131
|
|
|
Ral GTPase activating protein catalytic subunit alpha 1 |
GARNL1, GRIPE, NEDHRIT, RalGAPalpha1, TULIP1, p240 |
|
132
|
|
|
Ribosomal protein L10a pseudogene 2 |
RPL10A_5_900 |
|
133
|
|
|
Ring finger protein 144B |
IBRDC2, PIR2, bA528A10.3, p53RFP |
|
134
|
|
|
Ring finger protein 214 |
- |
|
135
|
|
|
RAS guanyl releasing protein 3 |
GRP3 |
|
136
|
|
|
RAB3 GTPase activating non-catalytic protein subunit 2 |
MARTS1, RAB3-GAP150, RAB3GAP150, SPG69, WARBM2, p150 |
Abnormal dermatoglyphic pattern, Agenesis of corpus callosum, Brachycephaly, Cardiomyopathy, Cataract, Cataract-intellectual disability-hypogonadism syndrome, Central visual impairment, Cerebral cortical atrophy, Congenital clubfoot, Congenital epicanthus, Congenital hypoplasia of penis, Congenital pectus carinatum, Congenital pectus excavatum, Congestive heart failure, Cryptorchidism, Developmental delay, Dwarfism, Fundus coloboma, High palate, Hydronephrosis, Hypogonadotropic hypogonadism, Hypoplasia of corpus callosum, Hypoplasia of the maxilla, Mental retardation, Spastic diplegia, Macrotia, Martsolf syndrome, Micro syndrome, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Multiple congenital anomalies, Nervous system diseases, Optic atrophy, Pachygyria, Penis agenesis, Polymicrogyria, Posteriorly rotated ear, Retinal coloboma, Scoliosis, Spastic paraplegia, Tracheomalacia, Warburg micro syndromeView all (29 more) |
137
|
|
|
RAD54 homolog B |
RDH54 |
|
138
|
|
|
Ribosomal protein L36 |
L36, eL36 |
|
139
|
|
|
Ring finger and CHY zinc finger domain containing 1 |
ARNIP, CHIMP, PIRH2, PRO1996, RNF199, ZCHY, ZNF363 |
|
140
|
|
|
Rotatin |
MSSP |
Agenesis of corpus callosum, Arachnoid cyst, Cerebellar atrophy, Cerebral atrophy, Congenital microcephaly, Cortical dysplasia, Craniosynostosis, Cryptorchidism, Duodenal atresia, Dwarfism, Dysarthria, Dyssomnia, Eczema, Hypoplasia of corpus callosum, Hypoplasia of the optic nerve, Hypospadias, Mental retardation, Lobar holoprosencephaly, Microcephalic cortical malformations-short stature, Microcephaly, Microcephaly, short stature, and polymicrogyria with or without seizures, Microphthalmos, Microstomia, Pachygyria, Pelvic kidney, Periventricular nodular heterotopia, Polymicrogyria, Proptosis, Renal aplasia, Sensorineural hearing loss, Sleep disorders, Stereotyped behaviorView all (17 more) |