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"
641 to 650 of 679 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

641
Nucleoporin 214
CAIN, CAN, IIAE9
Brain disease, Congenital facial anomaly, Developmental delay, Developmental disability, Lymphoblastic leukemia, Myeloid leukemia

642
Nucleoporin 35
MP-44, MP44, NP44, NUP53
Scoliosis

643
Nucleoporin 37
MCPH24, p37
Primary microcephaly, Idiopathic steroid-resistant nephrotic syndrome, Genetic steroid-resistant nephrotic syndrome, Hereditary steroid-resistant nephrotic syndrome, Microcephaly

644
Nucleoporin 42
CG1, NLP-1, NLP1, NLP_1, NUPL2, UIP1, hCG1
Obstructive pulmonary disease

645
Nucleoporin 50
NPAP60, NPAP60L
Amyotrophic lateral sclerosis, Schizophrenia

646
Nucleoporin 54
DYT37
Dystonia, Metabolic syndrome, Diabetes mellitus type 2

647
Nucleoporin 62
IBSN, SNDI, p62
Biliary cirrhosis, Hearing loss, Leigh syndrome, Biliary cholangitis

648
Nucleoporin 62 C-terminal like
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Pancreatitis

649
Nucleoporin 85
FROUNT, NPHS17, Nup75
Alzheimer disease, Idiopathic steroid-resistant nephrotic syndrome, Genetic steroid-resistant nephrotic syndrome, Tourette syndrome, Hereditary steroid-resistant nephrotic syndrome, Nephrotic syndrome, Peripheral arterial disease, Seckel syndrome, Systemic sclerosis, Diabetes mellitus type 2

650
Nucleoporin 88
FADS4
Fetal akinesia deformation sequence, Metabolic syndrome, Pena-shokeir syndrome , Rheumatoid arthritis, Diabetes mellitus type 2