271
|
|
|
Eukaryotic translation initiation factor 2 alpha kinase 2 |
DYT33, EIF2AK1, LEUDEN, PKR, PPP1R83, PRKR |
|
272
|
|
|
Eukaryotic translation initiation factor 4E nuclear import factor 1 |
4E-T, Clast4 |
|
273
|
|
|
Endoplasmic reticulum oxidoreductase 1 beta |
ERO1LB, Ero1beta |
|
274
|
|
|
Exosome component 5 |
CABAC, RRP41B, RRP46, Rrp46p, hRrp46p, p12B |
|
275
|
|
|
EMSY transcriptional repressor, BRCA2 interacting |
C11orf30, GL002 |
Asthma, Breast cancer, Mammary neoplasms, Breast carcinoma, Dermatitis, Eczema, Eosinophilia, Marfan syndrome, Sclerocystic ovaries, Polycystic ovary syndrome, Prostate cancer, Prostate cancer, hereditary |
276
|
|
|
Endoplasmic reticulum-golgi intermediate compartment 1 |
AMC2, AMCN, ERGIC-32, ERGIC32, NET24 |
Arthrogryposis multiplex congenita, Congenital clubfoot, Congenital contracture, Congenital torticollis, Gastric ulcer, Hemiplegia/hemiparesis, Inflammatory bowel disease, Intestinal atresia, Micrognathism, Micromelia, Myocardial infarction, Myopathy, Neurogenic arthrogryposis multiplex congenita |
277
|
|
|
Endosome-lysosome associated apoptosis and autophagy regulator 1 |
EIG121, KIAA1324 |
|
278
|
|
|
Ectopic P-granules 5 autophagy tethering factor |
HEEW1, KIAA1632, VICIS |
Agenesis of corpus callosum, Albinism, Antibody deficiency syndrome, Breast cancer, Cardiomyopathy, Cataract, Cerebellar hypoplasia, Cerebral cortical atrophy, Congestive heart failure, Developmental delay, Dwarfism, Dyssomnia, Hearing loss, High palate, Hypopigmentation disorder, Immunologic deficiency syndromes, Impervious ureter, Left ventricular hypertrophy, Mental retardation, Microcephaly, Micrognathism, Motor delay, Myocardial diseases, Myopathy, Neuronal heterotopia, Nystagmus, Ocular albinism, Optic atrophy, Penile hypospadias, Schizencephaly, Sleep disorders, Vici syndromeView all (17 more) |
279
|
|
|
Epidermal growth factor receptor pathway substrate 15 like 1 |
EPS15R |
|
280
|
|
|
Ectonucleotide pyrophosphatase/phosphodiesterase family member 5 |
NPP-5, NPP5 |
|