GlyCosmos Portal

Displaying entries **401 - 425** of **748** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
431727	alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B	mgat4b
100333333	mgat4 family member C	mgat4c
724006	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	mgat5	proteinuria
101884072	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B	mgat5b
569613	malectin	mlec
100003089	matrix metallopeptidase 21	mmp21
570584	monooxygenase, DBH-like 1	moxd1
447806	mannose-P-dolichol utilization defect 1a	mpdu1a	congenital disorder of glycosylation If
415220	mannose-P-dolichol utilization defect 1b	mpdu1b	congenital disorder of glycosylation If
100003330	melanocortin 2 receptor accessory protein 2a	mrap2a
101884805	melanocortin 2 receptor accessory protein 2b	mrap2b
798441	myostatin b	mstnb
393526	methylthioadenosine phosphorylase	mtap	biliary tract benign neoplasm common bile duct neoplasm diaphyseal medullary stenosis with malignant fibrous histiocytoma pancreatic cancer
30667	melatonin receptor 1A a	mtnr1aa
30668	melatonin receptor 1Bb	mtnr1bb
406207	microsomal triglyceride transfer protein	mttp
30686	MYC proto-oncogene, bHLH transcription factor a	myca
393141	MYC proto-oncogene, bHLH transcription factor b	mycb
791161	NALCN channel auxiliary factor 2	nalf2
336746	napsin A aspartic peptidase	napsa
336844	nicalin	ncln
561437	neuron-derived neurotrophic factor	ndnf
100329944	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1a	ndst1a	DiGeorge syndrome autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia congenital diaphragmatic hernia intellectual disability newborn respiratory distress syndrome
570459	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1b	ndst1b	DiGeorge syndrome autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia congenital diaphragmatic hernia intellectual disability newborn respiratory distress syndrome
793524	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2a	ndst2a	autism spectrum disorder azoospermia intellectual disability

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