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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 **3001 - 3025** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▼
DOID:8437	intestinal obstruction	ACSBG1 CD55 GGT1 PTGES PTGS2 SDHA SDHB SDHC SDHD	1604 23205 2678 5743 6389 6390 6391 6392 9536	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:4610	intestinal benign neoplasm Aliases: intestinal tumors intestine growth neoplasm of intestinal tract	B4GALNT1 CEACAM5 DCN EFNA1 GPX1 GPX2 HPGDS PIK3CA PIK3CB PIK3CD PIK3CG PLA2G2A PRSS8 PTGDS PTGS2 SHMT1 SMC3 TIGAR	1048 1634 1942 2583 27306 2876 2877 5290 5291 5293 5294 5320 5652 57103 5730 5743 6470 9126	Homo sapiens (human)	DisGeNET DisGeNET
DOID:10155	intestinal cancer Aliases: malignant intestinal tumors malignant neoplasm of intestine	B4GALNT1 CEACAM5 DCN EFNA1 GPX1 GPX2 HPGDS PIK3CA PIK3CB PIK3CD PIK3CG PLA2G2A PRSS8 PTGDS PTGS2 SHMT1 SMC3 TIGAR	1048 1634 1942 2583 27306 2876 2877 5290 5291 5293 5294 5320 5652 57103 5730 5743 6470 9126	Homo sapiens (human)	DisGeNET DisGeNET
DOID:456	ascariasis Aliases: Ascariasis - roundworm	CAT CHIT1 CYP1A1 SIGLEC1	1118 1543 6614 847	Homo sapiens (human)	DisGeNET DisGeNET
DOID:10486	intestinal atresia	SLC2A2 SLC2A5 SLC5A1	6514 6518 6523	Homo sapiens (human)	DisGeNET
DOID:3669	intermittent claudication Aliases: Charcot's syndrome	ABO ACE AGXT ALDH7A1 BAD CALR CD14 CHI3L1 CYP1A1 CYP1A2 CYP2C19 DLD ENPP1 GPX1 ICAM1 KLRB1 LIPC PCYT1A SIRT2 SLC2A10 SRD5A1 VCAM1 VCAN XYLT1 XYLT2	1116 1462 1543 1544 1557 1636 1738 189 22933 28 2876 3383 3820 3990 501 5130 5167 572 64131 64132 6715 7412 81031 811 929	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:3892	insulinoma Aliases: Insulin-Producing tumor of Islet cells Islet cell adenoma	ABO ACO2 ACSS2 CAT CD44 CHGA DHCR24 ENPP1 G6PC1 G6PC2 GAD1 GAD2 GCK GPD2 HK1 INPPL1 INS KL LGALS3 MCAT MRC1 NCAM1 PCYT1A PDHX PIK3CG PKD1 PLA2G15 PTEN PYGM SDHA SDHB SDHD SLC2A2 SLC2A3 TKT TNKS	1113 1718 23659 2538 2571 2572 2645 27349 28 2820 3098 3630 3636 3958 4360 4684 50 5130 5167 5294 5310 55902 5728 57818 5837 6389 6390 6392 6514 6515 7086 8050 847 8658 9365 960	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:8469	influenza Aliases: Influenza with other manifestations flu influenza with non-respiratory manifestation	ABO AGA AKR1C4 APRT ARSF B3GAT1 B3GNT3 BST2 CD14 CD177 CD248 CD38 CD44 CD48 CD55 CEL CLEC10A CLEC7A CLEC9A CPT2 DDOST DLAT DPEP1 ENO1 FCN2 FUT2 GAD1 GAL3ST1 GALNS GAPDH GGT1 GLA GLDC GOLPH3 GPI HACD1 ICAM1 IL18R1 ISYNA1 KLRB1 KLRD1 LGALS9 MBL2 MMUT MPPE1 MRC1 NAGA NEU1 NPL PARP12 PARP9 PDIA3 PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PKM PRKAA2 PRNP PRSS8 PSMD10 PTEN PTGS1 PTGS2 SDC1 SELL SFTPD SIGLEC1 SLC27A5 SLC35A1 SPHK2 ST3GAL3 ST6GAL1 TECR UGT1A10 UGT1A3 UGT1A4 UGT1A5 UGT1A6 UGT1A7 UGT1A8 UGT1A9	10331 10462 10559 1056 10998 1109 1376 1604 1650 1737 175 1800 2023 2220 2524 2571 2588 2597 2678 27087 2717 2731 28 2821 283420 2923 3383 353 3820 3824 3965 4153 416 4360 4594 4668 4758 51477 5290 5291 5293 5294 5310 5315 54575 54576 54577 54578 54579 54600 54657 54659 5563 5621 5652 56848 57124 57126 5716 5728 5742 5743 6382 6402 64083 6441 64581 64761 6480 6487 65258 6614 684 80896 83666 8809 9200 929 9514 952 9524 960 962	Homo sapiens (human)	DisGeNET
DOID:3008	invasive ductal carcinoma Aliases: Infiltrating ductal carcinoma of breast Invasive ductal carcinoma, NST ductal adenocarcinoma	ABO ADH4 AKT1 ALDOA ASAH1 ATP6AP2 CD14 CD44 CHI3L1 CTSA CYP19A1 DCN DHCR24 DHRS11 DPEP1 ENO1 FUT3 GAL3ST1 GPX3 HMMR HPGDS HPSE HSD17B12 HSD17B1 HSD17B7 IDH1 KL KLB LGALS1 LGALS3 MCAT MGAT5 MGLL NAMPT NEU1 PCNA PDIA3 PFKFB4 PIK3CA PIK3CB PIK3CD PIK3CG PIP5K1C PLCB2 POFUT1 PRKAA2 PSMD10 PTEN PTGS2 RGN SDC1 SELE SLC35B2 SMUG1 ST8SIA1 SULF2 UGCG VTCN1	10135 10159 10855 1116 11343 127 152831 1588 1634 1718 1800 2023 207 226 23396 23509 23583 2525 27306 27349 28 2878 2923 3161 3292 3417 347734 3956 3958 4249 427 4758 5111 51144 51478 5210 5290 5291 5293 5294 5330 5476 5563 55959 5716 5728 5743 6382 6401 6489 7357 79154 79679 9104 929 9365 9514 960	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET Alliance of Genome Resources
DOID:12336	male infertility	ACE ACSBG2 ACSL6 ALDH2 ANXA5 ATP6V0A2 CAT CCDC115 CLC CLEC7A COMT CTNS CYP17A1 CYP19A1 CYP1A1 CYP1B1 CYP2B6 ENO1 ENO4 GALNTL5 GBA2 GPX3 HPGDS LDHC MPG OGG1 PDHA2 PDIA3 PGAM4 PIK3CA PIK3CB PIK3CD PIK3CG PPT1 RGN SRGN	1178 1312 1497 1543 1545 1555 1586 1588 1636 168391 2023 217 23305 23545 27306 2878 2923 308 387712 3948 4350 441531 4968 5161 5290 5291 5293 5294 5538 5552 57704 64581 81616 84317 847 9104	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:5223	infertility	ABO ACOT7 BAAT CD14 CD44 CYP17A1 EFNA5 GBA2 H6PD HJV HSD17B1 HSD17B3 KL PLCB1 PLCZ1	11332 148738 1586 1946 23236 28 3292 3293 570 57704 89869 929 9365 9563 960	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:8568	infectious mononucleosis Aliases: Filatov's disease Gammaherpesviral mononucleosis Monocytic angina Pfeiffer's disease glandular fever mononucleosis	KLRD1 NCAM1	3824 4684	Homo sapiens (human)	DisGeNET
DOID:782	renal infectious disease	ACE CYP2C9 DCN GLA HSPG2 MMUT PKM PLA2R1 SDC1 SDC2 SFTPD SLC3A1 TM7SF2 UMOD	1559 1634 1636 22925 2717 3339 4594 5315 6382 6383 6441 6519 7108 7369	Homo sapiens (human)	DisGeNET DisGeNET
DOID:3156	hypomelanosis of Ito Aliases: Bloch-Siemans syndrome Incontinentia pigmenti achromians syndrome Ito's nevus incontinentia pigmenti achromians nevus of Ito	ACACA CD38 CEL CHIT1 CLEC7A COLEC11 CYP1B1 CYP51A1 G6PD IL1R1 MASP1 MPG NSDHL PARP9 SFTPD SLC27A5 SMUG1	1056 10998 1118 1545 1595 23583 2539 31 3554 4350 50814 5648 6441 64581 78989 83666 952	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET
DOID:12305	Bloch-Sulzberger syndrome Aliases: Incontinentia pigmenti Incontinentia pigmenti syndrome	ACACA CD38 CEL CHIT1 CLEC7A COLEC11 CYP1B1 CYP51A1 G6PD IL1R1 MASP1 MPG NSDHL PARP9 SFTPD SLC27A5 SMUG1	1056 10998 1118 1545 1595 23583 2539 31 3554 4350 50814 5648 6441 64581 78989 83666 952	Homo sapiens (human)	DisGeNET DisGeNET Alliance of Genome Resources
DOID:10646	schizotypal personality disorder	COMT	1312	Homo sapiens (human)	DisGeNET DisGeNET
DOID:3401	inappropriate ADH syndrome Aliases: SIADH syndrome of Inappropriate Antidiuretic Hormone Secretion syndrome of inappropriate secretion of ADH syndrome of inappropriate secretion of antidiuretic hormone syndrome of inappropriate vasopressin secretion	ACE COMT	1312 1636	Homo sapiens (human)	DisGeNET
DOID:10937	impulse control disorder	APRT COMT PAFAH1B1 PLCD1 PLCG1	1312 353 5048 5333 5335	Homo sapiens (human)	DisGeNET
DOID:12400	kleptomania Aliases: Pathological stealing	APRT COMT PAFAH1B1 PLCD1 PLCG1	1312 353 5048 5333 5335	Homo sapiens (human)	DisGeNET
DOID:8504	impetigo	GALNS	2588	Homo sapiens (human)	DisGeNET
DOID:0111147	angioimmunoblastic T-cell lymphoma	DLAT GAPDH IDH1 IDH2 PIK3CA PIK3CB PIK3CD PIK3CG PLCG1 SMUG1 STS	1737 23583 2597 3417 3418 412 5290 5291 5293 5294 5335	Homo sapiens (human)	DisGeNET
DOID:1557	hypersensitivity reaction type III disease Aliases: immune complex disease	CD22 MASP2	10747 933	Homo sapiens (human)	DisGeNET
DOID:0060656	autosomal recessive congenital ichthyosis 1 Aliases: ARCI1	ACE ALDH3A2 ALOX12B AMY2B CERS3 COG7 DGAT1 EBP ELOVL4 GBA1 HSD17B6 LPIN2 MPDU1 PNPLA2 PNPLA6 SGPL1 STS SULT2B1	10682 10908 1636 204219 224 242 2629 280 412 57104 6785 6820 8630 8694 8879 91949 9526 9663	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET
DOID:1699	obsolete congenital ichthyosiform erythroderma	ACE ADH5 ALDH3A1 ALDH3A2 ALOX12B AMY2B CD44 CERS3 COG7 DGAT1 EBP ELOVL4 FCER2 GBA1 HSD17B6 LPIN2 MPDU1 MRC1 NSDHL PIGA PNPLA2 PNPLA6 PRSS8 SGPL1 STS SULT2B1	10682 10908 128 1636 204219 218 2208 224 242 2629 280 412 4360 50814 5277 5652 57104 6785 6820 8630 8694 8879 91949 9526 960 9663	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET
DOID:2734	keratosis follicularis Aliases: DARIER-WHITE DISEASE Darier's disease	ACE AKR1B1 ALDH3A2 ALDH7A1 ALOX12B ALPL AMY2B APRT CANX CERS3 DGAT1 EBP ELOVL4 ENPP1 GBA1 GLA GNPTAB HPGDS HSD17B6 ICAM1 LPIN2 MPDU1 NCAM1 NT5E PKD1 PLA2G1B PNPLA2 PNPLA6 POGLUT1 PTEN PTGS2 SELE SELL SELP SGPL1 SMUG1 STS SULT2B1 XYLT1 XYLT2	10682 10908 1636 204219 224 231 23583 242 249 2629 2717 27306 280 3383 353 412 4684 4907 501 5167 5310 5319 56983 57104 5728 5743 6401 6402 6403 64131 64132 6785 6820 79158 821 8630 8694 8879 9526 9663	Homo sapiens (human)	DisGeNET DisGeNET DisGeNET DisGeNET DisGeNET

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