|
201
|
|
|
REV1 DNA directed polymerase |
AIBP80, REV1L |
|
|
202
|
|
|
Rh family C glycoprotein |
C15orf6, PDRC2, RHGK, SLC42A3 |
|
|
203
|
|
|
RAB14, member RAS oncogene family |
FBP, RAB-14 |
|
|
204
|
|
|
Ras related dexamethasone induced 1 |
AGS1, DEXRAS1, MGC:26290 |
|
|
205
|
|
|
RAB23, member RAS oncogene family |
HSPC137 |
Acquired kyphoscoliosis, Acrocephaly, Anodontia, Atrial septal defect, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Carpenter syndrome, Cerebral atrophy, Congenital camptodactyly, Congenital clubfoot, Congenital epicanthus, Congenital exomphalos, Congenital kyphoscoliosis, Congenital omphalocele, Coronal craniosynostosis, Craniosynostosis, Cryptorchidism, Dwarfism, Gastrointestinal stromal tumor, Hearing loss, High palate, Hydronephrosis, Hypoplasia of the maxilla, Mental retardation, Microcornea, Micrognathism, Multiple congenital anomalies, Obesity, Optic atrophy, Patent ductus arteriosus, Polydactyly, Polysplenia, Precocious puberty, Pulmonary stenosis, Sagittal craniosynostosis, Scoliosis, Spina bifida occulta, Syndactyly of fingers, Syndactyly of the toes, Synostotic posterior plagiocephaly, Tetralogy of fallot, Transposition of great vessels, Postaxial hand polydactyly, Ventricular septal defectView all (30 more) |
|
206
|
|
|
Rap guanine nucleotide exchange factor 6 |
KIA001LB, PDZ-GEF2, PDZGEF2, RA-GEF-2, RAGEF2 |
|
|
207
|
|
|
Regulator of telomere elongation helicase 1 |
C20orf41, DKCA4, DKCB5, NHL, PFBMFT3, RTEL |
Alopecia, Anemia, Asthma, Bronchiectasis, Cataract, Central nervous system neoplasms, Cerebellar hypoplasia, Cerebral cortical atrophy, Cirrhosis, Colonic neoplasms, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Crohn disease, Dermatitis, Developmental delay, Diabetes mellitus, Diffuse interstitial pulmonary fibrosis, Dwarfism, Dyskeratosis congenita, Esophageal stenosis, Gastroesophageal reflux disease, Glioblastoma, Glioma, Honeycomb lung, Hoyeraal-hreidarsson syndrome, Hypodontia, Hypoplasia of the maxilla, Immunologic deficiency syndromes, Leukopenia, Leukoplakia, Liver failure, Lung neoplasms, Lung cancer, Lymphoma, Malabsorption syndrome, Mental retardation, Microcephaly, Nail dystrophy, Nasopharyngeal carcinoma, Neoplasms, Osteoporosis, Palmoplantar keratoderma, Pancreatic neoplasm, Periodontitis, Pulmonary fibrosis, Hamman-rich syndrome, Pulmonary fibrosis and/or bone marrow failure, Respiratory tract diseases, Scoliosis, Taurodontism, Ulcerative colitisView all (37 more) |
|
208
|
|
|
RAB4B, member RAS oncogene family |
- |
|
|
209
|
|
|
Receptor interacting serine/threonine kinase 4 |
ANKK2, ANKRD3, CHANDS, DIK, NKRD3, PKK, PPS2, RIP4 |
Absent eyebrow, Alopecia, Ambiguous genitalia, Anodontia, Anonychia, Bartsocas-papas syndrome, Chand syndrome, Congenital ankyloblepharon, Curly hair, ankyloblepharon, nail dysplasia syndrome, Hypohidrosis, Mental retardation, Microcephaly, Micrognathism, Microstomia, Nail diseases, Nail dysplasia, Osseous ankylosis, Syndactyly, Syndactyly of fingers, Syndactyly of the toes, Talipes, Thumb aplasiaView all (7 more) |
|
210
|
|
|
Ras and Rab interactor 2 |
MACS, RASSF4 |
Alopecia, Aortic aneurysm, Brachydactyly, Breast carcinoma, Congenital exomphalos, Cryptorchidism, Dwarfism, High palate, Hypogonadism, Impaired cognition, Macrocephaly, alopecia, cutis laxa, and scoliosis, Mental disorders, Myopia, Premature menopause, Psychosis, Rin2 syndrome, ScoliosisView all (2 more) |
