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
223774	ALG12 alpha-1,6-mannosyltransferase	Alg12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
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
98660	ATPase, Na+/K+ transporting, alpha 2 polypeptide	Atp1a2	alcohol use disorder alternating hemiplegia of childhood benign neonatal seizures developmental and epileptic encephalopathy 98 epilepsy familial hemiplegic migraine 2 familial hemiplegic migraine hyperhomocysteinemia hypertension migraine with aura nervous system disease
232975	ATPase, Na+/K+ transporting, alpha 3 polypeptide	Atp1a3	alcohol use disorder alternating hemiplegia of childhood bipolar disorder developmental and epileptic encephalopathy 99 dystonia 12 epilepsy familial hemiplegic migraine nervous system disease
12015	BCL2-associated agonist of cell death	Bad	Alzheimer's disease Parkinsonism acute kidney failure brain ischemia breast cancer colon cancer diabetic neuropathy endometrial cancer gastric ulcer glaucoma high grade glioma hypertension hypothyroidism impotence intermittent claudication lung non-small cell carcinoma macular degeneration middle cerebral artery infarction obesity osteoarthritis pancreatic cancer prostate carcinoma prostatic hypertrophy pulmonary fibrosis renal cell carcinoma traumatic brain injury type 2 diabetes mellitus visual epilepsy
231841	BRCA1-associated ATM activator 1	Brat1
109880	Braf transforming gene	Braf	Langerhans-cell histiocytosis Noonan syndrome 7 Noonan syndrome with multiple lentigines 3 bile duct adenoma cancer cardiofaciocutaneous syndrome 1 cardiofaciocutaneous syndrome cardiomyopathy cholangiocarcinoma colon carcinoma colorectal adenocarcinoma colorectal cancer dysembryoplastic neuroepithelial tumor endometrial carcinoma familial melanoma germinoma high grade glioma intrahepatic cholangiocarcinoma lung cancer malignant astrocytoma melanoma pancreatic acinar cell adenocarcinoma pancreatic cancer pleomorphic xanthoastrocytoma prostate adenocarcinoma thyroid gland papillary carcinoma
59048	C1GALT1-specific chaperone 1	C1galt1c1	Tn polyagglutination syndrome hemolytic-uremic syndrome
67389	C1q and tumor necrosis factor related 12	C1qtnf12
213819	CAS1 domain containing 1	Casd1
12494	CD38 antigen	Cd38	type 1 diabetes mellitus type 2 diabetes mellitus
74343	CREB regulated transcription coactivator 2	Crtc2	type 2 diabetes mellitus
101351	EGF domain specific O-linked N-acetylglucosamine transferase	Eogt	Adams-Oliver syndrome
77781	EPM2A interacting protein 1	Epm2aip1
192193	ER degradation enhancer, mannosidase alpha-like 1	Edem1	cystic fibrosis
108687	ER degradation enhancer, mannosidase alpha-like 2	Edem2
66967	ER degradation enhancer, mannosidase alpha-like 3	Edem3	congenital disorder of glycosylation type II
74155	ERBB receptor feedback inhibitor 1	Errfi1	endometrial cancer osteoarthritis
75578	FGGY carbohydrate kinase domain containing	Fggy
269952	GDP-D-glucose phosphorylase 1	Gdpgp1

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