Genes | GeDiPNet - Gene Disease Pathway & Associations

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12421 to 12430 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
12421	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
12422	6601	SMARCC2	SWI/SNF related BAF chromatin remodeling complex subunit C2	BAF170, CRACC2, CSS8, Rsc8	Coffin-siris syndrome, Intellectual developmental disorder, Neurodevelopmental disorder
12423	6602	SMARCD1	SWI/SNF related BAF chromatin remodeling complex subunit D1	BAF60A, CRACD1, CSS11, Rsc6p	Coffin-siris syndrome, Neurodevelopmental disorder
12424	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
12425	6604	SMARCD3	SWI/SNF related BAF chromatin remodeling complex subunit D3	BAF60C, CRACD3, Rsc6p	Multiple myeloma
12426	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)
12427	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)
12428	27127	SMC1B	Structural maintenance of chromosomes 1B	SMC1BETA, SMC1L2	Colorectal cancer, Gonadal dysgenesis, Rheumatoid arthritis, Urinary bladder neoplasms
12429	10592	SMC2	Structural maintenance of chromosomes 2	CAP-E, CAPE, SMC-2, SMC2L1	Alzheimer disease, Aortic stenosis, Basal cell carcinoma, Biliary tract cancer, Breast cancer, Cancer, Cervical cancer, Colorectal cancer, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Hepatocellular carcinoma, Keratinocyte carcinoma, Liver cirrhosis View all (14 more)
12430	9126	SMC3	Structural maintenance of chromosomes 3	BAM, BMH, CDLS3, CSPG6, HCAP, SMC3L1	Autism, Cornelia de lange syndrome, De lange syndrome, Desbuquois syndrome, Intellectual developmental disorder, Myeloid leukemia, Neurodevelopmental disorder, Neuromuscular disease, Wiedemann-steiner syndrome

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