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1001
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Solute carrier family 25 member 22 |
DEE3, EIEE3, GC-1, GC1, NET44 |
Autism, Cerebellar atrophy, Cerebral atrophy, Choreoathetosis, Clonic seizures, Congenital exomphalos, Developmental delay, Developmental regression, Dyskinetic syndrome, Dysphagia, Dyssomnia, Epileptic encephalopathy, Episodic ataxia, Eyelid myoclonias, Febrile seizures, Focal seizures, Focal tonic seizures, Hypoplasia of corpus callosum, Hypotonic seizures, Malignant migrating partial seizures of infancy, Mental retardation, Microcephaly, Myoclonic encephalopathy, Myoclonic seizures, Hypotonia, Pachygyria, Penis agenesis, Precocious puberty, Renal dysplasia, Seizure, Sleep disorders, Spasms x-linked, Strabismus, Ureterocele, Ventricular septal defect, West syndromeView all (21 more) |
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1002
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Smad nuclear interacting protein 1 |
NEDHCS, PML1, PMRED |
Aortic valve sclerosis, Bicuspid aortic valve, Congenital exomphalos, Developmental delay, Epilepsy, Horizontal nystagmus, Hypoplasia of corpus callosum, Macroglossia, Macrostomia, Psychomotor retardation, epilepsy, and craniofacial dysmorphism, Strabismus |
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1003
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Succinyl-CoA:glutarate-CoA transferase |
C7orf10, DERP13, GA3, ORF19 |
Abdominal migraine, Acne, Common migraine, Confusional migraine, Glutaric acidemia, Hemicrania migraine, Hypertension, Migraine, Pancreatic neoplasm, Pancreatic carcinoma, Pancreatic cancer, Prostate cancer, Prostate cancer, hereditary, Status migrainosus |
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1004
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SEM1 26S proteasome subunit |
C7orf76, DSS1, ECD, PSMD15, SHFD1, SHFM1, SHSF1, Shfdg1 |
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1005
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SREBF pathway regulator in golgi 1 |
C12orf49, LUR1, POST1, SPRING |
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1006
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SHC binding and spindle associated 1 |
PAL |
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1007
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SAFB like transcription modulator |
Met |
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1008
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Suppression of tumorigenicity 7 |
ETS7q, FAM4A, FAM4A1, HELG, RAY1, SEN4, TSG7 |
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1009
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Sorting nexin 22 |
- |
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1010
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Sperm flagellar 2 |
CT122, KPL2, SPGF43 |
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