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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 **226 - 250** of **4649** in total

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Disease ID	Disease Name ▼	Gene Symbol	Gene ID	Organism	Source
DOID:2562	suppurative periapical periodontitis Aliases: Apical abscess Dentoalveolar abscess Periapical abscess Suppurative apical periodontitis	ELANE	1991	Homo sapiens (human)	Alliance of Genome Resources
DOID:11506	suppurative otitis media Aliases: Otitis media with effusion - purulent Purulent otitis media	IFNG TLR2 TLR4	3458 7097 7099	Homo sapiens (human)	Alliance of Genome Resources
DOID:9007	sudden infant death syndrome Aliases: Cot death Crib death SIDS Sudden death of nonspecific cause in infancy	SCN5A SLC6A4 VEGFA	6331 6532 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060175	succinic semialdehyde dehydrogenase deficiency Aliases: 4-hydroxybutyric aciduria SSADH gamma-hydroxybutyric aciduria	ALDH5A1	7915	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:9973	substance dependence	CREB1 FOSB	1385 2354	Homo sapiens (human)	Alliance of Genome Resources
DOID:302	substance abuse	ADRA2A DRD4 HTR1A HTR1B NRG1 SLC6A4	150 1815 3084 3350 3351 6532	Homo sapiens (human)	Alliance of Genome Resources
DOID:13560	subserous uterine fibroid Aliases: subserous leiomyoma of uterus	TNRC6B	23112	Homo sapiens (human)	Alliance of Genome Resources
DOID:12897	submandibular gland disease	FN1	2335	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111169	subcortical band heterotopia Aliases: HeCo band heterotopia double cortex syndrome heterotopic cortex subcortical laminar heterotopia	WDR75	84128	Homo sapiens (human)	Alliance of Genome Resources
DOID:8970	subacute sclerosing panencephalitis Aliases: Immunosuppressive measles encephalitis Van Bogaert's sclerosing leukoencephalitis subacute sclerosing leukoencephalopathy	ACE IFNL1	1636 282618	Homo sapiens (human)	Alliance of Genome Resources
DOID:8645	subacute delirium	ACHE HTR1A	3350 43	Homo sapiens (human)	Alliance of Genome Resources
DOID:4751	striatonigral degeneration	NUP62	23636	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070352	stress-induced childhood-onset neurodegeneration with variable ataxia and seizures Aliases: CONDSIAS	ADPRS BPHL PARG	54936 670 8505	Homo sapiens (human)	Alliance of Genome Resources
DOID:540	strabismus	BMP4	652	Homo sapiens (human)	Alliance of Genome Resources
DOID:9637	stomatitis	CAT	847	Homo sapiens (human)	Alliance of Genome Resources
DOID:76	stomach disease Aliases: Gastropathy stomach disorder	CALCA HLA-DQB1 MUC5AC PTEN	3119 4586 5728 796	Homo sapiens (human)	Alliance of Genome Resources
DOID:5517	stomach carcinoma Aliases: cancer of the stomach carcinoma of stomach gastric carcinoma	AZGP1 BCOR BRCA1 ERBB2 ERBB3 ERBB4 FGFR2 GRB7 KDM4C KMT2C KRAS MDC1 MMP1 MMP2 MMP9 MRE11 MUTYH PARP1 RNF43 SLC3A2 SPARC SPINT1 TNFAIP3 XPO1 XRCC1	142 2064 2065 2066 2263 23081 2886 3845 4312 4313 4318 4361 4595 54880 54894 563 58508 6520 6678 6692 672 7128 7514 7515 9656	Homo sapiens (human)	Alliance of Genome Resources
DOID:10534	stomach cancer Aliases: gastric cancer gastric neoplasm	ABL1 ACE ACVR1B ADAR ADGRB1 ADM AKR1B1 ANXA1 APC ARID1A ARPC1B ASPM ATM ATP4B BAMBI BAX BCOR BGN BRCA1 BST2 CALR CASP9 CCL5 CCN3 CD1D CD274 CD8A CDK12 CES1 CHRNA3 COL6A3 CSF1R CTNNB1 CUX1 CXCR4 CYP1A1 CYP2E1 DAXX DDR2 DICER1 DOCK6 EEF1E1 EEF2 EFNB1 EFNB2 EPHB1 ERBB2 ERCC5 ERCC6 EZH2 FGFR2 FGFR4 FOXA1 FOXM1 FUBP1 FUT11 GDA GLDC GPX1 GPX3 GSE1 HDAC2 HLA-DQA1 IDH2 IGFBP3 IL10 IL1RN IL5 IL6 IL6R IL6ST IL7R JAK1 KDM6A KDR KIF18A KMT2C KMT2D KRAS LRP1B LRRN1 MAP3K1 MAP4K4 MKI67 MMP9 MUTYH NBEA NCOA2 NFKB1 NTRK3 NUF2 PARP1 PCNA PDCD1 PIK3CA PTCH1 PTEN PTPN11 RAC1 RGN RICTOR RNF43 RUNX1 RUNX3 SETD2 SGCE SHH SLC7A5 SMO SOD2 SPOP SRC STAT3 STIM1 TBX3 TEP1 TERT TET2 TFF1 TMEM260 TNFRSF11A TP53 TTR UBR5 XPO1 XRCC1	10095 103 10499 1066 1136 1293 133 142 1436 1499 1523 1543 1571 1616 1636 170384 1938 1947 1948 2047 2064 2073 2074 2146 2263 2264 2305 231 23199 23405 25 253260 25805 259266 26960 2731 2876 2878 29072 29126 301 3066 3117 3169 324 3418 3486 3557 3567 3569 3570 3572 3575 3586 3716 3791 3845 4214 4288 4318 4595 472 4790 4856 4916 4921 496 5111 5133 51366 51755 5290 53353 54790 54880 54894 54916 5727 5728 575 57572 57633 5781 581 58508 5879 633 6352 6469 6608 6648 6714 672 6774 6786 684 6926 7011 7015 7031 7157 7276 7403 7514 7515 7852 8085 811 8140 81930 8289 83540 8405 842 861 864 8792 8880 8910 91 9104 912 925 9448 9521 9615	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111561	stiff skin syndrome Aliases: SSKS	FBN1	2200	Homo sapiens (human)	Alliance of Genome Resources
DOID:1701	steroid inherited metabolic disorder	HSD17B7	51478	Homo sapiens (human)	Alliance of Genome Resources
DOID:9452	steatotic liver disease Aliases: Fatty change of liver SLD Steatosis of liver alcoholic fatty liver fatty liver disease hepatic lipidosis hepatic steatosis	ABCA1 ABCC2 ABCC3 ACACA ACACB ACOX1 ADIPOQ ADRB2 AHCY ALPL APOA1 APOB APOE CAT CCL5 CD163 CDIPT CPE CPS1 CTSB CYP2E1 DGAT2 FGFR1 G6PC1 GCK GGT1 GPX1 HADHA HADHB HFE HSPA5 HTR2A HTR2B IL10 IL13RA2 IL6 INS INSR LDLR LEP LGALS3 LRP6 MC4R NFKB1 NOX4 NR3C2 OPA1 PLAU PNPLA3 PPARA PPARG PPARGC1A PTEN PTGS2 RELA SEC63 SHC1 SIRT1 SLCO1A2 UCP2	10423 10891 11231 1244 1363 1373 1508 154 1571 19 191 2260 23411 249 2538 2645 2678 2876 3030 3032 3077 31 32 3309 335 3356 3357 338 348 3569 3586 3598 3630 3643 3949 3952 3958 4040 4160 4306 4790 4976 50507 51 5328 5465 5468 5728 5743 5970 6352 6464 6579 7351 80339 84649 847 8714 9332 9370	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111556	steatocystoma multiplex Aliases: multiple sebaceous cysts sebocystomatosis	KRT17	3872	Homo sapiens (human)	Alliance of Genome Resources
DOID:1824	status epilepticus Aliases: Grand mal status	ABAT ABCB1 ABCC2 ABCC8 ABCG2 ACAN ADAM10 ADAM9 ANK3 APEX1 APOD AQP1 AQP4 ATM BAX BDNF CASP6 CCL2 CCR5 CFL1 CKMT1A CKMT1B CNR1 CX3CL1 CYP11A1 DAB1 DMD DPYSL2 GABRB3 GHSR GRIA1 GRIA2 GRIK1 GRIN1 GRIN2A GRN GSK3B H2AX HCN1 HRH3 HSD11B1 HSPA1A IDH2 IL6ST KCNC4 KCNJ11 KCNK3 MEF2C MMP9 MTOR NLGN1 NLGN2 NR3C1 NT5E NTF3 OGG1 OLIG2 PGF PLAT PLAU PLAUR PTGS2 PTPRZ1 RELA RELN SLC6A8 SLC8A1 SLC8A2 SLC8A3 SOCS3 SOD2 SRC SSTR4 TFAM TNF XRN2	102 10215 1072 11255 1159 1234 1244 1268 1583 1600 1756 176 18 1808 22803 22871 2475 2562 2693 288 2890 2891 2896 2897 2902 2903 2908 2932 3014 328 3290 3303 3418 347 348980 3572 358 361 3749 3767 3777 4208 4318 472 4907 4908 4968 5228 5243 5327 5328 5329 548596 5649 5743 57555 5803 581 5970 627 6347 6376 6535 6543 6546 6547 6648 6714 6754 6833 7019 7124 839 8754 9021 9429	Homo sapiens (human)	Alliance of Genome Resources
DOID:9362	status asthmaticus Aliases: Asthma with status asthmaticus Severe asthma attack	IL5 MPO	3567 4353	Homo sapiens (human)	Alliance of Genome Resources

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