1711
|
|
|
RNA polymerase II, I and III subunit K |
ABC10-alpha, RPABC4, RPB10alpha, RPB12, RPB7.0, hRPB7.0, hsRPB10a |
Curated: Interstitial lung disease
Unreviewed: Breast neoplasm, Liver carcinoma, Polycystic ovary syndrome
|
1712
|
|
|
RNA polymerase II subunit K pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
1713
|
|
|
RNA polymerase II subunit K pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
1714
|
|
|
RNA polymerase II, I and III subunit L |
RBP10, RPABC5, RPB10, RPB10beta, RPB7.6, hRPB7.6 |
Curated: N/A
Unreviewed: Hepatocellular carcinoma, Male infertility, Multiple sclerosis, Prostatic neoplasm, Uterine polyp
|
1715
|
|
|
RNA polymerase II subunit L pseudogene 1 |
POLR2LP |
Curated: N/A
Unreviewed: N/A
|
1716
|
|
|
RNA polymerase II subunit M |
GCOM1, GRINL1A, Gdown, Gdown1 |
Curated: Asthma, Atrial fibrillation, Hypertension, Osteoarthritis
Unreviewed: DiGeorge Syndrome, Shprintzen Syndrome
|
1717
|
|
|
POLR2M pseudogene 1 |
GCOM2, GLURR2, GRINL1B |
Curated: N/A
Unreviewed: Leukemia
|
1718
|
|
|
RNA polymerase III subunit A |
ADDH, C160, HLD7, RPC1, RPC155, WDRTS, hRPC155 |
Curated: Bipolar disorder, Cerebellar ataxia, Desbuquois syndrome, Hypomyelinating leukodystrophy, Leukodystrophy, Movement disorder, Nonalcoholic fatty liver disease, Spastic ataxia, Tremor-ataxia-central hypomyelination syndrome, Wiedemann-rautenstrauch syndrome, POLR3A-related disorder
Unreviewed: Acanthosis Nigricans, Acquired Kyphoscoliosis, Agenesis Of Corpus Callosum, Amyotrophy, Anodontia, Arnold-Chiari malformation, Ataxia, Atrophy, Attention Deficit Hyperactivity Disorder, Autoimmune Diseases, Basal ganglia disease, Cataract, Cerebellar ataxia and hypogonadotropic hypogonadism, Cerebellar atrophy, Cerebellar diseases, Cerebellar Hypoplasia, Cerebral cortical atrophy, Cervical Vertebral Dysplasia, Cockayne Syndrome, Cognition disorder, Colonic neoplasm, Congenital kyphoscoliosis, Congenital malformation of the left heart, Connective Tissue Disease, Corpus callosum agenesis, Craniofacial abnormalities, Cryptorchidism, Dandy-Walker Syndrome, Demyelinating diseases, Developmental Delay, Developmental regression, Diabetes Mellitus, Dwarfism, Dysarthria, Dysautonomia, Dysmyelinating Leukodystrophy With Oligodontia, Dysphagia, Dystonia, Ectropion, Entropion, Fatty Liver, Focal Seizures, Frontal bossing, Gastrointestinal disease, Gastrointestinal Diseases, Growth disorder, Gynecomastia, Headache, Hearing loss, Hereditary elliptocytosis, Hereditary spastic paraplegia, Hydrocephalus, Hydronephrosis, Hyperopia, Hyperthyroidism, Hypodontia, Hypogonadism, Hypogonadotropic Hypogonadism, Hypomyelinating Leukodystrophy, With Hypodontia And Hypogonadotropic Hypogonadism, Hypomyelinating Leukodystrophy-Ataxia-Hypodontia-Hypomyelination Syndrome, Hypomyelination-Cerebellar Atrophy-Hypoplasia Of The Corpus Callosum Syndrome, Hypomyelination-Hypogonadotropic Hypogonadism-Hypodontia Syndrome, Hypoplasia Of Corpus Callosum, Hypoplasia Of Optic Disc, Hypospadias, Hypotrichosis, Isolated Somatotropin Deficiency, Lagopthalmos, Laryngomalacia, Leukemia, Leukoencephalopathy, Lipoatrophy, Lipodystrophy, Lipoma, Long QT Syndrome, Macrocephaly, Malignant Neoplasm, Mental retardation, Metachromatic leukodystrophy, Micrognathism, Microstomia, Myopia, Neoplasms, Nervous system disease, Neurodegenerative disorder, Neurodegenerative Disorders, Nystagmus, Odontoleukodystrophy, Oligodontia, Optic Atrophy, Osteopenia, Otitis media, Parkinson disease, Pelizaeus-Merzbacher disease, Periodontal disease, Pituitary dwarfism, Polymicrogyria, Posteriorly Rotated Ear, Pulmonary Stenosis, Retinitis Pigmentosa, Scleroderma, Scoliosis, Seizures, Short femur, Somatotropin Deficiency, Spastic Ataxia, Spastic paraplegia, Spastic tetraparesis, Stomach neoplasms, Submucous cleft of soft and hard palate, Supranuclear gaze palsy, Syndactyly Of The Toes, Synophrys, Synovitis, Systemic sclerosis, Tremor, Tremor-Ataxia-Central Hypomyelination Syndrome, Trichohepatoenteric Syndrome, Vesicoureteral Reflux, Wiedemann-Rautenstrauch Syndrome
|
1719
|
|
|
RNA polymerase III subunit B |
C128, CMT1I, HLD8, INMAP, RPC2 |
Curated: Alzheimer disease, Central nervous system cancer, Cerebellar ataxia, Charcot-marie-tooth disease, Dementia, Desbuquois syndrome, Glioblastoma, Glioma, Hypogonadotropic hypogonadism, Hypomyelinating leukodystrophy, Intellectual developmental disorder, Leukodystrophy, Neurodevelopmental disorder, Parkinson disease, Tourette syndrome, Tremor-ataxia-central hypomyelination syndrome, POLR3B-related disorder
Unreviewed: Addison`s Disease, Adrenal Cortical Hypofunction, Anodontia, Asthma, Ataxia, Autism, Cataract, Central Nervous System Neoplasms, Cerebellar atrophy, Cerebellar diseases, Cerebellar Hypoplasia, Cerebral cortical atrophy, Cognition disorder, Coronary Heart Disease, Corpus callosum agenesis, Craniofacial abnormalities, Cryptorchidism, Demyelinating diseases, Developmental Delay, Developmental disability, Dwarfism, Dysarthria, Dysphagia, Endosteal Sclerosis-Cerebellar Hypoplasia Syndrome, Epilepsy, Graves ophthalmopathy, Gynecomastia, Hereditary elliptocytosis, Horizontal nystagmus, Hypodontia, Hypogonadism, Hypogonadotropic Hypogonadism, Hypomyelinating Leukodystrophy WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM, Hypomyelinating Leukodystrophy, With Hypodontia And Hypogonadotropic Hypogonadism, Hypomyelination-Hypogonadotropic Hypogonadism-Hypodontia Syndrome, Hypoplasia Of Corpus Callosum, Language development disorders, Learning disorders, Leukoencephalopathy, Lung Cancer, Lung carcinoma, Lung neoplasms, Mental retardation, Metachromatic leukodystrophy, Myopia, Neoplasms, Oligodontia, Penis Agenesis, Peripheral nervous system disease, Physiologic Amenorrhea, Pituitary dwarfism, Polymicrogyria, Rufous oculocutaneous albinism, Tooth abnormalities, Trichohepatoenteric Syndrome
|
1720
|
|
|
RNA polymerase III subunit C |
C82, RPC3, RPC62 |
Curated: Gout
Unreviewed: Gouty arthritis
|