GlyCosmos Portal

Displaying entries **276 - 300** of **320** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
100497898	polypeptide N-acetylgalactosaminyltransferase 17	galnt17
100488804	polypeptide N-acetylgalactosaminyltransferase 18	galnt18
100488284	polypeptide N-acetylgalactosaminyltransferase 2	galnt2	congenital disorder of glycosylation type II
100488466	polypeptide N-acetylgalactosaminyltransferase 3	galnt3	hyperphosphatemic familial tumoral calcinosis
780162	polypeptide N-acetylgalactosaminyltransferase 4	galnt4
101733275	polypeptide N-acetylgalactosaminyltransferase 5	galnt5
100497888	polypeptide N-acetylgalactosaminyltransferase 6	galnt6.1
100498043	polypeptide N-acetylgalactosaminyltransferase 6, gene 3	galnt6.3
407859	polypeptide N-acetylgalactosaminyltransferase 7	galnt7
100490061	polypeptide N-acetylgalactosaminyltransferase 9	galnt9
100487935	polypeptide N-acetylgalactosaminyltransferase like 6	galntl6
734090	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	plod3	hepatocellular carcinoma hypothyroidism
496411	protein O-fucosyltransferase 1	pofut1	Dowling-Degos disease
779585	protein O-fucosyltransferase 2	pofut2	Down syndrome
493476	protein O-glucosyltransferase 1	poglut1
100158594	protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)	pomgnt1	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2O congenital muscular dystrophy-dystroglycanopathy type A3 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy retinitis pigmentosa
496628	protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)	pomgnt2	congenital muscular dystrophy-dystroglycanopathy type A8 muscular dystrophy-dystroglycanopathy type C8
548704	protein phosphatase 1 regulatory subunit 3B	ppp1r3b	alcohol use disorder
448158	protein phosphatase 1 regulatory subunit 3C gene 2	ppp1r3c.2	alcohol use disorder
496958	protein phosphatase 1, catalytic subunit, beta isozyme	ppp1cb	Noonan syndrome-like disorder with loose anagen hair 2 cancer
407879	protein phosphatase 1, catalytic subunit, gamma isozyme	ppp1cc	cancer congestive heart failure type 2 diabetes mellitus
448433	protein-O-mannosyltransferase 1	pomt1	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2K cardiomyopathy cleft lip congenital muscular dystrophy-dystroglycanopathy type A1 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy muscular dystrophy
100490100	protein-O-mannosyltransferase 2	pomt2	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy congenital muscular dystrophy-dystroglycanopathy type A2 lissencephaly muscular dystrophy-dystroglycanopathy type B2 muscular dystrophy-dystroglycanopathy muscular dystrophy
100489267	provisional ortholog of UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7	XB5969542
100496837	provisional ortholog of core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1	XB5871033	autoimmune disease of blood

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