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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 **15451 - 15475** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:0050830	peripheral artery disease	ADIPOQ B2M CCN1 NPY1R NPY2R NPY5R P2RY12 SERPINE1	3491 4886 4887 4889 5054 567 64805 9370	Homo sapiens (human)	Alliance of Genome Resources
DOID:9120	amyloidosis Aliases: amyloid disease	ADIPOQ APCS CSF1 GOT1 SERPINE1 TNF TNFRSF1A TREM1 TTR	1435 2805 325 5054 54210 7124 7132 7276 9370	Homo sapiens (human)	Alliance of Genome Resources
DOID:7998	hyperthyroidism Aliases: overactive thyroid	ADIPOQ ANXA1 ANXA2 ANXA5 APOA1 APOA2 APOC3 BDH1 CAT CP CS CTSL CTSV GPX1 HLA-DQB1 IGF1R IL10 MCM7 NR1D1 PCSK1 PPARGC1A SERPINA7 SERPINE1 SLC34A1 SLC9A1 SOD1 TSHR UCP3 UGT1A1 VIM	10891 1356 1431 1514 1515 2876 301 302 308 3119 335 336 345 3480 3586 4176 5054 5122 54658 622 6548 6569 6647 6906 7253 7352 7431 847 9370 9572	Homo sapiens (human)	Alliance of Genome Resources
DOID:3312	bipolar disorder Aliases: Manic Bipolar Affective disorder Manic Depressive disorder Manic bipolar I disorder bipolar depression bipolar disorder manic phase manic depression manic disorder mixed bipolar disorder	ADIPOQ AKT1 ANK3 AVPR1B BMAL1 BRD1 CAMK2A CCL2 CDC42 CHRM2 CHRNB3 CLOCK COMT CS ERBB4 ETV1 GABRA3 GABRA5 GAD1 GAD2 GRIN2A GRIN2B GRK3 GRN GSK3B HLA-DRA HTR2C IMPA2 KAT6B L1CAM MBL2 NCAM1 NGF NRG1 NTRK2 PER3 PTGS1 PTGS2 RELN SLC18A1 SLC6A4 SNCA SRSF3 SSTR5 SYNE1 TNFRSF11B TTK VWF	1129 1142 1312 1431 157 2066 207 2115 23345 23522 23774 2556 2558 2571 2572 288 2896 2903 2904 2932 3084 3122 3358 3613 3897 406 4153 4684 4803 4915 4982 553 5649 5742 5743 6347 6428 6532 6570 6622 6755 7272 7450 815 8863 9370 9575 998	Homo sapiens (human)	Alliance of Genome Resources
DOID:2526	prostate adenocarcinoma	ADIPOQ AKT1 AKT2 AKT3 AR BIN1 CD9 CLU CREB3L4 GRB2 IGF1R IKBKB INSR JUN KDR MAP2K1 MYC NCOA2 PAM PDGFA PDGFRA PIK3CB PRKCQ RAF1 RELA STAT1	10000 10499 1191 148327 207 208 274 2885 3480 3551 3643 367 3725 3791 4609 5066 5154 5156 5291 5588 5604 5894 5970 6772 928 9370	Homo sapiens (human)	Alliance of Genome Resources
DOID:11714	gestational diabetes Aliases: GDM Gestational diabetes mellitus Maternal gestational diabetes mellitus	ADIPOQ AHSG ANGPTL6 APOD ATP2B4 CALB1 CCL2 CDKAL1 CYP24A1 CYP27B1 CYP2R1 DCN DNAH8 GAD2 GCK GGT1 GPX1 HNF1A ICAM1 IGF1R IL10 IL6 INHBA INS INSR ITPR1 ITPR2 ITPR3 LEP MET OGG1 PLAT RBP4 RYR1 RYR2 RYR3 SRRM1 TRPV5 TRPV6	10250 120227 1591 1594 1634 1769 197 2572 2645 2678 2876 3383 347 3480 3569 3586 3624 3630 3643 3708 3709 3710 3952 4233 493 4968 5327 54901 55503 56302 5950 6261 6262 6263 6347 6927 793 83854 9370	Homo sapiens (human)	Alliance of Genome Resources
DOID:1580	diffuse scleroderma Aliases: diffuse systemic sclerosis systemic sclerosis, diffuse	ADIPOQ AGT FCGR2A HLA-DQA1 IL10 IL13 IL6 IRAK1 KDR STAT4 TAP1 TLR2	183 2212 3117 3569 3586 3596 3654 3791 6775 6890 7097 9370	Homo sapiens (human)	Alliance of Genome Resources
DOID:13378	Kawasaki disease Aliases: Kawasaki's disease MLNS acute febrile MCLS acute febrile mucocutaneous lymph node syndrome mucocutaneous lymph node syndrome	ADIPOQ AGER BTNL2 CCR2 CCR5 CD40 CD40LG CLU FLT1 HMGB1 HP HSPA1A HSPA1L MBL2 MMP9 NPPB SELP TIMP1 TLR4 TNF VEGFA	1191 1234 177 2321 3146 3240 3303 3305 4153 4318 4879 56244 6403 7076 7099 7124 729230 7422 9370 958 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:13207	proliferative diabetic retinopathy Aliases: PDR	ADIPOQ AGER BCOR CALD1 CALU CAT CCL2 CCN1 COL5A2 COL6A3 CORO1C ENPP2 FLT1 IL6R PDGFB PPARG PTPN1 RBP4 SERPINE1 SERPINF1 SLIT2 SRSF6 TIMM44 VEGFA	10469 1290 1293 177 2321 23603 3491 3570 5054 5155 5168 5176 5468 54880 5770 5950 6347 6431 7422 800 813 847 9353 9370	Homo sapiens (human)	Alliance of Genome Resources
DOID:1287	cardiovascular system disease Aliases: disease of subdivision of hemolymphoid system	ADIPOQ AGER AGT APOA4 APOB CCL2 CD40LG CFH DBI ENPP1 FGB FTO GHRL GIPR GPX1 GPX3 GYS1 HP HSPA1A LIPG MPO PLAUR PPARG PPARGC1A PTGS2 TLR9 UBR1	10891 1622 177 183 197131 2244 2696 2876 2878 2997 3075 3240 3303 337 338 4353 5167 51738 5329 54106 5468 5743 6347 79068 9370 9388 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060180	colitis	ADIPOQ ADRB3 ANXA1 APOA4 ARRB1 BMP6 CAT CCKBR CCL2 CCR1 CD40 CHUK CRHR2 CXCR2 HAVCR1 HLA-B HP HPR ICAM1 ICOS IKBKB IL10 IL17A KDR LCT MIF MSH2 MUC2 NOD2 NOS2 NOS3 NTRK1 NTRK2 PPARGC1A PTGS2 RELA SELL SELP SI TACR1 TACR2 TFF1 TLR3 TLR4 VCAM1	10891 1147 1230 1395 155 26762 29851 301 3106 3240 3250 337 3383 3551 3579 3586 3605 3791 3938 408 4282 4436 4583 4843 4846 4914 4915 5743 5970 6347 6402 6403 64127 6476 654 6865 6869 7031 7098 7099 7412 847 887 9370 958	Homo sapiens (human)	Alliance of Genome Resources
DOID:12361	Graves' disease Aliases: Grave's disease Graves disease exophthalmic goiter	ADIPOQ ADRB2 BTNL2 C4A C4B CAT CD40 CD40LG CTLA4 CYP1A1 DNMT1 FAS GC HLA-B HLA-DQA1 HLA-DQB1 HLA-DRB1 HLA-DRB3 ICAM1 IFNG IGF1R IL10 IL13 IL17A IL23R IL2 IL3 IL6 IL6R ITGB3 LTA OGG1 SERPINE1 SLC25A16 TG TNF TP53 TSHR VEGFA	149233 1493 154 1543 1786 2638 3106 3117 3119 3123 3125 3383 3458 3480 355 3558 3562 3569 3570 3586 3596 3605 3690 4049 4968 5054 56244 7038 7124 7157 720 721 7253 7422 8034 847 9370 958 959	Homo sapiens (human)	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 ADRA1A ADRA1B ADRA1D ADRB2 ADRB3 AKR1C3 AKT2 AMH AR ATP5F1B CAPN10 CD36 COMT CYP17A1 CYP19A1 CYP1A1 FST GPX3 HSD17B7 HSD3B1 HSD3B2 MMP2 NCOA2 NCOA4 NCOR1 NGFR NR3C1 NR3C2 PECAM1 PGR RARRES2 SERPINE1 VEGFA	10468 10499 11132 1312 146 147 148 154 1543 155 1586 1588 208 268 2878 2908 3283 3284 367 4306 4313 4804 5054 506 51478 5175 5241 5919 7422 8031 8644 9370 948 9611	Homo sapiens (human)	Alliance of Genome Resources
DOID:3454	brain infarction	ADIPOQ ADM ADNP ALDH2 CACNA2D1 CALCRL CD8A CFH CTSB CYP11B1 CYP11B2 CYP2R1 GPNMB GZMB HGF HIF1A HLA-DQA1 HMGB1 HTR2B ICAM1 IGF2 IL15 IL2 KCNK6 MDK MMP14 MMP8 MMP9 MSI1 NES PARG PDGFB PRCP SCN7A TBXAS1 TNF TPCN2	10203 10457 10763 120227 133 1508 1584 1585 217 219931 23394 3002 3075 3082 3091 3117 3146 3357 3383 3481 3558 3600 4192 4317 4318 4323 4440 5155 5547 6332 6916 7124 781 8505 925 9370 9424	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080952	AMED syndrome Aliases: AMEDS	ADH5	128	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060892	late onset Parkinson's disease Aliases: late onset Parkinson disease	ADH1C ATXN2 ATXN3 EIF4G1 GBA1 HLA-DRA LRRK1 MAPT PMPCB PSAP TBP UQCRC1	126 1981 2629 3122 4137 4287 5660 6311 6908 7384 79705 9512	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050741	alcohol dependence Aliases: alcoholism	ADH1B ADH1C ADH4 ADRA2A AGO1 AGO2 AHR ALDH2 ANGPT1 AR BDNF BMAL1 BPTF CACNA1C CCK CHRNA3 CHRNB3 COMT CPE CREB1 CYP2C9 CYP2E1 CYP3A5 DRD1 DRD2 DRD4 FMN1 FOS FOSB GABBR1 GABRA2 GABRB3 GABRG2 GAD1 GAD2 GDNF GEMIN4 GGT1 GGTLC1 GGTLC2 GRIN2A GRM8 HTR1A HTR1B HTR2A HTR3A IGF1R IL1RN INSR INSRR KCNB2 LEP NCAM1 NGF NGFR NR3C2 NRXN3 NUCB2 OPRD1 OPRK1 OPRM1 PDE4B PER2 POMC PRL RPS6KB1 SLC29A1 SLC6A1 SLC6A2 SLC6A4 TAS2R16 XRCC5	1136 1142 125 126 127 1312 1363 1385 150 1559 1571 1577 1812 1813 1815 196 2030 217 2186 2353 2354 2550 2555 2562 2566 2571 2572 26523 2668 2678 27161 284 2903 2918 3350 3351 3356 3359 342184 3480 3557 3643 3645 367 3952 406 4306 4684 4803 4804 4925 4985 4986 4988 50628 50833 5142 5443 5617 6198 627 6529 6530 6532 7520 775 885 8864 91227 92086 9312 9369	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111305	familial febrile seizures 4 Aliases: FEB4 familial febrile convulsions 4	ADGRV1	84059	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110839	Usher syndrome type 2C Aliases: USH2C Usher syndrome IIC Usher syndrome type IIC	ADGRV1 PDZD7 SLC4A7	79955 84059 9497	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060250	idiopathic scoliosis	ADGRG6 DNAH10 KATNB1 MBTPS1 ODAD3 PRMT5 PTK7 PTPN11 RUNX3 SLC39A8 SLC6A9	10300 10419 115948 196385 57211 5754 5781 64116 6536 864 8720	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111863	X-linked congenital bilateral absence of vas deferens Aliases: CBAVDX	ADGRG2	10149	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080924	bilateral perisylvian polymicrogyria	ADGRG1	9289	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080922	bilateral frontoparietal polymicrogyria	ADGRG1	9289	Homo sapiens (human)	Alliance of Genome Resources
DOID:1554	vibratory urticaria	ADGRE2	30817	Homo sapiens (human)	Alliance of Genome Resources
DOID:1094	attention deficit hyperactivity disorder Aliases: ADHD attention deficit disorder hyperkinetic disorder	ADGRE1 ADGRE5 ADGRL1 ADGRL2 ADGRL3 ADGRL4 ADRA2A AR BAIAP2 BDNF BRINP1 CALY CDH2 CHRNB2 COMT DBH DOCK3 DRD4 DRD5 FOXP2 GIT1 GRIN2B GRM8 HMGCR HTR1B LGALS3 MEF2A MEF2C MEF2D MMP9 NF1 NTRK2 PER1 PTCHD1 SLC6A2 SLC6A3 SLC6A4 SNAP25 TACR1 TPH1 UST VEGFA VPS4A	1000 10090 10458 1141 1312 139411 150 1620 1621 1795 1815 1816 2015 22859 23266 23284 27183 28964 2904 2918 3156 3351 367 3958 4205 4208 4209 4318 4763 4915 50632 5187 627 64123 6530 6531 6532 6616 6869 7166 7422 93986 976	Homo sapiens (human)	Alliance of Genome Resources

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