Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Showing genes starting with "S"

551 to 560 of 1203 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
551	55206	SBNO1	Strawberry notch homolog 1	MOP3, Sno	Alzheimer disease, Insomnia, Osteoarthritis, Schizophrenia, Diabetes mellitus, type 2, Uterine fibroid, Venous thromboembolism
552	55209	SETD5	SET domain containing 5	MRD23, SETD5A	Attention deficit hyperactivity disorder, Autism, Congenital heart disease, Developmental disability, Global developmental delay, Hearing impairment, Hyperphosphatasia with intellectual disability syndrome, Intellectual developmental disorder, Intellectual developmental disorder dysmorphic facial, Irritable bowel syndrome, Metabolic syndrome, Neurodevelopmental disorders, Non-specific syndromic intellectual disability, Polymicrogyria, Diabetes mellitus, type 2, Uranostaphyloschisis View all (1 more)
553	55240	STEAP3	STEAP3 metalloreductase	AHMIO2, STMP3, TSAP6, dudlin-2, dudulin-2, pHyde	Hypochromic microcytic anemia, Colorectal cancer, Hyperopia, Lewy body disease, Hypochromic sideroblastic anemia, Skin disease
554	55244	SLC47A1	Solute carrier family 47 member 1	MATE1	Brain aneurysm, Kidney disease, Gout
555	55304	SPTLC3	Serine palmitoyltransferase long chain base subunit 3	C20orf38, LCB 3, LCB2B, LCB3, SPT 3, SPT3, SPTLC2L, dJ718P11, dJ718P11.1, hLCB2b	Cerebral amyloid angiopathy, Peripheral neuropathy, Sensory neuropathy
556	55315	SLC29A3	Solute carrier family 29 member 3	ENT3, HCLAP, HJCD, PHID	Asthma, Congenital heart disease, Major depressive disorder, Desbuquois syndrome, Diabetes mellitus type 1, Digestive system neoplasm, Dysosteosclerosis, Hearing impairment, Hearing loss, Congenital heart defect, Hepatomegaly, Hypertrichosis, Hypogonadism, Depression, Obesity View all (2 more)
557	55342	STRBP	Spermatid perinuclear RNA binding protein	HEL162, ILF3L, SPNR, p74	Astrocytoma, Central nervous system cancer, Dementia, Glioblastoma, Glioma, Insomnia, Metabolic syndrome, Oligodendroglioma, Diabetes mellitus, type 2
558	55343	SLC35C1	Solute carrier family 35 member C1	CDG2C, FUCT1	Alzheimer disease, Attention deficit hyperactivity disorder, Congenital disorder of glycosylation, Desbuquois syndrome, Leukocyte adhesion deficiency, Diabetes mellitus, type 2
559	55351	STK32B	Serine/threonine kinase 32B	HSA250839, STK32, STKG6, YANK2	Alzheimer disease, Celiac disease, Essential tremor, Schizophrenia, Spermatocele
560	55356	SLC22A15	Solute carrier family 22 member 15	FLIPT1, PRO34686	Colorectal neoplasm

«««...54 555657 58...»»»