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 **126 - 150** of **662** in total

« First

‹ Prev

1

2

3

4

5

6

7

8

9

10

…

Next ›

Last »
Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
68947	carbohydrate sulfotransferase 8	Chst8
71367	carbohydrate sulfotransferase 9	Chst9
269941	chondroitin sulfate synthase 1	Chsy1	temtamy preaxial brachydactyly syndrome
78923	chondroitin sulfate synthase 3	Chsy3
211286	ceroid-lipofuscinosis, neuronal 5	Cln5	neuronal ceroid lipofuscinosis 5
232370	calsyntenin 3	Clstn3
12833	collagen, type VI, alpha 1	Col6a1	Bethlem myopathy Ullrich congenital muscular dystrophy congenital muscular dystrophy muscular dystrophy
234407	collagen beta(1-O)galactosyltransferase 1	Colgalt1	brain small vessel disease 3
269132	collagen beta(1-O)galactosyltransferase 2	Colgalt2
12846	catechol-O-methyltransferase	Comt	Parkinsonism alcohol dependence alcohol use disorder amphetamine abuse attention deficit hyperactivity disorder autism spectrum disorder bipolar disorder breast cancer bulimia nervosa cannabis abuse cannabis dependence cocaine dependence cognitive disorder drug dependence endometrial cancer eumycotic mycetoma fibromyalgia heroin dependence hypertension intermittent explosive disorder leiomyoma lung cancer morphine dependence neonatal abstinence syndrome nicotine dependence obesity obsessive-compulsive disorder opiate dependence ovarian cancer pathological gambling polycystic ovary syndrome pre-eclampsia prostate cancer psoriasis renal cell carcinoma schizophrenia uremia urinary bladder cancer vitiligo withdrawal disorder
71883	coenzyme Q2 4-hydroxybenzoate polyprenyltransferase	Coq2	coenzyme Q10 deficiency disease glucose intolerance multiple system atrophy nephrotic syndrome primary coenzyme Q10 deficiency 1
230027	coenzyme Q3 methyltransferase	Coq3
12894	carnitine palmitoyltransferase 1a, liver	Cpt1a	alcoholic hepatitis carnitine palmitoyltransferase I deficiency end stage renal disease lipid metabolism disorder lymphangioleiomyomatosis metabolic dysfunction-associated steatohepatitis obesity type 2 diabetes mellitus
74343	CREB regulated transcription coactivator 2	Crtc2	type 2 diabetes mellitus
12952	cryptochrome circadian regulator 1	Cry1	delayed sleep phase syndrome
12974	citrate synthase	Cs	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
234356	chondroitin sulfate N-acetylgalactosaminyltransferase 1	Csgalnact1
78752	chondroitin sulfate N-acetylgalactosaminyltransferase 2	Csgalnact2
74245	chitobiase	Ctbs
320685	dCMP deaminase	Dctd
67880	dicarbonyl L-xylulose reductase	Dcxr	pentosuria
232449	deoxyribose-phosphate aldolase	Dera
67800	diacylglycerol O-acyltransferase 2	Dgat2	chronic kidney disease metabolic dysfunction-associated steatotic liver disease premature menopause steatotic liver disease
71755	dihydrodiol dehydrogenase	Dhdh
209692	dehydrogenase E1 and transketolase domain containing 1	Dhtkd1	2-aminoadipic 2-oxoadipic aciduria Charcot-Marie-Tooth disease axonal type 2Q

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements