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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	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **1351 - 1375** of **4621** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲
DOID:0111083	Fanconi anemia complementation group D2 Aliases: FA4 FAD2 FANCD2 Fanconi pancytopenia type 4	FUT1 NTHL1	2523 4913	Homo sapiens (human)
DOID:4160	differentiating neuroblastoma	CHAT	1103	Homo sapiens (human)
DOID:0110477	autosomal recessive nonsyndromic deafness 2 Aliases: DFNB2 autosomal recessive deafness 2	ACO2 ACOX1 ARSA CD109 CHSY1 COG4 LRTOMT OTOA OTOG PSAP TECTA	135228 146183 220074 22856 25839 340990 410 50 51 5660 7007	Homo sapiens (human)
DOID:0060127	gamma heavy chain disease Aliases: Franklin's disease	ASAH2	56624	Homo sapiens (human)
DOID:0110800	hereditary spastic paraplegia 48 Aliases: SPG48 autosomal recessive spastic paraplegia 48 autosomal recessive spastic paraplegia type 48	B4GALNT1 CYP2B6 CYP2U1 CYP39A1 CYP7B1 FAR1 GBA2 L1CAM MAG PCYT2 PLA2G6 PNPLA6 SELENOI SLC33A1 ST3GAL5	10908 113612 1555 2583 3897 4099 51302 57704 5833 8398 84188 85465 8869 9197 9420	Homo sapiens (human)
DOID:874	bacterial pneumonia Aliases: Pneumonia due to other gram-negative bacteria gram-negative pneumonia	CAT CD44 CHI3L1 CYP2J2 IL1RL1 MBL2 NAMPT SFTPA1 SFTPA2 SFTPC SFTPD TLR2 TLR6 TNF	10135 10333 1116 1573 4153 6440 6441 653509 7097 7124 729238 847 9173 960	Homo sapiens (human)
DOID:0080570	congenital disorder of glycosylation It Aliases: congenital disorder of glycosylation 1t	PGM1	5236	Homo sapiens (human)
DOID:11383	cryptorchidism Aliases: Cryptorchism Undescended testicle Undescended testis undescended testicles	AKR1C2 AKR1C4 ALG12 ALG8 ANXA5 ATP6V0A2 ATP6V1A B3GALNT2 B3GLCT B4GALT7 B4GAT1 CD44 CHST14 COG1 COG5 COLEC10 COLEC11 COMT CRPPA CYP11A1 CYP11B1 CYP17A1 CYP19A1 DAG1 DHDDS EBP EXT2 FIG4 FKRP FKTN G6PC3 GMPPB GPC3 GPC6 HACD1 HIBCH HPGDS HPSE2 HS6ST1 HSD17B3 HSD3B2 INPPL1 LARGE1 LFNG MASP1 MTM1 MTMR14 OCRL OGT PGK2 PIGN PIK3C2A PIK3CA PMM2 PNPLA6 POMGNT1 POMGNT2 POMK POMT1 POMT2 PTDSS1 PTGDS RXYLT1 SGPL1 SLC26A2 SLC35D1 SMC3 SRD5A2 STS STT3B TGDS	10082 10329 10466 10584 10585 10682 10908 11041 1109 11285 113189 1312 145173 148789 1583 1584 1586 1588 1605 1646 1836 201595 2132 2218 23169 23483 23545 23556 26275 2719 27306 29925 29954 308 3284 3293 3636 3955 412 4534 4952 523 5232 5286 5290 5373 55624 5648 5730 60495 64419 6716 729920 78989 79053 79087 79147 79947 84197 8473 84892 8879 9126 9200 9215 92579 9382 9394 960 9791 9896	Homo sapiens (human)
DOID:4308	polyradiculoneuropathy	B3GAT1 MAG	27087 4099	Homo sapiens (human)
DOID:13619	extrahepatic cholestasis Aliases: extrahepatic biliary Stasis extrahepatic obstructive biliary disease	ALPP ATRNL1 CYP27A1 CYP7A1 CYP8B1 HMGCS2 LGALS1	1581 1582 1593 250 26033 3158 3956	Homo sapiens (human)
DOID:5684	spondyloepimetaphyseal dysplasia, Sponastrime type Aliases: Spondylar and nasal Alterations-Striated Metaphyses syndrome sponastrime dysplasia	CTNS CYP51A1 EHHADH GPX3 IGF2R NAGLU OCRL SLC2A2 VNN1 VNN2	1497 1595 1962 2878 3482 4669 4952 6514 8875 8876	Homo sapiens (human)
DOID:4906	small intestine adenocarcinoma Aliases: small intestinal adenocarcinoma	HPGDS MRC1 PIK3CA PIK3CB PIK3CD PIK3CG PTEN SMUG1 UGT1A1	23583 27306 4360 5290 5291 5293 5294 54658 5728	Homo sapiens (human)
DOID:2596	larynx cancer	ACACA ACAN ACE ACSS2 ADH1B ADH1C ADH5 ADH7 AKR1A1 ALDH2 ALG1 ANXA5 CAT CD14 CD44 CMAS CYP1A1 CYP1B1 CYP2B6 CYP2C19 CYP2E1 DCN FUT4 GAPDH GPX1 HADH HK2 HPGDS HYAL1 INPP4B INPPL1 LGALS1 MTAP NTHL1 OGG1 OGT PDIA3 PIK3CA PIK3CB PIK3CD PIK3CG PLA2G15 PTEN PTGS2 SHMT1 SIGLEC7 SLC2A3 SMUG1 SULT1E1 UGT1A1 UGT1A7 VCAN VTCN1	10327 125 126 128 131 1462 1543 1545 1555 1557 1571 1634 1636 176 217 23583 23659 2526 2597 27036 27306 2876 2923 3033 308 3099 31 3373 3636 3956 4507 4913 4968 5290 5291 5293 5294 54577 54658 55902 55907 56052 5728 5743 6470 6515 6783 79679 847 8473 8821 929 960	Homo sapiens (human)
DOID:0110745	type 1 diabetes mellitus 6 Aliases: IDDM6 Insulin-Dependent Diabetes Mellitus 6	ABO ACAN ACE ACOT7 ACSL1 ADH5 AGA AGPAT1 AKR1A1 AKR1B1 ALDH2 ALDH3A2 ALOX12 ALOX15B ALOX5 AMY2A ANXA5 APRT B3GAT1 B4GALNT1 B4GALT1 BAAT CAT CBR1 CD14 CD1D CD209 CD38 CD44 CD48 CD74 CDH13 CEACAM5 CEPT1 CHAT CHST3 CLEC16A CSGALNACT1 CYP21A2 CYP24A1 CYP27A1 CYP27B1 CYP2E1 CYP2R1 CYP7A1 DCN DDOST DGCR2 DHCR7 DLAT EFNA1 ENO2 ENPP1 FASN FCER2 FCGR3B FCN2 FKRP FUT2 G6PC1 G6PC2 G6PD GAD1 GAD2 GAL3ST1 GALNT3 GBA3 GCK GLA GLB1 GLO1 GLUL GPI GPX1 GPX3 GYS1 HK1 HK2 HMGCS2 HPGDS HPRT1 HPSE2 HPSE HSD11B1 HSD11B2 HSD17B4 HSPG2 ICAM1 IGF2R IL18R1 IL18RAP IL1R1 IL1RL1 INPP5D INPPL1 IPPK ISYNA1 KL KLRC3 KLRD1 LDHC LGALS1 LGALS3 LIPC LPL LY6G6D LYPD5 MASP2 MBL2 MGAT1 MGAT5 MICA MIOX NAAA NAMPT NCAM1 OGA PARP1 PDHX PFKFB3 PGM1 PGP PIK3CA PIK3CB PIK3CD PIK3CG PIP4K2C PLA2G6 PLA2G7 PNPLA3 PRKAA2 PRKCSH PTEN PTGS2 REG1B RENBP SCD SDC2 SELE SELL SELP SIRT2 SIRT6 SLC2A12 SLC2A2 SLC2A3 SLC2A4 SLC2A8 SLC35A1 SLC35G1 SLC37A4 SLC5A1 SOAT1 ST3GAL4 SULT1E1 TKT TM7SF2 UGT1A1 UMOD VCAM1 VCAN VTCN1 XYLT1 XYLT2	100507436 1012 10135 10327 10390 1048 10554 10559 10724 10747 10855 1103 11332 120227 128 142 1462 154091 1571 1581 1589 1591 1593 159371 1594 1634 1636 1650 1717 1737 175 176 1942 2026 217 2180 2194 2208 2215 2220 224 22933 231 23274 239 240 247 2524 2538 2539 2542 2571 2572 2583 2591 2645 2683 27087 27163 2717 2720 27306 2739 2752 279 28 2821 283871 284348 2876 2878 2997 29988 308 30835 3098 3099 3158 3251 3290 3291 3295 3339 3383 3482 353 3554 3635 3636 3823 3824 3948 3956 3958 3990 4023 4153 4245 4249 4684 51477 51548 5167 5209 5236 5290 5291 5293 5294 54658 55586 5563 55790 5589 570 5728 5743 57733 57818 58530 5968 5973 60495 6319 6383 6401 6402 6403 64131 64132 64768 6484 6514 6515 6517 6523 6646 6783 7086 7108 7369 7412 79147 7941 79679 79837 80339 8050 8398 847 873 8807 8809 912 9173 929 9365 9469 9514 952 960 962 972 9993	Homo sapiens (human)
DOID:13137	Werdnig-Hoffmann disease Aliases: HMN (Hereditary motor Neuropathy) Proximal type I SMA1 Spinal muscular atrophy 1 hereditary motor neuropathy proximal type I infantile muscular atrophy progressive muscular atrophy of infancy	APRT HEXA HSPG2	3073 3339 353	Homo sapiens (human)
DOID:1184	nephrotic syndrome	ACAT1 ACE ALG1 ALOX5 CALR CHST14 CNTN1 COQ2 CYP2C19 CYP3A4 CYP3A5 DGAT1 DGKE EXT1 FCGR3B GLA GLO1 GPAM GPC3 GPC5 GPX1 GPX3 HPSE HSD11B2 HSPG2 IL1R1 KL LCAT LGALS1 LIPC LTA4H LYZ MLYCD PIK3CA PIK3CB PIK3CD PIK3CG PKD1 PLA2G7 PLA2R1 PLB1 PLCE1 PMM2 PPARGC1A PTGS2 SDC1 SDC2 SGPL1 SLC17A5 SOAT2 STS TREH VCAM1	10855 10891 11181 113189 1272 151056 1557 1576 1577 1636 2131 2215 2262 22925 23417 240 26503 2717 2719 27235 2739 2876 2878 3291 3339 3554 38 3931 3956 3990 4048 4069 412 51196 5290 5291 5293 5294 5310 5373 56052 5743 57678 6382 6383 7412 7941 811 8435 8526 8694 8879 9365	Homo sapiens (human)
DOID:4265	angiomyoma Aliases: vascular leiomyoma	SDHB	6390	Homo sapiens (human)
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)
DOID:0111680	essential fructosuria Aliases: fructokinase deficiency hepatic fructokinase deficiency ketohexokinase deficiency	KHK	3795	Homo sapiens (human)
DOID:14228	oligospermia	ANXA5 CYP17A1 CYP2R1 EPHX2 HPGDS LCT LDHC PARP1 PGAM1 PRPS2 SRD5A2 SRGN STS TEX101	120227 142 1586 2053 27306 308 3938 3948 412 5223 5552 5634 6716 83639	Homo sapiens (human)
DOID:2843	long QT syndrome Aliases: LQT long Q-T syndrome	ACADM ACSBG1 ALG10 ALG10B CNTN3 CYP1A1 KCNQ1 PTEN SCD SLC2A5 SQLE	144245 1543 23205 34 3784 5067 5728 6319 6518 6713 84920	Homo sapiens (human)
DOID:3227	tracheal stenosis Aliases: Stenosis of trachea	EBP IDUA	10682 3425	Homo sapiens (human)
DOID:12733	hypercementosis Aliases: Cementation hyperplasia	ENPP1	5167	Homo sapiens (human)
DOID:12969	central nervous system leukemia Aliases: Leukemia of the CNS	ICAM1 NCAM1	3383 4684	Homo sapiens (human)
DOID:0110776	hereditary spastic paraplegia 25 Aliases: SPG25 autosomal recessive spastic paraplegia 25 autosomal recessive spastic paraplegia type 25	B4GALNT1 CYP2B6 CYP2U1 CYP39A1 CYP7B1 FAR1 GBA2 L1CAM MAG PCYT2 PLA2G6 PNPLA6 SELENOI SLC33A1 ST3GAL5	10908 113612 1555 2583 3897 4099 51302 57704 5833 8398 84188 85465 8869 9197 9420	Homo sapiens (human)

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