Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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8971 to 8980 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8971
Nuclear FMR1 interacting protein 2
182-FIP, 82-FIP, FIP-82, NUFP2, PIG1
Attention deficit hyperactivity disorder, Breast cancer, Gout, Migraine, Prostate cancer, Schizophrenia, Scoliosis, Substance abuse, Diabetes mellitus type 2

8972
Nuclear GTPase, germinal center associated
C8orf80, HMFN0672, SLIP-GC, SLIPGC
Color vision deficiency, Venous thromboembolism

8973
Nuclear mitotic apparatus protein 1
NMP-22, NUMA
Alzheimer disease, Deafness, Allergic contact dermatitis, Diabetic ketoacidosis, Diabetes mellitus type 1

8974
NUMB endocytic adaptor protein
C14orf41, S171, c14_5527
Bipolar disorder, Hypertension, Kidney cancer, Scoliosis

8975
NUMB like endocytic adaptor protein
CAG3A, CTG3a, NBL, NUMB-R, NUMBLIKE, NUMBR, TNRC23
Angioedema, Gestational diabetes, Lung cancer, Schizophrenia, Squamous cell carcinoma

8976
Nucleoporin 107
GAMOS7, NPHS11, NUP84, ODG6, ODG6; GAMOS7
46,xy gonadal dysgenesis, Benign prostatic hyperplasia, Idiopathic steroid-resistant nephrotic syndrome, Focal segmental glomerulosclerosis, Galloway-mowat syndrome, Genetic steroid-resistant nephrotic syndrome, Global developmental delay, Gonadal dysgenesis, Hereditary steroid-resistant nephrotic syndrome, Nephrotic syndrome, Ovarian dysgenesis

8977
Nucleoporin 133
GAMOS8, NPHS18, hNUP133
Diabetes mellitus, Idiopathic steroid-resistant nephrotic syndrome, Galloway-mowat syndrome, Genetic steroid-resistant nephrotic syndrome, Hereditary steroid-resistant nephrotic syndrome, Nephrotic syndrome, Post-traumatic stress disorder, Diabetes mellitus type 2

8978
Nucleoporin 153
HNUP153, N153
Cholecystolithiasis, Congenital pulmonary artery atresia, Gallstones, Ovarian epithelial cancer, Obesity, Ovarian cancer

8979
Nucleoporin 155
ATFB15, N155
Alzheimer disease, Atrial fibrillation, Hereditary atrial fibrillation

8980
Nucleoporin 160
NPHS19
Alzheimer disease, Coronary artery disease, Idiopathic steroid-resistant nephrotic syndrome, Genetic steroid-resistant nephrotic syndrome, Hereditary steroid-resistant nephrotic syndrome, Hypertension, Insomnia, Major depressive disorder, Mood disorder, Myocardial infarction, Nephrotic syndrome, Neurotic disorder, Obesity, Osteoarthritis, Osteopetrosis
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