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"
321 to 330 of 682 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

321
NIPA like domain containing 4
ARCI6, ICHTHYIN, ICHYN, NIPA4, SLC57A6
Congenital ichthyosis, Congenital ichthyosiform erythroderma, Congenital nonbullous ichthyosiform erythroderma, Erythrokeratodermia variabilis, Lamellar ichthyosis

322
NIPBL cohesin loading factor
CDLS, CDLS1, IDN3, IDN3-B, Scc2
Bone disease, Brachydactyly, Congenital diaphragmatic hernia, Congenital heart disease, Congenital hypoplasia of lung, Cornelia de lange syndrome, Craniofacial abnormalities, Cryptorchidism, De lange syndrome, Desbuquois syndrome, Global developmental delay, Headache, Congenital heart defect, Intellectual developmental disorder, Intellectual disability
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323
Nipsnap homolog 1
-
Breast cancer, Iga nephropathy

324
Nipsnap homolog 2
GBAS
Macular telangiectasia, Diabetes mellitus type 2

325
Nipsnap homolog 3B
FP944, NIPSNAP3, SNAP1
Hypoalphalipoproteinemia, Obesity

326
Nischarin
I-1, IR1, IRAS, hIRAS
Bradycardia, Breast neoplasms, Congestive heart failure, Diverticular disease, Gout, Heart failure, Hypotension, Schizophrenia

327
Nitrilase 1
-
Brain small vessel disease

328
Nitrilase family member 2
HEL-S-8a
Alzheimer disease, Visual impairment

329
Sodium/potassium transporting ATPase interacting 1
FAM77C
Color vision deficiency, Osteoarthritis

330
Sodium/potassium transporting ATPase interacting 2
FAM77B, NKAIP2, TCBA, TCBA1
Alzheimer disease, Anemia, Atrial fibrillation, Attention deficit hyperactivity disorder, Adrenal gland neoplasms, Biliary atresia, Bipolar disorder, Celiac disease, Central nervous system cancer, Color vision deficiency, Delirium, dementia, and cognitive disorders, Essential tremor, Glioma, Hypotension, Insomnia
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