Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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8491 to 8500 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8491
Necdin, MAGE family member
HsT16328, PWCR
Carcinoma, Oligodendroglioma, Prader-willi syndrome, Psychiatric disorders

8492
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

8493
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

8494
N-myc downstream regulated 1
CAP43, CMT4D, DRG-1, DRG1, GC4, HMSNL, NDR1, NMSL, PROXY1, RIT42, RTP, TARG1, TDD5
Astrocytoma, Breast neoplasms, Non-small-cell lung carcinoma, Pancreatic ductal carcinoma, Renal cell carcinoma, Charcot-marie-tooth disease, Dejerine-sottas disease, Glioblastoma, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Kidney neoplasms, Liver neoplasms, Melanoma, Mouth neoplasms, Hereditary motor and sensory neuropathy
View all (7 more)

8495
NDRG family member 2
SYLD
Cataract, Colonic neoplasms, Exostoses, Nonalcoholic fatty liver disease, Psoriasis, Transient ischemic attack

8496
NDRG family member 3
-
Melanoma, Non-melanoma skin carcinoma

8497
NDRG family member 4
BDM1, SMAP-8, SMAP8
Achromatopsia, Autism, Schizophrenia

8498
N-deacetylase and N-sulfotransferase 1
HSST, MRT46, NST1
Nonsyndromic intellectual disability, Cleft lip and palate, Craniofacial abnormalities, Eye abnormalities, Gastrointestinal stromal tumor, Global developmental delay, Intellectual developmental disorder, Cortical development malformation, Osteoarthritis

8499
N-deacetylase and N-sulfotransferase 2
HSST2, N-HSST 2, NST2
Myocardial infarction, Prostatic neoplasms, Schizophrenia

8500
N-deacetylase and N-sulfotransferase 3
HSST3
Bipolar disorder, Kidney disease, Keratoconus, Metabolic syndrome, Neurotic disorder, Willis-ekbom disease, Schizophrenia, Diabetes mellitus type 2