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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 **15526 - 15550** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:9498	pulmonary eosinophilia	ADAM8 IL10 IL1RN IL5	101 3557 3567 3586	Homo sapiens (human)	Alliance of Genome Resources
DOID:4483	rhinitis	ADAM33 BDKRB1 BDKRB2 BDNF C3 C3AR1 C5AR1 CCL11 CCL1 CCL24 CCL7 CCR2 CCR3 CD14 CD28 CDC42 CRHR1 CRHR2 CTLA4 CX3CL1 CYSLTR1 CYSLTR2 FCER1A HLA-DQA1 HLA-DQB1 IL13 IL16 IL17A IL1RL1 IL1RN IL22 IL23R IL2 IL4 IL4R IL9 LEP MBL2 MIF MUC5AC NGF NGFR NOD2 NOS2 NTRK1 OPA1 PTGDR2 SERPINE1 SFTPD TAP1 TGFB1 TLR2 TLR6 TNF VEGFA	10333 10800 11251 1232 1394 1395 149233 1493 2205 3117 3119 3557 3558 3565 3566 3578 3596 3603 3605 3952 4153 4282 4586 4803 4804 4843 4914 4976 5054 50616 57105 623 624 627 6346 6354 6356 6369 6376 64127 6441 6890 7040 7097 7124 718 719 728 729230 7422 80332 9173 929 940 998	Homo sapiens (human)	Alliance of Genome Resources
DOID:7596	asbestos-related lung carcinoma	ADAM28 RARB	10863 5915	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060075	estrogen-receptor positive breast cancer	ADAM28 PIK3CA	10863 5290	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080434	developmental and epileptic encephalopathy 61 Aliases: DEE61 early infantile epileptic encephalopathy 61	ADAM22	53616	Homo sapiens (human)	Alliance of Genome Resources
DOID:3310	atopic dermatitis Aliases: Atopic neurodermatitis Besnier's prurigo allergic dermatitis atopic eczema	ADAM17 APOE BDNF C3 CCL28 CCR2 CCR3 CCR5 CD40 CDSN CLDN1 CMA1 CTLA4 CTSE CX3CL1 DOCK8 F2 FCGR2A HAVCR1 IFNG IL13 IL13RA1 IL13RA2 IL17A IL21R IL25 IL2 IL4 IL4R IL5 MBL2 NGF NGFR NTRK1 RELB SELP SHOC2 TGFB1 TLR2 TLR4 TNF TNFAIP6 TRAF3IP2 TSLP WASL	1041 10758 1215 1232 1234 1493 1510 2147 2212 26762 3458 348 3558 3565 3566 3567 3596 3597 3598 3605 4153 4803 4804 4914 50615 56477 5971 627 6376 6403 64806 6868 7040 7097 7099 7124 7130 718 729230 8036 81704 85480 8976 9076 958	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050589	inflammatory bowel disease	ADAM17 ADIPOQ AGER AGT ALPI ANKZF1 ANO6 B2M CD40LG EGFR EPB41 EPB41L1 EPB41L2 EPB41L3 FGF23 HSPA5 ICAM1 IGF2 IGFBP3 IL10 IL16 IL1RN IL21R IL2 IL2RA KLKB1 LTF MST1 MUC2 NOS2 NPSR1 PDGFB PDZD2 PIK3C3 RAB11A RAB11B RUNX3 SLC11A1 SLC6A14 ST6GALNAC1 STAT3 TGFB1 THEMIS TNF VEGFA	11254 177 183 1956 196527 2035 2036 2037 23037 23136 248 3309 3383 3481 3486 3557 3558 3559 3586 3603 3818 387129 387357 4057 4485 4583 4843 50615 5155 5289 55139 55808 567 6556 6774 6868 7040 7124 7422 8074 864 8766 9230 9370 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060258	reticulate acropigmentation of Kitamura Aliases: RAPK	ADAM10	102	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110050	Alzheimer's disease 18 Aliases: AD18 Alzheimer disease 18 Alzheimer's disease 18, late onset	ADAM10	102	Homo sapiens (human)	Alliance of Genome Resources
DOID:83	cataract	ADAM10 AKR1B1 ALDH18A1 ANXA1 B2M BCOR BRCA2 CASP9 CAT CCK CCL11 CDKN1B CRIM1 CRYAA CRYAB CTH DNASE2B FAS FDFT1 G6PD GALK1 GCLC GCNT2 GPX1 HSF4 INTS1 LIM2 LSS MAP2K1 MMP3 NFE2L2 NR3C1 OGG1 PIK3C2A PIKFYVE PON1 PSMC3 RBM24 SIPA1L3 SLC2A14 SLC2A3 SLC45A2 SLC9A1 SOD1 SORD TRPM3 VPS13B WFS1	102 1027 1409 1410 144195 1491 157680 200576 221662 2222 23094 231 2539 2584 26173 2651 2729 2876 2908 301 3299 355 3982 4047 4314 4780 4968 51151 51232 5286 5444 54880 5604 567 5702 5832 58511 6356 6515 6548 6647 6652 675 7466 80036 842 847 885	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081292	traumatic brain injury	ADAM10 AHR APP BAD CAPN1 CD163 CIT CYP2D7 DRD1 DRD2 FTO FUBP1 GRIA1 LAMP2 LCN2 MAPT MMP2 NFE2L2 NGF NOX1 PDE10A TGFB1 TP53	102 10846 11113 1564 1812 1813 196 27035 2890 351 3920 3934 4137 4313 4780 4803 572 7040 7157 79068 823 8880 9332	Homo sapiens (human)	Alliance of Genome Resources
DOID:13096	Sneddon syndrome Aliases: Idiopathic livedo reticularis with systemic involvement	ADA2	51816	Homo sapiens (human)	Alliance of Genome Resources
DOID:106	pleural tuberculosis Aliases: Pearly disease Tuberculosis of pleura Tuberculous pleurisy Tuberculous pleuritis tuberculous pleurisy in primary progressive tuberculosis	ADA2 CCR2 CCR5 IL1RN MMP9 TLR4 TNC	1234 3371 3557 4318 51816 7099 729230	Homo sapiens (human)	Alliance of Genome Resources
DOID:11294	arteriovenous malformation Aliases: Arteriovenous hemangioma Cirsoid aneurysm Racemose Angioma Racemose aneurysm Racemose hemangioma	ACVRL1 ENG GLMN MAP2 MMP9 RASA1 TEK	11146 2022 4133 4318 5921 7010 94	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060688	arteriovenous malformations of the brain Aliases: cerebral arteriovenous malformation intracranial arteriovenous malformation	ACVRL1 ENG FLT1 IL6 KDR KRAS LEMD3 NOTCH4 PITPNM3 SARS1 VEGFA	2022 2321 23592 3569 3791 3845 4855 6301 7422 83394 94	Homo sapiens (human)	Alliance of Genome Resources
DOID:1270	hereditary hemorrhagic telangiectasia Aliases: Osler hemorrhagic telangiectasia syndrome Osler-Weber-Rendu disease Rendu-Osler-Weber disease	ACVRL1 BMP10 ENG GDF2 SMAD4 TGFB1 TNF	2022 2658 27302 4089 7040 7124 94	Homo sapiens (human)	Alliance of Genome Resources
DOID:224	transient cerebral ischemia Aliases: TIA TIA - Transient ischaemic attack Transient cerebral ischaemia Transient ischemic attacks transient ischemic attack	ACVRL1 ADAMTS1 ADAMTS4 AGER AGT AHR AIFM1 ANK1 ANK2 APOE AQP4 ATF2 ATP5F1B BACE1 BAX C3 CAMK2A CASP7 CASP9 CBL CCL2 CCNH CCR6 CDK5 CHKA CREB1 CSF3 CX3CL1 DAXX DBN1 DLL4 DUSP16 EIF2S1 ELANE ELK1 ENTPD1 EP300 EPO ERCC6 ESR1 F11R F12 FADD FAS FGFR1 FGFR2 FMR1 FTO G6PD GAD1 GAD2 GHSR GLRX GLUL GOT1 GPX3 GRIN2A GRIN2B H2AX HAVCR2 HIF1A HNRNPA2B1 HNRNPAB HRH2 HSF1 HSPA5 HSPA8 HSPB1 HTT ICAM1 IFNB1 IKBKB IL10 IL1RN ITGAM ITGB3 ITPR1 JAK1 KCNK2 KDM1A KLF5 KMT2A LCN2 LMNA LPAR1 LTBP1 MADD MAP2K4 MBD3 MBP MCFD2 MDM2 MECP2 MFF MMP2 MMP9 MT1E MT1H MT2A MTOR NAMPT NEFH NEFL NEFM NF1 NFKB1 NGFR NOS1 NOS3 NOTCH1 NOX1 NRG1 NRP1 NRXN1 OGG1 OPA1 OPTN PARP1 PAWR PCNA PLAT PLAU PLXND1 PPARG PPP1R15A PPP1R9A PTAFR PTEN PTGER4 PTGIS PTPN13 RACK1 ROBO1 ROBO2 RPS6 SEMA3E SERPINE1 SERPINF1 SIN3A SIRT6 SLC12A2 SLC17A6 SLC17A8 SLIT2 SMPD3 SOD1 SOD2 STAT3 TERT TFPI TIAL1 TNF TNFRSF1A TRPC6 UCP2 VWF WNK1 WNK2 XRCC1	10133 10135 1020 10399 1119 1235 1385 1386 142 1440 1616 1627 177 183 1902 196 1965 1991 2002 2033 2056 2074 2099 2161 2260 2263 23028 23129 2332 23621 23645 246213 2475 2539 2571 2572 25942 2693 27035 2745 2752 2805 286 287 2878 2903 2904 3014 3064 3084 3091 3181 3182 3274 3297 3309 3312 3315 3383 3456 348 355 3551 3557 3586 361 3684 3690 3708 3716 3776 3934 4000 4052 4155 4193 4204 4297 4313 4318 4493 4496 4502 4741 4744 4747 4763 4790 4804 4842 4846 4851 4968 4976 5054 506 5074 50848 5111 51548 5176 5327 5328 53615 54567 5468 55512 55607 56947 57084 5724 5728 5734 5740 5783 581 6091 6092 6194 6347 6376 6416 65125 65268 6558 6647 6648 6774 688 7015 7035 7073 7124 7132 718 7225 7351 7450 7515 79068 80824 815 840 842 84868 8567 867 8772 8829 902 90411 9131 9353 9378 94 9507 9510 953 9723	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060856	right atrial isomerism Aliases: Ivemark syndrome asplenia with cardiovascular anomalies	ACVR2B CFC1 CFC1B	55997 653275 93	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050545	visceral heterotaxy Aliases: heterotaxia situs ambiguus	ACVR2B BICC1 CC2D1A CC2D2A CCDC39 CFAP53 CFC1 CFC1B DNAAF3 DNAH11 DNAH5 DRC1 FOXH1 GDF1 IFT74 MEGF8 MMP21 NODAL ODAD2 OSBPL1A PCSK5 PHKA2 PKD1L1 PSME4 SLIT2 TBC1D32 TMEM67	114876 118856 168507 1767 1954 220136 221322 23198 2657 339829 352909 4838 5125 5256 54862 55130 55997 57545 653275 80114 80173 8701 8928 91147 92749 93 9353	Homo sapiens (human)	Alliance of Genome Resources
DOID:4258	Weissenbacher-Zweymuller syndrome Aliases: Piere-Robin syndrome Pierre Robin Malformation	ACVR2A TFRC	7037 92	Homo sapiens (human)	Alliance of Genome Resources
DOID:3883	Lynch syndrome Aliases: COCA 1 HNPCC - hereditary nonpolyposis colon cancer Hereditary Defective Mismatch Repair syndrome Hereditary non-polyposis colon cancer Hereditary non-polyposis colon cancer syndrome Hereditary non-polyposis colorectal cancer Hereditary non-polyposis colorectal cancer syndrome Hereditary nonpolyposis colon cancer Hereditary nonpolyposis colon cancer syndrome Hereditary nonpolyposis colorectal cancer syndrome hereditary nonpolyposis colorectal cancer hereditary nonpolyposis colorectal neoplasm	ACVR2A CA12 CA9 E2F4 KRAS MARCKS MLH1 MRE11 MSH2 MSH6 PMS1 RNASEL RNASET2 SLC22A9 SMAD4 TCF4 TGFBR1 TGFBR2	114571 1874 2956 3845 4082 4089 4292 4361 4436 5378 6041 6925 7046 7048 768 771 8635 92	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050787	juvenile polyposis syndrome	ACVR2A ACVR2B BMP2 BMP4 BMPR1A BMPR1B HIVEP1 HIVEP2 HIVEP3 SMAD4 SMAD5	3096 3097 4089 4090 59269 650 652 657 658 92 93	Homo sapiens (human)	Alliance of Genome Resources
DOID:14323	Marfan syndrome Aliases: Marfan's syndrome	ACVR2A ACVR2B BMP2 BMP4 BMP6 BMP7 FBN1 MATN3 MMP12 MMP14 MMP2 TGFBR2	2200 4148 4313 4321 4323 650 652 654 655 7048 92 93	Homo sapiens (human)	Alliance of Genome Resources
DOID:1790	malignant mesothelioma Aliases: Diffuse malignant Mesothelioma advanced malignant mesothelioma asbestos-related malignant mesothelioma malignant tumor of Mesothelium	ACVR1B MCAM SETD2 XRCC1	29072 4162 7515 91	Homo sapiens (human)	Alliance of Genome Resources
DOID:5409	lung small cell carcinoma	ACVR1B APOA1 APOC3 ATM ATRX CDKN1B CHRNA3 CHRNA5 CHRNA9 CHRNB4 CSF1R CYP24A1 DLL4 E2F1 EEF2 FAT1 FOXA1 GRP ITGB1 KDM6A KMT2D LAMA3 LAMB3 LAMC2 MTOR NOTCH1 PBRM1 PTK2 RARB RICTOR SKP2 XPO5	1027 1136 1138 1143 1436 1591 1869 1938 2195 2475 253260 2922 3169 335 345 3688 3909 3914 3918 472 4851 54567 546 55193 55584 5747 57510 5915 6502 7403 8085 91	Homo sapiens (human)	Alliance of Genome Resources

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