|
221
|
|
|
Ras interacting protein 1 |
RAIN |
|
|
222
|
|
|
Rhomboid like 2 |
RRP2 |
|
|
223
|
|
|
Ring finger protein 125 |
TNORS, TRAC-1, TRAC1 |
Anxiety disorder, Cerebral cortical atrophy, Cerebral palsy, Congenital hemihypertrophy, Gastroesophageal reflux disease, Hydrocephalus, Hypertrichosis, Hypoglycemia, Hypoinsulinemia, Keratoconjunctivitis sicca, Macrocephaly, Macroglossia, Malocclusion, Mental retardation, Osteopenia, Raynaud phenomenon, Scoliosis, Stomatitis, Tenorio syndromeView all (4 more) |
|
224
|
|
|
Required for meiotic nuclear division 1 homolog |
C6orf96, COXPD11, RMD1, bA351K16, bA351K16.3 |
Breast cancer, Mammary neoplasms, Breast carcinoma, Cerebral cortical atrophy, Combined oxidative phosphorylation deficiency, Developmental delay, Dysmorphic features, Fatty liver, Hypoplasia of corpus callosum, Marfan syndrome, Mitochondrial diseases, Myopathy, Pachygyria, Renal cyst, Renal dysplasia, Renal hypoplasia, Renal insufficiencyView all (2 more) |
|
225
|
|
|
Ring finger protein 31 |
HOIP, IMD115, Paul, ZIBRA |
|
|
226
|
|
|
RNA binding motif protein 28 |
ANES, NOP4 |
Acquired kyphoscoliosis, Adrenocorticotropin deficient adrenal insufficiency, Alopecia, Alopecia, neurologic defects, and endocrinopathy syndrome, Amyotrophy, Congenital kyphoscoliosis, Dwarfism, Gynecomastia, Hypodontia, Hypogonadism, Hypogonadotropic hypogonadism, Isolated somatotropin deficiency, Lipoatrophy, Lipodystrophy, Melanocytic nevus, Mental retardation, Microcephaly, Motor neuron atrophy, Adrenal insufficiency, Hypothyroidism, Somatotropin deficiencyView all (6 more) |
|
227
|
|
|
RNA binding motif protein 23 |
CAPERbeta, PP239, RNPC4 |
|
|
228
|
|
|
Ring finger and WD repeat domain 3 |
FANCW, RNF201 |
Anemia, Arnold-chiari malformation, Astigmatism, Atrial septal defect, Azoospermia, Cafe-au-lait spot, Camptodactyly of fingers, Cataract, Choanal atresia, Congenital arteriovenous malformation, Congenital epicanthus, Congenital exomphalos, Congenital hypoplasia of radius, Cranial nerve paralysis, Cryptorchidism, Developmental delay, Dolichocephaly, Duodenal atresia, Dwarfism, Fanconi anemia, Frontal bossing, High palate, Hirschsprung disease, Hydrocephalus, Hypertrophic cardiomyopathy, Hypogonadism, Hypospadias, Imperforate anus, Isolated somatotropin deficiency, Leukopenia, Meckel diverticulum, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Multiple myeloma, Myelodysplasia, Myelodysplastic syndrome, Nystagmus, Patent ductus arteriosus, Polysplenia, Proptosis, Ptosis, Renal hypoplasia, Renal insufficiency, Scoliosis, Somatotropin deficiency, Spina bifida, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Testicular neoplasms, Testicular germ cell tumor, Tetralogy of fallot, Thumb aplasiaView all (40 more) |
|
229
|
|
|
Ring finger protein 220 |
C1orf164, HLD23 |
|
|
230
|
|
|
Replication timing regulatory factor 1 |
- |
|
