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

12411 to 12420 of 15448 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
12411	4093	SMAD9	SMAD family member 9	MADH6, MADH9, PPH2, SMAD8, SMAD8/9, SMAD8A, SMAD8B	Aortic stenosis, Aortic valve disease, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Coronary artery disease, Pulmonary hypertension, Pulmonary arterial hypertension, Myocardial infarction, Prostate cancer
12412	60682	SMAP1	Small ArfGAP 1	SMAP-1	Color vision deficiency, Ocular hypotension
12413	64744	SMAP2	Small ArfGAP2	SMAP1L	Pancreatic cancer
12414	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
12415	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)
12416	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)
12417	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
12418	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
12419	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
12420	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)

«««...1240 124112421243 1244...»»»