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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 **4476 - 4500** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:0081212	autosomal recessive intellectual developmental disorder 48	Slc6a17	613226	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0081212	autosomal recessive intellectual developmental disorder 48	Slc6a17	229706	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110661	congenital myasthenic syndrome 20 Aliases: CMS20 congenital myasthenic syndrome 20 presynaptic	Slc5a7	85426	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111199	autosomal dominant distal hereditary motor neuronopathy 7 Aliases: DHMN7A DHMNVPy HMN VIIA HMN7A Harper-Young myopath dHMN7 distal hereditary motor neuronopathy type 7 distal hereditary motor neuropathy type VIIA distal spinal muscular atrophy with vocal cord paralysis distal spinal muscular atrophy with vocal cord paralysis type 7A	Slc5a7	85426	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110661	congenital myasthenic syndrome 20 Aliases: CMS20 congenital myasthenic syndrome 20 presynaptic	Slc5a7	63993	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111199	autosomal dominant distal hereditary motor neuronopathy 7 Aliases: DHMN7A DHMNVPy HMN VIIA HMN7A Harper-Young myopath dHMN7 distal hereditary motor neuronopathy type 7 distal hereditary motor neuropathy type VIIA distal spinal muscular atrophy with vocal cord paralysis distal spinal muscular atrophy with vocal cord paralysis type 7A	Slc5a7	63993	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112185	thyroid dyshormonogenesis 1 Aliases: TDH1 genetic defect in thyroid hormonogenesis 1 iodide accumulation, transport, or trapping defect	Slc5a5	114613	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050718	vitamin metabolic disorder	Slc5a5 Slc5a6	114613 170551	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9432	renal glycosuria Aliases: renal diabetes	Slc5a2	64522	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9432	renal glycosuria Aliases: renal diabetes	Slc5a2	246787	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050718	vitamin metabolic disorder	Slc5a12 Slc5a6 Slc5a8	216225 241612 330064	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080785	Brown-Vialetto-Van Laere syndrome 1	Slc52a3	69698	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080632	Fazio-Londe disease Aliases: riboflavin transporter deficiency neuronopathy	Slc52a3	69698	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080632	Fazio-Londe disease Aliases: riboflavin transporter deficiency neuronopathy	Slc52a3	311536	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080785	Brown-Vialetto-Van Laere syndrome 1	Slc52a3	311536	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080786	Brown-Vialetto-Van Laere syndrome 2	Slc52a2	52710	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8454	riboflavin deficiency Aliases: ariboflavinosis vitamin B2 deficiency	Slc52a2	52710	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050694	Brown-Vialetto-Van Laere syndrome	Slc52a2 Slc52a3	52710 69698	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8454	riboflavin deficiency Aliases: ariboflavinosis vitamin B2 deficiency	Slc52a2	362942	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080786	Brown-Vialetto-Van Laere syndrome 2	Slc52a2	362942	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050694	Brown-Vialetto-Van Laere syndrome	Slc52a2 Slc52a3	311536 362942	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110839	Usher syndrome type 2C Aliases: USH2C Usher syndrome IIC Usher syndrome type IIC	Slc4a7	117955	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111620	corneal dystrophy-perceptive deafness syndrome Aliases: CDPD CDPD1 Harboyan syndrome corneal dystrophy and perceptive deafness corneal dystrophy with progressive deafness corneal endothelial dystrophy and perceptive deafness	Slc4a11	269356	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060649	congenital hereditary endothelial dystrophy of cornea Aliases: CHED	Slc4a11	269356	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110919	hereditary spherocytosis type 4 Aliases: HS4 SPH4 hereditary spherocytosis 4	Slc4a1	24779	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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