|
521
|
|
|
GTF2I repeat domain containing 1 |
BEN, CREAM1, GTF3, MUSTRD1, RBAP2, WBS, WBSCR11, WBSCR12, hMusTRD1alpha1 |
Abnormal dermatoglyphic pattern, Abnormal spinal segmentation, Accessory kidney, Aneurysm of aortic arch, Anxiety disorder, Arnold-chiari malformation, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Bicuspid aortic valve, Bladder diverticulum, Blepharophimosis, Camptodactyly of fingers, Cataract, Cerebral cortical atrophy, Cholelithiasis, Congenital anomaly of neck, Congenital epicanthus, Congenital exomphalos, Congenital hypoplasia of penis, Congenital keratoglobus, Congenital pectus excavatum, Congestive heart failure, Cornea plana, Cryptorchidism, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Dysgraphia, Gastroesophageal reflux disease, Glaucoma, Hearing loss, Hypercalcemia, Hypertension, Hypertrophic cardiomyopathy, Hypodontia, Hypogonadotropic hypogonadism, Hypothyroidism, Lupus erythematosus, Macroglossia, Macrostomia, Macrotia, Malabsorption syndrome, Mental depression, Mental retardation, Microcephaly, Microdontia, Micrognathism, Mitral valve prolapse, Multiple renal cysts, Myocardial infarction, Myopathy, Myopia, Nephrocalcinosis, Nephrolithiasis, Nystagmus-induced head nodding, Obesity, Obsessive-compulsive disorder, Osteopenia, Osteoporosis, Osteosclerosis, Otitis media, Overriding aorta, Patent ductus arteriosus, Pelvic kidney, Peptic ulcer, Peripheral pulmonary artery stenosis, Phakomatosis pigmentovascularis, Polycystic ovary syndrome, Posterior embryotoxon, Precocious puberty, Pulmonary stenosis, Radioulnar synostosis, Rectal prolapse, Renal hypoplasia, Renal insufficiency, Schizophrenia, Scoliosis, Spina bifida occulta, Strabismus, Stroke, Supravalvar aortic stenosis, Tetralogy of fallot, Ventricular septal defect, Vesicoureteral reflux, Williams syndromeView all (72 more) |
|
522
|
|
|
Golgi SNAP receptor complex member 2 |
Bos1, EPM6, GS27, MYOS |
Action myoclonus-renal failure syndrome, Atrial fibrillation, Cardiovascular diseases, Coronary artery disease, Dentatorubral pallidoluysian atrophy, Dysarthria, Hypotonic seizures, Inclusion-body disease, May-white syndrome, Myoclonic epilepsy, Oral cleft, Paroxysmal atrial fibrillation, Progressive myoclonic epilepsy, Scoliosis |
|
523
|
|
|
Growth differentiation factor 3 |
KFS3, MCOP7, MCOPCB6 |
Neoplasm, Microphthalmia with coloboma, Congenital coloboma of iris, Congenital ocular coloboma, Congenital torticollis, Ectopic anus, Embryonal neoplasm, Fundus coloboma, Tumor, Hemiplegia/hemiparesis, Hypoplasia of optic disc, Impaired cognition, Imperforate anus, Isolated klippel-feil syndrome, Isolated microphthalmia-anophthalmia-coloboma, Klippel feil syndrome, Microphthalmia, Microphthalmos, Neck webbing, Nystagmus, Retinal coloboma, Scoliosis, Spina bifida, Sprengel deformity, Ventricular septal defectView all (10 more) |
|
524
|
|
|
Guanine deaminase |
CYPIN, GAH, GUANASE, NEDASIN |
|
|
525
|
|
|
Guanylate cyclase activator 1C |
GCAP3 |
|
|
526
|
|
|
G protein subunit alpha 14 |
HG1I |
Anemia, Angioblastoma, Angioma, Cholecystolithiasis, Cholelithiasis, Esotropia, Fibrinogen deficiency, Hemangioma of the lip, Hypertrichosis, Hypofibrinogenemia, Kaposiform hemangioendothelioma, Pyogenic granuloma, Skin neoplasms |
|
527
|
|
|
Growth regulating estrogen receptor binding 1 |
- |
|
|
528
|
|
|
Granule associated Rac and RHOG effector 1 |
KIAA0355, MiniBAR |
|
|
529
|
|
|
GIT ArfGAP 2 |
CAT-2, CAT2, PKL |
|
|
530
|
|
|
GINS complex subunit 1 |
IMD55, PSF1 |
|
