|
3261
|
|
|
RAS related 2 |
NS12, TC21 |
|
|
3262
|
|
|
Integrin subunit alpha 11 |
HsT18964 |
|
|
3263
|
|
|
Chloride channel accessory 4 |
CaCC, CaCC2 |
|
|
3264
|
|
|
IKAROS family zinc finger 3 |
AIO, AIOLOS, IMD84, ZNFN1A3 |
Asthma, Lymphocytic leukemia, B-cell lymphoma, Biliary cirrhosis, Dermatitis, Digestive system neuroendocrine neoplasm, Esophagus neoplasm, Immunoglobulin a deficiency, Lymphoblastic leukemia, Lupus erythematosus, Polycystic ovary syndrome, Rheumatoid arthritis, Selective immunoglobulin a deficiency |
|
3265
|
|
|
IKAROS family zinc finger 2 |
ANF1A2, HELIOS, ICHAD, IMDIA, ZNF1A2, ZNFN1A2 |
|
|
3266
|
|
|
Muscle RAS oncogene homolog |
M-RAs, NS11, R-RAS3, RRAS3 |
Abnormal dermatoglyphic pattern, Atrial septal defect, Brachydactyly, Camptodactyly of fingers, Cardiofaciocutaneous syndrome, Cardiovascular diseases, Carotid artery disease, Carotid atherosclerosis, Congenital pectus carinatum, Congenital pectus excavatum, Coronary arteriosclerosis, Coronary artery disease, Coronary heart disease, Costello syndrome, Cryptorchidism, Developmental delay, Diabetes mellitus, Dwarfism, Dysarthria, Hearing loss, High palate, Hypogonadotropic hypogonadism, Leopard syndrome, Cystic hygroma, Melanocytic nevus, Micrognathism, Moyamoya disease, Narcolepsy, Neck webbing, Noonan syndrome, Noonan-like syndrome with loose anagen hair, Nystagmus, Posteriorly rotated ear, Proptosis, Ptosis, Pulmonary stenosis, Radioulnar synostosis, Scoliosis, StrabismusView all (24 more) |
|
3267
|
|
|
Activating transcription factor 5 |
ATFX, HMFN0395 |
|
|
3268
|
|
|
Coat protein complex I subunit gamma 1 |
COPG, IMD128 |
|
|
3269
|
|
|
Pleckstrin homology like domain family A member 1 |
DT1P1B11, PHRIP, TDAG51 |
|
|
3270
|
|
|
Poly(U) binding splicing factor 60 |
FIR, RoBPI, SIAHBP1, VRJS |
8q24.3 microdeletion syndrome, Aortic coarctation, Atrioventricular septal defect, Attention deficit hyperactivity disorder, Bilateral renal hypoplasia, Branchioma, Camptodactyly of fingers, Cerebral atrophy, Clinodactyly, Renal agenesis, Developmental dysplasia of the hip, Congenital epicanthus, Hypoplastic aortic arch, Short femur, Congenital ocular coloboma, Congenital pectus excavatum, Developmental delay, Dwarfism, Dysmorphic features, Dysphagia, Exocrine pancreatic insufficiency, Exotropia, Fundus coloboma, Gastroesophageal reflux disease, Tourette syndrome, Heart septal defects, Hemifacial hypoplasia, Hyperopia, Hypertrichosis, Hypoplasia of corpus callosum, Hypoplasia of the optic nerve, Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome, Isolated somatotropin deficiency, Mental retardation, Mesothelioma, Microcephaly, Micrognathism, Micromelia, Microphthalmos, Multiple congenital anomalies, Myopia, Partial or complete agenesis of corpus callosum, Patent ductus arteriosus, Pelvic kidney, Penile hypospadias, Persistent truncus arteriosus, Polydactyly, Posteriorly rotated ear, Ptosis, Radial polydactyly, Renal aplasia, Renal cyst, Renal hypoplasia, Retinal coloboma, Scoliosis, Spina bifida occulta, Strabismus, Strawberry nevus of skin, Submucosal cleft palate, Supernumerary mesiodens tooth, Talipes, Thymus hyperplasia, Ventricular septal defect, Chromosome 8q24.3 deletion syndrome, Vertical talus, Vesicoureteral refluxView all (51 more) |
