GlyCosmos Portal

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

Displaying entries **9726 - 9750** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:11832	visual epilepsy Aliases: epilepsy, visual	Appl Dop2R Egfr Eno GluRIA L2HGDH Nrx-IV Ptp99A Sh TkR99D dnc futsch htl nAChRalpha1 nAChRalpha2 nAChRbeta1 nAChRbeta2 smo wfs1	31002 31309 32780 33007 33196 33351 35156 37455 38545 38742 39387 42160 42679 42918 42919 42920 43469 43551 5740544	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:824	periodontitis Aliases: chronic pericementitis	Appl Nep1 Nep4 Octbeta2R	31002 31547 41549 42449	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:1289	neurodegenerative disease Aliases: degenerative disease	Appl AttC Dro Drs FIG4 Gga GluRIA Nmdar1 Nup50 Sarm Tpi drpr ft ptc st	31002 31902 33627 33658 35784 35851 36484 36635 38218 38419 38742 38895 39836 40665 43582	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0081292	traumatic brain injury	Appl Dop1R1 Dop2R GluRIA	31002 33007 38742 41726	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:1561	cognitive disorder Aliases: cognitive disease	Appl Nmdar1 nAChRalpha6	31002 34304 40665	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:11758	iron deficiency anemia	Appl Mvl Tsf2 scb	31002 36692 39435 42490	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080348	Alzheimer's disease 1 Aliases: Alzheimer's disease 1, early onset	Appl Pxn	31002 38326	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0070028	APP-related cerebral amyloid angiopathy Aliases: Amyloidosis, Cerebroarterial, App-Related Amyloidosis, Hereditary, With Cerebral Hemorrhage, Dutch Variant Cerebral Amyloid Angiopathy, App-Related, Arctic Variant Cerebral Amyloid Angiopathy, App-Related, Dutch Variant Cerebral Amyloid Angiopathy, App-Related, Flemish Variant Cerebral Amyloid Angiopathy, App-Related, Iowa Variant Cerebral Amyloid Angiopathy, App-Related, Italian Variant HCHWAD	Appl	31002	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080930	primary localized cutaneous amyloidosis 1 Aliases: familial primary localized cutaneous amyloidosis-1	Osmr	310132	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	Hmgcr Ser rumi tn tw	31024 326122 37190 42803 43275	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0050560	Walker-Warburg syndrome Aliases: HARD syndrome cerebroocular dysplasia-muscular dystrophy syndrome	CG15651 CG3253 Col4a1 rt tw	31024 33727 37375 37861 39297	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:9884	muscular dystrophy	CG15651 Dg Msp300 rt tn tw	31024 36773 37190 37375 3771968 39297	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0112374	muscular dystrophy-dystroglycanopathy Aliases: MDDG	Dg Gmppb rt tw	31024 36773 39297 40599	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0050453	lissencephaly	Dg rt tw	31024 36773 39297	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0111240	congenital muscular dystrophy-dystroglycanopathy type A2 Aliases: MDDGA2 Walker-Warburg syndrome or muscle-eye-brain disease, POMT2-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A2	tw	31024	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0110298	autosomal recessive limb-girdle muscular dystrophy type 2N Aliases: LGMD2N muscular dystrophy-dystroglycanopathy (limb-girdle) type C 2 muscular dystrophy-dystroglycanopathy limb-girdle POMT2-related	tw	31024	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0112380	muscular dystrophy-dystroglycanopathy type B2 Aliases: MDDGB2 congenital muscular dystrophy POMT2-related	tw	31024	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080010	bone structure disease	Qrfpr	310327	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080620	familial glucocorticoid deficiency	Nnt	310378	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:13099	Moyamoya disease Aliases: progressive intracranial arterial occlusion	ACTA1 ACTA2 ACTB ACTBL2 ACTC1 ACTG1 ANO1 HLA-A RNF213	3105 345651 55107 57674 58 59 60 70 71	Homo sapiens (human)	Alliance of Genome Resources
DOID:419	scleroderma Aliases: dermatosclerosis	HLA-A	3105	Homo sapiens (human)	Alliance of Genome Resources
DOID:525	central nervous system vasculitis	HLA-A	3105	Homo sapiens (human)	Alliance of Genome Resources
DOID:1761	Melkersson-Rosenthal syndrome Aliases: Cheilitis granulomatosa of Mescher-Melkersson-Rosenthal Melkersson's syndrome	HLA-A	3105	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111694	familial adult myoclonic epilepsy 7 Aliases: BAFME7 FAME7 FCMTE7 benign adult familial myoclonic epilepsy 7 familial cortical myoclonic tremor and epilepsy 7	Rapgef2	310533	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9415	allergic asthma Aliases: extrinsic asthma with acute exacerbation extrinsic asthma with status asthmaticus	EPX HLA-B HLA-C HLA-DPA1 HLA-DPB1 HLA-DRB1	3106 3107 3113 3115 3123 8288	Homo sapiens (human)	Alliance of Genome Resources

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