|
341
|
|
|
Exoribonuclease 1 |
3'HEXO, HEXO, HXAL, SEMDGC, SEMDGS, THEX1 |
|
|
342
|
|
|
Endothelial cell adhesion molecule |
NEDIHSS, W117m |
|
|
343
|
|
|
Exonuclease 1 |
HEX1, hExoI |
|
|
344
|
|
|
Exocyst complex component 3 like 4 |
C14orf73 |
|
|
345
|
|
|
Elongation factor Tu GTP binding domain containing 2 |
MFDGA, MFDM, SNRNP116, Snrp116, Snu114, U5-116KD |
Atrial septal defect, Choanal atresia, Congenital epicanthus, Developmental delay, Dwarfism, Dysmorphic features, Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate, Hearing loss, Hypoplasia of the maxilla, Mandibulofacial dysostosis, Mandibulofacial dysostosis-microcephaly syndrome, Mental retardation, Microcephaly, Micrognathism, Microtia, Multiple congenital anomalies, Polydactyly, Trigonocephaly, Ventricular septal defectView all (4 more) |
|
346
|
|
|
EGF like and EMI domain containing 1, pseudogene |
C3orf50, NCRNA00259 |
|
|
347
|
|
|
Endothelin converting enzyme like 1 |
DA5D, DINE, ECEX, XCE |
Arthrogryposis multiplex congenita, Astigmatism, Brachydactyly, Congenital camptodactyly, Distal arthrogryposis, Dwarfism, Dysmorphic features, Elbow flexion contracture, High palate, Micrognathism, Multiple congenital anomalies, Ptosis, Scoliosis |
|
348
|
|
|
Eukaryotic translation initiation factor 2 alpha kinase 3 |
PEK, PERK, WRS |
Brachydactyly, Congenital epicanthus, Congenital heart defects, Pancreatic hypoplasia, Developmental delay, Diabetes mellitus, Dwarfism, Epiphyseal dysplasia, Exocrine pancreatic insufficiency, Grand mal status epilepticus, High palate, Hyperglycemia, Hyperopia, Hyperuricemia, Hypoglycemia, Hypothyroidism, Insulin-resistant diabetes mellitus, Ketosis, Kidney disease, Liver failure, Malformation of cortical development, Mental retardation, Microcephaly, Microdontia, Motor delay, Multiple epiphyseal dysplasia, Myocardial ischemia, Neutropenia, Nonconvulsive status epilepticus, Osteopenia, Osteoporosis, Petit mal status, Progressive supranuclear ophthalmoplegia, Progressive supranuclear palsy, Renal insufficiency, Renal tubular disorder, Status epilepticus, Supranuclear palsy, Wolcott-rallison syndromeView all (24 more) |
|
349
|
|
|
Eukaryotic translation initiation factor 4E family member 2 |
4E-LP, 4EHP, EIF4EL3, IF4e, h4EHP |
|
|
350
|
|
|
Ectonucleoside triphosphate diphosphohydrolase 1 |
ATP-DPH, ATPDase, CD39, NTPDase-1, SPG64 |
|
