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 **626 - 650** of **662** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
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
231841	BRCA1-associated ATM activator 1	Brat1
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
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
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
102580	ALG9 alpha-1,2-mannosyltransferase	Alg9	congenital disorder of glycosylation Il 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
320438	ALG6 alpha-1,3-glucosyltransferase	Alg6	congenital disorder of glycosylation Ic congenital disorder of glycosylation type I
66248	ALG5 dolichyl-phosphate beta-glucosyltransferase	Alg5	congenital disorder of glycosylation type I polycystic kidney disease
208624	ALG3 alpha-1,3- mannosyltransferase	Alg3	congenital disorder of glycosylation Id congenital disorder of glycosylation
56737	ALG2 alpha-1,3/1,6-mannosyltransferase	Alg2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
223774	ALG12 alpha-1,6-mannosyltransferase	Alg12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
207958	ALG11 alpha-1,2-mannosyltransferase	Alg11	congenital disorder of glycosylation Ip
380959	ALG10 alpha-1,2-glucosyltransferase	Alg10b	long QT syndrome 2 nonsyndromic deafness
208211	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	Alg1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
11875	ADP-ribosyltransferase 5	Art5
109978	ADP-ribosyltransferase 4	Art4
109979	ADP-ribosyltransferase 3	Art3
11872	ADP-ribosyltransferase 2b	Art2b
11871	ADP-ribosyltransferase 2a	Art2a
11870	ADP-ribosyltransferase 1	Art1
100206	ADP-ribosylserine hydrolase	Adprs	stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
234072	ADP-ribosylhydrolase like 1	Adprhl1
56297	ADP-ribosylation factor-like 6	Arl6	Bardet-Biedl syndrome 1 Bardet-Biedl syndrome 3 Bardet-Biedl syndrome ciliopathy retinitis pigmentosa 55
11843	ADP-ribosylation factor 4	Arf4

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