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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 **10701 - 10725** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:3869	childhood medulloblastoma Aliases: pediatric Medulloblastoma	Ddx3y	26900	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050457	Sertoli cell-only syndrome Aliases: DEL CASTILLO SYNDROME Germinal Cell Aplasia	Ddx3y	26900	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112196	spondylometaepiphyseal dysplasia, short limb-hand type Aliases: SMED short limb-abnormal calcification type SMED short limb-hand type SMED type 2 SMED, type II SMED-SL SMED-SL/AC spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome spondylometaepiphyseal dysplasia short limb-hand type	Ddr2	18214	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5627	adenosquamous gallbladder carcinoma Aliases: Adenosquamous carcinoma of the gallbladder	Ddr2	18214	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050427	xeroderma pigmentosum	Ddb1	13194	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111258	pentosuria Aliases: L-xylulose reductase deficiency L-xylulosuria PNTSU essential pentosuria xylitol dehydrogenase deficiency	Dcxr	67880	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111258	pentosuria Aliases: L-xylulose reductase deficiency L-xylulosuria PNTSU essential pentosuria xylitol dehydrogenase deficiency	Dcxr	171408	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050890	synucleinopathy Aliases: Synucleinopathies alpha Synucleinopathies	Dctn1	29167	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060486	Perry syndrome Aliases: parkinsonism with alveolar hypoventilation and mental depression	Dctn1	29167	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111202	autosomal dominant distal hereditary motor neuronopathy 14 Aliases: DHMN7B HMN VIIB HMN7B Harper-Young myopathy distal hereditary motor neuronopathy type 7B distal hereditary motor neuropathy type VIIB distal spinal muscular atrophy with vocal cord paralysis type 7B	Dctn1	29167	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060193	amyotrophic lateral sclerosis type 1 Aliases: ALS1 amyotrophic lateral sclerosis 1	Dctn1 Sncg Sod2 Vegfa	24787 29167 64347 83785	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:231	motor neuron disease	Dctn1 Nos1 Vwa1	24598 29167 298683	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060486	Perry syndrome Aliases: parkinsonism with alveolar hypoventilation and mental depression	Dctn1	13191	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111202	autosomal dominant distal hereditary motor neuronopathy 14 Aliases: DHMN7B HMN VIIB HMN7B Harper-Young myopathy distal hereditary motor neuronopathy type 7B distal hereditary motor neuropathy type VIIB distal spinal muscular atrophy with vocal cord paralysis type 7B	Dctn1	13191	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050890	synucleinopathy Aliases: Synucleinopathies alpha Synucleinopathies	Dctn1	13191	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060193	amyotrophic lateral sclerosis type 1 Aliases: ALS1 amyotrophic lateral sclerosis 1	Dctn1 Nefh Sncg Sod1 Sod2 Vegfa	13191 20618 20655 20656 22339 380684	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:231	motor neuron disease	Dctn1 Kif5b Sod1 Vapa Vwa1	13191 16573 20655 246228 30960	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050632	oculocutaneous albinism	Dct Nsf Oca2 Slc45a2 Tyr Tyrp1	13190 18195 18431 22173 22178 22293	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060445	congenital stromal corneal dystrophy Aliases: CSCD congenital hereditary stromal dystrophy	Dcn	29139	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060445	congenital stromal corneal dystrophy Aliases: CSCD congenital hereditary stromal dystrophy	Dcn	13179	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4428	dyslexia	Dclk1 Drd4	13175 13491	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080585	Van Maldergem syndrome 1	Dchs1	308912	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080585	Van Maldergem syndrome 1	Dchs1	233651	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111153	congenital mirror movement disorder Aliases: familial congenital controlateral synkinesia familial congenital mirror movements hereditary congenital controlateral synkinesia hereditary congenital mirror movements isolated congenital controlateral synkinesia isolated congenital mirror movements	Dcc	25311	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111153	congenital mirror movement disorder Aliases: familial congenital controlateral synkinesia familial congenital mirror movements hereditary congenital controlateral synkinesia hereditary congenital mirror movements isolated congenital controlateral synkinesia isolated congenital mirror movements	Dcc Ntn1	13176 18208	Mus musculus (house mouse)	Alliance of Genome Resources

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