3591
|
|
|
Striatin 3 |
PPP2R6B, S/G2NA, SG2NA |
Curated: Colorectal cancer
Unreviewed: Bladder carcinoma, Bladder Neoplasm, Hepatocellular carcinoma, Urinary bladder cancer, Vitiligo, Vitiligo-associated SYSTEMIC LUPUS ERYTHEMATOSUS
|
3592
|
|
|
Striatin 4 |
PPP2R6C, ZIN, zinedin |
Curated: N/A
Unreviewed: Arachnodactyly, Asthma, Autism, Endometrial neoplasm, Glioma, Hepatocellular carcinoma, Limb-girdle muscular dystrophy, Lung carcinoma, Malignant Neoplasm, Myopia, Neoplasms, Nervous System Disorder, Pancreatic cancer, Pancreatic carcinoma, Prostatic Neoplasms, Scoliosis
|
3593
|
|
|
Steroid sulfatase |
ARSC, ARSC1, ASC, ES, SSDD, XLI |
Curated: Rheumatoid arthritis, Attention deficit hyperactivity disorder, Autism, Fatty liver, Fatty liver, alcoholic, Alcoholic hepatitis, Diabetes mellitus type 2, Obesity, X-linked ichthyosis with steryl-sulfatase deficiency
Unreviewed: 46, XX Gonadal Sex Reversal, Achromatopsia, Adenocarcinoma, Alopecia, Male Pattern, Alzheimer disease, Amyloidosis, Anaplastic Oligoastrocytoma, Androgen-Insensitivity Syndrome, Angioimmunoblastic T-cell lymphoma, Aortic valve calcification, Aortic Valve Disease, Aortic Valve Insufficiency, Aortic Valve Sclerosis, Arterial Occlusive Disease, Arteriosclerosis, Arthritis, Asthma, Astrocytoma, Ataxia-oculomotor apraxia, Atherosclerosis, Atrial Fibrillation, Attention Deficit Hyperactivity Disorder, Auditory perceptual disorder, Autism Spectrum Disorder, Azoospermia, B-Cell Lymphoma, Benign Prostatic Hyperplasia, Bladder carcinoma, Bladder Neoplasm, Brachytelephalangic Chondrodysplasia Punctata, Brain Infarction, Brain Neoplasms, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Cat Eye Syndrome, Catalepsy, Cataract, Cervical Cancer, Cervical Intraepithelial Neoplasia, Cervical Tumor, Cervix carcinoma, Cholangiocarcinoma, Cholangitis, Cholesteatoma, Chondrodysplasia Punctata, Chronic Obstructive Pulmonary Disease, Cirrhosis, Colitis, Colonic Neoplasms, Colorectal adenoma, Colorectal Cancer, Complete Atrioventricular Block, Congenital Chromosomal Disease, Congenital Ichthyosis, Congenital Nonbullous Ichthyosiform Erythroderma, Congestive Heart Failure, Corneal Dystrophy, Coronary artery disease, Coronary Heart Disease, Cryopyrin-Associated Periodic Syndromes, Cryptorchidism, Cystic Fibrosis, Dermatologic Disorders, Developmental Delay, Diabetes Mellitus, Diabetic cardiomyopathy, Diabetic Nephropathy, Diffuse Lymphoma, Down Syndrome, Ductal carcinoma, Dwarfism, Dysphasia, Eczema, Encephalitis, Endometrial Cancer, Endometrial carcinoma, Endometrial Hyperplasia, Endometrial Neoplasms, Endometriosis, Epidermodysplasia Verruciformis, Epidermolysis Bullosa, Epithelial ovarian carcinoma, Esophageal Cancer, Fatty Liver, Fibroadenoma, Fibrosarcoma, Gastric Varix, Gastroparesis, Glioblastoma, Glioma, Heart Failure, Hepatic Encephalopathy, Hereditary Hemochromatosis, Hodgkin Disease, Huntington Disease, Hyperandrogenism, Hyperkeratosis, Hypertension, Hypogonadism, Hypohidrosis, Hypoparathyroidism, Hypoparathyroidism-deafness-renal disease syndrome, Ichthyosis, Ichthyosis Congenita, Ichthyosis Vulgaris, Ichthyosis, X-Linked, Immune Thrombocytopenic Purpura, Inborn Errors Of Metabolism, Inflammatory Bowel Disease, Intestinal Diseases, Intraepithelial Neoplasia, Kallmann Syndrome, Kawasaki disease, Kidney Disease, Kidney Failure, Language Disorders, Laryngeal Carcinoma, Leukemia, Liposarcoma, Lissencephaly, Liver Cancer, Liver carcinoma, Liver Cirrhosis, Lung Cancer, Lung carcinoma, Lung Neoplasms, Lymphoma, Malignant Neoplasm, Malignant Neoplasm Of Testis, Mammary Neoplasms, Melanocytic nevus, Melanoma, Meningioma, Mental retardation, Mental Retardation, X-Linked, Metabolic Diseases, Metabolic Syndrome, Migraine, Minimal Brain Dysfunction, Mood Disorder, Multiple Sulfatase Deficiency, Myelodysplastic Syndrome, Myelofibrosis, Myocardial Ischemia, Neoplasms, Nephrocalcinosis, Nephronophthisis, Nephrotic Syndrome, Neurilemmoma, Neurodevelopmental Disorders, Nocturnal enuresis, Nystagmus, Ocular albinism, Oestrogen Receptor Positive Breast Cancer, Oligospermia, Osteoglophonic dwarfism, Osteopenia, Osteosarcoma, Otitis media, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pancreatic adenocarcinoma, Papilloma, Patent ductus arteriosus, Penile Hypospadias, Periodontitis, Peritoneal Fibrosis, Pituitary Neoplasms, Placental Steroid Sulfatase Deficiency, Polycystic Ovary Syndrome, Prader-Willi Syndrome, Prostate cancer, Prostatic neoplasm, Prostatic Neoplasms, Psoriasis, Renal aplasia, Renal Carcinoma, Renal Insufficiency, Renpenning Syndrome, Retinal Diseases, Sarcoma, Schizophrenia, Sclerosing Cholangitis, Seminoma, Sheldon-Hall syndrome, Smith-Lemli-Opitz Syndrome, Smith-Magenis Syndrome, Speech Disorders, Steroid Sulfatase Deficiency Disease, Stomach Carcinoma, Stomach Neoplasms, Stroke, Syndromic Ichthyosis, X-Linked, Thrombophilia, Tremor, Trichohepatoenteric Syndrome, Urinary bladder cancer, Usher Syndrome, Vasculitis, Vulval varices, XX Males
|
3594
|
|
|
Steroid sulfatase (microsomal) pseudogene 1 |
STS-Y, STSP |
Curated: N/A
Unreviewed: N/A
|
3595
|
|
|
STT3 oligosaccharyltransferase complex catalytic subunit A |
CDG1WAD, CDG1WAR, ITM1, STT3-A, TMC |
Curated: Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Congenital disorder of glycosylation, Major depressive disorder, Schizophrenia, STT3A-congenital disorder of glycosylation, congenital disorder of glycosylation, type Iw, autosomal dominant
Unreviewed: Alzheimer disease, Attention Deficit Hyperactivity Disorder, Bipolar Disorder, Breast neoplasm, Carcinogenesis, Cerebellar atrophy, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Colon Carcinoma, Colonic Neoplasms, Cryptorchidism, Development Disorder, Developmental Delay, Developmental disability, Epidermodysplasia Verruciformis, Follicular Thyroid Carcinoma, Glomerulonephritis, Glycogen storage disease, Mental Depression, Mental retardation, Microcephaly, Mucoepidermoid Carcinoma, Nasal polyp, Penis Agenesis, Renal cell carcinoma, Seizures, Skin cancer, Skin carcinoma
|
3596
|
|
|
STT3A antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
3597
|
|
|
STT3 oligosaccharyltransferase complex catalytic subunit B |
CDG1X, SIMP, STT3-B |
Curated: Graft versus host disease, Congenital disorder of glycosylation, Diabetic retinopathy, Gout, Schizophrenia
Unreviewed: Bone disease, Cerebellar atrophy, Colorectal neoplasm, Cryptorchidism, Developmental Delay, Glycogen storage disease, Hypertrophic cardiomyopathy, Intellectual developmental disorder, Lymphatic metastasis, Mental retardation, Microcephaly, Optic Atrophy, Osteoarthritis, Penis Agenesis
|
3598
|
|
|
STIP1 homology and U-box containing protein 1 |
CHIP, HSPABP2, NY-CO-7, SCA48, SCAR16, SDCCAG7, UBOX1 |
Curated: Spinocerebellar ataxia, Cerebellar ataxia
Unreviewed: Alopecia, Alzheimer disease, Amyotrophic Lateral Sclerosis, Anxiety Disorder, Apraxia, Arachnodactyly, Arteriosclerosis, Ataxia, Ataxia, sensory, autosomal dominant, Atherosclerosis, Atrophy, Atrophy Of Corpus Callosum, Attention Deficit Hyperactivity Disorder, Autonomic nervous system disease, Bardet-Biedl Syndrome, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cerebellar Ataxia, Cerebellar ataxia and hypogonadotropic hypogonadism, Cerebellar atrophy, Cerebellar diseases, Cerebellar Hypoplasia, Cerebral Ischemia, Cognition disorder, Colorectal Cancer, Colorectal neoplasm, Congestive Heart Failure, Delayed menarche, Dementia, Developmental Delay, Diabetes, Diabetes Mellitus, Distal amyotrophy, Dysarthria, Dysphagia, Epilepsy, Gastrointestinal stromal tumor, Glaucoma, Glioma, Gordon Holmes syndrome, Head and neck cancer, Head And Neck Carcinoma, Heart Failure, Hematologic Neoplasms, Hematological Disease, Hepatoblastoma, Hepatocellular carcinoma, Hereditary breast and ovarian cancer syndrome, Hereditary elliptocytosis, Horizontal nystagmus, Huntington disease, Huntington Disease-Like, Hypertension, Hypogonadism, Hypothyroidism, Impaired Cognition, Iridocyclitis, Kaufman-McKusick Syndrome, Kidney Disease, Leukemia, Lung Cancer, Lung carcinoma, Lupus Erythematosus, Lymphocytic Leukemia, Malignant Neoplasm, Mammary Neoplasms, Mesothelioma, Metabolic Diseases, Miller Dieker Syndrome, Mouth neoplasm, Movement Disorders, Multiple myeloma, Myelodysplastic Syndrome, Myelofibrosis, Myeloid leukemia, Neoplasms, Neurodegenerative disorder, Neurodegenerative Disorders, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Osteopenia, Ovarian cancer, Ovarian Carcinoma, Ovarian Epithelial carcinoma, Pancreatic cancer, Pancreatic carcinoma, Pancreatitis, Papillary thyroid carcinoma, Parkinson disease, Persistent truncus arteriosus, Physiologic Amenorrhea, Polycystic Ovary Syndrome, Prostate cancer, Rheumatoid arthritis, Schizophrenia, Spastic ataxia, Spastic Paraplegia, Spinocerebellar Ataxia, Stomach Carcinoma, Stomach Neoplasms, Triple Negative Breast Neoplasms, Ulcerative colitis, Uveitis
|
3599
|
|
|
STUB1 divergent transcript |
LA16c-313D11.9, LINC02867 |
Curated: N/A
Unreviewed: N/A
|
3600
|
|
|
STUB1 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|