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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 **11251 - 11275** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲	Source
DOID:3021	acute kidney failure	Ace Adrb2 Ager Ambp Avpr1a Azgp1 Bad Bax Clu Ece1 Egf Egfr Egln1 Epo Fas Fga Fn1 Gpt Gpx4 Gsr Havcr1 Hbegf Hp Hspa8 Icam1 Igf1r Il1rn Lcn2 Met Mpo Mtor Ndufb8 Nfe2l2 Nos3 Pkd2 Plat Pparg Proc Procr Ptafr Ptger4 Ptgs2 Ren1 Serpinc1 Slc22a1 Slc22a2 Tgfa Thbd Timd2 Tlr4 Tnfrsf1a Tnfrsf1b Uts2r Wnt4	112405 11421 11555 11596 11699 11905 12007 12015 12028 12759 13645 13649 13856 14102 14161 14268 14782 15200 15439 15481 15894 16001 16181 16819 171283 171284 17295 17523 18024 18127 18764 18791 19016 19123 19124 19204 19219 19225 19701 20517 20518 217369 21802 21824 21898 21937 21938 22417 230857 54140 56717 625249 67264 76282	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080338	familial erythrocytosis 3 Aliases: ECYT3	Egln1	112405	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112124	X-linked retinitis pigmentosa and sinorespiratory infections Aliases: primary ciliary dyskinesia-retinitis pigmentosa syndrome	Rpgr	19893	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060610	megacystis-microcolon-intestinal hypoperistalsis syndrome Aliases: Berdon syndrome Megacystis microcolon intestinal hypoperistalsis syndrome megacystis-microcolon-intestinal hypoperistalsis syndrome, MMIH visceral myopathy	Chrm3	12671	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050638	transthyretin amyloidosis Aliases: ATTR amyloidosis ATTRm amyloidosis Amyloidosis, hereditary, transthyretin-related Corino de Andrade's disease Familial transthyretin amyloidosis TTR amyloidosis familial amyloid polyneuropathy paramyloidosis transthyretin-related hereditary amyloidosis	Ttr	22139	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060746	basal laminar drusen Aliases: cuticular drusen drusen of bruch membrane early adult-onset grouped drusen	Cfh Cfhr4	12628 214403	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1273	respiratory syncytial virus infectious disease Aliases: RSV respiratory syncytial virus	Ace2 Ccr5 Cd28 H2-D1 H2-K1 H2-M2 H2-M3 H2-Q10 H2-Q1 H2-Q2 H2-Q6 H2-Q7 Icam1 Ifng Il10 Il17a Il5ra Il9 Ngf Ngfr Pdcd1 Sftpb Sftpd Tacr1 Tlr4 Tlr7 Tlr8 Tslp	110557 12487 12774 14964 14972 14990 14991 15006 15007 15013 15018 15894 15978 16153 16171 16192 16198 170743 170744 18049 18053 18566 20388 20390 21336 21898 53603 70008	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14264	benign neonatal seizures Aliases: benign familial neonatal seizures benign neonatal convulsions	Atp1a2 Kcnq2 Kcnq3	110862 16536 98660	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2320	obstructive lung disease Aliases: respiratory airway obstruction	A2m Mmp1a	232345 83995	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050766	choreaacanthocytosis Aliases: Levine-Critchley syndrome choreo-acanthocytosis	Vps13a Vps13c	271564 320528	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14687	diastrophic dysplasia	Slc26a2	13521	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13934	facial paralysis Aliases: Facial Palsy	Tubb2a Tubb2b Tubb3 Tubb4a Tubb4b Tubb5 Tubb6	22151 22152 22153 22154 227613 67951 73710	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:384	Wolff-Parkinson-White syndrome Aliases: Anomalous A-V excitation Wolff-Parkinson-White pattern anomalous atrioventricular excitation	Bmpr1a Map3k7 Myh6 Prkag2 Prkag3	108099 12166 17888 241113 26409	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060653	lethal congenital contracture syndrome 3 Aliases: Israeli Bedouin type B multiple contracture syndrome	Pip5k1c	18717	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5016	hepatocellular clear cell carcinoma Aliases: Clear cell carcinoma of the Liver cells Hepatocellular carcinoma, clear cell type	Idh1 Idh2 Lep Lepr	15926 16846 16847 269951	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9976	heroin dependence	Abcb1a Abcb1b Ache Adra1a Aldh2 Ankk1 Bche Bdnf Chrm2 Comt Cyp2c29 Drd1 Drd2 Drd3 Drd4 Fas Gabbr1 Gabrb3 Gabrg2 Gad1 Gdnf Gria1 Grin2a Grm2 Htr3a Ngf Npy1r Oprd1 Oprk1 Oprm1 Penk Pomc Slc6a3 Th	108068 11423 11549 11669 12038 12064 12846 13095 13162 13488 13489 13490 13491 14102 14402 14406 14415 14573 14799 14811 15561 18049 18166 18386 18387 18390 18619 18669 18671 18976 21823 243764 244859 54393	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110433	dilated cardiomyopathy 1E Aliases: CDCD2 CMD1E dilated cardiomyopathy with conduction defect 2 dilated cardiomyopathy with conduction disorder and arrhythmia	Scn5a	20271	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110651	long QT syndrome 10 Aliases: LQT10	Scn4b	399548	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070068	autosomal dominant intellectual developmental disorder 38 Aliases: MRD38 PRELDS autosomal dominant mental retardation 38 autosomal dominant non-syndromic intellectual disability 38 psychomotor retardation, epilepsy, and language disability syndrome	Eef1a2	13628	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050741	alcohol dependence Aliases: alcoholism	Adh1 Adra2a Ago2 Aldh2 Angpt1 Ankk1 Bdnf Cacna1c Chrna3 Chrnb3 Comt Cpe Cyp2c29 Drd1 Drd2 Fos Gabbr1 Gabra2 Gabrb3 Gabrg2 Gad1 Gdnf Ggt1 Grin2a Grm8 Htr1a Htr1b Htr2a Htr3a Igf1r Il1rn Insr Insrr Kcnb2 Lep Ncam1 Ngf Ngfr Nrxn3 Nucb2 Oprd1 Oprk1 Oprm1 Per2 Pomc Rgs6 Rps6kb1 Slc29a1 Slc6a1 Slc6a2 Slc6a4 Tas2r118	108043 110834 11522 11551 11600 11669 12064 12288 12846 12876 13095 13488 13489 14281 14395 14402 14406 14415 14573 14598 14811 14823 15550 15551 15558 15561 15567 16001 16181 16337 16846 17967 18049 18053 18191 18386 18387 18390 18627 18976 20538 232333 23920 239528 244859 387347 50779 53322 54393 63959 72508 98741	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110497	autosomal recessive nonsyndromic deafness 39 Aliases: DFNB39 autosomal recessive deafness 39	Hgf	15234	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5295	intestinal disease	Bax Bmpr1a Slc10a2 Sod2	12028 12166 20494 20656	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060903	thrombosis	Ace2 Apoh C5ar1 Cd40lg F11 F2 F3 F5 Fcgr2b Fcgr3 Fgb Hrg Itga2 Itgam Mmp1a Mmp9 P2ry12 Pik3cb Proc Serpinc1 Vtn	109821 110135 11818 11905 12273 14061 14066 14067 14130 14131 16398 16409 17395 19123 21947 22370 70008 70839 74769 83995 94175	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060449	gelatinous drop-like corneal dystrophy Aliases: GDCD corneal amyloidosis primary familial amyloidosis of the cornea subepithelial amyloidosis of the cornea	Clu Tacstd2	12759 56753	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14291	Noonan syndrome with multiple lentigines Aliases: Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome Generalized lentiginosis Gorlin syndrome II LEOPARD syndrome Lentiginosis profusa syndrome Moynahan syndrome Multiple lentigines syndrome Progressive cardiomyopathic lentiginosis	Ptpn11	19247	Mus musculus (house mouse)	Alliance of Genome Resources

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