1241
|
|
|
General transcription factor IIH subunit 2B (pseudogene) |
- |
Curated: N/A
Unreviewed: N/A
|
1242
|
|
|
GTF2H2 family member C |
GTF2H2C_2 |
Curated: N/A
Unreviewed: Glioma
|
1243
|
|
|
GTF2H2 family member C, copy 2 |
GTF2H2D |
Curated: N/A
Unreviewed: N/A
|
1244
|
|
|
General transcription factor IIH subunit 3 |
BTF2, P34, TFB4, TFIIH |
Curated: Breast cancer, Alzheimer disease
Unreviewed: Ataxia Telangiectasia, Carcinoma Of The Head And Neck, CNS Disorder, Cockayne Syndrome, Congenital heart defects, Cortical cataract, Dermatologic Disorders, Development Disorder, Diffuse Panbronchiolitis, Endometrial neoplasm, Esophageal squamous cell carcinoma, Hamartoma, Hereditary Motor Neuropathy, Lung Cancer, Lung carcinoma, Malignant Neoplasm, Melanoma, Multiple polyposis syndrome, Neoplasms, Parkinson disease, Polycystic ovary syndrome, Polycythemia vera, Prostate cancer, Pruritus, Skin cancer, Sleep Apnea, Spinal Muscular Atrophy, Stomach neoplasms, Tongue carcinoma, Trichothiodystrophy, Xeroderma Pigmentosum, Xeroderma Pigmentosum-Cockayne Syndrome Complex
|
1245
|
|
|
General transcription factor IIH subunit 4 |
P52, TFB2, TFIIH |
Curated: Multiple sclerosis, Non-small cell lung carcinoma, Rheumatoid arthritis, Sarcoidosis, Schizophrenia, Squamous cell carcinoma
Unreviewed: Adenocarcinoma, Age-related macular degeneration, Anaplastic Lymphoma, Asthma, Ataxia Telangiectasia, Bladder carcinoma, Bladder Neoplasm, Breast Cancer, Breast Carcinoma, Carcinoma, Carcinoma Of The Head And Neck, Cervical Intraepithelial Neoplasia, CNS Disorder, Cockayne Syndrome, Colon Carcinoma, Congenital Contractural Arachnodactyly, Cortical cataract, Dermatologic Disorders, Development Disorder, Diabetes, Diabetes Mellitus, Diffuse Lymphoma, Diffuse Panbronchiolitis, Fatigue syndrome, Fibroadenoma, Gastritis, Glioblastoma, Graves Disease, Hamartoma, Hereditary Motor Neuropathy, Hodgkin Disease, Hodgkin Lymphoma, Keratoconus, Leukemia, Lung Cancer, Lung carcinoma, Lung neoplasms, Lymphoma, Macular degeneration, Malignant Neoplasm, Melanoma, Multiple Sclerosis, Neoplasms, Osteopetrosis, Parkinson disease, Prostate cancer, Renal Carcinoma, Rotator cuff syndrome, Skin cancer, Sleep Apnea, Spinal Muscular Atrophy, Stomach Carcinoma, Stomach Neoplasms, T-Cell Lymphoma, Tongue carcinoma, Trichothiodystrophy, Triple Negative Breast Neoplasms, Urinary bladder cancer, Uterine disease, Uveal Melanoma, Vitiligo, Xeroderma Pigmentosum, Xeroderma Pigmentosum-Cockayne Syndrome Complex
|
1246
|
|
|
General transcription factor IIH subunit 5 |
C6orf175, TFB5, TFIIH, TGF2H5, TTD, TTD-A, TTD3, TTDA, bA120J8.2 |
Curated: Color vision deficiency, Colorectal cancer, Hearing loss, Systemic sclerosis, Trichothiodystrophy
Unreviewed: Ablepharon macrostomia syndrome, Age-related macular degeneration, Anemia, Asthma, Astigmatism, Bronchospasm, Carcinoma, Carcinoma Of The Head And Neck, Cardiomyopathy, Cataract, Cerebral cortical atrophy, CNS Disorder, Cockayne Syndrome, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Congenital Epicanthus, Congenital exfoliative erythroderma, Congenital Exomphalos, Congenital Nonbullous Ichthyosiform Erythroderma, Cortical cataract, Craniosynostosis, Cryptorchidism, Dental Enamel Hypoplasia, Dermatologic Disorders, Development Disorder, Developmental Delay, Diabetes, Diabetes Mellitus, Diffuse Panbronchiolitis, Dwarfism, Dysarthria, Ectropion, Eczema, Esotropia, Exfoliative Dermatitis, Gonadal Dysgenesis, Hamartoma, Hereditary Motor Neuropathy, Hypoplasia of mandible relative to maxilla, Ichthyosis, Impaired social reciprocity, Keratoconjunctivitis Sicca, Malignant Neoplasm, Melanoma, Mental retardation, Microcephaly, Microcornea, Microphthalmos, Myopia, Neoplasms, Nervous System Diseases, Neutropenia, Nystagmus, Osteopenia, Osteosclerosis, Ovarian cancer, Ovarian neoplasm, Pancreatic carcinoma, Paraplegia, Partial Agenesis Of Corpus Callosum, Periodontitis, Periventricular Leukomalacia, Progeria, Prostate cancer, Retinoblastoma, Seizure, Sensorineural hearing loss, Skin cancer, Sleep Apnea, Spinal Muscular Atrophy, Squamous cell carcinoma, Tongue carcinoma, Ventricular septal defect, Xeroderma Pigmentosum, Xeroderma Pigmentosum-Cockayne Syndrome Complex
|
1247
|
|
|
General transcription factor IIi |
BAP135, BTKAP1, DIWS, GTFII-I, IB291, SPIN, TFII-I, WBS, WBSCR6 |
Curated: Eczema, Atrial fibrillation, Autism, Autoimmune musculoskeletal system disorder, Breast cancer, Basal cell carcinoma, Cardiovascular disease, Obstructive pulmonary disease, Connective tissue disease, Crohn disease, Hypertension, Heart failure, Inflammatory bowel disease, Kidney disease, Myeloid leukemia, Metabolic syndrome, Migraine, Sjogren syndrome, Skin disease, Systemic lupus erythematosus, Diabetes mellitus type 2, Ulcerative colitis, Williams syndrome
Unreviewed: 11p11.2 Deletion Syndrome, Abnormal dermatoglyphic pattern, Abnormal spinal segmentation, Accessory Kidney, Anemia, Anencephaly, Aneurysm Of Aortic Arch, Angioimmunoblastic T-cell lymphoma, Anxiety Disorder, Arnold-Chiari malformation, Astrocytoma, Atrial Fibrillation, Atrial Septal Defect, Attention Deficit Hyperactivity Disorder, Autism Spectrum Disorder, Beckwith-Wiedemann Syndrome, Bicuspid aortic valve, Bladder Diverticulum, Blepharophimosis, Breast Cancer, Breast Carcinoma, Breast neoplasm, Camptodactyly of fingers, Cardiovascular Diseases, Cataract, Central hypothyroidism, Cerebral cortical atrophy, Cholelithiasis, Chronic Obstructive Pulmonary Disease, Cognition disorder, Cognitive disorder, Colorectal neoplasm, Congenital Anomaly Of Neck, Congenital Epicanthus, Congenital Exomphalos, Congenital Hypoplasia Of Penis, Congenital Keratoglobus, Congenital Pectus Excavatum, Congestive Heart Failure, Cornea Plana, Cryptorchidism, Developmental regression, Diabetes Mellitus, Diffuse idiopathic skeletal hyperostosis, Dwarfism, Dysarthria, Dysgraphia, Dyslexia, Dysmorphic Features, Epithelioma, Facial dysmorphism syndrome, Gastroesophageal Reflux Disease, Glaucoma, Hearing Loss, Hematologic Neoplasms, Hypercalcemia, Hypertrophic cardiomyopathy, Hypodontia, Hypogonadotropic Hypogonadism, Hypothyroidism, Impaired Cognition, Intellectual developmental disorder, Leukemia, Lupus Erythematosus, Lupus Nephritis, Macroglossia, Macrostomia, Macrotia, Malabsorption Syndrome, Memory disorders, Mental Depression, Mental retardation, Microcephaly, Microdontia, Micrognathism, Mitral Valve Prolapse, Multiple renal cysts, Multiple Sclerosis, Myasthenia gravis, Myeloid Leukemia, Myocardial Infarction, Myopathy, Myopia, Nephrocalcinosis, Nephrolithiasis, Neuromyelitis Optica, Nystagmus-induced head nodding, Obesity, Obsessive-Compulsive Disorder, Osteopenia, Osteoporosis, Osteosclerosis, Otitis media, Overriding aorta, Paroxysmal atrial fibrillation, Patent ductus arteriosus, Peeling Skin Syndrome, Pelvic kidney, Peptic Ulcer, Peripheral pulmonary artery stenosis, Phakomatosis pigmentovascularis, Polycystic Ovary Syndrome, Posterior embryotoxon, Precocious puberty, Promyelocytic Leukemia, Prostatic neoplasm, Proteinuria, Pulmonary Stenosis, Radioulnar Synostosis, Rectal Prolapse, Renal hypoplasia, Renal Insufficiency, Rhabdomyosarcoma, Rheumatoid arthritis, Scleroderma, Scoliosis, Seasonal Affective Disorder, Separation Anxiety Disorder, Sjogren`s Syndrome, Spina bifida occulta, Strabismus, Stroke, Supravalvar aortic stenosis, Systemic sclerosis, Tetralogy of Fallot, Thymic Carcinoma, Thymic tumor, Thymoma, Thyroid Carcinoma, Ventricular septal defect, Vesicoureteral Reflux, Williams Syndrome
|
1248
|
|
|
GTF2I antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
1249
|
|
|
General transcription factor IIi pseudogene 1 |
WBSCR7 |
Curated: N/A
Unreviewed: Williams Syndrome
|
1250
|
|
|
General transcription factor IIi pseudogene 10 |
- |
Curated: N/A
Unreviewed: N/A
|