|
161
|
|
|
NOP53 ribosome biogenesis factor |
GLTSCR2, PICT-1, PICT1 |
|
|
162
|
|
|
Neurexophilin 1 |
NPH1, Nbla00697 |
|
|
163
|
|
|
5', 3'-nucleotidase, cytosolic |
DNT, DNT1, HEL74, P5N2, PN-I, PN-II, UMPH2, cdN, dNT-1 |
|
|
164
|
|
|
Neuregulin 1 |
ARIA, GGF, GGF2, HGL, HRG, HRG1, HRGA, MST131, MSTP131, NDF, NRG1-IT2, SMDF |
Arthritis, Asthma, Bipolar disorder, Breast cancer, Mammary neoplasms, Breast carcinoma, Chronic obstructive pulmonary disease, Colonic aganglionosis, Congenital intestinal aganglionosis, Congestive heart failure, Dermatitis, Gastric ulcer, Heart failure, Hirschsprung disease, Hypothyroidism, Juvenile arthritis, Lung carcinoma, Lung neoplasms, Lung adenocarcinoma, Lung cancer, Marfan syndrome, Mental depression, Movement disorders, Myocardial infarction, Oral cleft, Sclerocystic ovaries, Papillary thyroid carcinoma, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Polycystic ovary syndrome, Schizophrenia, Status marmoratus, Still disease, Thyroid carcinomaView all (19 more) |
|
165
|
|
|
Nuclear receptor subfamily 4 group A member 1 |
GFRP1, HMR, N10, NAK-1, NGFIB, NP10, NUR77, TR3 |
|
|
166
|
|
|
Nudix hydrolase 2 |
APAH1, IDDPN |
|
|
167
|
|
|
N-deacetylase and N-sulfotransferase 1 |
HSST, MRT46, NST1 |
Absence of septum pellucidum, Autism, Central visual impairment, Cerebral atrophy, Cortical dysplasia, Developmental delay, Dyskinetic syndrome, Dyssomnia, Gastrointestinal stromal tumor, Hypoplasia of corpus callosum, Mental retardation, Malformation of cortical development, Mental depression, Microcephaly, Motor delay, Myocardial infarction, Non-syndromic intellectual disability, Polymicrogyria, Salaam seizures, Seizure, Sleep disorders, Stereotyped behaviorView all (7 more) |
|
168
|
|
|
NLR family pyrin domain containing 9 |
CLR19.1, NALP9, NOD6, PAN12 |
|
|
169
|
|
|
NLR family pyrin domain containing 14 |
CLR11.2, GC-LRR, NALP14, NOD5, PAN8 |
|
|
170
|
|
|
N-acetyltransferase 8 like |
CML3, NACED, NAT8-LIKE |
|
