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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 **13476 - 13500** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:1799	islet cell tumor Aliases: Islet cell neoplasm endocrine pancreas cancer islet cell tumour malignant pancreatic Endocrine tumor malignant pancreatic Endocrine tumour malignant tumor of endocrine pancreas malignant tumour of endocrine pancreas pancreatic Endocrine neoplasm	Atrx Pcsk1	18548 22589	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1115	sarcoma Aliases: connective and soft tissue neoplasm tumor of soft tissue and skeleton	Atrx Ccl2 Fus Hspb1 Kdr Met Pdhx Ptprb Srebf2 Trp53	15507 16542 17295 19263 20296 20788 22059 22589 233908 27402	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3907	lung squamous cell carcinoma Aliases: Epidermoid cell carcinoma of the lung	Atrx Bsg Chrna5 Chrnb4 Clptm1l Csf1r Ctnnb1 Ddr2 Fap Fgf9 Fgfr4 Frzb Gpx1 Idh1 Idh2 Lamc2 Ptch1 Ptpn13 Ptprj Sftpb Slc7a5 Src	108015 110835 12215 12387 12978 14089 14180 14186 14775 15926 16782 18214 19206 19249 19271 20378 20388 20539 20779 218335 22589 269951	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14264	benign neonatal seizures Aliases: benign familial neonatal seizures benign neonatal convulsions	Atpalpha	48971	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0050635	alternating hemiplegia of childhood Aliases: AHC	Atpalpha	48971	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:863	nervous system disease	Atpalpha	48971	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0111558	Charcot-Marie-Tooth disease type 2DD Aliases: ATP1A1-related CMT2 ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2 CMT2DD Charcot-Marie-Tooth disease, axonal, type 2DD Charcot-Marie-Tooth neuropathy, type 2DD	Atpalpha	48971	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0090056	dystonia 12	Atpalpha	48971	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0070385	developmental and epileptic encephalopathy 99 Aliases: DEE99 early infantile epileptic encephalopathy 99	Atpalpha	48971	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:4500	hypokalemia Aliases: hypopotassemia potassium deficiency disorder	Atpalpha	48971	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0070384	developmental and epileptic encephalopathy 98 Aliases: DEE98 early infantile epileptic encephalopathy 98	Atpalpha	48971	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0111182	familial hemiplegic migraine 2 Aliases: FHM2 Familial hemiplegic migraine-2 MHP2	Atpalpha	48971	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0060178	familial hemiplegic migraine	Atpalpha cac	32158 48971	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:3312	bipolar disorder Aliases: Manic Bipolar Affective disorder Manic Depressive disorder Manic bipolar I disorder bipolar depression bipolar disorder manic phase manic depression manic disorder mixed bipolar disorder	Atpalpha Egfr Fas2 Grd Msp300 Nrg SerT enok kdn mAChR-A nAChRalpha1 nAChRbeta1 nAChRbeta2 per sgg vn	31248 31251 31364 31579 31792 37455 3771968 37859 37892 37895 38545 38657 39984 42918 42920 48971	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:10024	migraine with aura Aliases: classic migraine	Atpalpha Dop2R Tbh cac	31718 32158 33007 48971	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:10003	sensorineural hearing loss Aliases: High Frequency Hearing Loss High frequency deafness Perceptive deafness Perceptive hearing loss Perceptive hearing loss or deafness Sensorineural Deafness Sensory hearing loss central hearing loss high-frequency hearing loss	Atpalpha Ctl2 Rh5 Rh6 dysc nrv1 nrv2 scb wfs1	33952 33953 34615 36692 39533 41889 42679 43440 48971	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0070231	benign recurrent intrahepatic cholestasis 1 Aliases: BRIC type 1 BRIC1 Summerskill syndrome	Atp8b1	291555	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070228	intrahepatic cholestasis of pregnancy 1 Aliases: ICP1 pregnancy related cholestasis 1	Atp8b1	291555	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070226	progressive familial intrahepatic cholestasis 1 Aliases: FIC1 deficiency PFIC1	Atp8b1	291555	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111272	occipital horn syndrome Aliases: EDS IX Ehlers-Danlos syndrome type 9 Ehlers-Danlos syndrome type IX X-linked cutis laxa	Atp7a	24941	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1838	Menkes disease Aliases: COPPER TRANSPORT DISEASE Menkes kinky-hair syndrome steely hair syndrome	Atp7a	24941	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111196	X-linked distal spinal muscular atrophy 3 Aliases: ATP7A-related distal motor neuropathy DSMAX SMAX3 X-linked dHMN3 X-linked dSMA3 X-linked distal hereditary motor neuropathy type 3 X-linked recessive distal spinal muscular atrophy	Atp7a	24941	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:896	metal metabolism disorder Aliases: inborn metal metabolism disorder	Atp7a	24941	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:893	Wilson disease Aliases: Cerebral pseudosclerosis Westphal pseudosclerosis Westphal-Strumpell syndrome Wilson's disease hepatolenticular degeneration	Atp7a Hmgcr	24941 25675	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3144	cutis laxa Aliases: loose skin	Atp7a Fbln5 Ltbp1	24941 29158 59107	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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