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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 **7026 - 7050** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0110370	retinitis pigmentosa 55 Aliases: RP55	Arl6	56297	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13641	exfoliation syndrome Aliases: Pseudoexfoliation glaucoma Pseudoexfoliation syndrome	ACVR1 APOE CLU EDN1 ELN LOXL1 LYST MMP1 MMP9 OPTN PON1 SOD2 STRA6 TLR4	10133 1130 1191 1906 2006 348 4016 4312 4318 5444 64220 6648 7099 90	Homo sapiens (human)	Alliance of Genome Resources
DOID:5082	liver cirrhosis Aliases: Cirrhosis cirrhosis of liver	C06G1.1 C53D5.5 T03D8.6 W01F3.2 acn-1 daf-2 fbn-1 let-23 parp-1 pat-3 pgp-1 pgp-3 pxn-1 pxn-2 scav-2 scav-3 skn-1 srp-3 ver-1 ver-3 ver-4 zmp-2 zmp-4	171619 174462 175182 175383 175410 175504 176076 176673 176787 177343 178215 178672 179991 180351 180364 180780 181288 181289 181326 181720 186632 191484 266823	Caenorhabditis elegans	Alliance of Genome Resources
DOID:8997	polycythemia vera Aliases: Osler-Vaquez syndrome Polycythaemia rubra vera Proliferative polycythaemia chronic erythremia	Snmp2	38868	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0111188	myofibrillar myopathy 9 Aliases: Edstrom myopathy HIBM-ERF HMERF Hereditary inclusion body myopathy with early respiratory failure MFM-titinopathy MFM9 MPRM Myofibrillar myopathy-titinopathy autosomal dominant distal myopathy with early respiratory failure hereditary myopathy with early respiratory failure myofibrillar myopathy 9 with early respiratory failure proximal myopathy with early respiratory muscle involvement	TTN	7273	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111238	congenital muscular dystrophy-dystroglycanopathy type A13 Aliases: MDDGA13 Walker-Warburg syndrome or muscle-eye-brain disease, B3GNT1-related Walker-Warburg syndrome or muscle-eye-brain disease, B4GNT1-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A13	bgnt-1.4 bgnt-1.5	182795 3565692	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2566	corneal dystrophy	Tacstd2	494343	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2043	hepatitis B Aliases: chronic hepatitis B hepatitis B infection	Ugt301D1 Ugt302K1 Ugt303A1 Ugt304A1 Ugt316A1 Ugt35A1 Ugt35C1 Ugt35E1 Ugt35E2 Ugt36D1 Ugt36E1 Ugt36F1 Ugt37A1 Ugt37A3 Ugt37C1 Ugt37D1 Ugt37E1 Ugt49B2	35105 35137 35138 35139 35307 40079 41334 41574 42538 53501 53502 53503 53504 53506 53507 53511 53512 53583	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:9206	Barrett's esophagus Aliases: Barrett esophagus Barrett's esophagus with esophagitis Barrett's oesophagus Barrett's ulcer of esophagus Barretts syndrome ulcerative esophagitis	b3gat2.L b3gat2.S bmp4.S	108716933 399322 733177	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:2997	Sertoli-Leydig cell tumor	Inha	24504	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3265	chronic granulomatous disease Aliases: Bridges-Good syndrome CGD Congenital dysphagocytosis Quie syndrome	CYBB IFNG TLR5 TLR9	1536 3458 54106 7100	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111442	optic atrophy 9 Aliases: OPA9	Aco2	79250	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1470	major depressive disorder Aliases: clinical depression major depression recurrent major depression single major depressive episode unipolar depression	5-HT1A 5-HT1B ChT Nrx-IV SerT Syn mAChR-A nAChRalpha1 nAChRbeta1 nAChRbeta2 vn	37191 37196 37892 37895 38545 38657 39387 41247 42245 42918 42920	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:3526	cerebral infarction Aliases: CVA - Cerebral infarction Cerebral infarct	Acer Ance ItgaPS4 ItgaPS5 Nmdar1 Spn28Dc scb	34091 34189 34805 36692 36693 37732 40665	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0081335	Becker disease	clh-1	174821	Caenorhabditis elegans	Alliance of Genome Resources
DOID:13088	periventricular leukomalacia	Mbp Tnf	17196 21926	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050858	Marshall-Smith syndrome	NFIX	4784	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112196	spondylometaepiphyseal dysplasia, short limb-hand type Aliases: SMED short limb-abnormal calcification type SMED short limb-hand type SMED type 2 SMED, type II SMED-SL SMED-SL/AC spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome spondylometaepiphyseal dysplasia short limb-hand type	Ddr2	18214	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110672	congenital myasthenic syndrome 21 Aliases: CMS21 congenital myasthenic syndrome 21, presynaptic	Slc18a3	60422	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0081140	agammaglobulinemia 8A	TCF3	6929	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110529	autosomal recessive nonsyndromic deafness 84A Aliases: DFNB84A autosomal recessive deafness 84A autosomal recessive deafness 84A with vestibular dysfunction	Ptprq	237523	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050429	Hailey-Hailey disease Aliases: BENIGN CHRONIC PEMPHIGUS Pemphigus, Benign Familial	Atp2b1 Atp2b2 Atp2b4	11941 381290 67972	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060856	right atrial isomerism Aliases: Ivemark syndrome asplenia with cardiovascular anomalies	Acvr2b	25366	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080736	Ehlers-Danlos syndrome musculocontractural type 1	Chst14	691394	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10024	migraine with aura Aliases: classic migraine	Atp1a2 Cacna1a Dbh Drd2	24212 24318 25398 25699	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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