Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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8371 to 8380 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8371
NEDD8 activating enzyme E1 subunit 1
A-116A10.1, APPBP1, HPP1, NEDFIH, ula-1
Neurodevelopmental disorder

8372
Nuclear assembly factor 1 ribonucleoprotein
PFBMFT7
Glioma, Lung cancer, Myeloproliferative disorder, Pulmonary fibrosis, Telomere-related pulmonary fibrosis and/or bone marrow failure, Schizophrenia, Squamous cell carcinoma

8373
Alpha-N-acetylgalactosaminidase
D22S674, GALB
Alpha-n-acetylgalactosaminidase deficiency, Arthrogryposis multiplex congenita, Pena-shokeir syndrome , Schindler disease

8374
N-acetylglucosamine kinase
GNK, HSA242910
Prostatic neoplasms

8375
N-acetyl-alpha-glucosaminidase
CMT2V, MPS-IIIB, MPS3B, NAG, UFHSD
Asthma, Charcot-marie-tooth disease, Desbuquois syndrome, Hypertrichosis, Intellectual developmental disorder, Mucopolysaccharidosis, Parkinson disease, Prostatic neoplasms, Sanfilippo syndrome, Schizophrenia, Intellectual disability, Spastic ataxia, Diabetes mellitus type 2

8376
N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase
APAA, UCE
Kawasaki disease, Scoliosis, Vasculitis

8377
N-acetylglutamate synthase
AGAS, ARGA
Amino acid metabolism disorder, Urea cycle disorder, Esophageal atresia, Hyperammonemia

8378
Nuclear apoptosis inducing factor 1
C9orf90, bA379C10.2
Gout

8379
NLR family apoptosis inhibitory protein
BIRC1, NLRB1, psiNAIP
Proximal spinal muscular atrophy, Spinal muscular atrophy

8380
Sodium leak channel, non-selective
CLIFAHDD, CanIon, IHPRF, IHPRF1, INNFD, VGCNL1, bA430M15.1
Arthrogryposis multiplex congenita, Distal arthrogryposis, Autism, Bipolar disorder, Congenital contracture of limbs and face, hypotonia, developmental delay syndrome, Congenital limbs-face contractures-hypotonia-developmental delay syndrome, Congenital neurologic anomalies, Developmental disability, Digitotalar dysmorphism, Eating disorder, Temporal lobe epilepsy, Global developmental delay, Intellectual developmental disorder, Major depressive disorder, Neurodevelopmental disorder
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