GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Gene Symbol

Gene ID

Organism

Source

Display
results per page.

Clear

Submissions

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 **15276 - 15300** of **15957** in total

« First

‹ Prev

…

608

609

610

611

612

613

614

615

616

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:0060203	amyotrophic lateral sclerosis type 12 Aliases: ALS12 amyotrophic lateral sclerosis 12	OPTN	10133	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081294	neuronal intranuclear inclusion disease	OPTN	10133	Homo sapiens (human)	Alliance of Genome Resources
DOID:5408	Paget's disease of bone Aliases: Paget disease of bone Paget's bone disease osseous Paget's disease osteitis deformans	INPP5D OPTN SQSTM1 TNFRSF11A TNFRSF11B VCP	10133 3635 4982 7415 8792 8878	Homo sapiens (human)	Alliance of Genome Resources
DOID:1067	open-angle glaucoma Aliases: Wide-angle glaucoma glaucoma simplex open angle glaucoma pigmentary glaucoma	ADRB2 APOC3 APOE GMDS IL10 IL2 MYOC OPTN PON1 TAP1 TNF	10133 154 2762 345 348 3558 3586 4653 5444 6890 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:13544	low tension glaucoma Aliases: Normal tension glaucoma	ADRB1 APOE BDNF EDN1 HSPD1 MYOC OPTN SLC1A1 SLC1A3 SOD1 TLR4 TNF TP53	10133 153 1906 3329 348 4653 627 6505 6507 6647 7099 7124 7157	Homo sapiens (human)	Alliance of Genome Resources
DOID:1070	primary open angle glaucoma Aliases: chronic simple glaucoma	ACVR1 ADIPOQ ADRB2 APOE BDNF COL6A3 CYP1B1 EDN1 ELN GLUL LAMB2 LOXL1 MBL2 MMP1 MMP9 MYOC NOS3 OGG1 OPA1 OPTN PON1 SOD2 THBS1 TLR4 TNF TP53 WDR36	10133 1293 134430 154 1545 1906 2006 2752 348 3913 4016 4153 4312 4318 4653 4846 4968 4976 5444 627 6648 7057 7099 7124 7157 90 9370	Homo sapiens (human)	Alliance of Genome Resources
DOID:13948	bladder neck obstruction Aliases: Obstruction of bladder neck or vesicourethral orifice	ADRA1A COL1A1 COL3A1 CYP19A1 ELN HIF1A HTR2A NGF NOS3 OPTN SOD2	10133 1277 1281 148 1588 2006 3091 3356 4803 4846 6648	Homo sapiens (human)	Alliance of Genome Resources
DOID:576	proteinuria	ACE ADD3 AGER AGTR1 ALB B2M C6 CD55 CFH CLU COL4A5 F7 HAVCR1 HIF1A ICAM1 IFNB1 IL1RN IL6 LAMB2 LEPR MGAT5 MMP2 MYH9 NCKAP5 NPHS1 NPHS2 NPNT NPPB OPTN OSGEP PLA2G7 PON1 SDC1 SERPINA1 SLC9A1 SNRPD1 SORCS1 TGFB1 TLR9 TMEM67 TRPC6 VEGFA VTN	10133 114815 1191 120 1287 1604 1636 177 185 213 2155 255743 26762 3075 3091 3383 344148 3456 3557 3569 3913 3953 4249 4313 4627 4868 4879 5265 54106 5444 55644 567 6382 6548 6632 7040 7225 729 7422 7448 7827 7941 91147	Homo sapiens (human)	Alliance of Genome Resources
DOID:13641	exfoliation syndrome Aliases: Pseudoexfoliation glaucoma Pseudoexfoliation syndrome	ACVR1 APOE CLU EDN1 ELN LOXL1 LYST MMP1 MMP9 OPTN PON1 SOD2 STRA6 TLR4	10133 1130 1191 1906 2006 348 4016 4312 4318 5444 64220 6648 7099 90	Homo sapiens (human)	Alliance of Genome Resources
DOID:332	amyotrophic lateral sclerosis Aliases: ALS Lou Gehrig's disease motor neuron disease, bulbar	APOE AQP4 ATP13A2 ATP13A3 ATP13A5 BPTF C3 C5AR1 C9orf72 CASP9 CCR2 CHMP2B DCTN1 DPP6 EIF2AK2 EPG5 EPO EWSR1 FUS GDNF GOT1 GRN GSK3A GSK3B HDAC4 HMGB1 IGF1R IGF2R ITIH4 ITPR2 KDR KEAP1 KIF1B LCN2 LRRK2 MAP4 MAPT MMP1 MMP2 MMP9 MSTN NEFH NEFL NEFM NFE2L2 NRG1 OPTN PGF PON2 PON3 PPARGC1A PSMC4 PSMC5 PTGS2 PTPRZ1 SARM1 SERPINF1 SLC11A2 SLC1A2 SOD1 SOD3 SQSTM1 TARDBP TFAM UBQLN1 UBQLN2 UBQLN3 UBQLN4 UNC13A VAPA VAPB VEGFA ZNF106	10133 10891 120892 1639 1804 203228 2056 2130 2186 23025 23095 23098 23400 23435 2521 25978 2660 2668 2805 2896 2931 2932 29978 29979 3084 3146 344905 348 3480 3482 361 3700 3709 3791 3934 4134 4137 4312 4313 4318 4741 4744 4747 4780 4891 50613 5176 5228 5445 5446 5610 56893 5704 5705 5743 57724 5803 64397 6506 6647 6649 7019 718 728 729230 7422 79572 842 8878 9217 9218 9759 9817	Homo sapiens (human)	Alliance of Genome Resources
DOID:12858	Huntington's disease Aliases: HD Huntington disease Huntington's chorea	ABAT ACHE AGTR1 APOA4 ATF2 BAX BCHE BDNF CASP9 CAT CNR2 CREB1 CREBBP CTSH DNAJB2 DRD1 E2F1 EIF2AK2 ELK1 F2 FAS FASLG FKBP11 FOXP1 GIT1 GLUL GPX1 GPX6 GRIK2 GRIN2A GRIN2B HSF1 HTT IL6 IL6R ITPR1 LCP1 LEP MAP2 MBP MMP9 MTNR1A NCOR1 ND3 NFE2L2 NGFR NOG NOS3 NPY2R NRF1 OPTN PACSIN2 PARP1 PLS1 PLS3 PPARD PPARGC1A PPP1R9A PRKAA1 PTGS2 QPRT RRS1 SETDB1 SIN3A SIRT1 SLC18A3 SLC1A2 SRSF6 SYNE3 TBP TFAM TRIP10 UCP2 WIPI1 WIPI2 YBX2 ZDHHC13	10133 10891 11252 1269 1385 1386 1387 142 1512 161176 18 1812 185 1869 2002 2147 23212 23411 23475 257202 25942 26100 27086 2752 2876 28964 2898 2903 2904 3064 3297 3300 337 355 356 3569 3570 3708 3936 3952 4133 4155 43 4318 4537 4543 4780 4804 4846 4887 4899 51087 51303 5357 5358 54503 5467 55062 55607 5562 5610 5743 581 590 627 6431 6506 6572 6908 7019 7351 842 847 9241 9322 9611 9869	Homo sapiens (human)	Alliance of Genome Resources
DOID:891	progressive myoclonus epilepsy Aliases: PME progressive myoclonic epilepsy	EPM2A OPTN SCARB2 SEMA6B	10133 10501 7957 950	Homo sapiens (human)	Alliance of Genome Resources
DOID:1686	glaucoma	ACE2 AGO2 APOA4 ATF2 BAD BAX BDNF CCR5 CDKN1B CFH EEF2 EPO EPOR FAS FOXC1 HDAC1 HEPH HLA-DQB1 HLA-DRB1 JUN LGR4 LINGO1 MAS1 MMP9 MUC5AC NEFH NGF NGFR NTRK1 NTRK2 OPTN PITX2 PTGS1 PTPN11 RFTN1 SERPINE1 SH3PXD2B SNCG SQSTM1 TNF VEGFA WDR36	10133 1027 1234 134430 1386 1938 2056 2057 2296 23180 27161 285590 3065 3075 3119 3123 337 355 3725 4142 4318 4586 4744 4803 4804 4914 4915 5054 5308 55366 572 5742 5781 581 59272 627 6623 7124 7422 84894 8878 9843	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:0070033	autosomal dominant intellectual developmental disorder 3 Aliases: MRD3 autosomal dominant mental retardation 3 autosomal dominant non-syndromic intellectual disability 3	CDH15	1013	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050888	syndromic intellectual disability	AGAP1 AGAP2 AGAP5 AGAP9 AUTS2 BRPF1 DOT1L DYRK1A EZH2 FRY FRYL KDM5B OPHN1 PDZD8 PRPF19 PSMC3 UNC79 ZMYND8	10129 10765 116986 116987 118987 1859 2146 23613 26053 27339 285527 4983 5702 57578 642517 729092 7862 84444	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111180	French Canadian Leigh disease Aliases: French Canadian type COX deficiency French Canadian type Leigh syndrome French Canadian type cytochrome c oxidase deficiency Saguenay Lac saint Jean type COX deficiency Saguenay Lac saint Jean type Leigh syndrome mitochondrial complex IV deficiency nuclear type 5	LRPPRC	10128	Homo sapiens (human)	Alliance of Genome Resources
DOID:3652	Leigh disease Aliases: Infantile necrotizing encephalomyelopathy Leigh syndrome juvenile subacute necrotizing encephalomyelopathy	LRPPRC ND3 ND5 SDHA SDHC SOD2 SURF1	10128 4537 4540 6389 6391 6648 6834	Homo sapiens (human)	Alliance of Genome Resources
DOID:14250	Down syndrome Aliases: Complete trisomy 21 syndrome Down's syndrome Down's syndrome - trisomy 21 Downs syndrome G Trisomy trisomy 21 syndrome	ACTR1A CBS CTSS DBN1 DOP1A DOP1B DSCAM DSCAML1 DYRK1A HSPD1 IGFBP3 MMP9 MTHFD1 PCNT POFUT2 RELN RPLP0 SNAP25 SOD1 SRSF4 SYNJ1 SYNJ2 TIMP1 TUBA1A	10121 1520 1627 1826 1859 23033 23275 3329 3486 4318 4522 5116 5649 57453 6175 6429 6616 6647 7076 7846 875 8867 8871 9980	Homo sapiens (human)	Alliance of Genome Resources
DOID:4247	coronary restenosis	BCHE CDH13 CXCR3 ITGB2 LOX MBL2 MYC NPY5R SPP1 TNF TP53 UCP3	1012 2833 3689 4015 4153 4609 4889 590 6696 7124 7157 7352	Homo sapiens (human)	Alliance of Genome Resources
DOID:2871	endometrial carcinoma Aliases: carcinoma of the Endometrium endometrioid carcinoma endometrioid carcinoma of female Reproductive system	APC AURKB BSG CD82 CDH13 ERAP1 FGF7 GRB2 GSK3B HDAC3 HRAS JUN MMP8 MMP9 NCOA1 NCOR2 NOS3 POLE PRKCA PTGS1 PTK2 RUNX3 SFN SMAD4 SPARC TFF1 TIMP1 TP53 WNT2 WNT4 WNT5A	1012 2252 2810 2885 2932 324 3265 3725 3732 4089 4317 4318 4846 51752 5426 54361 5578 5742 5747 6678 682 7031 7076 7157 7472 7474 864 8648 8841 9212 9612	Homo sapiens (human)	Alliance of Genome Resources
DOID:303	substance-related disorder	CDH13 FASLG GSK3B HTR2C KCNMA1 KCNU1 PTEN SLC18A2	1012 157855 2932 3358 356 3778 5728 6571	Homo sapiens (human)	Alliance of Genome Resources
DOID:2349	arteriosclerosis Aliases: Arteriosclerotic vascular disease	ABCG5 ABCG8 ACAT1 AKR1B1 ALDH3A1 ALOX5 ALPL APOA1 APOB APOH B2M CCL5 CD36 CDH13 CHI3L1 EGR1 ESR1 F13A1 F7 FURIN HGF HP HSPD1 IFNGR1 IGFBP3 IL10 IL15 IL6ST ITGA2 ITGA7 KDR LCAT LDLR LEPR LMNA LOX MAP3K7 MET MMP12 MMP13 MMP14 MMP1 MMP2 MMP3 MMP9 MSR1 NME2 NOTCH4 NPPC PAPPA PON1 PPARG PTGER4 PTGS2 RELA SERPINA1 TBXAS1 TGFB1 TGFBR2 TLR4 TNFRSF14	1012 1116 1958 2099 2155 2162 218 231 240 249 3082 3240 3329 335 338 3459 3486 350 3572 3586 3600 3673 3679 3791 38 3931 3949 3953 4000 4015 4233 4312 4313 4314 4318 4321 4322 4323 4481 4831 4855 4880 5045 5069 5265 5444 5468 567 5734 5743 5970 6352 64240 64241 6885 6916 7040 7048 7099 8764 948	Homo sapiens (human)	Alliance of Genome Resources
DOID:3459	breast carcinoma Aliases: Mammary carcinoma carcinoma of breast	ABCE1 ABCG2 ADAM28 AFDN AMACR APEX1 ATM ATP7B BIN1 BRCA1 CA9 CADM1 CD46 CD59 CD82 CD9 CDC25A CDC25B CDH13 CTCF CYP24A1 DCN DDR1 EGFR ENO2 EP300 ESR1 FAS FZD1 FZD2 HDAC1 HLA-DRB1 IGF2R KDM6B KDR KLK6 KMT2D LZTS1 MDC1 MMP14 MRE11 MSH2 MSH6 NCOA1 NCOA3 NME1 PDGFRA PDGFRB PLCG1 PLK1 PLK3 POLE PRSS8 RHOA SNW1 SRD5A1 SRD5A2 STAT1 TFRC THOC5 TIMP3 TWIST1 VEGFC WNT2 ZFHX3	1012 10664 10863 11178 1263 1591 1634 1956 2026 2033 2099 22938 23135 23600 23705 2535 274 2956 3065 3123 328 3482 355 3732 3791 387 4179 4301 4323 4361 4436 463 472 4830 5156 5159 5335 5347 540 5426 5652 5653 6059 6715 6716 672 6772 7037 7078 7291 7424 7472 768 780 8085 8202 8321 8563 8648 928 9429 9656 966 993 994	Homo sapiens (human)	Alliance of Genome Resources
DOID:11054	urinary bladder cancer Aliases: bladder cancer tumor of the bladder	AKT1 ALOX12 AMACR APEX1 AREG BAX BRCA1 CA9 CASP9 CD44 CD82 CD9 CDC25A CDC25B CDH13 CDH1 CDKN1B CHEK2 COL6A3 COMT CTNNA1 CTNNB1 CTSB CXCR2 CYP1A1 CYP1B1 CYP2C9 DNMT1 E2F1 EEF1E1 EGFR ENO2 ERBB2 ERBB3 ERBB4 EZH2 F2 FAS FASLG FGFR2 FGFR3 FN1 HK1 HRAS HSPA1A ICAM1 IFNG IGFBP3 IL1RN IL2 JUP KDM5B KDR KIT KRAS KRT5 MAP2K4 MDM2 MGMT MKI67 MLH1 MMP13 MMP1 MMP2 MMP9 MRE11 MSH2 MSH6 MTR MUC1 MUC5B MYC NCSTN NME1 NME2 NOS3 PHB1 PLAU PLK1 PPARG PRKCA PTEN PTGS2 RB1 RELA RHOA RUNX3 SERPINE1 SFN SLC11A1 SMAD4 SOD2 SPARC SPP1 TERT TFF1 TGFBR1 THBS1 TIMP3 TLR2 TMEFF2 TNFRSF10A TOP2A TP53 TYMP TYMS VEGFA VEGFC VEGFD WIF1 WNT7B XRCC1	1012 1027 10765 11197 11200 1293 1312 1495 1499 1508 1543 1545 1559 1786 1869 1890 1956 2026 2064 2065 2066 207 2146 2147 2261 2263 2277 2335 23385 23600 23671 239 2810 2956 3098 3265 328 3303 3383 3458 3486 355 3557 3558 356 3579 3728 3732 374 3791 3815 3845 3852 387 4089 4193 4255 4288 4292 4312 4313 4318 4322 4361 4436 4548 4582 4609 4830 4831 4846 5054 5245 5328 5347 5468 5578 5728 5743 581 5925 5970 6416 6556 6648 6678 6696 672 7015 7031 7046 7057 7078 7097 7153 7157 727897 7298 7422 7424 7477 7515 768 842 864 8797 928 9521 960 993 994 999	Homo sapiens (human)	Alliance of Genome Resources

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements