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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 **13326 - 13350** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:18	urinary system disease Aliases: Non-neoplastic urinary tract disease urinary tract disease	Bmp4	12159	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080313	cleft palate-lateral synechia syndrome Aliases: CPLS syndrome syngnathia	Bmp4	12159	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060887	ossification of the posterior longitudinal ligament of spine Aliases: OPLL	Bmp4 Enpp1	12159 18605	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5394	prolactinoma Aliases: PITUITARY ADENOMA, PROLACTIN-SECRETING Prolactinoma of Pituitary gland familial prolactinoma	Bmp4 Myc Npy5r Ptgs2	12159 17869 18168 19225	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080207	CAKUT2 Aliases: Congenital anomalies of the kidney and urinary tract 2	Bmp4 Mmp9 Timp1	12159 17395 21857	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080205	CAKUT Aliases: Congenital anomalies of the kidney and urinary tract Renal or urinary tract malformation	Bmp4 Hspa1a Lifr	12159 16880 193740	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11963	esophagitis Aliases: acute esophagitis	Bmp4 Il4ra Ptgs2 Slc7a5 Tnf	12159 16190 19225 20539 21926	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1882	atrial heart septal defect Aliases: atrial septal defect atrioseptal defect auricular septal defect congenital atrial septal defect interatrial septal defect interauricular septal defect	Bmp4 Gata4 Myh6 Tbx20	12159 14463 17888 57246	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13515	tuberous sclerosis Aliases: Bourneville's disease Epiloia Tuberose sclerosis Tuberous sclerosis syndrome cerebral sclerosis	Bmp4 Eif4ebp1 Mmp9 Tsc1	12159 13685 17395 64930	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13976	peptic esophagitis Aliases: Peptic reflux disease Reflux oesophagitis reflux esophagitis	Bmp4 Egfr F11r Il13 Il5 Tjp1 Tnf	12159 13649 16163 16191 16456 21872 21926	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050651	atrioventricular septal defect Aliases: AVCD AVSD ECD atrioventricular canal defect endocardial cushion defect	Bmp4 Creld1 Dnah11 Gata4 Glyr1	12159 13411 14463 171508 74022	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111535	progressive osseous heteroplasia Aliases: POH ectopic ossification familial type familial ectopic ossification osteoma cutis	Bmp4 Ctnnb1 Gnas Sparc Spp1	12159 12387 14683 20692 20750	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:182	calcinosis Aliases: Pathologically calcified structure pathologic calcification	Bmp4 Ctnnb1 Erbb2 Gpx1 Sparc Spp1	12159 12387 13866 14775 20692 20750	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111029	hemochromatosis type 1 Aliases: HFE1 symptomatic form of HFE-related hereditary hemochromatosis symptomatic form of classic hemochromatosis symptomatic form of hemochromatosis type 1	Bmp2 Hfe	12156 15216	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110965	brachydactyly type A2 Aliases: BDA2 Mohr-Wriedt type brachydactyly brachymesophalangy II	Bmp2 Gdf5	12156 14563	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050591	tooth agenesis Aliases: familial tooth agenesis hypodontia oligodontia selective tooth agenesis	Bmp2 Bmp4 Eda Grem2 Lrp6 Tspear Wnt10a Wnt10b	12156 12159 13607 16974 22409 22410 23893 252974	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080494	ovarian dysgenesis 2	Bmp15	12155	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5426	primary ovarian insufficiency Aliases: hypergonadotropic hypogonadism premature ovarian failure premature ovarian insufficiency	Bbs9 Bmp15 Dis3 Fanca Mlh1 Mov10 Msh6 Npm1 Usp36	12155 14087 17350 17454 17688 18148 319845 72344 72662	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110342	osteogenesis imperfecta type 13 Aliases: OI13 osteogenesis imperfecta type XIII	Bmp1	12153	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1591	renovascular hypertension	ACE ADM ADRB1 AGTR1 AGTR2 AVPR1A CAMK2D CMA1 CXCR3 DYRK1A EIF4G2 FN1 G6PD HAVCR1 LAMA2 LCN2 MPO NOS1 PDGFA PRL PTGER3 PTGS1 RELA REN SLC9A1 SLC9A3 SPP1	1215 133 153 1636 185 1859 186 1982 2335 2539 26762 2833 3908 3934 4353 4842 5154 552 5617 5733 5742 5970 5972 6548 6550 6696 817	Homo sapiens (human)	Alliance of Genome Resources
DOID:11984	hypertrophic cardiomyopathy Aliases: hypertrophic obstructive cardiomyopathy	ACE2 ACE ACTB ADGRL4 ADM AGT AHR CACNB2 CD36 CMA1 CS CTSL CYP1A1 CYP1B1 CYP2E1 DNMT1 DSP EDN1 EPHX2 FHL1 HRAS HTR2B ICAM1 IGF1R KRAS LAMP2 MAP3K7 MMP1 MMP2 MMP9 MYBPC3 MYH7 NPPA NPPB NRAS ORAI1 ORAI3 PKD1 PTPN11 SDHD SLC25A6 STIM1 STIM2 TNNI3 VCL XIRP1	1215 133 1431 1514 1543 1545 1571 1636 165904 1786 183 1832 1906 196 2053 2273 293 3265 3357 3383 3480 3845 3920 4312 4313 4318 4607 4625 4878 4879 4893 5310 57620 5781 59272 60 6392 64123 6786 6885 7137 7414 783 84876 93129 948	Homo sapiens (human)	Alliance of Genome Resources
DOID:3082	interstitial lung disease Aliases: ILD	AP3B1 BDNF CCL2 CCR2 CCR5 CD28 CMA1 HGF IL1A IL1RN IL2 IL4R KIT MMP9 MPO MUC1 NGF NOS2 NR3C1 SERPINE1 SFTPA1 SFTPB SFTPC SFTPD TGFB1 TLR9	1215 1234 2908 3082 3552 3557 3558 3566 3815 4318 4353 4582 4803 4843 5054 54106 627 6347 6439 6440 6441 653509 7040 729230 8546 940	Homo sapiens (human)	Alliance of Genome Resources
DOID:11335	sarcoidosis Aliases: Boeck sarcoid lymphogranulomatosis	ACE AGTR1 BTNL2 CCR2 CCR5 CD14 CFH CMA1 CTLA4 HLA-B HLA-DQB1 HLA-DRB1 HP IL23R PTGS2 SFTPD SLC11A1	1215 1234 149233 1493 1636 185 3075 3106 3119 3123 3240 56244 5743 6441 6556 729230 929	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110348	osteogenesis imperfecta type 12 Aliases: OI12 osteogenesis imperfecta type XII	SP7	121340	Homo sapiens (human)	Alliance of Genome Resources
DOID:1712	aortic valve stenosis Aliases: Aortic stenosis Rheumatic aortic stenosis rheumatic aortic valve stenosis	ADRB1 APOB BAMBI EGR1 ELN ENO3 LGALS3 MMP1 NFATC1 NPPC OGT SP7 TNF TNFRSF11B	121340 153 1958 2006 2027 25805 338 3958 4312 4772 4880 4982 7124 8473	Homo sapiens (human)	Alliance of Genome Resources

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