Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "N"
141 to 150 of 682 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

141
-
-
Auditory neuropathy, Blindness, Dysarthria, Leber hereditary optic neuropathy, Leigh syndrome, Melas syndrome, Mitochondrial disease, Optic atrophy, Paresthesia, Parkinson disease, Spinal muscular atrophy

142
NDC1 transmembrane nucleoporin
NET3, TMEM48
Global developmental delay, Major depressive disorder, Mood disorder, Neurodevelopmental disorder, Polyneuropathy, Uranostaphyloschisis

143
NDC80 kinetochore complex component
HEC, HEC1, HsHec1, KNTC2, TID3, hsNDC80
Hepatocellular carcinoma

144
NudE neurodevelopment protein 1
HOM-TES-87, LIS4, MHAC, NDE, NUDE, NUDE1
Aortic aneurysm, Intestinal pseudo-obstruction, Congenital aneurysm of ascending aorta, Connective tissue disease, Thoracic aortic aneurysm and aortic dissection, Hydranencephaly, Intellectual developmental disorder, Left ventricular disease, Lissencephaly, Macrogyria, Megacystis microcolon intestinal hypoperistalsis syndrome, Microcephaly, Microhydranencephaly, Microlissencephaly, Myopia
View all (7 more)

145
NudE neurodevelopment protein 1 like 1
EOPA, MITAP1, NDE1L1, NDE2, NUDEL
Juvenile arthritis, Color vision deficiency, Juvenile idiopathic arthritis, Non-organic psychosis, Oligoarticular juvenile idiopathic arthritis, Psoriasis, Psychotic disorders, Schizophrenia

146
Nedd4 family interacting protein 1
N4WBP5
Ankylosing spondylitis, Asthma, Eczema, Biliary cirrhosis, Breast cancer, Cancer, Corneal astigmatism, Crohn disease, Dementia, Inflammatory bowel disease, Multiple sclerosis, Biliary cholangitis, Psoriasis, Respiratory system disease, Sclerosing cholangitis
View all (4 more)

147
Nedd4 family interacting protein 2
N4WBP5A
Major depressive disorder

148
Necdin, MAGE family member
HsT16328, PWCR
Carcinoma, Oligodendroglioma, Prader-willi syndrome, Psychiatric disorders

149
Neuron derived neurotrophic factor
C4orf31, HH25, NORD
Endometriosis, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Migraine, Obesity, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Sheehan syndrome

150
Norrin cystine knot growth factor NDP
EVR2, FEVR, ND
Atrophia bulborum heritaria, Coats disease, Exudative retinopathy, Exudative vitreoretinopathy, Hearing impairment, Hyperplasia, Nystagmus, Primary aldosteronism, Retinal detachment, Retinitis pigmentosa, Retinopathy of prematurity, Schizophrenia, Myopia