Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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8381 to 8390 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8381
NALCN channel auxiliary factor 1
FAM155A, NLF-1, NLF1
Alzheimer disease, Anorexia nervosa, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Breast cancer, Central nervous system cancer, Colorectal cancer, Conduct disorder, Dementia, Diverticular disease, Diverticulitis, Eating disorder, Glioblastoma
View all (16 more)

8382
NALCN channel auxiliary factor 2
CXorf63, FAM155B, TED, TMEM28, bB57D9.1
Gestational diabetes, Tooth agenesis

8383
Nicotinamide phosphoribosyltransferase
1110035O14Rik, PBEF, PBEF1, VF, VISFATIN
Colitis, Colorectal neoplasms, Allergic contact dermatitis, Mouth neoplasms, Obesity, Squamous cell carcinoma, Transient ischemic attack

8384
Nanog homeobox retrogene P8
NANOGP1, PN8
Bronchopulmonary dysplasia, Keratoconus

8385
Nanos C2HC-type zinc finger 1
EC_Rep1a, NOS-1, NOS1, SPGF12, ZC2HC12A
Male infertility single gene azoospermia, Mesothelioma, Spermatogenic failure

8386
Nanos C2HC-type zinc finger 2
NOS2, ZC2HC12B
Alzheimer disease, Male infertility, Neurotic disorder, Diabetes mellitus type 2

8387
Nanos C2HC-type zinc finger 3
NANOS1L, NOS3, ZC2HC12C
Breast cancer

8388
N-acetylneuraminate synthase
HEL-S-100, SAS, SEMDCG, SEMDG
Bone disease, Desbuquois syndrome, Developmental disability, Spondyloepimetaphyseal dysplasia

8389
Nucleosome assembly protein 1 like 1
NAP1, NAP1L, NRP
Obesity

8390
Nucleosome assembly protein 1 like 2
BPX
Cortical development malformation