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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 **5226 - 5250** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:0050559	Fukuyama congenital muscular dystrophy	Dag1 Fktn	13138 246179	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112374	muscular dystrophy-dystroglycanopathy Aliases: MDDG	Dag1 Pomt1 Pomt2	13138 217734 99011	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D Aliases: Alpha-sarcoglycanopathy DMDA2 Duchenne-like autosomal recessive muscular dystrophy type 2 LGMD2D muscular dystrophy, limb-girdle, type 2D primary adhalinopathy	Dag1 Sgca	13138 20391	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111232	congenital muscular dystrophy-dystroglycanopathy type A9 Aliases: MDDGA9 Walker-Warburg syndrome or muscle-eye-brain disease DAG1-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A9	Dag1	13138	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110293	autosomal recessive limb-girdle muscular dystrophy type 2P Aliases: LGMD2P MDDGC9 muscular dystrophy-dystroglycanopathy (limb-girdle) type C9 muscular dystrophy-dystroglycanopathy limb-girdle DAG1-related	Dag1	13138	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090145	dopamine beta-hydroxylase deficiency Aliases: congenital dopamine beta-hydroxylase deficiency noradrenaline deficiency norepinephrine deficiency	Dbh Hspa5 Slc6a2 Slc6a3	13162 13166 14828 20538	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090145	dopamine beta-hydroxylase deficiency Aliases: congenital dopamine beta-hydroxylase deficiency noradrenaline deficiency norepinephrine deficiency	Dbh Slc6a3	24898 25699	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
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:0080585	Van Maldergem syndrome 1	Dchs1	233651	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:4428	dyslexia	Dclk1 Drd4	13175 13491	Mus musculus (house mouse)	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:0060445	congenital stromal corneal dystrophy Aliases: CSCD congenital hereditary stromal dystrophy	Dcn	29139	Rattus norvegicus (Norway rat)	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:231	motor neuron disease	Dctn1 Kif5b Sod1 Vapa Vwa1	13191 16573 20655 246228 30960	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: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:231	motor neuron disease	Dctn1 Nos1 Vwa1	24598 29167 298683	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:0060486	Perry syndrome Aliases: parkinsonism with alveolar hypoventilation and mental depression	Dctn1	29167	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: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

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