|
551
|
|
|
Strawberry notch homolog 1 |
MOP3, Sno |
|
|
552
|
|
|
SET domain containing 5 |
MRD23, SETD5A |
Anxiety disorder, Astigmatism, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Blepharophimosis, Brachycephaly, Camptodactyly of fingers, Cataract, Cerebral cortical atrophy, Choanal atresia, Congenital diaphragmatic hernia, Congenital hypoplasia of penis, Congenital malrotation of intestine, Congenital pectus excavatum, Cornelia de lange syndrome, Cryptorchidism, Cutis marmorata, Developmental delay, Dwarfism, Dysmorphic features, Dyssomnia, Febrile seizures, Foot polydactyly, Gastroesophageal reflux disease, Glaucoma, Hearing loss, Hemianopsia, High palate, Hyperopia, Hypoplasia of nipple, Hypospadias, Mental retardation, Intellectual disability-facial dysmorphism syndrome, Intestinal volvulus, Macrotia, Microcephaly, Microcornea, Micrognathism, Micromelia, Microphthalmos, Multicystic renal dysplasia, Multiple congenital anomalies, Myopia, Nervous system diseases, Neurodevelopmental disorders, Nystagmus, Obsessive-compulsive disorder, Oligodactyly, Phthisis bulbi, Physiologic amenorrhea, Ptosis, Radioulnar synostosis, Renal insufficiency, Scoliosis, Sleep disorders, Speech disorders, Strabismus, Syndactyly of the toes, Synophrys, Talipes, Uterine anomalies, Ventricular septal defect, Vesicoureteral refluxView all (49 more) |
|
553
|
|
|
STEAP3 metalloreductase |
AHMIO2, STMP3, TSAP6, dudlin-2, dudulin-2, pHyde |
|
|
554
|
|
|
Solute carrier family 47 member 1 |
MATE1 |
|
|
555
|
|
|
Serine palmitoyltransferase long chain base subunit 3 |
C20orf38, LCB 3, LCB2B, LCB3, SPT 3, SPT3, SPTLC2L, dJ718P11, dJ718P11.1, hLCB2b |
|
|
556
|
|
|
Solute carrier family 29 member 3 |
ENT3, HCLAP, HJCD, PHID |
Alopecia, Anemia, Arcus senilis, Autoimmune diabetes, Autoinflammatory disease, Azoospermia, Bronchiectasis, Cervical lymphadenopathy, Clinodactyly, Congenital camptodactyly, Congenital heart defects, Developmental regression, Diabetes mellitus, Brittle diabetes mellitus, Dwarfism, Dysosteosclerosis, Elbow flexion contracture, Episcleritis, Gynecomastia, H syndrome, Hearing loss, Histiocytosis, Histiocytosis with joint contractures and sensorineural deafness, Hydrocephalus, Hypertrichosis, Hypogonadism, Hypogonadotropic hypogonadism, Ichthyosis, Isolated somatotropin deficiency, Lipodystrophy, Macrocephaly, Malabsorption syndrome, Mental depression, Mental retardation, Nystagmus, Optic atrophy, Osteosclerosis, Penis agenesis, Proptosis, Psoriasiform eczema, Rhinitis, Scleroderma, Sinus histiocytosis, Somatotropin deficiency, Ventricular septal defect, Vitiligo, Vulval varicesView all (32 more) |
|
557
|
|
|
Spermatid perinuclear RNA binding protein |
HEL162, ILF3L, SPNR, p74 |
|
|
558
|
|
|
Solute carrier family 35 member C1 |
CDG2C, FUCT1 |
Anxiety disorder, Autism, Brachydactyly, Bronchiolitis, Cerebral cortical atrophy, Congenital disorder of glycosylation, Developmental delay, Dwarfism, Febrile seizures, Mental retardation, Leukocyte adhesion deficiency, Microcephaly, Neutrophilia, Obsessive-compulsive disorder, Otitis media, PeriodontitisView all (1 more) |
|
559
|
|
|
Serine/threonine kinase 32B |
HSA250839, STK32, STKG6, YANK2 |
|
|
560
|
|
|
Solute carrier family 22 member 15 |
FLIPT1, PRO34686 |
|
