|
401
|
|
|
Non-SMC condensin I complex subunit G |
CAPG, CHCG, NY-MEL-3, YCG1 |
|
|
402
|
|
|
NOC3 like DNA replication regulator |
AD24, C10orf117, FAD24 |
|
|
403
|
|
|
Nuclear receptor binding SET domain protein 1 |
ARA267, KMT3B, SOTOS, SOTOS1, STO |
5q35 microduplication syndrome, Accessory kidney, Adenocarcinoma, Atrial septal defect, Autism, Beckwith-wiedemann syndrome, Congenital clubfoot, Developmental dysplasia of the hip, Congenital hypoplasia of penis, Congenital pectus carinatum, Craniosynostosis, Cryptorchidism, Deletion 5q36, Developmental delay, Dolichocephaly, Dwarfism, Dysmorphic features, Frontal bossing, Hearing loss, Heart septal defects, High palate, Hyperinsulinemic hypoglycemia, Hyperopia, Hypoglycemia, Hypoplasia of corpus callosum, Hypospadias, Impaired cognition, Mental retardation, Leukemia, Lung diseases, Macrocephaly, Macrotia, Malocclusion, Microcephaly, Micrognathism, Monosomy 5q35, Multiple congenital anomalies, Multiple renal cysts, Myeloid leukemia, Myopia, Hypotonia, Nervous system neoplasms, Nephroblastoma, Nystagmus, Obesity, Osteopenia, Otitis media, Partial agenesis of corpus callosum, Patent ductus arteriosus, Patent foramen ovale, Precocious puberty, Sacrococcygeal teratoma, Scoliosis, Sotos` syndrome, Specific learning disorder, Strabismus, Syndactyly of fingers, Talipes transversoplanus, Talipes valgus, Uranostaphyloschisis, Ventricular septal defect, Vesicoureteral reflux, Weaver syndromeView all (48 more) |
|
404
|
|
|
NFKB inhibitor zeta |
I-kappa-B-zeta, IKBZ, INAP, IkappaB-zeta, MAIL, ikB-zeta, ikappaBzeta |
|
|
405
|
|
|
Nucleoredoxin |
NRX, RRS2, TRG-4 |
Abnormal spinal segmentation, Alopecia, Ankyloglossia, Atrial septal defect, Bicuspid aortic valve, Brachydactyly, Camptodactyly of fingers, Clinodactyly, Colonic neoplasms, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Absent uvula, Congenital camptodactyly, Congenital epicanthus, Congenital exomphalos, Rib fusion, Congenital hypoplasia of penis, Congenital omphalocele, Congenital pectus carinatum, Congenital pectus excavatum, Cryptorchidism, Developmental delay, Dwarfism, Ectopic anus, Fingernail dysplasia, Frontal bossing, Hydronephrosis, Hypodontia, Macrocephaly, Macrostomia, Mental retardation, Mesomelia, Micrognathism, Multicystic renal dysplasia, Oral cleft, Otitis media, Phakomatosis pigmentovascularis, Posteriorly rotated ear, Proptosis, Ptosis, Robinow syndrome, Scoliosis, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Tetralogy of fallot, Ventricular septal defectView all (33 more) |
|
406
|
|
|
NR2F2 antisense RNA 1 |
- |
|
|
407
|
|
|
Nucleolar protein with MIF4G domain 1 |
C7orf3, PPP1R113, SGD1 |
|
|
408
|
|
|
Nitric oxide synthase 2 pseudogene 1 |
NOS2C |
|
|
409
|
|
|
N-deacetylase and N-sulfotransferase 4 |
N-HSST, N-HSST 4, NDST-4, NHSST4 |
|
|
410
|
|
|
Nuclear casein kinase and cyclin dependent kinase substrate 1 |
JC7, NUCKS |
|
