GlyCosmos Portal

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

Displaying entries **11376 - 11400** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
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: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:0050426	Stevens-Johnson syndrome	Clu H2-Ab1 H2-D1 H2-K1 H2-M2 H2-Q10 H2-Q1 H2-Q2 H2-Q4 H2-Q6 H2-Q7 H2-T3 Tnf	110557 12759 14961 14964 14972 14990 15006 15007 15013 15015 15018 15043 21926	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080226	autosomal dominant intellectual developmental disorder 56 Aliases: autosomal dominant intellectual developmental disorder-56 autosomal dominant mental retardation 56	Cltc	67300	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110828	Usher syndrome type 3 Aliases: USH3	Clrn1	229320	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110373	retinitis pigmentosa 61 Aliases: RP61	Clrn1	229320	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110841	Usher syndrome type 3A Aliases: USH3A Usher syndrome type IIIA	Clrn1	229320	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050921	pharynx squamous cell carcinoma	Clptm1l	316916	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9261	nasopharynx carcinoma Aliases: Nasopharyngeal carcinoma malignant Nasopharyngeal tumor malignant neoplasm of nasopharynx nasopharynx cancer	Clptm1l Cxcr4 Erbb3 Fgfr4 Grin2a Kdr Ppia Ppial4d Tp53 Vegfa	100360977 24409 24842 25114 25518 25589 29496 316916 60628 83785	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050921	pharynx squamous cell carcinoma	Clptm1l	218335	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:0110728	neuronal ceroid lipofuscinosis 5 Aliases: CLN5 neuronal ceroid lipofuscinosis 5 variable age of onset	Cln5	211286	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:10605	short bowel syndrome Aliases: acquired short bowel syndrome short gut syndrome	Clmp Insr Lep Lepr	16337 16846 16847 71566	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:10605	short bowel syndrome Aliases: acquired short bowel syndrome short gut syndrome	Clmp Lep Lepr	24536 25608 286939	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1928	Williams-Beuren syndrome Aliases: Fanconi Schlesinger syndrome WBS	Clip2 Dlg4 Fzd3 Fzd9 Limk1 Lox Src	13385 14365 14371 16885 16948 20779 269713	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	Clcnkb	79430	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:445	Bartter disease Aliases: Aldosteronism with hyperplasia of the adrenal cortex Bartter's syndrome	Clcnkb	79430	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110144	Bartter disease type 3 Aliases: BARTS3 Bartter syndrome type 3 classic Bartter syndrome	Clcnkb	79430	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050450	Gitelman syndrome Aliases: HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA	Clcnkb Slc12a3	54300 79430	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:445	Bartter disease Aliases: Aldosteronism with hyperplasia of the adrenal cortex Bartter's syndrome	Clcnkb Slc12a1	20495 56365	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

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