Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "S"

911 to 920 of 1631 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
911	6594	SMARCA1	SNF2 related chromatin remodeling ATPase 1	ISWI, NURF140, SNF2L, SNF2L1, SNF2LB, SNF2LT, SWI, SWI2, hSNF2L	Intellectual developmental disorder, x-linked, Neurodevelopmental disorder, Prostatic neoplasms, Schizophrenia, X-linked intellectual disability
912	6595	SMARCA2	SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2	BAF190, BIS, BRM, NCBRS, SAMRCA2, SNF2, SNF2L2, SNF2LA, SWI2, Sth1p, hBRM, hSNF2a	Alzheimer disease, Asthma, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Blepharophimosis intellectual disability syndrome, Blepharophimosis-intellectual disability syndrome, Adenoid cystic carcinoma, Coffin-siris syndrome, Color vision deficiency, Colorectal cancer, Developmental disability, Dyslexia, Gastric cancer, Intellectual developmental disorder View all (11 more)
913	6597	SMARCA4	SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4	BAF190, BAF190A, BRG1, CSS4, MRD16, OTSC12, RTPS2, SNF2, SNF2-beta, SNF2L4, SNF2LB, SWI2, hSNF2b	Alzheimer disease, Amyotrophic lateral sclerosis, Atherosclerosis, Eczema, Atrial septal defect, Autism, Burkitt lymphoma, Small cell carcinoma, Cardiovascular disease, Carotid atherosclerosis, Central nervous system cancer, Cerebral palsy, Cerebrovascular disorder, Coffin-siris syndrome, Coronary artery disease View all (33 more)
914	8467	SMARCA5	SNF2 related chromatin remodeling ATPase 5	ISWI, SNF2H, WCRF135, hISWI, hSNF2H	Neurodevelopmental disorder, Extraskeletal ewing sarcoma, Global developmental delay, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Partial epilepsy, Schizophrenia, Diabetes mellitus type 2
915	56916	SMARCAD1	SNF2 related chromatin remodeling ATPase with DExD box 1	ADERM, BASNS, ETL1, HEL1, HRZ, TYS	Absence of fingerprints-congenital milia syndrome, Androgenetic alopecia, Atrial fibrillation, Bipolar disorder, Ectodermal dysplasia, Major depressive disorder, Neurodevelopmental disorder, Prostatic neoplasms, Schizophrenia
916	50485	SMARCAL1	SNF2 related chromatin remodeling annealing helicase 1	HARP, HHARP	Atrioventricular septal defect, Hemolytic uremic syndrome, Congenital microcephaly, Desbuquois syndrome, Focal glomerulosclerosis, Kidney disease, Nephrotic syndrome, Nonalcoholic fatty liver disease, Steroid-resistant nephrotic syndrome, Diabetes mellitus type 2
917	6598	SMARCB1	SWI/SNF related BAF chromatin remodeling complex subunit B1	BAF47, CSS3, INI-1, INI1, MRD15, PPP1R144, RDT, RTPS1, SNF5, SNF5L1, SWNTS1, Sfh1p, Snr1, hSNFS	Atrial fibrillation, Atypical teratoid rhabdoid tumor, Autism, Cardiomyopathy, Coffin-siris syndrome, Color vision deficiency, Neurodevelopmental disorder, Dementia, Desbuquois syndrome, Developmental disability, Dilated cardiomyopathy, Meningioma, Heart failure, Hematologic disease, Hypertrophic cardiomyopathy View all (5 more)
918	6599	SMARCC1	SWI/SNF related BAF chromatin remodeling complex subunit C1	BAF155, CRACC1, HYC5, Rsc8, SRG3, SWI3	Alzheimer disease, Autism, Color vision deficiency, Congenital hydrocephalus, Dementia, Global developmental delay, Gout, Hydrocephalus, Liver cirrhosis, Lung neoplasms, Diabetes mellitus type 2
919	6601	SMARCC2	SWI/SNF related BAF chromatin remodeling complex subunit C2	BAF170, CRACC2, CSS8, Rsc8	Coffin-siris syndrome, Intellectual developmental disorder, Neurodevelopmental disorder
920	6602	SMARCD1	SWI/SNF related BAF chromatin remodeling complex subunit D1	BAF60A, CRACD1, CSS11, Rsc6p	Coffin-siris syndrome, Neurodevelopmental disorder

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