Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "S"

1101 to 1110 of 1631 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1101	6659	SOX4	SRY-box transcription factor 4	CSS10, EVI16, IDDSDF	Atrial fibrillation, Adenoid cystic carcinoma, Basal cell carcinoma, Cardiomegaly, Coffin-siris syndrome, Congestive heart failure, Developmental delay, Heart failure, Intellectual developmental disorder speech dysmorphic, Intellectual developmental disorder, Liver cirrhosis, Liver neoplasms, Intellectual disability, Neurodevelopmental disorder, Salivary gland neoplasms
1102	6660	SOX5	SRY-box transcription factor 5	L-SOX5, L-SOX5B, L-SOX5F, LAMSHF	12p12.1 microdeletion syndrome, Anorexia nervosa, Anxiety disorder, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Azoospermia, Bipolar disorder, Color vision deficiency, Colorectal cancer, Coronary artery disease, Crohn disease, Developmental and epileptic encephalopathy, Tourette syndrome, Hemorrhoid View all (22 more)
1103	55553	SOX6	SRY-box transcription factor 6	HSSOX6, SOXD, TOLCAS	Atrial fibrillation, Basal cell carcinoma, Bipolar disorder, Bone fracture, Cardiovascular disease, Colorectal cancer, Neurodevelopmental disorder, Coronary artery disease, Melanoma, Generalized anxiety disorder, Hypertension, Intellectual developmental disorder, Major depressive disorder, Metabolic syndrome, Mood disorder View all (8 more)
1104	83595	SOX7	SRY-box transcription factor 7	-	Autism, Brain aneurysm, Congenital heart disease, Neurotic disorder, Systemic lupus erythematosus, Tetralogy of fallot, Diabetes mellitus type 2
1105	30812	SOX8	SRY-box transcription factor 8	-	Multiple sclerosis, Neurodevelopmental disorder, Non-neoplastic peripheral nervous system disease, Peripheral nervous system disease, Peripheral neuropathy, Polycystic ovary syndrome
1106	6662	SOX9	SRY-box transcription factor 9	CMD1, CMPD1, ENH13, SRA1, SRXX2, SRXY10, TES, TESCO	46, xx ovotesticular disorder of sex development, 46, xx sex reversal, 46, xy complete gonadal dysgenesis, 46, xy partial gonadal dysgenesis, Anonychia, Autism, Bent bone dysplasia, Campomelic dysplasia, Camptomelic dysplasia, Carcinoma, Congenital hand deformities, Connective tissue disease, Cooks syndrome, Craniofacial abnormalities, Desbuquois syndrome View all (5 more)
1107	6667	SP1	Sp1 transcription factor	-	Schizophrenia, Colorectal neoplasms, Hyperglycemia, Hypospadias, Metabolic syndrome, Non-organic psychosis, Osteoporosis, Parkinson disease, Progressive supranuclear palsy, Psychotic disorders, Skin neoplasms, Diabetes mellitus type 2
1108	3431	SP110	SP110 nuclear body protein	IFI41, IFI75, IPR1, VODI	Cholangiocarcinoma, Lymphocytic leukemia, Colorectal cancer, Esophageal squamous cell carcinoma, Hepatic veno occlusive disease with immunodeficiency, Inflammatory bowel disease, Obesity, Obsessive-compulsive disorder, Sclerosing cholangitis, Tuberculoma
1109	11262	SP140	SP140 nuclear body protein	LYSP100, LYSP100-A, LYSP100-B	Ankylosing spondylitis, Cholangiocarcinoma, Lymphocytic leukemia, Colorectal cancer, Crohn disease, Hepatic veno occlusive disease with immunodeficiency, Hodgkin lymphoma, Inflammatory bowel disease, Leukemia, Lymphocytic b-cell leukemia, Liver cirrhosis, Lymphoid leukemia, Multiple myeloma, Multiple sclerosis, Non-hodgkins lymphoma View all (4 more)
1110	93349	SP140L	SP140 nuclear body protein like	-	Lymphoid leukemia, Major depressive disorder, Multiple myeloma, Sarcoidosis

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