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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 **326 - 350** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:1273	respiratory syncytial virus infectious disease Aliases: RSV respiratory syncytial virus	ACE2 CCR5 CD28 HLA-G ICAM1 IFNG IL10 IL17A IL5RA IL6 IL9 NGF NGFR PDCD1 SFTPA1 SFTPB SFTPC SFTPD TACR1 TLR4 TLR7 TLR8 TSLP	1234 3135 3383 3458 3568 3569 3578 3586 3605 4803 4804 51284 51311 5133 59272 6439 6440 6441 653509 6869 7099 85480 940	Homo sapiens (human)	Alliance of Genome Resources
DOID:14069	cerebral malaria Aliases: Malarial encephalitis	ACE2 NRG1	3084 59272	Homo sapiens (human)	Alliance of Genome Resources
DOID:4492	avian influenza Aliases: avian flu bird flu	ACE2 PTGS2	5743 59272	Homo sapiens (human)	Alliance of Genome Resources
DOID:437	myasthenia gravis	ACHE ADRB2 CHRM1 CXCR3 FAS HLA-DQA1 HLA-DQB1 HLA-DRB1 IL2RB MUSK	1128 154 2833 3117 3119 3123 355 3560 43 4593	Homo sapiens (human)	Alliance of Genome Resources
DOID:9470	bacterial meningitis	ACHE BCHE BDNF CD46 CHI3L1 MMP9 NGF PARP1 TREM1	1116 142 4179 43 4318 4803 54210 590 627	Homo sapiens (human)	Alliance of Genome Resources
DOID:2297	leptospirosis Aliases: Fort Bragg fever Leptospirosis icterohaemorrhagica Rat Catcher's Yellows Weil's disease nanukayami fever spirochetal jaundice	ACHE BCHE F2 MBL2	2147 4153 43 590	Homo sapiens (human)	Alliance of Genome Resources
DOID:10487	Hirschsprung's disease Aliases: Hirschsprung disease aganglionic megacolon congenital megacolon macrocolon pelvirectal achalasia total intestinal aganglionosis	ACHE CD14 EDNRB ERBB2 GDNF GFRA1 IHH ITGB1 KIT NGFR NTRK1 PINK1 RET SHH SLC2A1 STX1A WNT8B	1910 2064 2668 2674 3549 3688 3815 43 4804 4914 5979 6469 65018 6513 6804 7479 929	Homo sapiens (human)	Alliance of Genome Resources
DOID:8645	subacute delirium	ACHE HTR1A	3350 43	Homo sapiens (human)	Alliance of Genome Resources
DOID:6088	acute stress disorder Aliases: traumatic stress disorder	ACHE	43	Homo sapiens (human)	Alliance of Genome Resources
DOID:12978	Plasmodium vivax malaria Aliases: Malaria by Plasmodium vivax Vivax Malaria	ACKR1	2532	Homo sapiens (human)	Alliance of Genome Resources
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:2600	laryngeal carcinoma Aliases: cancer of larynx carcinoma of larynx	ACKR3 CXCR4 KMT2C UBR5 XRCC1	51366 57007 58508 7515 7852	Homo sapiens (human)	Alliance of Genome Resources
DOID:13268	porphyria Aliases: Hematoporphyria Porphyrinopathy disorder of porphyrin and hem metabolism disorder of porphyrin metabolism	ACO1 ALAS1 EPO GBE1 IREB2	2056 211 2632 3658 48	Homo sapiens (human)	Alliance of Genome Resources
DOID:1724	duodenal ulcer Aliases: Curling Ulcer Curling's ulcers Stress Ulcer	ACO1 CFTR SLC11A2 STAT3 TFRC VEGFA	1080 48 4891 6774 7037 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:14330	Parkinson's disease Aliases: Parkinson disease paralysis agitans	ACO1 AKL1 ARK1 HMG1 HMG2 HSF1 INP53 OGG1 PBS2 PGI1 PGK1 PRK1 PSD1 RRN3 SMF3 SMY2 SYH1 TIF4631 YAK1	850370 850721 851013 851171 852351 852470 852495 852806 853071 853300 853313 853734 854276 854713 854900 854942 855552 855711 855999	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1289	neurodegenerative disease Aliases: degenerative disease	ACO1 BUD2 FIG4 HRR25 MTM1 NTE1 OSI1 RHO1 RPN1 TPI1	851013 851620 853173 853770 853792 854943 855392 855897 856294 856422	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:331	central nervous system disease	ACO1 CSC1 ISW1 PHM7	850942 851013 852547 854070	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1891	optic nerve disease Aliases: disorder of the second nerve optic nerve disorder optic neuropathy	ACO1	851013	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0050883	infantile cerebellar-retinal degeneration	ACO1	851013	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111442	optic atrophy 9 Aliases: OPA9	ACO1	851013	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1891	optic nerve disease Aliases: disorder of the second nerve optic nerve disorder optic neuropathy	ACO2 AGER EDN1	177 1906 50	Homo sapiens (human)	Alliance of Genome Resources
DOID:1289	neurodegenerative disease Aliases: degenerative disease	ACO2 AIMP1 APLP2 BCL11A BCL11B CAT CLEC16A DEGS1 DEGS2 DVL1 DVL3 DYNC1H1 EPO FAT4 FIG4 FUS GC GGA2 GGA3 GRIA1 GRIA2 GRIA3 GRIA4 GRIK1 GRIK2 GRIK3 GRIN1 HNRNPA1 HNRNPA1L2 HNRNPA2B1 HNRNPA3 HPDL HTT KIF5B LATS1 LATS2 LRRK2 MAPT MARK2 MARK3 MARS2 MEGF10 MEGF11 MTMR10 MTMR11 NFKB1 NFKB2 NPLOC4 NRDC NUP50 PACSIN2 PEAR1 PLA2G6 PNPLA6 PNPLA7 PON1 PON2 PON3 PRKAG2 PRKAG3 PSMA3 PSMA5 PSMB1 PSMC4 PSMD2 PTCH1 PTCH2 RASA1 RHOA RHOB RHOC SARM1 SCNN1A SCNN1B SCNN1D SCNN1G SDHA SLC17A6 SLC17A8 SLC1A1 SLC1A2 SLC1A3 SLC1A4 SLC1A5 SLC1A6 SLC1A7 STK4 TARDBP TBP TPI1 TRAK1 TRAK2 TRPC4 TRPC5 TSPAN3 TSPAN7 UBQLN1 UBQLN2 UBQLN4 UBR1 UFD1 VAPA VAPB VCP YAP1 YBX2	10099 10413 10762 10903 10908 11252 120892 123099 144983 1778 1855 1857 197131 2011 2056 220988 22906 23062 23098 23163 23274 23435 246213 2521 2638 26524 2890 2891 2892 2893 2897 2898 2899 2902 29978 29979 3064 3178 3181 334 375033 375775 3799 387 388 389 4137 4140 4790 4791 4898 50 51087 51422 53335 53632 5444 5445 5446 54893 55666 5684 5686 5689 56893 5704 5708 57084 5727 5921 6337 6338 6339 6340 6389 64919 6505 6506 6507 6509 6510 6511 6512 66008 6789 6908 7102 7167 7223 7224 7353 7415 79633 8398 84465 84466 847 84842 8560 8643 9113 9217 9218 9255 92935 9896	Homo sapiens (human)	Alliance of Genome Resources
DOID:331	central nervous system disease	ACO2 GRIA1 GRIA2 GRIA3 GRIA4 HGF IL6 IRF2BP1 IRF2BP2 IRF2BPL SMARCA1 SMARCA5 TAOK1 TAOK2 TMEM63A TMEM63B TMEM63C	26145 2890 2891 2892 2893 3082 3569 359948 50 55362 57156 57551 64207 6594 8467 9344 9725	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050883	infantile cerebellar-retinal degeneration	ACO2	50	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111442	optic atrophy 9 Aliases: OPA9	ACO2	50	Homo sapiens (human)	Alliance of Genome Resources

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