GlyCosmos Portal

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **7501 - 7525** of **15957** in total

« First

‹ Prev

…

297

298

299

300

301

302

303

304

305

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼	Source
DOID:0050886	Troyer syndrome Aliases: SPG20 autosomal recessive spastic paraplegia 20 autosomal recessive spastic paraplegia Troyer type autosomal recessive spastic paraplegia type 20 childhood-onset spastic paraparesis with distal muscle wasting hereditary spastic paraplegia 20 spastic paraplegia 20 spastic paraplegia type 20	Spart	229285	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5679	retinal disease	Aqp4 Cept1 Gfap Il10 Map2k3 Opn4 Prph2 Thy1	11829 14580 16153 19133 21838 26397 30044 99712	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111141	delayed sleep phase syndrome Aliases: DSPD	Cry1	12952	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8712	neurofibromatosis	Nf1	18015	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090141	cortisone reductase deficiency 1 Aliases: CORTRD1	H6pd	100198	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112367	Coffin-Siris syndrome 8 Aliases: CSS8	Smarcc2	68094	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11573	listeriosis Aliases: Infection by Listeria monocytogenes Listeria infection	Il15 Il1rn	16168 16181	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050789	tarsal-carpal coalition syndrome	Nog	18121	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050958	spinocerebellar ataxia type 7	Atxn7	246103	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:680	tauopathy	Cd2ap Enah Map4 Mapt	12488 13800 17758 17762	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111331	intellectual disability-severe speech delay-mild dysmorphism syndrome Aliases: FOXP1 Haploinsufficiency FOXP1 syndrome FOXP1-Related Neurodevelopmental Disorder Mental retardation with language impairment and with or without autistic features	Foxp1	108655	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9159	gas gangrene Aliases: Gas bacillus infection	Gsn	227753	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8499	night blindness Aliases: nyctalopia	Nyx Rho	212541 236690	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3827	congenital diaphragmatic hernia Aliases: Diaphragmatic Hernia	Ace Agtr2 Atp7a Bmp4 Cbl Ep300 Frem1 Gata4 Htr2a Igf2 Igfbp3 Lcn2 Lrp1 Myrf Ndst1 Nos3 Nr2f2 Pdgfra Pls3 Sftpb Slc6a4 Slit2 Slit3 Sod1 Sod2 Tnf Vegfa	102866 11421 11609 11819 11977 12159 12402 14463 15531 15558 15567 16002 16009 16819 16971 18127 18595 20388 20563 20564 20655 20656 21926 22339 225908 328572 329872	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9408	acute myocardial infarction	Arhgap17 Bax C3 Cacng4 Dsc2 Fos Gp6 Gsk3b Ifng Il10 Il17a Il1rl1 Il4 Itgam Pf4 Serping1 Tnf	12028 12258 12266 13506 14281 15978 16153 16171 16189 16409 17082 21926 243816 54377 56637 56744 70497	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111650	ectodermal dysplasia 13 Aliases: ECTD13 ectodermal dysplasia 13, hair/tooth type	Kremen1	84035	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080944	familial Behcet-like autoinflammatory syndrome Aliases: A20 haploinsufficiency	Tnfaip3	21929	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112106	chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia Aliases: X-linked dominant chondrodysplasia, Chassaing-Lacombe type X-linked dominant chondrodysplasia-hydrocephaly-microphthalmia syndrome	Hdac6	15185	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2835	polycythemia due to hypoxia	Pxk	218699	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050981	spinocerebellar ataxia type 34	Elovl4	83603	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080288	spinocerebellar ataxia 46	Pld3	18807	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110678	congenital myasthenic syndrome 4A Aliases: CMS Ia1 CMS1A1 CMS4A congenital myasthenic syndrome 4A slow-channel congenital myasthenic syndrometype Ia1	Chrne	11448	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111494	combined oxidative phosphorylation deficiency 4 Aliases: COXPD4	Tufm	233870	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14415	Legg-Calve-Perthes disease Aliases: Calve - Perthes' disease Coxa plana Juvenile osteochond-hip/pelvis Juvenile osteochondrosis of hip and/or pelvis Perthe's disease Perthes disease juvenile osteochondrosis of hip and pelvis osteochondrosis of Legg-Calve-Perthes pseudocoxalgia	Col2a1	12824	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:12297	Vogt-Koyanagi-Harada disease Aliases: Harada's disease Vogt-Koyanagi syndrome uveomeningoencephalitic syndrome	H2-Aa H2-Ab1 H2-Eb1 Ifng Itgb2 Itgb2l Tnf	14960 14961 14969 15978 16414 16415 21926	Mus musculus (house mouse)	Alliance of Genome Resources

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements