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311
|
|
|
RB transcriptional corepressor 1 |
OSRC, PPP1R130, RB, p105-Rb, p110-RB1, pRb, pp110 |
13q14 deletion syndrome, Abnormal dermatoglyphic pattern, Adrenal cancer, Adrenal neoplasia, Adrenocortical carcinoma, Anaplastic carcinoma, Benign neoplasm of bladder, Urinary bladder cancer, Bladder neoplasm, Bladder carcinoma, Brachydactyly, Breast adenocarcinoma, Breast cancer, Mammary neoplasms, Breast carcinoma, Camptodactyly of fingers, Hereditary cancer syndrome, Carcinoma, Cataract, Cerebral ischemia, Colorectal cancer, Congenital coloboma of iris, Congenital epicanthus, Dwarfism, Erythroleukemia, Esophagus neoplasm, Ewing sarcoma, Gastrointestinal stromal tumor, Hereditary retinoblastoma, Holoprosencephaly, Hypoplasia of corpus callosum, Hypotrichosis, Leukemia, Lymphoblastic leukemia, Leukocoria, Liver carcinoma, Lung carcinoma, Lung neoplasms, Lung cancer, Lymphoma, Marfan syndrome, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Monosomy 13q14, Myeloid leukemia, Neck webbing, Neoplasms, Non-hereditary retinoblastoma, Osteosarcoma, Pancreatic neoplasm, Pancreatic cancer, Pineal gland neoplasm, Prostatic neoplasms, Prostate cancer, Ptosis, Retinoblastoma, Sarcoma, Sezary syndrome, Stevens-johnson syndrome, Syndactyly of fingers, Trigonocephaly, Trilateral retinoblastoma, Vulvar adenocarcinoma of mammary gland, Woolly hair, with or without hypotrichosisView all (51 more) |
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312
|
|
|
RB binding protein 8, endonuclease |
COM1, CTIP, JAWAD, JWDS, RIM, SAE2, SCKL2 |
Benign tumor of pancreas, Breast carcinoma, Camptodactyly of fingers, Cerebellar hypoplasia, Congenital microcephaly, Craniosynostosis, Developmental delay, Dwarfism, Glaucoma, Hypospadias, Impaired cognition, Jawad syndrome, Mental retardation, Microcephaly, Microcephaly-digital anomalies syndrome, Microdontia, Microglossia, Micrognathism, Microphthalmos, Myasthenia gravis, Pancreatic neoplasm, Pancreatic carcinoma, Pancreatic cancer, Scoliosis, Seckel syndromeView all (10 more) |
|
313
|
|
|
RB transcriptional corepressor like 2 |
BRUWAG, P130, Rb2 |
|
|
314
|
|
|
RNA binding motif protein 3 |
IS1-RNPL, RNPL |
|
|
315
|
|
|
Relaxin family peptide receptor 1 |
LGR7, RXFPR1 |
|
|
316
|
|
|
RNA binding motif single stranded interacting protein 1 |
C2orf12, HCC-4, MSSP, MSSP-1, MSSP-2, MSSP-3, SCR2, YC1 |
|
|
317
|
|
|
RNA binding motif protein Y-linked family 1 member A1 |
RBM, RBM1, RBM2, RBMY, RBMY1C, YRRM1, YRRM2 |
|
|
318
|
|
|
Retinol binding protein 1 |
CRABP-I, CRBP, CRBP1, CRBPI, RBPC, hCRBP1 |
|
|
319
|
|
|
Retinol binding protein 3 |
D10S64, D10S65, D10S66, IRBP, RBPI, RP66 |
Autoimmune diseases, Capsular cataract, Cataract, Colorectal cancer, Congenital hypoplasia of penis, Diabetes mellitus, Disorder of eye, Glaucoma, Hearing loss, Hyperinsulinism, Hypogonadism, Keratoconus, Mental retardation, Night blindness, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinal dystrophy, Retinitis pigmentosa, Rod-cone dystrophy, UveitisView all (7 more) |
|
320
|
|
|
Retinol binding protein 4 |
MCOPCB10, RDCCAS |
Anaplastic carcinoma, Carcinoma, Microphthalmia with coloboma, Comedonal acne, Congenital coloboma of iris, Congenital ocular coloboma, Congestive heart failure, Disorder of eye, Fundus coloboma, Gastric cancer, Heart failure, Keratomalacia, Kidney disease, Microphthalmos, Miscarriage, Myocardial infarction, Night blindness, Sclerocystic ovaries, Patent ductus arteriosus, Peripheral retinal atrophy, Polycystic ovary syndrome, Progressive retinal dystrophy, Retinal coloboma, Retinal dystrophy, Retinal dystrophy, iris coloboma, and comedogenic acne syndrome, Retinitis pigmentosa, Retinol deficiency, Stomach neoplasms, Syndromic microphthalmia, Vitamin a deficiency, Xerotic keratitisView all (16 more) |
