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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **6626 - 6650** of **7942** in total

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Disease ID	Disease Name ▲	Gene Symbol	Gene ID	Organism	Source
DOID:0050770	polycystic liver disease Aliases: congenital cystic liver disease congenital hepatic cyst fibrocystic liver disease	alg8.S	431849	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0050770	polycystic liver disease Aliases: congenital cystic liver disease congenital hepatic cyst fibrocystic liver disease	ALG8 GTB1 ROT2	851807 852530 854233	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0050770	polycystic liver disease Aliases: congenital cystic liver disease congenital hepatic cyst fibrocystic liver disease	Alg8 Ucp2	293129 54315	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050770	polycystic liver disease Aliases: congenital cystic liver disease congenital hepatic cyst fibrocystic liver disease	algn-8	174542	Caenorhabditis elegans	Alliance of Genome Resources
DOID:11612	polycystic ovary syndrome Aliases: Multicystic ovaries PCOS Polycystic Ovarian disease Polycystic ovaries Stein-Leventhal synd. Stein-Leventhal syndrome polycystic ovary	ACACA ACAN ACE ADIPOQ ADRB3 AGPAT2 AKR1B1 AKR1C1 AKR1C2 AKR1C3 AKT2 ALDH1A3 ANXA5 APRT ARSD BAAT CAT CD44 CHST3 COMT CPT1A CPT2 CYP11A1 CYP11B1 CYP17A1 CYP19A1 CYP1A1 CYP1B1 CYP21A2 CYP2B6 CYP2R1 CYP51A1 DCN DHCR7 DHRS11 ENPP1 FADS1 FADS2 FBXO44 FUT7 G6PC1 GGT1 GPX1 GPX3 GYS2 H6PD HACD1 HAS1 HAS2 HAS3 HMMR HPGDS HSD11B1 HSD11B2 HSD17B1 HSD17B2 HSD17B4 HSD17B6 HSD17B7 HSD3B1 HSD3B2 ICAM1 IL1R1 ISYNA1 ITLN1 LALBA LCT LGALS3 LPCAT2 LPIN1 LPL MANEA MELTF MGAT5B MIOX MPG NAMPT NANS NEIL2 PAFAH1B1 PAPSS2 PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PLA2G7 PLAUR PNPLA2 PNPLA3 PPT1 PRKAA2 PTEN PTGS2 RENBP SCD SFTPC SLC2A4 SLC33A1 SLC35G1 SLC37A4 SRD5A1 SRD5A2 STS SULT1E1 VCAM1 VCAN	10135 10555 120227 1312 1374 1376 1462 146664 1543 1545 155 1555 1583 1584 1586 1588 1589 159371 1595 1634 1636 1645 1646 1717 176 208 220 231 23175 2529 252969 2538 2542 2678 27306 2876 2878 2998 3036 3037 3038 308 31 3161 3283 3284 3290 3291 3292 3294 3295 3383 353 3554 3906 3938 3958 3992 4023 412 414 4241 4350 5048 51477 51478 5167 5290 5291 5293 5294 5310 5329 54187 54947 5538 55586 55600 5563 570 57104 5728 5743 5973 6319 6440 6517 6715 6716 6783 7412 79154 7941 79694 80339 847 8630 8644 9060 9197 9200 93611 9370 9415 9469 9563 960	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:11612	polycystic ovary syndrome Aliases: Multicystic ovaries PCOS Polycystic Ovarian disease Polycystic ovaries Stein-Leventhal synd. Stein-Leventhal syndrome polycystic ovary	YPR1	851974	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:11612	polycystic ovary syndrome Aliases: Multicystic ovaries PCOS Polycystic Ovarian disease Polycystic ovaries Stein-Leventhal synd. Stein-Leventhal syndrome polycystic ovary	Adipoq Akt2 Comt	11450 11652 12846	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11612	polycystic ovary syndrome Aliases: Multicystic ovaries PCOS Polycystic Ovarian disease Polycystic ovaries Stein-Leventhal synd. Stein-Leventhal syndrome polycystic ovary	Akt2 Comt	24267 25233	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:8997	polycythemia vera Aliases: Osler-Vaquez syndrome Polycythaemia rubra vera Proliferative polycythaemia chronic erythremia	ACE ACO1 ACSL6 AKR1C4 ALOX5 BPGM CALR CAT CD177 CD33 CD38 CEL CH25H CHI3L1 CHIT1 CYB5R3 CYP1A1 CYP2B6 ENPP1 FH FUT1 G6PD HPGDS ICAM1 IDH1 IDH2 IL18R1 ISYNA1 LGALS1 LGALS3 LPL PCYT1A PIGA PIK3CA PIK3CB PIK3CD PIK3CG PKLR PLAUR PTEN SDC1 SMUG1 SOAT1	1056 1109 1116 1118 1543 1555 1636 1727 2271 23305 23583 240 2523 2539 27306 3383 3417 3418 3956 3958 4023 48 5130 51477 5167 5277 5290 5291 5293 5294 5313 5329 57126 5728 6382 6646 669 811 847 8809 9023 945 952	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:8432	polycythemia Aliases: Erythrocythemia	ACE ACO1 ACSL6 AKR1C4 ALOX5 BPGM CALR CD177 CD33 CEL CH25H CHI3L1 CHIT1 CYB5R3 CYP1A1 CYP2B6 ENPP1 FH FUT1 G6PD HPGDS HPRT1 IDH1 IDH2 IL18R1 ISYNA1 LGALS1 LGALS3 PIK3CA PIK3CB PIK3CD PIK3CG PKLR PLAUR SMUG1 SOAT1	1056 1109 1116 1118 1543 1555 1636 1727 2271 23305 23583 240 2523 2539 27306 3251 3417 3418 3956 3958 48 51477 5167 5290 5291 5293 5294 5313 5329 57126 6646 669 811 8809 9023 945	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:1148	polydactyly Aliases: postaxial polydactyly	ACHE DHCR7 EBP GPC3 HADHB INPP5E PIGX PIK3CA PNPLA6 PTEN SC5D UMOD	10682 10908 1717 2719 3032 43 5290 54965 56623 5728 6309 7369	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:8488	polyhydramnios	AGRN ALG12 ALG8 ALPL B3GLCT CHAT CNTN1 COMT DHCR7 DPM2 EBP FIG4 FUT8 GBA1 GBE1 GPC3 HACD1 HSD17B4 HSPG2 INPPL1 MTM1 MTMR14 PAFAH1B1 PIGN PIGY PMM2 SLC26A2 SLC35D1	10682 1103 1272 1312 145173 1717 1836 23169 23556 249 2530 2629 2632 2719 3295 3339 3636 375790 4534 5048 5373 64419 79053 79087 84992 8818 9200 9896	Homo sapiens (human)	DisGeNET
DOID:853	polymyalgia rheumatica	ICAM1 MBL2 PIK3CA PIK3CB PIK3CD PIK3CG SMUG1	23583 3383 4153 5290 5291 5293 5294	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:1389	polyneuropathy	ACACA ACE ACOT7 AGRN AKR1A1 AKR1B1 APRT ARSA B3GAT1 CANX CAT CD14 CD55 CHAT CHIT1 CNTN1 COMT CPT1C CYP17A1 CYP19A1 CYP2C8 CYP2U1 CYP3A5 CYP7B1 DAG1 DEGS1 DGAT2 ENO2 FIG4 FUCA1 GAD1 GCK GFRA1 GFRA2 GLA GPX1 HADHA HADHB HPGDS IDH1 IDH2 IGF2R LPIN1 LTC4S LYZ MAG MGLL MTM1 MTMR2 NAMPT NCAN NGLY1 NT5E NTNG1 PGM3 PGP PIK3CA PIK3CB PIK3CD PIK3CG PMM2 PNP PNPLA6 PRNP PRPS1 PSAP PTEN PTGIS RGN RPIA SARM1 SCP2 SGPL1 SLC2A4 SPTLC1 SPTLC3 ST3GAL4 TKT TPI1 TYMP	10135 10327 10558 10908 1103 1118 11332 11343 113612 126129 1272 1312 1463 1558 1577 1586 1588 1604 1605 1636 1890 2026 22854 22934 23098 231 23175 2517 2571 2645 2674 2675 27087 2717 27306 283871 2876 3030 3032 31 3417 3418 3482 353 375790 4056 4069 4099 410 4534 4860 4907 5238 5290 5291 5293 5294 5373 55304 55768 5621 5631 5660 5728 5740 6342 6484 6517 7086 7167 821 84649 847 8560 8879 8898 9104 929 9420 9896	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET
DOID:9042	polyp of corpus uteri Aliases: endometrial/uterine polyp polyp of Endometrium polyp of the Uterus polyp, uterus	CYP19A1 PTEN PTGS2 SDC1	1588 5728 5743 6382	Homo sapiens (human)	DisGeNET DisGeNET
DOID:7439	polyp of middle ear Aliases: polyp - middle ear polyp of the middle ear	CLEC10A CLEC12B CLEC5A CLEC6A CLEC7A LY75 MGLL MRC1 PIK3CA PIK3CB PIK3CD PIK3CG PSMD10 PTGS2 STS	10462 11343 23601 387837 4065 412 4360 5290 5291 5293 5294 5716 5743 64581 93978	Homo sapiens (human)	DisGeNET
DOID:4308	polyradiculoneuropathy	B3GAT1 MAG	27087 4099	Homo sapiens (human)	DisGeNET
DOID:9230	pompholyx Aliases: Cheiropompholyx DYSHYDROTIC ECZEMA Vesicular eczema of hands and/or feet dyshidrosis	ANXA5 CHI3L1 CYP4F3 ELOVL7 IDH1 IDH2 IDH3B IL1RL2 KLRB1 SULT1E1	1116 308 3417 3418 3420 3820 4051 6783 79993 8808	Homo sapiens (human)	DisGeNET
DOID:0112333	pontocerebellar hypoplasia type 16 Aliases: PCH16	MINPP1	9562	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060270	pontocerebellar hypoplasia type 2D	ATP6V0A2 ATP6V1A B3GALNT2 B4GAT1 CRPPA DAG1 DHCR24 DLST FIG4 FKRP FKTN HSPG2 LARGE1 NSDHL PAFAH1B1 PCCA PCCB PIGP PIGQ POMGNT1 POMGNT2 POMK POMT1 POMT2 RXYLT1 SDC2 STS TMTC3	10329 10585 11041 148789 160418 1605 1718 1743 2218 23545 29954 3339 412 5048 50814 5095 5096 51227 523 55624 6383 729920 79147 84197 84892 9091 9215 9896	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET
DOID:0060276	pontocerebellar hypoplasia type 7	ATP6V0A2 ATP6V1A B3GALNT2 B4GAT1 CRPPA DAG1 DHCR24 DLST FIG4 FKRP FKTN HSPG2 LARGE1 NSDHL PAFAH1B1 PIGP PIGQ POMGNT1 POMGNT2 POMK POMT1 POMT2 RXYLT1 SDC2 STS TMTC3	10329 10585 11041 148789 160418 1605 1718 1743 2218 23545 29954 3339 412 5048 50814 51227 523 55624 6383 729920 79147 84197 84892 9091 9215 9896	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:0060277	pontocerebellar hypoplasia type 8	ATP6V0A2 ATP6V1A B3GALNT2 B4GAT1 CRPPA DAG1 DHCR24 DLST FIG4 FKRP FKTN HSPG2 LARGE1 NSDHL PAFAH1B1 PIGP PIGQ POMGNT1 POMGNT2 POMK POMT1 POMT2 RXYLT1 SDC2 STS TMTC3	10329 10585 11041 148789 160418 1605 1718 1743 2218 23545 29954 3339 412 5048 50814 51227 523 55624 6383 729920 79147 84197 84892 9091 9215 9896	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:0060278	pontocerebellar hypoplasia type 9	ATP6V0A2 ATP6V1A B3GALNT2 B4GAT1 CRPPA DAG1 DHCR24 DLST FIG4 FKRP FKTN HSPG2 LARGE1 NSDHL PAFAH1B1 PIGP PIGQ POMGNT1 POMGNT2 POMK POMT1 POMT2 RXYLT1 SDC2 STS TMTC3	10329 10585 11041 148789 160418 1605 1718 1743 2218 23545 29954 3339 412 5048 50814 51227 523 55624 6383 729920 79147 84197 84892 9091 9215 9896	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET
DOID:0060055	popliteal pterygium syndrome Aliases: facio-genito-popliteal syndrome popliteal web syndrome	B3GLCT POFUT2	145173 23275	Homo sapiens (human)	DisGeNET
DOID:0060263	porencephaly	COLGALT1	79709	Homo sapiens (human)	DisGeNET DisGeNET

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