|
61
|
|
|
Ras association domain family member 8 |
C12orf2, HOJ1 |
|
|
62
|
|
|
Ring finger protein 139 |
HRCA1, RCA1, TRC8 |
|
|
63
|
|
|
Recombination signal binding protein for immunoglobulin kappa J region like |
RBPL, RBPSUHL, SUHL |
|
|
64
|
|
|
Ring finger protein 13 |
DEE73, EIEE73, RZF |
Cataract, Central visual impairment, Congenital microcephaly, Developmental delay, Epileptic encephalopathy, Hearing loss, Hypoplasia of corpus callosum, Mental retardation, Microcephaly, Myocardial infarction, Scoliosis, Visual cortex disease |
|
65
|
|
|
Ring finger protein 157 |
- |
|
|
66
|
|
|
Rhophilin Rho GTPase binding protein 1 |
ODF5, RHOPHILIN, RHPN |
|
|
67
|
|
|
RecQ mediated genome instability 2 |
BLAP18, C16orf75 |
Ankylosing spondylitis, Arthritis, Asthma, Autoimmune diseases, Celiac disease, Cholangitis, Crohn disease, Diabetes mellitus, Eczema, Immune system diseases, Inflammatory bowel disease, Intrauterine growth restriction, congenital multiple caf -au-lait macules-increased sister chromatid exchange syndrome, Leprosy, Multiple sclerosis, Oligoarticular arthritis, Pauciarticular chronic arthritis, Seronegative polyarthritis, Biliary cirrhosis, Psoriasis, Psoriasis vulgaris, Rheumatoid arthritis, Sclerosing cholangitis, Still disease, Ulcerative colitisView all (9 more) |
|
68
|
|
|
RAB39B, member RAS oncogene family |
BGMR, MRX72, WSMN, WSN, XLID72 |
Attention deficit hyperactivity disorder, Autism, Developmental delay, Dolichocephaly, Dysarthria, Dyskinetic syndrome, Epilepsy, Facial paralysis, Frontal bossing, Neurosensory hearing impairment, Mental retardation, Macrocephaly, Meckel diverticulum, Mental retardation, x-linked, Movement disorders, Non-syndromic intellectual disability, x-linked, Obesity, Parkinson disease, Waisman syndrome, Seizure, Speech disorders, Stereotyped behavior, Strabismus, Syndactyly of the toesView all (9 more) |
|
69
|
|
|
Ribosomal protein L3 pseudogene 2 |
RPL3-Hom, RPL3_1_679 |
|
|
70
|
|
|
Relaxin 3 |
H3, RXN3, ZINS4, insl7 |
|
