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 **51 - 75** of **449** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
304646	MGAT4 family, member D	Mgat4d
24577	MYC proto-oncogene, bHLH transcription factor	Myc	Burkitt lymphoma acute lymphoblastic leukemia acute promyelocytic leukemia angiosarcoma breast cancer cancer chronic lymphocytic leukemia clear cell renal cell carcinoma coronary restenosis demyelinating disease hepatitis C hepatocellular carcinoma hyperparathyroidism leiomyoma liver cirrhosis lung adenocarcinoma lung cancer nephroblastoma obesity osteoporosis polycystic kidney disease 1 polycystic kidney disease prolactinoma prostate adenocarcinoma prostate cancer prostatic hypertrophy pulmonary hypertension renal cell carcinoma rhabdoid cancer thyroid gland papillary carcinoma urinary bladder cancer
114104	N-acylsphingosine amidohydrolase 2	Asah2	cardiomyopathy
29633	N-deacetylase and N-sulfotransferase 1	Ndst1	DiGeorge syndrome autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia congenital diaphragmatic hernia intellectual disability newborn respiratory distress syndrome
114002	N-deacetylase and N-sulfotransferase 2	Ndst2	autism spectrum disorder azoospermia intellectual disability
295430	N-deacetylase and N-sulfotransferase 3	Ndst3	autism spectrum disorder azoospermia intellectual disability
362035	N-deacetylase and N-sulfotransferase 4	Ndst4	autism spectrum disorder azoospermia intellectual disability
364682	NHL repeat containing E3 ubiquitin protein ligase 1	Nhlrc1	Lafora disease
154968	O-GlcNAcase	Oga	type 2 diabetes mellitus
26295	O-linked N-acetylglucosamine (GlcNAc) transferase	Ogt	aortic valve stenosis congestive heart failure diabetes mellitus non-syndromic X-linked intellectual disability 106 type 2 diabetes mellitus
298282	OMA1 zinc metallopeptidase	Oma1
83516	PPARG coactivator 1 alpha	Ppargc1a	Alzheimer's disease Huntington's disease Parkinson's disease abdominal obesity-metabolic syndrome age related macular degeneration amblyopia amyotrophic lateral sclerosis cardiovascular system disease chronic obstructive pulmonary disease colitis congenital hypothyroidism diabetic retinopathy dilated cardiomyopathy heart disease hyperglycemia hyperthyroidism kidney cancer kidney failure macular degeneration malignant fibrous histiocytoma melanoma metabolic dysfunction-associated steatotic liver disease myocardial infarction nephrotic syndrome obesity placental insufficiency prediabetes syndrome primary biliary cholangitis renal fibrosis sciatic neuropathy steatotic liver disease type 2 diabetes mellitus
60433	RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	Rfng
362924	ST3 beta-galactoside alpha-2,3-sialyltransferase 1	St3gal1
64442	ST3 beta-galactoside alpha-2,3-sialyltransferase 2	St3gal2
64445	ST3 beta-galactoside alpha-2,3-sialyltransferase 3	St3gal3	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
363040	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	St3gal4
83505	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	St3gal5	salt and pepper syndrome
304023	ST3 beta-galactoside alpha-2,3-sialyltransferase 6	St3gal6
287920	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 1	St6galnac1	inflammatory bowel disease
303692	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2	St6galnac2
29758	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 3	St6galnac3
407764	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 4	St6galnac4
365984	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5	St6galnac5
407765	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 6	St6galnac6

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