GlyCosmos Portal

Mus musculus (house mouse)

Summary

Taxonomy ID: 10090
PubChem Taxonomy: 10090

Genes (662) Glycans (1270) Glycoproteins (13000) Lectins (276) Pathways (1335)

Displaying entries **26 - 50** of **662** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
11676	aldolase C, fructose-bisphosphate	Aldoc	autoimmune disease of the nervous system borna disease hepatocellular carcinoma
208211	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	Alg1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
380959	ALG10 alpha-1,2-glucosyltransferase	Alg10b	long QT syndrome 2 nonsyndromic deafness
207958	ALG11 alpha-1,2-mannosyltransferase	Alg11	congenital disorder of glycosylation Ip
223774	ALG12 alpha-1,6-mannosyltransferase	Alg12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
67574	asparagine-linked glycosylation 13	Alg13	developmental and epileptic encephalopathy 36
66789	asparagine-linked glycosylation 14	Alg14	congenital myasthenic syndrome 15
56737	ALG2 alpha-1,3/1,6-mannosyltransferase	Alg2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
208624	ALG3 alpha-1,3- mannosyltransferase	Alg3	congenital disorder of glycosylation Id congenital disorder of glycosylation
66248	ALG5 dolichyl-phosphate beta-glucosyltransferase	Alg5	congenital disorder of glycosylation type I polycystic kidney disease
320438	ALG6 alpha-1,3-glucosyltransferase	Alg6	congenital disorder of glycosylation Ic congenital disorder of glycosylation type I
381903	ALG8 alpha-1,3-glucosyltransferase	Alg8	congenital disorder of glycosylation Ih congenital disorder of glycosylation type I polycystic liver disease
102580	ALG9 alpha-1,2-mannosyltransferase	Alg9	congenital disorder of glycosylation Il congenital disorder of glycosylation type I
11722	amylase 1, salivary	Amy1
100043688	amylase 2a2	Amy2a2
100043686	amylase 2a3	Amy2a3
100043684	amylase 2a4	Amy2a4
109959	amylase 2a5	Amy2a5
30924	angiopoietin-like 3	Angptl3	alcohol use disorder familial hypobetalipoproteinemia 2
11815	apolipoprotein D	Apod	Alzheimer's disease gestational diabetes obesity status epilepticus type 2 diabetes mellitus vasculogenic impotence
11821	adenine phosphoribosyl transferase	Aprt	adenine phosphoribosyltransferase deficiency hepatocellular carcinoma
11843	ADP-ribosylation factor 4	Arf4
56297	ADP-ribosylation factor-like 6	Arl6	Bardet-Biedl syndrome 1 Bardet-Biedl syndrome 3 Bardet-Biedl syndrome ciliopathy retinitis pigmentosa 55
11870	ADP-ribosyltransferase 1	Art1
11871	ADP-ribosyltransferase 2a	Art2a