|
321
|
|
|
Solute carrier family 39 member 6 |
LIV-1, LIV1, ZIP6 |
|
|
322
|
|
|
SAM pointed domain containing ETS transcription factor |
PDEF, bA375E1.3 |
|
|
323
|
|
|
SAMM50 sorting and assembly machinery component |
CGI-51, OMP85, SAM50, TOB55, TRG-3, YNL026W |
|
|
324
|
|
|
Sulfotransferase family 4A member 1 |
BR-STL-1, BRSTL1, DJ388M5.3, NST, SULTX3, hBR-STL-1 |
|
|
325
|
|
|
SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 |
CHBL2, DCIP, HDDC1, MOP-5, SBBI88, hSAMHD1 |
Acquired porencephaly, Aicardi goutieres syndrome, Aortic aneurysm, Arrhinencephaly, Arthritis, Arthropathy, Autoinflammatory disease, Brain atrophy, Cerebral atrophy, Chilblain lupus erythematosus, Chilblain lesions, Cutis marmorata, Degeneration of the striatum, Demyelinating neuropathy, Deoxyguanosine kinase deficiency, Developmental delay, Developmental regression, Diabetes mellitus, Dwarfism, Enchondroma, Glaucoma, Glaucoma, congenital, Hemiplegia/hemiparesis, Hypertrophic cardiomyopathy, Hypoplasia of corpus callosum, Hypothyroidism, Lymphocytic leukemia, Leukodystrophy, Leukoencephalopathy, Lipoatrophy, Lipodystrophy, Microcephaly, Moyamoya disease, Myositis, Alloimmune thrombocytopenia, Nystagmus, Panniculitis, Penis agenesis, Plagiocephaly, Porencephalic cyst, Pseudo-torch syndrome, Ptosis, Raynaud phenomenon, Scoliosis, Spastic quadriplegia, VasculitisView all (31 more) |
|
326
|
|
|
SIN3 transcription regulator family member A |
CHR15DELq24, DEL15Q24, WITKOS |
15q24 microdeletion syndrome, Agenesis of corpus callosum, Aqueductal stenosis, Arachnodactyly, Attention deficit hyperactivity disorder, Autism spectrum disorder, Autism, Brachydactyly, Camptodactyly of fingers, Clinodactyly, Communicating hydrocephalus, Congenital coloboma of iris, Congenital diaphragmatic hernia, Congenital epicanthus, Congenital hydrocephalus, Congenital microcephaly, Corpus callosum malformation, Cryptorchidism, Developmental delay, Developmental regression, Dwarfism, Dysmorphic features, Dysplastic corpus callosum, Dyssomnia, Fetal cerebral ventriculomegaly, Gastrointestinal atresia, High palate, Hydrocephalus, Hydrocephalus ex-vacuo, Hyperopia, Hypogonadism, Hypoplasia of corpus callosum, Hypoplasia of thumb, Hypospadias, Immunologic deficiency syndromes, Mental retardation, Intestinal atresia, Isolated somatotropin deficiency, Macrotia, Microcephaly, Microlissencephaly, Microphthalmos, Microstomia, Nystagmus, Obesity, Obstructive hydrocephalus, Penis agenesis, Scoliosis, Sleep disorders, Somatotropin deficiency, Strabismus, Syndactyly of the toes, Witteveen-kolk syndromeView all (38 more) |
|
327
|
|
|
SH2B adaptor protein 1 |
PSM, SH2B |
Aortic valve insufficiency, Arachnodactyly, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Chromosome 16p11.2 deletion syndrome, Coloboma of optic disc, Congenital diaphragmatic hernia, Developmental delay, Distal 16p11.2 microdeletion syndrome, Dwarfism, Gastroesophageal reflux disease, Hirschsprung disease, Hyperinsulinism, Hyperuricemia, Inflammatory bowel disease, Kidney disease, Language disorders, Macrocephaly, Mental retardation, Micrognathism, Microphthalmos, Microstomia, Migraine, Myopia, Hypotonia, Obesity, Proximal 16p11.2 microdeletion syndrome, Psychosis, Renal agenesis, Rod-cone dystrophy, Scoliosis, Strabismus, Syndromic microphthalmia, Syringomyelia, Vesicoureteral refluxView all (21 more) |
|
328
|
|
|
Sushi, nidogen and EGF like domains 1 |
IRE-BP1, SST3, Snep |
|
|
329
|
|
|
Spermatogenesis associated serine rich 2 like |
DNAPTP6, SGNP |
|
|
330
|
|
|
Signal induced proliferation associated 1 like 1 |
E6TP1, SPAR1 |
|
