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"
221 to 230 of 679 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

221
NIMA related kinase 10
CILD44
Asthma, Breast cancer, Cancer, Cannabis abuse, Cardiovascular disease, Cataract, Ciliary dyskinesia, Colorectal cancer, Dementia, Estrogen-receptor negative breast cancer, Hoarding disorder, Hypertrophic cardiomyopathy, Alzheimer disease, Lung cancer, Ovarian epithelial cancer
View all (9 more)

222
NIMA related kinase 11
-
Atherosclerosis, Insomnia

223
NIMA related kinase 2
HsPK21, NEK2A, NLK1, PPP1R111, RP67
Hepatocellular carcinoma, Non-small-cell lung carcinoma, Retinitis pigmentosa

224
NIMA related kinase 4
NRK2, STK2, pp12301
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Kidney disease, Ciliopathy, Kidney failure, Osteoarthritis

225
NIMA related kinase 5
-
Crohn disease, Inflammatory bowel disease, Ulcerative colitis

226
NIMA related kinase 6
SID6-1512
Androgenetic alopecia, Asthma, Atrial fibrillation, Autoimmune disease, Pharyngeal disorder, Hypothyroidism, Major depressive disorder, Nasal disorder, Polycystic ovary syndrome, Prostate cancer, Rhinitis, Scoliosis, Thyroid disease, Upper respiratory tract disorder, Vitiligo

227
NIMA related kinase 7
-
Alzheimer disease, Central nervous system cancer, Dementia, Glioblastoma, Glioma, Insomnia, Major depressive disorder, Optic atrophy, Diabetes mellitus type 2

228
NIMA related kinase 8
JCK, NEK12A, NPHP9, PKD8, RHPD2
Polycystic kidney disease, Kidney disease, Nephronophthisis

229
NIMA related kinase 9
APUG, LCCS10, NC, NERCC, NERCC1
Arthrogryposis with perthes disease and gaze palsy, Congenital deformity of clavicle, Congenital deformity of elbow, Congenital deformity of forearm, Congenital deformity of scapula, Congenital deformity of wrist, Congenital dislocation of elbow, Congenital glenohumeral joint dislocation, Congenital joint contractures, Congenital omphalocele, Coronary artery disease, Desbuquois syndrome, Lethal congenital contracture syndrome

230
Negative elongation factor complex member A
NELF-A, P/OKcl.15, WHSC2
Alzheimer disease, Breast cancer, Wolf-hirschhorn syndrome