|
271
|
|
|
RAB5B, member RAS oncogene family |
- |
|
|
272
|
|
|
RAB27A, member RAS oncogene family |
GS2, HsT18676, RAB27, RAM |
Acrocephalopolydactyly, Glioma, Griscelli syndrome, Histiocytosis haematophagic, Hyperlipidemia, Hypopigmentation disorder, Hypopigmentation-immunodeficiency disease, Immunologic deficiency syndromes, Neutropenia, Pancytopenia, Piebaldism, Seizure |
|
273
|
|
|
RAB27B, member RAS oncogene family |
C25KG |
|
|
274
|
|
|
RAB5C, member RAS oncogene family |
L1880, RAB5CL, RAB5L, RABL |
|
|
275
|
|
|
Rac family small GTPase 1 |
MIG5, MRD48, Rac-1, TC-25, p21-Rac1 |
Autism, Basal cell neoplasm, Bicuspid aortic valve, Carcinoma, Carcinoma of the head and neck, Cardiomyopathy, Cerebellar hypoplasia, Congenital exomphalos, Congenital sensorineural hearing loss, Congestive heart failure, Cryptorchidism, Developmental delay, Diabetes mellitus, Eczema, Hearing loss, Heart failure, Hypoplasia of corpus callosum, Hypospadias, Liver carcinoma, Macrocephaly, Malignant uterine corpus neoplasm, Melanoma, Mental depression, Mental retardation, Microcephaly, Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrome, Motor delay, Myocardial infarction, Otitis media, Patent ductus arteriosus, Patent foramen ovale, Plagiocephaly, Polymicrogyria, Scoliosis, Skin carcinoma, Stereotyped behavior, Tracheobronchomalacia, Ventricular septal defectView all (23 more) |
|
276
|
|
|
Rac family small GTPase 2 |
EN-7, Gx, HSPC022, IMD73A, IMD73B, IMD73C, p21-Rac2 |
Breast cancer, Graves disease, Heart diseases, Immunologic deficiency syndromes, Lymphoma, Lymphopenia, Melanoma, Myelomonocytic leukemia, Neutrophil immunodeficiency syndrome, Neutrophilia, Severe combined immunodeficiency disease, Urachal cyst |
|
277
|
|
|
Rac family small GTPase 3 |
- |
|
|
278
|
|
|
RAD9 checkpoint clamp component A |
RAD9 |
|
|
279
|
|
|
RAD21 cohesin complex component |
CDLS4, HR21, HRAD21, MCD1, MGS, NXP1, SCC1, hHR21 |
Anxiety disorder, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Barrett esophagus, Brachycephaly, Camptodactyly of fingers, Cataract, Cerebral cortical atrophy, Choanal atresia, Colorectal cancer, Congenital diaphragmatic hernia, Congenital hypoplasia of penis, Congenital malrotation of intestine, Congenital muscular hypertrophy-cerebral syndrome, Congenital pectus excavatum, Cornelia de lange syndrome, Cryptorchidism, Cutis marmorata, Developmental delay, Dwarfism, Dyssomnia, Endometrial cancer, Endometrial carcinoma, Gastroesophageal reflux disease, Glaucoma, Hearing loss, High palate, Hypoplasia of nipple, Hypospadias, Mental retardation, Intestinal pseudoobstruction, Intestinal volvulus, Leukemia, Leukemia, megakaryoblastic, of down syndrome, Lung neoplasms, Lung cancer, Lung carcinoma, Macrotia, Megaduodenum, Microcephaly, Microcornea, Micrognathism, Micromelia, Monocytic leukemia, Multicystic renal dysplasia, Mungan syndrome, Myeloid leukemia, Myopia, Nervous system diseases, Nystagmus, Obsessive-compulsive disorder, Oligodactyly, Phthisis bulbi, Physiologic amenorrhea, Ptosis, Pulmonary stenosis, Radioulnar synostosis, Renal hypoplasia, Renal insufficiency, Schizoaffective disorder, Sleep disorders, Speech disorders, Strabismus, Syndactyly of the toes, Synophrys, Talipes, Tricuspid valve insufficiency, Uterine anomalies, Ventricular septal defect, Vesicoureteral refluxView all (56 more) |
|
280
|
|
|
RAD23 nucleotide excision repair protein A |
HHR23A, HR23A |
|
