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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 **13876 - 13900** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:2349	arteriosclerosis Aliases: Arteriosclerotic vascular disease	Abcg5 Abcg8 Akr1b1 Alpl Apob Apoh Cd36 Cdh13 Chi3l1 Egr1 Esr1 F13a1 F7 Furin Hgf Hp Hspd1 Ifngr1 Igfbp3 Il10 Il15 Il6st Itga2 Itga7 Kdr Lcat Ldlr Lepr Lmna Lox Map3k7 Met Mmp12 Mmp13 Mmp1a Mmp2 Mmp9 Msr1 Notch4 Pappa Pon1 Pparg Ptger4 Ptgs2 Rela Serpina1a Serpina1b Serpina1c Serpina1d Serpina1e Tgfb1 Tgfbr2 Tlr4 Tnfrsf14 Tnfsf10	11647 11677 11818 12491 12554 12654 13653 13982 14068 15234 15439 15510 15979 16009 16153 16168 16195 16398 16404 16542 16816 16835 16847 16905 16948 17295 17381 17386 17390 17395 18132 18491 18550 18979 19016 19219 19225 19697 20288 20700 20701 20702 20703 20704 21803 21813 21898 22035 230979 238055 26409 27409 67470 74145 83995	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112329	pontocerebellar hypoplasia type 2F Aliases: PCH2F	TSEN15	116461	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies Aliases: FENIB	Serpine1 Serpine2 Serpini1	116459 24617 29366	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070168	spermatogenic failure 3 Aliases: SPGF3	SLC26A8 SRSF6	116369 6431	Homo sapiens (human)	Alliance of Genome Resources
DOID:2861	congenital nonspherocytic hemolytic anemia Aliases: HNSHA congenital nonspherocytic hemolytic anaemia hereditary nonspherocytic hemolytic anaemia hereditary nonspherocytic hemolytic anemia	Ak1 G6pd2 G6pdx Gpi1 Hk1	11636 14380 14381 14751 15275	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:583	hemolytic anemia Aliases: ANEMIA HEMOLYTIC	A2m Abo Ak1 Fcgr2b Fcgr3 G6pd2 G6pdx Gclc Hp Pgk1 Rhag	11636 14130 14131 14380 14381 14629 15439 18655 19743 232345 80908	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112009	pituitary adenoma 1 Aliases: PITA1 pituitary adenoma 1, multiple types	Aip	11632	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080628	alopecia-mental retardation syndrome 1	Ahsg	11625	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080227	autosomal dominant intellectual developmental disorder 55 Aliases: autosomal dominant intellectual developmental disorder-55 with seizures autosomal dominant mental retardation 55	NUS1	116150	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080553	congenital disorder of glycosylation Iaa Aliases: congenital disorder of glycosylation 1aa	NUS1	116150	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111039	hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase Aliases: hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency	Ahcy Ahcyl	11615 269378	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8455	pyridoxine deficiency anemia Aliases: vitamin B6 deficiency syndrome	Ahcy Ahcyl	11615 269378	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9279	hyperhomocysteinemia	Ahcy Ahcyl Atp1a1 Atp1a2 Bche Ccl2 Ece1 Ednra F10 F12 F2 F8 G6pd2 G6pdx Gpx1 Gria1 Grin2a Grin2b Icam1 Ngf Sod2	11615 11928 12038 13617 14058 14061 14069 14380 14381 14775 14799 14811 14812 15894 18049 20296 20656 230857 269378 58992 98660	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060038	specific developmental disorder	BCL11A BCL11B FOXP1 FOXP2 FOXP4	116113 27086 53335 64919 93986	Homo sapiens (human)	Alliance of Genome Resources
DOID:11049	meconium aspiration syndrome Aliases: Neonatal aspiration of meconium meconium aspiration	Agtr2 Atf2	11609 11909	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3891	placental insufficiency	Agtr1a Emp2 Epo Grin1 Grin2a Grin2b Itga2 Pdx1 Ppargc1a	11607 13731 13856 14810 14811 14812 16398 18609 19017	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1073	renal hypertension	Agtr1a Cyp2c29 Hspa8 Mmp2 Mmp9 Nos3 Tnf	11607 13095 15481 17390 17395 18127 21926	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4780	anti-basement membrane glomerulonephritis Aliases: anti-GBM glomerulonephritis	Agtr1a Bax Ccl2 Cd40lg Cd80 Clu Csf1 Csf1r Ctla4 Fcgr4 H2-Eb1 Il10 Il17a Il1rn Il4 Itga4 Mapk14 Mmp12 Pdcd1 Pf4 Selp Slit2 Tnf	11607 12028 12477 12519 12759 12977 12978 14969 16153 16171 16181 16189 16401 17381 18566 20296 20344 20563 21926 21947 246256 26416 56744	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:12705	Friedreich ataxia Aliases: Friedreich's ataxia Friedreich's tabes	Agtr1a Agtr1b	11607 11608	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:6713	cerebrovascular disease Aliases: CVA cerebrovascular disorder stroke	Agtr1a Agtr1b Arhgef7 G6pd2 G6pdx Glce Lmna P2ry12 Sele	11607 11608 14380 14381 16905 20339 54126 70839 93683	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9620	vesicoureteral reflux Aliases: vesico-ureteral reflux	Agtr1a Agtr1b Agtr2 Csf1 Havcr1 Ifng Igf1r Robo2 Timd2 Tnxb Upk3a	11607 11608 11609 12977 15978 16001 171283 171284 22270 268902 81877	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110657	congenital myasthenic syndrome 8 Aliases: CMS8 congenital myasthenic syndrome 8 with pre- and postsynaptic defects congenital myasthenic syndrome due to agrin deficiency	Agrn	11603	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050876	Caroli disease	Angpt2	11601	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3247	rhabdomyosarcoma	Angpt2 Cad	11601 69719	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:299	adenocarcinoma	Angpt2 Notch1 Notch2 Notch3 Ptgs2 Tnni3	11601 18128 18129 18131 19225 21954	Mus musculus (house mouse)	Alliance of Genome Resources

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