|
311
|
|
|
ELOVL fatty acid elongase 7 |
- |
|
|
312
|
|
|
Enhancer of mRNA decapping 3 |
LSM16, MRT50, YJDC, YJEFN2, hYjeF_N2-15q23 |
Absence of septum pellucidum, Autism, Central visual impairment, Cerebral atrophy, Cortical dysplasia, Developmental delay, Dyskinetic syndrome, Dyssomnia, Hypoplasia of corpus callosum, Mental retardation, Mental depression, Microcephaly, Motor delay, Non-syndromic intellectual disability, Polymicrogyria, Salaam seizures, Seizure, Sleep disorders, Stereotyped behaviorView all (4 more) |
|
313
|
|
|
EF-hand domain family member D1 |
MST133, MSTP133, PP3051, SWS2 |
|
|
314
|
|
|
Endonuclease/exonuclease/phosphatase family domain containing 1 |
HSPC107 |
|
|
315
|
|
|
EGF like domain multiple 8 |
C6orf8, NG3 |
|
|
316
|
|
|
Elongation factor for RNA polymerase II |
C19orf17, ELL1, MEN, PPP1R68 |
|
|
317
|
|
|
- |
- |
|
|
318
|
|
|
Ess-2 spliceosome associated protein |
DGCR13, DGCR14, DGS-H, DGS-I, DGSH, DGSI, ES2, ESS-2, Es2el, bis1 |
Blepharophimosis, Conotruncal anomaly face syndrome, Digeorge syndrome, Dwarfism, Mental retardation, Microcephaly, Mood swings, Paranoia, Pierre-robin syndrome, Posterior embryotoxon, Pulmonary dysgenesis, Schizophrenia, Shprintzen syndrome, Specific learning disorder, Velopharyngeal insufficiency, Ventricular septal defectView all (1 more) |
|
319
|
|
|
Eosinophil peroxidase |
EPO, EPP, EPX-PEN, EPXD |
|
|
320
|
|
|
Eomesodermin |
TBR2 |
Agenesis of corpus callosum, Anxiety disorder, Autoimmune nervous system disorder, Urinary bladder cancer, Bladder neoplasm, Breast cancer, Cerebellar hypoplasia, Colonic neoplasms, Congenital microcephaly, Digestive system neuroendocrine neoplasm, Immune disorders, nervous system, Microcephaly-polymicrogyria-corpus callosum agenesis syndrome, Polymicrogyria |
