GlyCosmos Portal

Displaying entries **551 - 575** of **662** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
64383	sirtuin 2	Sirt2	cocaine dependence high grade glioma intermittent claudication metabolic dysfunction-associated steatotic liver disease
75387	sirtuin 4	Sirt4	metabolic dysfunction-associated steatotic liver disease
50721	sirtuin 6	Sirt6	metabolic dysfunction-associated steatotic liver disease obesity progeria transient cerebral ischemia
54338	solute carrier family 23 (nucleobase transporters), member 2	Slc23a2
27376	solute carrier family 25 (mitochondrial carrier, dicarboxylate transporter), member 10	Slc25a10	mitochondrial DNA depletion syndrome 19 mitochondrial DNA depletion syndrome mitochondrial complex I deficiency myoclonic-atonic epilepsy
67863	solute carrier family 25 (mitochondrial carrier oxoglutarate carrier), member 11	Slc25a11	paraganglioma
50799	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	Slc25a13	adult-onset type II citrullinemia citrullinemia common bile duct disease intrahepatic cholestasis neonatal-onset type II citrullinemia
56017	solute carrier family 2, (facilitated glucose transporter), member 8	Slc2a8
213053	solute carrier family 39 (zinc transporter), member 14	Slc39a14	hypermanganesemia with dystonia 2
20532	solute carrier family 3, member 1	Slc3a1	cystinuria
17254	solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2	Slc3a2	adenoid cystic carcinoma lung adenocarcinoma lung non-small cell carcinoma lung pleomorphic carcinoma stomach carcinoma tongue squamous cell carcinoma transitional cell carcinoma
20597	sphingomyelin phosphodiesterase 1, acid lysosomal	Smpd1	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
100340	sphingomyelin phosphodiesterase, acid-like 3B	Smpdl3b
71726	single-strand selective monofunctional uracil DNA glycosylase	Smug1
20322	sorbitol dehydrogenase	Sord	autosomal recessive distal hereditary motor neuronopathy 8 cataract diabetic neuropathy obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
75622	sperm acrosome associated 3	Spaca3
278203	sperm acrosome associated 5	Spaca5
20690	sperm adhesion molecule 1	Spam1
217116	spermatogenesis associated 20	Spata20	oligoasthenoteratozoospermia
20442	ST3 beta-galactoside alpha-2,3-sialyltransferase 1	St3gal1
20444	ST3 beta-galactoside alpha-2,3-sialyltransferase 2	St3gal2
20441	ST3 beta-galactoside alpha-2,3-sialyltransferase 3	St3gal3	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
20443	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	St3gal4
20454	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	St3gal5	salt and pepper syndrome
54613	ST3 beta-galactoside alpha-2,3-sialyltransferase 6	St3gal6

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