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3441
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Pogo transposable element derived with ZNF domain |
MRD37, WHSUS, ZNF280E, ZNF635, ZNF635m |
Astigmatism, Autism, Autism spectrum disorder, Brachycephaly, Brachydactyly, Central visual impairment, Cerebellar atrophy, Cerebral atrophy, Cerebral cortical atrophy, Congenital coloboma of iris, Congenital diaphragmatic hernia, Congenital heart defects, Developmental delay, Dwarfism, Dyscognitive seizures, Dysmorphic features, Expressive language delay, Febrile seizures, Gastroesophageal reflux disease, Hearing loss, High palate, Hyperopia, Hypoglycemic seizures, Hypoplasia of corpus callosum, Hypothyroidism, Macrostomia, Malocclusion, Mental retardation, Microcephaly, Microstomia, Movement disorders, Multiple congenital anomalies, Myopia, Neurodevelopmental disorders, Obesity, Obsessive-compulsive disorder, Optic atrophy, Posteriorly rotated ear, Rod-cone dystrophy, Seizure, Sensorineural hearing loss, Sleep apnea, Stereotyped behavior, Strabismus, Subcortical cerebral atrophy, Vitiligo, White-sutton syndromeView all (32 more) |
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3442
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Collagen beta(1-O)galactosyltransferase 2 |
C1orf17, ColGalT 2, GLT25D2 |
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3443
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Plexin D1 |
CHTD9, PLEXD1 |
Arthrogryposis multiplex congenita, Autism, Brachydactyly, Cafe-au-lait spot, Camptodactyly of fingers, Breast aplasia, Congenital clubfoot, Congenital epicanthus, Dysphagia, Facial paralysis, Heart failure, High palate, Hypogonadotropic hypogonadism, Microdontia, Micrognathism, Mobius syndrome, Moebius syndrome, Motor delay, Persistent truncus arteriosus, Ptosis, Strabismus, Syndactyly of fingersView all (7 more) |
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3444
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Fli-1 proto-oncogene, ETS transcription factor |
BDPLT21, EWSR2, FLI-1, SIC-1 |
Agenesis of corpus callosum, Anemia, Annular pancreas, Anorexia, Aortic coarctation, Aortic valve sclerosis, Attention deficit hyperactivity disorder, Bipolar disorder, Bleeding disorder, Brain neoplasms, Cardiovascular abnormalities, Cataract, Cerebral atrophy, Clinodactyly, Congenital coloboma of iris, Congenital epicanthus, Congenital malrotation of intestine, Corneal astigmatism, Cryptorchidism, Developmental delay, Duodenal atresia, Dwarfism, Ectopic anus, Ectropion, Eczema, Endometrial neoplasms, Ewing sarcoma, Extra-osseous ewing`s sarcoma, Extraskeletal ewing sarcoma, Frontal bossing, Hydronephrosis, Hypoplastic left heart syndrome, Isolated delta-storage pool disease, Jacobsen syndrome, Macrocephaly, Major affective disorder, Medulloblastoma, Medullomyoblastoma, Mental retardation, Microcornea, Multicystic renal dysplasia, Myopia, Neck webbing, Neoplasm of scrotum, Ovarian neoplasm, Pachygyria, Pancreatic neoplasm, Pancreatitis, Paris-trousseau thrombocytopenia, Peripheral primitive neuroectodermal tumor, Precocious puberty, Proptosis, Ptosis, Schizophrenia, Scoliosis, Skeletal ewing sarcoma, Spina bifida, Spinal cord neoplasms, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Talipes, Trigonocephaly, Ventricular septal defect, VitiligoView all (50 more) |
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3445
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PHD finger protein 8 |
JHDM1F, KDM7B, MRXSSD, ZNF422 |
Cryptorchidism, Dysmorphic features, Mental disorders, Mental retardation, Mental retardation, x-linked, Multiple congenital anomalies, Polydactyly, Psychosis, Scoliosis, Syndromic mental retardation, x-linked, Synophrys |
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3446
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Lysine demethylase 6B |
JMJD3, NEDCFSA, NEDSST |
Adenocarcinoma, Apraxia, Autism, Camptodactyly of fingers, Congenital epicanthus, Congenital pectus excavatum, Cryptorchidism, Developmental delay, Esotropia, Exotropia, Hemangioma, Hypoplasia of nipple, Mental retardation, Macrostomia, Macrotia, MalocclusionView all (1 more) |
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3447
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Erythrocyte membrane protein band 4.1 like 3 |
4.1B, DAL-1, DAL1 |
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3448
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Microtubule associated serine/threonine kinase 2 |
MAST205, MTSSK |
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3449
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FLII actin remodeling protein |
CMD2J, FLI, FLIL, Fli1 |
Anxiety disorder, Attention deficit hyperactivity disorder, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Developmental delay, Dwarfism, Dyssomnia, Frontal bossing, Gastroesophageal reflux disease, Hearing loss, Hypercholesterolemia, Hypothyroidism, Malocclusion, Mental retardation, Microcephaly, Microcornea, Micrognathism, Myopia, Obesity, Otitis media, Precocious puberty, Retinal detachment, Scoliosis, Sleep disorders, Smith-magenis syndrome, Speech disorders, Stereotyped behavior, Strabismus, Syndactyly of the toes, Synophrys, TaurodontismView all (17 more) |
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3450
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Zinc finger ZZ-type and EF-hand domain containing 1 |
ZZZ4 |
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