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 **401 - 425** of **662** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
26903	dysferlin	Dysf	Miyoshi muscular dystrophy 1 autosomal recessive limb-girdle muscular dystrophy type 2B distal myopathy with anterior tibial onset distal myopathy limb-girdle muscular dystrophy muscular dystrophy
233115	dpy-19 like C-mannosyltransferase 3	Dpy19l3
244745	dpy-19 like C-mannosyltransferase 1	Dpy19l1
381510	dpy-19 like 4	Dpy19l4
320752	dpy-19 like 2	Dpy19l2	spermatogenic failure 9
13481	dolichyl-phosphate mannosyltransferase subunit 2, regulatory	Dpm2	congenital disorder of glycosylation Iu congenital disorder of glycosylation type I
13480	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	Dpm1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
13478	dolichyl-phosphate N-acetylglucosaminephosphotransferase 1	Dpagt1	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
235339	dihydrolipoamide S-acetyltransferase	Dlat	lactic acidosis pyruvate decarboxylase deficiency
71755	dihydrodiol dehydrogenase	Dhdh
67880	dicarbonyl L-xylulose reductase	Dcxr	pentosuria
67800	diacylglycerol O-acyltransferase 2	Dgat2	chronic kidney disease metabolic dysfunction-associated steatotic liver disease premature menopause steatotic liver disease
232449	deoxyribose-phosphate aldolase	Dera
209692	dehydrogenase E1 and transketolase domain containing 1	Dhtkd1	2-aminoadipic 2-oxoadipic aciduria Charcot-Marie-Tooth disease axonal type 2Q
320685	dCMP deaminase	Dctd
12952	cryptochrome circadian regulator 1	Cry1	delayed sleep phase syndrome
94192	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1	C1galt1	autoimmune disease of blood
12833	collagen, type VI, alpha 1	Col6a1	Bethlem myopathy Ullrich congenital muscular dystrophy congenital muscular dystrophy muscular dystrophy
269132	collagen beta(1-O)galactosyltransferase 2	Colgalt2
234407	collagen beta(1-O)galactosyltransferase 1	Colgalt1	brain small vessel disease 3
230027	coenzyme Q3 methyltransferase	Coq3
71883	coenzyme Q2 4-hydroxybenzoate polyprenyltransferase	Coq2	coenzyme Q10 deficiency disease glucose intolerance multiple system atrophy nephrotic syndrome primary coenzyme Q10 deficiency 1
12974	citrate synthase	Cs	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
78923	chondroitin sulfate synthase 3	Chsy3
269941	chondroitin sulfate synthase 1	Chsy1	temtamy preaxial brachydactyly syndrome

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