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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 **9401 - 9425** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲	Source
DOID:0090067	Fuhrmann syndrome	Wnt7a	22421	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2234	focal epilepsy Aliases: localisation-related epilepsy partial epilepsy	Cnr1 Depdc5 Mmp9	12801 17395 277854	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081060	X-linked nephrogenic diabetes insipidus Aliases: nephrogenic diabetes insipidus type 1	Avpr2	12000	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080072	intestinal pseudo-obstruction Aliases: Chronic intestinal pseudo-obstruction neuronal intestinal dysplasia	Nup35 Spry2	24064 69482	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8481	rheumatic myocarditis Aliases: Rheumatic degeneration of myocardium Rheumatic fever with myocarditis Rheumatoid myocarditis active rheumatic fever with myocarditis acute rheumatic carditis acute rheumatic myocarditis	Gsn Icam1 Sele Vcam1	15894 20339 22329 227753	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090056	dystonia 12	Atp1a3 Pla2g6	232975 53357	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111996	immunodeficiency 51 Aliases: CANDF5 IMD51 familial candidiasis 5	Il17ra	16172	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5052	melioidosis Aliases: Nightcliff gardener's disease Pseudoglanders Whitmore's disease acute and fulminating melioidosis subacute and chronic melioidosis	Ifna11 Ifna12 Ifna13 Ifna16 Ifna1 Ifna4 Ifna9 Plaur Serpinf1 Tlr5 Trem1	15962 15964 15967 15972 18793 20317 230396 230398 242519 53791 58217	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:6846	familial melanoma	Braf Mc1r Mitf	109880 17199 17342	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080019	metaphyseal dysplasia Aliases: Bakwin-Krida syndrome Pyle's disease Pyle-Cohn syndrome	Sfrp4	20379	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111239	congenital muscular dystrophy-dystroglycanopathy type A10 Aliases: MDDGA10 Walker-Warburg syndrome or muscle-eye-brain disease, TMEM5-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A10	Rxylt1	216395	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8634	prostate carcinoma in situ Aliases: PIN III carcinoma in situ of prostate grade III PIN	Areg Aurkb Carm1 Creb3l4 Csf1r Esr1 Esr2 Fgf6 Fgf8 Flt1 Fzd4 Hdac1 Lrp1 Map2k4 Phb1 Prss8 Ptgs2 Rela Rxra Smad4 St14	11839 12978 13982 13983 14177 14179 14254 14366 16971 17128 18673 19143 19225 19697 20181 20877 26398 433759 59035 76560 78284	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080425	developmental and epileptic encephalopathy 47 Aliases: DEE47 early infantile epileptic encephalopathy 47	Fgf10 Fgf16 Fgf5 Fgf6 Fgf7	14165 14176 14177 14178 80903	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080771	beta-thalassemia major Aliases: Cooley's anemia	Pon1	18979	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1949	cholecystitis Aliases: acute and chronic cholecystitis acute cholecystitis acute on chronic cholecystitis chronic cholecystitis	Abcb4	18670	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080037	Worth syndrome Aliases: Worth's syndrome autosomal dominant endosteal hyperostosis autosomal dominant osteosclerosis benign form of Worth hyperostosis corticalis generalisata with torus platinus	Lrp5	16973	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090129	carnitine palmitoyltransferase I deficiency Aliases: CPT I deficiency CPT1A deficiency L-CPT1 deficiency carnitine palmitoyl transferase 1A deficiency carnitine palmitoyl transferase IA deficiency hepatic CPT deficiency type I hepatic carnitine palmitoyl transferase 1 deficiency hepatic carnitine palmitoyl transferase I deficiency	Cpt1a	12894	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080212	polycystic kidney disease 4	Pkhd1	241035	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112025	female-restricted syndromic X-linked intellectual disability 99 Aliases: MRXS99F X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability female-restricted syndromic X-linked mental retardation 99	Usp9x	22284	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060748	familial temporal lobe epilepsy 1 Aliases: ETL1 partial epilepsy with auditory features	Lgi1	56839	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090093	hypogonadotropic hypogonadism 21 with or without anosmia	Flrt3	71436	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060540	Hermansky-Pudlak syndrome 2	Ap3b1	11774	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080430	developmental and epileptic encephalopathy 65 Aliases: DEE65 early infantile epileptic encephalopathy 65	Cyfip2	76884	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:12306	vitiligo	C4b Comt Ctla4 Esr1 Foxd3 H2-Aa H2-Ab1 H2-Eb1 Hgf Hspa1a Ifng Il13 Il17a Il1a Il2 Il4 Mbl2 Myg1 Ncstn Sod2 Tgfb1 Tlr2 Tlr4 Tnf Tyr	12268 12477 12846 13982 14960 14961 14969 15221 15234 15978 16163 16171 16175 16183 16189 17195 193740 20656 21803 21898 21926 22173 24088 59287 60315	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3082	interstitial lung disease Aliases: ILD	Ap3b1 Bdnf Ccl2 Ccr5 Cd28 Cma1 Cxcl9 Hgf Il1a Il1rn Il2 Il4ra Kit Mmp9 Mpo Muc1 Ngf Nr3c1 Sftpb Sftpd Tgfb1 Tlr9	11774 12064 12487 12774 14815 15234 16175 16181 16183 16190 16590 17228 17329 17395 17523 17829 18049 20296 20388 20390 21803 81897	Mus musculus (house mouse)	Alliance of Genome Resources

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