|
41
|
|
|
Small nucleolar RNA host gene 31 |
- |
|
|
42
|
|
|
SLC7A14 antisense RNA 1 |
- |
|
|
43
|
|
|
SMIM15 antisense RNA 1 |
CTC-436P18.1 |
|
|
44
|
|
|
SIRPG antisense RNA 1 |
- |
|
|
45
|
|
|
SCN1A and SCN9A antisense RNA 1 |
SCN1A-NAT, SCN1ANAT |
Autism, Developmental dysplasia of the hip, Developmental delay, Dysmorphic features, Epilepsy, Epilepsy with febrile seizures plus, Epileptic encephalopathy, Erythermalgia, Febrile convulsions, Febrile seizures, Frontal bossing, Generalized epilepsy with febrile seizures plus, Hemimegalencephaly, Hemiplegic migraine, Leukemia, Malformation of cortical development, Megalencephaly, Mental retardation, Mesial temporal lobe epilepsy with hippocampal sclerosis, Movement disorders, Neuropathy, Obesity, Paroxysmal extreme pain disorder, Polymicrogyria, Small fiber neuropathy, Spasms x-linked, Speech delay, TalipesView all (13 more) |
|
46
|
|
|
Syntaxin 6 |
- |
|
|
47
|
|
|
Solute carrier family 17 member 2 |
NPT3 |
|
|
48
|
|
|
Serine and arginine repetitive matrix 1 |
160-KD, POP101, SRM160 |
|
|
49
|
|
|
Sprouty RTK signaling antagonist 2 |
IGAN3, hSPRY2 |
|
|
50
|
|
|
Splicing factor 3b subunit 4 |
AFD1, Hsh49, SAP49, SF3b49 |
Acrofacial dysostosis, Aqueductal stenosis, Arrhinencephaly, Clinodactyly, Congenital clubfoot, Congenital hypoplasia of radius, Dwarfism, Dysmorphic features, Gastroschisis, Hearing loss, Hirschsprung disease, Hydrocephalus, Hypoplasia of rib, Hypoplasia of the epiglottis, Hypoplasia of the maxilla, Laryngeal hypoplasia, Macrostomia, Microcephaly, Micrognathism, Microtia, Multiple congenital anomalies, Nager syndrome, Osteochondrodysplasia, Phocomelia, Polymicrogyria, Posteriorly rotated ear, Ptosis, Radioulnar synostosis, Renal aplasia, Scoliosis, Skeletal dysplasia, Sprengel deformity, Stenosis of external auditory canal, Syndactyly of fingers, Syndactyly of the toes, Tetralogy of fallot, Thumb aplasia, Trismus, Urticaria, Uterine anomalies, Velopharyngeal insufficiencyView all (26 more) |
