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"
511 to 520 of 679 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

511
Nuclear receptor subfamily 2 group E member 3
ESCS, PNR, RNR, RP37, rd7
Retinitis pigmentosa, Cone-rod dystrophy, Goldmann-favre syndrome, Gout, Leber congenital amaurosis, Optic atrophy

512
Nuclear receptor subfamily 2 group F member 1
BBOAS, BBSOAS, COUP-TFI, COUPTF1, EAR-3, EAR3, ERBAL3, SVP44, TCFCOUP1, TFCOUP1
Autism, Bosch-boonstra-schaaf optic atrophy syndrome, Breast neoplasms, Optic atrophy, Ovarian cysts, Retinitis pigmentosa

513
Nuclear receptor subfamily 2 group F member 2
ARP-1, ARP1, CHTD4, COUPTF2, COUPTFB, COUPTFII, NF-E3, SRXX5, SVP40, TFCOUP2
46,xx sex reversal, Atrioventricular septal defect, Congenital heart disease, Endometriosis, Female infertility, Neurodevelopmental disorder, Tetralogy of fallot

514
Nuclear receptor subfamily 2 group F member 6
EAR-2, EAR2, ERBAL2
Breast neoplasms, Endometriosis, Hypogonadism, Breast cancer, Triple negative breast cancer

515
Nuclear receptor subfamily 3 group C member 1
GCCR, GCR, GCRST, GR, GRL
Anorexia nervosa, Asthma, Atrial fibrillation, Atrial flutter, Bipolar disorder, Breast cancer, Ischemic heart disease, Obstructive airway disease, Coronary artery disease, Cushing syndrome, Galactokinase deficiency, Bipolar depression, Major depressive disorder, Endometriosis, Glucocorticoid receptor deficiency/resistance
View all (18 more)

516
Nuclear receptor subfamily 3 group C member 2
MCR, MLR, MR, NR3C2VIT
Alzheimer disease, Atrial fibrillation, Autism, Pseudohypoaldosteronism, Dilated cardiomyopathy, Cervical cancer, Congestive heart failure, Major depressive disorder, Endometriosis, Heart failure, Hypertension, Early-onset hypertension with severe exacerbation in pregnancy, Insomnia, Keratoconus, Myocardial infarction
View all (5 more)

517
Nuclear receptor subfamily 4 group A member 1
GFRP1, HMR, N10, NAK-1, NGFIB, NP10, NUR77, TR3
Major depressive disorder, Endometriosis, Essential tremor, Diabetes mellitus type 2, Kidney disease, Myocardial ischemia, Oligodendroglioma, Pancreatic neoplasms, Proteinuria

518
Nuclear receptor subfamily 4 group A member 2
HZF-3, IDLDP, NOT, NURR1, RNR1, TINUR
Juvenile arthritis, Psoriatic arthritis, Autism, Dopa-responsive dystonia, Bipolar disorder, Colorectal neoplasms, Neurodevelopmental disorder, Dermatologic disorder, Developmental delay with language impairment and movement disorder, Developmental disability, Epilepsy, Intellectual developmental disorder language neurodegenerative, Juvenile idiopathic arthritis, Major depressive disorder, Non-specific syndromic intellectual disability
View all (6 more)

519
Nuclear receptor subfamily 4 group A member 3
CHN, CSMF, MINOR, NOR1
Juvenile arthritis, Rheumatoid arthritis, Chondrosarcoma, Extraskeletal myxoid chondrosarcoma, Hypercholesterolemia, Diabetes mellitus type 2, Juvenile idiopathic arthritis, Lung cancer, Oligoarticular juvenile idiopathic arthritis, Squamous cell carcinoma, Systemic lupus erythematosus, Diabetes mellitus type 1

520
Nuclear receptor subfamily 5 group A member 1
AD4BP, ELP, FTZ1, FTZF1, POF7, SF-1, SF1, SPGF8, SRXX4, SRXY3, hSF-1
46,xy gonadal dysgenesis, 46,xx ovotesticular disorder of sex development, 46,xx sex reversal, 46,xy partial gonadal dysgenesis, 46,xy sex reversal, 46, xy disorder of sex development, Endometriosis, Gonadal dysgenesis, Male infertility, Male infertility single gene azoospermia, Premature ovarian failure, Ovarian neoplasms, Spermatogenic failure, Swyer syndrome, Testicular azoospermia