|
501
|
|
|
NFS1 cysteine desulfurase |
COXPD52, HUSSY-08, IscS, NIFS |
|
|
502
|
|
|
Nuclear export mediator factor |
IDDSAPN, NY-CO-1, RQC2, SDCCAG1 |
|
|
503
|
|
|
Neuralized E3 ubiquitin protein ligase 1 |
NEUR1, NEURL, RNF67, bA416N2.1, neu, neu-1 |
|
|
504
|
|
|
Nexilin F-actin binding protein |
CDM2M, CMH20, NELIN |
|
|
505
|
|
|
NLR family pyrin domain containing 12 |
CLR19.3, FCAS2, NALP12, PAN6, PYPAF7, RNO, RNO2 |
|
|
506
|
|
|
NIMA related kinase 9 |
APUG, LCCS10, NC, NERCC, NERCC1 |
Arthrogryposis multiplex congenita, Arthrogryposis, perthes disease, and upward gaze palsy, Asthma, Atrial septal defect, Cataract, Comedone, Congenital camptodactyly, Congenital clubfoot, Pulmonary hypoplasia, Congenital hypoplasia of thymus, Congenital omphalocele, Coronary artery disease, Dermatitis, Hamartoma, High palate, Hydrops fetalis, Ichthyosis, Lethal congenital contracture syndrome, Microcephaly, Micrognathism, Nevus comedonicus, Overriding aorta, Pena shokeir syndrome, Phakomatosis pigmentovascularis, Pulmonary stenosis, Radial polydactyly, Scoliosis, Skeletal dysplasia, Spina bifida occulta, Syndactyly of fingers, Syndactyly of the toes, Ventricular septal defectView all (17 more) |
|
507
|
|
|
NADH:ubiquinone oxidoreductase complex assembly factor 2 |
B17.2L, MC1DN10, MMTN, NDUFA12L, mimitin |
Anemia, Central nervous system inborn metabolic diseases, Cerebellar ataxia, Developmental delay, Diabetes mellitus, Dysarthria, Dysphagia, Epileptic encephalopathy, Hearing loss, Hypertrichosis, Hypertrophic cardiomyopathy, Hypoglycemia, Mental retardation, Isolated complex i deficiency, Leigh syndrome, Leigh syndrome with leukodystrophy, Leukodystrophy, Leukoencephalopathy, Microcephaly, Mitochondrial complex deficiency, Mitochondrial myopathy, Mood swings, Multiple congenital anomalies, Nervous system diseases, Nystagmus, Optic atrophy, Parkinson disease, Ptosis, Respiratory failure, Retinitis pigmentosa, Schizophrenia, Strabismus, Ventricular septal defectView all (18 more) |
|
508
|
|
|
Nuclear assembly factor 1 ribonucleoprotein |
PFBMFT7 |
|
|
509
|
|
|
Noggin |
SYM1, SYNS1, SYNS1A |
Cubitus valgus, Elbow ankylosis, Anonychia, Brachydactyly, Camptodactyly of fingers, Carpal synostosis, Clinodactyly, Dislocated radial head, Congenital pectus excavatum, Dwarfism, Hearing loss, Hyperopia, Hypoplasia of lower limb, Multiple synostoses syndrome, Ovarian failure, Proximal symphalangism, Stapes ankylosis with broad thumb and toes, Strabismus, Symphalangism, Symphalangism-brachydactyly syndrome, Syndactyly of fingers, Syndactyly of the toes, Tarsal coalition, Tarsal-carpal coalition syndrome, Teunissen cremers syndromeView all (10 more) |
|
510
|
|
|
NUMB like endocytic adaptor protein |
CAG3A, CTG3a, NBL, NUMB-R, NUMBLIKE, NUMBR, TNRC23 |
|
