Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "N"

91 to 100 of 533 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
91	221078	NSUN6	NOP2/Sun RNA methyltransferase 6	4933414E04Rik, ARL5B-AS1, MRT82, NOPD1	Breast cancer, Mammary neoplasms, Breast carcinoma, Marfan syndrome, Schizophrenia
92	221294	NT5DC1	5'-nucleotidase domain containing 1	C6orf200, LP2642, NT5C2L1	Age-related macular degeneration, Melanoma, Metaphyseal chondrodysplasia, Myopia, Narcolepsy
93	222698	NKAPL	NFKB activating protein like	C6orf194, bA424I5.1	Rheumatoid arthritis, Schizophrenia
94	22795	NID2	Nidogen 2	NID-2	Breast cancer, Goldenhar syndrome
95	22854	NTNG1	Netrin G1	Lmnt1, NetG1, NetrinG1	Bipolar disorder, Camptodactyly of fingers, Cerebral cortical atrophy, Colorectal cancer, Colorectal neoplasms, Developmental regression, Gastroesophageal reflux disease, Macrostomia, Manic disorder, Mental retardation, Microcephaly, Movement disorders, Nephrolithiasis, Rett syndrome, Schizophrenia, Syndromic mental retardation View all (1 more)
96	22861	NLRP1	NLR family pyrin domain containing 1	AIADK, CARD7, CIDED, CLR17.1, DEFCAP, DEFCAP-L/S, JRRP, MSPC, NAC, NALP1, PP1044, SLEV1, VAMAS1	Autoimmune hemolytic anemia, Autoinflammation with arthritis and dyskeratosis, Autoinflammatory disease, Carcinoma, Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome, Corneal neovascularization, Ectodermal dysplasia, Hypereosinophilia, Hyperkeratosis, Keratoconjunctivitis sicca, Limbal stem cell deficiency, Macular amyloidosis, Palmoplantar carcinoma, Palmoplantar keratoderma, Parakeratosis View all (7 more)
97	22871	NLGN1	Neuroligin 1	NL1, NLG1	Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Diabetes mellitus, Leukemia, Motion sickness, Schizophrenia
98	22978	NT5C2	5'-nucleotidase, cytosolic II	GMP, NT5B, PNT5, SPG45, SPG65, cN-II	Anxiety disorder, Attention deficit hyperactivity disorder, Bipolar disorder, Cardiovascular diseases, Development disorder, Developmental delay, Dysplastic corpus callosum, Hypertension, Hypoplasia of corpus callosum, Lymphoblastic leukemia, Malignant neoplasm, Mental depression, Mental retardation, Motor delay, Myopia View all (5 more)
99	23054	NCOA6	Nuclear receptor coactivator 6	AIB3, ASC2, NRC, PRIP, RAP250, TRBP	Breast cancer, Coronary artery disease, Endometrioma, Endometriosis, Melanoma
100	23057	NMNAT2	Nicotinamide nucleotide adenylyltransferase 2	C1orf15, PNAT2	Cerebellar hypoplasia, Dysmorphic features, Erythromelalgia, Hydrocephalus, Hydropic placenta, Hydrops fetalis, Lupus erythematosus, Cystic hygroma, Micrognathism, Multiple congenital anomalies, Polyneuropathy

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