPR LIPC LMNA LPL LTA MAPK8IP1 MAPK9 MT2A MTNR1B MTOR NOS2 P2RY12 PCK1 PCSK2 PDX1 PIK3C2G PKLR PLA2G7 PLAT PNPLA3 PON1 PON2 PPARD PPARG PPARGC1A PPP1R3A PRKAA2 PTPN1 PTPRD RBP4 RRAD SERPINF1 SGCG SHBG SLC2A1 SLC2A2 SLC2A4 SOD1 SOD2 SOD3 SORBS1 SPHK1 SRC SREBF1 SREBF2 STAT3 TLR4 UCP3 VPS26A WFS1 XRCC1	1056 10580 10891 11132 116519 1268 1363 150 1543 155 1559 1585 1636 177 1803 1813 19 197 208 2099 2155 217 229 231 2475 253559 2642 2645 2690 2739 2820 2864 2878 3077 3091 3099 3117 3156 3172 3290 3304 338 3458 347 3482 3486 3551 3557 356 3569 3586 3630 3636 3643 3651 3667 3673 3767 3784 3952 3953 3990 4000 4023 4049 4502 4544 4843 5105 51167 51206 5126 5167 51738 5176 5243 5288 5313 5327 5444 5445 5467 5468 54901 5506 5563 558 55937 5601 5770 5789 590 5950 6236 6445 6462 64805 6513 6514 6517 6647 6648 6649 6714 6720 6721 6774 6833 685 6868 6927 7099 7352 7466 7515 776 79068 7941 80339 842 844 8660 8877 9370 9479 948 952 9559 9945	Homo sapiens (human)	Alliance of Genome Resources
DOID:3393	coronary artery disease Aliases: CHD Coronary disease coronary arteriosclerosis coronary heart disease	ABCA1 ABCC6 ACAT2 ACE ADIPOQ ADRB3 AGER AGTR1 AHSG APOA5 APOB APOC3 APOE APOM ARHGAP31 BCHE BRINP3 BTNL2 C1orf167 CBS CCR2 CD40LG CLCN6 CPE CUBN CYP2R1 ECE1 EDN1 EPHX2 ESR1 F2 F7 FCGR2A FCGR3A FGB FTO GCK GPX1 HMGCR HNF1A HSPD1 IL10 IL1RL1 IRS1 KALRN KL LEPR LIPC LIPG LPL LRP8 LTA LUM MLXIPL MMP12 MMP1 MMP3 MMP9 MYLK NOD2 NOS3 NPPA NR3C1 OGG1 OLR1 PECAM1 PLA2G7 PNPLA3 PON1 PON2 PPARA PTPN1 PTPRD RBP4 SELE SERPINE1 SOAT2 SOD3 SREBF1 TLL1 TLR4 TNF TP53 XRCC1	116519 1185 120227 1363 155 1636 177 185 1889 19 1906 197 2053 2099 2147 2155 2212 2214 2244 2645 284498 2876 2908 3156 3329 338 339479 345 348 3586 3667 368 39 3953 3990 4023 4049 4060 4312 4314 4318 4321 4638 4846 4878 4968 4973 5054 51085 5175 5444 5445 5465 55937 56244 57514 5770 5789 590 5950 6401 64127 6649 6720 6927 7092 7099 7124 7157 729230 7515 7804 79068 7941 8029 80339 8435 875 8997 9173 9365 9370 9388 959	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:1387	hypolipoproteinemia Aliases: Hypolipoproteinaemia	ABCA1 APOA1	19 335	Homo sapiens (human)	Alliance of Genome Resources
DOID:1388	Tangier disease Aliases: familial alpha-lipoprotein deficiency familial high density lipoprotein deficiency	ABCA1	19	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080957	primary hypoalphalipoproteinemia 1 Aliases: familial HDL deficiency familial hypoalphalipoproteinemia	ABCA1	19	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060713	autosomal recessive congenital ichthyosis 4B Aliases: ARCI4B harlequin ichthyosis harlequin type ichthyosis congenita harlequin type ichthyosis fetalis	ABCA12	26154	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060712	autosomal recessive congenital ichthyosis 4A Aliases: ARCI4A ICR2B ichthyosis congenita IIB lamellar ichthyosis 2	ABCA12	26154	Homo sapiens (human)	Alliance of Genome Resources

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