189951
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Trio Rho guanine nucleotide exchange factor |
ARHGEF23, MEBAS, MRD44, MRD63, tgat |
Curated: Anaphylaxis, Angioedema, Asthma, Color vision deficiency, Deafness, Developmental delay, Essential tremor, Gout, Intellectual developmental disorder, Myeloid leukemia, Liver neoplasms, Major depressive disorder, Neuroblastoma, Neurodevelopmental disorder, Neuropathy, Peripheral neuropathy, Prostate cancer, syndromic intellectual disability
Unreviewed: Adenocarcinoma, Arthritis, Atrioventricular septal defect, Attention Deficit Hyperactivity Disorder, Autism, Autism spectrum disorder, B-Cell Lymphoma, beta Thalassemia, Bladder carcinoma, Bladder Neoplasm, Brachydactyly, Breast neoplasm, Camptodactyly of fingers, Cardiovascular disease, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Cirrhosis, Clinodactyly, Colorectal Cancer, Congenital Epicanthus, Congenital Microcephaly, Congenital Pectus Excavatum, Congenital ptosis, Coronary Heart Disease, Developmental Delay, Developmental disability, Dysmorphic Features, Dyssomnia, Ectodermal dysplasia, Encephalitis, Epilepsy, Fibromyxosarcoma, Glioblastoma, Hearing loss, Hepatocellular carcinoma, High palate, Hypercalcemia, Hypertension, Hypodontia, Hypophosphatasia, Leukemia, Liposarcoma, Liver Cancer, Liver carcinoma, Liver Cirrhosis, Lung neoplasms, Lymphatic metastasis, Macrotia, Malignant Neoplasm, Malignant Peripheral Nerve Sheath Tumor, Mental Depression, Mental retardation, Metastatic Melanoma, Metastatic Prostate Carcinoma, Microcephaly, Micrognathism, Mosaic variegated aneuploidy, Motor delay, Multiple Congenital Anomalies, Myeloid Leukemia, Neoplasms, Neurodevelopmental Disorders, Obsessive-Compulsive Disorder, Osteoporosis, Proteinuria, Sarcoma, Schizophrenia, Scoliosis, Sleep Disorders, Spasms X-Linked, Specific Learning Disorder, Spinocerebellar Ataxia, Stereotyped Behavior, Strabismus, Syndactyly Of The Toes, Synophrys, Thyroid Hormone Resistance, Triple negative breast cancer, Urinary bladder cancer, Urinary bladder neoplasms, Uterine neoplasm, Uveal Melanoma
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189952
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TRIO and F-actin binding protein |
DFNB28, HRIHFB2122, TAP68, TARA, dJ37E16.4 |
Curated: Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Glaucoma, Hearing loss, Hereditary hearing loss, Meniere disease, Nephrolithiasis, Open angle glaucoma, Osteoarthritis, hearing loss, autosomal recessive
Unreviewed: Carcinogenesis, Colorectal Cancer, Diabetes Mellitus, Glioblastoma, Glioma, Malignant Neoplasm, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness, Renal cell carcinoma, Schizophrenia, Skin neoplasm, Stomach neoplasms
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189953
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Thyroid hormone receptor interactor 10 |
CIP4, HSTP, STOT, STP, TRIP-10 |
Curated: N/A
Unreviewed: Adenocarcinoma, Adenoma, Bile duct carcinoma, Brain Neoplasms, Breast Cancer, Breast Carcinoma, Bulbospinal Atrophy, X-Linked, Carcinoma, Cholangiocarcinoma, Colorectal Cancer, Diabetic Nephropathy, Duchenne muscular dystrophy, Huntington Disease, Hypertension, Kawasaki disease, Laryngeal neoplasm, Liver Cancer, Liver carcinoma, Lung adenocarcinoma, Lung carcinoma, Lymphocytic Leukemia, Malignant Neoplasm, Mammary Neoplasms, Myocardial Ischemia, Nasopharyngeal Carcinoma, Neoplasms, Neuronal Ceroid Lipofuscinosis, Oestrogen Receptor Positive Breast Cancer, Pancreatic neoplasm, Prostate cancer, Pulmonary Fibrosis, Renal Carcinoma, Squamous cell carcinoma, Triple negative breast cancer, Triple Negative Breast Neoplasms
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189954
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TRIP10 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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189955
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Thyroid hormone receptor interactor 11 |
ACG1A, CEV14, GMAP-210, GMAP210, ODCD, ODCD1, TRIP-11, TRIP230 |
Curated: Achondrogenesis, Connective tissue disease, Desbuquois syndrome, Major depressive disorder, Spondylometaphyseal dysplasia, TRIP11-related skeletal dysplasia
Unreviewed: Acromelia, Brachydactyly, Congenital Exomphalos, Congenital genu recurvatum, Congenital Hypoplasia Of Radius, Congenital Pectus Carinatum, Cystic hygroma, Defect Of Skull Ossification, Dentinogenesis Imperfecta, Developmental delay, Dwarfism, Eosinophilia, Frontal bossing, Hepatitis b, Hernia, Femoral, Hydrops Fetalis, Hypertension, Hypoglycemia, Hypoplasia Of Lower Limb, Hypotonia, Hypoxia, Kidney Cancer, Kidney neoplasm, Leukemia, Lung disease, Macrocephaly, Mesomelia, Micrognathism, Micromelia, Motor delay, Myeloid leukemia, Neoplasms, Odontochondrodysplasia, Osteochondrodysplasia, Osteoporosis, Patent ductus arteriosus, Polycystic kidney disease, Pyle Metaphyseal Dysplasia, Renal Carcinoma, Renal cell carcinoma, Retinoblastoma, Rhizomelia, Scoliosis, Short clavicles, Skeletal Dysplasia, Spondylometaphyseal dysplasia with dentinogenesis imperfecta, Strabismus, Strudwick Syndrome, Thoracic hypoplasia
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189956
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Thyroid hormone receptor interactor 12 |
MRD49, TRIP-12, TRIPC, ULF |
Curated: Clark-baraitser syndrome, Color vision deficiency, Neurodevelopmental disorder, Intellectual developmental disorder, Metabolic syndrome, Non-specific syndromic intellectual disability, Diabetes mellitus type 2, complex neurodevelopmental disorder
Unreviewed: Atrial Septal Defect, Autism, Autism Spectrum Disorder, Breast neoplasm, Carcinogenesis, Carcinoma Of The Head And Neck, Clinodactyly, Congenital abnormalities, Congenital Epicanthus, Developmental Delay, Developmental disability, Dysmorphic Features, Epilepsy, Facial dysmorphism, Facial dysmorphism syndrome, Gata2 deficiency, Hereditary breast and ovarian cancer syndrome, High palate, Language development disorders, Learning Disorders, Macrostomia, Meconium ileus, Mental retardation, Micrognathism, Myeloid leukemia, Neuroblastoma, Neurodevelopmental Disorders, Obesity, Seizures, Strabismus, Temporomandibular Joint Disorders, Trigonocephaly
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189957
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Thyroid hormone receptor interactor 13 |
16E1BP, MVA3, OOMD9, OZEMA9 |
Curated: Aneuploidy, Hepatocellular carcinoma, Female infertility, Mosaic variegated aneuploidy, Oocyte maturation defect, Post-traumatic stress disorder, Squamous cell carcinoma, Wilms tumor
Unreviewed: Adenocarcinoma, Ambiguous Genitalia, Aniridia, Aortic Aneurysm, Aortic Coarctation, Aortic Valve Insufficiency, Athetoid cerebral palsy, Atrial Septal Defect, Bartter syndrome, Bladder carcinoma, Bladder Neoplasm, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cafe-au-lait spot, Camptodactyly of fingers, Carcinogenesis, Carcinoma Of The Head And Neck, Cataract, Cerebellar Hypoplasia, Chordoma, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Congenital Epicanthus, Dandy-Walker Syndrome, Developmental Delay, Duodenal Atresia, Dwarfism, Embryonal Neoplasm, Epithelial ovarian carcinoma, Esophageal squamous cell carcinoma, Esophagus Neoplasm, Extrapyramidal dyskinesia, Frontal bossing, Glaucoma, Glioblastoma, Glioma, Head and neck cancer, Head And Neck Carcinoma, Head and neck neoplasm, Hematologic Neoplasms, Hemolytic anemia, Holoprosencephaly, Hypertension, Hypothyroidism, Infertility, Intestinal Polyposis, Kidney Failure, Liver carcinoma, Liver neoplasms, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung Neoplasms, Lymphatic Metastasis, Lymphoblastic Leukemia, Lymphocytic Leukemia, Malignant Neoplasm, Melanoma, Mental retardation, Mesothelioma, Microcephaly, Micrognathism, Microphthalmos, Mosaic Variegated Aneuploidy, Multicystic renal dysplasia, Multiple myeloma, Muscular dystrophy, Myelodysplasia, Myelodysplastic Syndrome, Necrosis, Neoplasm, Neoplasms, Nephroblastoma, Ovarian cancer, Ovarian Epithelial carcinoma, Papillary thyroid cancer, Pontoneocerebellar hypoplasia, Prostate cancer, Prostatic neoplasm, Renal cell carcinoma, Rhabdomyosarcoma, Schizophrenia, Stomach disease, Stomach Neoplasms, Subaortic Stenosis, Thyroid cancer, Thyroid Carcinoma, Thyroid Neoplasm, Tumor, Urinary bladder cancer, Urinary bladder neoplasms, Vaginal Neoplasms
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189958
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Thyroid hormone receptor interactor 4 |
ASC-1, ASC1, HsT17391, MDCDC, SMABF1, ZC2HC5 |
Curated: Alzheimer disease, Centronuclear myopathy, Congenital muscular dystrophy, Pericarditis, Spinal muscular atrophy
Unreviewed: Amyotrophic lateral sclerosis, Amyotrophy, Arthrogryposis multiplex congenita, Breast Cancer, Breast Carcinoma, Carcinogenesis, Cardiomyopathy, Cerebellar hypoplasia, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Congenital alveolar dysplasia, Congenital Muscular Dystrophy-Respiratory Failure-Skin Abnormalities-Joint Hyperlaxity Syndrome, Congenital myopathy, Congenital Pectus Excavatum, Cryptorchidism, Cystinuria, Developmental Delay, Diaphragmatic Eventration, Dilated cardiomyopathy, Dysphagia, Gastroesophageal Reflux Disease, Glioblastoma, Glioma, High palate, Hypohidrosis, Melanoma, Microstomia, Minicore myopathy with external ophthalmoplegia, Motor delay, Muscular dystrophy, Muscular Dystrophy, Congenital, Myopathy, Myotonia congenita, Nasopharyngeal carcinoma, Neoplasms, Neuromuscular Diseases, Patent ductus arteriosus, Peripheral axonal neuropathy, Peripheral nervous system disease, Phrynoderma, Polyneuropathy, Prostate cancer, Pulmonary hypoplasia, Renal cell carcinoma, Schizophrenia, Scoliosis, Spinal Muscular Atrophy, Spinal Muscular Atrophy With Congenital Bone Fractures, Uterine neoplasm
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189959
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- |
C4TRIPq32.1q32.2 |
Curated: N/A
Unreviewed: N/A
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189960
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Thyroid hormone receptor interactor 6 |
OIP-1, OIP1, TRIP-6, TRIP6i2, ZRP-1 |
Curated: Alzheimer disease, Gastroesophageal reflux disease
Unreviewed: Breast neoplasm, Colonic neoplasm, Colonic Neoplasms, Colorectal Cancer, Ewing sarcoma, Glioblastoma, Glioma, Intracranial vasospasm, Liver carcinoma, Malignant Neoplasm, Mesothelioma, Nasopharyngeal Cancer, Nasopharyngeal carcinoma, Neoplasms, Neural Tube Defect, Paget disease
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