301
|
|
|
Retinoic acid receptor responder 2 pseudogene 8 |
- |
Curated: N/A
Unreviewed: N/A
|
302
|
|
|
Retinoic acid receptor responder 2 pseudogene 9 |
- |
Curated: N/A
Unreviewed: N/A
|
303
|
|
|
Arginyl-tRNA synthetase 1 |
ArgRS, DALRD1, HLD9, RARS |
Curated: Hypomyelinating leukodystrophy, Leukodystrophy, hypomyelinating leukodystrophy 9
Unreviewed: 5q-syndrome, Anemia, Anemia With Ringed Sideroblasts, Brain atrophy, Brain disease, Breast Cancer, Breast Carcinoma, Cerebral Atrophy, Chronic obstructive pulmonary disease, Colorectal neoplasm, Congenital Chromosomal Disease, Demyelinating diseases, Developmental Delay, Dysarthria, Eosinophilia, Epileptic encephalopathy, Head and neck cancer, Head And Neck Carcinoma, Hypomyelinating Leukodystrophy, Hypoplasia Of Corpus Callosum, Intellectual developmental disorder, Leukemia, Leukoencephalopathy With Brainstem And Spinal Cord Involvement And Lactate Elevation, Lymphocytic Leukemia, Malignant Neoplasm, Mental retardation, Metachromatic leukodystrophy, Microcephaly, Multiple myeloma, Myelodysplastic syndrome, Myelodysplastic-Myeloproliferative Diseases, Myelofibrosis, Myeloid leukemia, Myelomonocytic Leukemia, Myeloproliferative disorder, Nasopharyngeal Carcinoma, Neoplasms, Neurodegenerative Disorders, Neurodevelopmental Disorders, Nystagmus, Pelizaeus-Merzbacher disease, Pontoneocerebellar hypoplasia, Pseudobulbar Palsy, Thrombocythemia, Thrombocytosis, Uterine neoplasm
|
304
|
|
|
Arginyl-tRNA synthetase 1 pseudogene 1 |
RARSP1 |
Curated: N/A
Unreviewed: N/A
|
305
|
|
|
Arginyl-tRNA synthetase 2, mitochondrial |
ArgRS, DALRD2, PCH6, PRO1992, RARSL |
Curated: Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Neurodevelopmental disorder, Congenital disorder of glycosylation, Mitochondrial disease, Non-specific syndromic intellectual disability, Pontocerebellar hypoplasia
Unreviewed: Brain disease, Brainstem Atrophy, Cardiomyopathy, Cerebellar atrophy, Cerebellar Hypoplasia, Cerebral Atrophy, Developmental and epileptic encephalopathy, Developmental Delay, Edema, Epilepsy, Epileptic encephalopathy, Focal Clonic Seizures, Hydrops Fetalis, Infantile Spasms, Lactic acidosis, Leukoencephalopathy With Brainstem And Spinal Cord Involvement And Lactate Elevation, Meibomian Cyst, MELAS Syndrome, MERRF Syndrome, Microcephaly, Mitochondrial Diseases, Mitochondrial encephalomyopathy, Mitochondrial Respiratory Chain Deficiencies, Myoclonic epilepsy, Myoclonic epilepsy with ragged red fibers, Neurodegenerative Disorders, Neurodevelopmental Disorders, PEHO Syndrome, Pontoneocerebellar hypoplasia, Scoliosis, Seizures, West Syndrome
|
306
|
|
|
RAS p21 protein activator 1 |
CM-AVM, CMAVM, CMAVM1, GAP, PKWS, RASA, RASGAP, p120, p120GAP, p120RASGAP |
Curated: Arteriovenous hemangioma, Arteriovenous malformations, Basal cell carcinoma, Capillary malformation-arteriovenous malformation, Carcinoma, Squamous cell carcinoma, Developmental venous anomaly, Hereditary hemorrhagic telangiectasia, Hydrops fetalis, Klippel-trenaunay syndrome, Noonan syndrome, Parkes weber syndrome, Port-wine stain, Prostate cancer, Diabetes mellitus type 2
Unreviewed: N/A
|
307
|
|
|
RAS p21 protein activator 2 |
GAP1M |
Curated: Asthma, Breast cancer, Melanoma, Metabolic syndrome, Multiple myeloma, Noonan syndrome, Osteoarthritis, Ovarian cancer, Ovarian serous carcinoma, Scoliosis, Diabetes mellitus type 2
Unreviewed: Abnormal dermatoglyphic pattern, Brachydactyly, Breast Cancer, Breast Carcinoma, Camptodactyly of fingers, Capillary Malformation-Arteriovenous Malformation, Carcinogenesis, Cardiofaciocutaneous syndrome, Colon Carcinoma, Colorectal Cancer, Congenital Pectus Carinatum, Congenital Pectus Excavatum, Costello syndrome, Creutzfeldt-Jakob disease, Cryptorchidism, Cystic hygroma, Dwarfism, Dysarthria, Fatal Insomnia, Head and neck cancer, Head And Neck Carcinoma, Hearing Loss, High palate, Hypogonadotropic Hypogonadism, Insomnia, LEOPARD Syndrome, Leukemia, Liposarcoma, Liver Cancer, Lung Cancer, Lung carcinoma, Lung neoplasms, Lymphoblastic Leukemia, Malignant Neoplasm, Medullary thyroid cancer, Megalencephaly, Polymicrogyria, Polydactyly, Hydrocephalus Syndrome, Melanocytic nevus, Micrognathism, Neck Webbing, Neoplasms, Neurofibromatosis, Noonan Syndrome, Noonan-Like Syndrome With Loose Anagen Hair, Nystagmus, Obesity, Prion disease, Proptosis, Prostate cancer, Prostatic neoplasm, Ptosis, Radioulnar Synostosis, Sezary syndrome, Strabismus
|
308
|
|
|
RASA2 intronic transcript 1 |
- |
Curated: N/A
Unreviewed: N/A
|
309
|
|
|
RAS p21 protein activator 3 |
GAP1IP4BP, GAPIII |
Curated: Alzheimer disease, Melanoma, Major depressive disorder, Schizophrenia
Unreviewed: Anemia, Colorectal Neoplasms, Edema, Erythroblastic Leukemia, Growth disorder, Liver carcinoma, Pancytopenia
|
310
|
|
|
RASA3 intronic transcript 1 |
- |
Curated: N/A
Unreviewed: N/A
|