|
461
|
|
|
Nectin cell adhesion molecule 4 |
EDSS1, LNIR, PRR4, PVRL4, nectin-4 |
|
|
462
|
|
|
NUAK family kinase 2 |
ANPH2, SNARK |
|
|
463
|
|
|
Neuropilin and tolloid like 2 |
BTCL2, NEOT2 |
|
|
464
|
|
|
Nuclear receptor coactivator 3 |
ACTR, AIB-1, AIB1, CAGH16, CTG26, KAT13B, RAC3, SRC-3, SRC3, TNRC14, TNRC16, TRAM-1, bHLHe42, pCIP |
Adenocarcinoma, Anaplastic astrocytoma, Astrocytoma, Bone neoplasms, Breast cancer, Mammary neoplasms, Breast carcinoma, Carcinoma, Fibrillary astrocytoma, Gemistocytic astrocytoma, Grade i astrocytoma, Intracranial astrocytoma, Leukemia, Lung carcinoma, Malignant bone neoplasm, Marfan syndrome, Oligoastrocytoma, Prostatic neoplasms, Prostate cancer, Protoplasmic astrocytomaView all (5 more) |
|
465
|
|
|
Nuclear receptor interacting protein 1 |
CAKUT3, RIP140 |
Breast cancer, Mammary neoplasms, Breast carcinoma, Congenital anomalies of kidney and urinary tract, Congestive heart failure, Ectopic kidney, Endometrial neoplasms, Endometrial carcinoma, Heart failure, Hydronephrosis, Marfan syndrome, Myocardial infarction, Renal cyst, Schizophrenia, Vesicoureteral reflux |
|
466
|
|
|
N-alpha-acetyltransferase 10, NatA catalytic subunit |
ARD1, ARD1A, ARD1P, DXS707, LZMS, MAA, MCOPS1, NATD, OGDNS, TE2, hARD1 |
Acquired kyphoscoliosis, Atrial septal defect, Autism, Bicuspid aortic valve, Camptodactyly of fingers, Capillary malformation, Cataract, Cerebral atrophy, Ciliary body coloboma, Clinodactyly, Coloboma of optic disc, Congenital ankyloblepharon, Congenital camptodactyly, Congenital coloboma of iris, Congenital epicanthus, Short clavicles, Congenital kyphoscoliosis, Congenital pectus excavatum, Cryptorchidism, Cutis laxa, Developmental delay, Dwarfism, Frontal bossing, Fundus coloboma, Glaucoma, High palate, Hirschsprung disease, Hydronephrosis, Hypospadias, Imperforate anus, Spastic diplegia, Lung adenocarcinoma, Macrotia, Mental retardation, Microcephaly, Microcornea, Microphthalmia, Syndromic microphthalmia, Microphthalmos, Motor delay, Neck webbing, Nystagmus, Ogden syndrome, Oral cleft, Otitis media, Proptosis, Ptosis, Rectal prolapse, Renal hypoplasia, Retinal coloboma, Scoliosis, Speech disorders, Stereotyped behavior, Supraventricular tachycardia, Syndactyly, Syndactyly of fingers, Torsades de pointes, Ventricular septal defect, Ventricular tachycardiaView all (44 more) |
|
467
|
|
|
NUF2 component of NDC80 kinetochore complex |
CDCA1, CT106, NUF2R |
|
|
468
|
|
|
NACA family member 4, pseudogene |
FKSG17, NACAP1 |
|
|
469
|
|
|
Neurocalcin delta |
- |
|
|
470
|
|
|
NLR family CARD domain containing 5 |
CLR16.1, NOD27, NOD4 |
|
