|
201
|
|
|
Extended synaptotagmin 1 |
FAM62A, MBC2 |
|
|
202
|
|
|
Exosome component 2 |
RRP4, Rrp4p, SHRF, hRrp4p, p7 |
Alopecia, Brachydactyly, Cerebellar atrophy, Corneal dystrophy, Dwarfism, Hearing loss, Hypothyroidism, Liver neoplasms, Liver cancer, Mental retardation, Motor delay, Myopia, Posteriorly rotated ear, Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome, Rod-cone dystrophy, Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome(shrf)View all (1 more) |
|
203
|
|
|
ETHE1 persulfide dioxygenase |
HSCO, YF13H12 |
|
|
204
|
|
|
Enhancer of mRNA decapping 4 |
GE1, Ge-1, HEDL5, HEDLS, RCD-8, RCD8 |
|
|
205
|
|
|
EP300 interacting inhibitor of differentiation 1 |
C15orf3, CRI1, EID-1, IRO45620, PNAS-22, PTD014, RBP21 |
|
|
206
|
|
|
EMAP like 2 |
ELP70, EMAP-2, EMAP2 |
|
|
207
|
|
|
EBF transcription factor 3 |
COE3, EBF-3, HADDS, O/E-2, OE-2 |
Allanson pantzar mcleod syndrome, Apraxia, Astigmatism, Autism, Camptodactyly of fingers, Congenital epicanthus, Cryptorchidism, Developmental delay, Developmental regression, Dolichocephaly, Dysarthria, Dysmorphic features, Dysphagia, Esotropia, Exotropia, Gastroesophageal reflux disease, Hypodontia, Hypotonia, ataxia, and delayed development syndrome, Mental retardation, Micropenis, Mobius syndrome, Movement disorders, Hypotonia, Neurodevelopmental disorders, Neurogenic urinary bladder, Obsolete prominent epicanthal folds, Penis agenesis, Pierre-robin syndrome, Posteriorly rotated ear, Stereotyped behavior, Strabismus, Synophrys, Vesicoureteral refluxView all (18 more) |
|
208
|
|
|
EH domain binding protein 1 like 1 |
- |
|
|
209
|
|
|
ELMO domain containing 2 |
9830169G11Rik |
|
|
210
|
|
|
ELKS/RAB6-interacting/CAST family member 2 |
CAST, CAST1, ELKSL, SPBC110, Spc110 |
|
