|
291
|
|
|
Ral guanine nucleotide dissociation stimulator |
RGDS, RGF, RalGEF |
|
|
292
|
|
|
RAN, member RAS oncogene family |
ARA24, Gsp1, TC4 |
|
|
293
|
|
|
RAN binding protein 1 |
HTF9A |
|
|
294
|
|
|
RAN binding protein 2 |
ADANE, ANE1, IIAE3, NUP358, TRP1, TRP2 |
|
|
295
|
|
|
Ran GTPase activating protein 1 |
Fug1, RANGAP, SD |
|
|
296
|
|
|
RAP1A, member of RAS oncogene family |
C21KG, G-22K, KREV-1, KREV1, RAP1, SMGP21 |
Abnormal dermatoglyphic pattern, Aortic coarctation, Cerebral cortical atrophy, Congenital diaphragmatic hernia, Congenital hypoplasia of penis, Congenital ocular coloboma, Cryptorchidism, Dwarfism, Hearing loss, Heart septal defects, High palate, Hydrocephalus, Hydronephrosis, Hypodontia, Hypospadias, Kabuki syndrome, Macrotia, Microcephaly, Microcornea, Microdontia, Nystagmus, Obesity, Osteoporosis, Precocious puberty, Ptosis, Schizophrenia, Scoliosis, StrabismusView all (13 more) |
|
297
|
|
|
RAP1B, member of RAS oncogene family |
K-REV, RAL1B, THC11 |
Abnormal dermatoglyphic pattern, Aortic coarctation, Cerebral cortical atrophy, Congenital diaphragmatic hernia, Congenital hypoplasia of penis, Congenital ocular coloboma, Cryptorchidism, Dwarfism, Hearing loss, Heart septal defects, High palate, Hydrocephalus, Hydronephrosis, Hypodontia, Hypospadias, Kabuki syndrome, Macrotia, Microcephaly, Microcornea, Microdontia, Nystagmus, Obesity, Precocious puberty, Ptosis, Scoliosis, StrabismusView all (11 more) |
|
298
|
|
|
RAP1 GTPase activating protein |
RAP1GA1, RAP1GAP1, RAP1GAPII, RAPGAP |
|
|
299
|
|
|
RAP2A, member of RAS oncogene family |
K-REV, KREV, RAP2, RbBP-30 |
|
|
300
|
|
|
Receptor associated protein of the synapse |
CMS11, CMS4C, FADS, FADS2, RAPSYN, RNF205 |
Akinesia, Amyotrophy, Arthrogryposis multiplex congenita, Autoimmune diseases, Pulmonary hypoplasia, Myasthenic syndrome, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Facial paralysis, Fetal akinesia deformation sequence, High palate, Lethal multiple pterygium syndrome, Limb-girdle muscular dystrophy, Cystic hygroma, Mental depression, Micrognathism, Mood disorder, Multiple pterygium syndrome, Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency, Myasthenic syndrome, congenital, with facial dysmorphism, associated with acetylcholine receptor deficiency, Myopathy, Hypotonia, Pena shokeir syndrome, Posteriorly rotated ear, Pterygium, Ptosis, Respiratory failure, ScoliosisView all (14 more) |
