Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "S"

911 to 920 of 1624 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
911	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
912	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)
913	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, Lung neoplasms, Diabetes mellitus type 2
914	6601	SMARCC2	SWI/SNF related BAF chromatin remodeling complex subunit C2	BAF170, CRACC2, CSS8, Rsc8	Coffin-siris syndrome, Intellectual developmental disorder, Neurodevelopmental disorder
915	6602	SMARCD1	SWI/SNF related BAF chromatin remodeling complex subunit D1	BAF60A, CRACD1, CSS11, Rsc6p	Coffin-siris syndrome, Neurodevelopmental disorder
916	6603	SMARCD2	SWI/SNF related BAF chromatin remodeling complex subunit D2	BAF60B, CRACD2, PRO2451, Rsc6p, SGD2	Severe congenital neutropenia, Myeloid leukemia, Neutropenia, Specific granule deficiency
917	6604	SMARCD3	SWI/SNF related BAF chromatin remodeling complex subunit D3	BAF60C, CRACD3, Rsc6p	Multiple myeloma
918	6605	SMARCE1	SWI/SNF related BAF chromatin remodeling complex subunit E1	BAF57, CSS5	Asthma, Eczema, Adenoid cystic carcinoma, Cardiovascular disease, Cleft face, Coffin-siris syndrome, Crohn disease, Dermatitis, Desbuquois syndrome, Meningioma, Inflammatory bowel disease, Intellectual developmental disorder, Periodontal disease, Periodontitis, Respiratory system disease View all (4 more)
919	8243	SMC1A	Structural maintenance of chromosomes 1A	CDLS2, DEE85, DXS423E, EIEE85, SB1.8, SMC1, SMC1L1, SMC1alpha, SMCB	Rett syndrome, Adenoid cystic carcinoma, Cerebellar atrophy, Congenital muscular hypertrophy-cerebral syndrome, Congenital neurologic anomalies, Congenital pes cavus, Congestive heart failure, Cornelia de lange syndrome, De lange syndrome, Desbuquois syndrome, Developmental and epileptic encephalopathy, Dysarthria, Epilepsy, Global developmental delay, Heart failure View all (9 more)
920	27127	SMC1B	Structural maintenance of chromosomes 1B	SMC1BETA, SMC1L2	Colorectal cancer, Gonadal dysgenesis, Rheumatoid arthritis, Urinary bladder neoplasms

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