|
281
|
|
|
Solute carrier family 9 member A8 |
NHE-8, NHE8 |
|
|
282
|
|
|
SAM and SH3 domain containing 1 |
CAPOK, DUH, DUH1, SH3D6A, dJ323M4.1 |
Alopecia, Carcinoma, Diabetic nephropathy, Dyschromatosis, Dyschromatosis universalis hereditaria, Lentiginosis profusa, Leukemia, Multinodular goiter, Nail dystrophy, Palmoplantar keratoderma, Pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome, Rotator cuff syndrome |
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283
|
|
|
SZT2 subunit of KICSTOR complex |
C1orf84, DEE18, EIEE18, KIAA0467, KICS1, SZT2A, SZT2B |
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Cerebral atrophy, Cryptorchidism, Developmental delay, Developmental regression, Dwarfism, Dyskinetic syndrome, Epilepsy, Epileptic encephalopathy, Gastroesophageal reflux disease, Hypodontia, Mental retardation, Microcephaly, Non-specifi epileptic encephalopathy, Nystagmus, Optic atrophy, Ptosis, Status epilepticusView all (5 more) |
|
284
|
|
|
Spectrin repeat containing nuclear envelope protein 1 |
8B, AMC3, AMCM, ARCA1, C6orf98, CPG2, EDMD4, KASH1, MYNE1, Nesp1, SCAR8, dJ45H2.2 |
Amyotrophy, Arthrogryposis multiplex congenita, Ataxia, Atrioventricular block, Attention deficit hyperactivity disorder, Bipolar disorder, Breast cancer, Mammary neoplasms, Breast carcinoma, Cardiomyopathy, Cerebellar ataxia, Cerebellar atrophy, Colorectal cancer, Colorectal neoplasms, Congenital clubfoot, Congenital muscular dystrophy, Congenital pectus excavatum, Cryptorchidism, Depressed bipolar disorder, Development disorder, Developmental delay, Developmental regression, Distal arthrogryposis, Dysarthria, Elbow flexion contracture, Emery-dreifuss muscular dystrophy, Emery-dreifuss muscular dystrophy, x-linked, Endometriosis, Horizontal nystagmus, Hyperopia, Hypertrophic cardiomyopathy, Ichthyosis, Limb-girdle muscular dystrophy, Lipodystrophy, Marfan syndrome, Mental depression, Mental retardation, Motor delay, Muscular dystrophy, Myogenic arthrogryposis multiplex congenita, Nasopharyngeal carcinoma, Nystagmus, Obesity, Peripheral axonal neuropathy, Ptosis, Schizophrenia, Scoliosis, Spinocerebellar ataxia, Sprengel deformity, Strabismus, Uterine fibroids, Plexiform leiomyoma, Ventricular septal hypertrophy, Vocal cord paralysisView all (39 more) |
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285
|
|
|
Structural maintenance of chromosomes flexible hinge domain containing 1 |
BAMS, FSHD2 |
Arrhinia, Cataract, Choanal atresia, Arrhinia with choanal atresia and microphthalmia syndrome, Congenital coloboma of iris, Congenital hypoplasia of penis, Congenital ocular coloboma, Cryptorchidism, Facioscapulohumeral dystrophy, Facioscapulohumeral muscular dystrophy, Gynecomastia, Hearing loss, High palate, Hypogonadism, Hypoplasia of the olfactory bulb, Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome, Microphthalmos, Muscular dystrophy, Penis agenesis, Physiologic amenorrhea, Submucosal cleft palate, Syndromic microphthalmiaView all (7 more) |
|
286
|
|
|
Sad1 and UNC84 domain containing 1 |
UNC84A |
|
|
287
|
|
|
SLIT-ROBO Rho GTPase activating protein 2 |
ARHGAP34, FNBP2, SRGAP2A, SRGAP3 |
|
|
288
|
|
|
Sperm antigen with calponin homology and coiled-coil domains 1 like |
CYTSA, GBBB2, OBLFC1, TBHS, TBHS1 |
Agenesis of corpus callosum, Anxiety disorder, Aortic coarctation, Atrial septal defect, Autism, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Cerebral cortical atrophy, Congenital epicanthus, Congenital exomphalos, Pulmonary hypoplasia, Congenital omphalocele, Congenital pectus excavatum, Craniosynostosis, Cryptorchidism, Developmental delay, Dwarfism, Dysphagia, Ectopic kidney, Female pseudohermaphroditism, Frontal bossing, Agenesis of gallbladder, Hearing loss, Hiatal hernia, High palate, Hypertelorism syndrome, Hypospadias, Imperforate anus, Laryngeal cleft, Macrostomia, Mental retardation, Micrognathism, Multicystic renal dysplasia, Oculomaxillofacial dysostosis, Opitz gbbb syndrome, Oral cleft, Patent ductus arteriosus, Posteriorly rotated ear, Proptosis, Ptosis, Pulmonary arterial hypertension, Spade-like hand, Strabismus, Syndactyly of fingers, Teebi syndrome, Tetralogy of fallot, Ventricular septal defectView all (33 more) |
|
289
|
|
|
SIK family kinase 3 |
L19, QSK, SEMDK, SIK-3 |
Allergic rhinitis, Annular pancreas, Arnold-chiari malformation, Asthma, Atrial fibrillation, Atrial septal defect, Brachydactyly, Breast cancer, Breast carcinoma, Congenital pectus excavatum, Coronary heart disease, Developmental delay, Diabetes, Diabetes mellitus, Eczema, Elbow flexion contracture, Frontal bossing, Heart failure, High palate, Hydrocephalus, Immunologic deficiency syndromes, Malignant neoplasm, Mesomelia, Metabolic syndrome, Patent ductus arteriosus, Platybasia, Congenital hypertrophic pyloric stenosis, Rhizomelia, Spondyloenchondrodysplasia, Stroke, Syndactyly of the toesView all (16 more) |
|
290
|
|
|
Sirtuin 3 |
SIR2L3 |
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