Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "S"

961 to 970 of 1203 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
961	6857	SYT1	Synaptotagmin 1	BAGOS, P65, SVP65, SYT	Baker-gordon syndrome, Choreoathetosis, Congenital epicanthus, Developmental delay, Dyskinetic syndrome, Dysmorphic features, Gastroesophageal reflux disease, Hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome, Lupus erythematosus, Mental retardation, Micrognathism, Movement disorders, Hypotonia, Nystagmus, Scoliosis View all (3 more)
962	6860	SYT4	Synaptotagmin 4	HsT1192	Melanoma
963	6906	SERPINA7	Serpin family A member 7	TBG, TBGQTL	Congenital isolated thyroxine-binding globulin deficiency, Inborn errors of metabolism, Reduction of thyroxine-binding globulin x-linked
964	692088	SNORD50B	Small nucleolar RNA, C/D box 50B	U50', U50B	Benign neoplasm, Malignant neoplasm, Neoplasms
965	692157	SNORA16B	Small nucleolar RNA, H/ACA box 16B	U98b	Creutzfeldt-jakob disease
966	692200	SNORD103C	Small nucleolar RNA, C/D box 103C	HBII-251, SNORD85	Schizophrenia
967	710	SERPING1	Serpin family G member 1	C1IN, C1INH, C1NH, HAE1, HAE2	Angioedema, C1 inhibitor deficiency, Complement component deficiency, Dermatographic urticaria, Dysphagia, Hereditary c1 esterase inhibitor deficiency, Liver cirrhosis, Liver fibrosis, Lung neoplasms, Lung cancer, Lupus erythematosus, Lupus nephritis, Narcolepsy, Peripheral axonal neuropathy
968	724107	SPG32	-	SPG29	Spastic paraplegia
969	724110	SPG34	-	-	Spastic paraplegia, x-linked
970	727676	SNORD118	Small nucleolar RNA, C/D box 118	LCC, U8	Developmental delay, Dysarthria, Leukodystrophy, Leukoencephalopathy, Leukoencephalopathy with calcifications and cysts, Leukoencephalopathy, brain calcifications, and cysts

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