|
841
|
|
|
Spermine synthase |
MRSR, MRXSSR, SPMSY, SRS, SpS |
Acquired kyphoscoliosis, Arachnodactyly, Bipolar disorder, Brachycephaly, Congenital camptodactyly, Congenital clubfoot, Congenital kyphoscoliosis, Congenital pectus carinatum, Congenital pectus excavatum, Cryptorchidism, Dwarfism, Dysarthria, Ectopic kidney, Epilepsy, High palate, Hypospadias, Macrocephaly, Malocclusion, Mental retardation, Mental retardation, x-linked, Microstomia, Mood disorder, Myoclonic seizures, Myopia, Neck webbing, Osteoporosis, Patchy hypo- and hyperpigmentation, Proptosis, Rheumatoid arthritis, Smith-magenis syndrome, Synophrys, Testicular atrophyView all (17 more) |
|
842
|
|
|
Snail family transcriptional repressor 1 |
SLUGH2, SNA, SNAH, SNAIL, SNAIL1, dJ710H13.1 |
Nonmedullary thyroid carcinoma, Amyotrophic lateral sclerosis, Breast cancer, Mammary neoplasms, Breast carcinoma, Cholestasis, Gastric cancer, Lateral sclerosis, Marfan syndrome, Papillary thyroid carcinoma, Stomach neoplasms, Thyroid cancer |
|
843
|
|
|
Synaptosome associated protein 25 |
CMS18, DEE117, RIC-4, RIC4, SEC9, SNAP, SNAP-25, SUP, bA416N4.2, dJ1068F16.2 |
Acquired kyphoscoliosis, Arthrogryposis multiplex congenita, Bipolar disorder, Bulbar palsy, Developmental dysplasia of the hip, Congenital kyphoscoliosis, Myasthenic syndrome, Congenital pectus carinatum, Developmental delay, Diabetes mellitus, Distal amyotrophy, Dysarthria, Dysphagia, Epilepsy, Esotropia, Gastroesophageal reflux disease, Tourette syndrome, Hearing loss, High palate, Manic disorder, Melancholia, Mental depression, Mental retardation, Motor delay, Myasthenia gravis, Neurodevelopmental disorders, Nystagmus, Polyneuropathy, Psychosis, Ptosis, Schizoaffective disorder, Schizophreniform disorders, Sleep apnea, Sudden episodic apnea, Tonic-clonic epilepsyView all (20 more) |
|
844
|
|
|
Synuclein beta |
- |
|
|
845
|
|
|
Synuclein alpha |
NACP, PARK1, PARK4, PD1 |
Abnormal male sexual function, Akinesia, Anxiety disorder, Cerebral cortical atrophy, Congenital clubfoot, Degenerative diseases, central nervous system, Delusions, Dementia, Dementia of frontal lobe, Dementia with lewy body, Dysarthria, Dysautonomia, Dyskinetic syndrome, Dysphagia, Dyssomnia, Female sexual dysfunction, Gastroparesis, Gaucher disease, Hallucinations, Hepatolenticular degeneration, Hereditary parkinson`s disease, Lewy body disease, Male sexual dysfunction, Mental depression, Neurodegenerative disorders, Neurogenic urinary bladder, Panic disorder, Paranoia, Parkinson disease, Parkinsonian disease, Parkinsonian-pyramidal syndrome, Ramsay hunt paralysis syndrome, Restless legs syndrome, Schizophrenia, Sleep disorders, Social communication disorderView all (21 more) |
|
846
|
|
|
Synuclein gamma |
BCSG1, SR |
|
|
847
|
|
|
Small nuclear ribonucleoprotein polypeptides B and B1 |
CCMS, COD, SNRPB1, Sm-B/B', SmB/B', SmB/SmB', snRNP-B |
Acquired porencephaly, Atrial septal defect, Congenital alveolar dysplasia, Camptodactyly of fingers, Cerebrocostomandibular syndrome, Cerebrocostomandibular-like syndrome, Cleft soft palate, Developmental dysplasia of the hip, Congenital epicanthus, Dwarfism, Ectopic kidney, Elbow flexion contracture, Gastric cancer, Gastroesophageal reflux disease, Glossoptosis, Hearing loss, High palate, Horseshoe kidney, Hydranencephaly, Meningomyelocele, Mental retardation, Microcephaly, Micrognathism, Multicystic renal dysplasia, Neck webbing, Patent ductus arteriosus, Porencephalic cyst, Posteriorly rotated ear, Renal cyst, Scoliosis, Stomach neoplasms, Thoracic hypoplasia, Tracheomalacia, Ventricular septal defectView all (19 more) |
|
848
|
|
|
Small nuclear ribonucleoprotein polypeptide B2 |
Msl1, U2B'' |
|
|
849
|
|
|
Small nuclear ribonucleoprotein D3 polypeptide |
SMD3, Sm-D3 |
|
|
850
|
|
|
Small nuclear ribonucleoprotein polypeptide E |
HYPT11, SME, Sm-E, snRNP-E |
|
