951
|
|
|
RecQ mediated genome instability 2 |
BLAP18, C16orf75 |
Curated: Ankylosing spondylitis, Asthma, Autoimmune disease, Bulimia, Celiac disease, Cholecystolithiasis, Colorectal cancer, Crohn disease, Dementia, Gallstones, Inflammatory bowel disease, Multiple sclerosis, Obesity, Oligoarticular juvenile idiopathic arthritis, Oligodendroglioma, Pancreatic cancer, Polyarticular juvenile idiopathic arthritis, Biliary cholangitis, Psoriasis, Psoriasis vulgaris, Sclerosing cholangitis, Juvenile idiopathic arthritis, Systemic lupus erythematosus, Hypertension, Diabetes mellitus type 1, Diabetes mellitus type 2, Ulcerative colitis
Unreviewed: Ankylosing Spondylitis, Arthritis, Autoimmune Diseases, Biliary Cirrhosis, Bloom Syndrome, Breast neoplasm, Carcinogenesis, Cholangitis, Crohn Disease, Dermatomyositis, Diabetes Mellitus, Eczema, Hepatocellular carcinoma, Immune System Diseases, Inflammatory Bowel Disease, Intrauterine Growth Restriction, Congenital Multiple Caf -Au-Lait Macules-Increased Sister Chromatid Exchange Syndrome, Leprosy, Multiple Sclerosis, Myotonic dystrophy, Oligoarticular Arthritis, Pauciarticular chronic arthritis, Rheumatoid arthritis, Sclerosing Cholangitis, Seronegative polyarthritis, Still Disease
|
952
|
|
|
RMI2 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
953
|
|
|
Required for meiotic nuclear division 1 homolog |
C6orf96, COXPD11, RMD1, bA351K16, bA351K16.3 |
Curated: Breast neoplasms, Combined oxidative phosphorylation deficiency, Congenital neurologic anomalies, Mitochondrial disease, Nephronophthisis, Perrault syndrome, Uterine fibroid, Xx gonadal dysgenesis syndrome
Unreviewed: B-Cell Lymphoma, Brain disease, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cardiomyopathy, Cerebral cortical atrophy, Combined Oxidative Phosphorylation Deficiency, Congenital lactic acidosis, Cyst, Deafness, Developmental Delay, Dilated cardiomyopathy, Dysautonomia, Dysmorphic Features, Epileptic encephalopathy, Fatty Liver, Gonadal dysgenesis, Hearing loss, Hypoaldosteronism, Hypoplasia Of Corpus Callosum, Kidney Failure, Lactic acidosis, Leukodystrophy, Leukoencephalopathy, Mammary Neoplasms, Marfan Syndrome, Mitochondrial complex deficiency, Mitochondrial Diseases, Multiple system atrophy, Myeloid Leukemia, Myopathy, Neoplasms, Non-Hodgkin lymphoma, Osteoporosis, Pachygyria, Renal cyst, Renal dysplasia, Renal hypoplasia, Renal Insufficiency, Thrombosis
|
954
|
|
|
Required for meiotic nuclear division 5 homolog A |
CTLH, GID2, GID2A, RMD5, p44CTLH |
Curated: Hypertrophic cardiomyopathy, Rheumatoid arthritis, Schizophrenia
Unreviewed: Breast neoplasm, Congenital Cerebral Hernia, Dwarfism, Encephalocele, Lymphoma, Mouth neoplasm, Neoplasms, Pancreatic neoplasm, Squamous cell carcinoma
|
955
|
|
|
Required for meiotic nuclear division 5 homolog B |
GID2, GID2B |
Curated: Dyskeratosis congenita
Unreviewed: Dwarfism, Dyskeratosis Congenita
|
956
|
|
|
Ribonuclease MRP subunit p24 |
C18orf21, HsT3108, PNAS-124, PNAS-131, XTP13 |
Curated: N/A
Unreviewed: Torsades de Pointes
|
957
|
|
|
RMP24 pseudogene 1 |
C18orf21, C18orf21P1 |
Curated: N/A
Unreviewed: N/A
|
958
|
|
|
Ribonuclease MRP subunit p64 |
ANXD3, C3orf17, NEPRO, NET17 |
Curated: Anauxetic dysplasia
Unreviewed: Anauxetic Dysplasia, Osteochondrodysplasia, Skeletal Dysplasia
|
959
|
|
|
RNA component of mitochondrial RNA processing endoribonuclease |
CHH, NME1, RMRPR, RRP2 |
Curated: cartilage-hair hypoplasia
Unreviewed: Alopecia, Anauxetic Dysplasia, Anemia, Aplastic anemia, B-Cell Lymphoma, Bladder carcinoma, Bladder Neoplasm, Bone Disease, Bone marrow failure syndrome, Brachycephaly, Brachydactyly, Breast Cancer, Breast Carcinoma, Breast neoplasm, Bronchiectasis, Cardiomyopathy, Cartilage-Hair Hypoplasia, Cholangiocarcinoma, Colorectal neoplasm, Congenital Central Hypoventilation, Congenital Epicanthus, Congenital Hypogonadotropic Hypogonadism, Congenital Hypoplastic Anemia, Congenital Neutropenia, Congenital Pectus Carinatum, Diabetes Mellitus, Dwarfism, Dyskeratosis Congenita, Eosinophilia, Epidermal nevus, Epidermodysplasia Verruciformis, Esophageal Atresia, Esophageal Carcinoma, Esophageal neoplasm, Esophageal squamous cell carcinoma, Esophagus Neoplasm, Exfoliative Dermatitis, Glioma, Glucose-6-Phosphate Transport Defect, Gonadotropin Deficiency, Growth disorder, Heart Block, Heart failure, Heart Septal Defects, Hepatocellular carcinoma, Hermansky-Pudlak Syndrome, Hirschsprung Disease, Hodgkin Disease, Hydrocephalus, Hypertension, Hypodontia, Hypogonadism, Hypospadias, Hypothyroidism, Hypotrichosis, Hypoxia, Immunologic Deficiency Syndromes, Impaired Cognition, Intervertebral Disc Degeneration, Intervertebral disc disease, Intervertebral Disc Disorder, Intestinal Obstruction, Kallmann Syndrome, Kidney Disease, Leukemia, Liver carcinoma, Liver disease, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung neoplasms, Lymphatic metastasis, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoma, Lymphopenia, Lymphoproliferative syndrome, Macrotia, Macular corneal dystrophy, Malabsorption Syndrome, Malignant Neoplasm, Mental retardation, Mesomelia, Metaphyseal chondrodysplasia, Metaphyseal dysplasia, METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS, Micromelia, Mucopolysaccharidosis, Myopia, Neoplasms, Nephrotic Syndrome, Neuroblastoma, Neutropenia, Oculocutaneous albinism, Omenn Syndrome, Osteochondrodysplasia, Penile Hypospadias, Pyle Metaphyseal Dysplasia, Rheumatoid arthritis, Rhizomelia, Scoliosis, Severe combined immunodeficiency disease, Shwachman Syndrome, Skeletal Dysplasia, Skin Neoplasms, Spina Bifida, Stomach Carcinoma, Stomach Neoplasms, Strabismus, T-Cell Lymphoma, Testotoxicosis, Thyroiditis, Tracheal Stenosis, Urinary bladder cancer, Urinary bladder neoplasms
|
960
|
|
|
RNA component of mitochondrial RNA processing endoribonuclease pseudogene 5 |
- |
Curated: N/A
Unreviewed: N/A
|