|
741
|
|
|
ST3 beta-galactoside alpha-2,3-sialyltransferase 1 |
Gal-NAc6S, SIAT4A, SIATFL, ST3GalA, ST3GalA.1, ST3GalIA, ST3GalIA,1, ST3O |
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742
|
|
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ST3 beta-galactoside alpha-2,3-sialyltransferase 4 |
CGS23, NANTA3, SAT3, SIAT4, SIAT4C, ST-4, ST3GalA.2, ST3GalIV, STZ, gal-NAc6S |
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743
|
|
|
Solute carrier family 13 member 3 |
ARLIAK, NADC3, NaC3, SDCT2 |
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744
|
|
|
ST3 beta-galactoside alpha-2,3-sialyltransferase 3 |
DEE15, EIEE15, MRT12, SIAT6, ST3GALII, ST3Gal III, ST3GalIII, ST3N |
Absence of septum pellucidum, Amyotrophic lateral sclerosis, Attention deficit hyperactivity disorder, Autism, Central visual impairment, Cerebral atrophy, Cortical dysplasia, Developmental delay, Developmental regression, Diabetes mellitus, Dyskinetic syndrome, Dyssomnia, Epileptic encephalopathy, Hypoplasia of corpus callosum, Mental retardation, Mental depression, Microcephaly, Motor delay, Non-syndromic intellectual disability, Polymicrogyria, Salaam seizures, Schizophrenia, Seizure, Sleep disorders, Spasms syndrome, Stereotyped behavior, West syndromeView all (12 more) |
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745
|
|
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ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 |
GD3S, SIAT8, SIAT8-A, SIAT8A, ST8SiaI |
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746
|
|
|
STIL centriolar assembly protein |
MCPH7, SIL |
|
|
747
|
|
|
SIM bHLH transcription factor 1 |
bHLHe14 |
6q16 microdeletion syndrome, Attention deficit hyperactivity disorder, Autism, Brachycephaly, Breast cancer, Mammary neoplasms, Breast carcinoma, Camptodactyly of fingers, Congenital epicanthus, Developmental delay, Dwarfism, High palate, Hyperglycemia, Hyperinsulinism, Macrocephaly, Macrotia, Marfan syndrome, Microcephaly, Myopia, Nystagmus, Obesity, Prader-willi-like syndrome, StrabismusView all (8 more) |
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748
|
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|
Signal-induced proliferation-associated 1 |
SPA1 |
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749
|
|
|
SIX homeobox 1 |
BOS3, DFNA23, TIP39 |
Anterior segment anomalies, Bor syndrome, Branchial clefts-congenital disorder, Branchioma, Branchiooculofacial syndrome, Branchiootic syndrome, Branchiootorenal syndrome, Cholesteatoma, Developmental dysplasia of the hip, Congenital malrotation of intestine, Deafness, Developmental delay, Endometrial neoplasms, Endometrial carcinoma, Euthyroid goiter, Facial paralysis, Fistula of branchial cleft, Hearing loss, High palate, Hydronephrosis, Malrotation of kidney, Melnick-fraser syndrome, Microdontia, Micrognathism, Microtia, Multicystic renal dysplasia, Nephroblastoma, Non-syndromic sensorineural deafness, Polycystic kidney disease, Prostate cancer, Renal agenesis, Renal dysplasia, Renal insufficiency, Renal steatosis, Stenosis of external auditory canal, Vesicoureteral reflux, Wilms tumorView all (22 more) |
|
750
|
|
|
SIX homeobox 3 |
HPE2 |
Agenesis of corpus callosum, Alobar holoprosencephaly, Ambiguous genitalia, Arrhinencephaly, Arrhinia, Asthma, Cerebellar hypoplasia, Cerebral cortical atrophy, Choanal atresia, Complete atrioventricular canal defect, Congenital coloboma of iris, Congenital hypoplasia of penis, Cyclocephaly, Developmental delay, Diabetes insipidus, Duodenal atresia, Dwarfism, Fused incisors, Hemangioma, Holoprosencephaly, Hypothyroidism, Liver neoplasms, Liver cancer, Lobar holoprosencephaly, Mental retardation, Microcephaly, Microform holoprosencephaly, Microphthalmos, Midline interhemispheric variant of holoprosencephaly, Panhypopituitarism, Renal agenesis, Schizencephaly, Scoliosis, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly, Single ventricle defect, Strabismus, Submucosal cleft palate, Tetralogy of fallotView all (24 more) |
