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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 **12976 - 13000** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:2596	larynx cancer	Cxcr4 Gpx1 Vegfa	12767 14775 22339	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2600	laryngeal carcinoma Aliases: cancer of larynx carcinoma of larynx	Ackr3 Cxcr4	12767 12778	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050073	invasive aspergillosis	Cxcr3 Cyp2c29 Mbl2 Ptx3 Tlr4	12766 13095 17195 19288 21898	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9675	pulmonary emphysema	Ccl11 Ccl2 Ccr5 Clptm1l Csf3 Cxcl9 Cxcr3 Ednra Egr1 Elane Ephx1 Fga Fstl1 Fut8 Gclc Itgb6 Jun Kl Mmp1a Mmp2 Mmp9 Nfe2l2 Ptgs2 Ptma Serpina1a Serpina1b Serpina1c Serpina1d Serpina1e Smo Tgfb1 Tlr4	12766 12774 12985 13617 13653 13849 14161 14314 14629 16420 16476 16591 17329 17390 17395 18024 19225 19231 20292 20296 20700 20701 20702 20703 20704 21803 218335 21898 319757 50701 53618 83995	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:559	acute pyelonephritis	Cxcr2 Rbp4	12765 19662	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:823	periapical periodontitis Aliases: Apical periodontitis	Ccl2 Ccl7 Cxcr2 Il17a Tnfrsf11b	12765 16171 18383 20296 20306	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4930	nasal cavity adenocarcinoma Aliases: adenocarcinoma of the nasal cavity	Clu	12759	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060449	gelatinous drop-like corneal dystrophy Aliases: GDCD corneal amyloidosis primary familial amyloidosis of the cornea subepithelial amyloidosis of the cornea	Clu Tacstd2	12759 56753	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4251	conjunctival disease	Clu Tnfaip6	12759 21930	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8691	mycosis fungoides Aliases: mycosis fungoides lymphoma	Clu H2-Ab1 Sod2	12759 14961 20656	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11656	cicatricial pemphigoid Aliases: Cicatricial pemphigoid with ocular involvement Ocular pemphigoid benign mucous membrane pemphigoid benign mucous membrane pemphigoid with ocular involvement ocular pemphigus	Clu H2-Ab1 H2-Eb1 Il1rn Tnf	12759 14961 14969 16181 21926	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:535	sleep disorder Aliases: Non-organic sleep disorder	Clock Ghrhr Igf1r Ins1 Insr Insrr Nf1 Npsr1 Tfap2b	12753 14602 16001 16333 16337 18015 21419 23920 319239	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110721	neuronal ceroid lipofuscinosis 1 Aliases: CLN1 neuronal ceroid lipofuscinosis 1 variable age of onset	Cln3 Ppt1	12752 19063	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14503	neuronal ceroid lipofuscinosis Aliases: hereditary ceroid lipofuscinosis	Atp13a2 Atp13a3 Atp13a5 Cln3 Ctsd Ppt1 Ppt2 Sod2	12752 13033 19063 20656 224088 268878 54397 74772	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080059	autosomal recessive spinocerebellar ataxia 7 Aliases: SCAR7	Tpp1	12751	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110726	neuronal ceroid lipofuscinosis 2 Aliases: CLN2 neuronal ceroid lipofuscinosis 2 variable age at onset	Tpp1	12751	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110146	Bartter disease type 4b Aliases: BARTS4B Bartter syndrome, type 4b, digenic neonatal Bartter syndrome type 4B with sensorineural deafness	Clcnka Clcnkb	12733 56365	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110144	Bartter disease type 3 Aliases: BARTS3 Bartter syndrome type 3 classic Bartter syndrome	Clcnka Clcnkb	12733 56365	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050450	Gitelman syndrome Aliases: HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA	Clcnka Clcnkb Slc12a3 Wnk4	12733 20497 56365 69847	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080353	X-linked recessive hypophosphatemic rickets	Clcn5	12728	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:447	renal tubular transport disease Aliases: inborn renal tubular transport disorder	Clcn5	12728	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111798	X-linked nephrolithiasis type I Aliases: NPHL1 X-linked nephrolithiasis with renal failure X-linked recessive urolithiasis type 1 XRN nephrolithiasis 1 nephrolithiasis X-linked recessive type 1	Clcn5	12728	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110731	neuronal ceroid lipofuscinosis 3 Aliases: Batten disease CLN3 juvenile neuronal ceroid lipofuscinosis	Clcn3 Clcn6 Cln3 Ppt1	12725 12752 19063 26372	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111815	low molecular weight proteinuria with hypercalciuric nephrocalcinosis	Clcn3 Clcn5	12725 12728	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050699	Dent disease Aliases: Dent disease 1 Dent disease 2 Dent's disease	Clcn3 Clcn5	12725 12728	Mus musculus (house mouse)	Alliance of Genome Resources

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