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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 **801 - 825** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:4467	clear cell renal cell carcinoma Aliases: Clear cell carcinoma of kidney clear cell kidney carcinoma conventional (Clear cell) renal cell carcinoma conventional renal cell carcinoma renal clear cell carcinoma	ACKR3 AGER BAX CXCR4 DDR1 ENG EP300 F2 FTO GATA2 IGF1R KAT8 MMP12 MYC PAK4 PDGFB SETD2 SMARCB1 SRSF4 SRSF5 SRSF6 SRSF7 TP53	10298 177 2022 2033 2147 2624 29072 3480 4321 4609 5155 57007 581 6429 6430 6431 6432 6598 7157 780 7852 79068 84148	Homo sapiens (human)	Alliance of Genome Resources
DOID:3744	cervical squamous cell carcinoma Aliases: squamous cell carcinoma of cervix squamous cell carcinoma of the Cervix Uteri	ADAR BAX BIRC2 CCR4 CD82 CSF1R FGF7 FGFR3 FOS PDPN TMBIM6 TNFRSF4 TNFSF4 TP53 TYMP	103 10630 1233 1436 1890 2252 2261 2353 329 3732 581 7009 7157 7292 7293	Homo sapiens (human)	Alliance of Genome Resources
DOID:11166	Human papillomavirus infectious disease Aliases: HPV	ADAR CD274 EGFR FGFR3 HLA-DPB1 HLA-DRB1 IL1RL1 TLR3 TLR9	103 1956 2261 29126 3115 3123 54106 7098 9173	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050629	Aicardi-Goutieres syndrome Aliases: AGS Cree encephalitis	ADAR SAMHD1	103 25939	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060257	dyschromatosis symmetrica hereditaria Aliases: reticulate acropigmentation of Dohi	ADAR	103	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060250	idiopathic scoliosis	ADGRG6 DNAH10 KATNB1 MBTPS1 ODAD3 PRMT5 PTK7 PTPN11 RUNX3 SLC39A8 SLC6A9	10300 10419 115948 196385 57211 5754 5781 64116 6536 864 8720	Homo sapiens (human)	Alliance of Genome Resources
DOID:10907	microcephaly Aliases: Microcephalus microencephaly	AARS1 AARS2 ASPM AUTS2 CARS1 CDK5RAP2 CHKA CHKB CIT COPB2 DHX37 EFTUD2 ETNK1 ETNK2 EXOC7 KATNB1 KIF20B MAPKBP1 MFSD2A NSD1 ODF2 PSMB1 PUS7 SLC25A19 TUBA1A TUBB WDR62	10300 11113 1119 1120 16 203068 23005 23265 259266 26053 284403 4957 54517 55224 55500 55755 5689 57505 57647 60386 64324 7846 833 84879 9276 9343 9585	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112236	lissencephaly 6 Aliases: LIS6	KATNB1	10300	Homo sapiens (human)	Alliance of Genome Resources
DOID:2476	hereditary spastic paraplegia Aliases: French settlement disease Strumpell-Lorrain disease familial spastic paraplegia hereditary spastic paraparesis	ALDH18A1 AP5Z1 ATL2 ATL3 ATP13A2 ATP13A3 ATP13A5 BSCL2 CAPN1 CAPN3 DNM1 DNM2 ERLIN1 ERLIN2 HSPD1 KIF5B L2HGDH NIPAL1 NIPAL4 PNPLA6 PNPLA7 PSMC4 RTN1 RTN2 RTN3 RTN4 SEC23IP SPAST	10313 10613 10908 11160 11196 152519 1759 1785 23400 25923 26580 3329 344905 348938 375775 3799 5704 57142 5832 6252 6253 64225 6683 79572 79944 823 825 9907	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110765	hereditary spastic paraplegia 12 Aliases: SPG12 autosomal dominant spastic paraplegia 12 autosomal dominant spastic paraplegia type 12	RTN1 RTN2 RTN3 RTN4	10313 57142 6252 6253	Homo sapiens (human)	Alliance of Genome Resources
DOID:3910	lung adenocarcinoma Aliases: bronchogenic lung adenocarcinoma nonsmall cell adenocarcinoma	ABCE1 ADAM28 AKR1A1 ALX4 APOC3 ATRX AZGP1 BTK CADM1 CALR CBX5 CD44 CDC73 CDH1 CHD4 CHRNA3 CHRNA5 CHRNB4 CLPTM1L COL10A1 CSF1R CXCR4 CYP24A1 DLL4 E2F1 EEF2 EGF EGFR EHMT2 ERBB2 ERBB3 ERBB4 ERCC6 ERGIC3 ESCO2 EZH2 FAS FGF9 FGFR4 FOXA1 FOXP1 FUBP1 GPX3 HSP90B1 IDH1 IDH2 IGF2R IKZF1 IL1R2 KMT2C KRAS LRP1B MAP2K1 MAP4K4 MKI67 MSH2 MUC1 MUC4 MYC NOTCH1 NUF2 PLCG1 PLOD2 PRDM1 PTCH1 PTPN13 PTPRB PTPRJ RARB RBM10 RNF43 RUNX1 SDC1 SERPINA3 SETD2 SLC1A5 SLC3A2 SLC7A5 SNRPB SNRPE SOX30 SPOP SRC TERT TIMP3 UBR5 XPO1 XRCC1 ZFHX3	10320 10327 10863 10919 11063 1108 1136 1138 1143 12 1300 1436 157570 1591 1869 1938 1950 1956 2064 2065 2066 2074 2146 2254 2264 23468 23705 27086 2878 29072 3169 3417 3418 345 3482 355 3845 4288 4436 4582 4585 4609 463 4851 51366 51614 5335 53353 5352 54567 546 54894 5604 563 5727 5783 5787 5795 58508 5915 60529 6059 6382 639 6510 6520 6628 6635 6714 695 7015 7078 7184 7514 7515 7850 7852 79577 81037 811 8140 8241 83540 8405 861 8880 9448 960 999	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 ABCG2 ABO BAX BCR CAST CD46 CD79B CD86 CFB CREBBP CSF3 CSPG4 CYP1A1 CYP3A5 DPYD ENG EZH2 F3 FAS FGA FLT3 GNB1 GPI GPX1 HDAC1 HDAC2 HDAC4 HFE HK1 HLA-DQA1 HLA-DQB1 IFNG IKZF1 IL10 IRF4 KDM2B KDM3B KDM6A KMT2A KRAS MEFV MTR MYC NBN NOS3 NOTCH3 NRAS NUP214 PON1 PTEN SNRPE TERT TYMS XRCC1	10320 1244 1387 1440 1464 1543 1577 1806 2022 2146 2152 2243 2322 2782 28 2821 2876 3065 3066 3077 3098 3117 3119 3458 355 3586 3662 3845 4179 4210 4297 4548 4609 4683 4846 4854 4893 51780 5243 5444 5728 581 613 629 6635 7015 7298 7403 7515 8021 831 84678 942 9429 974 9759	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080630	B-lymphoblastic leukemia/lymphoma Aliases: B lymphoblastic leukemia/lymphoma B-ALL precursor B lymphoblastic lymphoma/leukemia	ABL1 AKR1C3 BRD2 CYP3A5 F13A1 F3 FLT3 IKZF1 STAT5A TFPI TNFSF13 TP53	10320 1577 2152 2162 2322 25 6046 6776 7035 7157 8644 8741	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081155	common variable immunodeficiency 13	IKZF1	10320	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050560	Walker-Warburg syndrome Aliases: HARD syndrome cerebroocular dysplasia-muscular dystrophy syndrome	B4GAT1 COL4A1 CRPPA FKRP FKTN POMGNT1 POMT1 POMT2 RXYLT1	10329 10585 11041 1282 2218 29954 55624 729920 79147	Homo sapiens (human)	Glyco-Disease Genes Database Glyco-Disease Genes Database Alliance of Genome Resources
DOID:0111239	congenital muscular dystrophy-dystroglycanopathy type A10 Aliases: MDDGA10 Walker-Warburg syndrome or muscle-eye-brain disease, TMEM5-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A10	RXYLT1	10329	Homo sapiens (human)	Alliance of Genome Resources
DOID:2945	severe acute respiratory syndrome Aliases: SARS SARS-CoV infection	ABO ACE2 ANPEP BPI C5AR1 CASP9 CCL2 CCL5 CD14 CD4 CD68 CD9 CEACAM8 CLCF1 CLEC4M FGF7 FSHB HLA-B HLA-DRA HLA-DRB1 HP IFNG IL10 IL1R1 IL6 ITGA2B LHB MSR1 PECAM1 PLAT POMC PRL RAB31 SERPINA3 STAT1 TGFB1 THBD TLR2 TNF TSHB	10332 1088 11031 12 2252 23529 2488 28 290 3106 3122 3123 3240 3458 3554 3569 3586 3674 3972 4481 5175 5327 5443 5617 59272 6347 6352 671 6772 7040 7056 7097 7124 7252 728 842 920 928 929 968	Homo sapiens (human)	Alliance of Genome Resources
DOID:2957	pulmonary tuberculosis	ABCB1 ADA2 ADIPOQ AKT1 ALOX5 ATF3 C3 CCL1 CCL2 CCL5 CCR5 CD14 CD163 CD1D CD209 CD274 CD36 CD86 CLEC4M EGFR EREG GBE1 HAVCR2 HLA-DPB1 HLA-DQB1 HLA-DRB1 IL13 IL15 IL1RN IL4R IL6 IL6R ITIH4 JUN KIR3DS1 LTA MARCO MBL2 MIF NOD2 NOS2 PDCD1 PDCD1LG2 PLAUR SFTPA1 SLC11A1 TAP1 TLR1 TLR2 TLR4 TLR9 TNF TREM1	10332 1234 1956 2069 207 240 2632 29126 30835 3115 3119 3123 3557 3566 3569 3570 3596 3600 3700 3725 3813 4049 4153 4282 467 4843 5133 51816 5243 5329 54106 54210 6346 6347 6352 64127 653509 6556 6890 7096 7097 7099 7124 718 80380 84868 8685 912 929 9332 9370 942 948	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050598	extrapulmonary tuberculosis	CD209 CLEC4M EREG	10332 2069 30835	Homo sapiens (human)	Alliance of Genome Resources
DOID:874	bacterial pneumonia Aliases: Pneumonia due to other gram-negative bacteria gram-negative pneumonia	CAT CSF3 CYP2J2 F2 IL1RL1 ITGB3 MBL2 MMP9 MPO PDPN PECAM1 SFTPA1 SFTPA2 SFTPB SFTPC SFTPD TLR2 TLR6 TNF TREM1	10333 10630 1440 1573 2147 3690 4153 4318 4353 5175 54210 6439 6440 6441 653509 7097 7124 729238 847 9173	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:399	tuberculosis	BTNL2 CCL1 CD209 CD274 CYP2B6 CYP2C19 EREG HLA-A HLA-B HLA-DQB1 HLA-DRB1 IFNG IFNGR1 IL22 IRAK3 KIR3DL1 KIR3DS1 KLRK1 NFE2L2 NRG1 PDCD1 SLC11A1 SPP1 TLR1 TLR2 TLR6 TNF TNFRSF1B	10333 11213 1555 1557 2069 22914 29126 30835 3084 3105 3106 3119 3123 3458 3459 3811 3813 4780 50616 5133 56244 6346 6556 6696 7096 7097 7124 7133	Homo sapiens (human)	Alliance of Genome Resources
DOID:8677	perinatal necrotizing enterocolitis Aliases: ENTEROCOLITIS NECROTIZING Necrotizing enterocolitis in fetus OR newborn Perinatal necrotising enterocolitis Pseudomembranous enterocolitis in newborn necrotizing enterocolitis	CD14 CD40 CD40LG EGF HBEGF IL10 IL10RB IL6 MUC2 PARP1 PLAUR PTAFR TJP1 TLR1 TLR2 TLR3 TLR4 TLR5 TLR6 TLR7 TLR9 TNF	10333 142 1839 1950 3569 3586 3588 4583 51284 5329 54106 5724 7082 7096 7097 7098 7099 7100 7124 929 958 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:13564	aspergillosis Aliases: Infection due to Aspergillus	AGER CD209 CLEC1A CLEC7A IL15 TLR1 TLR6	10333 177 30835 3600 51267 64581 7096	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060000	infective endocarditis	TLR6	10333	Homo sapiens (human)	Alliance of Genome Resources

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