GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Gene Symbol

Gene ID

Organism

Source

Display
results per page.

Clear

Submissions

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 **8001 - 8025** of **15957** in total

« First

‹ Prev

…

317

318

319

320

321

322

323

324

325

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼	Source
DOID:2841	asthma Aliases: bronchial hyperreactivity chronic obstructive asthma chronic obstructive asthma with acute exacerbation chronic obstructive asthma with status asthmaticus	ABCB1 ABO ACE ACSL3 ADAM33 ADAM8 ADH5 ADORA1 ADORA2A ADRB2 AGER AGTR1 AGTR2 ALOX5 AMBP BDKRB2 BDNF BMPR1B BMPR2 C3 C3AR1 C5 C5AR1 CAT CCL11 CCL1 CCL24 CCL2 CCL5 CCL7 CCR2 CCR3 CCR4 CCR5 CCR9 CD14 CD209 CD28 CD40 CD86 CDH1 CFTR CHAT CHI3L1 CHIA CHML CHRM1 CHRM2 CHRM3 CLCA1 CMA1 CRHR1 CRHR2 CSF2 CSF2RB CSF3 CTLA4 CX3CL1 CXCR3 CYP2E1 CYSLTR1 CYSLTR2 DCN DEFB1 DPP10 EDN1 EDNRB EGFR EGR1 EPX F2 F2RL1 F7 FAS FCER1A FCGR2A FCGR3A FGA GATA3 GC GSTO2 HAVCR1 HDAC2 HLA-B HLA-DPA1 HLA-DPB1 HLA-DQA1 HLA-DQA2 HLA-DQB1 HLA-DRA HLA-DRB1 HLA-DRB3 HLA-G HMGCR HP ICAM1 IFNG IFNGR1 IFNL1 IL10 IL12B IL13 IL13RA1 IL13RA2 IL15 IL16 IL17A IL18R1 IL19 IL1A IL1RL1 IL1RN IL21 IL22 IL2 IL2RA IL2RB IL3 IL4 IL4R IL5 IL5RA IL6 IL9 IL9R IRAK3 ITGB3 ITGB6 ITPR1 KDR LEP LGALS3 LTA4H LTA MBL2 MEFV MIF MMP9 MPO MUC1 MUC2 MUC5AC MUC5B MUC7 MYLK NFE2L2 NGF NOD2 NOS1 NOS2 NOS3 NPSR1 NR3C1 NTF3 NTRK1 ORMDL1 ORMDL2 P2RY12 PARP1 PDGFB PGF PLA2G4A PLA2G7 PLAU PRF1 PRG2 PRMT5 PROC PTGDR2 PTGDR PTGER3 PTGS2 RHOA RUNX3 SERPINA1 SERPINE1 SFTPA1 SFTPA2 SFTPB SFTPC SFTPD SLC18A3 SLC22A1 SLC5A7 SLC6A4 SOD2 STAT1 STAT4 STAT6 TACR1 TACR2 TAP1 TBXA2R TGFB1 THBD TLR10 TLR1 TLR2 TLR3 TLR4 TLR6 TLR9 TNC TNF TRPA1 VEGFA	101 10333 10419 1080 10800 10803 1103 1116 11213 1122 11251 1128 1129 1131 1179 119391 1215 1232 1233 1234 128 134 135 1394 1395 142 1437 1439 1440 1493 154 1571 1634 1636 1672 177 185 186 1906 1910 1956 1958 2147 2150 2155 2181 2205 2212 2214 2243 240 259 2625 2638 26762 27159 28 282618 2833 2908 29095 29949 3066 30835 3106 3113 3115 3117 3118 3119 3122 3123 3125 3135 3156 3240 3371 3383 3458 3459 355 3552 3557 3558 3559 3560 3562 3565 3566 3567 3568 3569 3578 3581 3586 3593 3596 3597 3598 3600 3603 3605 3690 3694 3708 3791 387 387129 3952 3958 4048 4049 4153 4210 4282 4318 4353 4582 4583 4586 4589 4638 4780 4803 4842 4843 4846 4908 4914 5054 50616 5155 5228 5243 5265 5321 5328 54106 5551 5553 5624 57105 5729 5733 5743 57628 59067 60482 624 627 6346 6347 6352 6354 6356 6369 6376 64127 6439 6440 6441 64805 6532 653509 6572 658 6580 659 6648 6772 6775 6778 6865 6869 6890 6915 7040 7056 7096 7097 7098 7099 7124 718 719 727 727897 728 729230 729238 7422 7941 80332 81793 8288 847 864 8809 8989 9173 929 940 94101 942 958 999	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080924	bilateral perisylvian polymicrogyria	ADGRG1	9289	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070218	familial hyperinsulinemic hypoglycemia 2 Aliases: Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency HHF2 hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia	KCNJ11	3767	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110334	osteogenesis imperfecta type 1 Aliases: OI1 osteogenesis imperfecta type I	COL1A1	1277	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112007	growth hormone secreting pituitary adenoma 2 Aliases: GH-secreting pituitary adenoma 2 PITA2 X-linked acromegaly acromegaly due to pituitary adenoma 2	GPR101	83550	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110009	achromatopsia 7 Aliases: ACHM7	ATF6	22926	Homo sapiens (human)	Alliance of Genome Resources
DOID:2999	granulosa cell tumor Aliases: Granulosa cell neoplasm Granulosa cell tumor, adult type Granulosa cell tumour, sarcomatoid malignant granulosa cell neoplasm	AMH CTNNB1 FSHR KIT LHCGR MGMT PTGS2 ST14 VEGFA	1499 2492 268 3815 3973 4255 5743 6768 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:5408	Paget's disease of bone Aliases: Paget disease of bone Paget's bone disease osseous Paget's disease osteitis deformans	INPP5D OPTN SQSTM1 TNFRSF11A TNFRSF11B VCP	10133 3635 4982 7415 8792 8878	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050476	Barth syndrome Aliases: 3-methylglutaconicaciduria type 2 3-methylglutaconicaciduria type II MGA Type 2 MGA type II	MEST	4232	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060198	amyotrophic lateral sclerosis type 6 Aliases: ALS6 amyotrophic lateral sclerosis 6, with or without frontotemporal dementia autosomal recessive amyotrophic lateral sclerosis 6	EWSR1 FUS	2130 2521	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080144	childhood acute lymphocytic leukemia Aliases: Childhood Acute Lymphoblastic Leukemia	CTCF	10664	Homo sapiens (human)	Alliance of Genome Resources
DOID:1584	acute chest syndrome Aliases: acute chest syndrome in sickle cell disease	HBB NOS3 VEGFA	3043 4846 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:384	Wolff-Parkinson-White syndrome Aliases: Anomalous A-V excitation Wolff-Parkinson-White pattern anomalous atrioventricular excitation	BMPR1A MAP3K7 PRKAG2 PRKAG3	51422 53632 657 6885	Homo sapiens (human)	Alliance of Genome Resources
DOID:8398	osteoarthritis Aliases: Osteoarthrosis and allied disorder degenerative arthritis degenerative joint disease hypertrophic arthritis osteoarthrosis	ACAN ADAM12 ADAMTS14 ADAMTS5 AGER ASPN ATP7A BAD BAG6 BAX BMP2 BMP7 BMPR1A CASP9 CCR4 CD36 CILP CLEC3B COL11A1 COL1A1 COL2A1 COL9A1 DDR2 EFEMP2 EGR1 ENPP1 EPAS1 ERRFI1 ESR1 FCGR2A FGFR1 FLT1 FN1 FRZB GDF5 GHR HBP1 HFE HIF1A IGF1R IGF2 IGFBP3 IHH IL1A IL4R IL5 INS JAG1 LEP MATN3 MMP13 MMP1 MMP2 MMP3 MMP8 MMP9 NCOR2 NFATC1 NGF PECAM1 POMC PTGS2 SERPINA1 TGFBR1 TNFRSF10A TNFRSF10B TNFRSF10C TNFRSF10D TNFRSF11B	11096 1233 1277 1280 1297 1301 140766 176 177 182 1958 2034 2099 2212 2260 2321 2335 2487 2690 26959 30008 3077 3091 3480 3481 3486 3549 3552 3566 3567 3630 3952 4148 4312 4313 4314 4317 4318 4322 4772 4803 4921 4982 5167 5175 5265 538 54206 5443 54829 572 5743 581 650 655 657 7046 7123 7917 8038 8200 842 8483 8793 8794 8795 8797 948 9612	Homo sapiens (human)	Alliance of Genome Resources
DOID:1852	intrahepatic cholestasis Aliases: neonatal intrahepatic cholestasis	ABCB11 ABCB4 ENTPD1 HSD3B7 SLC22A1 SLC22A2 SLC25A12 SLC25A13	10165 5244 6580 6582 80270 8604 8647 953	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110838	Usher syndrome type 2A Aliases: USH2A Usher syndrome type IIA	PDZD7 USH2A	7399 79955	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070423	early onset progressive encephalopathy with brain atrophy and thin corpus callosum Aliases: PEBAT early-onset progressive encephalopathy with brain atrophy and thin corpus callosum	TBCD	6904	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111898	CK syndrome Aliases: X-linked intellectual disability-microcephaly-cortical malformation-thin habitus syndrome	NSDHL	50814	Homo sapiens (human)	Alliance of Genome Resources
DOID:4947	cholangiocarcinoma Aliases: adult primary Cholangiocarcinoma adult primary cholangiocellular carcinoma cholangiosarcoma	ABCC2 ADRB2 ALB ALOX5 ANXA2 APC APOA1 ASPH EPO EPOR EZH2 FASLG FSCN1 GNAS HDAC6 HGF IL1R2 IL4R IL6 INS KIT KRT7 MDM2 MET MFSD4A MGMT MKI67 MMP2 MMP9 MUC16 MUC1 MUC2 MUC3A MUC4 MUC5AC MUC5B MUC6 NCAM1 NOS2 NOTCH1 OGG1 OSBP2 OSBPL7 PANX2 PAWR PPIA PPP3CA PREX2 PRSS2 PRSS56 PTGS2 REG1A RNF43 RUNX3 SLC4A4 SLC7A5 SOCS3 SOX2 TGFB1 TGFBR2 THBS1 TNC TNFAIP3 TTR UGT1A9 WDHD1 WNT9A	10013 11169 114881 1244 148808 154 2056 2057 213 2146 23762 240 2778 302 3082 324 335 3371 356 3566 3569 3630 3815 3855 4193 4233 4255 4288 4313 4318 444 4582 4583 4584 4585 4586 4588 4684 4843 4851 4968 5074 54600 5478 54894 5530 5645 56666 5743 5967 646960 6624 6657 7040 7048 7057 7128 7276 727897 7483 7850 80243 8140 864 8671 9021 94025	Homo sapiens (human)	Alliance of Genome Resources
DOID:7188	autoimmune thyroiditis Aliases: Chronic Lymphocytic Thyroiditis Hashimoto thyroiditis Hashimoto's Disease Hashimoto's syndrome Hashimoto's thyroiditis Lymphocytic Thyroiditis	CTLA4 HLA-DQA1 HLA-DQB1 HLA-DRA HLA-DRB1 IFNG IL4 LRP2 MBL2 TG TLR3	1493 3117 3119 3122 3123 3458 3565 4036 4153 7038 7098	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112051	non-syndromic X-linked intellectual disability 30 Aliases: MRX30 MRX47 X-linked mental retardation 30 X-linked mental retardation 30/47 X-linked mental retardation 47	PAK3	5063	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080380	nephrotic syndrome type 5 Aliases: nephrotic syndrome type 5, with or without ocular abnormalities	LAMB2	3913	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111844	X-linked intellectual developmental disorder 108 Aliases: MRX108	SLC9A7	84679	Homo sapiens (human)	Alliance of Genome Resources
DOID:4648	familial retinoblastoma Aliases: Hereditary Retinoblastoma	RB1	5925	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110648	long QT syndrome 6 Aliases: LQT6	KCNE2	9992	Homo sapiens (human)	Alliance of Genome Resources

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements