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"
561 to 570 of 682 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

561
NSFL1 cofactor
P47, UBX1, UBXD10, UBXN2C, dJ776F14.1
Metabolic syndrome, Sjogren syndrome, Diabetes mellitus type 2

562
Neuronal vesicle trafficking associated 2
CALY3, HMP19
Duchenne muscular dystrophy, Psychiatric disorders

563
NSL1 component of MIS12 kinetochore complex
C1orf48, DC8, MIS14
Color vision deficiency, Leprosy, Multiple sclerosis, Diabetes mellitus type 1, Diabetes mellitus type 2

564
Neutral sphingomyelinase activation associated factor
FAN, GRAMD5
Essential tremor

565
NSE1 component of SMC5/6 complex
NSE1
Asthma, Eczema, Peripheral arterial disease

566
NSE2 SUMO ligase component of SMC5/6 complex
C8orf36, MMS21, NSE2, ZMIZ7
Alzheimer disease, Behcet disease, Central nervous system cancer, Obstructive pulmonary disease, Desbuquois syndrome, Glioblastoma, Glioma, Global developmental delay, Metabolic syndrome, Oligodendroglioma, Psoriasis, Seckel syndrome, Diabetes mellitus type 2

567
NSE3 component of SMC5/6 complex
HCA4, LICS, MAGEG1, MAGEL3, NDNL2, NSE3
Lung disease

568
NMDA receptor synaptonuclear signaling and neuronal migration factor
HH9, NELF
Carcinoma, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Liver cirrhosis, Male infertility single gene azoospermia, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Pituitary stalk interruption syndrome, Sheehan syndrome

569
Nuclear speckle splicing regulatory protein 1
CCDC55, HSPC095, NEDSSBA, NSrp70
Obstructive pulmonary disease, Neurodevelopmental disorder

570
NOP2/Sun RNA methyltransferase 2
MISU, MRT5, SAKI, TRM4
Autism, Nonsyndromic intellectual disability, Dubowitz syndrome, Intellectual developmental disorder, Hypertension