|
431
|
|
|
Nuclear receptor subfamily 2 group C member 2 |
TAK1, TR4 |
|
|
432
|
|
|
NUT family member 2A |
FAM22A |
|
|
433
|
|
|
NALCN channel auxiliary factor 1 |
FAM155A, NLF-1, NLF1 |
|
|
434
|
|
|
Neuroblastoma associated transcript 1 |
CASC14, NBAT-1 |
|
|
435
|
|
|
NUT family member 2B |
FAM22B, bA119F19.1 |
|
|
436
|
|
|
Nuclear receptor subfamily 1 group H member 2 |
LXR-b, LXRB, NER, NER-I, RIP15, UNR |
|
|
437
|
|
|
Nuclear receptor binding SET domain protein 2 |
KMT3F, KMT3G, MMSET, RAUST, REIIBP, TRX5, WHS, WHSC1 |
Absence of septum pellucidum, Agenesis of corpus callosum, Aplasia cutis congenita, Arachnodactyly, Atrial septal defect, Axenfeld anomaly, Breast cancer, Mammary neoplasms, Breast carcinoma, Congenital anomaly of eye, Congenital clubfoot, Congenital coloboma of iris, Congenital diaphragmatic hernia, Congenital epicanthus, Rib fusion, Congenital keratoglobus, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Frontal bossing, Congenital gallbladder anomaly, Gastroesophageal reflux disease, Hemangioma, Hypodontia, Hypoplasia of thumb, Hypospadias, Immunologic deficiency syndromes, Mental retardation, Lymphoblastic leukemia, Marfan syndrome, Microcephaly, Micrognathism, Microtia, Movement disorders, Multicystic renal dysplasia, Nystagmus, Optic atrophy, Osteoporosis, Otitis media, Pitt-rogers-danks syndrome, Polydactyly, Precocious puberty, Primary tethered cord syndrome, Proptosis, Ptosis, Radioulnar synostosis, Retinal diseases, Rieger syndrome, Sclerocornea, Scoliosis, Situs inversus, Stenosis of external auditory canal, Stereotyped behavior, Strabismus, Ventricular septal defect, Wolf-hirschhorn syndromeView all (42 more) |
|
438
|
|
|
Negative elongation factor complex member A |
NELF-A, P/OKcl.15, WHSC2 |
Agenesis of corpus callosum, Aplasia cutis congenita, Arachnodactyly, Atrial septal defect, Breast carcinoma, Congenital clubfoot, Congenital coloboma of iris, Congenital diaphragmatic hernia, Congenital epicanthus, Rib fusion, Congenital keratoglobus, Cryptorchidism, Developmental delay, Dolichocephaly, Frontal bossing, Congenital gallbladder anomaly, Hemangioma, Hypodontia, Hypoplasia of thumb, Hypospadias, Mental retardation, Microcephaly, Micrognathism, Microtia, Movement disorders, Multicystic renal dysplasia, Nystagmus, Optic atrophy, Osteoporosis, Otitis media, Polydactyly, Primary tethered cord syndrome, Proptosis, Ptosis, Retinal diseases, Sclerocornea, Scoliosis, Situs inversus, Strabismus, Wolf-hirschhorn syndromeView all (25 more) |
|
439
|
|
|
NPHS2 stomatin family member, podocin |
PDCN, SRN1 |
Alport syndrome, x-linked, Alport syndrome, Genetic steroid-resistant nephrotic syndrome, Glomerular hyalinosis, Glomerulosclerosis, Hematuria, Hyperlipidemia, Hypertensive nephropathy, Hypoalbuminemia, Kidney disease, Nephritis, Nephrosis, Nephrotic syndrome, Renal glomerular disease |
|
440
|
|
|
Nucleoporin 37 |
MCPH24, p37 |
|
