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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 **13526 - 13550** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:0050328	congenital hypothyroidism	Atp5pd Duox1 Duox2 G6pd Ghr Inhbb Nefl Nefm Ngfr Ppargc1a Slc5a5 Trhr Tshr	114613 24377 24588 24596 25196 25235 25360 25570 266807 641434 79107 83516 83613	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060332	mitochondrial complex V (ATP synthase) deficiency nuclear type 3 Aliases: MC5DN3	Atp5f1e	245958	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070463	mitochondrial complex V (ATP synthase) deficiency nuclear type 5 Aliases: MC5DN5	Atp5f1d	245965	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111498	combined oxidative phosphorylation deficiency 22 Aliases: COXPD22	Atp5f1a	65262	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070462	mitochondrial complex V (ATP synthase) deficiency nuclear type 4B Aliases: MC5DN4B	Atp5f1a	65262	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070461	mitochondrial complex V (ATP synthase) deficiency nuclear type 4A Aliases: MC5DN4A	Atp5f1a	65262	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:8725	vascular dementia Aliases: Multi Infarct Dementia multifocal dementia	Atp5f1a Avp Bdnf Cdk5 Creb1 Epo Fgfr1 Grin1 Grin2a Grin2b Gsk3b Igf1r Mmp2 Nefl Nox1 Pon2 Snca Sncg Tnf Tp53	114243 140908 24221 24225 24335 24408 24409 24410 24835 24842 25718 29219 296851 64347 65262 79114 81646 81686 83613 84027	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070461	mitochondrial complex V (ATP synthase) deficiency nuclear type 4A Aliases: MC5DN4A	Atp5f1a	11946	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070462	mitochondrial complex V (ATP synthase) deficiency nuclear type 4B Aliases: MC5DN4B	Atp5f1a	11946	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111498	combined oxidative phosphorylation deficiency 22 Aliases: COXPD22	Atp5f1a	11946	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8725	vascular dementia Aliases: Multi Infarct Dementia multifocal dementia	Atp5f1a Avp Bdnf Epo Fgfr1 Flt1 Gclm Gpx1 Grin1 Grin2a Grin2b Gsk3b Hspa1a Igf1r Mapt Mmp2 Mtor Nefl Nox1 Pon2 Rps6 Snca Sncg Srebf2 Tnf Trp53	11946 11998 12064 13856 14182 14254 14630 14775 14810 14811 14812 16001 17390 17762 18039 193740 20104 20617 20618 20788 21926 22059 237038 330260 56637 56717	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0040090	autoimmune gastritis	Atp4b	24217	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:8929	atrophic gastritis Aliases: gastric atrophy	Atp4b	24217	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0040090	autoimmune gastritis	Atp4b	11945	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8929	atrophic gastritis Aliases: gastric atrophy	Atp4b H2-Ab1 H2-Eb1 Ptpn11	11945 14961 14969 19247	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:543	dystonia Aliases: dystonic disease	Atp2b4 Bche Gnal Penk Tor1a Tor1b Tor2a Tor3a	12038 14680 18619 30931 30933 30934 30935 381290	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050564	autosomal dominant nonsyndromic deafness Aliases: autosomal dominant deafness	Atp2b2 Col11a1 Epha10 Grhl2 Map1b	11941 12814 17755 230735 252973	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110467	autosomal recessive nonsyndromic deafness 12 Aliases: DFNB12 autosomal recessive deafness 12	Atp2b2 Cdh23	11941 22295	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:2734	keratosis follicularis Aliases: DARIER-WHITE DISEASE Darier's disease	Atp2a2	11938	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050606	acrokeratosis verruciformis Aliases: Acrokeratosis verruciformis of Hopf Hopf disease	Atp2a2	11938	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2856	euthyroid sick syndrome Aliases: Sick-euthyroid syndrome	Atp2a2	11938	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14221	abdominal obesity-metabolic syndrome 1 Aliases: dysmetabolic syndrome X metabolic syndrome X	Atp2a2 Bax Fas Lep Lpl	11938 12028 14102 16846 16956	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050692	Brody myopathy	Atp2a1 Atp2a2 Atp2a3	11937 11938 53313	Mus musculus (house mouse)	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	Atp1b1 Ednrb Ifng Il2 Ngf Opn4 Ptgds Scarb1 Slc44a4 Sod2 Tnf	116562 192223 24787 24835 25073 25526 25650 25712 294255 310738 50672	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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