GlyCosmos Portal

Displaying entries **576 - 600** of **662** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
20454	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	St3gal5	salt and pepper syndrome
20443	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	St3gal4
20441	ST3 beta-galactoside alpha-2,3-sialyltransferase 3	St3gal3	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
20444	ST3 beta-galactoside alpha-2,3-sialyltransferase 2	St3gal2
20442	ST3 beta-galactoside alpha-2,3-sialyltransferase 1	St3gal1
75859	RIKEN cDNA 4930568D16 gene	4930568D16Rik
19719	RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	Rfng
67013	OMA1 zinc metallopeptidase	Oma1
108155	O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase)	Ogt	aortic valve stenosis congestive heart failure diabetes mellitus non-syndromic X-linked intellectual disability 106 type 2 diabetes mellitus
106821	O-acyl-ADP-ribose deacylase 1	Oard1
76055	O-GlcNAcase	Oga	type 2 diabetes mellitus
18145	NPC intracellular cholesterol transporter 1	Npc1	Niemann-Pick disease type C1 Niemann-Pick disease
105193	NHL repeat containing 1	Nhlrc1	Lafora disease
268395	N-methylpurine-DNA glycosylase	Mpg
64580	N-deacetylase/N-sulfotransferase (heparin glucosaminyl) 4	Ndst4	autism spectrum disorder azoospermia intellectual disability
83398	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	Ndst3	autism spectrum disorder azoospermia intellectual disability
17423	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	Ndst2	autism spectrum disorder azoospermia intellectual disability
15531	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1	Ndst1	DiGeorge syndrome autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia congenital diaphragmatic hernia intellectual disability newborn respiratory distress syndrome
54447	N-acylsphingosine amidohydrolase 2	Asah2	cardiomyopathy
94181	N-acetylneuraminic acid synthase (sialic acid synthase)	Nans	spondyloepimetaphyseal dysplasia, Genevieve-type
214505	N-acetylglucosamine-1-phosphotransferase, gamma subunit	Gnptg	glycoproteinosis mucolipidosis III gamma
27426	N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase	Nagpa
432486	N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits	Gnptab	mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucolipidosis
17939	N-acetyl galactosaminidase, alpha	Naga	Fabry disease Kanzaki disease Schindler disease type 1 angiokeratoma neuroaxonal dystrophy
71001	MGAT4 family, member E	Mgat4e

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