GlyCosmos Portal

Rattus norvegicus (Norway rat)

Summary

Taxonomy ID: 10116
PubChem Taxonomy: 10116

Genes (449) Glycans (773) Glycoproteins (2935) Lectins (166) Pathways (1070)

Displaying entries **401 - 425** of **449** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
298690	Beta-1,3-galactosyltransferase 6	B3galt6	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome spondyloepimetaphyseal dysplasia with joint laxity type 1
288161	Beta-1,3-galactosyltransferase 5	B3galt5	pancreatic cancer
171079	Beta-1,3-galactosyltransferase 4	B3galt4
686081	Beta-1,3-galactosyltransferase 2	B3galt2
366064	Beta-1,3-galactosyltransferase 1	B3galt1
291212	beta-1,3-N-acetylgalactosaminyltransferase 2	B3galnt2	congenital muscular dystrophy-dystroglycanopathy type A11
310508	beta-1,3-N-acetylgalactosaminyltransferase 1 (globoside blood group)	B3galnt1
24212	ATPase Na+/K+ transporting subunit alpha 2	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
79255	activating transcription factor 4	Atf4	borna disease prostate carcinoma pulmonary venoocclusive disease
25389	activating transcription factor 3	Atf3	prostate cancer pulmonary tuberculosis
114104	N-acylsphingosine amidohydrolase 2	Asah2	cardiomyopathy
259167	ADP-ribosyltransferase 5	Art5
293152	ADP-ribosyltransferase 2b	Art2b
79120	ADP-ribosylation factor 4	Arf4
292072	adenine phosphoribosyl transferase	Aprt	adenine phosphoribosyltransferase deficiency hepatocellular carcinoma
25239	apolipoprotein D	Apod	Alzheimer's disease gestational diabetes obesity status epilepticus type 2 diabetes mellitus vasculogenic impotence
497039	amylase 2a3	Amy2a3
367083	ALG9, alpha-1,2-mannosyltransferase	Alg9	congenital disorder of glycosylation Il congenital disorder of glycosylation type I
293129	ALG8, alpha-1,3-glucosyltransferase	Alg8	congenital disorder of glycosylation Ih congenital disorder of glycosylation type I polycystic liver disease
362547	ALG6, alpha-1,3-glucosyltransferase	Alg6	congenital disorder of glycosylation Ic congenital disorder of glycosylation type I
295051	ALG5, dolichyl-phosphate beta-glucosyltransferase	Alg5	congenital disorder of glycosylation type I polycystic kidney disease
287983	ALG3, alpha-1,3- mannosyltransferase	Alg3	congenital disorder of glycosylation Id congenital disorder of glycosylation
313231	ALG2, alpha-1,3/1,6-mannosyltransferase	Alg2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
362031	ALG14, UDP-N-acetylglucosaminyltransferase subunit	Alg14	congenital myasthenic syndrome 15
300284	ALG13, UDP-N-acetylglucosaminyltransferase subunit like 1	Alg13l1	developmental and epileptic encephalopathy 36

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