|
511
|
|
|
Neuralized E3 ubiquitin protein ligase 3 |
LINCR, RNF132 |
|
|
512
|
|
|
Neuronal regeneration related protein |
C5orf13, D4S114, P311, PRO1873, PTZ17, SEZ17 |
|
|
513
|
|
|
N-deacetylase and N-sulfotransferase 3 |
HSST3 |
|
|
514
|
|
|
Neurexin 3 |
C14orf60 |
|
|
515
|
|
|
Neurexin 1 |
Hs.22998, PTHSL2, SCZD17 |
Amyotrophic lateral sclerosis, Auditory processing disorder, Autism, Autism spectrum disorder, Bipolar disorder, Brachycephaly, Celiac disease, Cerebral cortical atrophy, Chromosome 2p16.3 deletion syndrome, Cryptorchidism, Developmental regression, Diabetes mellitus, Dysphagia, Epileptic encephalopathy, Frontal bossing, Gastroesophageal reflux disease, Gluten intolerance, Mental retardation, Language development disorders, Macrostomia, Malocclusion, Mental depression, Multiple congenital anomalies, Narcolepsy, Obesity, Pitt-hopkins syndrome, Pitt-hopkins-like syndrome, Plagiocephaly, Precocious puberty, Pulmonary stenosis, Schizophrenia, Scoliosis, Social communication disorder, Speech delay, Stereotyped behavior, Strabismus, Tricuspid valve insufficiency, Ventricular septal defectView all (23 more) |
|
516
|
|
|
Neurexin 2 |
- |
|
|
517
|
|
|
N-myristoyltransferase 2 |
- |
|
|
518
|
|
|
Netrin 1 |
MRMV4, NET1, NTN1L |
Agenesis of corpus callosum, Cerebral palsy, Congenital mirror movements, Dysgenesis of the hippocampus, Hypogonadotropic hypogonadism, Mental retardation, Mirror movements, Oral cleft, Rheumatoid arthritis, Specific learning disorder, Subarachnoid hemorrhage |
|
519
|
|
|
Natural cytotoxicity triggering receptor 1 |
CD335, LY94, NK-p46, NKP46 |
|
|
520
|
|
|
Aminopeptidase puromycin sensitive |
AAP-S, MP100, PSA |
|
